CNMD
Leukocyte cell-derived chemotaxin 1
Also known as: BRICD3, CHM-I, CHM1, CNMD_HUMAN, LECT1, MYETS1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75829
- Gene
- CNMD
- Ensembl
- ENSG00000136110
- Chromosome
- 13
- Canonical length
- 334 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins, Predicted secreted proteins
- Secretome location
- Secreted to extracellular matrix
OverviewNCBI Gene
This gene encodes a glycosylated transmembrane protein that is cleaved to form a mature, secreted protein. The N-terminus of the precursor protein shares characteristics with other surfactant proteins and is sometimes called chondrosurfactant protein although no biological activity has yet been defined for it. The C-terminus of the precursor protein contains a 25 kDa mature protein called leukocyte cell-derived chemotaxin-1 or chondromodulin-1. The mature protein promotes chondrocyte growth and inhibits angiogenesis. This gene is expressed in the avascular zone of prehypertrophic cartilage and its expression decreases during chondrocyte hypertrophy and vascular invasion. The mature protein likely plays a role in endochondral bone development by permitting cartilaginous anlagen to be vascularized and replaced by bone. It may be involved also in the broad control of tissue vascularization during development. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
334 residues, UniProt reviewed canonical sequence.
>O75829|CNMD
1 MTENSDKVPI ALVGPDDVEF CSPPAYATLT VKPSSPARLL KVGAVVLISG AVLLLFGAIG
61 AFYFWKGSDS HIYNVHYTMS INGKLQDGSM EIDAGNNLET FKMGSGAEEA IAVNDFQNGI
121 TGIRFAGGEK CYIKAQVKAR IPEVGAVTKQ SISSKLEGKI MPVKYEENSL IWVAVDQPVK
181 DNSFLSSKVL ELCGDLPIFW LKPTYPKEIQ RERREVVRKI VPTTTKRPHS GPRSNPGAGR
241 LNNETRPSVQ EDSQAFNPDN PYHQQEGESM TFDPRLDHEG ICCIECRRSY THCQKICEPL
301 GGYYPWPYNY QGCRSACRVI MPCSWWVARI LGMVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CNMD 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.47
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 12 nTPM
- retina: 7.7 nTPM
- basal ganglia: 6.4 nTPM
- salivary gland: 6.3 nTPM
- spinal cord: 3.4 nTPM
- thyroid gland: 3.1 nTPM
Single-cell type
- müller glia: 109 nCPM
- retinal amacrine cells: 23 nCPM
- early primary spermatocytes: 16 nCPM
- epicardial cells: 16 nCPM
- oligodendrocyte progenitor cells: 16 nCPM
- retinal pigment epithelial cells: 8.5 nCPM
Immune cell
- T-reg: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- basal ganglia: 10 nTPM
- choroid plexus: 7 nTPM
- spinal cord: 5.9 nTPM
- white matter: 5.7 nTPM
- medulla oblongata: 5.3 nTPM
- thalamus: 5.2 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)
- 1.24
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cartilage development
- cell differentiation
- negative regulation of angiogenesis
- negative regulation of endothelial cell proliferation
- proteoglycan metabolic process
- skeletal system development
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CNMD as an antibody target. Whether an autoantibody or antibody against CNMD could matter depends on whether native CNMD is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CNMD is annotated as secreted, so native CNMD circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label CNMD as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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