KEGG   Homo sapiens (human): 4692
Entry
4692              CDS       T01001                                 
Symbol
NDN, HsT16328, PWCR
Name
(RefSeq) necdin, MAGE family member
  KO
K19482  necdin
Organism
hsa  Homo sapiens (human)
Disease
H00478  Prader-Willi syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99995 Signaling proteins
    4692 (NDN)
SSDB
Motif
Pfam: MAGE
Other DBs
NCBI-GeneID: 4692
NCBI-ProteinID: NP_002478
OMIM: 602117
HGNC: 7675
Ensembl: ENSG00000182636
UniProt: Q99608 X5D982
Position
15:complement(23685400..23687305)
AA seq 321 aa
MSEQSKDLSDPNFAAEAPNSEVHSSPGVSEGVPPSATLAEPQSPPLGPTAAPQAAPPPQA
PNDEGDPKALQQAAEEGRAHQAPSAAQPGPAPPAPAQLVQKAHELMWYVLVKDQKKMIIW
FPDMVKDVIGSYKKWCRSILRRTSLILARVFGLHLRLTSLHTMEFALVKALEPEELDRVA
LSNRMPMTGLLLMILSLIYVKGRGARESAVWNVLRILGLRPWKKHSTFGDVRKLITEEFV
QMNYLKYQRVPYVEPPEYEFFWGSRASREITKMQIMEFLARVFKKDPQAWPSRYREALEE
ARALREANPTAHYPRSSVSED
NT seq 966 nt   +upstreamnt  +downstreamnt
atgtcagaacaaagtaaggatctgagcgaccctaactttgcagccgaggcccccaactcc
gaggtgcacagcagccctggggtttcggagggggttcctccgtccgcgaccctggcagag
ccgcagagccctcctctaggcccgacggccgctccgcaggccgcgccgcctccccaggcc
ccgaacgacgagggcgacccgaaggccctgcagcaggctgcggaggagggccgcgcccac
caggccccgagcgcggcccagccgggcccggcaccgccagccccggcgcagctggtgcag
aaggcgcacgagctcatgtggtacgtgctggtcaaggaccagaagaagatgatcatctgg
tttccagacatggtgaaagatgtcatcggcagctacaagaagtggtgcaggagcatcctc
cggcgcaccagcctcatcctcgcccgggtgttcgggctgcacctgaggctaaccagcctg
cacaccatggagtttgcgctggtcaaagcgctggagcccgaggagctggacagggtggcg
ctgagcaaccgcatgcccatgacaggcctcctgctcatgatcctgagcctcatctacgtg
aagggccgcggcgccagagagagcgccgtctggaacgtgctgcgcatcctggggctgcgg
ccctggaagaagcactccaccttcggggacgtgcggaagctcatcactgaggagttcgtc
caaatgaattacctgaagtaccagcgcgtcccatacgtggagccgcccgaatacgagttc
ttttggggctcccgggccagccgcgaaatcaccaagatgcaaatcatggagttcctggcc
agggtctttaagaaagacccccaggcctggccctcccgatacagagaagctctggaggag
gccagagctctgcgggaggctaatcccactgcccactaccctcgcagcagtgtctctgag
gactag

  All links  
Ontology (1)   
   KEGG BRITE (1)   
Disease (2)   
   KEGG DISEASE (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (15)   
   KEGG ORTHOLOGY (1)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (4)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (23)   
   RefSeq(nuc) (1)   
   GenBank (11)   
   EMBL (11)   
Protein domain (1)   
   Pfam (1)   
All databases (47)   

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