KEGG   Homo sapiens (human): 8738
Entry
8738              CDS       T01001                                 
Symbol
CRADD, MRT34, RAIDD
Name
(RefSeq) CASP2 and RIPK1 domain containing adaptor with death domain
  KO
K02832  CASP2 and RIPK1 domain containing adaptor with death domain
Organism
hsa  Homo sapiens (human)
Disease
H00768  Autosomal recessive intellectual developmental disorder
H01911  Syndromic autosomal recessive mental retardation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99995 Signaling proteins
    8738 (CRADD)
SSDB
Motif
Pfam: CARD Death
Other DBs
NCBI-GeneID: 8738
NCBI-ProteinID: NP_001307028
OMIM: 603454
HGNC: 2340
Ensembl: ENSG00000169372
UniProt: P78560 Q53XL1 Q8IY43
Structure
LinkDB
Position
12:93677375..93894840
AA seq 199 aa
MEARDKQVLRSLRLELGAEVLVEGLVLQYLYQEGILTENHIQEINAQTTGLRKTMLLLDI
LPSRGPKAFDTFLDSLQEFPWVREKLKKAREEAMTDLPAGDRLTGIPSHILNSSPSDRQI
NQLAQRLGPEWEPMVLSLGLSQTDIYRCKANHPHNVQSQVVEAFIRWRQRFGKQATFQSL
HNGLRAVEVDPSLLLHMLE
NT seq 600 nt   +upstreamnt  +downstreamnt
atggaggccagagacaaacaagtactccgctcacttcgcctggagctgggtgcagaggta
ttggtggagggactggttcttcagtacctctaccaggaaggaatcttgacggaaaaccat
attcaagaaatcaatgctcaaaccacaggcctccggaaaacaatgctcctgctggatatc
ctaccttccaggggccctaaagcatttgatacattcctagattccctacaggagtttccc
tgggtcagggagaagctgaagaaggcaagggaagaggccatgaccgacctgcctgcaggt
gacagattgactgggatcccctcgcacatcctcaacagctccccatcagaccggcagatt
aaccagctggcccagaggctgggccctgagtgggagcccatggtgctgtctctgggactg
tcccagacggatatctaccgctgtaaggccaaccacccccacaacgtgcagtcgcaggtg
gtggaggccttcatccgttggcggcagcgcttcgggaagcaggccaccttccagagcctg
cacaacgggctgcgggctgtggaggtggacccctcgctgctcctgcacatgttggagtga

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