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CSNK1A1

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protein-coding gene in the species Homo sapiens

faili seletus: Visualisation de la protéine Cristallisée CSNK1A1

Välised allikad

Freebase
/m/03np4r_
Ensembl transcript ID
ENST00000261798[1]
ENST00000377843[1]
ENST00000503350[1]
ENST00000504676[1]
ENST00000515435[1]
ENST00000515748[1]
ENST00000515768[1]
ENST00000523203[1]
ENST00000606299[1]
ENST00000606719[1]
ENST00000606826[1]
ENST00000657001[1]
ENST00000657462[1]
ENST00000670598[1]
ENST00000657706[1]
ENST00000662268[1]
ENST00000661952[1]
Entrez Gene ID
1452[2]
Ensembl gene ID
ENSG00000113712[1]
UMLS CUI
C1332795[3]
HGNC gene symbol
CSNK1A1[2]
OMIM ID
600505[4]
HGNC ID
2451[2]
RefSeq RNA ID
NM_001025105[2]
NM_001271741[2]
NM_001271742[2]
NM_001892[2]

üksikjuht nähtusest

geen[1]

mille alamklass

protein-coding gene[5]

found in taxon

Homo sapiens[1]

encodes

Casein kinase 1 alpha 1[6]
casein kinase I isoform alpha[7]

genetic association

söögitoruvähk[8]

määramismeetod: Ülegenoomne assotsiatsiooniuuring, TAS

chromosome

human chromosome 5[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

reverse strand[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

148872949[1]

chromosome: human chromosome 5

genomic assembly: Genome assembly GRCh37

148871760[1]

chromosome: human chromosome 5

genomic assembly: Genome assembly GRCh37

149492982[1]

chromosome: human chromosome 5

genomic assembly: genome assembly GRCh38

genomic end

148884233[1]

chromosome: human chromosome 5

genomic assembly: Genome assembly GRCh37

148931007[1]

chromosome: human chromosome 5

genomic assembly: Genome assembly GRCh37

149551471[1]

chromosome: human chromosome 5

genomic assembly: genome assembly GRCh38

cytogenetic location

5q32[2]

HomoloGene ID

111694[2]

Gene Atlas image

ortholog

Csnk1a1[9][10]

found in taxon: koduhiir

Csnk1a1[9]

found in taxon: rändrott

CkIalpha[9][10]

found in taxon: Harilik äädikakärbes

kin-19[10]

found in taxon: varbuss

expressed in

stromal cell of endometrium[11]

järjekorranumber: 1

islet of Langerhans[11]

järjekorranumber: 2

Sapipõis[11]

järjekorranumber: 3

ganglionic eminence[11]

järjekorranumber: 4

Silelihased[11]

järjekorranumber: 5

epithelium of colon[11]

järjekorranumber: 6

ventricular zone[11]

järjekorranumber: 7

Nibu[11]

järjekorranumber: 8

Achilleuse kõõlus[11]

järjekorranumber: 9

Maolukuti[11]

järjekorranumber: 10

täpne vaste

http://identifiers.org/ncbigene/1452[12]

Viited

  1. ↑ 1,00 1,01 1,02 1,03 1,04 1,05 1,06 1,07 1,08 1,09 1,10 1,11 1,12 1,13 1,14 1,15 1,16 1,17 1,18 1,19 1,20 1,21 1,22 1,23 1,24 1,25 1,26 1,27 ensembl Release 106, ENSG00000113712
  2. ↑ 2,0 2,1 2,2 2,3 2,4 2,5 2,6 2,7 2,8 NCBI Gene, 15. mai 2022, 1452
  3. ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
  4. ↑ Online Mendelian Inheritance in Man, 19. august 2019
  5. ↑ NCBI homo sapiens annotation release 107, NCBI Gene, 2. oktoober 2016, 1452
  6. ↑ UniProt, 6. juuli 2017, P48729
  7. ↑ H0Y9X2, 20. märts 2016, UniProt, inglise keel
  8. ↑ Phenocarta, Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_5041&ncbiId=1452, http://www.genome.gov/gwastudies/index.cfm?gene=CSNK1A1, 25. mai 2020
  9. ↑ 9,0 9,1 9,2 HomoloGene build68, 111694
  10. ↑ 10,0 10,1 10,2 Orthologous MAtrix, https://omabrowser.org/oma/vps/P48729/
  11. ↑ 11,00 11,01 11,02 11,03 11,04 11,05 11,06 11,07 11,08 11,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000113712
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
Pärit leheküljelt "https://et.wikipedia.org/wiki/Eri:AboutTopic/Q5048388"