KANSL1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | KANSL1 , KAT8 regulatory NSL complex subunit 1, NSL1, KIAA1267, MSL1v1, CENP-36, hMSL1v1, KDVS | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 612452; MGI: 1923969; HomoloGene: 9140; GeneCards: KANSL1; OMA:KANSL1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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KAT8 regulatory NSL complex subunit 1 is a protein that in humans is encoded by the KANSL1 gene. [5] [6]
Spermatid perinuclear RNA-binding protein is a protein that in humans is encoded by the STRBP gene.
SECIS-binding protein 2 is a protein that in humans is encoded by the SECISBP2 gene.
Myotubularin-related protein 6 is a protein that in humans is encoded by the MTMR6 gene.
CCR4-NOT transcription complex subunit 8 is a protein that in humans is encoded by the CNOT8 gene. It is a subunit of the CCR4-Not deadenylase complex.
Adaptin ear-binding coat-associated protein 2 is a protein that in humans is encoded by the NECAP2 gene.
Synaptotagmin-3 is a protein that in humans is encoded by the SYT3 gene.
Beta-taxilin is a protein that in humans is encoded by the TXLNB gene.
Histone deacetylase complex subunit SAP130 is an enzyme that in humans is encoded by the SAP130 gene.
Histone deacetylase 11 is a 39kDa histone deacetylase enzyme that in humans is encoded by the HDAC11 gene on chromosome 3 in humans and chromosome 6 in mice.
Lethal(3)malignant brain tumor-like 2 protein is a protein that in humans is encoded by the L3MBTL2 gene.
LisH domain-containing protein ARMC9 is a protein that in humans is encoded by the ARMC9 gene.
BRCA1-A complex subunit MERIT40 is a protein that in humans is encoded by the BABAM1 gene.
Spartan (SPRTN) is a protein that in humans is encoded by the SPRTN gene. It is involved in DNA repair. Ruijs-Aalfs syndrome is an autosomal recessive genetic disorder. Characteristics of this disorder are features of premature aging, chromosome instability and development of hepatocellular carcinoma. Ruijs-Aalfs syndrome arises as a result of mutations in the SPRTN gene that encodes a metalloproteinase employed in the repair of protein-linked DNA breaks.
Secretory carrier-associated membrane protein 5 is a protein that in humans is encoded by the SCAMP5 gene.
KANSL3, or KAT8 regulatory NSL complex subunit 3 is a protein that in humans is encoded by the KANSL3 gene.
Zinc finger protein 471 is a protein that in humans is encoded by the ZNF471 gene.
Zinc finger protein 34 is a protein that in humans is encoded by the ZNF34 gene.
Ankyrin repeat domain-containing protein 13C is a protein that in humans is encoded by the ANKRD13C gene.
Kelch-like protein 18 is a protein that in humans is encoded by the KLHL18 gene.
60S ribosomal protein L10-like is a protein that in humans is encoded by the RPL10L gene.