HCCS
protein-coding gene in the species Homo sapiens
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HCCS
Summary
HCCS is a gene[1].
Key Facts
- HCCS's instance of is recorded as gene[2].
- HCCS is a type of protein-coding gene[3].
- HCCS's HomoloGene ID is recorded as 3897[4].
- HCCS's genomic start is recorded as 11111301[5].
- HCCS's genomic start is recorded as 11129421[6].
- HCCS's genomic end is recorded as 11141198[7].
- HCCS's genomic end is recorded as 11123086[8].
- HCCS's ortholog is recorded as Hccs[9].
- HCCS's ortholog is recorded as CYT2[10].
- HCCS's ortholog is recorded as Hccs[11].
- HCCS's ortholog is recorded as hccsb[12].
- HCCS's ortholog is recorded as cchl-1[13].
- HCCS's ortholog is recorded as hccsa.1[14].
- HCCS's ortholog is recorded as Cchl[15].
- HCCS's encodes is recorded as Holocytochrome c synthase[16].
- HCCS's found in taxon is recorded as Homo sapiens[17].
- HCCS's chromosome is recorded as human X chromosome[18].
- HCCS's genetic association is recorded as microphthalmia–dermal aplasia–sclerocornea syndrome[19].
- HCCS's strand orientation is recorded as forward strand[20].
- HCCS's exact match is recorded as http://identifiers.org/ncbigene/3052[21].
- HCCS's cytogenetic location is recorded as Xp22.2[22].
- HCCS's expressed in is recorded as Skeletal muscle tissue of biceps brachii[23].
- HCCS's expressed in is recorded as gastrocnemius muscle[24].
- HCCS's expressed in is recorded as muscle of thigh[25].
- HCCS's expressed in is recorded as right ventricle[26].