KCTD5 - potassium channel tetramerization domain containing 5 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 54442

About KCTD5

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:2,682,523-2,709,030 (from NCBI)

This gene has 5 transcripts (splice variants), 219 orthologues and 3 paralogues. Ubiquitous expression in colon (RPKM 15.1), esophagus (RPKM 11.8) and 25 other tissues.

Summary

Enables identical protein binding activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

KCTD5 Products (1)

mRNA Protein Name
NM_018992.4 NP_061865.1 BTB/POZ domain-containing protein KCTD5
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
27152988 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17239418 GOA
enables protein-containing complex binding IDA
IDA: Inferred from direct assay
23209302 GOA
Cellular Component GO Annotation Evidence References Source
located in cytosol IDA
IDA: Inferred from direct assay
18573101 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

KCTD5 Protein Structure

BTB_2

BTB_2: BTB/POZ domain (46 - 135)

  • 0
  • 100
  • 200
  • 234 a.a.
Protein Preferred Names Protein Names

BTB/POZ domain-containing protein KCTD5

  • potassium channel tetramerisation domain containing 5

KCTD5 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
KCTD5 Q9NXV2 GIT2 Homo sapiens Q14161 21988832
Intra
KCTD5 Q9NXV2 KCTD5 Homo sapiens Q9NXV2
EM
27152988
Intra
KCTD5 Q9NXV2 KCTD5 Homo sapiens Q9NXV2
GMS
27152988
Intra
KCTD5 Q9NXV2 CD1A Homo sapiens P06126 21988832
Intra
KCTD5 Q9NXV2 Rep78 Adeno-associated virus 2 Q89268
IF
17239418
Intra
KCTD5 Q9NXV2 Rep78 Adeno-associated virus 2 Q89268 17239418
Cross
KCTD5 Q9NXV2 Rep68 Adeno-associated virus 2 P03132 17239418
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Scalp-Ear-Nipple Syndrome
  • Finlay-Marks Syndrome

  • Sen Syndrome

  • SENS

  • Scalp Ear Nipple Syndrome

  • Hereditary Syndrome Of Lumpy Scalp, Odd Ears And Rudimentary Nipples

  • Hereditary Syndrome Of Lumpy Scalp, Odd Ears, And Rudimentary Nipples

  • Indian Childhood Cirrhosis

Branchiooculofacial Syndrome
  • Branchio-Oculo-Facial Syndrome

  • BOFS

  • Bof Syndrome

  • Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome

  • Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome

  • Branchial Clefts With Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, And Premature Aging

  • Branchial Clefts With Characteristic Facies Growth Retardation Imperforate Nasolacrimal Duct And Premature Aging

  • Bofs Syndrome

  • Lip Pseudocleft-Hemagiomatous Branchial Cyst Syndrome

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
Macaca mulatta KCTD5 VGNC VGNC:73876
Mus musculus KCTD5 MGD MGI:1916509
Canis familiaris KCTD5 VGNC VGNC:42309
Felis catus KCTD5 VGNC VGNC:97472
Rattus norvegicus KCTD5 RGD RGD:1304990
Bos taurus KCTD5 VGNC VGNC:30513
Others KCTD5 NCBI