KANSL3 - KAT8 regulatory NSL complex subunit 3 Gene

Homo sapiens

Also known as NSL3; Rcd1; KIAA1310

Gene ID: 55683 | Gene type: protein coding

About KANSL3

Cytogenetic location: 2q11.2 Genomic coordinates (GRCh38): 2:96,580,494-96,638,312 (from NCBI)

This gene has 21 transcripts (splice variants), 203 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 20.0), ovary (RPKM 12.2) and 25 other tissues.

Summary

Involved in histone H4-K16 acetylation; histone H4-K5 acetylation; and histone H4-K8 acetylation. Located in nucleoplasm. Part of Histone Acetyltransferase complex. [provided by Alliance of Genome Resources, Apr 2022]

KANSL3 Products(8)

mRNA	Protein	Name
NM_001115016.3	NP_001108488.1	KAT8 regulatory NSL complex subunit 3 isoform 1
NM_001349256.2	NP_001336185.1	KAT8 regulatory NSL complex subunit 3 isoform 2
NM_001349257.2	NP_001336186.1	KAT8 regulatory NSL complex subunit 3 isoform 3
NM_001349258.2	NP_001336187.1	KAT8 regulatory NSL complex subunit 3 isoform 4
NM_001349259.2	NP_001336188.1	KAT8 regulatory NSL complex subunit 3 isoform 5
NM_001349260.2	NP_001336189.1	KAT8 regulatory NSL complex subunit 3 isoform 6
NM_001349261.2	NP_001336190.1	KAT8 regulatory NSL complex subunit 3 isoform 7
NM_001349262.2	NP_001336191.1	KAT8 regulatory NSL complex subunit 3 isoform 7

KANSL3 Protein Structure

Abhydrolase_5

0
200
400
600
800
878 a.a.

Protein Preferred Names

Protein Names

KAT8 regulatory NSL complex subunit 3

NSL complex protein NSL3

Related Diseases

Diseases

Alias

Mixed Cerebral Palsy

Cerebral Palsy, Mixed

Maxillonasal Dysplasia, Binder Type

Binder Syndrome	Binder Type Maxillonasal Dysplasia
Maxillonasal Dysplasia	Maxillonasal Dysostosis

Nodular Ganglioneuroblastoma

Ganglioneuroblastoma, Nodular

Discitis

Osteogenesis Imperfecta, Type Iv

Osteogenesis Imperfecta Type 4	Osteogenesis Imperfecta Type Iv
OI4	Oi, Type Iv
Osteogenesis Imperfecta With Normal Sclerae	Oi Type Iv
Oi Type 4	Osteogenesis Imperfecta With Normal Sclera
Common Variable Oi With Normal Sclerae	Osteogenesis Imperfecta 4
Oi-Iv

Osteogenesis Imperfecta, Type Iii

Osteogenesis Imperfecta Type Iii	OI3
Oi, Type Iii	Osteogenesis Imperfecta Type 3
Oi Type Iii	Oi Type 3
Progressive Deforming Osteogenesis Imperfecta	Severe Osteogenesis Imperfecta
Osteogenesis Imperfecta, Progressively Deforming, With Normal Sclerae	Progressively Deforming Osteogenesis Imperfecta With Normal Sclera
Osteogenesis Imperfecta, Progressively Deforming With Normal Sclerae	Progressively Deforming Oi
Osteogenesis Imperfecta 3	Oi-Iii
Progressively Deforming Osteogenesis Imperfecta With Normal Sclerae

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS07069	KANSL3 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	KANSL3	RGD	RGD:1309220
Mus musculus	KANSL3	MGD	MGI:1918055
Felis catus	KANSL3	VGNC	VGNC:63021
Macaca mulatta	KANSL3	VGNC	VGNC:73907
Canis familiaris	KANSL3	VGNC	VGNC:42206
Bos taurus	KANSL3	VGNC	VGNC:30395

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