RN7SL338P
pseudogene in the species Homo sapiens
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RN7SL338P
Summary
RN7SL338P is a pseudogene[1].
Key Facts
- RN7SL338P's instance of is recorded as pseudogene[2].
- RN7SL338P's instance of is recorded as gene[3].
- RN7SL338P is a type of pseudogene[4].
- RN7SL338P's genomic start is recorded as 35049271[5].
- RN7SL338P's genomic end is recorded as 35049563[6].
- RN7SL338P's found in taxon is recorded as Homo sapiens[7].
- RN7SL338P's chromosome is recorded as human chromosome 9[8].
- RN7SL338P's strand orientation is recorded as forward strand[9].
- RN7SL338P's exact match is recorded as http://identifiers.org/ncbigene/106479347[10].
- RN7SL338P's cytogenetic location is recorded as 9p13.3[11].
- RN7SL338P's expressed in is recorded as sural nerve[12].
- RN7SL338P's expressed in is recorded as bone marrow cell[13].
- RN7SL338P's expressed in is recorded as Achilles tendon[14].
- RN7SL338P's expressed in is recorded as epithelium of colon[15].
- RN7SL338P's expressed in is recorded as muscle of thigh[16].
- RN7SL338P's expressed in is recorded as skeletal muscle tissue[17].
- RN7SL338P's expressed in is recorded as lymph node[18].
- RN7SL338P's expressed in is recorded as urinary bladder[19].
- RN7SL338P's expressed in is recorded as blood[20].
- RN7SL338P's expressed in is recorded as corpus callosum[21].