MYH9 - myosin heavy chain 9 Gene

Homo sapiens

Also known as MHA; FTNS; EPSTS; BDPLT6; DFNA17; MATINS; NMMHCA; NMHC-II-A; NMMHC-IIA

Gene ID: 4627 | Gene type: protein coding

About MYH9

Cytogenetic location: 22q12.3 Genomic coordinates (GRCh38): 22:36,281,280-36,387,967 (from NCBI)

This gene has 23 transcripts (splice variants), 279 orthologues, 43 paralogues and is associated with 100 phenotypes. Ubiquitous expression in spleen (RPKM 146.6), lung (RPKM 134.4) and 25 other tissues.

Summary

This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a Myosin IIA heavy chain that contains an IQ domain and a Myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]

MYH9 Products(1)

mRNA	Protein	Name
NM_002473.6	NP_002464.1	myosin-9

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables ADP binding	IDA IDA: Inferred from direct assay	15065866	GOA
enables ATP binding	IDA IDA: Inferred from direct assay	15065866	GOA
enables actin binding	IDA IDA: Inferred from direct assay	15065866	GOA
contributes to actin filament binding	IDA IDA: Inferred from direct assay	24072716	GOA
enables actin filament binding	IDA IDA: Inferred from direct assay	12237319	GOA
enables identical protein binding	IPI IPI: Inferred from physical interaction	22483112	GOA
enables integrin binding	IDA IDA: Inferred from direct assay	10822899	GOA
contributes to microfilament motor activity	IDA IDA: Inferred from direct assay	24072716	GOA
enables microfilament motor activity	IDA IDA: Inferred from direct assay	12237319	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	2732579	GOA
enables protein domain specific binding	IPI IPI: Inferred from physical interaction	23325791	GOA
enables protein homodimerization activity	IDA IDA: Inferred from direct assay	12237319	GOA
enables protein-membrane adaptor activity	IMP IMP: Inferred from mutant phenotype	16403913	GOA

Biological Process GO Annotation	Evidence	Reference	Source
involved in actin cytoskeleton organization	IMP IMP: Inferred from mutant phenotype	15869600	GOA
acts upstream of or within actin filament-based movement	IDA IDA: Inferred from direct assay	15845534	GOA
involved in actin filament-based movement	IDA IDA: Inferred from direct assay	12237319	GOA
involved in actomyosin structure organization	IDA IDA: Inferred from direct assay	24072716	GOA
involved in angiogenesis	IDA IDA: Inferred from direct assay	16403913	GOA
involved in blood vessel endothelial cell migration	IMP IMP: Inferred from mutant phenotype	16403913	GOA
involved in cytokinetic process	IMP IMP: Inferred from mutant phenotype	15774463	GOA
involved in lysosome localization	IMP IMP: Inferred from mutant phenotype	2732579	GOA
involved in membrane protein ectodomain proteolysis	IDA IDA: Inferred from direct assay	16186248	GOA
involved in monocyte differentiation	IEP IEP: Inferred from expression pattern	1912569	GOA
involved in negative regulation of actin filament severing	IMP IMP: Inferred from mutant phenotype	23325791	GOA
involved in plasma membrane repair	IDA IDA: Inferred from direct assay	27325790	GOA
involved in platelet formation	IMP IMP: Inferred from mutant phenotype	12237319	GOA
involved in protein transport	IMP IMP: Inferred from mutant phenotype	16403913	GOA
involved in regulated exocytosis	IMP IMP: Inferred from mutant phenotype	2732579	GOA
involved in regulation of cell shape	IMP IMP: Inferred from mutant phenotype	11029059	GOA
involved in regulation of plasma membrane repair	IMP IMP: Inferred from mutant phenotype	2732579	GOA

Cellular Component GO Annotation	Evidence	Reference	Source
part of COP9 signalosome	IDA IDA: Inferred from direct assay	18850735	GOA
located in actin cytoskeleton	IDA IDA: Inferred from direct assay	15869600	GOA
located in actomyosin	IDA IDA: Inferred from direct assay	24072716	GOA
located in actomyosin contractile ring	IDA IDA: Inferred from direct assay	11029059	GOA
located in cell leading edge	IDA IDA: Inferred from direct assay	12421915	GOA
located in cleavage furrow	IDA IDA: Inferred from direct assay	7699007	GOA
located in cytoplasm	IDA IDA: Inferred from direct assay	7699007	GOA
located in cytoplasmic side of plasma membrane	IDA IDA: Inferred from direct assay	15064761	GOA
located in cytosol	IDA IDA: Inferred from direct assay	14508515	GOA
located in immunological synapse	IDA IDA: Inferred from direct assay	15064761	GOA
part of myosin II complex	IDA IDA: Inferred from direct assay	24072716	GOA
located in myosin II filament	IDA IDA: Inferred from direct assay	24072716	GOA
located in nucleus	IDA IDA: Inferred from direct assay	14508515	GOA
located in plasma membrane	IDA IDA: Inferred from direct assay	16186248	GOA
part of protein-containing complex	IDA IDA: Inferred from direct assay	12421915	GOA
located in ruffle	IDA IDA: Inferred from direct assay	16403913	GOA
located in stress fiber	IDA IDA: Inferred from direct assay	7699007	GOA
located in uropod	IDA IDA: Inferred from direct assay	15064761	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

MYH9 Protein Structure

Myosin_N

Myosin_head

Myosin_tail_1

0
400
800
1200
1600
1960 a.a.

Protein Preferred Names

Protein Names

myosin-9

cellular myosin heavy chain, type A

Related Diseases

Diseases

Alias

Macrothrombocytopenia And Granulocyte Inclusions With Or Without Nephritis Or Sensorineural Hearing Loss

Fechtner Syndrome	May-Hegglin Anomaly
Sebastian Syndrome	Epstein Syndrome
Macrothrombocytopenia With Leukocyte Inclusions	Myh9-Related Disorder
Macrothrombocytopenia And Progressive Sensorineural Deafness	MATINS
Bdplt6	Mha
Dohle Leukocyte Inclusions With Giant Platelets	Giant Platelet Syndrome With Thrombocytopenia
Sbs	Sebastian Platelet Syndrome
Epstns	Ftns
Bleeding Disorder, Platelet-Type, 6	Macrothrombocytopenia With Dispersed Leukocytic Inclusions
Macrothrombocytopenia, Nephritis, And Deafness	Macrothrombocytopenia, Nephritis, Deafness, And Leukocyte Inclusions
Alport Syndrome With Macrothrombocytopenia, Formerly	Apsm, Formerly
Myh9 Related Thrombocytopenia	Myh9 Related Disorders
Myh9-Rd	Myh9-Related Disease
Myh9-Related Syndrome	Myh9-Related Syndromic Thrombocytopenia
Autosomal Dominant Myh9 Spectrum Disorders	Myh9-Related Macrothrombocytopenias
Myh9rd	Alport Syndrome, With Macrothrombocytopenia
Bleeding Disorder Platelet-Type 6	Macrothrombocytopathy, Nephritis, And Deafness
Macrothrombocytopathy-Nephritis-Deafness	Mpsd
Epsteins Syndrome	May-Hegglin Disorder
Macrothrombocytopenia, Granulocyte Inclusions With/Without Nephritis Or Sensorineural Hearing Loss

Deafness, Autosomal Dominant 17

DFNA17	Autosomal Dominant Nonsyndromic Deafness 17
Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17	Autosomal Dominant Deafness 17
Late-Onset Progressive Hereditary Hearing Impairment Due To Cochleosaccular Degeneration	Nonsyndromic Hereditary Deafness Dfna17
Deafness, Autosomal Dominant, 17	Cochleosaccular Degeneration
Deafness, Autosomal Dominant, Type 17	Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts

Myh-9 Related Disease

Myh9-Related Disease	Myh9-Rd
Myh9-Related Disorder	Myh9-Related Syndrome
Myh9-Related Syndromic Thrombocytopenia	Sebastian Syndrome

Pseudosarcomatous Fibromatosis

Nodular Fasciitis	Pseudosarcomatous Fasciitis
Fasciitis - Nodular	Fasciitis Nodular

Thrombocytopenia

Low Platelet Count	Low Platelets
Decreased Platelets	Platelet Dysfunction Nos

Autosomal Recessive Nonsyndromic Deafness

Deafness, Autosomal Recessive, Nonsyndromic

Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb

Autosomal Recessive Isolated Neurosensory Deafness Type Dfnb	Autosomal Recessive Isolated Neurosensory Hearing Loss Type Dfnb
Autosomal Recessive Isolated Sensorineural Deafness Type Dfnb	Autosomal Recessive Isolated Sensorineural Hearing Loss Type Dfnb
Autosomal Recessive Non-Syndromic Neurosensory Deafness Type Dfnb	Autosomal Recessive Non-Syndromic Neurosensory Hearing Loss Type Dfnb
Autosomal Recessive Non-Syndromic Sensorineural Hearing Loss Type Dfnb

Deafness, Autosomal Recessive

Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna

Autosomal Dominant Isolated Neurosensory Deafness Type Dfna	Autosomal Dominant Isolated Neurosensory Hearing Loss Type Dfna
Autosomal Dominant Isolated Sensorineural Deafness Type Dfna	Autosomal Dominant Isolated Sensorineural Hearing Loss Type Dfna
Autosomal Dominant Non-Syndromic Neurosensory Deafness Type Dfna	Autosomal Dominant Non-Syndromic Neurosensory Hearing Loss Type Dfna
Autosomal Dominant Non-Syndromic Sensorineural Hearing Loss Type Dfna

Rare Genetic Deafness

Rare Genetic Hearing Loss

End Stage Renal Disease

End Stage Renal Failure	End-Stage Kidney Disease
Kidney Failure, Chronic	Chronic Kidney Disease Stage 5

Alport Syndrome

Hereditary Nephritis	Alport Syndrome, X-Linked
Hemorrhagic Hereditary Nephritis	Congenital Hereditary Hematuria
Hemorrhagic Familial Nephritis	Familial Nephritis
Thin Basement Membrane Disease	Thin Basement Membrane Nephropathy
Hematuria-Nephropathy-Deafness Syndrome	Hematuric Hereditary Nephritis
Hereditary Familial Congenital Hemorrhagic Nephritis	Hereditary Hematuria Syndrome
Hereditary Interstitial Pyelonephritis	Alport Deafness-Nephropathy
Alport Hearing Loss-Nephropathy	Alports Syndrome
Nephritis, Hereditary

Deafness, Autosomal Recessive 63

DFNB63	Autosomal Recessive Nonsyndromic Deafness 63
Autosomal Recessive Deafness 63	Deafness, Autosomal Recessive, 63
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 63	Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 63
Deafness, Autosomal Recessive, Type 63

Hemangioma, Capillary Infantile

HCI	Capillary Infantile Hemangioma
Hemangioma, Hereditary Capillary	Hemangioma, Capillary Infantile, Susceptibility To
Hemangioma, Capillary Infantile, Somatic	Hemangioma Hereditary Capillary

Bernard-Soulier Syndrome

Giant Platelet Syndrome	BSS
Von Willebrand Factor Receptor Deficiency	Bdplt1
Platelet Glycoprotein Ib Deficiency	Bernard-Soulier Syndrome, Type A1
Bernard-Soulier Syndrome, Type B	Bernard Soulier Syndrome
Deficiency Of Platelet Glycoprotein 1b	Hemorrhagiparous Thrombocytic Dystrophy
Bernard-Soulier Syndrome Type C	Bleeding Disorder, Platelet-Type, 1
Glycoprotein Ib, Platelet, Deficiency Of	Giant Platelet Disorder, Isolated
Giant Platelet Disease	Macrothrombocytopenia, Familial Bernard-Soulier Type
Bernard-Soulier Syndrome, Type C	Bernard - Soulier Thrombopathy
Hemorrhagic Dystrophic Thrombocytopenia	Thrombopathy, Bernard-Soulier
Platelet Glycoprotein 1b, Deficiency Of	Hemorrhagioparous Thrombocytic Dystrophy
Bernard-Soulier Syndrome Type A1	Bernard-Soulier Syndrome Type B
Bleeding Disorder Platelet-Type 1	Gpd
Macrothrombocytopenia, Familial, Bernard-Soulier Type

Sensorineural Hearing Loss

Sensory Hearing Loss	Sensorineural Deafness
Sensorineural Hearing Loss Disorder	Hearing Loss, Sensorineural
Central Hearing Loss	High Frequency Deafness
High Frequency Hearing Loss	High-Frequency Hearing Loss
Perceptive Deafness	Perceptive Hearing Loss
Perceptive Hearing Loss Or Deafness	Hearing Loss Sensorineural
Deafness Sensorineural	Hearing Loss High-Frequency
Hearing Loss, Central	Hearing Loss, High-Frequency

Blood Platelet Disease

Platelet Disorder	Blood Platelet Disorders
Thrombocytopathy	Platelet Dysfunction
Platelet Disorders	Qualitative Platelet Deficiency

Fasciitis

Hypertension, Essential

Essential Hypertension	Hypertension
High Blood Pressure	Hypertension, Essential, Susceptibility To
Hypertensive Disease	Primary Hypertension
EHT	Hypertension, Salt-Sensitive Essential, Susceptibility To
Hyperpiesia	Idiopathic Hypertension
Hypertensive Disorder	Hypertension, Essential, Susceptibility To, 3
Hypertension, Essential 3	Hypertension, Essential, Salt-Sensitive
Hypertension, Essential, Susceptibility To, 6	Hypertension, Essential 6
Hypertension, Salt-Sensitive Essential	Hypertension, Susceptibility To
Hypertension, Essential, Susceptibility To, 4	Hypertension, Essential 4
Hypertension, Essential, Susceptibility To, 2	Hypertension, Essential 2
Hypertension, Essential, Susceptibility To, 1	Hypertension, Essential 1
Hypertension, Essential, Susceptibility To, 5	Hypertension, Essential 5
Htn	Vascular Hypertensive Disorder
Systemic Primary Arterial Hypertension	Hbp - [High Blood Pressure]
Systemic Arterial Hypertensive Disorder	Elevated Blood Pressure
Arterial Hypertension Nos	Hypertension Nos
Benign Hypertension	Systemic Arterial Hypertension
Systemic Hypertension	Artery Htn
Benign Htn	Vascular Htn
Vascular Hypertension	Cholesterol Hypertension
Cholesterol Htn	Idiopathic Htn
Malignant Hypertension	Malignant Htn
Raised Blood Pressure	Cardiovascular Hypertension
Primary Htn - [Hypertension]	High Arterial Tension
High Blood Pressure Disorder	Ht - [Hypertension]
Htn - [Hypertension]	Hypertensive Vascular Disease
Hypertensive Vascular Degeneration

Ankrd26-Related Thrombocytopenia

Thrombocytopenia 2

Thc2

Focal Segmental Glomerulosclerosis

Familial Idiopathic Steroid-Resistant Nephrotic Syndrome	Focal Glomerulosclerosis
Fsgs	Segmental Glomerulosclerosis
Glomerulosclerosis, Focal Segmental	Fgs
Focal Glomerular Sclerosis	Familial Idiopathic Nephrotic Syndrome
Focal Sclerosis With Hyalinosis	Glomerulosclerosis, Focal
Glomerulosclerosis Focal	Glomerulosclerosis, Segmental, Focal
Focal Segmental Glomerulosclerosis, Not Otherwise Specified

Body Mass Index Quantitative Trait Locus 11

OBESITY	Obesity, Susceptibility To
Leanness, Inherited	Obesity, Susceptibility To, Bmiq11
Obesity, Mild, Early-Onset	Obesity, Association With
Obesity, Early-Onset, Susceptibility To	Obesity, Severe
Obesity, Severe, And Type Ii Diabetes	Obesity, Late-Onset
Obesity , Susceptibility To	BMIQ11
Obesity Bmiq11	Obesity, Early-Onset
Simple Obesity Nos	Excess Fat
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified	Adiposis

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

Glomerulonephritis

Bright'S Disease

Bladder Exstrophy

Exstrophy Of The Bladder

Classic Exstrophy Of The Bladder

Nephrotic Syndrome

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

Acquired Thrombocytopenia

Secondary Thrombocytopenia

Intravascular Fasciitis

Intravascular Pseudosarcomatous Fasciitis

Ischemic Fasciitis

Atypical Decubital Fibroplasia

Autosomal Dominant Alport Syndrome

Alport Syndrome, Autosomal Dominant	Alport Syndrome Dominant Type
Renal Failure And Sensorineural Hearing Loss	Alport Syndrome, Dominant Type

Proliferative Fasciitis

X-Linked Alport Syndrome

Nephropathy And Deafness, X-Linked

Autosomal Recessive Alport Syndrome

Alport Syndrome, Recessive Type	Alport Syndrome, Autosomal Recessive
Alport Syndrome Autosomal Recessive	Alport Syndrome Recessive Type
Nephropathy And Deafness

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

Cataract

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

Hematuria, Benign Familial

Benign Familial Hematuria	BFH
Thin Membrane Nephropathy	Tmn
Thin Basement Membrane Nephropathy	Thin-Basement-Membrane Nephropathy
Hematuria, Familial Benign	Hematuria Benign Familial
Hematuria, Benign, Familial	Thin Basement Membrane Disease

Renal Hypertension

Hypertension Renal

Hypertension, Renal

Lens Disease

Lens Diseases

Febrile Seizures, Familial, 1

FEB1	Convulsions, Familial Febrile, 1
Familial Febrile Seizures 1	Familial Febrile Convulsions 1

Amegakaryocytic Thrombocytopenia, Congenital

Congenital Amegakaryocytic Thrombocytopenia	CAMT
Thrombocytopenia, Congenital Amegakaryocytic	Congenital Amegakaryocytic Thrombocytopenic Purpura
Thrombocytopenia Congenital Amegakaryocytic	Thrombocytopenia, Amegakaryocytic, Congenital

Glanzmann Thrombasthenia 1

Glanzmann Thrombasthenia	Thrombasthenia Of Glanzmann And Naegeli
Glanzmann'S Thrombasthenia	Bdplt2
Platelet Glycoprotein Iib-Iiia Deficiency	Deficiency Of Platelet Fibrinogen Receptor
GT1	Gt
Platelet Fibrinogen Receptor Deficiency	Glycoprotein Complex Iib-Iiia Deficiency
Deficiency Of Glycoprotein Complex Iib-Iiia	Glycoprotein Iib/Iiia Defect
Glanzmann Thrombasthenia, Type A	Thrombasthenia
Bleeding Disorder, Platelet-Type, 2	Gp Iib-Iiia Complex Deficiency
Deficiency Of Gp Iib-Iiia Complex	Platelet-Type Bleeding Disorder 2
Thrombocytasthenia	Deficiency Of Gp 2b 3a Complex
Diacyclothrombopathia 2b 3a	Glanzmann Thrombasthenia Type A
Platelet Fibrinogen Receptor, Deficiency Of	Platelet Glycoprotein 2b 3a Deficiency
Glanzmann Disease	Glanzmann-Naegeli Disorder
Hereditary Hemorrhagic Thrombasthenia	Hereditary Thrombasthenia
Bleeding Disorder Platelet-Type 2

Sleeping Sickness

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

Cleft Palate, Isolated

Cleft Palate	Isolated Cleft Palate
CPI	Cp
Palatoschisis	Cleft Palate Isolated
Uranostaphyloschisis	Congenital Fissure Of Palate
Cleft Of Secondary Palate

Autosomal Dominant Nonsyndromic Deafness

Autosomal Dominant Deafness

Hermansky-Pudlak Syndrome

Hps	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
Hermanski-Pudlak Syndrome	Hermansky Pudlak Syndrome
Platelet Storage Pool Deficiency

Cardiomyopathy, Familial Hypertrophic, 1

Asymmetric Septal Hypertrophy	Familial Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 1	CMH1
Hypertrophic Cardiomyopathy 19	CMH
Ventricular Hypertrophy, Hereditary	Ash
Hypertrophic Subaortic Stenosis, Idiopathic	Cardiomyopathy, Familial Hypertrophic
Cardiomyopathy, Hypertrophic, 1, Digenic	Cardiomyopathy, Familial Hypertrophic 1
Hcm	Hereditary Ventricular Hypertrophy
Idiopathic Hypertrophic Subaortic Stenosis	Hypertrophic Cardiomyopathy
Cardiomyopathy, Hypertrophic, Familial	Cardiomyopathy, Hypertrophic, 1
Familial Asymmetric Septal Hypertrophy	Heritable Hypertrophic Cardiomyopathy
Fhc	Cardiomyopathy, Hypertrophic, Familial, Type 1

Hypertrophic Cardiomyopathy

Hypertrophic Obstructive Cardiomyopathy	Cardiomyopathy, Hypertrophic
Cardiomyopathy Hypertrophic Obstructive	Cardiomyopathy, Hypertrophic, Familial
Idiopathic Myocardial Hypertrophy	Idiopathic Hypertrophic Cardiomyopathy
Obstructive Idiopathic Hypertrophic Cardiomyopathy	Obstructive Cardiomyopathy
Idiopathic Hypertrophic Subaortic Stenosis	Muscular Subaortic Stenosis
Hypertrophic Obstructive Subaortic Stenosis

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS08908	MYH9 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	MYH9	MGD	MGI:107717
Bos taurus	MYH9	VGNC	VGNC:31798
Felis catus	MYH9	VGNC	VGNC:68382
Canis familiaris	MYH9	VGNC	VGNC:43540
Macaca mulatta	MYH9	VGNC	VGNC:75102
Rattus norvegicus	MYH9	RGD	RGD:3140