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SH3PXD2B

SH3 and PX domains 2B

HCNC Approved Symbol
SH3PXD2B (HGNC:29242)
Genomic Coordinates
5:172,325,181 - 172,454,525 (5q35.1)
Synonyms
FLJ20831, KIAA1295
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Frank-ter Haar syndrome
249420AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SH3PXD2B gene.

Frequently observed phenotypes

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

No Results