Homo sapiens Protein: CRADD | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-586447.3 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | CRADD | ||||||||||||||||||
Protein Name | CASP2 and RIPK1 domain containing adaptor with death domain | ||||||||||||||||||
Synonyms | MRT34; RAIDD; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000439068 | ||||||||||||||||||
InnateDB Gene | IDBG-51368 (CRADD) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Apoptotic adaptor molecule specific for caspase-2 and FASL/TNF receptor-interacting protein RIP. In the presence of RIP and TRADD, CRADD recruits caspase-2 to the TNFR-1 signalling complex. | ||||||||||||||||||
Subcellular Localization | Cytoplasm {ECO:0000250}. Nucleus {ECO:0000250}. | ||||||||||||||||||
Disease Associations | Mental retardation, autosomal recessive 34 (MRT34) [MIM:614499]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRT34 is a non-syndromic form. Affected individuals have mildly delayed development and significantly impaired cognitive function, precluding independent living and self-care. Speech is rudimentary, but articulate; autism is not present. {ECO:0000269PubMed:22279524}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Constitutively expressed in most tissues, with particularly high expression in adult heart, testis, liver, skeletal muscle, fetal liver and kidney. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 26 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 |
IPR000488
Death domain IPR001315 CARD domain IPR011029 Death-like domain |
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PFAM |
PF00531
PF00619 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00005
SM00114 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | P78560 | ||||||||||||||||||
PhosphoSite | PhosphoSite-P78560 | ||||||||||||||||||
TrEMBL | Q53XL1 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 8738 | ||||||||||||||||||
UniGene | Hs.719191 | ||||||||||||||||||
RefSeq | |||||||||||||||||||
HUGO | HGNC:2340 | ||||||||||||||||||
OMIM | 603454 | ||||||||||||||||||
CCDS | CCDS9048 | ||||||||||||||||||
HPRD | 04584 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AK314861 BC017042 BT009837 CH471054 CR407643 U79115 U84388 | ||||||||||||||||||
GenPept | AAB42217 AAC50952 AAH17042 AAP88839 BAG37377 CAG28571 EAW97497 | ||||||||||||||||||