RN7SL692P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL692P
Summary
RN7SL692P is a pseudogene[1].
Key Facts
- RN7SL692P's instance of is recorded as pseudogene[2].
- RN7SL692P's instance of is recorded as gene[3].
- RN7SL692P is a type of pseudogene[4].
- RN7SL692P's genomic start is recorded as 92974827[5].
- RN7SL692P's genomic end is recorded as 92975114[6].
- RN7SL692P's found in taxon is recorded as Homo sapiens[7].
- RN7SL692P's chromosome is recorded as human chromosome 1[8].
- RN7SL692P's strand orientation is recorded as reverse strand[9].
- RN7SL692P's exact match is recorded as http://identifiers.org/ncbigene/106479476[10].
- RN7SL692P's cytogenetic location is recorded as 1p22.1[11].
- RN7SL692P's expressed in is recorded as testicle[12].
- RN7SL692P's expressed in is recorded as monocyte[13].
- RN7SL692P's expressed in is recorded as skeletal muscle tissue[14].
- RN7SL692P's expressed in is recorded as bone marrow[15].
- RN7SL692P's expressed in is recorded as urinary bladder[16].
- RN7SL692P's expressed in is recorded as islet of Langerhans[17].
- RN7SL692P's expressed in is recorded as lymph node[18].
- RN7SL692P's expressed in is recorded as duodenum[19].
- RN7SL692P's expressed in is recorded as blood[20].
- RN7SL692P's expressed in is recorded as muscle of leg[21].