1. Gene
  2. DRC7 - dynein regulatory complex subunit 7 Gene

DRC7 - dynein regulatory complex subunit 7 Gene

中文名称:动力蛋白调节复合物亚基 7

种属: Homo sapiens

同用名: FAP50; CFAP50; CCDC135; C16orf50

基因 ID: 84229 | 基因类型: protein coding

关于 DRC7

Cytogenetic location: 16q21 Genomic coordinates (GRCh38): 16:57,694,806-57,731,805 (from NCBI)

This gene has 10 transcripts (splice variants) and 139 orthologues. Restricted expression toward testis (RPKM 24.8).

功能概要

预测参与有鞭毛的精子活动。位于细胞质中。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to be involved in flagellated sperm motility. Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

DRC7 基因产物(3)

mRNA Protein Name
NM_001289162.2 NP_001276091.1 dynein regulatory complex subunit 7 isoform a
NM_001289163.2 NP_001276092.1 dynein regulatory complex subunit 7 isoform b
NM_032269.6 NP_115645.4 dynein regulatory complex subunit 7 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
24407287 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

dynein regulatory complex subunit 7

coiled-coil domain containing 135

DRC7 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
DRC7 Q8IY82 MBIP Homo sapiens Q9NS73-5 25416956
种属内
DRC7 Q8IY82 NEK7 Homo sapiens Q8TDX7 32814053
种属内
DRC7 Q8IY82 NEK7 Homo sapiens Q8TDX7 32814053
种属内
DRC7 Q8IY82 NEK7 Homo sapiens Q8TDX7 32814053
种属内
DRC7 Q8IY82 EFHC2 Homo sapiens Q5JST6 32296183
种属内
DRC7 Q8IY82 EFHC2 Homo sapiens Q5JST6 32296183
种属内
DRC7 Q8IY82 DLST Homo sapiens P36957 32814053
种属内
DRC7 Q8IY82 DLST Homo sapiens P36957 32814053
种属内
DRC7 Q8IY82 DLST Homo sapiens P36957 32814053
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
Polycystic Kidney Disease 2 With Or Without Polycystic Liver Disease

Polycystic Kidney Disease 2

PKD2

Polycystic Kidney Disease, Adult, Type Ii

Apkd2

Polycystic Kidney Disease, Type 2

Adpkd2

Adult Polycystic Kidney Disease Type 2

Autosomal Dominant Polycystic Kidney Disease 2

Pkd-2

Polycystic Kidney Disease Adult Type Ii

Polycystic Kidney Type 2 Autosomal Dominant Disease

Kidney Disease, Polycystic, Type 2

Bardet-Biedl Syndrome 1

BBS1

Bardet-Biedl Syndrome 1, Modifier Of

Bardet-Biedl Syndrome

BBS

Bardet-Biedl Syndrome, Type 1

Laurence-Moon-Bardet-Biedl Syndrome

Primary Ciliary Dyskinesia

Immotile Cilia Syndrome

Kartagener Syndrome

Dextrocardia Bronchiectasis And Sinusitis

Pcd

Ciliary Motility Disorders

Ciliary Motility Disorder

Immotile Ciliary Syndrome

Ciliary Dyskinesia Primary

Ics

Polynesian Bronchiectasis

Dextrocardia-Bronchiectasis-Sinusitis Syndrome

Immotile Cilia Syndrome, Kartagener Type

Primary Ciliary Dyskinesia And Situs Inversus

Primary Ciliary Dyskinesia, Kartagener Type

Siewert Syndrome

Dyskinesia, Ciliary, Primary

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
Felis catus DRC7 VGNC VGNC:61625
Bos taurus DRC7 VGNC VGNC:28206
Macaca mulatta DRC7 VGNC VGNC:71905
Canis familiaris DRC7 VGNC VGNC:40092
Rattus norvegicus DRC7 RGD RGD:1565601
Mus musculus DRC7 MGD MGI:2685616