RAB33B Chromosome 4

RAB33B, member RAS oncogene family
18 variants 18 Health Risk

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What This Gene Does
This gene encodes a small GTP-binding protein of the Rab GTPase family, whose members function in vesicle transport during protein secretion and endocytosis. Rab GTPases are active, membrane-associated proteins that recruit effector proteins in the GTP-bound state and inactive cytosolic proteins when in a GDP-bound state. The protein encoded by this gene is ubiquitously expressed and has been implicated in Golgi to endoplasmic reticulum cycling of Golgi enzymes. In addition, this protein regulates Golgi homeostasis and coordinates intra-Golgi retrograde trafficking. Allelic variants in this gene have been associated with Dyggve-Melchior-Clausen syndrome and Smith-McCort dysplasia 2, which are autosomal recessive spondyloepimetaphyseal dysplasias characterized by skeletal abnormalities. [provided by RefSeq, Sep 2016]
Gene Info
Gene Group
RAB, member RAS oncogene GTPases
Locus Type
gene with protein product
Location
4q31.1
Ensembl
ENSG00000172007
Associated Conditions (4)
Smith-McCort dysplasia 2
RAB33B-related disorder
Inborn genetic diseases
See cases
Key Variants
All Variants (18)
RSID Category Clinical Significance Conditions
RS1085307129 Health Risk Conflicting classifications of pathogenicity Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS138534367 Health Risk Conflicting classifications of pathogenicity Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS140381459 Health Risk Conflicting classifications of pathogenicity Smith-McCort dysplasia 2, RAB33B-related disorder, Smith-McCort dysplasia 2
RS142541603 Health Risk Conflicting classifications of pathogenicity Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS568007401 Health Risk Conflicting classifications of pathogenicity Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS758182997 Health Risk Conflicting classifications of pathogenicity Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS769999843 Health Risk Conflicting classifications of pathogenicity Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS779490913 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS587776958 Health Risk Likely pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS1085307128 Health Risk Pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS1085307130 Health Risk Pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS1085307131 Health Risk Pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS1187861686 Health Risk Pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS1750416123 Health Risk Pathogenic Smith-McCort dysplasia 2, See cases, Smith-McCort dysplasia 2
RS2111067418 Health Risk Pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS2111087458 Health Risk Pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS886044716 Health Risk Pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
RS1561002040 Health Risk Pathogenic/Likely pathogenic Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
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