SEMA3C
Semaphorin-3C
Also known as: SEM3C_HUMAN, SEMAE, SemE
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99985
- Gene
- SEMA3C
- Ensembl
- ENSG00000075223
- Chromosome
- 7
- Canonical length
- 751 aa
- Protein class
- Predicted secreted proteins
- Subcellular location
- Golgi apparatus,Plasma membrane,Cytosol
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease. [provided by RefSeq, May 2017]
Canonical amino-acid sequenceUniProt
751 residues, UniProt reviewed canonical sequence.
>Q99985|SEMA3C
1 MAFRTICVLV GVFICSICVK GSSQPQARVY LTFDELRETK TSEYFSLSHH PLDYRILLMD
61 EDQDRIYVGS KDHILSLNIN NISQEALSVF WPASTIKVEE CKMAGKDPTH GCGNFVRVIQ
121 TFNRTHLYVC GSGAFSPVCT YLNRGRRSED QVFMIDSKCE SGKGRCSFNP NVNTVSVMIN
181 EELFSGMYID FMGTDAAIFR SLTKRNAVRT DQHNSKWLSE PMFVDAHVIP DGTDPNDAKV
241 YFFFKEKLTD NNRSTKQIHS MIARICPNDT GGLRSLVNKW TTFLKARLVC SVTDEDGPET
301 HFDELEDVFL LETDNPRTTL VYGIFTTSSS VFKGSAVCVY HLSDIQTVFN GPFAHKEGPN
361 HQLISYQGRI PYPRPGTCPG GAFTPNMRTT KEFPDDVVTF IRNHPLMYNS IYPIHKRPLI
421 VRIGTDYKYT KIAVDRVNAA DGRYHVLFLG TDRGTVQKVV VLPTNNSVSG ELILEELEVF
481 KNHAPITTMK ISSKKQQLYV SSNEGVSQVS LHRCHIYGTA CADCCLARDP YCAWDGHSCS
541 RFYPTGKRRS RRQDVRHGNP LTQCRGFNLK AYRNAAEIVQ YGVKNNTTFL ECAPKSPQAS
601 IKWLLQKDKD RRKEVKLNER IIATSQGLLI RSVQGSDQGL YHCIATENSF KQTIAKINFK
661 VLDSEMVAVV TDKWSPWTWA SSVRALPFHP KDIMGAFSHS EMQMINQYCK DTRQQHQQGD
721 ESQKMRGDYG KLKALINSRK SRNRRNQLPE SLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEMA3C 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
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 65 nTPM
Expression across tissuesHPA
Tissue
- urinary bladder: 65 nTPM
- prostate: 63 nTPM
- breast: 54 nTPM
- ovary: 52 nTPM
- adipose tissue: 50 nTPM
- cervix: 50 nTPM
Single-cell type
- mesothelial cells: 1,101 nCPM
- respiratory ionocytes: 1,008 nCPM
- urothelial cells: 931 nCPM
- schwann cells: 893 nCPM
- epididymal basal cells: 742 nCPM
- melanocytes: 720 nCPM
Immune cell
- basophil: 50 nTPM
- classical monocyte: 5.8 nTPM
- myeloid DC: 3.6 nTPM
- plasmacytoid DC: 3.3 nTPM
- neutrophil: 2.6 nTPM
- intermediate monocyte: 2.4 nTPM
Brain region
- pons: 42 nTPM
- hypothalamus: 33 nTPM
- white matter: 31 nTPM
- medulla oblongata: 28 nTPM
- cerebral cortex: 28 nTPM
- spinal cord: 26 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)
- 0.52
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.99
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- axon guidance
- blood vessel remodeling
- cardiac right ventricle morphogenesis
- dichotomous subdivision of terminal units involved in salivary gland branching
- immune response
- limb bud formation
- negative chemotaxis
- neural crest cell migration
- neural tube development
- outflow tract septum morphogenesis
- positive regulation of cardiac neural crest cell migration involved in outflow tract morphogenesis
- positive regulation of cell migration
- post-embryonic development
- pulmonary myocardium development
- response to xenobiotic stimulus
- semaphorin-plexin signaling pathway
- somitogenesis
- cardiac endothelial to mesenchymal transition
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SEMA3C 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 SEMA3C as an antibody target. Whether an autoantibody or antibody against SEMA3C could matter depends on whether native SEMA3C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEMA3C is annotated as secreted, so native SEMA3C 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 SEMA3C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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