RN7SL152P
pseudogene in the species Homo sapiens
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RN7SL152P
Summary
RN7SL152P is a pseudogene[1].
Key Facts
- RN7SL152P's instance of is recorded as pseudogene[2].
- RN7SL152P's instance of is recorded as gene[3].
- RN7SL152P is a type of pseudogene[4].
- RN7SL152P's genomic start is recorded as 140577925[5].
- RN7SL152P's genomic end is recorded as 140578222[6].
- RN7SL152P's found in taxon is recorded as Homo sapiens[7].
- RN7SL152P's chromosome is recorded as human chromosome 4[8].
- RN7SL152P's strand orientation is recorded as forward strand[9].
- RN7SL152P's exact match is recorded as http://identifiers.org/ncbigene/106480962[10].
- RN7SL152P's cytogenetic location is recorded as 4q31.1[11].
- RN7SL152P's expressed in is recorded as ganglionic eminence[12].
- RN7SL152P's expressed in is recorded as skeletal muscle tissue[13].
- RN7SL152P's expressed in is recorded as gallbladder[14].
- RN7SL152P's expressed in is recorded as superior frontal gyrus[15].
- RN7SL152P's expressed in is recorded as liver[16].
- RN7SL152P's expressed in is recorded as monocyte[17].
- RN7SL152P's expressed in is recorded as islet of Langerhans[18].
- RN7SL152P's expressed in is recorded as blood[19].
- RN7SL152P's expressed in is recorded as prefrontal cortex[20].
- RN7SL152P's expressed in is recorded as urinary bladder[21].