Homo sapiens (human): 23154
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Entry
23154 CDS
T01001
Symbol
NCDN, NEDIES
Name
(RefSeq) neurochondrin
Organism
hsa
Homo sapiens (human)
Disease
H02459
Syndromic neurodevelopmental disorder
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Ortholog
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Gene cluster
GFIT
Motif
Pfam:
Neurochondrin
Motif
Other DBs
NCBI-GeneID:
23154
NCBI-ProteinID:
NP_001014839
OMIM:
608458
HGNC:
17597
Ensembl:
ENSG00000020129
UniProt:
Q9UBB6
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Position
1:35557799..35566779
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AA seq
729 aa
AA seq
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MSCCDLAAAGQLGKASIMASDCEPALNQAEGRNPTLERYLGALREAKNDSEQFAALLLVT
KAVKAGDIDAKTRRRIFDAVGFTFPNRLLTTKEAPDGCPDHVLRALGVALLACFCSDPEL
AAHPQVLNKIPILSTFLTARGDPDDAARRSMIDDTYQCLTAVAGTPRGPRHLIAGGTVSA
LCQAYLGHGYGFDQALALLVGLLAAAETQCWKEAEPDLLAVLRGLSEDFQKAEDASKFEL
CQLLPLFLPPTTVPPECYRDLQAGLARILGSKLSSWQRNPALKLAARLAHACGSDWIPAG
SSGSKFLALLVNLACVEVRLALEETGTEVKEDVVTACYALMELGIQECTRCEQSLLKEPQ
KVQLVSVMKEAIGAVIHYLLQVGSEKQKEPFVFASVRILGAWLAEETSSLRKEVCQLLPF
LVRYAKTLYEEAEEANDLSQQVANLAISPTTPGPTWPGDALRLLLPGWCHLTVEDGPREI
LIKEGAPSLLCKYFLQQWELTSPGHDTSVLPDSVEIGLQTCCHIFLNLVVTAPGLIKRDA
CFTSLMNTLMTSLPALVQQQGRLLLAANVATLGLLMARLLSTSPALQGTPASRGFFAAAI
LFLSQSHVARATPGSDQAVLALSPEYEGIWADLQELWFLGMQAFTGCVPLLPWLAPAALR
SRWPQELLQLLGSVSPNSVKPEMVAAYQGVLVELARANRLCREAMRLQAGEETASHYRMA
ALEQCLSEP
NT seq
2190 nt
NT seq
+upstream
nt +downstream
nt
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
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