RN7SL182P
pseudogene in the species Homo sapiens
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RN7SL182P
Summary
RN7SL182P is a pseudogene[1].
Key Facts
- RN7SL182P's instance of is recorded as pseudogene[2].
- RN7SL182P's instance of is recorded as gene[3].
- RN7SL182P is a type of pseudogene[4].
- RN7SL182P's genomic start is recorded as 49083233[5].
- RN7SL182P's genomic end is recorded as 49083532[6].
- RN7SL182P's found in taxon is recorded as Homo sapiens[7].
- RN7SL182P's chromosome is recorded as human chromosome 3[8].
- RN7SL182P's strand orientation is recorded as forward strand[9].
- RN7SL182P's exact match is recorded as http://identifiers.org/ncbigene/106479287[10].
- RN7SL182P's cytogenetic location is recorded as 3p21.31[11].
- RN7SL182P's expressed in is recorded as bone marrow cell[12].
- RN7SL182P's expressed in is recorded as skeletal muscle tissue[13].
- RN7SL182P's expressed in is recorded as epithelium of colon[14].
- RN7SL182P's expressed in is recorded as ganglionic eminence[15].
- RN7SL182P's expressed in is recorded as muscle of thigh[16].
- RN7SL182P's expressed in is recorded as sural nerve[17].
- RN7SL182P's expressed in is recorded as cervix[18].
- RN7SL182P's expressed in is recorded as tonsil[19].
- RN7SL182P's expressed in is recorded as blood[20].
- RN7SL182P's expressed in is recorded as monocyte[21].