1. Gene
  2. CMIP - c-Maf inducing protein Gene

CMIP - c-Maf inducing protein Gene

中文名称:c-Maf 诱导蛋白

种属: Homo sapiens

同用名: TCMIP

基因 ID: 80790 | 基因类型: protein coding

关于 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.

功能概要

该基因编码在 T 细胞信号通路中发挥作用的 c-Maf 诱导蛋白。已经针对该基因描述了编码不同亚型的选择性剪接转录物变体。[RefSeq 提供,2011 年 8 月]

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 基因产物(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
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
20018188 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

CMIP 蛋白结构

LRR_6

LRR_6: Leucine Rich repeat (685 - 707)

LRR_6

LRR_6: Leucine Rich repeat (712 - 732)

  • 0
  • 200
  • 400
  • 600
  • 773 a.a.
蛋白主名 其他名称

C-Maf-inducing protein

tc-Mip

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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