RN7SL422P
pseudogene in the species Homo sapiens
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RN7SL422P
Summary
RN7SL422P is a pseudogene[1].
Key Facts
- RN7SL422P's instance of is recorded as pseudogene[2].
- RN7SL422P's instance of is recorded as gene[3].
- RN7SL422P is a type of pseudogene[4].
- RN7SL422P's genomic start is recorded as 67175775[5].
- RN7SL422P's genomic end is recorded as 67176035[6].
- RN7SL422P's found in taxon is recorded as Homo sapiens[7].
- RN7SL422P's chromosome is recorded as human chromosome 9[8].
- RN7SL422P's strand orientation is recorded as reverse strand[9].
- RN7SL422P's exact match is recorded as http://identifiers.org/ncbigene/106481038[10].
- RN7SL422P's cytogenetic location is recorded as 9q21.11[11].
- RN7SL422P's expressed in is recorded as bone marrow cell[12].
- RN7SL422P's expressed in is recorded as blood[13].
- RN7SL422P's expressed in is recorded as lactiferous gland[14].
- RN7SL422P's expressed in is recorded as primary visual cortex[15].
- RN7SL422P's expressed in is recorded as myometrium[16].
- RN7SL422P's expressed in is recorded as liver[17].
- RN7SL422P's expressed in is recorded as urinary bladder[18].
- RN7SL422P's expressed in is recorded as male reproductive system[19].
- RN7SL422P's expressed in is recorded as monocyte[20].
- RN7SL422P's expressed in is recorded as small intestine[21].