MFSD14B
Hippocampus abundant transcript-like protein 1
Also known as: FLJ14753, HIATL1, MF14B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5SR56
- Gene
- MFSD14B
- Ensembl
- ENSG00000148110
- Chromosome
- 9
- Canonical length
- 506 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
506 residues, UniProt reviewed canonical sequence.
>Q5SR56|MFSD14B
1 MSVEPPPELE EKAASEPEAG AMPEKRAGAQ AAGSTWLQGF GRPSVYHAAI VIFLEFFAWG
61 LLTTPMLTVL HETFSQHTFL MNGLIQGVKG LLSFLSAPLI GALSDVWGRK PFLLGTVFFT
121 CFPIPLMRIS PWWYFAMISV SGVFSVTFSV IFAYVADVTQ EHERSTAYGW VSATFAASLV
181 SSPAIGAYLS ASYGDSLVVL VATVVALLDI CFILVAVPES LPEKMRPVSW GAQISWKQAD
241 PFASLKKVGK DSTVLLICIT VFLSYLPEAG QYSSFFLYLR QVIGFGSVKI AAFIAMVGIL
301 SIVAQTAFLS ILMRSLGNKN TVLLGLGFQM LQLAWYGFGS QAWMMWAAGT VAAMSSITFP
361 AISALVSRNA ESDQQGVAQG IITGIRGLCN GLGPALYGFI FYMFHVELTE LGPKLNSNNV
421 PLQGAVIPGP PFLFGACIVL MSFLVALFIP EYSKASGVQK HSNSSSGSLT NTPERGSDED
481 IEPLLQDSSI WELSSFEEPG NQCTELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MFSD14B 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)
- 0.34
- Highest tissue expression
- 90 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 90 nTPM
- skin: 38 nTPM
- esophagus: 37 nTPM
- tonsil: 33 nTPM
- urinary bladder: 32 nTPM
- placenta: 31 nTPM
Single-cell type
- neutrophil progenitors: 443 nCPM
- neutrophils: 278 nCPM
- esophageal apical cells: 161 nCPM
- monocyte progenitors: 155 nCPM
- melanocytes: 151 nCPM
- urothelial cells: 110 nCPM
Immune cell
- intermediate monocyte: 8.5 nTPM
- neutrophil: 7.3 nTPM
- myeloid DC: 6.2 nTPM
- classical monocyte: 5.9 nTPM
- non-classical monocyte: 5.9 nTPM
- plasmacytoid DC: 5.1 nTPM
Brain region
- choroid plexus: 46 nTPM
- white matter: 36 nTPM
- medulla oblongata: 34 nTPM
- spinal cord: 33 nTPM
- midbrain: 33 nTPM
- basal ganglia: 31 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)
- 0.68
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MFSD14B as an antibody target. Whether an autoantibody or antibody against MFSD14B could matter depends on whether native MFSD14B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MFSD14B 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 MFSD14B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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