SAMD14
Sterile alpha motif domain-containing protein 14
Also known as: FLJ36890, SAM14_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IZD0
- Gene
- SAMD14
- Ensembl
- ENSG00000167100
- Chromosome
- 17
- Canonical length
- 417 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli fibrillar center
OverviewNCBI Gene
Predicted to enable actin filament binding activity. Predicted to be involved in actin filament organization; calcium-mediated signaling; and neuron projection development. Predicted to be active in several cellular components, including actin cytoskeleton; dendrite; and postsynaptic density. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
417 residues, UniProt reviewed canonical sequence.
>Q8IZD0|SAMD14
1 MASSKLREPV DEVFDLDLAV PETARLDSSL HKARAQLLAK GRRHRPSRSR LRDSASSAED
61 GEGSDGPGGK VTDGCGSPLH RLRSPLHSGP GSPAGGSFCL DPPGLRRSLD EDEPPPSPLT
121 RYRPLHNAAS HEGLAAASCS PPRSAPSSDS SPSFVRRHPR AEPHSEDDSR DASPPEPASP
181 TIGLDKKTRR KFLDLGVTLR RASTGKSRKE KGSNRLSMGS RESVEGSGRS GGSPFLPFSW
241 FTDSGKGSAS SGSTTSPTCS PKHEGFSPKK SASQESTLSD DSTPPSSSPK IPSGPWQEAK
301 CSYPYHTLSQ SSDEFLDEPL PPVHHWTSQQ VGQWLQSLNL EQYAAEFAAR QVDGPQLLQL
361 DGSKLKSLGL SNSHDRALVK RKLKEMAAAA EKERKAQEKA ARQREKLRRR EQEAKKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SAMD14 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)
- 0.65
- Highest tissue expression
- 67 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 67 nTPM
- cerebral cortex: 36 nTPM
- amygdala: 34 nTPM
- basal ganglia: 33 nTPM
- hippocampal formation: 31 nTPM
- hypothalamus: 17 nTPM
Single-cell type
- megakaryocytes: 235 nCPM
- platelets: 73 nCPM
- retinal bipolar cells: 61 nCPM
- epididymal principal cells: 41 nCPM
- cardiomyocytes: 37 nCPM
- retinal amacrine cells: 33 nCPM
Immune cell
- basophil: 0.6 nTPM
- eosinophil: 0.2 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 50 nTPM
- hippocampal formation: 41 nTPM
- cerebral cortex: 41 nTPM
- amygdala: 40 nTPM
- basal ganglia: 39 nTPM
- hypothalamus: 33 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)
- 0.72
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.13
- DepMap mean gene effect
- -0.11
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SAMD14 as an antibody target. Whether an autoantibody or antibody against SAMD14 could matter depends on whether native SAMD14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SAMD14 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 SAMD14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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