RN7SL291P
pseudogene in the species Homo sapiens
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RN7SL291P
Summary
RN7SL291P is a pseudogene[1].
Key Facts
- RN7SL291P's instance of is recorded as pseudogene[2].
- RN7SL291P's instance of is recorded as gene[3].
- RN7SL291P is a type of pseudogene[4].
- RN7SL291P's genomic start is recorded as 44772773[5].
- RN7SL291P's genomic end is recorded as 44773061[6].
- RN7SL291P's found in taxon is recorded as Homo sapiens[7].
- RN7SL291P's chromosome is recorded as human X chromosome[8].
- RN7SL291P's strand orientation is recorded as reverse strand[9].
- RN7SL291P's exact match is recorded as http://identifiers.org/ncbigene/106479328[10].
- RN7SL291P's cytogenetic location is recorded as Xp11.3[11].
- RN7SL291P's expressed in is recorded as sural nerve[12].
- RN7SL291P's expressed in is recorded as corpus callosum[13].
- RN7SL291P's expressed in is recorded as monocyte[14].
- RN7SL291P's expressed in is recorded as Achilles tendon[15].
- RN7SL291P's expressed in is recorded as stromal cell of endometrium[16].
- RN7SL291P's expressed in is recorded as prefrontal cortex[17].
- RN7SL291P's expressed in is recorded as gallbladder[18].
- RN7SL291P's expressed in is recorded as bone marrow[19].
- RN7SL291P's expressed in is recorded as skeletal muscle tissue[20].
- RN7SL291P's expressed in is recorded as liver[21].