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  2. ZCCHC7 - zinc finger CCHC-type containing 7 Gene

ZCCHC7 - zinc finger CCHC-type containing 7 Gene

中文名称:含锌指 CCHC 型 7

种属: Homo sapiens

同用名: AIR1; HSPC086

基因 ID: 84186 | 基因类型: protein coding

关于 ZCCHC7

This gene has 9 transcripts (splice variants), 203 orthologues and 3 paralogues. Ubiquitous expression in lymph node (RPKM 3.6), testis (RPKM 2.2) and 25 other tissues.

功能概要

启用 RNA 结合活性。位于胞质溶胶和核仁中。 [由基因组资源联盟提供,2022 年 4 月]

Enables RNA binding activity. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Apr 2022]

ZCCHC7 基因产物(4)

mRNA Protein Name
NM_001289119.2 NP_001276048.1 zinc finger CCHC domain-containing protein 7
NM_001289120.2 NP_001276049.1 zinc finger CCHC domain-containing protein 7
NM_001289121.2 NP_001276050.1 zinc finger CCHC domain-containing protein 7
NM_032226.3 NP_115602.2 zinc finger CCHC domain-containing protein 7
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
25416956 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

ZCCHC7 蛋白结构

zf-CCHC

zf-CCHC: Zinc knuckle (242 - 257)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 543 a.a.
蛋白主名 其他名称

zinc finger CCHC domain-containing protein 7

TRAMP-like complex RNA-binding factor ZCCHC7

ZCCHC7 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
Intra ZCCHC7 Q8N3Z6 q59gp6_human Homo sapiens Q59GP6
Y2H Prey Pooling
25416956
Intra ZCCHC7 Q8N3Z6 q59gp6_human Homo sapiens Q59GP6
Y2H Array
25416956
Intra ZCCHC7 Q8N3Z6 NEK6 Homo sapiens Q9HC98-4
Validated Y2H
32296183
Intra ZCCHC7 Q8N3Z6 GIPC2 Homo sapiens Q8TF65
Validated Y2H
32296183
Intra ZCCHC7 Q8N3Z6 TRIM41 Homo sapiens Q8WV44
Validated Y2H
32296183
Intra ZCCHC7 Q8N3Z6 CARD9 Homo sapiens Q9H257
Y2H Array
25416956
Intra ZCCHC7 Q8N3Z6 CARD9 Homo sapiens Q9H257
Y2H Prey Pooling
25416956
Intra ZCCHC7 Q8N3Z6 CARD9 Homo sapiens Q9H257
Validated Y2H
25416956
Intra ZCCHC7 Q8N3Z6 KIF9 Homo sapiens Q9HAQ2
Validated Y2H
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
Trichohepatoenteric Syndrome 1

Trichohepatoenteric Syndrome

Syndromic Diarrhea

Tricho-Hepato-Enteric Syndrome

Sd/The

Syndromic Diarrhea/Tricho-Hepato-Enteric Syndrome

THES1

Phenotypic Diarrhea

Thes

Phenotypic Diarrhea Of Infancy

Diarrhea, Syndromic

Diarrhea, Fatal Infantile, With Trichorrhexis Nodosa

Intractable Diarrhea With Phenotypic Anomalies

Syndromatic Diarrhea

Fatal Infantile Diarrhea With Trichorrhexis Nodosa

Pontocerebellar Hypoplasia, Type 1e

Pontocerebellar Hypoplasia Type 1

PCH1E

Norman Disease

Pch1

Pontocerebellar Hypoplasia With Anterior Horn Cell Disease

Pontocerebellar Hypoplasia With Infantile Spinal Muscular Atrophy

Pontocerebellar Hypoplasia Type 1e

Pontocerebellar Hypoplasia 1e

Doid:0112322

Doid:0112330

Pontocerebellar Hypoplasia

Pch

Congenital Pontocerebellar Hypoplasia

Opch

Hypoplasia, Pontocerebellar

Pontoneocerebellar Hypoplasia

Nonsyndromic Pontocerebellar Hypoplasia

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 ZCCHC7 RGD RGD:1310467
Canis familiaris ZCCHC7 VGNC VGNC:53504
Bos taurus ZCCHC7 VGNC VGNC:37122
Macaca mulatta ZCCHC7 VGNC VGNC:82088
Felis catus ZCCHC7 VGNC VGNC:103010
Mus musculus ZCCHC7 MGD MGI:2442912