PRAMEF22
PRAME family member 22
Also known as: PRA22_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for PRAMEF22 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
481 residues, UniProt reviewed canonical sequence.
>A3QJZ6|PRAMEF22
1 MRMSLQAPRR LLELAGQSLL GDQALAISIL DELPRELFPP LFVEAFTSRR CEVLKVMVQA
61 WPFPCLPLGS LMKTPDLEIL HYVVDGIDCL LAQKVRPRRW KLQVLELRDV DENFWTIWSG
121 ARPLSCSPEA MSKRQTVEDC PRTGEKQPLK VFMDVCLKEK FMDEDLSFFS GWVQHRRGSV
181 HLCCTKVVNY SMSILNFRNI LETVYPDSIQ VLEIWNMCWP CMIVEFSRYL SQMRNLRKLF
241 ISDGCRYLLS SDSQEQLVAE FSSVLLRLEY LQMLYVRRVC FFRGHLDQLI RCLRSPLETL
301 ALTYGFLEKV DLKCLPRYPS LSQLKQLNLS HGALRFIRLE PLRALLEKVA ATLQTLFLVD
361 CGIRDSKLRV ILPALSCCSN LTTFCFHGND TSMDGLKDLL RHTGRLSNLS LETYPAPRES
421 LDDRGRVISE LLTPLQAELM RILREVREPK RIFFGPVSCP CCGTSPTEQL EFNFCLWGRP
481 ALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRAMEF22 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
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)
- 1.91
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.36
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of apoptotic process
- negative regulation of cell differentiation
- negative regulation of DNA-templated transcription
- positive regulation of cell population proliferation
- proteasome-mediated ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PRAMEF22 as an antibody target. Whether an autoantibody or antibody against PRAMEF22 could matter depends on whether native PRAMEF22 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRAMEF22 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 PRAMEF22 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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