IER3IP1
Ilme
protein-coding gene in the species Homo sapiens
mille alamklass
protein-coding gene[5]
found in taxon
Homo sapiens[2]
encodes
Immediate early response 3 interacting protein 1[6]
genetic association
primary microcephaly-epilepsy-permanent neonatal diabetes syndrome[7]
chromosome
strand orientation
genomic start
genomic end
cytogenetic location
18q21.1[1]
HomoloGene ID
41106[1]
expressed in
täpne vaste
Viited
- ↑ 1,0 1,1 1,2 1,3 1,4 1,5 NCBI Gene, 15. mai 2022, 51124
- ↑ 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 ensembl Release 106, ENSG00000134049
- ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
- ↑ Online Mendelian Inheritance in Man, 19. august 2019
- ↑ NCBI homo sapiens annotation release 107, NCBI Gene, 3. oktoober 2016, 51124
- ↑ UniProt, 6. juuli 2017, Q9Y5U9
- ↑ Q9Y5U9, 13. august 2019, UniProt
- ↑ 8,0 8,1 HomoloGene build68, 41106
- ↑ 9,00 9,01 9,02 9,03 9,04 9,05 9,06 9,07 9,08 9,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000134049
- ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069