KEGG   Homo sapiens (human): 29081
Entry
29081             CDS       T01001                                 
Symbol
METTL5, HSPC133, MRT72
Name
(RefSeq) methyltransferase 5, N6-adenosine
  KO
K24418  rRNA N6-adenosine-methyltransferase METTL5
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
   03009 Ribosome biogenesis [BR:hsa03009]
    29081 (METTL5)
Ribosome biogenesis [BR:hsa03009]
 Eukaryotic type
  Pre-40S particles
   Export and cytoplasmic maturation factors
    29081 (METTL5)
SSDB
Motif
Pfam: MTS PrmA Methyltransf_31 Methyltransf_25 Cons_hypoth95 UPF0020 Methyltransf_11 Methyltransf_12 DNA_methylase BpsA_C Methyltransf_4 Ubie_methyltran Met_10 FtsJ FmrO N6_Mtase Methyltransf_16 TehB Methyltransf_9 N6-adenineMlase AdoMet_MTase Methyltransf_32
Other DBs
NCBI-GeneID: 29081
NCBI-ProteinID: NP_001280115
OMIM: 618628
HGNC: 25006
Ensembl: ENSG00000138382
UniProt: Q9NRN9
Structure
Position
2:complement(169811757..169824905)
AA seq 209 aa
MKKVRLKELESRLQQVDGFEKPKLLLEQYPTRPHIAACMLYTIHNTYDDIENKVVADLGC
GCGVLSIGTAMLGAGLCVGFDIDEDALEIFNRNAEEFELTNIDMVQCDVCLLSNRMSKSF
DTVIMNPPFGTKNNKGTDMAFLKTALEMARTAVYSLHKSSTREHVQKKAAEWKIKIDIIA
ELRYDLPASYKFHKKKSVDIEVDLIRFSF
NT seq 630 nt   +upstreamnt  +downstreamnt
atgaagaaagtaaggcttaaggaactagagagtcgcctgcaacaagtggatggatttgaa
aagcccaagctacttctggaacagtatcctaccaggccgcacattgcagcatgtatgctc
tatacaatccataacacttatgatgacattgaaaataaagtcgttgcagatctaggatgt
ggttgtggagtacttagcatcggaactgcaatgttaggagcagggttgtgtgttggattt
gacatagatgaagacgcattggaaatatttaataggaatgcagaagagtttgagttaaca
aatattgacatggttcaatgtgatgtgtgcttattatctaacagaatgtccaagtcattc
gatacagtaattatgaatcctccctttgggaccaaaaataataaagggacagatatggct
tttctaaagactgctttggaaatggcaagaacagcagtatattccttacacaaatcctca
actagagaacatgttcaaaagaaagctgcagaatggaaaatcaagatagatattatagca
gaacttcgatatgacctgccagcatcatacaagtttcacaaaaagaaatcagtggacatt
gaagtggacctaattcggttttccttttaa

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