Basic Information
TF
Full name: transferrin
Gene type: protein coding
HGNC ID: HGNC:11740
Gene location: 3q22.1
Gene resources
NCBI: https://www.ncbi.nlm.nih.gov/gene/7018
Alliance of genome: https://www.alliancegenome.org/gene/HGNC:11740
MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_001063.4
Protein resources
UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P02787
AlphaFold: https://alphafold.ebi.ac.uk/entry/P02787
MEME motif:
Clinical resources
Pathway resources
KEGG pathway: https://www.genome.jp/pathway/hsa04066+7018
Variant resources
Gene | Disease type | Variant type | NCBI dbSNP | Alleles | Variant location |
---|---|---|---|---|---|
TF | AMD | Intron Variant | rs4481157 | G>A | chr3:133745840 (GRCh38.p13) |