CMIP - c-Maf inducing protein Gene

Homo sapiens

Also known as TCMIP

Gene ID: 80790 | Gene type: protein coding

About CMIP

Cytogenetic location: 16q23.2-q23.3 Genomic coordinates (GRCh38): 16:81,444,808-81,711,762 (from NCBI)

This gene has 11 transcripts (splice variants) and 180 orthologues. Ubiquitous expression in brain (RPKM 12.0), small intestine (RPKM 8.6) and 25 other tissues.

Summary

This gene encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]

CMIP Products(2)

mRNA	Protein	Name
NM_030629.3	NP_085132.1	C-Maf-inducing protein isoform Tc-Mip
NM_198390.3	NP_938204.2	C-Maf-inducing protein isoform C-Mip

CMIP Protein Structure

LRR_6

0
200
400
600
773 a.a.

Protein Preferred Names

Protein Names

C-Maf-inducing protein

tc-Mip

Related Diseases

Diseases

Alias

Nephrotic Syndrome

Finnish Congenital Nephrotic Syndrome	Ns - [Nephrotic Syndrome]
Nephrosis Syndrome	Nephrosis Nos
Glomerular Lesion Nephrosis

Speech And Communication Disorders

Language Disorder	Communication Disorder
Language Disorders	Communication Disorders
Speech Language Disorder	Speech-Language Disorder
Communication Impairment	Speech And Language Disorder

Myasthenic Syndrome, Congenital, 11, Associated With Acetylcholine Receptor Deficiency

Congenital Myasthenic Syndrome 11	CMS11
Cms Ie	Cms1e
Myasthenic Syndrome, Congenital, Ie	Myasthenic Syndrome, Congenital, Ie, Formerly
Cms1e, Formerly	Cms Ie, Formerly
Congenital Myasthenic Syndrome 11 Associated With Acetylcholine Receptor Deficiency	Congenital Myasthenic Syndrome 1e
Myasthenic Syndrome, Congenital, Type 11, Associated With Acetylcholine Receptor Deficiency

Specific Language Impairment

Language Impairment, Specific

Reading Disorder

Specific Reading Disorder	Reading
Dyslexia	Developmental Reading Disorder

Lymphoepithelioma-Like Thymic Carcinoma

Lymphoepithelioma-Like Carcinoma Of The Thymus

Thymic Lymphoepithelioma-Like Carcinoma

Expressive Language Disorder

Developmental Expressive Language Disorder

Gastric Tubular Adenocarcinoma

Tubular Adenocarcinoma Of Stomach

Learning Disability

Learning Disabilities	Learning Disorders
Academic Skill Disorder	Learning Disorder

Speech Disorder

Speech Disorders

Dyslexia

Autism Spectrum Disorder

Asd	Autism Spectrum Disorders
Autistic Continuum	Pervasive Developmental Disorder
Pervasive Development Disorder	Autistic Behavior
Autistic Disorder	Autistic
Autistic Disorder Of Childhood Onset	Infantile Autism
Childhood Autism	Kanner Syndrome
Pervasive Developmental Delay Nos	Pervasive Developmental Disorder, Not Otherwise Specified

Autism

Autistic Disorder	Autism Susceptibility 1
Childhood Autism	Autistic Disorder Of Childhood Onset
Infantile Autism	Kanner'S Syndrome
Autistic

Benign Epilepsy With Centrotemporal Spikes

Rolandic Epilepsy	Benign Rolandic Epilepsy
Epilepsy, Rolandic	Bcects
Benign Childhood Epilepsy With Centrotemporal Spike	Sylvan Seizures
Becrs	Bects
Bre	Benign Epilepsy Of Childhood With Centrotemporal Spikes
Benign Familial Epilepsy Of Childhood With Rolandic Spikes	Centrotemporal Epilepsy

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

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS02859	CMIP Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	CMIP	VGNC	VGNC:60998
Macaca mulatta	CMIP	VGNC	VGNC:99501
Canis familiaris	CMIP	VGNC	VGNC:53321
Mus musculus	CMIP	MGD	MGI:1921690
Rattus norvegicus	CMIP	RGD	RGD:1306101
Bos taurus	CMIP	VGNC	VGNC:52187