KCND3
protein-coding gene in the species Homo sapiens
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KCND3
Summary
KCND3 is a gene[1]. KCND3 ranks in the top 2% of gene entities by monthly Wikipedia readership (18 views/month).[2]
Key Facts
- KCND3's instance of is recorded as gene[3].
- KCND3 is a type of protein-coding gene[4].
- KCND3's HomoloGene ID is recorded as 21036[5].
- KCND3's genomic start is recorded as 111770662[6].
- KCND3's genomic start is recorded as 112313284[7].
- KCND3's genomic end is recorded as 112531777[8].
- KCND3's genomic end is recorded as 111989668[9].
- KCND3's ortholog is recorded as Kcnd3[10].
- KCND3's ortholog is recorded as Kcnd3[11].
- KCND3's ortholog is recorded as kcnd3[12].
- KCND3's encodes is recorded as Potassium voltage-gated channel subfamily D member 3[13].
- KCND3's found in taxon is recorded as Homo sapiens[14].
- KCND3's chromosome is recorded as human chromosome 1[15].
- KCND3's genetic association is recorded as smallpox[16].
- KCND3's genetic association is recorded as spinocerebellar ataxia type 19/22[17].
- KCND3's genetic association is recorded as Brugada syndrome 9[18].
- KCND3's strand orientation is recorded as reverse strand[19].
- KCND3's exact match is recorded as http://identifiers.org/ncbigene/3752[20].
- KCND3's cytogenetic location is recorded as 1p13.2[21].
- KCND3's expressed in is recorded as cerebellar vermis[22].
- KCND3's expressed in is recorded as pars reticulata[23].
- KCND3's expressed in is recorded as lateral nuclear group of thalamus[24].
- KCND3's expressed in is recorded as pars compacta[25].
- KCND3's expressed in is recorded as paraflocculus of cerebellum[26].
- KCND3's expressed in is recorded as Brodmann area 23[27].
Why It Matters
KCND3 ranks in the top 2% of gene entities by monthly Wikipedia readership (18 views/month).[2]