KEGG   Homo sapiens (human): 135892
Entry
135892            CDS       T01001                                 
Symbol
TRIM50, TRIM50A
Name
(RefSeq) tripartite motif containing 50
  KO
K12024  tripartite motif-containing protein 50/73/74
Organism
hsa  Homo sapiens (human)
Disease
H01439  Williams-Beuren syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04121 Ubiquitin system [BR:hsa04121]
    135892 (TRIM50)
Ubiquitin system [BR:hsa04121]
 Ubiquitin ligases (E3)
  Single Ring-finger type E3
   TRIM/RBCC proteins
    135892 (TRIM50)
SSDB
Motif
Pfam: PRY SPRY zf-RING_UBOX zf-B_box zf-C3HC4_4 zf-C3HC4_3 zf-C3HC4 zf-C3HC4_2 zf-RING_2 RING_XB3-XBAT31 zf-RING_5 U-box Trimer_CC Prok-RING_4 zf-Nse zf-RING_6 Baculo_IE-1 ANCHR-like_BBOX
Other DBs
NCBI-GeneID: 135892
NCBI-ProteinID: NP_001268380
OMIM: 612548
HGNC: 19017
Ensembl: ENSG00000146755
UniProt: Q86XT4
Position
7:complement(73312536..73328082)
AA seq 487 aa
MAWQVSLPELEDRLQCPICLEVFKEPLMLQCGHSYCKGCLVSLSCHLDAELRCPVCRQAV
DGSSSLPNVSLARVIEALRLPGDPEPKVCVHHRNPLSLFCEKDQELICGLCGLLGSHQHH
PVTPVSTVYSRMKEELAALISELKQEQKKVDELIAKLVNNRTRIVNESDVFSWVIRREFQ
ELHHLVDEEKARCLEGIGGHTRGLVASLDMQLEQAQGTRERLAQAECVLEQFGNEDHHKF
IRKFHSMASRAEMPQARPLEGAFSPISFKPGLHQADIKLTVWKRLFRKVLPAPEPLKLDP
ATAHPLLELSKGNTVVQCGLLAQRRASQPERFDYSTCVLASRGFSCGRHYWEVVVGSKSD
WRLGVIKGTASRKGKLNRSPEHGVWLIGLKEGRVYEAFACPRVPLPVAGHPHRIGLYLHY
EQGELTFFDADRPDDLRPLYTFQADFQGKLYPILDTCWHERGSNSLPMVLPPPSGPGPLS
PEQPTKL
NT seq 1464 nt   +upstreamnt  +downstreamnt
atggcttggcaggtgagcctgccagagctggaggaccggcttcagtgtcccatctgcctg
gaggtcttcaaggagcccctgatgctgcagtgtggccactcttactgcaagggctgcctg
gtttccctgtcctgccacctggatgccgagctgcgctgccccgtgtgccggcaggcggtg
gacggcagcagctccctgcccaacgtctccctggccagggtgatcgaagccctgaggctc
cctggggacccggagcccaaggtctgcgtgcaccaccggaacccgctcagccttttctgc
gagaaggaccaggagctcatctgtggcctctgcggtctgctgggctcccaccaacaccac
ccggtcacgcccgtctccaccgtctacagccgcatgaaggaggagctcgcagccctcatc
tctgagctgaagcaggagcagaaaaaggtggatgagctcatcgccaaactggtgaacaac
cggacccgaatcgtcaatgagtcggatgtcttcagctgggtgatccgccgcgagttccag
gagctgcaccacctggtggatgaggagaaggcccgctgcctggaggggatagggggtcac
acccgtggcctggtggcctccctggacatgcagctggagcaggcccagggaacccgggag
cggctggcccaagccgagtgtgtgctggaacagttcggcaatgaggaccaccacaagttc
atccggaagttccactccatggcctccagagcagagatgccgcaggcccggcccttagaa
ggcgcattcagccccatctccttcaagccaggcctccaccaggctgacatcaagctgacc
gtgtggaaaaggctcttccggaaagttttgccagccccggagcctctcaagttggaccct
gccactgcccacccactcctggagctctccaagggcaacacggtggtgcagtgcgggctt
ctggcccagcggcgagccagccagcctgagcgcttcgactacagcacctgcgtcctggcc
agccgcggcttctcctgcggccgccactactgggaggtggtggtgggcagcaagagcgac
tggcgcctgggggtcatcaagggcacagccagccgtaagggcaagctgaacaggtccccc
gagcacggcgtgtggctgatcggcctgaaggagggccgggtgtacgaagcctttgcctgc
ccccgggtacccctgcccgtggccggccacccccaccgcatcgggctctacctgcactat
gagcagggcgaactcaccttcttcgatgccgaccgccccgatgacctgcggccgctctac
accttccaggccgacttccagggcaagctctaccccatcctggacacctgctggcacgag
aggggcagcaactcgctgcccatggtgctgcccccgcccagcgggcctggccccctcagc
cccgagcagcccaccaagctgtag

  All links  
Disease (1)   
   OMIM (1)   
Gene (10)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (13)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (11)   
DNA sequence (33)   
   RefSeq(nuc) (11)   
   GenBank (11)   
   EMBL (11)   
Protein domain (18)   
   Pfam (18)   
All databases (75)   

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