FAM169A
Soluble lamin-associated protein of 75 kDa
Also known as: F169A_HUMAN, KIAA0888, SLAP75
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y6X4
- Gene
- FAM169A
- Ensembl
- ENSG00000198780
- Chromosome
- 5
- Canonical length
- 670 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear membrane,Cytosol
OverviewNCBI Gene
Predicted to be located in nuclear inner membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
670 residues, UniProt reviewed canonical sequence.
>Q9Y6X4|FAM169A
1 MAFPVDMLEN CSHEELENSA EDYMSDLRCG DPENPECFSL LNITIPISLS NVGFVPLYGG
61 DQTQKILALF APEDSLTAVA LYLADQWWAI DDIVKTSVPS REGLKQVSTL GERVVLYVLN
121 RIIYRKQEME RNEIPFLCHS STDYAKILWK KGEAIGFYSV KPTGSICASF LTQSYQLPVL
181 DTMFLRKKYR GKDFGLHMLE DFVDSFTEDA LGLRYPLSSL MYTACKQYFE KYPGDHELLW
241 EVEGVGHWYQ RIPVTRALQR EALKILALSQ NEPKRPMSGE YGPASVPEYE ARTEDNQSSE
301 MQLTIDSLKD AFASTSEGHD KTSVSTHTRS GNLKRPKIGK RFQDSEFSSS QGEDEKTSQT
361 SLTASINKLE STARPSESSE EFLEEEPEQR GIEFEDESSD RDARPALETQ PQQEKQDGEK
421 ESELEPMNGE IMDDSLKTSL ITEEEDSTSE VLDEELKLQP FNSSEDSTNL VPLVVESSKP
481 PEVDAPDKTP RIPDSEMLMD EGTSDEKGHM EEKLSLLPRK KAHLGSSDNV ATMSNEERSD
541 GGFPNSVIAE FSEEPVSENL SPNTTSSLED QGEEGVSEPQ ETSTALPQSS LIEVELEDVP
601 FSQNAGQKNQ SEEQSEASSE QLDQFTQSAE KAVDSSSEEI EVEVPVVDRR NLRRKAKGHK
661 GPAKKKAKLTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FAM169A 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)
- 0.53
- Highest tissue expression
- 73 nTPM
Expression across tissuesHPA
Tissue
- retina: 73 nTPM
- epididymis: 18 nTPM
- cerebral cortex: 15 nTPM
- testis: 11 nTPM
- thyroid gland: 6.3 nTPM
- parathyroid gland: 5.1 nTPM
Single-cell type
- rod photoreceptor cells: 732 nCPM
- müller glia: 438 nCPM
- cone photoreceptor cells: 383 nCPM
- retinal bipolar cells: 299 nCPM
- retinal amacrine cells: 247 nCPM
- retinal horizontal cells: 188 nCPM
Immune cell
- MAIT T-cell: 1.1 nTPM
- naive CD8 T-cell: 1 nTPM
- naive CD4 T-cell: 0.8 nTPM
- gdT-cell: 0.7 nTPM
- memory CD8 T-cell: 0.7 nTPM
- memory CD4 T-cell: 0.4 nTPM
Brain region
- hypothalamus: 78 nTPM
- thalamus: 61 nTPM
- spinal cord: 60 nTPM
- white matter: 60 nTPM
- medulla oblongata: 55 nTPM
- basal ganglia: 54 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)
- 0.23
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.42
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- none
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FAM169A 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 FAM169A as an antibody target. Whether an autoantibody or antibody against FAM169A could matter depends on whether native FAM169A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FAM169A 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 FAM169A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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