PIRT
protein-coding gene in the species Homo sapiens
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PIRT
Summary
PIRT is a gene[1].
Key Facts
- PIRT's instance of is recorded as gene[2].
- PIRT is a type of protein-coding gene[3].
- PIRT's HomoloGene ID is recorded as 77645[4].
- PIRT's genomic start is recorded as 10725792[5].
- PIRT's genomic start is recorded as 10822470[6].
- PIRT's genomic end is recorded as 10741762[7].
- PIRT's genomic end is recorded as 10838087[8].
- PIRT's ortholog is recorded as Pirt[9].
- PIRT's ortholog is recorded as Pirt[10].
- PIRT's encodes is recorded as Phosphoinositide interacting regulator of transient receptor potential channels[11].
- PIRT's found in taxon is recorded as Homo sapiens[12].
- PIRT's chromosome is recorded as human chromosome 17[13].
- PIRT's strand orientation is recorded as reverse strand[14].
- PIRT's exact match is recorded as http://identifiers.org/ncbigene/644139[15].
- PIRT's cytogenetic location is recorded as 17p12[16].
- PIRT's expressed in is recorded as spinal ganglia[17].
- PIRT's expressed in is recorded as trigeminal ganglion[18].
- PIRT's expressed in is recorded as internal globus pallidus[19].
- PIRT's expressed in is recorded as hypothalamus[20].
- PIRT's expressed in is recorded as substantia nigra[21].
- PIRT's expressed in is recorded as spinal cord[22].
- PIRT's expressed in is recorded as C1 segment[23].
- PIRT's expressed in is recorded as medulla oblongata[24].
- PIRT's expressed in is recorded as superior vestibular nucleus[25].
- PIRT's expressed in is recorded as muscle layer of sigmoid colon[26].