CRYGN
protein-coding gene in the species Homo sapiens
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CRYGN
Summary
CRYGN is a gene[1].
Key Facts
- CRYGN's instance of is recorded as gene[2].
- CRYGN is a type of protein-coding gene[3].
- CRYGN's HomoloGene ID is recorded as 16986[4].
- CRYGN's genomic start is recorded as 151125921[5].
- CRYGN's genomic start is recorded as 151428832[6].
- CRYGN's genomic end is recorded as 151440813[7].
- CRYGN's genomic end is recorded as 151137899[8].
- CRYGN's ortholog is recorded as Crygn[9].
- CRYGN's ortholog is recorded as Crygn[10].
- CRYGN's ortholog is recorded as crygn1[11].
- CRYGN's ortholog is recorded as crygn2[12].
- CRYGN's encodes is recorded as Crystallin gamma N[13].
- CRYGN's found in taxon is recorded as Homo sapiens[14].
- CRYGN's chromosome is recorded as human chromosome 7[15].
- CRYGN's strand orientation is recorded as reverse strand[16].
- CRYGN's exact match is recorded as http://identifiers.org/ncbigene/155051[17].
- CRYGN's cytogenetic location is recorded as 7q36.1[18].
- CRYGN's expressed in is recorded as right lobe of thyroid gland[19].
- CRYGN's expressed in is recorded as left lobe of thyroid gland[20].
- CRYGN's expressed in is recorded as decidua[21].
- CRYGN's expressed in is recorded as canal of the cervix[22].
- CRYGN's expressed in is recorded as popliteal artery[23].
- CRYGN's expressed in is recorded as tibial arteries[24].
- CRYGN's expressed in is recorded as left uterine tube[25].
- CRYGN's expressed in is recorded as prefrontal cortex[26].