CMIP
C-Maf-inducing protein
Also known as: CMIP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IY22
- Gene
- CMIP
- Ensembl
- ENSG00000153815
- Chromosome
- 16
- Canonical length
- 773 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
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]
Canonical amino-acid sequenceUniProt
773 residues, UniProt reviewed canonical sequence.
>Q8IY22|CMIP
1 MDVTSSSGGG GDPRQIEETK PLLGGDVSAP EGTKMGAVPC RRALLLCNGM RYKLLQEGDI
61 QVCVIRHPRT FLSKILTSKF LRRWEPHHLT LADNSLASAT PTGYMENSVS YSAIEDVQLL
121 SWENAPKYCL QLTIPGGTVL LQAANSYLRD QWFHSLQWKK KIYKYKKVLS NPSRWEVVLK
181 EIRTLVDMAL TSPLQDDSIN QAPLEIVSKL LSENTNLTTQ EHENIIVAIA PLLENNHPPP
241 DLCEFFCKHC RERPRSMVVI EVFTPVVQRI LKHNMDFGKC PRLRLFTQEY ILALNELNAG
301 MEVVKKFIQS MHGPTGHCPH PRVLPNLVAV CLAAIYSCYE EFINSRDNSP SLKEIRNGCQ
361 QPCDRKPTLP LRLLHPSPDL VSQEATLSEA RLKSVVVASS EIHVEVERTS TAKPALTASA
421 GNDSEPNLID CLMVSPACST MSIELGPQAD RTLGCYVEIL KLLSDYDDWR PSLASLLQPI
481 PFPKEALAHE KFTKELKYVI QRFAEDPRQE VHSCLLSVRA GKDGWFQLYS PGGVACDDDG
541 ELFASMVHIL MGSCYKTKKF LLSLAENKLG PCMLLALRGN QTMVEILCLM LEYNIIDNND
601 TQLQIISTLE STDVGKRMYE QLCDRQRELK ELQRKGGPTR LTLPSKSTDA DLARLLSSGS
661 FGNLENLSLA FTNVTSACAE HLIKLPSLKQ LNLWSTQFGD AGLRLLSEHL TMLQVLNLCE
721 TPVTDAGLLA LSSMKSLCSL NMNSTKLSAD TYEDLKAKLP NLKEVDVRYT EAWLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CMIP can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 49 nTPM
- cerebral cortex: 49 nTPM
- small intestine: 46 nTPM
- duodenum: 38 nTPM
- hypothalamus: 33 nTPM
- esophagus: 32 nTPM
Single-cell type
- neutrophils: 902 nCPM
- platelets: 896 nCPM
- urothelial cells: 599 nCPM
- lactotrophs: 583 nCPM
- salivary basal cells: 582 nCPM
- monocytes: 549 nCPM
Immune cell
- basophil: 3 nTPM
- neutrophil: 2.4 nTPM
- eosinophil: 1 nTPM
- classical monocyte: 0.7 nTPM
- intermediate monocyte: 0.5 nTPM
- gdT-cell: 0.4 nTPM
Brain region
- hypothalamus: 140 nTPM
- cerebral cortex: 133 nTPM
- pons: 130 nTPM
- basal ganglia: 125 nTPM
- hippocampal formation: 122 nTPM
- amygdala: 113 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.15
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.26
- DepMap mean gene effect
- -0.32
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Leucine-rich repeat domain superfamily
- C-Maf-inducing protein
- C-Maf-inducing protein, PH domain
- C-Maf-inducing protein PH domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CMIP in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CMIP as an antibody target. Whether an autoantibody or antibody against CMIP could matter depends on whether native CMIP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CMIP is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CMIP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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