KEGG   Homo sapiens (human): 155368
Entry
155368            CDS       T01001                                 
Symbol
METTL27, WBSCR27
Name
(RefSeq) methyltransferase like 27
  KO
K24419  methyltransferase-like protein 27 [EC:2.1.1.-]
Organism
hsa  Homo sapiens (human)
Disease
H01439  Williams-Beuren syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09191 Unclassified: metabolism
   99980 Enzymes with EC numbers
    155368 (METTL27)
SSDB
Motif
Pfam: Methyltransf_25 Methyltransf_11 Methyltransf_23 Methyltransf_12 Methyltransf_31 Ubie_methyltran Methyltransf_9 MTS
Other DBs
NCBI-GeneID: 155368
NCBI-ProteinID: NP_689772
OMIM: 612546
HGNC: 19068
Ensembl: ENSG00000165171
UniProt: Q8N6F8
Position
7:complement(73834590..73842516)
AA seq 245 aa
MAQEEGGSLPEVRARVRAAHGIPDLAQKLHFYDRWAPDYDQDVATLLYRAPRLAVDCLTQ
ALPGPPHSALILDVACGTGLVAAELRAPGFLQLHGVDGSPGMLEQAQAPGLYQRLSLCTL
GQEPLPSPEGTFDAVLIVGALSDGQVPCNAIPELHVTKPGGLVCLTTRTNSSNLQYKEAL
EATLDRLEQAGMWEGLVAWPVDRLWTAGSWLPPSWRWYPASLPRMASSPALSTCTESGRR
PRLRK
NT seq 738 nt   +upstreamnt  +downstreamnt
atggcccaggaggagggtgggagcctgcccgaggtgcgggcgcgggtcagggccgcgcat
ggcatccccgacctggcccaaaagctccatttctatgaccgctgggctccggactacgac
caggatgtggccaccctgctgtaccgtgcgccccgcctcgcagtggactgcctcacacaa
gcccttccaggcccgccccacagtgccctgatcctggacgtggcctgtggcacaggccta
gtggctgccgagctgcgggctccaggcttcctccagctgcatggggtggatgggagccca
gggatgctggaacaggcccaggcccccggcctctatcagcgcctcagcctctgcaccctg
ggccaggagcctctgcccagcccggaagggaccttcgacgcggtgctgatagtcggtgcc
ctcagtgacggccaggtgccctgcaatgcgatacctgagctacatgtcaccaagccaggt
gggctggtgtgtctgaccaccaggaccaactcgtccaaccttcaatacaaggaggctctg
gaggccaccctggacaggctggagcaggctgggatgtgggaaggcctggtggcctggcct
gtggaccgcctgtggaccgctgggagctggctacctccgagctggaggtggtatccggca
tctctgccaaggatggcttcatctccggcattgtctacctgtaccgaaagtggaaggcga
cccaggttgaggaagtga

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