KEGG   Homo sapiens (human): 54496
Entry
54496             CDS       T01001                                 
Symbol
PRMT7, SBIDDS
Name
(RefSeq) protein arginine N-methyltransferase 7 isoform 1
  KO
K11438  type III protein arginine methyltransferase [EC:2.1.1.321]
Organism
hsa  Homo sapiens (human)
Disease
H02481  Syndromic disorder with short stature
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    54496 (PRMT7)
Enzymes [BR:hsa01000]
 2. Transferases
  2.1  Transferring one-carbon groups
   2.1.1  Methyltransferases
    2.1.1.321  type III protein arginine methyltransferase
     54496 (PRMT7)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Histone modification proteins
   HMTs (histone methyltransferases)
    PRMTs (protein arginine metyltransferases)
     54496 (PRMT7)
SSDB
Motif
Pfam: PRMT_C PrmA Methyltransf_25 Methyltransf_18 Methyltransf_4 tRNA-synt_2c TrmK Methyltransf_32 PCMT
Other DBs
NCBI-GeneID: 54496
NCBI-ProteinID: NP_001276947
OMIM: 610087
HGNC: 25557
UniProt: Q9NVM4
Position
16:68311019..68360870
AA seq 692 aa
MKIFCSRANPTTGSVEWLEEDEHYDYHQEIARSSYADMLHDKDRNVKYYQGIRAAVSRVK
DRGQKALVLDIGTGTGLLSMMAVTAGADFCYAIEVFKPMADAAVKIVEKNGFSDKIKVIN
KHSTEVTVGPEGDMPCRANILVTELFDTELIGEGALPSYEHAHRHLVEENCEAVPHRATV
YAQLVESGRMWSWNKLFPIHVQTSLGEQVIVPPVDVESCPGAPSVCDIQLNQVSPADFTV
LSDVLPMFSIDFSKQVSSSAACHSRRFEPLTSGRAQVVLSWWDIEMDPEGKIKCTMAPFW
AHSDPEEMQWRDHWMQCVYFLPQEEPVVQGSALYLVAHHDDYCVWYSLQRTSPEKNERVR
QMRPVCDCQAHLLWNRPRFGEINDQDRTDRYVQALRTVLKPDSVCLCVSDGSLLSVLAHH
LGVEQVFTVESSAASHKLLRKIFKANHLEDKINIIEKRPELLTNEDLQGRKVSLLLGEPF
FTTSLLPWHNLYFWYVRTAVDQHLGPGAMVMPQAASLHAVVVEFRDLWRIRSPCGDCEGF
DVHIMDDMIKRALDFRESREAEPHPLWEYPCRSLSEPWQILTFDFQQPVPLQPLCAEGTV
ELRRPGQSHAAVLWMEYHLTPECTLSTGLLEPADPEGGCCWNPHCKQAVYFFSPAPDPRA
LLGGPRTVSYAVEFHPDTGDIIMEFRHADTPD
NT seq 2079 nt   +upstreamnt  +downstreamnt
atgaagatcttctgcagtcgggccaatccgaccacggggtctgtggagtggctggaggag
gatgaacactatgattaccaccaggagattgcaaggtcatcttatgcagatatgctacat
gacaaagacagaaatgtaaaatactaccaaggtatccgggctgccgtgagcagggtgaag
gacagaggacagaaggccttggttctcgacattggcactggcacgggactcttgtcaatg
atggcggtcacagcaggtgccgacttctgctatgccatcgaggttttcaagcctatggct
gatgctgctgtgaagattgtggagaaaaatggctttagtgataagattaaggttatcaac
aagcattccaccgaggtgactgtaggtccagagggtgacatgccatgccgtgccaacatc
ctggtcacagagttgtttgacacagagctgatcggggagggggcgctgccctcctatgag
cacgcacacaggcatctcgtggaggaaaattgtgaggccgtgccccacagagccaccgtc
tatgcacagctggtggagtccgggaggatgtggtcgtggaacaagctatttcccatccac
gtgcagaccagcctcggagagcaggtcatcgtccctcccgttgacgtggagagctgccct
ggcgcaccctctgtctgtgacattcagctgaaccaggtgtcaccagccgactttacagtc
ctcagcgatgtgctgcccatgttcagcatagacttcagcaagcaagtcagtagctcagca
gcctgccatagcaggcggtttgaacctctgacatctggccgagctcaggtggttctctcg
tggtgggacattgaaatggaccctgaggggaagatcaagtgcaccatggcccccttctgg
gcacactcagacccagaggagatgcagtggcgggaccactggatgcagtgtgtgtacttc
ctgccacaagaggagcctgtggtgcagggctcagcgctctatctggtagcccaccacgat
gactactgcgtatggtacagcctgcagaggaccagccctgaaaagaatgagagagtccgc
cagatgcgccccgtgtgtgactgccaggctcacctgctctggaaccggcctcggtttgga
gagatcaatgaccaggacagaactgatcgatacgtccaggctctgaggaccgtgctgaag
ccagacagcgtgtgcctgtgtgtcagcgatggcagcctgctctccgtgctggcccatcac
ctgggggtggagcaggtgtttacagtcgagagttcagcagcttctcacaaactgttgaga
aaaatcttcaaggctaaccacttggaagataaaattaacatcatagagaaacggccggaa
ttattaacaaatgaggacctacagggcagaaaggtctctctcctcctgggcgagccgttc
ttcactaccagcctgctgccgtggcacaacctctacttctggtacgtgcggaccgctgtg
gaccagcacctggggccaggtgccatggtgatgccccaggcagcctcgctgcacgctgtg
gttgtggagttcagggacctgtggcggatccggagcccctgtggtgactgcgaaggcttc
gacgtgcacatcatggacgacatgattaagcgtgccctggacttcagggagagcagggaa
gctgagccccacccgctgtgggagtacccatgccgcagcctctccgagccctggcagatc
ctgacctttgacttccagcagccggtgcccctgcagcccctgtgtgccgagggcaccgtg
gagctcagaaggcccgggcagagccacgcagcggtgctatggatggagtaccacctgacc
ccggagtgcacgctcagcactggcctcctggagcctgcagaccccgaggggggctgctgc
tggaacccccactgcaagcaggccgtctacttcttcagccctgccccagatcccagagca
ctgctgggtggcccacggactgtcagctatgcagtggagtttcaccccgacacaggcgac
atcatcatggagttcaggcatgcagataccccagactga

  All links  
Disease (2)   
   OMIM (2)   
Gene (21)   
   RefGene (12)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (81)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (79)   
DNA sequence (127)   
   RefSeq(nuc) (103)   
   GenBank (12)   
   EMBL (12)   
Protein domain (9)   
   Pfam (9)   
All databases (240)   

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