CPSF1P1
pseudogene in the species Homo sapiens
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CPSF1P1
Summary
CPSF1P1 is a pseudogene[1].
Key Facts
- CPSF1P1's instance of is recorded as pseudogene[2].
- CPSF1P1's instance of is recorded as gene[3].
- CPSF1P1 is a type of pseudogene[4].
- CPSF1P1's genomic start is recorded as 32269381[5].
- CPSF1P1's genomic end is recorded as 32273110[6].
- CPSF1P1's found in taxon is recorded as Homo sapiens[7].
- CPSF1P1's chromosome is recorded as human chromosome 22[8].
- CPSF1P1's strand orientation is recorded as forward strand[9].
- CPSF1P1's exact match is recorded as http://identifiers.org/ncbigene/129099[10].
- CPSF1P1's cytogenetic location is recorded as 22q12.3[11].
- CPSF1P1's expressed in is recorded as testicle[12].
- CPSF1P1's expressed in is recorded as prefrontal cortex[13].
- CPSF1P1's expressed in is recorded as ganglionic eminence[14].
- CPSF1P1's expressed in is recorded as lymph node[15].
- CPSF1P1's expressed in is recorded as hepatobiliary system[16].
- CPSF1P1's expressed in is recorded as gallbladder[17].
- CPSF1P1's expressed in is recorded as islet of Langerhans[18].
- CPSF1P1's expressed in is recorded as superior frontal gyrus[19].
- CPSF1P1's expressed in is recorded as fallopian tube[20].
- CPSF1P1's expressed in is recorded as substantia nigra[21].