RN7SL449P
pseudogene in the species Homo sapiens
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RN7SL449P
Summary
RN7SL449P is a pseudogene[1].
Key Facts
- RN7SL449P's instance of is recorded as pseudogene[2].
- RN7SL449P's instance of is recorded as gene[3].
- RN7SL449P is a type of pseudogene[4].
- RN7SL449P's genomic start is recorded as 57618108[5].
- RN7SL449P's genomic end is recorded as 57618393[6].
- RN7SL449P's found in taxon is recorded as Homo sapiens[7].
- RN7SL449P's chromosome is recorded as human chromosome 17[8].
- RN7SL449P's strand orientation is recorded as forward strand[9].
- RN7SL449P's exact match is recorded as http://identifiers.org/ncbigene/106481045[10].
- RN7SL449P's cytogenetic location is recorded as 17q22[11].
- RN7SL449P's expressed in is recorded as corpus callosum[12].
- RN7SL449P's expressed in is recorded as skeletal muscle tissue[13].
- RN7SL449P's expressed in is recorded as epithelium of colon[14].
- RN7SL449P's expressed in is recorded as bone marrow cell[15].
- RN7SL449P's expressed in is recorded as ventricular zone[16].
- RN7SL449P's expressed in is recorded as lymph node[17].
- RN7SL449P's expressed in is recorded as tonsil[18].
- RN7SL449P's expressed in is recorded as monocyte[19].
- RN7SL449P's expressed in is recorded as placenta[20].
- RN7SL449P's expressed in is recorded as superior frontal gyrus[21].