TF (transferrin)

2007-02-01  

Identity

HGNC
LOCATION
3q22.1
LOCUSID
ALIAS
HEL-S-71p,PRO1557,PRO2086,TFQTL1
FUSION GENES

Other Information

Locus ID:

NCBI: 7018
MIM: 190000
HGNC: 11740
Ensembl: ENSG00000091513

Variants:

dbSNP: 7018
ClinVar: 7018
TCGA: ENSG00000091513
COSMIC: TF

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000091513ENST00000402696P02787
ENSG00000091513ENST00000414694F8WEK9
ENSG00000091513ENST00000461695H7C5E8
ENSG00000091513ENST00000466911C9JB55
ENSG00000091513ENST00000482271C9JVG0
ENSG00000091513ENST00000485977F8WC57
ENSG00000091513ENST00000494430F8WCI6

Expression (GTEx)

0
500
1000
1500
2000
2500

Pathways

PathwaySourceExternal ID
Mineral absorptionKEGGko04978
Mineral absorptionKEGGhsa04978
HIF-1 signaling pathwayKEGGhsa04066
HemostasisREACTOMER-HSA-109582
Platelet activation, signaling and aggregationREACTOMER-HSA-76002
Response to elevated platelet cytosolic Ca2+REACTOMER-HSA-76005
Platelet degranulationREACTOMER-HSA-114608
Vesicle-mediated transportREACTOMER-HSA-5653656
Membrane TraffickingREACTOMER-HSA-199991
Transmembrane transport of small moleculesREACTOMER-HSA-382551
Iron uptake and transportREACTOMER-HSA-917937
Transferrin endocytosis and recyclingREACTOMER-HSA-917977
Clathrin-mediated endocytosisREACTOMER-HSA-8856828
Cargo recognition for clathrin-mediated endocytosisREACTOMER-HSA-8856825
FerroptosisKEGGko04216
FerroptosisKEGGhsa04216

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA10004adalimumabChemicalClinicalAnnotationassociatedPD27115882
PA443815Crohn DiseaseDiseaseClinicalAnnotationassociatedPD27115882

References

Pubmed IDYearTitleCitations
378761472024"Hide and seek": Misleading transferrin variants in PMM2-CDG complicate diagnostics.0
379301352024Height of non-Hispanic white adults with homeostatic iron regulator HFE genotypes p.C282Y/p.C282Y and wt/wt.1
379646892024Evaluation of salivary transferrin in patients with oral squamous cell carcinoma.1
380489912024Cohort-Based Reference Values for Serum Ferritin and Transferrin and Longitudinal Determinants of Iron Status in European Children Aged 3-15 Years.0
378761472024"Hide and seek": Misleading transferrin variants in PMM2-CDG complicate diagnostics.0
379301352024Height of non-Hispanic white adults with homeostatic iron regulator HFE genotypes p.C282Y/p.C282Y and wt/wt.1
379646892024Evaluation of salivary transferrin in patients with oral squamous cell carcinoma.1
380489912024Cohort-Based Reference Values for Serum Ferritin and Transferrin and Longitudinal Determinants of Iron Status in European Children Aged 3-15 Years.0
365090212023COVID-19 compromises iron homeostasis: Transferrin as a target of investigation.3
371462462023The hepatic niche leads to aggressive natural killer cell leukemia proliferation through the transferrin-transferrin receptor 1 axis.2
375035772023Macromolecular Crowding Promotes Re-entrant Liquid-Liquid Phase Separation of Human Serum Transferrin and Prevents Surface-Induced Fibrillation.0
376942822023Transferrin promotes chondrogenic differentiation in condylar growth through inducing autophagy via ULK1-ATG16L1 axis.1
379589172023Meconium Transferrin and Ferritin as Markers of Homeostasis in the Developing Fetus.2
365090212023COVID-19 compromises iron homeostasis: Transferrin as a target of investigation.3
371462462023The hepatic niche leads to aggressive natural killer cell leukemia proliferation through the transferrin-transferrin receptor 1 axis.2

Citation

Dessen P

TF (transferrin)

Atlas Genet Cytogenet Oncol Haematol. 2007-02-01

Online version: http://atlasgeneticsoncology.org/gene/46020/tf-(transferrin)