RN7SL391P
pseudogene in the species Homo sapiens
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RN7SL391P
Summary
RN7SL391P is a pseudogene[1].
Key Facts
- RN7SL391P's instance of is recorded as pseudogene[2].
- RN7SL391P's instance of is recorded as gene[3].
- RN7SL391P is a type of pseudogene[4].
- RN7SL391P's genomic start is recorded as 6344554[5].
- RN7SL391P's genomic end is recorded as 6344837[6].
- RN7SL391P's found in taxon is recorded as Homo sapiens[7].
- RN7SL391P's chromosome is recorded as human chromosome 12[8].
- RN7SL391P's strand orientation is recorded as forward strand[9].
- RN7SL391P's exact match is recorded as http://identifiers.org/ncbigene/106481030[10].
- RN7SL391P's cytogenetic location is recorded as 12p13.31[11].
- RN7SL391P's expressed in is recorded as testicle[12].
- RN7SL391P's expressed in is recorded as epithelium of colon[13].
- RN7SL391P's expressed in is recorded as ventricular zone[14].
- RN7SL391P's expressed in is recorded as skeletal muscle tissue[15].
- RN7SL391P's expressed in is recorded as tonsil[16].
- RN7SL391P's expressed in is recorded as bone marrow cell[17].
- RN7SL391P's expressed in is recorded as urinary bladder[18].
- RN7SL391P's expressed in is recorded as gallbladder[19].
- RN7SL391P's expressed in is recorded as blood[20].
- RN7SL391P's expressed in is recorded as human kidney[21].