1. Gene
  2. ZMYM4 - zinc finger MYM-type containing 4 Gene

ZMYM4 - zinc finger MYM-type containing 4 Gene

中文名称:含锌指 MYM 型 4

种属: Homo sapiens

同用名: MYM; CDIR; ZNF262; ZNF198L3

基因 ID: 9202 | 基因类型: protein coding

关于 ZMYM4

Cytogenetic location: 1p34.3 Genomic coordinates (GRCh38): 1:35,268,709-35,422,058 (from NCBI)

This gene has 6 transcripts (splice variants), 132 orthologues and 18 paralogues. Ubiquitous expression in testis (RPKM 15.0), ovary (RPKM 10.1) and 25 other tissues.

功能概要

预测启用 DNA 结合活性。参与细胞骨架组织和细胞形态发生的调节。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable DNA binding activity. Involved in Cytoskeleton organization and regulation of cell morphogenesis. [provided by Alliance of Genome Resources, Apr 2022]

ZMYM4 基因产物(5)

mRNA Protein Name
NM_001350138.2 NP_001337067.1 zinc finger MYM-type protein 4 isoform 2
NM_001350139.2 NP_001337068.1 zinc finger MYM-type protein 4 isoform 3
NM_001350140.2 NP_001337069.1 zinc finger MYM-type protein 4 isoform 3
NM_001375653.1 NP_001362582.1 zinc finger MYM-type protein 4 isoform 4
NM_005095.3 NP_005086.2 zinc finger MYM-type protein 4 isoform 1
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 protein binding IPI
IPI: 通过物理相互作用推断
25416956 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cytoskeleton organization IMP
IMP: 通过突变表型推断
21834987 GOA
involved in regulation of cell morphogenesis IMP
IMP: 通过突变表型推断
21834987 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

ZMYM4 蛋白结构

zf-FCS

zf-FCS: MYM-type Zinc finger with FCS sequence motif (335 - 373)

zf-FCS

zf-FCS: MYM-type Zinc finger with FCS sequence motif (382 - 425)

zf-FCS

zf-FCS: MYM-type Zinc finger with FCS sequence motif (479 - 521)

zf-FCS

zf-FCS: MYM-type Zinc finger with FCS sequence motif (683 - 719)

zf-FCS

zf-FCS: MYM-type Zinc finger with FCS sequence motif (722 - 760)

DUF3504

DUF3504: Domain of unknown function (DUF3504) (1354 - 1527)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1548 a.a.
蛋白主名 其他名称

zinc finger MYM-type protein 4

cell death inhibiting RNA

ZMYM4 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
ZMYM4 Q5VZL5 ROR2 Homo sapiens A1L4F5 25416956
种属内
ZMYM4 Q5VZL5 ROR2 Homo sapiens A1L4F5 25416956
种属内
ZMYM4 Q5VZL5 ROR2 Homo sapiens A1L4F5 25416956
种属内
ZMYM4 Q5VZL5 UBQLN1 Homo sapiens Q9UMX0-2 25416956
种属内
ZMYM4 Q5VZL5 UBQLN1 Homo sapiens Q9UMX0-2 25416956
种属内
ZMYM4 Q5VZL5 RUNX1T1 Homo sapiens Q06455-4 25416956
种属内
ZMYM4 Q5VZL5 FHL2 Homo sapiens Q14192 25416956
种属内
ZMYM4 Q5VZL5 FHL2 Homo sapiens Q14192 25416956
种属内
ZMYM4 Q5VZL5 UBQLN1 Homo sapiens Q9UMX0 25416956
种属内
ZMYM4 Q5VZL5 UBQLN1 Homo sapiens Q9UMX0 25416956
种属内
ZMYM4 Q5VZL5 CTCF Homo sapiens P49711 25416956
种属内
ZMYM4 Q5VZL5 CTCF Homo sapiens P49711 25416956
种属内
ZMYM4 Q5VZL5 CTCF Homo sapiens P49711 25416956
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
Parkinson Disease 20, Early-Onset

Early-Onset Parkinson Disease 20

PARK20

Parkinson'S Disease 20

Early-Onset Parkinson'S Disease 20

Parkinson Disease, Type 20, Early-Onset

Non-Syndromic X-Linked Intellectual Disability

X-Linked Non-Syndromic Intellectual Disability

Non-Specific X-Linked Mental Retardation

X-Linked Non-Specific Intellectual Disability

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 ZMYM4 MGD MGI:1915035
Felis catus ZMYM4 VGNC VGNC:67260
Macaca mulatta ZMYM4 VGNC VGNC:78887
Rattus norvegicus ZMYM4 RGD RGD:1309545
Bos taurus ZMYM4 VGNC VGNC:37200
Canis familiaris ZMYM4 VGNC VGNC:48648