RPL7L1P2
pseudogene in the species Homo sapiens
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RPL7L1P2
Summary
RPL7L1P2 is a pseudogene[1].
Key Facts
- RPL7L1P2's instance of is recorded as pseudogene[2].
- RPL7L1P2's instance of is recorded as gene[3].
- RPL7L1P2 is a type of pseudogene[4].
- RPL7L1P2's genomic start is recorded as 51259429[5].
- RPL7L1P2's genomic end is recorded as 51260167[6].
- RPL7L1P2's found in taxon is recorded as Homo sapiens[7].
- RPL7L1P2's chromosome is recorded as human chromosome 7[8].
- RPL7L1P2's strand orientation is recorded as reverse strand[9].
- RPL7L1P2's exact match is recorded as http://identifiers.org/ncbigene/100420155[10].
- RPL7L1P2's cytogenetic location is recorded as 7p12.1[11].
- RPL7L1P2's expressed in is recorded as corpus callosum[12].
- RPL7L1P2's expressed in is recorded as skeletal muscle tissue[13].
- RPL7L1P2's expressed in is recorded as tonsil[14].
- RPL7L1P2's expressed in is recorded as Achilles tendon[15].
- RPL7L1P2's expressed in is recorded as liver[16].
- RPL7L1P2's expressed in is recorded as prefrontal cortex[17].
- RPL7L1P2's expressed in is recorded as zone of skin[18].
- RPL7L1P2's expressed in is recorded as stomach[19].
- RPL7L1P2's expressed in is recorded as skin of leg[20].
- RPL7L1P2's expressed in is recorded as lactiferous gland[21].