FIGNL1
Fidgetin-like protein 1
Also known as: FIGL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6PIW4
- Gene
- FIGNL1
- Ensembl
- ENSG00000132436
- Chromosome
- 7
- Canonical length
- 674 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a member of the AAA ATPase family of proteins. The encoded protein is recruited to sites of DNA damage where it plays a role in DNA double-strand break repair via homologous recombination. This protein has also been shown to localize to the centrosome and inhibit ciliogenesis, and may regulate the proliferation and differentiation of osteoblasts. [provided by RefSeq, Oct 2016]
Canonical amino-acid sequenceUniProt
674 residues, UniProt reviewed canonical sequence.
>Q6PIW4|FIGNL1
1 MQTSSSRSVH LSEWQKNYFA ITSGICTGPK ADAYRAQILR IQYAWANSEI SQVCATKLFK
61 KYAEKYSAII DSDNVESGLN NYAENILTLA GSQQTDSDKW QSGLSINNVF KMSSVQKMMQ
121 AGKKFKDSLL EPALASVVIH KEATVFDLPK FSVCGSSQES DSLPNSAHDR DRTQDFPESN
181 RLKLLQNAQP PMVTNTARTC PTFSAPVGES ATAKFHVTPL FGNVKKENHS SAKENIGLNV
241 FLSNQSCFPA ACENPQRKSF YGSGTIDALS NPILNKACSK TEDNGPKEDS SLPTFKTAKE
301 QLWVDQQKKY HQPQRASGSS YGGVKKSLGA SRSRGILGKF VPPIPKQDGG EQNGGMQCKP
361 YGAGPTEPAH PVDERLKNLE PKMIELIMNE IMDHGPPVNW EDIAGVEFAK ATIKEIVVWP
421 MLRPDIFTGL RGPPKGILLF GPPGTGKTLI GKCIASQSGA TFFSISASSL TSKWVGEGEK
481 MVRALFAVAR CQQPAVIFID EIDSLLSQRG DGEHESSRRI KTEFLVQLDG ATTSSEDRIL
541 VVGATNRPQE IDEAARRRLV KRLYIPLPEA SARKQIVINL MSKEQCCLSE EEIEQIVQQS
601 DAFSGADMTQ LCREASLGPI RSLQTADIAT ITPDQVRPIA YIDFENAFRT VRPSVSPKDL
661 ELYENWNKTF GCGKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FIGNL1 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)
- 0.47
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 12 nTPM
- ovary: 9.9 nTPM
- lymph node: 9.5 nTPM
- thymus: 9.3 nTPM
- smooth muscle: 9.1 nTPM
- retina: 8.8 nTPM
Single-cell type
- early primary spermatocytes: 43 nCPM
- erythrocyte progenitors: 27 nCPM
- leydig cells: 22 nCPM
- megakaryocyte progenitors: 21 nCPM
- differentiating spermatogonia: 20 nCPM
- monocyte progenitors: 17 nCPM
Immune cell
- non-classical monocyte: 6.2 nTPM
- naive B-cell: 4.1 nTPM
- T-reg: 4.1 nTPM
- NK-cell: 3.9 nTPM
- memory B-cell: 3.4 nTPM
- memory CD8 T-cell: 3.4 nTPM
Brain region
- cerebellum: 14 nTPM
- white matter: 12 nTPM
- basal ganglia: 11 nTPM
- pons: 11 nTPM
- hypothalamus: 10 nTPM
- cerebral cortex: 10 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)
- 0.79
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.52
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- ATP metabolic process
- cellular response to ionizing radiation
- male meiotic nuclear division
- microtubule severing
- negative regulation of apoptotic process
- negative regulation of intrinsic apoptotic signaling pathway
- osteoblast differentiation
- osteoblast proliferation
- regulation of cell cycle
- regulation of double-strand break repair via homologous recombination
Molecular functions
- ATP binding
- ATP hydrolysis activity
- hydrolase activity
- magnesium ion binding
- microtubule severing ATPase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- AAA+ ATPase domain
- ATPase, AAA-type, core
- ATPase, AAA-type, conserved site
- Spastin/Vps4, C-terminal
- P-loop containing nucleoside triphosphate hydrolase
- AAA ATPase, AAA+ lid domain
- Microtubule-severing AAA ATPase
- ATPase family associated with various cellular activities (AAA)
- Vps4 C terminal oligomerisation domain
- AAA+ lid domain
- Fidgetin-like 1, ATPase domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FIGNL1 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 FIGNL1 as an antibody target. Whether an autoantibody or antibody against FIGNL1 could matter depends on whether native FIGNL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FIGNL1 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 FIGNL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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