country

Product Name	Size / Unit Price	Qty

Total: USD 0.00 Checkout

ARRDC2 - arrestin domain containing 2 Gene

Also Known as PP2703; CLONE24945

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 27106

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_C

0
100
200
300
407 a.a.

Protein Preferred Names	Protein Names
arrestin domain-containing protein 2

ARRDC2 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	ARRDC2	Q8TBH0	EPN2	Homo sapiens	O95208-2	Y2H Prey Pooling	32296183
Intra	ARRDC2	Q8TBH0	EPN2	Homo sapiens	O95208-2	Y2H Array	32296183
Intra	ARRDC2	Q8TBH0	ZRANB1	Homo sapiens	Q9UGI0	Y2H Prey Pooling	32296183
Intra	ARRDC2	Q8TBH0	ZRANB1	Homo sapiens	Q9UGI0	Validated Y2H	32296183
Intra	ARRDC2	Q8TBH0	ZRANB1	Homo sapiens	Q9UGI0	Y2H Array	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

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

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS01031	ARRDC2 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

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