HMGN1P17
pseudogene in the species Homo sapiens
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HMGN1P17
Summary
HMGN1P17 is a pseudogene[1].
Key Facts
- HMGN1P17's instance of is recorded as pseudogene[2].
- HMGN1P17's instance of is recorded as gene[3].
- HMGN1P17 is a type of pseudogene[4].
- HMGN1P17's genomic start is recorded as 56381781[5].
- HMGN1P17's genomic end is recorded as 56382075[6].
- HMGN1P17's found in taxon is recorded as Homo sapiens[7].
- HMGN1P17's chromosome is recorded as human chromosome 5[8].
- HMGN1P17's strand orientation is recorded as forward strand[9].
- HMGN1P17's exact match is recorded as http://identifiers.org/ncbigene/100874443[10].
- HMGN1P17's cytogenetic location is recorded as 5q11.2[11].
- HMGN1P17's expressed in is recorded as human kidney[12].
- HMGN1P17's expressed in is recorded as gastric mucosa[13].
- HMGN1P17's expressed in is recorded as right lobe of thyroid gland[14].
- HMGN1P17's expressed in is recorded as ventricular zone[15].
- HMGN1P17's expressed in is recorded as ganglionic eminence[16].
- HMGN1P17's expressed in is recorded as left lobe of thyroid gland[17].
- HMGN1P17's expressed in is recorded as gallbladder[18].
- HMGN1P17's expressed in is recorded as bone marrow[19].
- HMGN1P17's expressed in is recorded as right coronary artery[20].
- HMGN1P17's expressed in is recorded as endometrium[21].