CMC4 - C-X9-C motif containing 4 Gene

Homo sapiens

Also known as p8; C6.1B; MTCP1; MTCP1B; MTCP1NB; p8MTCP1

Gene ID: 100272147 | Gene type: protein coding

About CMC4

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:155,061,622-155,071,136 (from NCBI)

This gene has 2 transcripts (splice variants) and 134 orthologues. Ubiquitous expression in heart (RPKM 14.9), fat (RPKM 9.7) and 25 other tissues.

Summary

This gene was identified by involvement in some t(X;14) translocations associated with mature T-cell proliferations. This region has a complex gene structure, with a common promoter and 5' exon spliced to two different sets of 3' exons that encode two different proteins. This gene represents the downstream 8 kDa protein that localizes to mitochondria.[provided by RefSeq, Mar 2009]

CMC4 Products(1)

mRNA	Protein	Name
NM_001018024.3	NP_001018024.1	cx9C motif-containing protein 4

CMC4 Protein Structure

MTCP1

0
68 a.a.

Protein Preferred Names

Protein Names

cx9C motif-containing protein 4

C-x(9)-C motif containing 4 homolog

Related Diseases

Diseases

Alias

Rhabdomyolysis-Myalgia Syndrome

Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii

Microcephalic Osteodysplastic Primordial Dwarfism Type Ii	Majewski Osteodysplastic Primordial Dwarfism Type Ii
MOPD2	Mopd Ii
Osteodysplastic Primordial Dwarfism Type Ii	Mopdii
Osteodysplastic Primordial Dwarfism Type 2	Osteodysplastic Primordial Dwarfism, Type Ii
Pcnt-Related Microcephalic Osteodysplastic Primordial Dwarfism	Microcephalic Osteodysplastic Primordial Dwarfism Type 2
Mopd 2	Microcephalic Osteodysplastic Primordial Dwarfism With Tooth Abnormalities
Mopd Type Ii	Microcephalic Osteodysplastic Primordial Dwarfism 2
Dwarfism, Primordial, Osteodysplastic, Microcephalic Type Ii

Moyamoya Disease 1

Moyamoya Disease	Spontaneous Occlusion Of The Circle Of Willis
Mymy	Progressive Intracranial Arterial Occlusion
Moyamoya Syndrome	MYMY1
Cerebrovascular Moyamoya Disease	Moya-Moya Disease
Progressive Intracranial Occlusive Arteropathy	Idiopathic Moyamoya Disease

Schimke Immunoosseous Dysplasia

Schimke Immuno-Osseous Dysplasia	SIOD
Immunoosseous Dysplasia, Schimke Type	Schimke Syndrome
Immunoosseous Dysplasia Schimke Type	Spondyloepiphyseal Dysplasia - Nephrotic Syndrome
Spondyloepiphyseal Dysplasia Nephrotic Syndrome	Spondyloepiphyseal Dysplasia-Nephrotic Syndrome

Cerebral Arterial Disease

Cerebral Arterial Diseases

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-RS02858	CMC4 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	CMC4	VGNC	VGNC:60997
Mus musculus	CMC4	MGD	MGI:5637812
Bos taurus	CMC4	VGNC	VGNC:27479
Rattus norvegicus	CMC4	RGD	RGD:7647017

Name
Email *

	Sorry, but the email address you supplied was invalid.