The TUBGCP2 gene homepage

General information
Gene symbol TUBGCP2
Gene name tubulin, gamma complex associated protein 2
Chromosome 10
Chromosomal band q26.3
Imprinted Unknown
Genomic reference NC_000010.10
Transcript reference NM_001256617.1
Exon/intron information NM_001256617.1 exon/intron table
Associated with diseases PAMDDFS
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 36
Unique public DNA variants reported 31
Individuals with public variants 10
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated May 05, 2025
Version TUBGCP2:250505

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001256617.1.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/TUBGCP2
HGNC HGNC:18599
Entrez Gene 10844
PubMed articles TUBGCP2
OMIM - Diseases PAMDDFS (Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures)
HGMD TUBGCP2
GeneCards TUBGCP2
NIH Genetic Testing Registry TUBGCP2
Orphanet TUBGCP2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00022142 10 transcript variant 1 NM_001256617.1 NP_001243546.1 36


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