RHOXF2
protein-coding gene in the species Homo sapiens
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RHOXF2
Summary
RHOXF2 is a gene[1].
Key Facts
- RHOXF2's instance of is recorded as gene[2].
- RHOXF2 is a type of protein-coding gene[3].
- RHOXF2's HomoloGene ID is recorded as 129688[4].
- RHOXF2's genomic start is recorded as 119292467[5].
- RHOXF2's genomic start is recorded as 120158613[6].
- RHOXF2's genomic end is recorded as 120165630[7].
- RHOXF2's genomic end is recorded as 119297945[8].
- RHOXF2's encodes is recorded as Rhox homeobox family member 2[9].
- RHOXF2's found in taxon is recorded as Homo sapiens[10].
- RHOXF2's chromosome is recorded as human X chromosome[11].
- RHOXF2's strand orientation is recorded as forward strand[12].
- RHOXF2's exact match is recorded as http://identifiers.org/ncbigene/84528[13].
- RHOXF2's cytogenetic location is recorded as Xq24[14].
- RHOXF2's expressed in is recorded as testicle[15].
- RHOXF2's expressed in is recorded as gonad[16].
- RHOXF2's expressed in is recorded as right testis[17].
- RHOXF2's expressed in is recorded as left testis[18].
- RHOXF2's expressed in is recorded as right uterine tube[19].
- RHOXF2's expressed in is recorded as blood[20].
- RHOXF2's expressed in is recorded as primary visual cortex[21].
- RHOXF2's expressed in is recorded as human kidney[22].
- RHOXF2's expressed in is recorded as human musculoskeletal system[23].
- RHOXF2's expressed in is recorded as intestine[24].