HMGN1P14
pseudogene in the species Homo sapiens
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HMGN1P14
Summary
HMGN1P14 is a pseudogene[1].
Key Facts
- HMGN1P14's instance of is recorded as pseudogene[2].
- HMGN1P14's instance of is recorded as gene[3].
- HMGN1P14 is a type of pseudogene[4].
- HMGN1P14's genomic start is recorded as 111846050[5].
- HMGN1P14's genomic end is recorded as 111846566[6].
- HMGN1P14's found in taxon is recorded as Homo sapiens[7].
- HMGN1P14's chromosome is recorded as human chromosome 5[8].
- HMGN1P14's strand orientation is recorded as reverse strand[9].
- HMGN1P14's exact match is recorded as http://identifiers.org/ncbigene/100874440[10].
- HMGN1P14's cytogenetic location is recorded as 5q22.1[11].
- HMGN1P14's expressed in is recorded as testicle[12].
- HMGN1P14's expressed in is recorded as gonad[13].
- HMGN1P14's expressed in is recorded as monocyte[14].
- HMGN1P14's expressed in is recorded as Achilles tendon[15].
- HMGN1P14's expressed in is recorded as Brodmann area 9[16].
- HMGN1P14's expressed in is recorded as gallbladder[17].
- HMGN1P14's expressed in is recorded as skeletal muscle tissue[18].
- HMGN1P14's expressed in is recorded as liver[19].
- HMGN1P14's expressed in is recorded as islet of Langerhans[20].
- HMGN1P14's expressed in is recorded as primary visual cortex[21].