TNMD
Tenomodulin
Also known as: BRICD4, ChM1L, myodulin, TEM, tendin, TNMD_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H2S6
- Gene
- TNMD
- Ensembl
- ENSG00000000005
- Chromosome
- X
- Canonical length
- 317 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a protein that is related to chondromodulin-I, which is a cartilage-specific glycoprotein that functions to stimulate chondrocyte growth and to inhibit tube formation of endothelial cells. This protein is also an angiogenesis inhibitor. Genetic variation in this gene is associated with a risk for type 2 diabetes, central obesity and serum levels of systemic immune mediators in a body size-dependent manner. This gene is also a candidate gene for age-related macular degeneration, though a direct link has yet to be demonstrated. [provided by RefSeq, Sep 2009]
Canonical amino-acid sequenceUniProt
317 residues, UniProt reviewed canonical sequence.
>Q9H2S6|TNMD
1 MAKNPPENCE DCHILNAEAF KSKKICKSLK ICGLVFGILA LTLIVLFWGS KHFWPEVPKK
61 AYDMEHTFYS NGEKKKIYME IDPVTRTEIF RSGNGTDETL EVHDFKNGYT GIYFVGLQKC
121 FIKTQIKVIP EFSEPEEEID ENEEITTTFF EQSVIWVPAE KPIENRDFLK NSKILEICDN
181 VTMYWINPTL ISVSELQDFE EEGEDLHFPA NEKKGIEQNE QWVVPQVKVE KTRHARQASE
241 EELPINDYTE NGIEFDPMLD ERGYCCIYCR RGNRYCRRVC EPLLGYYPYP YCYQGGRVIC
301 RVIMPCNWWV ARMLGRVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TNMD 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
- 1
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- seminal vesicle: 25 nTPM
- adipose tissue: 22 nTPM
- breast: 14 nTPM
- tongue: 5.4 nTPM
- ovary: 5.3 nTPM
- skeletal muscle: 3.5 nTPM
Single-cell type
- leydig cells: 11 nCPM
- ovarian stromal cells: 11 nCPM
- adipocytes: 10 nCPM
- hepatic stellate cells: 6.5 nCPM
- vascular endothelial cells: 5.1 nCPM
- retinal ganglion cells: 3.9 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 2.3 nTPM
- midbrain: 1.3 nTPM
- hypothalamus: 1.2 nTPM
- medulla oblongata: 1.2 nTPM
- thalamus: 0.7 nTPM
- pons: 0.6 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)
- 0.91
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.86
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
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
- endothelial cell morphogenesis
- negative regulation of angiogenesis
- negative regulation of endothelial cell proliferation
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TNMD as an antibody target. Whether an autoantibody or antibody against TNMD could matter depends on whether native TNMD is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TNMD 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 TNMD as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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