SERPINF2
Sign in to saveAlso known as A2AP, AAP, ALPHA-2-PI, API, PLI, serpin family F member 2, alpha2AP
protein-coding gene in the species Homo sapiens
Gene data
SERPINF2- Name
- serpin family F member 2
- Type
- protein-coding
- Position
- 1,742,069–1,755,271 (+)
- Aliases
- A2AP, AAP, ALPHA-2-PI, API, PLI, alpha2AP
- Ensembl
- ENSG00000167711
- RefSeq RNA
- NM_000934.4, NM_001165920.1, NM_001165921.2, XM_005256701.5, XM_017024765.2
- RefSeq protein
- NP_000925.2, NP_001159392.1, NP_001159393.1, XP_005256758.2, XP_016880254.1
This gene encodes a member of the serpin family of serine protease inhibitors. The protein is a major inhibitor of plasmin, which degrades fibrin and various other proteins. Consequently, the proper function of this gene has a major role in regulating the blood clotting pathway. Mutations in this gene result in alpha-2-plasmin inhibitor deficiency, which is characterized by severe hemorrhagic diathesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
serpin family F member 2
- Symbol
- SERPINF2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:1,742,069-1,755,271
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- 2R9Y.png
Show 9 more facts
- HomoloGene ID
- 719
- genomic start
- 1646130
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/5345
- chromosome
- human chromosome 17
- genomic end
- 1755265
- cytogenetic location
- 17p13.3
- Commons category
- Alpha 2-antiplasmin
- expressed in
- myometrium
Sources (6)
via Wikidata · CC0