RN7SL635P
pseudogene in the species Homo sapiens
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RN7SL635P
Summary
RN7SL635P is a pseudogene[1].
Key Facts
- RN7SL635P's instance of is recorded as pseudogene[2].
- RN7SL635P's instance of is recorded as gene[3].
- RN7SL635P is a type of pseudogene[4].
- RN7SL635P's genomic start is recorded as 65545401[5].
- RN7SL635P's genomic end is recorded as 65545696[6].
- RN7SL635P's found in taxon is recorded as Homo sapiens[7].
- RN7SL635P's chromosome is recorded as human chromosome 2[8].
- RN7SL635P's strand orientation is recorded as reverse strand[9].
- RN7SL635P's exact match is recorded as http://identifiers.org/ncbigene/106479454[10].
- RN7SL635P's cytogenetic location is recorded as 2p14[11].
- RN7SL635P's expressed in is recorded as testicle[12].
- RN7SL635P's expressed in is recorded as sural nerve[13].
- RN7SL635P's expressed in is recorded as ganglionic eminence[14].
- RN7SL635P's expressed in is recorded as gallbladder[15].
- RN7SL635P's expressed in is recorded as liver[16].
- RN7SL635P's expressed in is recorded as lymph node[17].
- RN7SL635P's expressed in is recorded as tonsil[18].
- RN7SL635P's expressed in is recorded as primary visual cortex[19].
- RN7SL635P's expressed in is recorded as islet of Langerhans[20].
- RN7SL635P's expressed in is recorded as monocyte[21].