RN7SL594P
pseudogene in the species Homo sapiens
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RN7SL594P
Summary
RN7SL594P is a pseudogene[1].
Key Facts
- RN7SL594P's instance of is recorded as pseudogene[2].
- RN7SL594P's instance of is recorded as gene[3].
- RN7SL594P is a type of pseudogene[4].
- RN7SL594P's genomic start is recorded as 25654595[5].
- RN7SL594P's genomic end is recorded as 25654881[6].
- RN7SL594P's found in taxon is recorded as Homo sapiens[7].
- RN7SL594P's chromosome is recorded as human chromosome 20[8].
- RN7SL594P's strand orientation is recorded as reverse strand[9].
- RN7SL594P's exact match is recorded as http://identifiers.org/ncbigene/106479439[10].
- RN7SL594P's cytogenetic location is recorded as 20p11.21[11].
- RN7SL594P's expressed in is recorded as bone marrow cell[12].
- RN7SL594P's expressed in is recorded as tonsil[13].
- RN7SL594P's expressed in is recorded as skeletal muscle tissue[14].
- RN7SL594P's expressed in is recorded as monocyte[15].
- RN7SL594P's expressed in is recorded as urinary bladder[16].
- RN7SL594P's expressed in is recorded as primary visual cortex[17].
- RN7SL594P's expressed in is recorded as blood[18].
- RN7SL594P's expressed in is recorded as kidney[19].
- RN7SL594P's expressed in is recorded as islet of Langerhans[20].
- RN7SL594P's expressed in is recorded as gastrocnemius muscle[21].