RN7SL399P
pseudogene in the species Homo sapiens
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RN7SL399P
Summary
RN7SL399P is a pseudogene[1].
Key Facts
- RN7SL399P's instance of is recorded as pseudogene[2].
- RN7SL399P's instance of is recorded as gene[3].
- RN7SL399P is a type of pseudogene[4].
- RN7SL399P's genomic start is recorded as 41730127[5].
- RN7SL399P's genomic end is recorded as 41730405[6].
- RN7SL399P's found in taxon is recorded as Homo sapiens[7].
- RN7SL399P's chromosome is recorded as human chromosome 17[8].
- RN7SL399P's strand orientation is recorded as reverse strand[9].
- RN7SL399P's exact match is recorded as http://identifiers.org/ncbigene/106479370[10].
- RN7SL399P's cytogenetic location is recorded as 17q21.2[11].
- RN7SL399P's expressed in is recorded as testicle[12].
- RN7SL399P's expressed in is recorded as endometrium[13].
- RN7SL399P's expressed in is recorded as hypothalamus[14].
- RN7SL399P's expressed in is recorded as liver[15].
- RN7SL399P's expressed in is recorded as duodenum[16].
- RN7SL399P's expressed in is recorded as smooth muscle tissue[17].
- RN7SL399P's expressed in is recorded as canal of the cervix[18].
- RN7SL399P's expressed in is recorded as islet of Langerhans[19].
- RN7SL399P's expressed in is recorded as gallbladder[20].
- RN7SL399P's expressed in is recorded as renal cortex[21].