DNMT1
protein-coding gene in the species Homo sapiens
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DNMT1
Summary
DNMT1 is a gene[1]. DNMT1 ranks in the top 1% of gene entities by monthly Wikipedia readership (62 views/month).[2]
Key Facts
- DNMT1's instance of is recorded as gene[3].
- DNMT1 is a type of protein-coding gene[4].
- DNMT1's HomoloGene ID is recorded as 124071[5].
- DNMT1's genomic start is recorded as 10244021[6].
- DNMT1's genomic start is recorded as 10133342[7].
- DNMT1's genomic end is recorded as 10231286[8].
- DNMT1's genomic end is recorded as 10341962[9].
- DNMT1's ortholog is recorded as Dnmt1[10].
- DNMT1's ortholog is recorded as Dnmt1[11].
- DNMT1's ortholog is recorded as dnmt1[12].
- DNMT1's encodes is recorded as DNA methyltransferase 1[13].
- DNMT1's found in taxon is recorded as Homo sapiens[14].
- DNMT1's chromosome is recorded as human chromosome 19[15].
- DNMT1's genetic association is recorded as hereditary sensory neuropathy-deafness-dementia syndrome[16].
- DNMT1's genetic association is recorded as autosomal dominant cerebellar ataxia, deafness and narcolepsy[17].
- DNMT1's strand orientation is recorded as reverse strand[18].
- DNMT1's exact match is recorded as http://identifiers.org/ncbigene/1786[19].
Why It Matters
DNMT1 ranks in the top 1% of gene entities by monthly Wikipedia readership (62 views/month).[2] DNMT1 has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[20] DNMT1 is known by 9 alternative names across languages and contexts.[21]