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TUBGCP2

tubulin gamma complex component 2

HCNC Approved Symbol
TUBGCP2 (HGNC:18599)
Genomic Coordinates
10:133,278,635 - 133,312,337 (10q26.3)
Synonyms
GCP2, Spc97p, SPBC97, hGCP2, ALP4
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
618737AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the TUBGCP2 gene.

Frequently observed phenotypes

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

No Results