C19orf12
protein-coding gene in the species Homo sapiens
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C19orf12
Summary
C19orf12 is a gene[1].
Key Facts
- C19orf12's instance of is recorded as gene[2].
- C19orf12 is a type of protein-coding gene[3].
- C19orf12's HomoloGene ID is recorded as 41744[4].
- C19orf12's genomic start is recorded as 30191721[5].
- C19orf12's genomic start is recorded as 29698937[6].
- C19orf12's genomic end is recorded as 29715789[7].
- C19orf12's genomic end is recorded as 30206364[8].
- C19orf12's ortholog is recorded as 1600014C10Rik[9].
- C19orf12's ortholog is recorded as LOC690000[10].
- C19orf12's ortholog is recorded as si:ch211-260e23.7[11].
- C19orf12's ortholog is recorded as zgc:101715[12].
- C19orf12's ortholog is recorded as si:ch211-260e23.8[13].
- C19orf12's ortholog is recorded as CG3740[14].
- C19orf12's ortholog is recorded as zgc:112052[15].
- C19orf12's ortholog is recorded as Nazo[16].
- C19orf12's encodes is recorded as Chromosome 19 open reading frame 12[17].
- C19orf12's found in taxon is recorded as Homo sapiens[18].
- C19orf12's chromosome is recorded as human chromosome 19[19].
- C19orf12's genetic association is recorded as neurodegeneration with brain iron accumulation 4[20].
- C19orf12's genetic association is recorded as hereditary spastic paraplegia 43[21].
- C19orf12's strand orientation is recorded as reverse strand[22].
- C19orf12's exact match is recorded as http://identifiers.org/ncbigene/83636[23].
- C19orf12's cytogenetic location is recorded as 19q12[24].
- C19orf12's expressed in is recorded as endothelial cell[25].
- C19orf12's expressed in is recorded as pancreatic epithelial cell[26].