RN7SL246P
pseudogene in the species Homo sapiens
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RN7SL246P
Summary
RN7SL246P is a pseudogene[1].
Key Facts
- RN7SL246P's instance of is recorded as pseudogene[2].
- RN7SL246P's instance of is recorded as gene[3].
- RN7SL246P is a type of pseudogene[4].
- RN7SL246P's genomic start is recorded as 45874035[5].
- RN7SL246P's genomic end is recorded as 45874330[6].
- RN7SL246P's found in taxon is recorded as Homo sapiens[7].
- RN7SL246P's chromosome is recorded as human chromosome 12[8].
- RN7SL246P's strand orientation is recorded as forward strand[9].
- RN7SL246P's exact match is recorded as http://identifiers.org/ncbigene/106480989[10].
- RN7SL246P's cytogenetic location is recorded as 12q12[11].
- RN7SL246P's expressed in is recorded as bone marrow cell[12].
- RN7SL246P's expressed in is recorded as sural nerve[13].
- RN7SL246P's expressed in is recorded as skeletal muscle tissue[14].
- RN7SL246P's expressed in is recorded as tonsil[15].
- RN7SL246P's expressed in is recorded as cervix[16].
- RN7SL246P's expressed in is recorded as human kidney[17].
- RN7SL246P's expressed in is recorded as primary visual cortex[18].
- RN7SL246P's expressed in is recorded as corpus callosum[19].
- RN7SL246P's expressed in is recorded as monocyte[20].
- RN7SL246P's expressed in is recorded as liver[21].