FAM98B
Protein FAM98B
Also known as: FA98B_HUMAN, FLJ38426
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q52LJ0
- Gene
- FAM98B
- Ensembl
- ENSG00000171262
- Chromosome
- 15
- Canonical length
- 433 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables identical protein binding activity and protein methyltransferase activity. Involved in positive regulation of cell population proliferation; positive regulation of gene expression; and protein methylation. Located in cytoplasm and nucleoplasm. Part of tRNA-splicing ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
433 residues, UniProt reviewed canonical sequence.
>Q52LJ0|FAM98B
1 MRGPEPGPQP TMEGDVLDTL EALGYKGPLL EEQALTKAAE GGLSSPEFSE LCIWLGSQIK
61 SLCNLEESIT SAGRDDLESF QLEISGFLKE MACPYSVLIS GDIKDRLKKK EDCLKLLLFL
121 STELQASQIL QNKKHKNSQL DKNSEVYQEV QAMFDTLGIP KSTTSDIPHM LNQVESKVKD
181 ILSKVQKNHV GKPLLKMDLN SEQAEQLERI NDALSCEYEC RRRMLMKRLD VTVQSFGWSD
241 RAKVKTDDIA RIYQPKRYAL SPKTTITMAH LLAAREDLSK IIRTSSGTSR EKTACAINKV
301 LMGRVPDRGG RPNEIEPPPP EMPPWQKRQE GGGGRGGWGG GGGGGGRGGG GGGGGRGGWG
361 GGGGGWGGGG GGGGGWGGGG GGGRGGFQGR GDYGGRGGYG GRGGYGGRGY GDPYGGGGGG
421 GGGGGGGGGY RRYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FAM98B 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)
- 0.5
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- thymus: 27 nTPM
- retina: 18 nTPM
- parathyroid gland: 18 nTPM
- cerebral cortex: 16 nTPM
- tongue: 15 nTPM
- colon: 14 nTPM
Single-cell type
- erythrocyte progenitors: 92 nCPM
- megakaryocyte progenitors: 69 nCPM
- megakaryocyte-erythroid progenitors: 62 nCPM
- corticotrophs: 46 nCPM
- neutrophil progenitors: 45 nCPM
- hematopoietic stem cells: 42 nCPM
Immune cell
- naive CD4 T-cell: 3.4 nTPM
- gdT-cell: 2.8 nTPM
- memory CD4 T-cell: 2.8 nTPM
- naive CD8 T-cell: 2.6 nTPM
- MAIT T-cell: 2.4 nTPM
- basophil: 2.3 nTPM
Brain region
- cerebellum: 30 nTPM
- white matter: 21 nTPM
- hypothalamus: 19 nTPM
- cerebral cortex: 18 nTPM
- basal ganglia: 17 nTPM
- spinal cord: 17 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)
- 0.65
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.44
- DepMap mean gene effect
- -0.31
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- positive regulation of cell population proliferation
- positive regulation of gene expression
- protein methylation
- tRNA splicing, via endonucleolytic cleavage and ligation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FAM98B 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 FAM98B as an antibody target. Whether an autoantibody or antibody against FAM98B could matter depends on whether native FAM98B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FAM98B 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 FAM98B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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