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SH3GL1

SH3 domain containing GRB2 like 1, endophilin A2

HCNC Approved Symbol
SH3GL1 (HGNC:10830)
Genomic Coordinates
19:4,360,370 - 4,400,547 (19p13.3)
Synonyms
SH3P8, SH3D2B, CNSA1, EEN, MGC111371
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Leukemia, acute myeloid
601626AD; SM

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SH3GL1 gene.

Frequently observed phenotypes

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

No Results