ZNF229
protein-coding gene in the species Homo sapiens
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ZNF229
Summary
ZNF229 is a gene[1].
Key Facts
- ZNF229's instance of is recorded as gene[2].
- ZNF229 is a type of protein-coding gene[3].
- ZNF229's HomoloGene ID is recorded as 130672[4].
- ZNF229's genomic start is recorded as 44417519[5].
- ZNF229's genomic start is recorded as 44921685[6].
- ZNF229's genomic end is recorded as 44448578[7].
- ZNF229's genomic end is recorded as 44952766[8].
- ZNF229's ortholog is recorded as house mouse[9].
- ZNF229's encodes is recorded as Zinc finger protein 229[10].
- ZNF229's found in taxon is recorded as Homo sapiens[11].
- ZNF229's chromosome is recorded as human chromosome 19[12].
- ZNF229's strand orientation is recorded as reverse strand[13].
- ZNF229's exact match is recorded as http://identifiers.org/ncbigene/7772[14].
- ZNF229's cytogenetic location is recorded as 19q13.31[15].
- ZNF229's expressed in is recorded as gonad[16].
- ZNF229's expressed in is recorded as testicle[17].
- ZNF229's expressed in is recorded as ventricular zone[18].
- ZNF229's expressed in is recorded as ganglionic eminence[19].
- ZNF229's expressed in is recorded as islet of Langerhans[20].
- ZNF229's expressed in is recorded as secondary oocyte[21].
- ZNF229's expressed in is recorded as stromal cell of endometrium[22].
- ZNF229's expressed in is recorded as retinal pigment epithelium[23].
- ZNF229's expressed in is recorded as smooth muscle tissue[24].
- ZNF229's expressed in is recorded as germinal epithelium[25].