Neidio i'r cynnwys

KRT41P

Ni chefnogir cynnwys y dudalen mewn ieithoedd eraill.
Creu erthygl

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pseudogene in Homo sapiens

Adnoddau allanol

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

enghraifft o'r canlynol

pseudogene[1]
genyn[4]

isddosbarth o'r canlynol

pseudogene[5]

found in taxon

Homo sapiens[1]

cromosom

cromosom dynol 17[1]

cynulliad genynnol: genome assembly GRCh38

strand orientation

edefyn ôl[1]

cynulliad genynnol: genome assembly GRCh38

genomic start

41406512[1]

cromosom: cromosom dynol 17

cynulliad genynnol: genome assembly GRCh38

genomic end

41411775[1]

cromosom: cromosom dynol 17

cynulliad genynnol: genome assembly GRCh38

cytogenetic location

17q21.2[3]

expressed in

skin of abdomen[6]

trefnolyn: 1

skin of leg[6]

trefnolyn: 2

aren[6]

trefnolyn: 3

human kidney[6]

trefnolyn: 4

renal cortex[6]

trefnolyn: 5

smooth muscle tissue[6]

trefnolyn: 6

lactiferous gland[6]

trefnolyn: 7

subcutaneous adipose tissue[6]

trefnolyn: 8

cysyniad o'r un fath

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

Cyfeiriadau

  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 Mehefin 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 Ionawr 2018, 8686
  5. ↑ NCBI homo sapiens annotation release 107, NCBI Gene, 12 Medi 2016, 8686
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 6.7 Bgee, 7 Mehefin 2024, https://www.bgee.org/gene/ENSG00000225438
  7. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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