Homo sapiens (human): 4692
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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)
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Paralog
Gene cluster
GFIT
Motif
Pfam:
MAGE
Motif
Other DBs
NCBI-GeneID:
4692
NCBI-ProteinID:
NP_002478
OMIM:
602117
HGNC:
7675
Ensembl:
ENSG00000182636
UniProt:
Q99608
X5D982
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All DBs
Position
15:complement(23685400..23687305)
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AA seq
321 aa
AA seq
DB search
MSEQSKDLSDPNFAAEAPNSEVHSSPGVSEGVPPSATLAEPQSPPLGPTAAPQAAPPPQA
PNDEGDPKALQQAAEEGRAHQAPSAAQPGPAPPAPAQLVQKAHELMWYVLVKDQKKMIIW
FPDMVKDVIGSYKKWCRSILRRTSLILARVFGLHLRLTSLHTMEFALVKALEPEELDRVA
LSNRMPMTGLLLMILSLIYVKGRGARESAVWNVLRILGLRPWKKHSTFGDVRKLITEEFV
QMNYLKYQRVPYVEPPEYEFFWGSRASREITKMQIMEFLARVFKKDPQAWPSRYREALEE
ARALREANPTAHYPRSSVSED
NT seq
966 nt
NT seq
+upstream
nt +downstream
nt
atgtcagaacaaagtaaggatctgagcgaccctaactttgcagccgaggcccccaactcc
gaggtgcacagcagccctggggtttcggagggggttcctccgtccgcgaccctggcagag
ccgcagagccctcctctaggcccgacggccgctccgcaggccgcgccgcctccccaggcc
ccgaacgacgagggcgacccgaaggccctgcagcaggctgcggaggagggccgcgcccac
caggccccgagcgcggcccagccgggcccggcaccgccagccccggcgcagctggtgcag
aaggcgcacgagctcatgtggtacgtgctggtcaaggaccagaagaagatgatcatctgg
tttccagacatggtgaaagatgtcatcggcagctacaagaagtggtgcaggagcatcctc
cggcgcaccagcctcatcctcgcccgggtgttcgggctgcacctgaggctaaccagcctg
cacaccatggagtttgcgctggtcaaagcgctggagcccgaggagctggacagggtggcg
ctgagcaaccgcatgcccatgacaggcctcctgctcatgatcctgagcctcatctacgtg
aagggccgcggcgccagagagagcgccgtctggaacgtgctgcgcatcctggggctgcgg
ccctggaagaagcactccaccttcggggacgtgcggaagctcatcactgaggagttcgtc
caaatgaattacctgaagtaccagcgcgtcccatacgtggagccgcccgaatacgagttc
ttttggggctcccgggccagccgcgaaatcaccaagatgcaaatcatggagttcctggcc
agggtctttaagaaagacccccaggcctggccctcccgatacagagaagctctggaggag
gccagagctctgcgggaggctaatcccactgcccactaccctcgcagcagtgtctctgag
gactag
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