RN7SL597P
pseudogene in the species Homo sapiens
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RN7SL597P
Summary
RN7SL597P is a pseudogene[1].
Key Facts
- RN7SL597P's instance of is recorded as pseudogene[2].
- RN7SL597P's instance of is recorded as gene[3].
- RN7SL597P is a type of pseudogene[4].
- RN7SL597P's genomic start is recorded as 41121876[5].
- RN7SL597P's genomic end is recorded as 41122171[6].
- RN7SL597P's found in taxon is recorded as Homo sapiens[7].
- RN7SL597P's chromosome is recorded as human chromosome 13[8].
- RN7SL597P's strand orientation is recorded as forward strand[9].
- RN7SL597P's exact match is recorded as http://identifiers.org/ncbigene/106479440[10].
- RN7SL597P's cytogenetic location is recorded as 13q14.11[11].
- RN7SL597P's expressed in is recorded as testicle[12].
- RN7SL597P's expressed in is recorded as ganglionic eminence[13].
- RN7SL597P's expressed in is recorded as bone marrow cell[14].
- RN7SL597P's expressed in is recorded as muscle tissue[15].
- RN7SL597P's expressed in is recorded as liver[16].
- RN7SL597P's expressed in is recorded as monocyte[17].
- RN7SL597P's expressed in is recorded as stromal cell of endometrium[18].
- RN7SL597P's expressed in is recorded as lymph node[19].
- RN7SL597P's expressed in is recorded as corpus callosum[20].
- RN7SL597P's expressed in is recorded as gallbladder[21].