RN7SL634P
pseudogene in the species Homo sapiens
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RN7SL634P
Summary
RN7SL634P is a pseudogene[1].
Key Facts
- RN7SL634P's instance of is recorded as pseudogene[2].
- RN7SL634P's instance of is recorded as gene[3].
- RN7SL634P is a type of pseudogene[4].
- RN7SL634P's genomic start is recorded as 104013642[5].
- RN7SL634P's genomic end is recorded as 104013933[6].
- RN7SL634P's found in taxon is recorded as Homo sapiens[7].
- RN7SL634P's chromosome is recorded as human chromosome 14[8].
- RN7SL634P's strand orientation is recorded as forward strand[9].
- RN7SL634P's exact match is recorded as http://identifiers.org/ncbigene/106481096[10].
- RN7SL634P's cytogenetic location is recorded as 14q32.33[11].
- RN7SL634P's expressed in is recorded as blood[12].
- RN7SL634P's expressed in is recorded as myometrium[13].
- RN7SL634P's expressed in is recorded as prefrontal cortex[14].
- RN7SL634P's expressed in is recorded as monocyte[15].
- RN7SL634P's expressed in is recorded as islet of Langerhans[16].
- RN7SL634P's expressed in is recorded as primary visual cortex[17].
- RN7SL634P's expressed in is recorded as liver[18].
- RN7SL634P's expressed in is recorded as gastrocnemius muscle[19].
- RN7SL634P's expressed in is recorded as hippocampus proper[20].
- RN7SL634P's expressed in is recorded as kidney[21].