1. Gene
  2. ILDR2 - immunoglobulin like domain containing receptor 2 Gene

ILDR2 - immunoglobulin like domain containing receptor 2 Gene

中文名称:含免疫球蛋白样结构域的受体 2

种属: Homo sapiens

同用名: C1orf32; dJ782G3.1

基因 ID: 387597 | 基因类型: protein coding

关于 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.

功能概要

预计在几个过程的上游或内部起作用,包括组织内细胞数量的稳态;胰岛素分泌;和对葡萄糖的反应。预测位于内质网膜。预计是膜的组成部分。 [由基因组资源联盟提供,2022 年 4 月]

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 基因产物(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 蛋白结构

LSR

LSR: Lipolysis stimulated receptor (LSR) (186 - 233)

  • 0
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  • 500
  • 600
  • 639 a.a.
蛋白主名 其他名称

immunoglobulin-like domain-containing receptor 2

angulin-3

重组 ILDR2 蛋白

目录号 产品名 蛋白编号 纯度
HY-P70864 ILDR2 Protein, Human (HEK293, His) Q71H61 (L21-E186) ≥95%

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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