TF - Gene browser

TF

transferrin

HCNC Approved Symbol: TF (HGNC:11740)
Genomic Coordinates: 3:133,661,998 - 133,796,641 (3q22.1)
Synonyms: PRO1557, PRO2086
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the TF gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results