1. Gene
  2. SLC25A33 - solute carrier family 25 member 33 Gene

SLC25A33 - solute carrier family 25 member 33 Gene

中文名称:溶质载体家族 25 成员 33

种属: Homo sapiens

同用名: PNC1; BMSC-MCP

基因 ID: 84275 | 基因类型: protein coding

关于 SLC25A33

Cytogenetic location: 1p36.22 Genomic coordinates (GRCh38): 1:9,539,465-9,585,173 (from NCBI)

This gene has 1 transcript (splice variant), 198 orthologues and 49 paralogues. Broad expression in testis (RPKM 27.8), fat (RPKM 18.2) and 23 other tissues.

功能概要

SLC25A33 属于线粒体载体蛋白的 SLC25 家族 (Haitina 等人,2006 [PubMed 16949250]) 。[OMIM 提供,2008 年 3 月]

SLC25A33 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]

SLC25A33 基因产物(1)

mRNA Protein Name
NM_032315.3 NP_115691.1 solute carrier family 25 member 33
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables pyrimidine nucleotide transmembrane transporter activity IDA
IDA: 通过直接分析推断
17596519 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

SLC25A33 蛋白结构

Mito_carr

Mito_carr: Mitochondrial carrier protein (8 - 120)

Mito_carr

Mito_carr: Mitochondrial carrier protein (127 - 216)

Mito_carr

Mito_carr: Mitochondrial carrier protein (230 - 317)

  • 0
  • 100
  • 200
  • 300
  • 321 a.a.
蛋白主名 其他名称

solute carrier family 25 member 33

bone marrow stromal cell mitochondrial carrier protein

关联疾病

疾病名称 别名
Schnyder Corneal Dystrophy

Schnyder Crystalline Corneal Dystrophy

SCCD

Corneal Dystrophy, Crystalline, Of Schnyder

Corneal Dystrophy, Schnyder Type

Corneal Dystrophy Crystalline Of Schnyder

Crystalline Stromal Dystrophy

Hereditary Crystalline Stromal Dystrophy Of Schnyder

Scd

Corneal Dystrophy, Schnyder

Schnyder Crystalline Dystrophy Sine Crystals

Dystrophy, Corneal, Crystalline, Schnyder

Orofaciodigital Syndrome Viii

Edwards Syndrome

Trisomy 18

Complete Trisomy 18 Syndrome

OFD8

Orofaciodigital Syndrome 8

Trisomy 18 Syndrome

Oral-Facial-Digital Syndrome With Hypoplastic Epiglottis

E3 Trisomy

Oral-Facial-Digital Syndrome Type 8

Orofaciodigital Syndrome Type 8

Ofds Viii

Oral-Facial-Digital Syndrome, Type Viii

Ofd Syndrome 8

Ofds 8

Oral Facial Digital Syndrome 8

Oral Facial Digital Syndrome Type 8

18 Trisomy

Chromosome 18 Trisomy

Trisomy 16-18

Trisomy E

Trisomy E Syndrome

Chromosome 18 Duplication

Oral-Facial-Digital Syndrome, Edwards Type

Orofaciodigital Syndrome, Edwards Type

Chromosome 18, Trisomy

Cleft Lip/Palate With Abnormal Thumbs And Microcephaly

Trisomy 18 Chromosome

Abnormal Autosomes 18

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
Mus musculus SLC25A33 MGD MGI:1917806
Bos taurus SLC25A33 VGNC VGNC:34759
Canis familiaris SLC25A33 VGNC VGNC:46307
Rattus norvegicus SLC25A33 RGD RGD:1583942
Felis catus SLC25A33 VGNC VGNC:65270