RN7SL262P
pseudogene in the species Homo sapiens
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RN7SL262P
Summary
RN7SL262P is a pseudogene[1].
Key Facts
- RN7SL262P's instance of is recorded as pseudogene[2].
- RN7SL262P's instance of is recorded as gene[3].
- RN7SL262P is a type of pseudogene[4].
- RN7SL262P's genomic start is recorded as 49152651[5].
- RN7SL262P's genomic end is recorded as 49152944[6].
- RN7SL262P's found in taxon is recorded as Homo sapiens[7].
- RN7SL262P's chromosome is recorded as human X chromosome[8].
- RN7SL262P's strand orientation is recorded as forward strand[9].
- RN7SL262P's exact match is recorded as http://identifiers.org/ncbigene/106479317[10].
- RN7SL262P's cytogenetic location is recorded as Xp11.23[11].
- RN7SL262P's expressed in is recorded as gonad[12].
- RN7SL262P's expressed in is recorded as right uterine tube[13].
- RN7SL262P's expressed in is recorded as ventricular zone[14].
- RN7SL262P's expressed in is recorded as ganglionic eminence[15].
- RN7SL262P's expressed in is recorded as lymph node[16].
- RN7SL262P's expressed in is recorded as skeletal muscle tissue[17].
- RN7SL262P's expressed in is recorded as pituitary gland[18].
- RN7SL262P's expressed in is recorded as corpus callosum[19].
- RN7SL262P's expressed in is recorded as anterior pituitary[20].
- RN7SL262P's expressed in is recorded as ovary[21].