TF - transferrin Gene

Homo sapiens

Also known as TFQTL1; PRO1557; PRO2086; HEL-S-71p

Gene ID: 7018 | Gene type: protein coding

About TF

Cytogenetic location: 3q22.1 Genomic coordinates (GRCh38): 3:133,661,998-133,796,641 (from NCBI)

This gene has 14 transcripts (splice variants), 170 orthologues, 3 paralogues and is associated with 2 phenotypes. Restricted expression toward liver (RPKM 1622.3).

Summary

This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009]

TF Products(3)

mRNA	Protein	Name
NM_001063.4	NP_001054.2	serotransferrin isoform 1 precursor
NM_001354703.2	NP_001341632.2	serotransferrin isoform 2
NM_001354704.2	NP_001341633.2	serotransferrin isoform 3

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables enzyme binding	IPI IPI: Inferred from physical interaction	37277838	GOA
enables ferrous iron binding	IDA IDA: Inferred from direct assay	18353247	GOA
enables iron chaperone activity	IDA IDA: Inferred from direct assay	18353247	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	14691533	GOA
enables transferrin receptor binding	IPI IPI: Inferred from physical interaction	9546397	GOA
enables transmembrane transporter binding	IPI IPI: Inferred from physical interaction	37277838	GOA

Biological Process GO Annotation	Evidence	Reference	Source
involved in cellular response to iron ion	IGI IGI: Inferred from genetic interaction	18353247	GOA
involved in intracellular iron ion homeostasis	IGI IGI: Inferred from genetic interaction	18353247	GOA
involved in multicellular organismal-level iron ion homeostasis	IMP IMP: Inferred from mutant phenotype	11113131	GOA
involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process	IDA IDA: Inferred from direct assay	37277838	GOA
involved in positive regulation of receptor-mediated endocytosis	IDA IDA: Inferred from direct assay	12704209	GOA
involved in positive regulation of receptor-mediated endocytosis	IGI IGI: Inferred from genetic interaction	18353247	GOA
involved in regulation of iron ion transport	IGI IGI: Inferred from genetic interaction	18353247	GOA

Cellular Component GO Annotation	Evidence	Reference	Source
part of HFE-transferrin receptor complex	IDA IDA: Inferred from direct assay	9546397	GOA
located in apical plasma membrane	IDA IDA: Inferred from direct assay	11208127	GOA
located in basal part of cell	IDA IDA: Inferred from direct assay	15880641	GOA
located in basal plasma membrane	IDA IDA: Inferred from direct assay	15880641	GOA
located in cell surface	IDA IDA: Inferred from direct assay	16195351	GOA
located in clathrin-coated pit	IDA IDA: Inferred from direct assay	12857860	GOA
located in cytoplasmic vesicle	IDA IDA: Inferred from direct assay	12857860	GOA
located in early endosome	IDA IDA: Inferred from direct assay	15880641	GOA
located in endocytic vesicle	IDA IDA: Inferred from direct assay	15229288	GOA
located in extracellular region	IDA IDA: Inferred from direct assay	9990067	GOA
located in extracellular region	IGI IGI: Inferred from genetic interaction	18353247	GOA
is active in extracellular space	IDA IDA: Inferred from direct assay	37277838	GOA
located in late endosome	IDA IDA: Inferred from direct assay	15880641	GOA
located in perinuclear region of cytoplasm	IDA IDA: Inferred from direct assay	15880641	GOA
located in recycling endosome	IDA IDA: Inferred from direct assay	15880641	GOA
located in vesicle	IDA IDA: Inferred from direct assay	18353773	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TF Protein Structure

Transferrin

0
200
400
600
698 a.a.

Protein Preferred Names

Protein Names

serotransferrin

beta-1 metal-binding globulin

TF Protein-protein interaction Information

Type Cross Intra	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Reference
Intra	TF	P02787	PGRMC2	Homo sapiens	O15173	Y2H Array	32296183
Intra	TF	P02787	PGRMC2	Homo sapiens	O15173	Y2H Prey Pooling	32296183
Intra	TF	P02787	RMDN3	Homo sapiens	Q96TC7	Validated Y2H	32296183
Intra	TF	P02787	RMDN3	Homo sapiens	Q96TC7	Y2H Array	32296183
Intra	TF	P02787	RMDN3	Homo sapiens	Q96TC7	Y2H Prey Pooling	32296183
Intra	TF	P02787	SORT1	Homo sapiens	Q99523	Validated Y2H	32296183
Intra	TF	P02787	SORT1	Homo sapiens	Q99523	Y2H Prey Pooling	32296183
Intra	TF	P02787	SORT1	Homo sapiens	Q99523	Y2H Array	32296183
Intra	TF	P02787	GPX8	Homo sapiens	Q8TED1	Validated Y2H	32296183
Intra	TF	P02787	GPX8	Homo sapiens	Q8TED1	Y2H Prey Pooling	32296183
Intra	TF	P02787	GPX8	Homo sapiens	Q8TED1	Y2H Array	32296183
Intra	TF	P02787	SPINT1	Homo sapiens	O43278-2	Y2H Prey Pooling	32296183
Intra	TF	P02787	SPINT1	Homo sapiens	O43278-2	Y2H Array	32296183
Intra	TF	P02787	SLC26A6	Homo sapiens	Q9BXS9-3	Validated Y2H	32296183
Intra	TF	P02787	SLC26A6	Homo sapiens	Q9BXS9-3	Y2H Array	32296183
Intra	TF	P02787	SLC26A6	Homo sapiens	Q9BXS9-3	Y2H Prey Pooling	32296183
Cross	TF	P02787	tbpB	Neisseria meningitidis serogroup B	Q9K0V0	GMS	22327295
Cross	TF	P02787	tbpB	Neisseria meningitidis serogroup B	Q9K0V0	SAXS	22327295
Intra	TF	P02787	AQP9	Homo sapiens	O43315	Y2H Array	32296183
Intra	TF	P02787	AQP9	Homo sapiens	O43315	Y2H Prey Pooling	32296183
Intra	TF	P02787	LEUTX	Homo sapiens	A8MZ59	Y2H Array	32296183
Intra	TF	P02787	LEUTX	Homo sapiens	A8MZ59	Y2H Prey Pooling	32296183
Intra	TF	P02787	GJB1	Homo sapiens	P08034	Y2H Prey Pooling	32296183
Intra	TF	P02787	GJB1	Homo sapiens	P08034	Validated Y2H	32296183
Intra	TF	P02787	GJB1	Homo sapiens	P08034	Y2H Array	32296183
Intra	TF	P02787	CPLX4	Homo sapiens	Q7Z7G2	Y2H Array	32296183
Intra	TF	P02787	CPLX4	Homo sapiens	Q7Z7G2	Y2H Prey Pooling	32296183
Intra	TF	P02787	CPLX4	Homo sapiens	Q7Z7G2	Validated Y2H	32296183
Intra	TF	P02787	HSD17B13	Homo sapiens	Q7Z5P4	Y2H Prey Pooling	32296183
Intra	TF	P02787	HSD17B13	Homo sapiens	Q7Z5P4	Validated Y2H	32296183
Intra	TF	P02787	HSD17B13	Homo sapiens	Q7Z5P4	Y2H Array	32296183
Intra	TF	P02787	GPR42	Homo sapiens	O15529	Y2H Prey Pooling	32296183
Intra	TF	P02787	GPR42	Homo sapiens	O15529	Y2H Array	32296183
Intra	TF	P02787	SLC10A6	Homo sapiens	Q3KNW5	Y2H Prey Pooling	32296183
Intra	TF	P02787	SLC10A6	Homo sapiens	Q3KNW5	Validated Y2H	32296183
Intra	TF	P02787	SLC10A6	Homo sapiens	Q3KNW5	Y2H Array	32296183
Intra	TF	P02787	TMEM52B	Homo sapiens	Q4KMG9	Y2H Prey Pooling	32296183
Intra	TF	P02787	TMEM52B	Homo sapiens	Q4KMG9	Y2H Array	32296183
Intra	TF	P02787	TMEM52B	Homo sapiens	Q4KMG9	Validated Y2H	32296183
Intra	TF	P02787	CLDN5	Homo sapiens	O00501	Y2H Array	32296183
Intra	TF	P02787	CLDN5	Homo sapiens	O00501	Y2H Prey Pooling	32296183
Intra	TF	P02787	ELOVL4	Homo sapiens	Q9GZR5	Y2H Prey Pooling	32296183
Intra	TF	P02787	ELOVL4	Homo sapiens	Q9GZR5	Validated Y2H	32296183
Intra	TF	P02787	ELOVL4	Homo sapiens	Q9GZR5	Y2H Array	32296183
Intra	TF	P02787	FAM210B	Homo sapiens	Q96KR6	Y2H Prey Pooling	32296183
Intra	TF	P02787	FAM210B	Homo sapiens	Q96KR6	Validated Y2H	32296183
Intra	TF	P02787	FAM210B	Homo sapiens	Q96KR6	Y2H Array	32296183
Intra	TF	P02787	GAST	Homo sapiens	P01350	Crosslink	19664057
Intra	TF	P02787	GAST	Homo sapiens	P01350	SPR	19664057
Intra	TF	P02787	GOLM1	Homo sapiens	Q8NBJ4	Y2H Prey Pooling	32296183
Intra	TF	P02787	GOLM1	Homo sapiens	Q8NBJ4	Validated Y2H	32296183
Intra	TF	P02787	GOLM1	Homo sapiens	Q8NBJ4	Y2H Array	32296183
Intra	TF	P02787	ERGIC3	Homo sapiens	Q9Y282	Validated Y2H	32296183
Intra	TF	P02787	ERGIC3	Homo sapiens	Q9Y282	Y2H Array	32296183
Intra	TF	P02787	ERGIC3	Homo sapiens	Q9Y282	Y2H Prey Pooling	32296183
Intra	TF	P02787	SYT2	Homo sapiens	Q8N9I0	Y2H Prey Pooling	32296183
Intra	TF	P02787	SYT2	Homo sapiens	Q8N9I0	Validated Y2H	32296183
Intra	TF	P02787	SYT2	Homo sapiens	Q8N9I0	Y2H Array	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant TF Proteins

Cat. No.	Product Name	Accession	Purity
HY-P70620	Transferrin Protein, Human (HEK293, His)	P02787/AAA61140.1/NP_001054.1 (V20-P698)	≥95%

Related Diseases

Diseases

Alias

Atransferrinemia

Familial Hypotransferrinemia	Congenital Atransferrinemia
Hypotransferrinemia, Familial	Congenital Hypotransferrinemia
ATRAF

Iron Overload In Africa

African Iron Overload	Bantu Siderosis
African Hemochromatosis	Hereditary Iron Overload And African Americans
African Nutritional Hemochromatosis	African Siderosis

Nutritional Deficiency Disease

Malnutrition	Nutritional Disorder
Nutritional Deficiency	Nutrition
Deficiency Diseases	Carbamoyl-Phosphate Synthase I Deficiency Disease
Nutrition Disorders

Iron Metabolism Disease

Iron Deficiency	Iron Disorder
Iron Metabolism Disorders	Disorder Of Iron Metabolism
Iron	Fe Deficiency
Iron Storage Disease	Iron Storage Disorder

Iron Deficiency Anemia

Iron-Deficiency Anemia	Fe Deficiency Anaemia
Ida - [Iron Deficiency Anemia]	Fe - [Iron] Deficiency Anemia Nos

Siderosis

Pulmonary Siderosis	Deposition Of Iron
Arc-Welders' Disease	Arc-Welders' Lung
Arc-Welders' Nodulation	Arc-Welders' Pneumoconiosis
Iron Oxide Lung	Iron Pneumoconiosis
Pneumoconiosis Siderotico	Siderotic Lung Disease
Steel Grinders' Disease	Welders' Lung
Welders' Siderosis	Lung Fibrosis With Siderosis

Protein-Energy Malnutrition

PEM	Protein Energy Malnutrition

Hemochromatosis, Type 1

Hemochromatosis	Hemochromatosis Type 1
Hereditary Hemochromatosis	Hh
HFE1	Hfe Hemochromatosis, Modifier Of
Symptomatic Form Of Classic Hemochromatosis	Symptomatic Form Of Hemochromatosis Type 1
Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis	Haemochromatosis
Iron Storage Disorder	Bronze Diabetes
Hereditary Haemochromatosis	Hlah
Hfe	Hemochromatosis, Hereditary
Diabetes Bronze	Classic Hemochromatosis
Hfe-Associated Hereditary Hemochromatosis	Hemochromatosis Classic
Bronzed Cirrhosis	Familial Hemochromatosis
Genetic Hemochromatosis	Hc
Pigmentary Cirrhosis	Primary Hemochromatosis
Troisier-Hanot-Chauffard Syndrome	Von Recklenhausen-Applebaum Disease
Hemochromatosis 1	Primary Hereditary Hemochromatosis
Bronze Cirrhosis

Microcytic Anemia

Iron-Refractory Iron Deficiency Anemia

Hfe Hemochromatosis

Hemochromatosis Type 1	Hfe-Associated Hemochromatosis
Hfe-Hh

Rare Hereditary Hemochromatosis

Iron Overload	Iron Overload Disease
Idiopathic Haemosiderosis	Hemosiderosis

Beta-Thalassemia

Beta Thalassemia	Cooley'S Anemia
Mediterranean Anemia	Beta Thalassemia Intermedia
Erythroblastic Anemia	Thalassemia, Hispanic Gamma-Delta-Beta
Thalassemia Major	Thalassemia Minor
Beta-Plus-Thalassemia	Thalassemia, Beta
Beta Thalassemia Major	Beta Thalassemia Minor
Thalassemias, Beta-	Microcytemia, Beta Type
Thalassemia, Beta Type	B-THAL
Mediterranean Anaemia	Beta Thalassaemia Syndrome
Mediterranean Disease	Beta Thalassaemia Disease

Haemophilus Influenzae

Deficiency Anemia

Anemia	Deficiency Anemias
Anaemia

Liver Cirrhosis

Cirrhosis	Cirrhosis Of Liver
CIRRH	Cryptogenic Cirrhosis
Cirrhosis, Cryptogenic	Cirrhosis Nos

Congenital Disorder Of Glycosylation, Type Ia

CDG1A	Cdg Ia
Phosphomannomutase 2 Deficiency	Jaeken Syndrome
Pmm2-Congenital Disorder Of Glycosylation	Congenital Disorder Of Glycosylation Type Ia
Cdgia	Congenital Disorder Of Glycosylation Ia
Congenital Disorder Of Glycosylation 1a	Carbohydrate-Deficient Glycoprotein Syndrome Type Ia
Cdgs1a	Pmm2-Cdg
Cdg-Ia	Congenital Disorder Of Glycosylation Type 1a
Carbohydrate-Deficient Glycoprotein Syndrome, Type Ia, Formerly	Pmm Deficiency
Cdg Syndrome Type Ia	Carbohydrate Deficient Glycoprotein Syndrome Type Ia
Cdg Syndrome Type 1a	Jaeken'S Syndrome
Pmm2 Deficiency	Glycosylation, Congenital Disorder Of, Type Ia

Dysentery

Infectious Diarrhea

Intracranial Hypotension

Alcohol Use Disorder

Alcohol Abuse	Alcoholism
Ethanol Abuse	Alcohol Addiction
Alcohol Dependence	Alcoholic Intoxication, Chronic
Alcohol-Related Disorders

Thalassemia

Sickle-Cell Thalassemia With Crisis	Sickle-Cell Thalassemia Without Crisis
Thalassemia Hb-S Disease With Crisis	Thalassemia Hb-S Disease Without Crisis
Thalassemias	Hereditary Leptocytosis
Haemoglobin Thalassaemia Disorder	Thalassaemia Syndrome
Thalassaemia Nos	Thalassemia Variants

Porphyria Cutanea Tarda

Hepatoerythropoietic Porphyria	HEP
Uroporphyrinogen Decarboxylase Deficiency	Pct
Pct, Type Ii	Porphyria, Hepatocutaneous Type
Urod Deficiency	Porphyria, Hepatoerythropoietic
Porphyria Cutanea Tarda, Susceptibility To	Familial Porphyria Cutanea Tarda
Porphyria Cutanea Tarda, Type Ii	Pct, 'Familial' Type
Porphyria, Hepatic	FPCT
Pct Type Ii	Porphyria Cutanea Tarda Type Ii
Porphyria Hepatocutaneous Type	Heterozygous Uroporphyrinogen Decarboxylase Deficiency
Urod - [Uroporphyrinogen Decarboxylase] Deficiency	Pct - [Porphyria Cutanea Tarda]

Hemosiderosis

Haemosiderosis

Iron Overload

Alzheimer Disease, Familial, 1

Alzheimer Disease	Alzheimer'S Disease
Presenile And Senile Dementia	AD1
Alzheimer Disease, Susceptibility To	Alzheimer Disease, Late-Onset, Susceptibility To
Alzheimer Disease 1, Familial	AD
Familial Alzheimer Disease	Alzheimer Disease, Late-Onset
Alzheimers Dementia	Alzheimer Dementia
Alzheimer Sclerosis	Alzheimer Syndrome
Alzheimer-Type Dementia	Dat
Primary Senile Degenerative Dementia	Sdat
Alzheimer Disease 1	Autosomal Dominant Alzheimer Disease
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy	Late Onset Alzheimer Disease
Alzheimers Disease	Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
Late-Onset Alzheimers Disease	Alzheimer'S Disease Pathway Kegg
Dementia Due To Alzheimer'S Disease	Alzheimer Disease Type 1
Alzheimers

Hyperferritinemia With Or Without Cataract

Hyperferritinemia-Cataract Syndrome	Hhcs
Hereditary Hyperferritinemia With Congenital Cataracts	Hyperferritinemia, Hereditary, With Congenital Cataracts
Bonneau-Beaumont Syndrome	HRFTC
Hereditary Hyperferritinemia-Cataract Syndrome	Cataract-Hyperferritinemia Syndrome
Hyperferritinemia Cataract Syndrome	Hereditary Hyperferritinemia Cataract Syndrome

Chronic Kidney Disease

Chronic Renal Disease	Chronic Kidney Failure
Ckd	Chronic Renal Failure
Kidney Failure, Chronic	Chronic Renal Failure Syndrome
Crf	Renal Failure - Chronic
Renal Failure Chronic	Chronic Kidney Diseases
Chronic Kidney Disease Stage 5	Ckd - [Chronic Kidney Disease]
Crf - [Chronic Renal Failure]	Chronic Kidney Impairment
Chronic Renal Impairment	Chronic Kidney Shutdown
Chronic Hypoxic Kidney Failure	Chronic Kidney Collapse
Chronic Renal Insufficiency	Chronic Kidney Toxaemia
Chronic Kidney Hypofunction	Chronic Renal Suppression
Chronic Renal Failure, Stage 5	Ckd - [Chronic Kidney Disease] Stage 5
End Stage Kidney Failure	End Stage Renal Failure
End Stage Kidney Disease	End Stage Renal Disease
End Stage Chronic Renal Failure	Esrf - [End Stage Renal Failure]
Esrd - [End Stage Renal Diseases]	Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²

Liver Disease

Liver Failure	Liver Diseases
Abnormality Of The Liver	Liver Dysfunction
Disorder Of Liver	Hepatic Disorder
Hepatic Disease	Disease Of Bilirubin Metabolism
Disorder Of Bilirubin Metabolism	Liver Decompensation
Liver Function Failure	Hepatic Failure Nos
Liver Failure Nos	End Stage Liver Disease
Decompensated Liver Failure	Decompensation Of Liver Function
Hepatic Decompensation	Hepatic Insufficiency
Liver Cell Necrosis With Hepatic Failure	Liver Insufficiency
Decompensated Liver Disease	End Stage Liver Failure
Liver Necrosis With Hepatic Failure

Cholera

Vibrio Cholerae Infection	Cholera - Vibrio Cholerae
Cholera Due To Vibrio Cholerae	Vibrio Cholerae
Cholera Syndrome	Asiatic Cholera
Epidemic Cholera

Hypochromic Microcytic Anemia

Anemia, Hypochromic Microcytic

Microcytic Hypochromic Anemia

Kidney Disease

Renal Failure	Kidney Failure
Kidney Diseases	Nephropathy
Abnormality Of The Kidney	Impaired Renal Function Disease
Renal Anomaly	Kidney Dysfunction
Renal Disease	Nephropathies
Renal Failure Adverse Event	Abnormal Renal Function

Substance Abuse

Substance-Related Disorders

Substance Abuse Problem

Congenital Disorder Of Glycosylation, Type In

Congenital Disorder Of Glycosylation	CDG1N
Congenital Disorders Of Glycosylation	Cdg In
Cdgin	Congenital Disorder Of Glycosylation 1n
Carbohydrate-Deficient Glycoprotein Syndrome	Cdg
Rft1-Cdg	Cdg-In
Congenital Disorder Of Glycosylation Type In	Carbohydrate Deficient Glycoprotein Syndrome
Cdg Syndrome	Congenital Disorder Of Glycosylation In
Carbohydrate-Deficient Glycoprotein Syndromes	Cdg Syndrome Type In
Carbohydrate Deficient Glycoprotein Syndrome Type In	Congenital Disorder Of Glycosylation Type 1n
Man5glcnac2-Pp-Dol Flippase Deficiency	Glycosylation, Congenital Disorder Of
Glycosylation, Congenital Disorder Of, Type In

Analbuminemia

ANALBA	Congenital Analbuminemia
Hypoalbuminemia

Adult Respiratory Distress Syndrome

Acute Respiratory Distress Syndrome	Ards
Non-Cardiogenic Pulmonary Edema	Acute Lung Injury
Respiratory Distress Syndrome, Adult	Shock Lung
Acute Respiratory Distress	Respiratory Distress Syndrome
Adult Rds	Ali
Increased-Permeability Pulmonary Edema	Stiff Lung
Respiratory Distress Syndrome Adult

Trypanosomiasis

Sleeping Sickness

African Trypanosomiasis	African Sleeping Sickness
Trypanosomiasis, Human East-African	Trypanosomiasis, East African
Trypanosomiasis African	Trypanosomiasis, African
Human African Trypanosomiasis

Congenital Hemolytic Anemia

Anemia Hemolytic Congenital	Anemia, Hemolytic, Congenital
Congenital Hemolytic Anaemia	Hereditary Hemolytic Anaemia
Hereditary Hemolytic Anemia

Interstitial Lung Disease

Ild	Lung Diseases, Interstitial
Lung Diseases Interstitial	Interstitial Lung Diseases

Hemolytic Anemia

Anemia, Hemolytic	Anemia Hemolytic
Anaemia Due To Other Disorders Of Glutathione Metabolism	Chronic Non Spherocytic Anaemia
G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia	Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia	Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
Favism Anaemia	Haemolytic Anaemia Due Tog6pd Deficiency
Favism	Pentose Phosphate Pathway Disorder Anaemia
Anaemia Due To Pentose Phosphate Pathway Defect

Hemoglobinopathy

Hemoglobinopathies

Lipoid Nephrosis

Minimal Change Disease	Minimal Change Glomerulonephritis
Nephrotic Syndrome With Lesion Of Minimal Change Glomerulonephritis	Nephrotic Syndrome With Lesion Of Minimal Change Nephrotic Syndrome
Idiopathic Minimal Change Nephrotic Syndrome	Mcns
Minimal Change Glomerulopathy	Minimal Change Nephrotic Syndrome
Nephrotic Syndrome Minimal Change	Nephrosis, Lipoid
Glomerulonephritis, Minimal Change	Nephrotic Syndrome, Minimal Change

Nephrotic Syndrome

Finnish Congenital Nephrotic Syndrome	Ns - [Nephrotic Syndrome]
Nephrosis Syndrome	Nephrosis Nos
Glomerular Lesion Nephrosis

Histoplasmosis

Darling Disease	Reticuloendotheliosis, X-Linked
Infection By Histoplasma Capsulatum	Histoplasma Infection
Reticuloendothelial Cytomycosis	Cytomycosis
Darling Histoplasmosis	African Histoplasmosis
Histoplasmosis Duboisii

Proctitis

Ulcerative Proctitis	Chronic Ulcerative Proctitis
Idiopathic Proctitis	Nonspecific Ulcerative Proctitis
Ulcerative Colitis Confined To Rectum	Ip - [Idiopathic Proctitis]
Chronic Ulcerative Proctitis Nos

Androgen Insensitivity Syndrome

Androgen Resistance Syndrome	AIS
Testicular Feminization Syndrome	Androgen Receptor Deficiency
Dhtr Deficiency	Dihydrotestosterone Receptor Deficiency
Ar Deficiency	Testicular Feminization
Tfm	Androgen Insensitivity
Androgen-Insensitivity Syndrome	Goldberg-Maxwell Syndrome
Complete Androgen Insensitivity Syndrome	Cais
Feminisation - Testicular	Goldberg - Maxwell Syndrome
Androgen Insensitivity Syndrome, Complete	Morris Syndrome
Ary	AR
Insensitivity Syndrome, Androgen	Androgen Insensitivity Nos

Osebold-Remondini Syndrome

Brachydactyly Type A6	Brachymesophalangy With Mesomelic Short Limbs And Carpal And Tarsal Osseous Abnormalities
Bda6	Brachydactyly, Type A6

Scrapie

Marasmus

Nutritional Marasmus

Nutritional Atrophy

Cystinosis

Cystine Storage Disease	Cystine Diathesis
Cystine Disease	Cystinoses
Protein Defect Of Cystin Transport	Cystin Transport, Protein Defect Of
Nephropathic Cystinosis	Protein Defect Of Cystine Transport

Diabetes Mellitus

Diabetes

Vitreoretinopathy, Neovascular Inflammatory

Proliferative Vitreoretinopathy	Adniv
Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy	VRNI
Pvr	Neovascular Inflammatory Vitreoretinopathy
Vitreoretinopathy, Neovascular Inflammatory, Autosomal Dominant	Retinitis Proliferans
Neovascular Inflammatory Vitreoretinopathy Autosomal Dominant	Vitreoretinopathy Proliferative
Vitreoretinopathy, Proliferative	Proliferative Vitreo-Retinopathy

Type 2 Diabetes Mellitus

Insulin Resistance	NIDDM
Type 2 Diabetes	Diabetes Mellitus, Non-Insulin-Dependent
T2D	Noninsulin-Dependent Diabetes Mellitus
Diabetes Mellitus, Type Ii	Maturity-Onset Diabetes
Insulin Resistance, Severe, Digenic	Diabetes Mellitus, Type 2
Diabetes Mellitus, Noninsulin-Dependent	Diabetes Mellitus, Noninsulin-Dependent, Association With
Diabetes Mellitus, Noninsulin-Dependent, Late Onset	Hypertension, Insulin Resistance-Related, Susceptibility To
Insulin Resistance, Susceptibility To	Non-Insulin-Dependent Diabetes Mellitus
Type Ii Diabetes Mellitus	Adult-Onset Diabetes Mellitus
Maturity-Onset Diabetes Mellitus	Diabetes Mellitus Type 2
Type Ii Diabetes	Type 2 Diabetes Mellitus, Susceptibility To
Diabetes, Type 2	Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To	Diabetes Mellitus, Type 2, Susceptibility To
Diabetes Mellitus, Noninsulin-Dependent, 2	Diabetes Mellitus, Type Ii, Susceptibility To
Hypertension, Insulin Resistance-Related	Adult-Onset Diabetes
Aodm	Diabetes Mellitus, Adult-Onset
Diabetes Mellitus Type Ii	Diabetes Mellitus Type 2, Susceptibility To
Diabetes, Type Ii, Susceptibility To	Diabetes Type 2
Diabetes Mellitus	Adult Onset Diabetes
Maturity Onset Diabetes	Nonketotic Diabetes
Non-Insulin Dependent Diabetes Mellitus	T2dm - [Type 2 Diabetes Mellitus]
Niddm - [Non Insulin Dependent Diabetes Mellitus]	Dm2
Dm Type Ii	Diabetic Type 2
Insulin Requiring Type 2 Diabetes	Noninsulin Dependent Diabetes
Non-Insulin-Dependent Diabetes Mellitus Without Complications	Diabetes Due To Insulin Secretory Defect
Diabetes Mellitus Due To Insulin Secretory Defect	Non-Insulin-Dependent Diabetes Of The Young
Senile Diabetes	Nonketotic Hyperglycaemia
Stable Diabetes

Cataract

Cataracts	Cat - [Cataract]
Cataract Form	Lens Opacity
Lens Opacities

Myelodysplastic Syndrome

Myelodysplastic Syndromes	Myelodysplasia
MDS	Myelodysplastic Syndrome Included
Myelodysplastic Syndrome, Susceptibility To, Included	Myelodysplastic Syndrome, Somatic
Myelodysplastic Syndrome, Susceptibility To

Alcohol Dependence

Alcoholism	Alcohol Dependence, Susceptibility To
Alcohol Dependence, Protection Against	Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against
Alcoholism, Susceptibility To	Alcoholic Intoxication, Chronic
Pharyngeal Neoplasms	Chronic Alcoholism
Dipsomania	Alcohol Addiction
Ethanol Dependence	Chronic Ethanolism
Chronic Alcoholic Disease Nos	Alcoholic Disease Nos
Alcoholic

Related Agents

Approval

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-18763	Indobufen	Inhibitor	99.98%	Unkown

Clinical Phase

Bioactive Molecules (5)

Cat. No.	Product Name	Effect	Purity	Phase
HY-P0171	Motixafortide	Antagonist	99.88%	Phase 3
HY-152963	Tisotumab vedotin		/	Phase 3
HY-19284	FR-146687	Inhibitor	/	Phase 2
HY-N1992	Theaflavin 3,3'-digallate	Inhibitor	99.73%	Phase 1
HY-153480	ARC19499	Inhibitor	93.65%	Phase 1

Inhibitory Antibodies (2)

Cat. No.	Product Name	Effect	Purity	Phase
HY-P99271	Tisotumab		≥95.0%	Phase 3
HY-P990090	Rademikibart	Inhibitor	/	Phase 3

Pre-clinical Phase

Bioactive Molecules (19)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-100388	SHP099	Inhibitor	99.80%	Unkown
HY-134094	Fluridone		99.79%	Unkown
HY-153480A	ARC19499 sodium	Inhibitor	93.65%	Unkown
HY-P5875A	P4pal10 TFA	Antagonist	98.25%	Unkown
HY-116170	SN34037		/	Unkown
HY-148880	VHLL-BCN		/	Unkown
HY-155951	JAK3-IN-14	Inhibitor	99.32%	Unkown
HY-156158	IDH2R140Q-IN-2	Inhibitor	/	Unkown
HY-162490	TF-S14	Inhibitor	/	Unkown
HY-169335	HIV-1 inhibitor-77	Inhibitor	/	Unkown
HY-18763A	Indobufen sodium	Inhibitor	/	Unkown
HY-18763S	Indobufen-d5	Inhibitor	/	Unkown
HY-N10308	TF-DG-cThea		/	Unkown
HY-N10310	TF-3-G-cThea		/	Unkown
HY-P5152	Scorpion toxin Tf2	Activator	/	Unkown
HY-P5875	P4pal10	Antagonist	/	Unkown
HY-RS14406	TF Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown
HY-13496	JNJ-28312141	Inhibitor	/	Unkown
HY-N10309	TF-3ʹ-G-cThea		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	TF	VGNC	VGNC:82716
Mus musculus	TF	MGD	MGI:98821
Rattus norvegicus	TF	RGD	RGD:3845
Canis familiaris	TF	NCBI
Macaca fascicularis	TF	NCBI	NCBI:101866521
Susscrofa domestica	TF	NCBI
Leporidae	TF	NCBI
Others	TF	NCBI