TNS2
Tensin-2
Also known as: C1-TEN, KIAA1075, TENC1, TENS2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q63HR2
- Gene
- TNS2
- Ensembl
- ENSG00000111077
- Chromosome
- 12
- Canonical length
- 1409 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene belongs to the tensin family. Tensin is a focal adhesion molecule that binds to actin filaments and participates in signaling pathways. This protein plays a role in regulating cell migration. Alternative splicing occurs at this locus and three transcript variants encoding three distinct isoforms have been identified. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
1409 residues, UniProt reviewed canonical sequence.
>Q63HR2|TNS2
1 MKSSGPVERL LRALGRRDSS RAASRPRKAE PHSFREKVFR KKPPVCAVCK VTIDGTGVSC
61 RVCKVATHRK CEAKVTSACQ ALPPVELRRN TAPVRRIEHL GSTKSLNHSK QRSTLPRSFS
121 LDPLMERRWD LDLTYVTERI LAAAFPARPD EQRHRGHLRE LAHVLQSKHR DKYLLFNLSE
181 KRHDLTRLNP KVQDFGWPEL HAPPLDKLCS ICKAMETWLS ADPQHVVVLY CKGNKGKLGV
241 IVSAYMHYSK ISAGADQALA TLTMRKFCED KVATELQPSQ RRYISYFSGL LSGSIRMNSS
301 PLFLHYVLIP MLPAFEPGTG FQPFLKIYQS MQLVYTSGVY HIAGPGPQQL CISLEPALLL
361 KGDVMVTCYH KGGRGTDRTL VFRVQFHTCT IHGPQLTFPK DQLDEAWTDE RFPFQASVEF
421 VFSSSPEKIK GSTPRNDPSV SVDYNTTEPA VRWDSYENFN QHHEDSVDGS LTHTRGPLDG
481 SPYAQVQRPP RQTPPAPSPE PPPPPMLSVS SDSGHSSTLT TEPAAESPGR PPPTAAERQE
541 LDRLLGGCGV ASGGRGAGRE TAILDDEEQP TVGGGPHLGV YPGHRPGLSR HCSCRQGYRE
601 PCGVPNGGYY RPEGTLERRR LAYGGYEGSP QGYAEASMEK RRLCRSLSEG LYPYPPEMGK
661 PATGDFGYRA PGYREVVILE DPGLPALYPC PACEEKLALP TAALYGLRLE REAGEGWASE
721 AGKPLLHPVR PGHPLPLLLP ACGHHHAPMP DYSCLKPPKA GEEGHEGCSY TMCPEGRYGH
781 PGYPALVTYS YGGAVPSYCP AYGRVPHSCG SPGEGRGYPS PGAHSPRAGS ISPGSPPYPQ
841 SRKLSYEIPT EEGGDRYPLP GHLASAGPLA SAESLEPVSW REGPSGHSTL PRSPRDAPCS
901 ASSELSGPST PLHTSSPVQG KESTRRQDTR SPTSAPTQRL SPGEALPPVS QAGTGKAPEL
961 PSGSGPEPLA PSPVSPTFPP SSPSDWPQER SPGGHSDGAS PRSPVPTTLP GLRHAPWQGP
1021 RGPPDSPDGS PLTPVPSQMP WLVASPEPPQ SSPTPAFPLA ASYDTNGLSQ PPLPEKRHLP
1081 GPGQQPGPWG PEQASSPARG ISHHVTFAPL LSDNVPQTPE PPTQESQSNV KFVQDTSKFW
1141 YKPHLSRDQA IALLKDKDPG AFLIRDSHSF QGAYGLALKV ATPPPSAQPW KGDPVEQLVR
1201 HFLIETGPKG VKIKGCPSEP YFGSLSALVS QHSISPISLP CCLRIPSKDP LEETPEAPVP
1261 TNMSTAADLL RQGAACSVLY LTSVETESLT GPQAVARASS AALSCSPRPT PAVVHFKVSA
1321 QGITLTDNQR KLFFRRHYPV NSITFSSTDP QDRRWTNPDG TTSKIFGFVA KKPGSPWENV
1381 CHLFAELDPD QPAGAIVTFI TKVLLGQRKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TNS2 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 150 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 150 nTPM
- blood vessel: 147 nTPM
- breast: 118 nTPM
- cervix: 106 nTPM
- ovary: 98 nTPM
- endometrium: 98 nTPM
Single-cell type
- leydig cells: 195 nCPM
- adipocytes: 152 nCPM
- pericytes: 152 nCPM
- vascular smooth muscle cells: 131 nCPM
- peritubular myoid cells: 131 nCPM
- podocytes: 130 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
- basal ganglia: 103 nTPM
- midbrain: 98 nTPM
- thalamus: 90 nTPM
- amygdala: 89 nTPM
- medulla oblongata: 87 nTPM
- white matter: 85 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)
- 0.5
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.26
- 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 homeostasis
- collagen metabolic process
- kidney development
- multicellular organism growth
- multicellular organismal-level homeostasis
- negative regulation of cell population proliferation
- negative regulation of insulin receptor signaling pathway
- peptidyl-tyrosine dephosphorylation
- response to muscle activity
Molecular functions
- identical protein binding
- kinase binding
- lipid binding
- protein tyrosine phosphatase activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SH2 domain
- Protein kinase C-like, phorbol ester/diacylglycerol-binding domain
- PTB/PI domain
- PH-like domain superfamily
- Tensin/EPS8 phosphotyrosine-binding domain
- Tensin phosphatase, C2 domain
- Protein-tyrosine phosphatase-like
- Tensin-type phosphatase domain
- Tensin, phosphotyrosine-binding domain
- Tensin-like, SH2 domain
- C2 domain superfamily
- SH2 domain superfamily
- C1-like domain superfamily
- Tensin Phosphatase
- SH2 domain
- Phorbol esters/diacylglycerol binding domain (C1 domain)
- Phosphotyrosine-binding domain
- C2 domain of PTEN tumour-suppressor protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TNS2 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 TNS2 as an antibody target. Whether an autoantibody or antibody against TNS2 could matter depends on whether native TNS2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TNS2 is annotated at the cell surface, where native TNS2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label TNS2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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