KEGG   Homo sapiens (human): 23154
Entry
23154             CDS       T01001                                 
Symbol
NCDN, NEDIES
Name
(RefSeq) neurochondrin
Organism
hsa  Homo sapiens (human)
Disease
H02459  Syndromic neurodevelopmental disorder
SSDB
Motif
Pfam: Neurochondrin
Other DBs
NCBI-GeneID: 23154
NCBI-ProteinID: NP_001014839
OMIM: 608458
HGNC: 17597
Ensembl: ENSG00000020129
UniProt: Q9UBB6
Position
1:35557799..35566779
AA seq 729 aa
MSCCDLAAAGQLGKASIMASDCEPALNQAEGRNPTLERYLGALREAKNDSEQFAALLLVT
KAVKAGDIDAKTRRRIFDAVGFTFPNRLLTTKEAPDGCPDHVLRALGVALLACFCSDPEL
AAHPQVLNKIPILSTFLTARGDPDDAARRSMIDDTYQCLTAVAGTPRGPRHLIAGGTVSA
LCQAYLGHGYGFDQALALLVGLLAAAETQCWKEAEPDLLAVLRGLSEDFQKAEDASKFEL
CQLLPLFLPPTTVPPECYRDLQAGLARILGSKLSSWQRNPALKLAARLAHACGSDWIPAG
SSGSKFLALLVNLACVEVRLALEETGTEVKEDVVTACYALMELGIQECTRCEQSLLKEPQ
KVQLVSVMKEAIGAVIHYLLQVGSEKQKEPFVFASVRILGAWLAEETSSLRKEVCQLLPF
LVRYAKTLYEEAEEANDLSQQVANLAISPTTPGPTWPGDALRLLLPGWCHLTVEDGPREI
LIKEGAPSLLCKYFLQQWELTSPGHDTSVLPDSVEIGLQTCCHIFLNLVVTAPGLIKRDA
CFTSLMNTLMTSLPALVQQQGRLLLAANVATLGLLMARLLSTSPALQGTPASRGFFAAAI
LFLSQSHVARATPGSDQAVLALSPEYEGIWADLQELWFLGMQAFTGCVPLLPWLAPAALR
SRWPQELLQLLGSVSPNSVKPEMVAAYQGVLVELARANRLCREAMRLQAGEETASHYRMA
ALEQCLSEP
NT seq 2190 nt   +upstreamnt  +downstreamnt
atgtcgtgttgtgacctggctgcggcgggacagttgggcaaggcgagcatcatggcctcg
gattgcgagccagctctgaaccaggcagagggccgaaaccccaccctggagcgctacctg
ggagccctccgtgaggccaagaatgacagcgagcagtttgcagccctgctgctagtgacc
aaggcagtcaaagcaggtgacatagatgccaaaactcggcggcggatcttcgatgctgtc
ggcttcaccttccccaatcgtctcctgaccaccaaggaggcgccggatggctgccctgac
catgttctgcgggctttgggtgtggccctgctggcctgcttctgcagtgaccctgaactg
gccgcccatccccaagtcctgaacaagattcccattcttagcaccttcctcacagcccgg
ggggacccggacgatgctgcccgccgctccatgattgatgacacctaccagtgcctgacg
gctgtagcaggcacacccagagggcctcggcacctcattgctggtggcaccgtgtctgcc
ctatgccaggcatacctggggcacggctatggctttgaccaggccctggcactcctggtg
gggctgctggctgctgccgagacacagtgctggaaggaggcggagcccgacctgctggcc
gtgttgcggggcctcagtgaggatttccagaaagctgaggatgccagcaagtttgagctc
tgccagctgctgcccctctttttgcccccgacaaccgtgccccctgaatgctaccgggat
ctgcaggccgggctggcacgcatcctgggaagcaagctgagctcctggcagcgcaaccct
gcactgaagctggcagcccgcctggcacacgcctgcggctccgactggatcccggcgggc
agctccgggagcaagttcctggccctgctggtgaatctggcgtgcgtggaagtgcggctg
gcactggaggagacgggcacggaggtgaaagaggatgtggtgaccgcctgctatgccctc
atggagttggggatccaggaatgcactcgctgtgagcagtcactgcttaaggagccacag
aaggtgcagctcgtgagcgtcatgaaggaggccataggggctgttatccactacctgctg
caggtggggtcagagaagcagaaggagccctttgtgtttgcctcggtgcggatcctgggt
gcctggctggccgaggagacctcatccttgcgtaaggaggtgtgccagctgctgcccttc
ctcgtccgctatgccaagaccctctacgaggaggccgaggaggccaatgacctttcccag
caggtggccaacctggccatctcccccaccaccccagggcccacctggccaggagacgct
ctccggctcctcctgcctggctggtgccacctgaccgttgaagatgggccccgggagatc
ctgatcaaggaaggggccccctcgcttctgtgcaagtatttcctgcagcagtgggaactc
acatcccctggccacgacacctcggtgctgcctgacagcgtggagattggcctgcagacc
tgctgccacatcttcctcaacctcgtggtcaccgcaccggggctgatcaagcgtgacgcc
tgcttcacatctctaatgaacaccctcatgacgtcgctaccagcactagtgcagcaacag
ggaaggctgcttctggctgctaatgtggccaccctggggctcctcatggcccggctcctt
agcacctctccagctcttcagggaacaccagcatcccgagggttcttcgcagctgccatc
ctcttcctatcacagtcccacgtggcgcgggccaccccgggctcagaccaggcagtgcta
gccctgtcccctgagtatgagggcatctgggccgacctgcaggagctctggttcctgggc
atgcaggccttcaccggctgtgtgcctctgctgccctggctggcccccgctgccctgcgc
tcccgctggccgcaggagctgctccagctgctaggcagtgtcagccccaactctgtcaag
cccgagatggtggccgcctatcagggtgtcctggtggagctggcgcgggccaaccggctg
tgccgggaggccatgaggctgcaggcgggcgaggagacggccagccactaccgcatggct
gccttggagcagtgcctgtcagagccctga

  All links  
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (29)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (17)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (21)   
   RefSeq(nuc) (3)   
   GenBank (9)   
   EMBL (9)   
Protein domain (1)   
   Pfam (1)   
All databases (60)   

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