1. Gene
  2. REEP5 - receptor accessory protein 5 Gene

REEP5 - receptor accessory protein 5 Gene

中文名称:受体辅助蛋白 5

种属: Homo sapiens

同用名: DP1; TB2; YOP1; POB16; Yip2e; D5S346; C5orf18

基因 ID: 7905 | 基因类型: protein coding

关于 REEP5

Cytogenetic location: 5q22.2 Genomic coordinates (GRCh38): 5:112,876,385-112,922,227 (from NCBI)

This gene has 7 transcripts (splice variants), 206 orthologues and 5 paralogues. Ubiquitous expression in thyroid (RPKM 89.7), brain (RPKM 63.5) and 25 other tissues.

功能概要

预计参与内质网组织和细胞内运输的调节。位于内质网管状网络中。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to be involved in endoplasmic reticulum organization and regulation of intracellular transport. Located in endoplasmic reticulum tubular network. [provided by Alliance of Genome Resources, Apr 2022]

REEP5 基因产物(1)

mRNA Protein Name
NM_005669.5 NP_005660.4 receptor expression-enhancing protein 5
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
16762630 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in endoplasmic reticulum tubular network IDA
IDA: 通过直接分析推断
23969831 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

REEP5 蛋白结构

TB2_DP1_HVA22

TB2_DP1_HVA22: TB2/DP1, HVA22 family (51 - 145)

  • 0
  • 100
  • 189 a.a.
蛋白主名 其他名称

receptor expression-enhancing protein 5

deleted in polyposis 1

REEP5 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
REEP5 Q00765 PITPNC1 Homo sapiens Q9UKF7-2 32296183
种属内
REEP5 Q00765 SNX1 Homo sapiens Q13596 32296183
种属内
REEP5 Q00765 RABAC1 Homo sapiens Q9UI14 35271311
种属内
REEP5 Q00765 RABAC1 Homo sapiens Q9UI14 33961781
种属内
REEP5 Q00765 RABAC1 Homo sapiens Q9UI14 28514442
种属内
REEP5 Q00765 ABHD4 Homo sapiens Q8TB40 32296183
种属内
REEP5 Q00765 PBX3 Homo sapiens Q96AL5 32296183
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
Transitional Papilloma

Transitional Cell Papilloma

Transitional Cell Papilloma, Benign

Diamond-Blackfan Anemia 5

DBA5

Rpl35a-Related Diamond-Blackfan Anemia

Anemia, Diamond-Blackfan, Type 5

Colorectal Cancer, Hereditary Nonpolyposis, Type 5

HNPCC5

Hereditary Nonpolyposis Colorectal Cancer Type 5

Hereditary Non-Polyposis Colorectal Cancer 5

Cancer, Colorectal, Nonpolyposis, Hereditary, Type 5

Muir-Torre Syndrome

MRTES

Keratoacanthoma

Muir-Torré Syndrome

Cutaneous Sebaceous Neoplasms And Keratoacanthomas, Multiple, With Gastrointestinal And Other Carcinomas

Cutaneous Sebaceous Neoplasms And Keratoacanthomas Multiple With Gastrointestinal And Other Carcinomas

Multiple Keratoacanthoma, Muir-Torre Type

Mts

Torre-Muir Syndrome

Retinitis Pigmentosa 77

RP77

Retinitis Pigmentosa, Type 77

Mismatch Repair Cancer Syndrome

Turcot Syndrome

Brain Tumor-Polyposis Syndrome 1

Btp1 Syndrome

Btps1

Childhood Cancer Syndrome

Cmmr-D Syndrome

Cmmrds

Constitutional Mismatch Repair Deficiency Syndrome

Mmr Deficiency

Cancer Syndrome, Mismatch Repair

Malignant Childhood Neoplasm

Lynch Syndrome

Hereditary Nonpolyposis Colon Cancer

Hereditary Nonpolyposis Colorectal Cancer

Hereditary Nonpolyposis Colorectal Carcinoma

Hereditary Nonpolyposis Colorectal Neoplasms

Familial Nonpolyposis Colon Cancer

Hnpcc

Coca 1

Hereditary Defective Mismatch Repair Syndrome

Hereditary Non-Polyposis Colon Cancer

Hereditary Non-Polyposis Colon Cancer Syndrome

Hereditary Non-Polyposis Colorectal Cancer

Hereditary Non-Polyposis Colorectal Cancer Syndrome

Hereditary Nonpolyposis Colon Cancer Syndrome

Hereditary Nonpolyposis Colorectal Cancer Syndrome

Hereditary Nonpolyposis Colorectal Neoplasm

Hnpcc - Hereditary Nonpolyposis Colon Cancer

Cancer Family Syndrome

Familial Nonpolyposis Colorectal Cancer

Colon Cancer, Familial Nonpolyposis

Colorectal Neoplasms, Hereditary Nonpolyposis

Cancer, Colorectal, Nonpolyposis, Hereditary

Colorectal Cancer, Hereditary Nonpolyposis, Type 1

Rectal Benign Neoplasm

Neoplasm Of Rectum

Rectal Tumor

Rectum Neoplasm

Neoplasm Of The Rectum

Rectal Neoplasms

Primary Rectal Cancer

Rectal Ampulla Cancer

Cancer Of The Rectum

Carcinoma Of Rectum

Primary Malignant Neoplasm Of Rectum

Rectal Cancer

Rectal Carcinoma

Spastic Paraplegia 10, Autosomal Dominant

SPG10

Hereditary Spastic Paraplegia 10

Autosomal Dominant Spastic Paraplegia Type 10

Spastic Paraplegia 10

Spastic Paraplegia 10 With Or Without Peripheral Neuropathy

Autosomal Dominant Spastic Paraplegia 10

Autosomal Dominant Spastic Paraplegia

Spastic Paraplegia, Autosomal Dominant

Paraplegia, Spastic, Autosomal Dominant, Type 10

Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia

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 REEP5 VGNC VGNC:76864
Mus musculus REEP5 MGD MGI:1270152
Felis catus REEP5 VGNC VGNC:64563
Bos taurus REEP5 VGNC VGNC:33855
Rattus norvegicus REEP5 RGD RGD:1306047
Canis familiaris REEP5 VGNC VGNC:45464