RELN
protein-coding gene in the species Homo sapiens
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RELN
Summary
RELN is a gene[1].
Key Facts
- RELN's instance of is recorded as gene[2].
- RELN is a type of protein-coding gene[3].
- RELN's Commons category is recorded as Reelin[4].
- RELN's HomoloGene ID is recorded as 3699[5].
- RELN's genomic start is recorded as 103112231[6].
- RELN's genomic start is recorded as 103471381[7].
- RELN's genomic end is recorded as 103629963[8].
- RELN's genomic end is recorded as 103989658[9].
- RELN's ortholog is recorded as Reln[10].
- RELN's ortholog is recorded as GUF1[11].
- RELN's ortholog is recorded as reln[12].
- RELN's encodes is recorded as reelin[13].
- RELN's found in taxon is recorded as Homo sapiens[14].
- RELN's chromosome is recorded as human chromosome 7[15].
- RELN's decreased expression in is recorded as schizophrenia[16].
- RELN's decreased expression in is recorded as bipolar disorder[17].
- RELN's genetic association is recorded as Alzheimer's disease[18].
- RELN's genetic association is recorded as otosclerosis[19].
- RELN's genetic association is recorded as multiple sclerosis[20].
- RELN's genetic association is recorded as schizophrenia[21].
- RELN's genetic association is recorded as Norman–Roberts syndrome[22].
- RELN's genetic association is recorded as familial temporal lobe epilepsy 7[23].
- RELN's strand orientation is recorded as reverse strand[24].
- RELN's exact match is recorded as http://identifiers.org/ncbigene/5649[25].
- RELN's cytogenetic location is recorded as 7q22.1[26].