Wicipedia

LAMA3

Creu erthygl

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protein-coding gene in the species Homo sapiens

Adnoddau allanol

dynodwr Freebase
/m/02kg6pw
Ensembl transcript ID
ENST00000592519[1]
ENST00000269217[1]
ENST00000313654[1]
ENST00000399516[1]
ENST00000585600[1]
ENST00000586709[1]
ENST00000586751[1]
ENST00000587184[1]
ENST00000588004[1]
ENST00000588164[1]
ENST00000588770[1]
ENST00000590104[1]
ENST00000591749[1]
ENST00000592442[1]
ENST00000649721[1]
Entrez Gene ID
3909[2]
UMLS CUI
C1416777[3]
Ensembl gene ID
ENSG00000053747[1]
dynodwr OMIM
600805[4]
dynodwr HGNC
6483[2]
HGNC gene symbol
LAMA3[2]
RefSeq RNA ID
XM_011525982[2]
NM_000227[2]
NM_001127717[2]
NM_001127718[2]
NM_001302996[2]
NM_198129[2]
NR_130106[2]
XM_011525978[2]
XM_011525979[2]
XM_011525980[2]
XM_011525981[2]
XM_017025743[2]
XM_017025744[2]
XM_047437503[5]
XM_047437504[5]
XM_047437505[5]
XM_047437506[5]

enghraifft o'r canlynol

genyn[1]

isddosbarth o'r canlynol

genyn codio-protein[6]

found in taxon

Homo sapiens[1]

amgodau

Laminin subunit alpha 3[7]
Laminin subunit alpha-3[8]

genetic association

sglerosis ochrol amyotroffig[9]

dull penderfynu: genome-wide association study, TAS

Laryngoonychocutaneous syndrome[10][11][12]
junctional epidermolysis bullosa Herlitz type[13]

cromosom

cromosom dynol 18[1]

cynulliad genynnol: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

edefyn blaen[1]

cynulliad genynnol: genome assembly GRCh38, Genome assembly GRCh37

genomic start

21269407[1]

cromosom: cromosom dynol 18

cynulliad genynnol: Genome assembly GRCh37

23689453[1]

cromosom: cromosom dynol 18

cynulliad genynnol: genome assembly GRCh38

genomic end

21535030[1]

cromosom: cromosom dynol 18

cynulliad genynnol: Genome assembly GRCh37

23956222[1]

cromosom: cromosom dynol 18

cynulliad genynnol: genome assembly GRCh38

cytogenetic location

18q11.2[2]

HomoloGene ID

18279[2]

Gene Atlas image

ortholog

Lama3[14]

found in taxon: Llygoden y tŷ

Lama3[14]

found in taxon: brown rat

expressed in

right lung[15]

trefnolyn: 1

skin of leg[15]

trefnolyn: 2

periodontal fiber[15]

trefnolyn: 3

skin of abdomen[15]

trefnolyn: 4

mucosa of sigmoid colon[15]

trefnolyn: 5

jejunal mucosa[15]

trefnolyn: 6

decidua[15]

trefnolyn: 7

sural nerve[15]

trefnolyn: 8

upper lobe of left lung[15]

trefnolyn: 9

minor salivary glands[15]

trefnolyn: 10

cysyniad o'r un fath

http://identifiers.org/ncbigene/3909[16]

Cyfeiriadau

  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 ensembl Release 106, ENSG00000053747
  2. ↑ 2.00 2.01 2.02 2.03 2.04 2.05 2.06 2.07 2.08 2.09 2.10 2.11 2.12 2.13 2.14 2.15 2.16 2.17 NCBI Gene, 15 Mai 2022, 3909
  3. ↑ UMLS 2023, 15 Mehefin 2023, inferred by common HGNC mappings on source and on Wikidata
  4. ↑ Online Mendelian Inheritance in Man, 19 Awst 2019
  5. ↑ 5.0 5.1 5.2 5.3 NCBI Gene, 10 Ebrill 2022, 3909
  6. ↑ Ensembl Release 87, ENSG00000053747
  7. ↑ UniProt, 6 Gorffennaf 2017, Q16787
  8. ↑ K7EPP3, 20 Mawrth 2016, UniProt, Saesneg
  9. ↑ Phenocarta, Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1., https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3909, http://www.genome.gov/gwastudies/index.cfm?gene=LAMA3, 25 Mai 2020
  10. ↑ Q16787, 13 Awst 2019, UniProt
  11. ↑ Open Targets Platform, 24 Awst 2023, https://platform.opentargets.org/evidence/ENSG00000053747/MONDO_0009513, inferred from an Open Targets association score over 0.7
  12. ↑ Open Targets Platform, 24 Awst 2023, https://platform.opentargets.org/evidence/ENSG00000053747/Orphanet_2407, inferred from an Open Targets association score over 0.7
  13. ↑ Open Targets Platform, 24 Awst 2023, https://platform.opentargets.org/evidence/ENSG00000053747/Orphanet_79404, inferred from an Open Targets association score over 0.7
  14. ↑ 14.0 14.1 HomoloGene build68, 18279
  15. ↑ 15.00 15.01 15.02 15.03 15.04 15.05 15.06 15.07 15.08 15.09 Bgee, 7 Mehefin 2024, https://www.bgee.org/gene/ENSG00000053747
  16. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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