IFIH1
protein-coding gene in the species Homo sapiens
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IFIH1
Summary
IFIH1 is a gene[1].
Key Facts
- IFIH1's instance of is recorded as gene[2].
- IFIH1 is a type of protein-coding gene[3].
- IFIH1's HomoloGene ID is recorded as 32535[4].
- IFIH1's genomic start is recorded as 163123589[5].
- IFIH1's genomic start is recorded as 162267074[6].
- IFIH1's genomic end is recorded as 163175213[7].
- IFIH1's genomic end is recorded as 162318684[8].
- IFIH1's ortholog is recorded as Ifih1[9].
- IFIH1's ortholog is recorded as Ifih1[10].
- IFIH1's ortholog is recorded as ifih1[11].
- IFIH1's encodes is recorded as Interferon induced with helicase C domain 1[12].
- IFIH1's found in taxon is recorded as Homo sapiens[13].
- IFIH1's chromosome is recorded as human chromosome 2[14].
- IFIH1's genetic association is recorded as type-1 diabetes[15].
- IFIH1's genetic association is recorded as type 1 diabetes mellitus 19[16].
- IFIH1's genetic association is recorded as Singleton-Merten syndrome 1[17].
- IFIH1's genetic association is recorded as Singleton Merten syndrome[18].
- IFIH1's genetic association is recorded as Aicardi-Goutieres syndrome[19].
- IFIH1's strand orientation is recorded as reverse strand[20].
- IFIH1's exact match is recorded as http://identifiers.org/ncbigene/64135[21].
- IFIH1's cytogenetic location is recorded as 2q24.2[22].
- IFIH1's expressed in is recorded as palpebral conjunctiva[23].
- IFIH1's expressed in is recorded as parotid gland[24].
- IFIH1's expressed in is recorded as jejunal mucosa[25].
- IFIH1's expressed in is recorded as monocyte[26].