1. Gene
  2. ARRDC2 - arrestin domain containing 2 Gene

ARRDC2 - arrestin domain containing 2 Gene

Homo sapiens

Also known as PP2703; CLONE24945

Gene ID: 27106 | Gene type: protein coding

About ARRDC2

This gene has 10 transcripts (splice variants), 217 orthologues and 5 paralogues. Ubiquitous expression in bone marrow (RPKM 25.3), fat (RPKM 16.5) and 24 other tissues.

Summary

Predicted to be involved in protein transport. Located in cytoplasmic vesicle and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ARRDC2 Products(3)

mRNA Protein Name
NM_001025604.3 NP_001020775.1 arrestin domain-containing protein 2 isoform 2
NM_001286826.2 NP_001273755.1 arrestin domain-containing protein 2 isoform 3
NM_015683.2 NP_056498.1 arrestin domain-containing protein 2 isoform 1

ARRDC2 Protein Structure

Arrestin_N

Arrestin_N: Arrestin (or S-antigen), N-terminal domain (19 - 158)

Arrestin_C

Arrestin_C: Arrestin (or S-antigen), C-terminal domain (181 - 306)

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  • 407 a.a.
Protein Preferred Names Protein Names

arrestin domain-containing protein 2

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, Autosomal Dominant 41

MRD41

Autosomal Dominant Non-Syndromic Intellectual Disability 41

Mental Retardation, Autosomal Dominant 41

Autosomal Dominant Intellectual Developmental Disorder 41

Autosomal Dominant Mental Retardation 41

Mental Retardation, Autosomal Dominant, Type 41

Ulna And Fibula, Absence Of, With Severe Limb Deficiency

Schinzel Phocomelia Syndrome

Aarrs

Limb/Pelvis-Hypoplasia/Aplasia Syndrome

LPHAS

Schinzel Type Phocomelia

Absence Of Ulna And Fibula With Severe Limb Deficiency

Al-Awadi/Raas-Rothschild Syndrome

Al Awadi-Raas-Rothschild Syndrome

Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome

Aplasia/Hypoplasia Of Limbs And Pelvis

Congenital Absence Of Ulna And Fibula

Severe Limb Deficit

Phocomelia, Schinzel Type

Al-Awadi-Raas-Rothschild Syndrome

Ulna And Fibula Absence Of With Severe Limb Deficiency

Limb Pelvis Hypoplasia Aplasia Syndrome

Limb/Pelvis/Uterus-Hypoplasia/Aplasia Syndrome

Ulna And Fibula, Absence Of, With Sever Limb Deficiency

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
Felis catus ARRDC2 VGNC VGNC:59944
Rattus norvegicus ARRDC2 RGD RGD:1309659
Canis familiaris ARRDC2 VGNC VGNC:38139
Bos taurus ARRDC2 VGNC VGNC:26172
Mus musculus ARRDC2 MGD MGI:1918057
Macaca mulatta ARRDC2 VGNC VGNC:69901