ILDR2 - immunoglobulin like domain containing receptor 2 Gene

Homo sapiens

Also known as C1orf32; dJ782G3.1

Gene ID: 387597 | Gene type: protein coding

About ILDR2

Cytogenetic location: 1q24.1 Genomic coordinates (GRCh38): 1:166,908,187-166,975,540 (from NCBI)

This gene has 9 transcripts (splice variants), 275 orthologues and 2 paralogues. Biased expression in testis (RPKM 6.6), brain (RPKM 4.2) and 3 other tissues.

Summary

Predicted to act upstream of or within several processes, including homeostasis of number of cells within a tissue; Insulin secretion; and response to glucose. Predicted to be located in endoplasmic reticulum membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ILDR2 Products(3)

mRNA	Protein	Name
NM_001410891.1	NP_001397820.1	immunoglobulin-like domain-containing receptor 2 isoform 2 precursor
NM_001410892.1	NP_001397821.1	immunoglobulin-like domain-containing receptor 2 isoform 3 precursor
NM_199351.3	NP_955383.1	immunoglobulin-like domain-containing receptor 2 isoform 1 precursor

ILDR2 Protein Structure

LSR

0
100
200
300
400
500
600
639 a.a.

Protein Preferred Names

Protein Names

immunoglobulin-like domain-containing receptor 2

angulin-3

Recombinant ILDR2 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P70864	ILDR2 Protein, Human (HEK293, His)	Q71H61 (L21-E186)	≥95%

Related Diseases

Diseases

Alias

Deafness, Autosomal Recessive 42

DFNB42	Autosomal Recessive Nonsyndromic Deafness 42
Autosomal Recessive Deafness 42	Deafness, Autosomal Recessive, 42
Congenital Neurosensory Deafness Autosomal Recessive 42	Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 42
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 42	Deafness, Autosomal Recessive, Type 42

Deafness, Autosomal Recessive 49

DFNB49	Autosomal Recessive Nonsyndromic Deafness 49
Autosomal Recessive Deafness 49	Deafness, Autosomal Recessive, 49
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 49	Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 49
Deafness, Autosomal Recessive, Type 49

Deafness, Autosomal Recessive 29

DFNB29	Autosomal Recessive Nonsyndromic Deafness 29
Autosomal Recessive Deafness 29	Deafness, Autosomal Recessive, 29
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 29	Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 29
Deafness, Autosomal Recessive, Type 29

Hermansky-Pudlak Syndrome 7

HPS7	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial
Delta Storage Pool Disease	Hermansky-Pudlak Syndrome, Type 7
Platelet Storage Pool Deficiency	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Astigmatism

Autosomal Recessive Nonsyndromic Deafness

Deafness, Autosomal Recessive, Nonsyndromic

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS06784	ILDR2 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	ILDR2	VGNC	VGNC:41998
Rattus norvegicus	ILDR2	RGD	RGD:1596420
Macaca mulatta	ILDR2	VGNC	VGNC:73619
Felis catus	ILDR2	VGNC	VGNC:107885
Mus musculus	ILDR2	MGD	MGI:1196370
Bos taurus	ILDR2	VGNC	VGNC:30174
Others	ILDR2	NCBI

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