FAM98A
Protein FAM98A
Also known as: DKFZP564F0522, FA98A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NCA5
- Gene
- FAM98A
- Ensembl
- ENSG00000119812
- Chromosome
- 2
- Canonical length
- 518 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Enables protein methyltransferase activity. Involved in positive regulation of cell population proliferation; positive regulation of gene expression; and protein methylation. Predicted to be located in cytoplasm and nucleus. Predicted to be part of tRNA-splicing ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
518 residues, UniProt reviewed canonical sequence.
>Q8NCA5|FAM98A
1 MECDLMETDI LESLEDLGYK GPLLEDGALS QAVSAGASSP EFTKLCAWLV SELRVLCKLE
61 ENVQATNSPS EAEEFQLEVS GLLGEMNCPY LSLTSGDVTK RLLIQKNCLL LLTYLISELE
121 AARMLCVNAP PKKAQEGGGS EVFQELKGIC IALGMSKPPA NITMFQFFSG IEKKLKETLA
181 KVPPNHVGKP LLKKPMGPAH WEKIEAINQA IANEYEVRRK LLIKRLDVTV QSFGWSDRAK
241 SQTEKLAKVY QPKRSVLSPK TTISVAHLLA ARQDLSKILR TSSGSIREKT ACAINKVLMG
301 RVPDRGGRPN EIEPPPPEMP PWQKRQDGPQ QQTGGRGGGR GGYEHSSYGG RGGHEQGGGR
361 GGRGGYDHGG RGGGRGNKHQ GGWTDGGSGG GGGYQDGGYR DSGFQPGGYH GGHSSGGYQG
421 GGYGGFQTSS SYTGSGYQGG GYQQDNRYQD GGHHGDRGGG RGGRGGRGGR GGRAGQGGGW
481 GGRGSQNYHQ GGQFEQHFQH GGYQYNHSGF GQGRHYTSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FAM98A 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)
- 0.54
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- testis: 47 nTPM
- skeletal muscle: 46 nTPM
- parathyroid gland: 45 nTPM
- tongue: 38 nTPM
- heart muscle: 38 nTPM
- smooth muscle: 34 nTPM
Single-cell type
- cardiomyocytes: 346 nCPM
- myonuclei: 109 nCPM
- sertoli cells: 91 nCPM
- plasma cells: 85 nCPM
- megakaryocyte progenitors: 74 nCPM
- late primary spermatocytes: 72 nCPM
Immune cell
- memory B-cell: 7.3 nTPM
- T-reg: 6.8 nTPM
- naive CD4 T-cell: 6.2 nTPM
- MAIT T-cell: 5.5 nTPM
- intermediate monocyte: 5.4 nTPM
- gdT-cell: 4.8 nTPM
Brain region
- white matter: 35 nTPM
- hippocampal formation: 30 nTPM
- cerebral cortex: 28 nTPM
- cerebellum: 27 nTPM
- basal ganglia: 25 nTPM
- thalamus: 25 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)
- 0.42
- gnomAD pLI
- 0.55
- gnomAD missense Z
- -0.06
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- lysosome localization
- positive regulation of cell population proliferation
- positive regulation of gene expression
- positive regulation of ruffle assembly
- protein methylation
- tRNA splicing, via endonucleolytic cleavage and ligation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
InteractionsUniProt · HPA
Protein binding partners of FAM98A 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 FAM98A as an antibody target. Whether an autoantibody or antibody against FAM98A could matter depends on whether native FAM98A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FAM98A 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 FAM98A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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