EIF1AXP2
pseudogene in the species Homo sapiens
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EIF1AXP2
Summary
EIF1AXP2 is a pseudogene[1].
Key Facts
- EIF1AXP2's instance of is recorded as pseudogene[2].
- EIF1AXP2's instance of is recorded as gene[3].
- EIF1AXP2 is a type of pseudogene[4].
- EIF1AXP2's genomic start is recorded as 65528830[5].
- EIF1AXP2's genomic end is recorded as 65529574[6].
- EIF1AXP2's found in taxon is recorded as Homo sapiens[7].
- EIF1AXP2's chromosome is recorded as human chromosome 14[8].
- EIF1AXP2's strand orientation is recorded as reverse strand[9].
- EIF1AXP2's exact match is recorded as http://identifiers.org/ncbigene/106479036[10].
- EIF1AXP2's cytogenetic location is recorded as 14q23.3[11].
- EIF1AXP2's expressed in is recorded as corpus callosum[12].
- EIF1AXP2's expressed in is recorded as granulocyte[13].
- EIF1AXP2's expressed in is recorded as tonsil[14].
- EIF1AXP2's expressed in is recorded as Achilles tendon[15].
- EIF1AXP2's expressed in is recorded as prefrontal cortex[16].
- EIF1AXP2's expressed in is recorded as primary visual cortex[17].
- EIF1AXP2's expressed in is recorded as stomach[18].
- EIF1AXP2's expressed in is recorded as left uterine tube[19].
- EIF1AXP2's expressed in is recorded as small intestine[20].
- EIF1AXP2's expressed in is recorded as right lobe of liver[21].