FEM1B
Protein fem-1 homolog B
Also known as: FEM1B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UK73
- Gene
- FEM1B
- Ensembl
- ENSG00000169018
- Chromosome
- 15
- Canonical length
- 627 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
This gene encodes an ankyrin repeat protein that belongs to the death receptor-associated family of proteins and plays a role in mediating apoptosis. The encoded protein is also thought to function in the replication stress-induced checkpoint signaling pathway via interaction with checkpoint kinase 1. [provided by RefSeq, Aug 2013]
Canonical amino-acid sequenceUniProt
627 residues, UniProt reviewed canonical sequence.
>Q9UK73|FEM1B
1 MEGLAGYVYK AASEGKVLTL AALLLNRSES DIRYLLGYVS QQGGQRSTPL IIAARNGHAK
61 VVRLLLEHYR VQTQQTGTVR FDGYVIDGAT ALWCAAGAGH FEVVKLLVSH GANVNHTTVT
121 NSTPLRAACF DGRLDIVKYL VENNANISIA NKYDNTCLMI AAYKGHTDVV RYLLEQRADP
181 NAKAHCGATA LHFAAEAGHI DIVKELIKWR AAIVVNGHGM TPLKVAAESC KADVVELLLS
241 HADCDRRSRI EALELLGASF ANDRENYDII KTYHYLYLAM LERFQDGDNI LEKEVLPPIH
301 AYGNRTECRN PQELESIRQD RDALHMEGLI VRERILGADN IDVSHPIIYR GAVYADNMEF
361 EQCIKLWLHA LHLRQKGNRN THKDLLRFAQ VFSQMIHLNE TVKAPDIECV LRCSVLEIEQ
421 SMNRVKNISD ADVHNAMDNY ECNLYTFLYL VCISTKTQCS EEDQCKINKQ IYNLIHLDPR
481 TREGFTLLHL AVNSNTPVDD FHTNDVCSFP NALVTKLLLD CGAEVNAVDN EGNSALHIIV
541 QYNRPISDFL TLHSIIISLV EAGAHTDMTN KQNKTPLDKS TTGVSEILLK TQMKMSLKCL
601 AARAVRANDI NYQDQIPRTL EEFVGFHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FEM1B 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)
- 0.24
- Highest tissue expression
- 68 nTPM
Expression across tissuesHPA
Tissue
- testis: 68 nTPM
- bone marrow: 57 nTPM
- skeletal muscle: 46 nTPM
- smooth muscle: 28 nTPM
- tongue: 26 nTPM
- cerebral cortex: 25 nTPM
Single-cell type
- early spermatids: 900 nCPM
- late primary spermatocytes: 378 nCPM
- late spermatids: 365 nCPM
- suprabasal keratinocytes: 113 nCPM
- thymic myoid cells: 112 nCPM
- melanocytes: 104 nCPM
Immune cell
- intermediate monocyte: 4.2 nTPM
- NK-cell: 3.7 nTPM
- non-classical monocyte: 3.6 nTPM
- naive CD4 T-cell: 3.5 nTPM
- memory CD8 T-cell: 3.3 nTPM
- classical monocyte: 3.1 nTPM
Brain region
- white matter: 70 nTPM
- cerebellum: 68 nTPM
- cerebral cortex: 59 nTPM
- basal ganglia: 58 nTPM
- pons: 58 nTPM
- hypothalamus: 55 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about FEM1B.
Disease | AllUniProt
Conditions FEM1B is implicated in, by any mechanism.
- Neurodevelopmental disorder with behavioral, ear, and skeletal abnormalities (NEDBES) MIM:621263
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 51 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Neurodevelopmental disorder with behavioral, ear, and skeletal abnormalities
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)
- 0.52
- gnomAD pLI
- 0.35
- gnomAD missense Z
- 3.62
- DepMap mean gene effect
- -0.21
- 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
- apoptotic process
- branching involved in prostate gland morphogenesis
- epithelial cell maturation involved in prostate gland development
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein ubiquitination
- regulation of DNA damage checkpoint
- regulation of extrinsic apoptotic signaling pathway via death domain receptors
- regulation of ubiquitin-protein transferase activity
- ubiquitin-dependent protein catabolic process via the C-end degron rule pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FEM1B 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 FEM1B as an antibody target. Whether an autoantibody or antibody against FEM1B could matter depends on whether native FEM1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FEM1B 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 FEM1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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