RN7SL67P
pseudogene in the species Homo sapiens
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RN7SL67P
Summary
RN7SL67P is a pseudogene[1].
Key Facts
- RN7SL67P's instance of is recorded as pseudogene[2].
- RN7SL67P's instance of is recorded as gene[3].
- RN7SL67P is a type of pseudogene[4].
- RN7SL67P's genomic start is recorded as 19303480[5].
- RN7SL67P's genomic end is recorded as 19303775[6].
- RN7SL67P's found in taxon is recorded as Homo sapiens[7].
- RN7SL67P's chromosome is recorded as human chromosome 12[8].
- RN7SL67P's strand orientation is recorded as forward strand[9].
- RN7SL67P's exact match is recorded as http://identifiers.org/ncbigene/106479248[10].
- RN7SL67P's cytogenetic location is recorded as 12p12.3[11].
- RN7SL67P's expressed in is recorded as testicle[12].
- RN7SL67P's expressed in is recorded as corpus callosum[13].
- RN7SL67P's expressed in is recorded as epithelium of colon[14].
- RN7SL67P's expressed in is recorded as bone marrow cell[15].
- RN7SL67P's expressed in is recorded as tonsil[16].
- RN7SL67P's expressed in is recorded as sural nerve[17].
- RN7SL67P's expressed in is recorded as kidney[18].
- RN7SL67P's expressed in is recorded as liver[19].
- RN7SL67P's expressed in is recorded as primary visual cortex[20].
- RN7SL67P's expressed in is recorded as prefrontal cortex[21].