IFITM2
Interferon-induced transmembrane protein 2
Also known as: 1-8D, DSPA2c, IFM2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q01629
- Gene
- IFITM2
- Ensembl
- ENSG00000185201
- Chromosome
- 11
- Canonical length
- 132 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm,Cell Junctions
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 and 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
132 residues, UniProt reviewed canonical sequence.
>Q01629|IFITM2
1 MNHIVQTFSP VNSGQPPNYE MLKEEQEVAM LGVPHNPAPP MSTVIHIRSE TSVPDHVVWS
61 LFNTLFMNTC CLGFIAFAYS VKSRDRKMVG DVTGAQAYAS TAKCLNIWAL ILGIFMTILL
121 IIIPVLVVQA QRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IFITM2 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
- 1,506 nTPM
Expression across tissuesHPA
Tissue
- spleen: 1,506 nTPM
- liver: 1,338 nTPM
- lung: 1,149 nTPM
- adipose tissue: 1,130 nTPM
- blood vessel: 933 nTPM
- fallopian tube: 814 nTPM
Single-cell type
- neutrophils: 3,451 nCPM
- decidual stromal cells: 339 nCPM
- platelets: 253 nCPM
- neutrophil progenitors: 208 nCPM
- nk-cells: 173 nCPM
- vascular endothelial cells: 158 nCPM
Immune cell
- neutrophil: 23,258 nTPM
- eosinophil: 3,762 nTPM
- basophil: 2,685 nTPM
- non-classical monocyte: 2,190 nTPM
- intermediate monocyte: 1,404 nTPM
- total PBMC: 1,352 nTPM
Brain region
- choroid plexus: 45 nTPM
- cerebral cortex: 44 nTPM
- hypothalamus: 39 nTPM
- thalamus: 33 nTPM
- medulla oblongata: 33 nTPM
- pons: 30 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)
- 1.89
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.31
- DepMap mean gene effect
- -0.19
- 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 response to interferon-beta
- defense response to virus
- host-mediated suppression of symbiont invasion
- immune response
- negative regulation of viral genome replication
- 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 IFITM2 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 IFITM2 as an antibody target. Whether an autoantibody or antibody against IFITM2 could matter depends on whether native IFITM2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IFITM2 is annotated at the cell surface, where native IFITM2 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 IFITM2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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