RN7SL79P
pseudogene in the species Homo sapiens
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RN7SL79P
Summary
RN7SL79P is a pseudogene[1].
Key Facts
- RN7SL79P's instance of is recorded as pseudogene[2].
- RN7SL79P's instance of is recorded as gene[3].
- RN7SL79P is a type of pseudogene[4].
- RN7SL79P's genomic start is recorded as 31465543[5].
- RN7SL79P's genomic end is recorded as 31465832[6].
- RN7SL79P's found in taxon is recorded as Homo sapiens[7].
- RN7SL79P's chromosome is recorded as human chromosome 17[8].
- RN7SL79P's strand orientation is recorded as forward strand[9].
- RN7SL79P's exact match is recorded as http://identifiers.org/ncbigene/106480943[10].
- RN7SL79P's cytogenetic location is recorded as 17q11.2[11].
- RN7SL79P's expressed in is recorded as testicle[12].
- RN7SL79P's expressed in is recorded as stomach[13].
- RN7SL79P's expressed in is recorded as liver[14].
- RN7SL79P's expressed in is recorded as superior frontal gyrus[15].
- RN7SL79P's expressed in is recorded as monocyte[16].
- RN7SL79P's expressed in is recorded as prefrontal cortex[17].
- RN7SL79P's expressed in is recorded as blood[18].
- RN7SL79P's expressed in is recorded as primary visual cortex[19].
- RN7SL79P's expressed in is recorded as human kidney[20].
- RN7SL79P's expressed in is recorded as gastrocnemius muscle[21].