MIEN1
protein-coding gene in the species Homo sapiens
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MIEN1
Summary
MIEN1 is a gene[1].
Key Facts
- MIEN1's instance of is recorded as gene[2].
- MIEN1 is a type of protein-coding gene[3].
- MIEN1's HomoloGene ID is recorded as 11969[4].
- MIEN1's genomic start is recorded as 39728496[5].
- MIEN1's genomic start is recorded as 37884749[6].
- MIEN1's genomic end is recorded as 37887040[7].
- MIEN1's genomic end is recorded as 39730532[8].
- MIEN1's ortholog is recorded as Mien1[9].
- MIEN1's ortholog is recorded as selenow2a[10].
- MIEN1's ortholog is recorded as selenow2b[11].
- MIEN1's ortholog is recorded as Mien1[12].
- MIEN1's encodes is recorded as Migration and invasion enhancer 1[13].
- MIEN1's found in taxon is recorded as Homo sapiens[14].
- MIEN1's chromosome is recorded as human chromosome 17[15].
- MIEN1's strand orientation is recorded as reverse strand[16].
- MIEN1's exact match is recorded as http://identifiers.org/ncbigene/84299[17].
- MIEN1's cytogenetic location is recorded as 17q12[18].
- MIEN1's expressed in is recorded as mucosa of transverse colon[19].
- MIEN1's expressed in is recorded as putamen[20].
- MIEN1's expressed in is recorded as caudate nucleus[21].
- MIEN1's expressed in is recorded as mucosa of ileum[22].
- MIEN1's expressed in is recorded as nucleus accumbens[23].
- MIEN1's expressed in is recorded as apex of heart[24].
- MIEN1's expressed in is recorded as C1 segment[25].
- MIEN1's expressed in is recorded as amygdala[26].