RN7SL446P
pseudogene in the species Homo sapiens
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RN7SL446P
Summary
RN7SL446P is a pseudogene[1].
Key Facts
- RN7SL446P's instance of is recorded as pseudogene[2].
- RN7SL446P's instance of is recorded as gene[3].
- RN7SL446P is a type of pseudogene[4].
- RN7SL446P's genomic start is recorded as 152264150[5].
- RN7SL446P's genomic end is recorded as 152264445[6].
- RN7SL446P's found in taxon is recorded as Homo sapiens[7].
- RN7SL446P's chromosome is recorded as human chromosome 4[8].
- RN7SL446P's strand orientation is recorded as reverse strand[9].
- RN7SL446P's exact match is recorded as http://identifiers.org/ncbigene/106479385[10].
- RN7SL446P's cytogenetic location is recorded as 4q31.3[11].
- RN7SL446P's expressed in is recorded as testicle[12].
- RN7SL446P's expressed in is recorded as gonad[13].
- RN7SL446P's expressed in is recorded as urinary bladder[14].
- RN7SL446P's expressed in is recorded as lymph node[15].
- RN7SL446P's expressed in is recorded as prefrontal cortex[16].
- RN7SL446P's expressed in is recorded as bone marrow cell[17].
- RN7SL446P's expressed in is recorded as monocyte[18].
- RN7SL446P's expressed in is recorded as stomach[19].
- RN7SL446P's expressed in is recorded as tonsil[20].
- RN7SL446P's expressed in is recorded as islet of Langerhans[21].