1. Gene
  2. LDLRAP1 - low density lipoprotein receptor adaptor protein 1 Gene

LDLRAP1 - low density lipoprotein receptor adaptor protein 1 Gene

Homo sapiens

Also known as ARH; ARH1; ARH2; FHCB1; FHCB2; FHCL4

Gene ID: 26119 | Gene type: protein coding

About LDLRAP1

Cytogenetic location: 1p36.11 Genomic coordinates (GRCh38): 1:25,543,606-25,590,400 (from NCBI)

This gene has 7 transcripts (splice variants), 285 orthologues, 11 paralogues and is associated with 3 phenotypes. Ubiquitous expression in spleen (RPKM 14.0), lymph node (RPKM 12.3) and 25 other tissues.

Summary

The protein encoded by this gene is a cytosolic protein which contains a phosphotyrosine binding (PTD) domain. The PTD domain has been found to interact with the cytoplasmic tail of the LDL receptor. Mutations in this gene lead to LDL receptor malfunction and cause the disorder autosomal recessive hypercholesterolaemia. [provided by RefSeq, Jul 2008]

LDLRAP1 Products(1)

mRNA Protein Name
NM_015627.3 NP_056442.2 low density lipoprotein receptor adapter protein 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables AP-1 adaptor complex binding IDA
IDA: Inferred from direct assay
12451172 GOA
enables AP-2 adaptor complex binding IDA
IDA: Inferred from direct assay
12451172 GOA
enables amyloid-beta binding IPI
IPI: Inferred from physical interaction
12805363 GOA
enables clathrin adaptor activity IDA
IDA: Inferred from direct assay
15728179 GOA
enables clathrin binding IDA
IDA: Inferred from direct assay
12221107 GOA
enables low-density lipoprotein particle receptor binding IPI
IPI: Inferred from physical interaction
12221107 GOA
enables phosphatidylinositol-4,5-bisphosphate binding IDA
IDA: Inferred from direct assay
12451172 GOA
enables phosphotyrosine residue binding IDA
IDA: Inferred from direct assay
12451172 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12221107 GOA
enables signaling adaptor activity IDA
IDA: Inferred from direct assay
12221107 GOA
enables signaling receptor complex adaptor activity IMP
IMP: Inferred from mutant phenotype
15166224 GOA
Biological Process GO Annotation Evidence Reference Source
involved in amyloid precursor protein metabolic process IMP
IMP: Inferred from mutant phenotype
12805363 GOA
involved in cellular response to cytokine stimulus IMP
IMP: Inferred from mutant phenotype
28257760 GOA
involved in cholesterol homeostasis IMP
IMP: Inferred from mutant phenotype
15166224 GOA
involved in low-density lipoprotein particle clearance IMP
IMP: Inferred from mutant phenotype
12417523 GOA
involved in positive regulation of low-density lipoprotein particle clearance IMP
IMP: Inferred from mutant phenotype
28257760 GOA
involved in positive regulation of receptor-mediated endocytosis IMP
IMP: Inferred from mutant phenotype
15166224 GOA
involved in positive regulation of receptor-mediated endocytosis involved in cholesterol transport IMP
IMP: Inferred from mutant phenotype
12417523 GOA
involved in positive regulation of vascular associated smooth muscle cell proliferation IMP
IMP: Inferred from mutant phenotype
28257760 GOA
involved in receptor internalization IMP
IMP: Inferred from mutant phenotype
15166224 GOA
involved in receptor-mediated endocytosis IDA
IDA: Inferred from direct assay
14528014 GOA
involved in receptor-mediated endocytosis involved in cholesterol transport IMP
IMP: Inferred from mutant phenotype
12417523 GOA
involved in regulation of protein binding IMP
IMP: Inferred from mutant phenotype
15166224 GOA
involved in regulation of protein localization to plasma membrane IMP
IMP: Inferred from mutant phenotype
12805363 GOA
Cellular Component GO Annotation Evidence Reference Source
located in basal plasma membrane IDA
IDA: Inferred from direct assay
12451172 GOA
located in cytoplasmic side of plasma membrane IDA
IDA: Inferred from direct assay
14528014 GOA
located in cytosol IDA
IDA: Inferred from direct assay
12451172 GOA
located in early endosome IDA
IDA: Inferred from direct assay
14528014 GOA
located in recycling endosome IDA
IDA: Inferred from direct assay
14528014 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

LDLRAP1 Protein Structure

PID

PID: Phosphotyrosine interaction domain (PTB/PID) (48 - 170)

  • 0
  • 100
  • 200
  • 308 a.a.
Protein Preferred Names Protein Names

low density lipoprotein receptor adapter protein 1

LDL receptor adaptor protein

LDLRAP1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra LDLRAP1 Q5SW96 AP2B1 Homo sapiens P63010-2
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 AP2B1 Homo sapiens P63010-2
BFG-2H
27107012
Intra LDLRAP1 Q5SW96 AP2B1 Homo sapiens P63010-2
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 AP1B1 Homo sapiens Q10567-3
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 AP1B1 Homo sapiens Q10567-3
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 PSD4 Homo sapiens Q8NDX1-2
Validated Y2H
25910212
Intra LDLRAP1 Q5SW96 PSD4 Homo sapiens Q8NDX1-2
Y2H Array
25910212
Intra LDLRAP1 Q5SW96 PSD4 Homo sapiens Q8NDX1-2
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 PSD4 Homo sapiens Q8NDX1-2
Validated Y2H
32296183
Intra LDLRAP1 Q5SW96 PSD4 Homo sapiens Q8NDX1-2
Y2H Bait-Prey Pool
25910212
Intra LDLRAP1 Q5SW96 PSD4 Homo sapiens Q8NDX1-2
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 ESPNL Homo sapiens Q6ZVH7
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 ESPNL Homo sapiens Q6ZVH7
Validated Y2H
32296183
Intra LDLRAP1 Q5SW96 ESPNL Homo sapiens Q6ZVH7
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 NOTO Homo sapiens A8MTQ0
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 NOTO Homo sapiens A8MTQ0
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 HOXC8 Homo sapiens P31273
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 HOXC8 Homo sapiens P31273
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 PAX5 Homo sapiens Q02548
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 PAX5 Homo sapiens Q02548
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 AP2B1 Homo sapiens P63010
Pull Down
12221107
Intra LDLRAP1 Q5SW96 FHL2 Homo sapiens Q14192
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 FHL2 Homo sapiens Q14192
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 HOXD8 Homo sapiens P13378
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 HOXD8 Homo sapiens P13378
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 MAPK8IP3 Homo sapiens Q9UPT6
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 MAPK8IP3 Homo sapiens Q9UPT6
Validated Y2H
32296183
Intra LDLRAP1 Q5SW96 MAPK8IP3 Homo sapiens Q9UPT6
BFG-2H
27107012
Intra LDLRAP1 Q5SW96 MAPK8IP3 Homo sapiens Q9UPT6
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 MAPK8IP3 Homo sapiens Q9UPT6
Complementation
32296183
Intra LDLRAP1 Q5SW96 MAGEA4 Homo sapiens P43358
Y2H Prey Pooling
32296183
Intra LDLRAP1 Q5SW96 MAGEA4 Homo sapiens P43358
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Validated Y2H
32296183
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Y2H Array
25416956
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Y2H Bait-Prey Pool
25910212
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Y2H Array
32296183
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Validated Y2H
25910212
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Y2H Prey Pooling
25416956
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Y2H Array
25910212
Intra LDLRAP1 Q5SW96 STN1 Homo sapiens Q9H668
Y2H Prey Pooling
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hypercholesterolemia, Familial, 4

Hypercholesterolemia, Autosomal Recessive

Arh

FHCL4

Autosomal Recessive Hypercholesterolemia

Arh1

Arh2

Autosomal Recessive Hypercholesterolemia 1

Autosomal Recessive Hypercholesterolemia 2

Fhcb1

Fhcb2

Hypercholesterolemia, Autosomal Recessive, 1, Formerly

Arh1, Formerly

Fhcb1, Formerly

Hypercholesterolemia, Autosomal Recessive, 2, Formerly

Arh2, Formerly

Fhcb2, Formerly

Familial Autosomal Recessive Hypercholesterolemia

Hypercholesterolemia, Familial, Autosomal Recessive

Hypercholesterolemia, Familial, Type 4

Familial Hypercholesterolemia

Hyperlipoproteinemia Type Iia

Familial Hyperbetalipoproteinaemia

Familial Hypercholesteremia

Fredrickson Type Iia Hyperlipoproteinemia

Fredrickson Type Iia Lipidaemia

Hyperbetalipoproteinemia

Type Ii Hyperlipidemia

Familial Hypercholesterolæmia

Familial Hypercholesterolaemia

Fh

Hypercholesterolemia Familial

Hyperlipoproteinemia Type Ii

Hypercholesterolemia, Familial

Homozygous Familial Hypercholesterolemia

Hofh

Xanthomatosis

Xanthomatosis, Susceptibility To

Xanthelasmatosis

Corneal Degeneration

Degenerative Corneal Opacity

Familial Hyperlipidemia

Familial Hyperlipoproteinemia

Hyperlipidaemia

Hyperlipoproteinemias

Hyperlipidemia

Hyperlipemia

Hyperlipidemias

Arcus Corneae

Arcus Senilis

Corneal Arcus

Arcus Of Cornea

Sea-Blue Histiocyte Disease

Sea-Blue Histiocytosis

Sea-Blue Histiocyte Syndrome

Histiocytosis, Sea-Blue

Inherited Lipemic Splenomegaly

SBHD

Sitosterolemia

Phytosterolemia

Beta-Sitosterolemia

Plant Sterol Storage Disease

Phytosterolæmia

Sitosterolæmia

Retention Of Dietary Cholesterol And Abnormal Retention Of Non-Cholesterol Sterols In The Body

Phytosterolaemia

Sitosterolaemia

Sitosterolemia With Xanthomatosis

Hypercholesterolemia, Familial, 1

Hypercholesterolemia

FHCL1

Fhc

Fh

Hyperlipoproteinemia, Type Ii

Hyperlipoproteinemia, Type Iia

Hyper-Low-Density-Lipoproteinemia

Hypercholesterolemic Xanthomatosis, Familial

Ldl Receptor Disorder

Hypercholesterolemia, Susceptibility To

Hypercholesterolemia, Familial, Modifier Of

Hypercholesterolemia, Familial, Due To Ldlr Defect, Modifier Of

Ldl Cholesterol Level Qtl2

Hyperlipoproteinemia Type Ii

Hypercholesterolemia, Familial, Type 1

High Cholesterol

Increased Cholesterol

Low-Density-Lipoid-Type Hyperlipoproteinemia

Pure Hypercholesterolaemia

Ldl - [Low Density Lipoprotein} Hyperlipoproteinemia

Group A Hyperlipidaemia

Pure Hypercholesterinaemia

Cholesterolaemia

Essential Cholesterolaemia

Essential Hypercholesterolaemia

Group A Hyperlipemia

Increased Low Density Lipoprotein

Low-Density-Lipoprotein-Type

Low-Density-Lipoprotein-Type Hyperlipoproteinemia

Cholesterol Ester Storage Disease
Lipoprotein Quantitative Trait Locus

Coronary Artery Disease

Coronary Artery Anomaly

Coronary Artery Disease, Susceptibility To

Myocardial Ischemia

Congenital Anomaly Of Coronary Artery

Coronary Arteriosclerosis

Coronary Disease

Coronary Heart Disease

Coronary Artery Disorder

LPAQTL

Lpa Deficiency, Congenital

Coronary Artery Abnormality

Coronary Artery Anomaly, Congenital

Chd

Coronary Syndrome

Congenital Malformations Of Coronary Vessels

Malformation Of Coronary Vessels

Congenital Coronary Artery Anomaly

Congenital Coronary Artery Deformity

Congenital Coronary Artery Disorder

Abnormal Coronary Artery

Congenital Coronary Artery Malposition

Congenital Coronary Disease

Congenital Anomaly Of Coronary Arteries

Lipid Metabolism Disorder

Dyslipidemia

Disorder Of Fatty Acid Metabolism

Lipid Metabolism Disorders

Fatty Acid Metabolism Disorder

Disorder Of Lipid Metabolism

Abnormality Of Lipid Metabolism

Lipid Metabolism, Inborn Errors

Dyslipidemias

Disorders Of Lipid Metabolism

Congenital Disorders Of Lipid Metabolism

Inherited Disorders Of Lipid Metabolism

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus LDLRAP1 VGNC VGNC:30830
Canis familiaris LDLRAP1 VGNC VGNC:42626
Rattus norvegicus LDLRAP1 RGD RGD:1563417
Felis catus LDLRAP1 VGNC VGNC:80251
Mus musculus LDLRAP1 MGD MGI:2140175