RAB33B Chromosome 4
RAB33B, member RAS oncogene family
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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
RS1085307129
Conflicting classifications of pathogenicity
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS138534367
Conflicting classifications of pathogenicity
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS140381459
Conflicting classifications of pathogenicity
Smith-McCort dysplasia 2, RAB33B-related disorder, Smith-McCort dysplasia 2
Health Risk
RS142541603
Conflicting classifications of pathogenicity
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS568007401
Conflicting classifications of pathogenicity
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS758182997
Conflicting classifications of pathogenicity
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS769999843
Conflicting classifications of pathogenicity
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS779490913
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS587776958
Likely pathogenic
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS1085307128
Pathogenic
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS1085307130
Pathogenic
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
RS1085307131
Pathogenic
Smith-McCort dysplasia 2, Smith-McCort dysplasia 2
Health Risk
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 |