KEGG   Homo sapiens (human): 6638
Entry
6638              CDS       T01001                                 
Symbol
SNRPN, HCERN3, PWCR, RT-LI, SM-D, SMN, SNRNP-N, SNURF-SNRPN, sm-N
Name
(RefSeq) small nuclear ribonucleoprotein polypeptide N
  KO
K11100  small nuclear ribonucleoprotein N
Organism
hsa  Homo sapiens (human)
Disease
H00478  Prader-Willi syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09192 Unclassified: genetic information processing
   99973 Transcription
    6638 (SNRPN)
SSDB
Motif
Pfam: LSM
Other DBs
NCBI-GeneID: 6638
NCBI-ProteinID: NP_003088
OMIM: 182279
HGNC: 11164
Ensembl: ENSG00000128739
UniProt: P63162 X5DP00
Structure
LinkDB
Position
15:24823637..24978723
AA seq 240 aa
MTVGKSSKMLQHIDYRMRCILQDGRIFIGTFKAFDKHMNLILCDCDEFRKIKPKNAKQPE
REEKRVLGLVLLRGENLVSMTVEGPPPKDTGIARVPLAGAAGGPGVGRAAGRGVPAGVPI
PQAPAGLAGPVRGVGGPSQQVMTPQGRGTVAAAAVAATASIAGAPTQYPPGRGTPPPPVG
RATPPPGIMAPPPGMRPPMGPPIGLPPARGTPIGMPPPGMRPPPPGIRGPPPPGMRPPRP
NT seq 723 nt   +upstreamnt  +downstreamnt
atgactgttggcaagagtagcaagatgctgcagcacattgactatagaatgagatgtatc
ctgcaagatggccgaatcttcattggcacctttaaggcttttgacaagcatatgaatttg
atcctctgtgattgtgatgagttcagaaagatcaagccaaagaatgcgaagcaaccagag
cgtgaagaaaagcgggttttgggtctggtgttgctgcgtggggagaacttggtatccatg
actgtggaggggccaccccccaaagatactggcattgctcgggtaccacttgctggagct
gctggaggccctggggttggtagggcagctggtagaggagtaccagctggtgtgccaatt
ccccaggcccctgctggattggcaggccctgtccgaggagttgggggaccatcccagcag
gtaatgactccacagggaagaggcactgtagcagctgctgctgttgctgcgactgccagt
attgctggagccccaacacagtacccaccaggacggggcactccgcccccacccgtcggc
agagcaaccccacctccaggcattatggctcctccacctggtatgagaccacccatgggc
ccaccaattgggcttccccctgctcgagggacgccaataggcatgccgcctccgggaatg
agaccccctccaccaggcattagaggtccacctcccccaggaatgcgtccaccaagacct
tag

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