CLSTN1

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Calsyntenin-1 is a protein that in humans is encoded by the CLSTN1 gene.[5][6]

AliasesCLSTN1, ALC-ALPHA, CDHR12, CSTN1, PIK3CD, XB31alpha, alcalpha1, alcalpha2, CST-1, calsyntenin 1
End9,823,984 bp[1]
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CLSTN1
Identifiers
AliasesCLSTN1, ALC-ALPHA, CDHR12, CSTN1, PIK3CD, XB31alpha, alcalpha1, alcalpha2, CST-1, calsyntenin 1
External IDsOMIM: 611321; MGI: 1929895; HomoloGene: 8814; GeneCards: CLSTN1; OMA:CLSTN1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014944
NM_001009566
NM_001302883

NM_001290989
NM_023051

RefSeq (protein)

NP_001009566
NP_001289812
NP_055759

NP_001277918
NP_075538

Location (UCSC)Chr 1: 9.73 – 9.82 MbChr 4: 149.67 – 149.73 Mb
PubMed search[3][4]
Wikidata
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Clinical relevance

Mutations in this gene have been shown associated to pathogenic mechanisms of Alzheimer's disease.[7]

Interactions

CLSTN1 has been shown to interact with APBA2[8][9] and Amyloid precursor protein.[8][9]

References

Further reading

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