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  2. GPR155 - G protein-coupled receptor 155 Gene

GPR155 - G protein-coupled receptor 155 Gene

中文名称:G 蛋白偶联受体 155

种属: Homo sapiens

同用名: DEP.7; PGR22; DEPDC3

基因 ID: 151556 | 基因类型: protein coding

关于 GPR155

This gene has 6 transcripts (splice variants), 274 orthologues and 3 paralogues. Ubiquitous expression in stomach (RPKM 11.2), brain (RPKM 8.6) and 24 other tissues.

功能概要

参与认知。位于细胞外外泌体。 [由基因组资源联盟提供,2022 年 4 月]

Involved in cognition. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

GPR155 基因产物(4)

mRNA Protein Name
NM_001033045.4 NP_001028217.1 integral membrane protein GPR155 isoform 1
NM_001267050.2 NP_001253979.1 integral membrane protein GPR155 isoform 1
NM_001267051.2 NP_001253980.1 integral membrane protein GPR155 isoform 2
NM_152529.7 NP_689742.4 integral membrane protein GPR155 isoform 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables cholesterol binding IDA
IDA: 通过直接分析推断
36007018 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cellular response to amino acid starvation IDA
IDA: 通过直接分析推断
36007018 GOA
involved in cellular response to cholesterol IDA
IDA: 通过直接分析推断
36007018 GOA
involved in cognition IMP
IMP: 通过突变表型推断
17519220 GOA
involved in positive regulation of TORC1 signaling IDA
IDA: 通过直接分析推断
36007018 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
is active in lysosomal membrane IDA
IDA: 通过直接分析推断
36007018 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

GPR155 蛋白结构

Mem_trans

Mem_trans: Membrane transport protein (45 - 189)

Mem_trans

Mem_trans: Membrane transport protein (204 - 360)

DEP

DEP: Domain found in Dishevelled, Egl-10, and Pleckstrin (DEP) (767 - 833)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 870 a.a.
蛋白主名 其他名称

integral membrane protein GPR155

G-protein coupled receptor PGR22

关联疾病

疾病名称 别名
Noonan Syndrome 13

NS13

Isolated Growth Hormone Deficiency, Type Ib

Isolated Growth Hormone Deficiency Type Ib

IGHD1B

Ighd Ib

Growth Hormone Deficiency, Isolated, Type Ib

Congenital Ighd Type Ib

Congenital Isolated Gh Deficiency Type Ib

Congenital Isolated Growth Hormone Deficiency Type Ib

Dwarfism Of Sindh

Pituitary Dwarfism I

Isolated Growth Hormone Deficiency Type 1b

Ighd 1b

Growth Hormone Deficiency, Isolated, 1b

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
Macaca mulatta GPR155 VGNC VGNC:72985
Felis catus GPR155 VGNC VGNC:62680
Rattus norvegicus GPR155 RGD RGD:1309162
Bos taurus GPR155 VGNC VGNC:29561
Canis familiaris GPR155 VGNC VGNC:41407
Mus musculus GPR155 MGD MGI:1915776
Others GPR155 NCBI