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IGF2

insulin like growth factor 2

HCNC Approved Symbol
IGF2 (HGNC:5466)
Genomic Coordinates
11:2,129,117 - 2,149,566 (11p15.5)
Synonyms
FLJ44734, IGF-II, C11orf43
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the IGF2 gene.

Frequently observed phenotypes

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

Facial hypoplasia
 1 (100.0%)
Failure to thrive
 1 (100.0%)
Simian line
 1 (100.0%)
Small for gestational age
 1 (100.0%)
IGF2 - Gene browser | 3billion