RN7SL448P
pseudogene in the species Homo sapiens
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RN7SL448P
Summary
RN7SL448P is a pseudogene[1].
Key Facts
- RN7SL448P's instance of is recorded as pseudogene[2].
- RN7SL448P's instance of is recorded as gene[3].
- RN7SL448P is a type of pseudogene[4].
- RN7SL448P's genomic start is recorded as 60899891[5].
- RN7SL448P's genomic end is recorded as 60900185[6].
- RN7SL448P's found in taxon is recorded as Homo sapiens[7].
- RN7SL448P's chromosome is recorded as human chromosome 17[8].
- RN7SL448P's strand orientation is recorded as forward strand[9].
- RN7SL448P's exact match is recorded as http://identifiers.org/ncbigene/106481843[10].
- RN7SL448P's cytogenetic location is recorded as 17q23.2[11].
- RN7SL448P's expressed in is recorded as testicle[12].
- RN7SL448P's expressed in is recorded as epithelium of colon[13].
- RN7SL448P's expressed in is recorded as muscle of thigh[14].
- RN7SL448P's expressed in is recorded as skeletal muscle tissue[15].
- RN7SL448P's expressed in is recorded as cervix[16].
- RN7SL448P's expressed in is recorded as urinary bladder[17].
- RN7SL448P's expressed in is recorded as prefrontal cortex[18].
- RN7SL448P's expressed in is recorded as sural nerve[19].
- RN7SL448P's expressed in is recorded as blood[20].
- RN7SL448P's expressed in is recorded as liver[21].