Basic Information
LCN9
Full name: lipocalin 9
Gene type: protein coding
HGNC ID: HGNC:17442
Gene location: 9q34.3
Gene resources
NCBI: https://www.ncbi.nlm.nih.gov/gene/392399
Alliance of genome: https://www.alliancegenome.org/gene/HGNC:17442
MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_001393661.1
Protein resources
UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/Q8WX39
AlphaFold: https://alphafold.ebi.ac.uk/entry/Q8WX39
MEME motif:
Clinical resources
Pathway resources
Variant resources
Gene | Disease type | Variant type | NCBI dbSNP | Alleles | Variant location |
---|---|---|---|---|---|
LCN9 | AMD | Missense Variant | rs200437673 | A>G | chr9:135663391 (GRCh38.p13) |