SPRYD3
protein-coding gene in the species Homo sapiens
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SPRYD3
Summary
SPRYD3 is a gene[1].
Key Facts
- SPRYD3's instance of is recorded as gene[2].
- SPRYD3 is a type of protein-coding gene[3].
- SPRYD3's HomoloGene ID is recorded as 13138[4].
- SPRYD3's genomic start is recorded as 53064316[5].
- SPRYD3's genomic start is recorded as 53458388[6].
- SPRYD3's genomic end is recorded as 53473204[7].
- SPRYD3's genomic end is recorded as 53079404[8].
- SPRYD3's ortholog is recorded as Spryd3[9].
- SPRYD3's ortholog is recorded as Spryd3[10].
- SPRYD3's ortholog is recorded as spryd3[11].
- SPRYD3's encodes is recorded as SPRY domain containing 3[12].
- SPRYD3's found in taxon is recorded as Homo sapiens[13].
- SPRYD3's chromosome is recorded as human chromosome 12[14].
- SPRYD3's strand orientation is recorded as reverse strand[15].
- SPRYD3's exact match is recorded as http://identifiers.org/ncbigene/84926[16].
- SPRYD3's cytogenetic location is recorded as 12q13.13[17].
- SPRYD3's expressed in is recorded as prefrontal cortex[18].
- SPRYD3's expressed in is recorded as right frontal lobe[19].
- SPRYD3's expressed in is recorded as nucleus accumbens[20].
- SPRYD3's expressed in is recorded as Brodmann area 9[21].
- SPRYD3's expressed in is recorded as cingulate gyrus[22].
- SPRYD3's expressed in is recorded as anterior cingulate cortex[23].
- SPRYD3's expressed in is recorded as islet of Langerhans[24].
- SPRYD3's expressed in is recorded as cardiac muscle tissue of right atrium[25].
- SPRYD3's expressed in is recorded as putamen[26].