RN7SL368P
pseudogene in the species Homo sapiens
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RN7SL368P
Summary
RN7SL368P is a pseudogene[1].
Key Facts
- RN7SL368P's instance of is recorded as pseudogene[2].
- RN7SL368P's instance of is recorded as gene[3].
- RN7SL368P is a type of pseudogene[4].
- RN7SL368P's genomic start is recorded as 43660500[5].
- RN7SL368P's genomic end is recorded as 43660776[6].
- RN7SL368P's found in taxon is recorded as Homo sapiens[7].
- RN7SL368P's chromosome is recorded as human chromosome 19[8].
- RN7SL368P's strand orientation is recorded as reverse strand[9].
- RN7SL368P's exact match is recorded as http://identifiers.org/ncbigene/106479357[10].
- RN7SL368P's cytogenetic location is recorded as 19q13.31[11].
- RN7SL368P's expressed in is recorded as bone marrow cell[12].
- RN7SL368P's expressed in is recorded as monocyte[13].
- RN7SL368P's expressed in is recorded as testicle[14].
- RN7SL368P's expressed in is recorded as blood[15].
- RN7SL368P's expressed in is recorded as sural nerve[16].
- RN7SL368P's expressed in is recorded as muscle of thigh[17].
- RN7SL368P's expressed in is recorded as ganglionic eminence[18].
- RN7SL368P's expressed in is recorded as gallbladder[19].
- RN7SL368P's expressed in is recorded as urinary bladder[20].
- RN7SL368P's expressed in is recorded as liver[21].