RN7SKP169
pseudogene in the species Homo sapiens
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RN7SKP169
Summary
RN7SKP169 is a pseudogene[1].
Key Facts
- RN7SKP169's instance of is recorded as pseudogene[2].
- RN7SKP169's instance of is recorded as gene[3].
- RN7SKP169 is a type of pseudogene[4].
- RN7SKP169's genomic start is recorded as 25963983[5].
- RN7SKP169's genomic end is recorded as 25964273[6].
- RN7SKP169's found in taxon is recorded as Homo sapiens[7].
- RN7SKP169's chromosome is recorded as human chromosome 22[8].
- RN7SKP169's strand orientation is recorded as reverse strand[9].
- RN7SKP169's exact match is recorded as http://identifiers.org/ncbigene/106480886[10].
- RN7SKP169's cytogenetic location is recorded as 22q12.1[11].
- RN7SKP169's expressed in is recorded as muscle of thigh[12].
- RN7SKP169's expressed in is recorded as skeletal muscle tissue[13].
- RN7SKP169's expressed in is recorded as prefrontal cortex[14].
- RN7SKP169's expressed in is recorded as liver[15].
- RN7SKP169's expressed in is recorded as urinary bladder[16].
- RN7SKP169's expressed in is recorded as right auricle of heart[17].
- RN7SKP169's expressed in is recorded as islet of Langerhans[18].
- RN7SKP169's expressed in is recorded as monocyte[19].
- RN7SKP169's expressed in is recorded as lung[20].
- RN7SKP169's expressed in is recorded as bone marrow cell[21].