NAP1L3 - nucleosome assembly protein 1 like 3 Gene

Homo sapiens

Also known as MB20; NPL3

Gene ID: 4675 | Gene type: protein coding

About NAP1L3

Cytogenetic location: Xq21.32 Genomic coordinates (GRCh38): X:93,670,930-93,673,578 (from NCBI)

This gene has 2 transcripts (splice variants), 207 orthologues and 18 paralogues.

Summary

This gene is intronless and encodes a member of the nucleosome assembly protein (NAP) family. This gene is linked closely to a region of genes responsible for several X-linked cognitive disability syndromes. [provided by RefSeq, Dec 2010]

NAP1L3 Products(1)

mRNA	Protein	Name
NM_004538.6	NP_004529.2	nucleosome assembly protein 1-like 3

NAP1L3 Protein Structure

NAP

0
100
200
300
400
506 a.a.

Protein Preferred Names

Protein Names

nucleosome assembly protein 1-like 3

Related Diseases

Diseases

Alias

Noonan Syndrome 8

NS8	Noonan Syndrome, Type 8

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-RS09027	NAP1L3 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	NAP1L3	VGNC	VGNC:43616
Macaca mulatta	NAP1L3	VGNC	VGNC:75130
Rattus norvegicus	NAP1L3	RGD	RGD:620990
Mus musculus	NAP1L3	MGD	MGI:1859565

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