KEGG   Homo sapiens (human): 221078
Entry
221078            CDS       T01001                                 
Symbol
NSUN6, 4933414E04Rik, ARL5B-AS1, MRT82, NOPD1
Name
(RefSeq) NOP2/Sun RNA methyltransferase 6
  KO
K21971  methyltransferase NSUN6 [EC:2.1.1.-]
Organism
hsa  Homo sapiens (human)
Disease
H00768  Autosomal recessive intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03016 Transfer RNA biogenesis [BR:hsa03016]
    221078 (NSUN6)
Transfer RNA biogenesis [BR:hsa03016]
 Eukaryotic type
  tRNA modification factors
   Methyltransferases
    221078 (NSUN6)
SSDB
Motif
Pfam: Methyltr_RsmB-F Methyltransf_31 FtsJ PUA PCMT BMT5-like Ubie_methyltran Methyltransf_23
Other DBs
NCBI-GeneID: 221078
NCBI-ProteinID: NP_872349
OMIM: 617199
HGNC: 23529
Ensembl: ENSG00000241058
Pharos: Q8TEA1(Tdark)
UniProt: Q8TEA1
Structure
Position
10:complement(18545561..18659327)
AA seq 469 aa
MSIFPKISLRPEVENYLKEGFMNKEIVTALGKQEAERKFETLLKHLSHPPSFTTVRVNTH
LASVQHVKNLLLDELQKQFNGLSVPILQHPDLQDVLLIPVIGPRKNIKKQQCEAIVGAQC
GNAVLRGAHVYAPGIVSASQFMKAGDVISVYSDIKGKCKKGAKEFDGTKVFLGNGISELS
RKEIFSGLPELKGMGIRMTEPVYLSPSFDSVLPRYLFLQNLPSALVSHVLNPQPGEKILD
LCAAPGGKTTHIAALMHDQGEVIALDKIFNKVEKIKQNALLLGLNSIRAFCFDGTKAVKL
DMVEDTEGEPPFLPESFDRILLDAPCSGMGQRPNMACTWSVKEVASYQPLQRKLFTAAVQ
LLKPEGVLVYSTCTITLAENEEQVAWALTKFPCLQLQPQEPQIGGEGMRGAGLSCEQLKQ
LQRFDPSAVPLPDTDMDSLREARREDMLRLANKDSIGFFIAKFVKCKST
NT seq 1410 nt   +upstreamnt  +downstreamnt
atgtctattttccctaagatatctttgagacctgaggttgaaaactatcttaaggaaggc
tttatgaataaggagattgtgactgctttaggtaaacaagaagcagaaaggaagtttgaa
actttgttaaagcacctgtcacatcctccatcatttacaactgtcagagtgaatacacat
ttagcctcagtacaacatgtgaaaaatctgttacttgatgaacttcagaagcagtttaat
ggattaagtgttcctattcttcaacatccagaccttcaagatgtgttacttattcctgtt
attggacccagaaagaatattaaaaaacaacagtgtgaagccattgttggagcccagtgt
ggcaatgcagttttaagaggagcccatgtctatgccccaggaattgtgtcagcatcacaa
tttatgaaagctggagatgttatttctgtatactctgatattaaaggaaaatgtaagaaa
ggagccaaagaatttgatggaacaaaagtatttcttggaaatgggatttctgaactaagc
cgcaaagaaatcttcagtggattacctgaactgaaaggcatgggcataagaatgacagaa
ccagtatatctcagcccttcatttgacagtgtactgccccgttacttatttttacaaaat
ttgccatctgccttagtaagtcatgtactaaatcctcaacctggagagaagattctagac
ttgtgtgcagcacctggagggaaaacaacacacattgcagcactaatgcatgatcaggga
gaagttatagcactggataaaatcttcaacaaagtagaaaaaatcaaacagaatgcctta
ttgttagggctgaattccatcagggcattttgttttgatggaacaaaggcggttaaactt
gatatggtggaggacacagaaggagaacctccatttctaccagaatcctttgaccgaatt
cttctggatgcaccctgtagtggaatgggacagagaccaaacatggcctgtacttggtct
gtgaaggaagtggcatcatatcagccattacagcgaaaactcttcactgcagcggttcag
ctgctgaagccagagggtgtgctggtttatagcacgtgcactataacactggccgaaaat
gaagaacaggttgcctgggccctgacaaaatttccttgccttcagcttcagccccaggaa
ccgcagattggaggagaaggaatgaggggagctgggctctcatgtgaacagttgaaacag
ctgcagcgatttgatccatcggctgtgccattaccggacactgacatggactctcttaga
gaggccagaagagaagacatgttgcgtctggctaataaggactctataggtttttttatt
gcaaaatttgtaaaatgcaaaagcacatag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (11)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
   PHAROS (1)   
Protein sequence (44)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (42)   
DNA sequence (72)   
   RefSeq(nuc) (42)   
   GenBank (15)   
   EMBL (15)   
3D Structure (4)   
   PDB (4)   
Protein domain (8)   
   Pfam (8)   
All databases (145)   

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