DRC7 - dynein regulatory complex subunit 7 Gene

Also Known as FAP50; CFAP50; CCDC135; C16orf50

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84229

About 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).

Summary

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

DRC7 Products (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
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
24407287 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

dynein regulatory complex subunit 7

  • coiled-coil domain containing 135

DRC7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
DRC7 Q8IY82 MBIP Homo sapiens Q9NS73-5 25416956
Intra
DRC7 Q8IY82 NEK7 Homo sapiens Q8TDX7 32814053
Intra
DRC7 Q8IY82 NEK7 Homo sapiens Q8TDX7 32814053
Intra
DRC7 Q8IY82 NEK7 Homo sapiens Q8TDX7 32814053
Intra
DRC7 Q8IY82 EFHC2 Homo sapiens Q5JST6 32296183
Intra
DRC7 Q8IY82 EFHC2 Homo sapiens Q5JST6 32296183
Intra
DRC7 Q8IY82 DLST Homo sapiens P36957 32814053
Intra
DRC7 Q8IY82 DLST Homo sapiens P36957 32814053
Intra
DRC7 Q8IY82 DLST Homo sapiens P36957 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
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

Diseases Alias
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

Orthologs Information

Species Symbol Source 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
Others DRC7 NCBI