CMIP - c-Maf inducing protein Gene

Also Known as TCMIP

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 80790

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

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	20018188	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

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

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

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