SEMA5A
Sign in to saveAlso known as semF, SEMAF, semaphorin 5A
Semaphorin-5A is a protein that in humans is encoded by the SEMA5A gene.
In the Vinony graph
Vinony's link graph records 5 inbound references to SEMA5A, and connects out to PubMed, human chromosome 5 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 5.
Vinony links it to 5 Wikipedia language editions.
Gene data
SEMA5A- Name
- semaphorin 5A
- Type
- protein-coding
- Position
- 9,035,033–9,546,142 (−)
- Aliases
- SEMAF, semF
- Ensembl
- ENSG00000112902
- RefSeq RNA
- NM_003966.3, XM_006714506.4, XM_006714507.4, XM_011514155.3, XM_011514156.3
- RefSeq protein
- NP_003957.2, XP_006714569.1, XP_006714570.1, XP_011512457.1, XP_011512458.1
This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.[provided by RefSeq, Jan 2010].
Gene Ontology
Biological process
Molecular function
Cellular component
Pathways
via MyGene.info
Gene · Ensembl
semaphorin 5A
- Symbol
- SEMA5A
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 5:9,035,033-9,546,142
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 9 more facts
- HomoloGene ID
- 2949
- exact match
- identifiers.org/ncbigene/9037
- genetic association
- Parkinson's disease
- found in taxon
- Homo sapiens
- genomic end
- 9546187
- genomic start
- 9035033
- chromosome
- human chromosome 5
- cytogenetic location
- 5p15.31
- expressed in
- decidua
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- Further reading
Semaphorin-5A is a protein that in humans is encoded by the SEMA5A gene.
Members of the semaphorin protein family, such as SEMA5A, are involved in axonal guidance during neural development.
Excerpted from Wikipedia’s “SEMA5A” article, available under the CC BY-SA 4.0 licence.