Homo sapiens Protein: RAB28 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-10089.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | RAB28 | ||||||||||||||||||
Protein Name | RAB28, member RAS oncogene family | ||||||||||||||||||
Synonyms | CORD18; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000328551 | ||||||||||||||||||
InnateDB Gene | IDBG-10083 (RAB28) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | |||||||||||||||||||
Subcellular Localization | Cell membrane {ECO:0000305}; Lipid-anchor {ECO:0000305}; Cytoplasmic side {ECO:0000305}. Cytoplasm, cytoskeleton, cilium basal body. Note=Expressed in the basal body and ciliary rootlet of the photoreceptors. {ECO:0000250}. | ||||||||||||||||||
Disease Associations | Cone-rod dystrophy 18 (CORD18) [MIM:615374]: A form of cone-rod dystrophy, an inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa. {ECO:0000269PubMed:23746546}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Isoform S is detected in most tissues investigated: cortex, liver, kidney, skeletal muscle, adipose tissue, testis, urothelium, lung, bone marrow and retinal pigment epithelium (RPE). Isoform L 2 is widely and abundantly expressed all tissues. Isoform 3 is highly expressed in heart, lung, bone marrow, retina, brain, and RPE. {ECO:0000269PubMed:23746546}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR001806
Small GTPase superfamily IPR002041 Ran GTPase IPR003578 Small GTPase superfamily, Rho type IPR003579 Small GTPase superfamily, Rab type IPR005225 Small GTP-binding protein domain IPR006689 Small GTPase superfamily, ARF/SAR type IPR006762 Gtr1/RagA G protein IPR013684 Mitochondrial Rho-like IPR020849 Small GTPase superfamily, Ras type IPR027417 P-loop containing nucleoside triphosphate hydrolase |
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PFAM |
PF00071
PF00025 PF04670 PF08477 |
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PRINTS |
PR00449
PR00627 PR00328 |
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PIRSF | |||||||||||||||||||
SMART |
SM00176
SM00174 SM00175 SM00173 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | P51157 | ||||||||||||||||||
PhosphoSite | PhosphoSite-P51157 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 9364 | ||||||||||||||||||
UniGene | Hs.603604 | ||||||||||||||||||
RefSeq | NP_001017979 | ||||||||||||||||||
HUGO | HGNC:9768 | ||||||||||||||||||
OMIM | 612994 | ||||||||||||||||||
CCDS | CCDS33961 | ||||||||||||||||||
HPRD | 06699 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC006226 AC006445 AC020729 AF498955 BC035054 CX165950 X94703 | ||||||||||||||||||
GenPept | AAH35054 AAM21103 CAA64364 | ||||||||||||||||||