NCAPH2 - non-SMC condensin II complex subunit H2 Gene

Homo sapiens

Also known as CAPH2

Gene ID: 29781 | Gene type: protein coding

About NCAPH2

Cytogenetic location: 22q13.33 Genomic coordinates (GRCh38): 22:50,508,224-50,524,780 (from NCBI)

This gene has 10 transcripts (splice variants) and 191 orthologues. Ubiquitous expression in bone marrow (RPKM 17.2), testis (RPKM 13.4) and 25 other tissues.

Summary

This gene encodes one of the non-SMC subunits of the condensin II complex. This complex plays an essential role in mitotic chromosome assembly. Alternate splicing of this gene results in multiple transcript variants.[provided by RefSeq, May 2010]

NCAPH2 Products(3)

mRNA	Protein	Name
NM_001185011.2	NP_001171940.1	condensin-2 complex subunit H2 isoform 3
NM_014551.5	NP_055366.3	condensin-2 complex subunit H2 isoform 1
NM_152299.4	NP_689512.2	condensin-2 complex subunit H2 isoform 2

NCAPH2 Protein Structure

CNDH2_N

0
100
200
300
400
500
605 a.a.

Protein Preferred Names

Protein Names

condensin-2 complex subunit H2

CAP-H2 subunit of the condensin II complex

Related Diseases

Diseases

Alias

Myopia 6

MYP6	Myopia, Susceptibility To
Myopia, Type 6

Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency

Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency	Fatal Infantile Cox Deficiency
Fatal Infantile Cytochrome C Oxidase Deficiency	Fatal Infantile Encephalocardiomyopathy

Mitochondrial Complex Iv Deficiency, Nuclear Type 2

Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 1	MC4DN2
Cemcox1	Mitochondrial Complex Ii Deficiency, Nuclear Type 4
MC2DN4	Mitochondrial Complex 2 Deficiency, Nuclear Type 4
Cytochrome C Oxidase Deficiency, Fatal Infantile, With Cardioencephalomyopathy	Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency 1
Cytochrome C Oxidase Deficiency With Fatal Infantile Cardioencephalomyopathy	Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency

Dilated Cardiomyopathy

Familial Dilated Cardiomyopathy	Primary Dilated Cardiomyopathy
Idiopathic Dilated Cardiomyopathy	Congestive Cardiomyopathy
Idiopathic Dilation Cardiomyopathy	Primary Familial Dilated Cardiomyopathy
Cardiomyopathy, Dilated	DCM
Cardiomyopathy, Familial Dilated	Dilated Cardiomyopathy, Familial
Hypokinetic Dilated Cardiomyopathy, Familial	Familial Idiopathic Cardiomyopathy
Fdc	Cardiomyopathy, Familial Idiopathic
Idiopathic Cardiomegaly	Dilated Congestive Cardiomyopathy
Chronic Dilated Cardiomyopathy	Ccm - [Congestive Cardiomyopathy]
Cocm - [Congestive Cardiomyopathy]	Dcm - [Dilated Cardiomyopathy]
Dilated-Hypokinetic Cardiomyopathy	Congestive Idiopathic Cardiomyopathy
Primary Idiopathic Dilated Cardiomyopathy

Pleural Empyema

Empyema	Pyothorax
Empyema, Pleural	Abscess Of Pleural Cavity
Abscess Of Thorax	Empyema Of Pleura
Empyema Of Pleura Without Fistula	Empyema With Fistula
Empyema With No Fistula	Empyema With Pleural Fistula
Empyema Without Mention Of Fistula	Empyema, Chest
Lung Empyema	Pleural Empyema With Fistula
Pleural Empyema With No Fistula	Purulent Pleurisy
Purulent Pleuritis	Thorax Abscess
Pyopneumothorax

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-RS09071	NCAPH2 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	NCAPH2	VGNC	VGNC:43644
Rattus norvegicus	NCAPH2	RGD	RGD:1565937
Macaca mulatta	NCAPH2	VGNC	VGNC:75018
Felis catus	NCAPH2	VGNC	VGNC:63735
Bos taurus	NCAPH2	VGNC	VGNC:31906
Mus musculus	NCAPH2	MGD	MGI:1289164

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