GPR89A - G protein-coupled receptor 89A Gene

中文名称：G 蛋白偶联受体 89A

种属: Homo sapiens

同用名: GPHR; GPR89; SH120; GPR89B; UNQ192

基因 ID: 653519 | 基因类型: protein coding

关于 GPR89A

Cytogenetic location: 1q21.1 Genomic coordinates (GRCh38): 1:145,607,988-145,670,650 (from NCBI)

This gene has 13 transcripts (splice variants), 201 orthologues and 1 paralogue. Ubiquitous expression in kidney (RPKM 15.4), testis (RPKM 12.4) and 25 other tissues.

功能概要

GPR89A 与 GPR89B 基因 (MIM 612806) 几乎相同。[OMIM 提供，2009 年 6 月]

GPR89A is a nearly identical copy of the GPR89B gene (MIM 612806).[supplied by OMIM, Jun 2009]

GPR89A 基因产物(2)

mRNA	Protein	Name
NM_001097612.2	NP_001091081.1	Golgi pH regulator A isoform 1
NM_001097613.3	NP_001091082.2	Golgi pH regulator A isoform 2

GPR89A 蛋白结构

GPHR_N

ABA_GPCR

0
100
200
300
400
455 a.a.

蛋白主名

其他名称

Golgi pH regulator A

protein GPR89

GPR89A 蛋白互作信息

分类	蛋白名称	蛋白编号	互作蛋白	互作蛋白种属	互作蛋白编号	实验方法	参考文献
种属内	GPR89B	P0CG08	WFS1	Homo sapiens	O76024	Validated Y2H	32814053
种属内	GPR89B	P0CG08	WFS1	Homo sapiens	O76024	Y2H Array	32814053
种属内	GPR89B	P0CG08	WFS1	Homo sapiens	O76024	Y2H Pooling	32814053

种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称

别名

Hemochromatosis, Type 2a

Hemochromatosis Type 2a	HFE2A
Juvenile Hemochromatosis	Hemochromatosis 2a
Hefe2	Hemochromatosis Type 2
Jh

Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb

Chromosome 1q21.1 Deletion Syndrome	1q21.1 Microdeletion Syndrome
Monosomy 1q21.1	1q21.1 Microdeletion
Chromosome 1q21.1 Microdeletion Syndrome	1q21.1 Contiguous Gene Deletion
1q21.1 Deletion	Del(1)(Q21)
1q21.1 Deletion Syndrome

Thrombocytopenia-Absent Radius Syndrome

Tar Syndrome	Radial Aplasia-Thrombocytopenia Syndrome
Absent Radii And Thrombocytopenia	TAR
Chromosome 1q21.1 Deletion Syndrome, 200-Kb	Thrombocytopenia Absent Radius Syndrome
Thrombocytopenia Absent Radii	Chromosome 1q21.1 Deletion Syndrome
Thrombocytopenia With Absent Radii Syndrome	Radial Aplasia-Amegakaryocytic Thrombocytopenia

Duodenal Atresia

Duodenal Stenosis

Familial Duodenal Atresia

Chromosome 1p36 Deletion Syndrome

1p36 Deletion Syndrome	Deletion 1p36
Monosomy 1p36	Subtelomeric 1p36 Deletion
Monosomy 1p36 Syndrome	Distal Monosomy 1p36
Del(1)(P36)	Deletion 1pter
Monosomy 1pter

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

Cat. No.	产品名	作用方式	纯度	是否罕见病
HY-RS05746	GPR89A Human Pre-designed siRNA Set A	Pre-designed Set	/	否

直系同源

种属	基因名	来源	基因 ID
Mus musculus	GPR89A	MGD	MGI:1914799

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MedChemExpress (MCE) 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务，不为任何个人或者非科研性质的、非用于药证申报使用等其他用途提供服务。

站点地图隐私声明

沪ICP备15051369号-4

上海工商

沪公网安备31011502019417

沪(浦)应急管危经许[2021]201709(QFYS)

营业执照（三证合一）

GPR89A - G protein-coupled receptor 89A Gene

关于 GPR89A

功能概要

GPR89A 基因产物(2)

GPR89A 蛋白结构

GPR89A 蛋白互作信息

关联疾病

直系同源

热门区域

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GPR89A - G protein-coupled receptor 89A Gene

关于 GPR89A

功能概要

GPR89A 基因产物(2)

GPR89A 蛋白结构

GPR89A 蛋白互作信息

关联疾病

相关产品

直系同源

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z