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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 (Low Density Lipoprotein Receptor Adaptor Protein 1) is a Protein Coding gene. Diseases associated with LDLRAP1 include Hypercholesterolemia, Familial, 4 and Homozygous Familial Hypercholesterolemia. Among its related pathways are Vesicle-mediated transport and Clathrin-mediated endocytosis. Gene Ontology (GO) annotations related to this gene include phosphatidylinositol-4,5-bisphosphate binding and amyloid-beta binding. An important paralog of this gene is NUMB.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0001540 | amyloid-beta binding | IPI | 12805363 |
GO:0001784 | phosphotyrosine residue binding | IDA | 12451172 |
GO:0005515 | protein binding | IPI | 12221107 |
GO:0005546 | phosphatidylinositol-4,5-bisphosphate binding | IDA | 12451172 |
GO:0030159 | receptor signaling complex scaffold activity | IMP | 15166224 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005737 | cytoplasm | IEA | -- |
GO:0005769 | early endosome | IDA,IEA | 14528014 |
GO:0005829 | cytosol | IDA | 12451172 |
GO:0005883 | neurofilament | IEA,ISS | 17727637 |
GO:0005886 | plasma membrane | TAS | -- |
SuperPathway | Contained pathways | ||
---|---|---|---|
1 | Lipoprotein metabolism | ||
2 | Clathrin-mediated endocytosis | ||
3 | Vesicle-mediated transport | ||
4 | Metabolism |
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5 | Statin Pathway |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006629 | lipid metabolic process | IEA | -- |
GO:0006897 | endocytosis | IEA | -- |
GO:0006898 | receptor-mediated endocytosis | IDA | 14528014 |
GO:0008202 | steroid metabolic process | IEA | -- |
GO:0008203 | cholesterol metabolic process | NAS | 12451172 |
Name | Status | Disease Links | Group | Role | Mechanism of Action | Clinical Trials |
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Name | Synonyms | Role | CAS Number | PubChem IDs | PubMed IDs |
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This gene was present in the common ancestor of chordates.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
chimpanzee (Pan troglodytes) |
Mammalia | LDLRAP1 33 32 |
|
OneToOne | |
cow (Bos Taurus) |
Mammalia | LDLRAP1 33 32 |
|
OneToOne | |
dog (Canis familiaris) |
Mammalia | LDLRAP1 33 32 |
|
OneToOne | |
mouse (Mus musculus) |
Mammalia | Ldlrap1 17 33 32 |
|
||
rat (Rattus norvegicus) |
Mammalia | Ldlrap1 32 |
|
||
oppossum (Monodelphis domestica) |
Mammalia | LDLRAP1 33 |
|
OneToOne | |
platypus (Ornithorhynchus anatinus) |
Mammalia | LDLRAP1 33 |
|
OneToOne | |
chicken (Gallus gallus) |
Aves | LDLRAP1 33 32 |
|
OneToOne | |
lizard (Anolis carolinensis) |
Reptilia | LDLRAP1 33 |
|
OneToOne | |
tropical clawed frog (Silurana tropicalis) |
Amphibia | ldlrap1 32 |
|
||
Str.11033 32 |
|
||||
African clawed frog (Xenopus laevis) |
Amphibia | Xl.8355 32 |
|
||
zebrafish (Danio rerio) |
Actinopterygii | ldlrap1b 33 32 |
|
OneToMany | |
ldlrap1a 33 |
|
OneToMany | |||
sbcb50 32 |
|
SNP ID | Clin | Chr 01 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
rs1007363567 | uncertain-significance, Familial hypercholesterolemia | 25,543,631(+) | G/A | 5_prime_UTR_variant, genic_upstream_transcript_variant, non_coding_transcript_variant, upstream_transcript_variant | |
rs1038619262 | uncertain-significance, Familial hypercholesterolemia | 25,568,729(+) | G/A | 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant | |
rs1044796585 | uncertain-significance, Familial hypercholesterolemia | 25,543,599(+) | G/A | 5_prime_UTR_variant, genic_upstream_transcript_variant, upstream_transcript_variant | |
rs1047410438 | uncertain-significance, Hypercholesterolemia, autosomal recessive | 25,566,907(+) | T/C | 3_prime_UTR_variant, coding_sequence_variant, intron_variant, missense_variant, non_coding_transcript_variant | |
rs1057515425 | uncertain-significance, Familial hypercholesterolemia | 25,543,662(+) | T/C | 5_prime_UTR_variant, genic_upstream_transcript_variant, non_coding_transcript_variant, upstream_transcript_variant |
Disorder | Aliases | PubMed IDs |
---|---|---|
hypercholesterolemia, familial, 4 |
|
|
homozygous familial hypercholesterolemia |
|
|
familial hypercholesterolemia |
|
|
xanthomatosis |
|
|
cholesterol ester storage disease |
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|