RPS7P12
pseudogene in the species Homo sapiens
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RPS7P12
Summary
RPS7P12 is a pseudogene[1].
Key Facts
- RPS7P12's instance of is recorded as pseudogene[2].
- RPS7P12's instance of is recorded as gene[3].
- RPS7P12 is a type of pseudogene[4].
- RPS7P12's genomic start is recorded as 134650830[5].
- RPS7P12's genomic end is recorded as 134651411[6].
- RPS7P12's found in taxon is recorded as Homo sapiens[7].
- RPS7P12's chromosome is recorded as human X chromosome[8].
- RPS7P12's strand orientation is recorded as forward strand[9].
- RPS7P12's exact match is recorded as http://identifiers.org/ncbigene/100270914[10].
- RPS7P12's cytogenetic location is recorded as Xq26.3[11].
- RPS7P12's expressed in is recorded as gonad[12].
- RPS7P12's expressed in is recorded as placenta[13].
- RPS7P12's expressed in is recorded as stromal cell of endometrium[14].
- RPS7P12's expressed in is recorded as smooth muscle tissue[15].
- RPS7P12's expressed in is recorded as fallopian tube[16].
- RPS7P12's expressed in is recorded as ganglionic eminence[17].
- RPS7P12's expressed in is recorded as left uterine tube[18].
- RPS7P12's expressed in is recorded as islet of Langerhans[19].
- RPS7P12's expressed in is recorded as canal of the cervix[20].
- RPS7P12's expressed in is recorded as gallbladder[21].