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KRT41P

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pseudogene in Homo sapiens

Välised allikad

Ensembl transcript ID
ENST00000393988[1]
UMLS CUI
C1825757[2]
HGNC gene symbol
KRT41P[3]
Entrez Gene ID
8686[3]
Ensembl gene ID
ENSG00000225438[1]
HGNC ID
6457[3]
Freebase
/m/0zbww7s

üksikjuht nähtusest

pseudogene[1]
geen[4]

mille alamklass

pseudogene[5]

found in taxon

Homo sapiens[1]

chromosome

human chromosome 17[1]

genomic assembly: genome assembly GRCh38

strand orientation

reverse strand[1]

genomic assembly: genome assembly GRCh38

genomic start

41406512[1]

chromosome: human chromosome 17

genomic assembly: genome assembly GRCh38

genomic end

41411775[1]

chromosome: human chromosome 17

genomic assembly: genome assembly GRCh38

cytogenetic location

17q21.2[3]

expressed in

skin of abdomen[6]

järjekorranumber: 1

skin of leg[6]

järjekorranumber: 2

neerud[6]

järjekorranumber: 3

human kidney[6]

järjekorranumber: 4

Neerukoor[6]

järjekorranumber: 5

Silelihased[6]

järjekorranumber: 6

lactiferous gland[6]

järjekorranumber: 7

subcutaneous adipose tissue[6]

järjekorranumber: 8

täpne vaste

http://identifiers.org/ncbigene/8686[7]

Viited

  1. ↑ 1,0 1,1 1,2 1,3 1,4 1,5 1,6 1,7 ensembl Release 106, ENSG00000225438
  2. ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
  3. ↑ 3,0 3,1 3,2 3,3 NCBI Gene, 15. mai 2022, 8686
  4. ↑ NCBI Gene, 6. jaanuar 2018, 8686
  5. ↑ NCBI homo sapiens annotation release 107, NCBI Gene, 12. september 2016, 8686
  6. ↑ 6,0 6,1 6,2 6,3 6,4 6,5 6,6 6,7 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000225438
  7. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
Pärit leheküljelt "https://et.wikipedia.org/wiki/Eri:AboutTopic/Q16886589"