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CBLIF

cobalamin binding intrinsic factor

HCNC Approved Symbol
CBLIF (HGNC:4268)
Genomic Coordinates
11:59,829,273 - 59,845,499 (11q12.1)
Synonyms
TCN3, IF, IFMH, INF, GIF
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the CBLIF gene.

Frequently observed phenotypes

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

Megaloblastic anemia
 2 (100.0%)
CBLIF - Gene browser | 3billion