TENM3
Teneurin-3
Also known as: KIAA1455, ODZ3, Ten-M3, TEN3, TEN3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P273
- Gene
- TENM3
- Ensembl
- ENSG00000218336
- Chromosome
- 4
- Canonical length
- 2699 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Cell Junctions,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the teneurin transmembrane protein family. The encoded protein may be involved in the regulation of neuronal development including development of the visual pathway. Mutations in this gene have been associated with microphthalmia and developmental dysplasia of the hip. [provided by RefSeq, Jan 2023]
Canonical amino-acid sequenceUniProt
2699 residues, UniProt reviewed canonical sequence.
>Q9P273|TENM3
1 MDVKERRPYC SLTKSRREKE RRYTNSSADN EECRVPTQKS YSSSETLKAF DHDSSRLLYG
61 NRVKDLVHRE ADEFTRQGQN FTLRQLGVCE PATRRGLAFC AEMGLPHRGY SISAGSDADT
121 ENEAVMSPEH AMRLWGRGVK SGRSSCLSSR SNSALTLTDT EHENKSDSEN EQPASNQGQS
181 TLQPLPPSHK QHSAQHHPSI TSLNRNSLTN RRNQSPAPPA ALPAELQTTP ESVQLQDSWV
241 LGSNVPLESR HFLFKTGTGT TPLFSTATPG YTMASGSVYS PPTRPLPRNT LSRSAFKFKK
301 SSKYCSWKCT ALCAVGVSVL LAILLSYFIA MHLFGLNWQL QQTENDTFEN GKVNSDTMPT
361 NTVSLPSGDN GKLGGFTQEN NTIDSGELDI GRRAIQEIPP GIFWRSQLFI DQPQFLKFNI
421 SLQKDALIGV YGRKGLPPSH TQYDFVELLD GSRLIAREQR SLLETERAGR QARSVSLHEA
481 GFIQYLDSGI WHLAFYNDGK NAEQVSFNTI VIESVVECPR NCHGNGECVS GTCHCFPGFL
541 GPDCSRAACP VLCSGNGQYS KGRCLCFSGW KGTECDVPTT QCIDPQCGGR GICIMGSCAC
601 NSGYKGESCE EADCIDPGCS NHGVCIHGEC HCSPGWGGSN CEILKTMCPD QCSGHGTYLQ
661 ESGSCTCDPN WTGPDCSNEI CSVDCGSHGV CMGGTCRCEE GWTGPACNQR ACHPRCAEHG
721 TCKDGKCECS QGWNGEHCTI EGCPGLCNSN GRCTLDQNGW HCVCQPGWRG AGCDVAMETL
781 CTDSKDNEGD GLIDCMDPDC CLQSSCQNQP YCRGLPDPQD IISQSLQSPS QQAAKSFYDR
841 ISFLIGSDST HVIPGESPFN KSLASVIRGQ VLTADGTPLI GVNVSFFHYP EYGYTITRQD
901 GMFDLVANGG ASLTLVFERS PFLTQYHTVW IPWNVFYVMD TLVMKKEEND IPSCDLSGFV
961 RPNPIIVSSP LSTFFRSSPE DSPIIPETQV LHEETTIPGT DLKLSYLSSR AAGYKSVLKI
1021 TMTQSIIPFN LMKVHLMVAV VGRLFQKWFP ASPNLAYTFI WDKTDAYNQK VYGLSEAVVS
1081 VGYEYESCLD LTLWEKRTAI LQGYELDASN MGGWTLDKHH VLDVQNGILY KGNGENQFIS
1141 QQPPVVSSIM GNGRRRSISC PSCNGQADGN KLLAPVALAC GIDGSLYVGD FNYVRRIFPS
1201 GNVTSVLELS SNPAHRYYLA TDPVTGDLYV SDTNTRRIYR PKSLTGAKDL TKNAEVVAGT
1261 GEQCLPFDEA RCGDGGKAVE ATLMSPKGMA VDKNGLIYFV DGTMIRKVDQ NGIISTLLGS
1321 NDLTSARPLT CDTSMHISQV RLEWPTDLAI NPMDNSIYVL DNNVVLQITE NRQVRIAAGR
1381 PMHCQVPGVE YPVGKHAVQT TLESATAIAV SYSGVLYITE TDEKKINRIR QVTTDGEISL
1441 VAGIPSECDC KNDANCDCYQ SGDGYAKDAK LSAPSSLAAS PDGTLYIADL GNIRIRAVSK
1501 NKPLLNSMNF YEVASPTDQE LYIFDINGTH QYTVSLVTGD YLYNFSYSND NDITAVTDSN
1561 GNTLRIRRDP NRMPVRVVSP DNQVIWLTIG TNGCLKSMTA QGLELVLFTY HGNSGLLATK
1621 SDETGWTTFF DYDSEGRLTN VTFPTGVVTN LHGDMDKAIT VDIESSSREE DVSITSNLSS
1681 IDSFYTMVQD QLRNSYQIGY DGSLRIIYAS GLDSHYQTEP HVLAGTANPT VAKRNMTLPG
1741 ENGQNLVEWR FRKEQAQGKV NVFGRKLRVN GRNLLSVDFD RTTKTEKIYD DHRKFLLRIA
1801 YDTSGHPTLW LPSSKLMAVN VTYSSTGQIA SIQRGTTSEK VDYDGQGRIV SRVFADGKTW
1861 SYTYLEKSMV LLLHSQRQYI FEYDMWDRLS AITMPSVARH TMQTIRSIGY YRNIYNPPES
1921 NASIITDYNE EGLLLQTAFL GTSRRVLFKY RRQTRLSEIL YDSTRVSFTY DETAGVLKTV
1981 NLQSDGFICT IRYRQIGPLI DRQIFRFSED GMVNARFDYS YDNSFRVTSM QGVINETPLP
2041 IDLYQFDDIS GKVEQFGKFG VIYYDINQII STAVMTYTKH FDAHGRIKEI QYEIFRSLMY
2101 WITIQYDNMG RVTKREIKIG PFANTTKYAY EYDVDGQLQT VYLNEKIMWR YNYDLNGNLH
2161 LLNPSNSARL TPLRYDLRDR ITRLGDVQYR LDEDGFLRQR GTEIFEYSSK GLLTRVYSKG
2221 SGWTVIYRYD GLGRRVSSKT SLGQHLQFFY ADLTYPTRIT HVYNHSSSEI TSLYYDLQGH
2281 LFAMEISSGD EFYIASDNTG TPLAVFSSNG LMLKQIQYTA YGEIYFDSNI DFQLVIGFHG
2341 GLYDPLTKLI HFGERDYDIL AGRWTTPDIE IWKRIGKDPA PFNLYMFRNN NPASKIHDVK
2401 DYITDVNSWL VTFGFHLHNA IPGFPVPKFD LTEPSYELVK SQQWDDIPPI FGVQQQVARQ
2461 AKAFLSLGKM AEVQVSRRRA GGAQSWLWFA TVKSLIGKGV MLAVSQGRVQ TNVLNIANED
2521 CIKVAAVLNN AFYLENLHFT IEGKDTHYFI KTTTPESDLG TLRLTSGRKA LENGINVTVS
2581 QSTTVVNGRT RRFADVEMQF GALALHVRYG MTLDEEKARI LEQARQRALA RAWAREQQRV
2641 RDGEEGARLW TEGEKRQLLS AGKVQGYDGY YVLSVEQYPE LADSANNIQF LRQSEIGRRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TENM3 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
- 1
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- placenta: 12 nTPM
- cerebral cortex: 6.8 nTPM
- thyroid gland: 5.7 nTPM
- adrenal gland: 4.8 nTPM
- parathyroid gland: 4.8 nTPM
- adipose tissue: 4.7 nTPM
Single-cell type
- cytotrophoblasts: 2,024 nCPM
- syncytiotrophoblasts: 1,527 nCPM
- adrenal cortex cells: 1,331 nCPM
- migrating cytotrophoblasts: 1,234 nCPM
- pituitary stem cells: 1,230 nCPM
- pituicytes/fscs: 1,090 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
- cerebral cortex: 113 nTPM
- basal ganglia: 106 nTPM
- hypothalamus: 87 nTPM
- thalamus: 79 nTPM
- amygdala: 76 nTPM
- midbrain: 76 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TENM3.
Disease | AllUniProt
Conditions TENM3 is implicated in, by any mechanism.
- Microphthalmia/Coloboma 9 (MCOPCB9) MIM:615145
- Microphthalmia, syndromic, 15 (MCOPS15) MIM:615145
Disease | GeneticClinVar
11 pathogenic / likely-pathogenic of 668 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Microphthalmia, isolated, with coloboma 9
- MICROPHTHALMIA, SYNDROMIC 15
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)
- 0.26
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.3
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
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
- camera-type eye morphogenesis
- homophilic cell adhesion via plasma membrane adhesion molecules
- neuron development
- positive regulation of neuron projection development
- regulation of homophilic cell adhesion
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- EGF-like domain
- YD repeat
- Carboxypeptidase-like, regulatory domain superfamily
- Teneurin intracellular, N-terminal
- Six-bladed beta-propeller, TolB-like
- Rhs repeat-associated core
- Tox-GHH domain
- WD40-repeat-containing domain superfamily
- Teneurin
- Teneurin, TTR-like domain
- Teneurin, NHL domain
- Teneurin-like, YD-shell
- Teneurin 1-4-like, FN-plug domain
- Teneurin-1-4-like, galactose-binding domain-like
- Teneurin Intracellular Region
- GHH signature containing HNH/Endo VII superfamily nuclease toxin
- Teneurin-3-like, galactose-binding domain-like
- Teneurin antibiotic-binding-like domain
- Teneurin 1-4, FN-plug domain
- Teneurin TTR-like domain
- Teneurin NHL domain
- Teneurin YD-shell
- Teneurin EGF domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TENM3 as an antibody target. Whether an autoantibody or antibody against TENM3 could matter depends on whether native TENM3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TENM3 is annotated at the cell surface, where native TENM3 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 TENM3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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