VIT
Vitrin
Also known as: VITRN_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6UXI7
- Gene
- VIT
- Ensembl
- ENSG00000205221
- Chromosome
- 2
- Canonical length
- 678 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to extracellular matrix
OverviewNCBI Gene
This gene encodes an extracellular matrix (ECM) protein. The protein may be associated with cell adhesion and migration. High levels of expression of the protein in specific parts of the brain suggest its likely role in neural development. [provided by RefSeq, Jun 2016]
Canonical amino-acid sequenceUniProt
678 residues, UniProt reviewed canonical sequence.
>Q6UXI7|VIT
1 MRTVVLTMKA SVIEMFLVLL VTGVHSNKET AKKIKRPKFT VPQINCDVKA GKIIDPEFIV
61 KCPAGCQDPK YHVYGTDVYA SYSSVCGAAV HSGVLDNSGG KILVRKVAGQ SGYKGSYSNG
121 VQSLSLPRWR ESFIVLESKP KKGVTYPSAL TYSSSKSPAA QAGETTKAYQ RPPIPGTTAQ
181 PVTLMQLLAV TVAVATPTTL PRPSPSAAST TSIPRPQSVG HRSQEMDLWS TATYTSSQNR
241 PRADPGIQRQ DPSGAAFQKP VGADVSLGLV PKEELSTQSL EPVSLGDPNC KIDLSFLIDG
301 STSIGKRRFR IQKQLLADVA QALDIGPAGP LMGVVQYGDN PATHFNLKTH TNSRDLKTAI
361 EKITQRGGLS NVGRAISFVT KNFFSKANGN RSGAPNVVVV MVDGWPTDKV EEASRLARES
421 GINIFFITIE GAAENEKQYV VEPNFANKAV CRTNGFYSLH VQSWFGLHKT LQPLVKRVCD
481 TDRLACSKTC LNSADIGFVI DGSSSVGTGN FRTVLQFVTN LTKEFEISDT DTRIGAVQYT
541 YEQRLEFGFD KYSSKPDILN AIKRVGYWSG GTSTGAAINF ALEQLFKKSK PNKRKLMILI
601 TDGRSYDDVR IPAMAAHLKG VITYAIGVAW AAQEELEVIA THPARDHSFF VDEFDNLHQY
661 VPRIIQNICT EFNSQPRNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against VIT 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)
- 0.36
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- tongue: 38 nTPM
- ovary: 36 nTPM
- adipose tissue: 34 nTPM
- blood vessel: 18 nTPM
- heart muscle: 18 nTPM
- urinary bladder: 17 nTPM
Single-cell type
- fibro-adipogenic progenitors: 352 nCPM
- leydig cells: 268 nCPM
- myosatellite cells: 222 nCPM
- fibroblasts: 213 nCPM
- bergmann glia: 145 nCPM
- goblet cells: 73 nCPM
Immune cell
- gdT-cell: 2.3 nTPM
- naive CD8 T-cell: 1.3 nTPM
- memory CD8 T-cell: 0.9 nTPM
- total PBMC: 0.6 nTPM
- NK-cell: 0.2 nTPM
- memory CD4 T-cell: 0.1 nTPM
Brain region
- cerebral cortex: 2.2 nTPM
- cerebellum: 1.8 nTPM
- basal ganglia: 1.2 nTPM
- choroid plexus: 1.2 nTPM
- thalamus: 0.9 nTPM
- white matter: 0.7 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)
- 1.59
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.77
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- extracellular matrix organization
- positive regulation of cell-substrate adhesion
- spinal cord development
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads VIT as an antibody target. Whether an autoantibody or antibody against VIT could matter depends on whether native VIT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
VIT is annotated as secreted, so native VIT 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 VIT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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