KANSL1 Protein, KAT8 regulatory NSL complex subunit 1

KANSL1

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KANSL1

Official Full Name KAT8 regulatory NSL complex subunit 1
Background This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The corresponding protein in Drosophila interacts with K(lysine) acetyltransferase 8, which is also a subunit of both the MLL1 and NSL1 complexes. [provided by RefSeq, Jun 2012]
Synonyms KANSL1; KAT8 regulatory NSL complex subunit 1; KDVS; NSL1; MSL1v1; CENP-36; hMSL1v1; KIAA1267; MSL1 homolog 1; centromere protein 36; NSL complex protein NSL1; non-specific lethal 1 homolog; male-specific lethal 1 homolog; MLL1/MLL complex subunit KANSL1;
 
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KANSL1 involved in several pathways and played different roles in them. We selected most pathways KANSL1 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with KANSL1 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein

KANSL1 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by KANSL1 itself. We selected most functions KANSL1 had, and list some proteins which have the same functions with KANSL1. You can find most of the proteins on our site.

Function Related Protein

KANSL1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with KANSL1 here. Most of them are supplied by our site. Hope this information will be useful for your research of KANSL1.

Panagopoulos, I; Gorunova, L; et al. Novel KAT6B-KANSL1 Fusion Gene Identified by RNA Sequencing in Retroperitoneal Leiomyoma with t(10;17)(q22;q21). PLoS One 10:-(2015).
Simioni, M; Araujo, TK; et al. Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation. JOURNAL OF HUMAN GENETICS 60:17-25(2015).

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