ST7L
Suppressor of tumorigenicity 7 protein-like
Also known as: FAM4B, FLJ20284, ST7L_HUMAN, ST7R, STLR
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDW4
- Gene
- ST7L
- Ensembl
- ENSG00000007341
- Chromosome
- 1
- Canonical length
- 575 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Centrosome
OverviewNCBI Gene
This gene was identified by its similarity to the ST7 tumor suppressor gene found in the chromosome 7q31 region. This gene is clustered in a tail-to-tail manner with the WNT2B gene in a chromosomal region known to be deleted and rearranged in a variety of cancers. Several transcript variants encoding many different isoforms have been described, but some have not been fully characterized. [provided by RefSeq, Feb 2011]
Canonical amino-acid sequenceUniProt
575 residues, UniProt reviewed canonical sequence.
>Q8TDW4|ST7L
1 MADRGGVGEA AAVGASPASV PGLNPTLGWR ERLRAGLAGT GASLWFVAGL GLLYALRIPL
61 RLCENLAAVT VFLNSLTPKF YVALTGTSSL ISGLIFIFEW WYFHKHGTSF IEQVSVSHLQ
121 PLMGGTESSI SEPGSPSRNR ENETSRQNLS ECKVWRNPLN LFRGAEYRRY TWVTGKEPLT
181 YYDMNLSAQD HQTFFTCDTD FLRPSDTVMQ KAWRERNPPA RIKAAYQALE LNNDCATAYV
241 LLAEEEATTI VDAERLFKQA LKAGETIYRQ SQQCQHQSPQ HEAQLRRDTN VLVYIKRRLA
301 MCARKLGRIR EAVKIMRDLM KEFPPLTMLN IHENLLESLL ELQAYPDVQA VLAKYDDISL
361 PKSAAICYTA ALLKTRTVSE KFSPETASRR GLSTAEINAV EAIHRAVEFN PHVPKYLLEM
421 KSLILPPEHI LKRGDSEAIA YAFFHLQHWK RIEGALNLLQ CTWEGTFRMI PYPLEKGHLF
481 YPYPSCTETA DRELLPTFHH VSVYPKKELP LFIHFTAGFC SSTAMIAILT HQFPEIMGIF
541 AKAVLGLWCP QPWASSGFEE NTQDLKSEDL GLSSGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ST7L 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 2
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 34 nTPM
Expression across tissuesHPA
Tissue
- testis: 34 nTPM
- thyroid gland: 7.1 nTPM
- retina: 6.3 nTPM
- skin: 5.8 nTPM
- bone marrow: 5.2 nTPM
- heart muscle: 5.1 nTPM
Single-cell type
- late spermatids: 530 nCPM
- early spermatids: 223 nCPM
- late primary spermatocytes: 219 nCPM
- cardiomyocytes: 175 nCPM
- myonuclei: 158 nCPM
- choroid plexus epithelial cells: 110 nCPM
Immune cell
- NK-cell: 3.8 nTPM
- naive CD4 T-cell: 2.5 nTPM
- memory B-cell: 2.4 nTPM
- MAIT T-cell: 1.9 nTPM
- memory CD4 T-cell: 1.8 nTPM
- plasmacytoid DC: 1.8 nTPM
Brain region
- cerebellum: 12 nTPM
- white matter: 11 nTPM
- basal ganglia: 10 nTPM
- cerebral cortex: 10 nTPM
- choroid plexus: 9.2 nTPM
- amygdala: 9 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)
- 0.87
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.58
- DepMap mean gene effect
- -0.13
- 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 components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ST7L as an antibody target. Whether an autoantibody or antibody against ST7L could matter depends on whether native ST7L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ST7L 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 ST7L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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