1. Gene
  2. ARRDC1 - arrestin domain containing 1 Gene

ARRDC1 - arrestin domain containing 1 Gene

Homo sapiens
Gene ID: 92714 | Gene type: protein coding

About ARRDC1

Cytogenetic location: 9q34.3 Genomic coordinates (GRCh38): 9:137,605,686-137,615,360 (from NCBI)

This gene has 12 transcripts (splice variants), 225 orthologues and 5 paralogues. Ubiquitous expression in stomach (RPKM 15.2), spleen (RPKM 13.5) and 25 other tissues.

Summary

Enables several functions, including Arrestin family protein binding activity; ubiquitin ligase-substrate adaptor activity; and ubiquitin protein ligase binding activity. Involved in several processes, including cellular protein metabolic process; extracellular vesicle biogenesis; and negative regulation of Notch signaling pathway. Located in cytoplasmic vesicle; extracellular vesicle; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ARRDC1 Products(2)

mRNA Protein Name
NM_001317968.2 NP_001304897.1 arrestin domain-containing protein 1 isoform 2
NM_152285.4 NP_689498.1 arrestin domain-containing protein 1 isoform 1

ARRDC1 Protein Structure

Arrestin_N

Arrestin_N: Arrestin (or S-antigen), N-terminal domain (7 - 139)

Arrestin_C

Arrestin_C: Arrestin (or S-antigen), C-terminal domain (163 - 284)

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  • 433 a.a.
Protein Preferred Names Protein Names

arrestin domain-containing protein 1

alpha-arrestin 1

Related Diseases

Diseases Alias
Methemoglobinemia And Ambiguous Genitalia

METAG

Methemoglobinemia Type Iv

Isolated 17,20-Lyase Deficiency, Pure

Methemoglobinemia Due To Deficiency Of Cytochrome B5

Methemoglobinemia Type 4

Methemoglobinemia Type Iv, Formerly

Methemoglobinemia Due To Deficiency Of Cytochrome B5, Formerly

Pure Isolated 17,20-Lyase Deficiency

Methemoglobinemia, Type Iv

Kleefstra Syndrome 1

9q Subtelomeric Deletion Syndrome

KLEFS1

Chromosome 9q34.3 Deletion Syndrome

9q- Syndrome

9q34 Deletion Syndrome

Kleefstra Syndrome Due To 9q34 Microdeletion

Kleefstra Syndrome

9q-Syndrome

9qstds

Kleefstra Syndrome Due To 9q Subtelomeric Deletion

Kleefstra Syndrome Due To Del(9)(Q34)

Kleefstra Syndrome Due To Monosomy 9q34

Chromosome 9q Subtelomeric Deletion Syndrome

Kleefstra Syndrome, Type 1

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 ARRDC1 VGNC VGNC:26171
Mus musculus ARRDC1 MGD MGI:2446136
Felis catus ARRDC1 VGNC VGNC:59943
Canis familiaris ARRDC1 VGNC VGNC:38138
Rattus norvegicus ARRDC1 RGD RGD:1309961
Macaca mulatta ARRDC1 VGNC VGNC:69920