RN7SL499P
pseudogene in the species Homo sapiens
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RN7SL499P
Summary
RN7SL499P is a pseudogene[1].
Key Facts
- RN7SL499P's instance of is recorded as pseudogene[2].
- RN7SL499P's instance of is recorded as gene[3].
- RN7SL499P is a type of pseudogene[4].
- RN7SL499P's genomic start is recorded as 231645998[5].
- RN7SL499P's genomic end is recorded as 231646273[6].
- RN7SL499P's found in taxon is recorded as Homo sapiens[7].
- RN7SL499P's chromosome is recorded as human chromosome 2[8].
- RN7SL499P's strand orientation is recorded as reverse strand[9].
- RN7SL499P's exact match is recorded as http://identifiers.org/ncbigene/106481059[10].
- RN7SL499P's cytogenetic location is recorded as 2q37.1[11].
- RN7SL499P's expressed in is recorded as testicle[12].
- RN7SL499P's expressed in is recorded as liver[13].
- RN7SL499P's expressed in is recorded as sural nerve[14].
- RN7SL499P's expressed in is recorded as tonsil[15].
- RN7SL499P's expressed in is recorded as monocyte[16].
- RN7SL499P's expressed in is recorded as kidney[17].
- RN7SL499P's expressed in is recorded as right lobe of liver[18].
- RN7SL499P's expressed in is recorded as blood[19].
- RN7SL499P's expressed in is recorded as cervix[20].
- RN7SL499P's expressed in is recorded as islet of Langerhans[21].