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SEMA5A

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Protein-coding gene in the species Homo sapiens
SEMA5A
Identifiers
AliasesSEMA5A, SEMAF, semF, semaphorin 5A
External IDsOMIM: 609297; MGI: 107556; HomoloGene: 2949; GeneCards: SEMA5A; OMA:SEMA5A - orthologs
Gene location (Human)
Chromosome 5 (human)
Chr.Chromosome 5 (human)
Chromosome 5 (human)Genomic location for SEMA5AGenomic location for SEMA5A
Band5p15.31Start9,035,033 bp
End9,546,075 bp
Gene location (Mouse)
Chromosome 15 (mouse)
Chr.Chromosome 15 (mouse)
Chromosome 15 (mouse)Genomic location for SEMA5AGenomic location for SEMA5A
Band15 B3.1|15 13.02 cMStart32,244,956 bp
End32,696,487 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • metanephric glomerulus

  • stromal cell of endometrium

  • periodontal fiber

  • synovial joint

  • nipple

  • olfactory bulb

  • sural nerve

  • parietal pleura

  • trigeminal ganglion

  • decidua
Top expressed in
  • molar

  • internal carotid artery

  • lateral septal nucleus

  • vas deferens

  • lateral geniculate nucleus

  • external carotid artery

  • medial geniculate nucleus

  • human fetus

  • ventricular zone

  • ventromedial nucleus
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

9037

20356

Ensembl

ENSG00000112902

ENSMUSG00000022231

UniProt

Q13591

Q62217
Q3UPZ0

RefSeq (mRNA)

NM_003966

NM_009154

RefSeq (protein)

NP_003957

NP_033180

Location (UCSC)Chr 5: 9.04 – 9.55 MbChr 15: 32.24 – 32.7 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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.

Semaphorin 5A also plays a role in autism, reducing the ability of neurons to form connections with other neurons in certain brain regions.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000112902Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000022231Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Adams RH, Betz H, Püschel AW (June 1996). "A novel class of murine semaphorins with homology to thrombospondin is differentially expressed during early embryogenesis". Mechanisms of Development. 57 (1): 33–45. doi:10.1016/0925-4773(96)00525-4. PMID 8817451. S2CID 17827262.
  6. Simmons AD, Püschel AW, McPherson JD, Overhauser J, Lovett M (January 1998). "Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate interval". Biochemical and Biophysical Research Communications. 242 (3): 685–691. doi:10.1006/bbrc.1997.8027. PMID 9464278.
  7. ^ "Entrez Gene: SEMA5A sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A".
  8. Mosca-Boidron AL, Gueneau L, Huguet G, Goldenberg A, Henry C, Gigot N, et al. (June 2016). "A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability". European Journal of Human Genetics. 24 (6): 838–843. doi:10.1038/ejhg.2015.211. PMC 4867450. PMID 26395558.
  9. Carulli D, de Winter F, Verhaagen J (2021). "Semaphorins in Adult Nervous System Plasticity and Disease". Frontiers in Synaptic Neuroscience. 13: 672891. doi:10.3389/fnsyn.2021.672891. PMC 8148045. PMID 34045951.

Further reading


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