IFITM1
Interferon-induced transmembrane protein 1
Also known as: 9-27, CD225, DSPA2a, IFI17, IFM1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P13164
- Gene
- IFITM1
- Ensembl
- ENSG00000185885
- Chromosome
- 11
- Canonical length
- 125 aa
- Protein class
- CD markers, Plasma proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Golgi apparatus,Plasma membrane
OverviewNCBI Gene
Interferon-induced transmembrane (IFITM) proteins are a family of interferon induced antiviral proteins. The family contains five members, including IFITM1, IFITM2 and IFITM3 that belong to the CD225 superfamily. The protein encoded by this gene restricts cellular entry by diverse viral pathogens, such as influenza A virus, Ebola virus and Sars-CoV-2. [provided by RefSeq, Nov 2021]
Canonical amino-acid sequenceUniProt
125 residues, UniProt reviewed canonical sequence.
>P13164|IFITM1
1 MHKEEHEVAV LGPPPSTILP RSTVINIHSE TSVPDHVVWS LFNTLFLNWC CLGFIAFAYS
61 VKSRDRKMVG DVTGAQAYAS TAKCLNIWAL ILGILMTIGF ILLLVFGSVT VYHIMLQIIQ
121 EKRGYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IFITM1 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)
- 0.53
- Highest tissue expression
- 1,087 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 1,087 nTPM
- spleen: 987 nTPM
- ovary: 914 nTPM
- choroid plexus: 896 nTPM
- cervix: 733 nTPM
- fallopian tube: 731 nTPM
Single-cell type
- epididymal efferent duct absorptive cells: 358 nCPM
- endometrial secretory cells: 264 nCPM
- epididymal principal cells: 251 nCPM
- neutrophils: 238 nCPM
- leydig cells: 177 nCPM
- ovarian stromal cells: 173 nCPM
Immune cell
- NK-cell: 4,695 nTPM
- total PBMC: 4,686 nTPM
- memory CD4 T-cell: 3,132 nTPM
- naive CD8 T-cell: 3,007 nTPM
- memory CD8 T-cell: 3,002 nTPM
- naive CD4 T-cell: 2,950 nTPM
Brain region
- medulla oblongata: 171 nTPM
- pons: 167 nTPM
- choroid plexus: 162 nTPM
- thalamus: 158 nTPM
- spinal cord: 139 nTPM
- cerebral cortex: 134 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)
- 1.78
- gnomAD pLI
- 0.14
- gnomAD missense Z
- 0.23
- 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
- cell surface receptor signaling pathway
- defense response to virus
- host-mediated suppression of symbiont invasion
- negative regulation of cell migration
- negative regulation of cell population proliferation
- negative regulation of viral genome replication
- ossification
- positive regulation of osteoblast differentiation
- response to interferon-alpha
- response to interferon-beta
- response to type II interferon
- response to virus
- type I interferon-mediated signaling pathway
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IFITM1 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 IFITM1 as an antibody target. Whether an autoantibody or antibody against IFITM1 could matter depends on whether native IFITM1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IFITM1 is annotated at the cell surface, where native IFITM1 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 IFITM1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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