1. Gene
  2. SBSN - suprabasin Gene

SBSN - suprabasin Gene

中文名称:上盆地

种属: Homo sapiens

同用名: UNQ698

基因 ID: 374897 | 基因类型: protein coding

关于 SBSN

Cytogenetic location: 19q13.12 Genomic coordinates (GRCh38): 19:35,523,367-35,528,311 (from NCBI)

This gene has 3 transcripts (splice variants) and 97 orthologues. Restricted expression toward skin (RPKM 753.6).

功能概要

位于细胞外外泌体。 [由基因组资源联盟提供,2022 年 4 月]

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

SBSN 基因产物(3)

mRNA Protein Name
NM_001166034.2 NP_001159506.1 suprabasin isoform 1 precursor
NM_001166035.2 NP_001159507.1 suprabasin isoform 3 precursor
NM_198538.4 NP_940940.1 suprabasin isoform 2 precursor
基因本体论
  • 分子功能
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
32296183 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
蛋白主名 其他名称

suprabasin

HLAR698

关联疾病

疾病名称 别名
Metal Allergy
Salivary Gland Adenoid Cystic Carcinoma

Cylindroma

Fuchs' Endothelial Dystrophy

Fuchs Endothelial Corneal Dystrophy

Fuchs Endothelial Dystrophy

Fuchs Dystrophy

Fced

Fuchs' Corneal Dystrophy

Fuchs' Endothelial Corneal Dystrophy

Fuchs Atrophy

Fuchs Corneal Dystrophy

Endoepithelial Corneal Dystrophy

Fecd

Late Hereditary Endothelial Dystrophy

Corneal Dystrophy, Fuchs Endothelial

Dystrophy, Corneal, Fuchs Endothelial

Corneal Dystrophy, Fuchs' Endothelial, 1

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
Rattus norvegicus SBSN RGD RGD:1562305
Bos taurus SBSN VGNC VGNC:34310
Mus musculus SBSN MGD MGI:2446326
Felis catus SBSN VGNC VGNC:64890