1. Gene
  2. KCTD9 - potassium channel tetramerization domain containing 9 Gene

KCTD9 - potassium channel tetramerization domain containing 9 Gene

Homo sapiens

Also known as BTBD27

Gene ID: 54793 | Gene type: protein coding

About KCTD9

Cytogenetic location: 8p21.2 Genomic coordinates (GRCh38): 8:25,427,847-25,458,433 (from NCBI)

This gene has 11 transcripts (splice variants), 266 orthologues and 3 paralogues. Ubiquitous expression in heart (RPKM 8.3), esophagus (RPKM 7.8) and 25 other tissues.

Summary

Enables cullin family protein binding activity; identical protein binding activity; and protein self-association. Predicted to be involved in intracellular signal transduction; protein homooligomerization; and protein ubiquitination. [provided by Alliance of Genome Resources, Apr 2022]

KCTD9 Products(1)

mRNA Protein Name
NM_017634.4 NP_060104.2 BTB/POZ domain-containing protein KCTD9

KCTD9 Protein Structure

KHA

KHA: KHA, dimerisation domain of potassium ion channel (1 - 64)

BTB_2

BTB_2: BTB/POZ domain (91 - 182)

Pentapeptide

Pentapeptide: Pentapeptide repeats (8 copies) (248 - 279)

Pentapeptide

Pentapeptide: Pentapeptide repeats (8 copies) (338 - 376)

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  • 100
  • 200
  • 300
  • 389 a.a.
Protein Preferred Names Protein Names

BTB/POZ domain-containing protein KCTD9

potassium channel tetramerisation domain containing 9

Related Diseases

Diseases Alias
Progressive Myoclonus Epilepsy 3

Cln14 Disease

Epm3

Neuronal Ceroid Lipofuscinosis 14

Pme Type 3

Progressive Myoclonic Epilepsy Due To Kctd7 Deficiency

Progressive Myoclonus Epilepsy Type 3

Epilepsy, Progressive Myoclonic 3

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

Progressive Myoclonus Epilepsy

Pme

Progressive Myoclonic Epilepsy

Myoclonic Epilepsies, Progressive

Unverricht-Lundborg 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
Rattus norvegicus KCTD9 RGD RGD:1312010
Canis familiaris KCTD9 VGNC VGNC:42312
Bos taurus KCTD9 VGNC VGNC:30516
Felis catus KCTD9 VGNC VGNC:63065
Macaca mulatta KCTD9 VGNC VGNC:84009
Mus musculus KCTD9 MGD MGI:2145579