RMI2
protein-coding gene in the species Homo sapiens
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RMI2
Summary
RMI2 is a gene[1].
Key Facts
- RMI2's instance of is recorded as gene[2].
- RMI2 is a type of protein-coding gene[3].
- RMI2's HomoloGene ID is recorded as 17543[4].
- RMI2's genomic start is recorded as 11249619[5].
- RMI2's genomic start is recorded as 11343476[6].
- RMI2's genomic end is recorded as 11445619[7].
- RMI2's genomic end is recorded as 11381662[8].
- RMI2's ortholog is recorded as Rmi2[9].
- RMI2's ortholog is recorded as Rmi2[10].
- RMI2's ortholog is recorded as rmi2[11].
- RMI2's encodes is recorded as RecQ mediated genome instability 2[12].
- RMI2's found in taxon is recorded as Homo sapiens[13].
- RMI2's chromosome is recorded as human chromosome 16[14].
- RMI2's strand orientation is recorded as forward strand[15].
- RMI2's exact match is recorded as http://identifiers.org/ncbigene/116028[16].
- RMI2's cytogenetic location is recorded as 16p13.13[17].
- RMI2's expressed in is recorded as ventricular zone[18].
- RMI2's expressed in is recorded as mucosa of ileum[19].
- RMI2's expressed in is recorded as ganglionic eminence[20].
- RMI2's expressed in is recorded as secondary oocyte[21].
- RMI2's expressed in is recorded as gonad[22].
- RMI2's expressed in is recorded as testicle[23].
- RMI2's expressed in is recorded as mucosa of transverse colon[24].
- RMI2's expressed in is recorded as placenta[25].
- RMI2's expressed in is recorded as rectum[26].