1. Gene
  2. ZNF595 - zinc finger protein 595 Gene

ZNF595 - zinc finger protein 595 Gene

中文名称:锌指蛋白 595

种属: Homo sapiens

基因 ID: 152687 | 基因类型: protein coding

关于 ZNF595

This gene has 5 transcripts (splice variants), 18 orthologues and 174 paralogues. Ubiquitous expression in placenta (RPKM 5.3), ovary (RPKM 4.1) and 25 other tissues.

功能概要

该基因编码属于 Cys2His2 锌指蛋白家族的一种蛋白质,其成员作为转录因子发挥作用,可以调节多种发育和细胞过程。该基因的可变剪接导致多个转录变体。[RefSeq 提供,2013 年 10 月]

This gene encodes a protein belonging to the Cys2His2 Zinc Finger Protein family, whose members function as transcription factors that can regulate a broad variety of developmental and cellular processes. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Oct 2013]

ZNF595 基因产物(4)

mRNA Protein Name
NM_001286052.2 NP_001272981.1 zinc finger protein 595 isoform b
NM_001286053.2 NP_001272982.1 zinc finger protein 595 isoform c
NM_001286054.2 NP_001272983.1 zinc finger protein 595 isoform c
NM_182524.4 NP_872330.1 zinc finger protein 595 isoform a
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

ZNF595 蛋白结构

KRAB

KRAB: KRAB box (4 - 44)

  • 0
  • 85 a.a.
蛋白主名 其他名称

zinc finger protein 595

ZNF595 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
ZNF595 Q8IYB9 KRTAP10-6 Homo sapiens P60371 32296183
种属内
ZNF595 Q8IYB9 KRTAP10-6 Homo sapiens P60371 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
Warburg Micro Syndrome 1

Warburg Micro Syndrome

Micro Syndrome

Warbm

WARBM1

Warburg Sjo Fledelius Syndrome

Warburg-Sjo-Fledelius Syndrome

Micro Syndrome 1

Microcephaly, Microcornea, Congenital Cataract, Intellectual Disability, Optic Atrophy And Hypogenitalism

Ciliary Dyskinesia, Primary, 4

Primary Ciliary Dyskinesia 4

CILD4

Ciliary Dyskinesia, Primary, 4, With Or Without Situs Inversus

Primary Ciliary Dyskinesia 4 With Or Without Situs Inversus

Primary Ciliary Dyskinesia, 4

Ciliary Dyskinesia, Primary, 8

Primary Ciliary Dyskinesia 8

CILD8

Ciliary Dyskinesia, Primary, 8, With Or Without Situs Inversus

Primary Ciliary Dyskinesia 8 With Or Without Situs Inversus

Warburg Micro Syndrome 3

WARBM3

Micro Syndrome 3

Warburg Micro Syndrome 2

WARBM2

Micro Syndrome 2

Wolf-Hirschhorn Syndrome

Pitt-Rogers-Danks Syndrome

WHS

Chromosome 4p16.3 Deletion Syndrome

Wittwer Syndrome

4p- Syndrome

Pitt Syndrome

4p Deletion Syndrome

Distal Deletion 4p

Distal Monosomy 4p

Telomeric Deletion 4p

Prds

4p Syndrome

Chromosome 4p Syndrome

Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation

Wolf Syndrome

Chromosome 4p Deletion Syndrome

Chromosome 4p Monosomy

Del Syndrome

Monosomy 4p

Partial Monosomy 4p

Chromosome 4 Short Arm Deletion

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 ZNF595 VGNC VGNC:79655