SLC22A14
Solute carrier family 22 member 14
Also known as: OCTL2, ORCTL4, S22AE_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y267
- Gene
- SLC22A14
- Ensembl
- ENSG00000144671
- Chromosome
- 3
- Canonical length
- 594 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Perinuclear theca,Connecting piece,Mid piece,Principal piece
OverviewNCBI Gene
This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 3. The encoded protein is a transmembrane protein which is thought to transport small molecules and since this protein is conserved among several species, it is suggested to have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Canonical amino-acid sequenceUniProt
594 residues, UniProt reviewed canonical sequence.
>Q9Y267|SLC22A14
1 MAGEENFKEE LRSQDASRNL NQHEVAGHPH SWSLEMLLRR LRAVHTKQDD KFANLLDAVG
61 EFGTFQQRLV ALTFIPSIMS AFFMFADHFV FTAQKPYCNT SWILAVGPHL SKAEQLNLTI
121 PQAPNGSFLT CFMYLPVPWN LDSIIQFGLN DTDTCQDGWI YPDAKKRSLI NEFDLVCGME
181 TKKDTAQIMF MAGLPIGSLI FRLITDKMGR YPAILLSLLG LIIFGFGTAF MNSFHLYLFF
241 RFGISQSVVG YAISSISLAT EWLVGEHRAH AIILGHCFFA VGAVLLTGIA YSLPHWQLLF
301 LVGGILVIPF ISYIWILPES PRWLMMKGKV KEAKQVLCYA ASVNKKTIPS NLLDELQLPR
361 KKVTRASVLD FCKNRQLCKV TLVMSCVWFT VSYTYFTLSL RMRELGVSVH FRHVVPSIME
421 VPARLCCIFL LQQIGRKWSL AVTLLQAIIW CLLLLFLPEG EDGLRLKWPR CPATELKSMT
481 ILVLMLREFS LAATVTVFFL YTAELLPTVL RATGLGLVSL ASVAGAILSL TIISQTPSLL
541 PIFLCCVLAI VAFSLSSLLP ETRDQPLSES LNHSSQIRNK VKDMKTKETS SDDVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC22A14 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 12
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- testis: 11 nTPM
- cerebellum: 1.3 nTPM
- cerebral cortex: 0.9 nTPM
- kidney: 0.5 nTPM
- amygdala: 0.3 nTPM
- basal ganglia: 0.3 nTPM
Single-cell type
- late spermatids: 174 nCPM
- early spermatids: 92 nCPM
- late primary spermatocytes: 48 nCPM
- proximal tubule cells: 16 nCPM
- endometrial glandular cells: 14 nCPM
- neutrophils: 13 nCPM
Immune cell
- neutrophil: 0.2 nTPM
- plasmacytoid DC: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebral cortex: 4.6 nTPM
- white matter: 3.1 nTPM
- cerebellum: 2.4 nTPM
- amygdala: 2.3 nTPM
- pons: 2.3 nTPM
- basal ganglia: 2.2 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)
- 1.26
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.14
- DepMap mean gene effect
- -0.01
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC22A14 as an antibody target. Whether an autoantibody or antibody against SLC22A14 could matter depends on whether native SLC22A14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC22A14 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 SLC22A14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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