Entity Details

Primary name CRADD_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP78560
EntryNameCRADD_HUMAN
FullNameDeath domain-containing protein CRADD
TaxID9606
Evidenceevidence at protein level
Length199
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesCRADD

GO terms

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GOName
GO:0002020 protease binding
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006919 activation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0006977 DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest
GO:0008625 extrinsic apoptotic signaling pathway via death domain receptors
GO:0030674 protein-macromolecule adaptor activity
GO:0042981 regulation of apoptotic process
GO:0043065 positive regulation of apoptotic process
GO:0070513 death domain binding
GO:0071260 cellular response to mechanical stimulus
GO:0097190 apoptotic signaling pathway
GO:2001235 positive regulation of apoptotic signaling pathway

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR000488 Death domainDomainDomain
IPR001315 CARD domainDomainDomain
IPR011029 Death-like domain superfamilyFamilyHomologous superfamily
IPR037926 CRADD, Death domainDomainDomain
IPR037939 Death domain-containing protein CRADDFamilyFamily
IPR042148 RAIDD, CARD domainDomainDomain

Diseases

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Disease IDSourceNameDescription
614499 OMIMMental retardation, autosomal recessive 34, with variant lissencephaly (MRT34)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. The disease is caused by variants affecting the gene represented in this entry.

Interactions

25 interactions

InteractorPartnerSourcesPublicationsLink
CRADD_HUMANCASP2_HUMANBioGRID, HPRD, IntAct, MINT11156409 11832478 15073321 16652156 23049853 25416956 27107012 29875129 31467278 31515488 32296183 8985253 details
CRADD_HUMANERG28_HUMANBioGRID, HPRD, IntAct16169070 details
CRADD_HUMANEF1A1_HUMANBioGRID, HPRD, IntAct16169070 details
CRADD_HUMANCCSE2_HUMANBioGRID, HPRD, IntAct16169070 details
CRADD_HUMANIL9R_HUMANBioGRID, IntAct21988832 details
CRADD_HUMANIMA5_HUMANBioGRID, IntAct21988832 details
CRADD_HUMANVTNC_HUMANBioGRID, IntAct21988832 details
CRADD_HUMANS35A3_HUMANBioGRID, IntAct21988832 details
CRADD_HUMANDCXR_HUMANBioGRID, IntAct21988832 details
CRADD_HUMANKCTD9_HUMANBioGRID, IntAct25416956 details
CRADD_HUMANBBS5_HUMANBioGRID, IntAct25416956 details
CRADD_HUMANDP13B_HUMANBioGRID, IntAct25416956 31515488 details
CRADD_HUMANTRI54_HUMANBioGRID, IntAct25416956 details
CRADD_HUMANWIF1_HUMANBioGRID, IntAct27107012 details
CRADD_HUMANACTN2_HUMANBioGRID, IntAct25910212 details
CRADD_HUMANPE2R4_HUMANBioGRID, MINT28298427 details
CRADD_HUMANTSHR_HUMANBioGRID, MINT28298427 details
CRADD_HUMANLRIF1_HUMANBioGRID, HPRD16169070 details
CRADD_HUMANRIPK1_HUMANBioGRID, HPRD8985253 9044836 details
CRADD_HUMANA4_HUMANBioGRID21832049 details
CRADD_HUMANPIDD1_HUMANBioGRID, HPRD, IntAct, MINT15073321 16360037 16652156 17159900 21415862 23049853 27773430 details
CRADD_HUMANRIF1_HUMANIntAct16169070 details
CRADD_HUMANTNR1A_HUMANBioGRID8985253 details
CRADD_HUMANCRYAB_HUMANBioGRID23049853 details
CRADD_HUMANCASP8_HUMANHPRD11002417 details