KCTD2
protein-coding gene in the species Homo sapiens
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KCTD2
Summary
KCTD2 is a gene[1].
Key Facts
- KCTD2's instance of is recorded as gene[2].
- KCTD2 is a type of protein-coding gene[3].
- KCTD2's HomoloGene ID is recorded as 82389[4].
- KCTD2's ortholog is recorded as Kctd2[5].
- KCTD2's ortholog is recorded as kctd2[6].
- KCTD2's ortholog is recorded as inso-1[7].
- KCTD2's encodes is recorded as Potassium channel tetramerization domain containing 2[8].
- KCTD2's found in taxon is recorded as Homo sapiens[9].
- KCTD2's exact match is recorded as http://identifiers.org/ncbigene/23510[10].
- KCTD2's cytogenetic location is recorded as 17q25.1[11].
- KCTD2's expressed in is recorded as cerebellar hemisphere[12].
- KCTD2's expressed in is recorded as cerebellar vermis[13].
- KCTD2's expressed in is recorded as prefrontal cortex[14].
- KCTD2's expressed in is recorded as cingulate gyrus[15].
- KCTD2's expressed in is recorded as Brodmann area 9[16].
- KCTD2's expressed in is recorded as oocyte[17].
- KCTD2's expressed in is recorded as amygdala[18].
- KCTD2's expressed in is recorded as gastrocnemius muscle[19].
- KCTD2's expressed in is recorded as Brodmann area 10[20].
- KCTD2's expressed in is recorded as nucleus accumbens[21].