Saltu al enhavo

NRG1

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protein-coding gene in the species Homo sapiens

Eksteraj rimedoj

identigilo de Freebase
/m/02rccpd
numero en Microsoft Academic
2778560701
Ensembl transcript ID
ENST00000631040[1]
ENST00000287842[1]
ENST00000356819[1]
ENST00000405005[1]
ENST00000517967[1]
ENST00000518084[1]
ENST00000518206[1]
ENST00000519240[1]
ENST00000519301[1]
ENST00000520407[1]
ENST00000520502[1]
ENST00000521670[1]
ENST00000522402[1]
ENST00000522569[1]
ENST00000523041[1]
ENST00000523079[1]
ENST00000523320[1]
ENST00000523534[1]
ENST00000523681[1]
ENST00000539990[1]
ENST00000614767[1]
ENST00000650919[1]
ENST00000650980[1]
ENST00000652698[1]
ENST00000650856[1]
ENST00000650964[1]
ENST00000651696[1]
ENST00000651807[1]
ENST00000651175[1]
ENST00000651335[1]
ENST00000652592[1]
ENST00000650967[1]
ENST00000650819[1]
ENST00000651333[1]
ENST00000652588[1]
ENST00000651149[1]
ENST00000650866[1]
Entrez Gene ID
3084[2]
Ensembl gene ID
ENSG00000157168[1]
UMLS CUI
C1367656[3]
CIViC gene ID
2593
OpenAlex ID
C2778560701[4]
identigilo laŭ Reta Mendela Heredo je Homoj
142445[5]
HGNC ID
7997[2]
HGNC gene symbol
NRG1[2]
RefSeq RNA ID
NM_001159995[2]
NM_001159996[2]
NM_001159999[2]
NM_001160001[2]
NM_001160002[2]
NM_001160004[2]
NM_001160005[2]
NM_001160007[2]
NM_001160008[2]
NM_004495[2]
NM_013956[2]
NM_013957[2]
NM_013958[2]
NM_013959[2]
NM_013960[2]
NM_013962[2]
NM_013964[2]
XM_011544512[2]
NM_001322197[2]
NM_001322201[2]
NM_001322202[2]
NM_001322205[2]
NM_001322206[2]
NM_001322207[2]
XM_017013367[2]
XM_017013368[2]
XM_017013371[2]
XM_017013372[2]

estas

geno[1]

subaro de

protein-kodanta geno[6]

en taksono

Homo sapiens[1]

kodas

Neuregulin 1[7]
Neuregulin 1 isoform HRG-beta2[8]
Neuregulin 1 type IV fetal B beta 1a[9]
Pro-neuregulin-1, membrane-bound isoform[10]
Neuregulin 1 variant fetal a IV 1[11]

rilato al geno

coronary artery disease[12]

determina metodo: tut-genara asociada studo, spurebla aŭtora aserto

tiroida kancero[13]

determina metodo: tut-genara asociada studo, spurebla aŭtora aserto

malsano de Hirschsprung[14]

determina metodo: tut-genara asociada studo, spurebla aŭtora aserto

kromosomo

homa kromosomo 8[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

orientiĝo de DNA-fadenoj

antaŭuma DNA-fadeno[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

komenco de geno

31496902[1]

kromosomo: homa kromosomo 8

genomic assembly: Genome assembly GRCh37

31639222[1]

kromosomo: homa kromosomo 8

genomic assembly: genome assembly GRCh38

fino de geno

32622548[1]

kromosomo: homa kromosomo 8

genomic assembly: Genome assembly GRCh37

32855666[1]

kromosomo: homa kromosomo 8

genomic assembly: genome assembly GRCh38

ĉelgenetika loko

8p12[2]

HomoloGene ID

8509[2]

Gene Atlas image

ortohomologa geno

Nrg1[15][16]

en taksono: Bruna rato

nrg1[15]

en taksono: Danio rerio

esprimata en

ventricular zone[17]

vicnumero: 1

ganglionic eminence[17]

vicnumero: 2

oocito[17]

vicnumero: 3

secondary oocyte[17]

vicnumero: 4

Monocito[17]

vicnumero: 5

Granulocito[17]

vicnumero: 6

stromal cell of endometrium[17]

vicnumero: 7

spinal ganglia[17]

vicnumero: 8

gonado[17]

vicnumero: 9

endothelial cell[17]

vicnumero: 10

plene kongruas kun

http://identifiers.org/ncbigene/3084[18]

Referenco

  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 1,28 1,29 1,30 1,31 1,32 1,33 1,34 1,35 1,36 1,37 1,38 1,39 1,40 1,41 1,42 1,43 1,44 1,45 ensembl Release 106, ENSG00000157168
  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 2,18 2,19 2,20 2,21 2,22 2,23 2,24 2,25 2,26 2,27 2,28 2,29 2,30 2,31 2,32 NCBI Gene, 15 maj. 2022, 3084
  3. ↑ UMLS 2023, 15 jun. 2023, inferred by common HGNC mappings on source and on Wikidata
  4. ↑ OpenAlex, 26 jan. 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  5. ↑ Reta Mendela Heredo je Homoj, 19 aŭg. 2019
  6. ↑ Ensembl Release 87, ENSG00000157168
  7. ↑ UniProt, 6 jul. 2017, Q02297
  8. ↑ Q7RTW3, 20 mar. 2016, UniProt, angla lingvo
  9. ↑ A6MW55, 20 mar. 2016, UniProt, angla lingvo
  10. ↑ E5RHQ1, 20 mar. 2016, UniProt, angla lingvo
  11. ↑ A5YAK6, 9 aŭg. 2016, UniProt, angla lingvo
  12. ↑ Phenocarta, Genetics of coronary artery calcification among African Americans, a meta-analysis, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_3393&ncbiId=3084, http://www.genome.gov/gwastudies/index.cfm?gene=NRG1, 25 maj. 2020
  13. ↑ Phenocarta, Discovery of common variants associated with low TSH levels and thyroid cancer risk, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1781&ncbiId=3084, http://www.genome.gov/gwastudies/index.cfm?gene=NRG1, 25 maj. 2020
  14. ↑ Phenocarta, Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10487&ncbiId=3084, http://www.genome.gov/gwastudies/index.cfm?gene=NRG1, 25 maj. 2020
  15. ↑ 15,0 15,1 HomoloGene build68, 8509
  16. ↑ Orthologous MAtrix, https://omabrowser.org/oma/vps/Q02297/
  17. ↑ 17,00 17,01 17,02 17,03 17,04 17,05 17,06 17,07 17,08 17,09 Bgee, 7 jun. 2024, https://www.bgee.org/gene/ENSG00000157168
  18. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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