Homo sapiens (human): 6638
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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)
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Paralog
Gene cluster
GFIT
Motif
Pfam:
LSM
Motif
Other DBs
NCBI-GeneID:
6638
NCBI-ProteinID:
NP_001336383
OMIM:
182279
HGNC:
11164
Ensembl:
ENSG00000128739
UniProt:
P63162
X5DP00
Structure
PDB
PDBj
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All DBs
Position
15:24823637..24978723
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AA seq
240 aa
AA seq
DB search
MTVGKSSKMLQHIDYRMRCILQDGRIFIGTFKAFDKHMNLILCDCDEFRKIKPKNAKQPE
REEKRVLGLVLLRGENLVSMTVEGPPPKDTGIARVPLAGAAGGPGVGRAAGRGVPAGVPI
PQAPAGLAGPVRGVGGPSQQVMTPQGRGTVAAAAVAATASIAGAPTQYPPGRGTPPPPVG
RATPPPGIMAPPPGMRPPMGPPIGLPPARGTPIGMPPPGMRPPPPGIRGPPPPGMRPPRP
NT seq
723 nt
NT seq
+upstream
nt +downstream
nt
atgactgttggcaagagtagcaagatgctgcagcacattgactatagaatgagatgtatc
ctgcaagatggccgaatcttcattggcacctttaaggcttttgacaagcatatgaatttg
atcctctgtgattgtgatgagttcagaaagatcaagccaaagaatgcgaagcaaccagag
cgtgaagaaaagcgggttttgggtctggtgttgctgcgtggggagaacttggtatccatg
actgtggaggggccaccccccaaagatactggcattgctcgggtaccacttgctggagct
gctggaggccctggggttggtagggcagctggtagaggagtaccagctggtgtgccaatt
ccccaggcccctgctggattggcaggccctgtccgaggagttgggggaccatcccagcag
gtaatgactccacagggaagaggcactgtagcagctgctgctgttgctgcgactgccagt
attgctggagccccaacacagtacccaccaggacggggcactccgcccccacccgtcggc
agagcaaccccacctccaggcattatggctcctccacctggtatgagaccacccatgggc
ccaccaattgggcttccccctgctcgagggacgccaataggcatgccgcctccgggaatg
agaccccctccaccaggcattagaggtccacctcccccaggaatgcgtccaccaagacct
tag
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