RN7SL498P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL498P
Summary
RN7SL498P is a pseudogene[1].
Key Facts
- RN7SL498P's instance of is recorded as pseudogene[2].
- RN7SL498P's instance of is recorded as gene[3].
- RN7SL498P is a type of pseudogene[4].
- RN7SL498P's genomic start is recorded as 6001733[5].
- RN7SL498P's genomic end is recorded as 6002030[6].
- RN7SL498P's found in taxon is recorded as Homo sapiens[7].
- RN7SL498P's chromosome is recorded as human chromosome 20[8].
- RN7SL498P's strand orientation is recorded as forward strand[9].
- RN7SL498P's exact match is recorded as http://identifiers.org/ncbigene/106479405[10].
- RN7SL498P's cytogenetic location is recorded as 20p12.3[11].
- RN7SL498P's expressed in is recorded as testicle[12].
- RN7SL498P's expressed in is recorded as bone marrow cell[13].
- RN7SL498P's expressed in is recorded as gonad[14].
- RN7SL498P's expressed in is recorded as monocyte[15].
- RN7SL498P's expressed in is recorded as primary visual cortex[16].
- RN7SL498P's expressed in is recorded as muscle tissue[17].
- RN7SL498P's expressed in is recorded as lymph node[18].
- RN7SL498P's expressed in is recorded as corpus callosum[19].
- RN7SL498P's expressed in is recorded as islet of Langerhans[20].
- RN7SL498P's expressed in is recorded as gallbladder[21].