Homo sapiens (human): 124512 Help Entry 124512            CDS       T01001                                  Symbol METTL23, C17orf95, MRT44 Name (RefSeq) methyltransferase 23, arginine   KO K23151   methyltransferase-like protein 23 [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    03110 Chaperones and folding catalysts [BR:hsa03110]     124512 (METTL23) Chaperones and folding catalysts [BR:hsa03110]  Other chaperones and cochaperones   Others    124512 (METTL23) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Methyltransf_16 Motif Other DBs NCBI-GeneID:  124512 NCBI-ProteinID:  NP_001073979 OMIM:  615262 HGNC:  26988 Ensembl:  ENSG00000181038 UniProt:  Q86XA0 LinkDB All DBs Position 17:76726041..76733881 Genome browser AA seq 190 aa AA seqDB search MYVWPCAVVLAQYLWFHRRSLPGKAILEIGAGVSLPGILAAKCGAEVILSDSSELPHCLE VCRQSCQMNNLPHLQVVGLTWGHISWDLLALPPQDIILASDVFFEPEDFEDILATIYFLM HKNPKVQLWSTYQVRSADWSLEALLYKWDMKCVHIPLESFDADKEDIAESTLPGRHTVEM LVISFAKDSL NT seq 573 nt NT seq  +upstreamnt  +downstreamnt atgtatgtttggccctgtgctgtggtcctggcccagtacctttggtttcacagaagatct ctgccaggcaaggccatcttagagattggagctggagtgagccttccaggaattttggct gccaaatgtggtgcagaagtaatactgtcagacagctcagaactgcctcactgtctggaa gtctgtcggcaaagctgccaaatgaataacctgccacatctgcaggtggtaggactaaca tggggtcatatatcttgggatcttctggctctaccaccacaagatattatccttgcatct gatgtgttctttgaaccagaagattttgaagacattttggctacaatatattttttgatg cacaagaatcccaaggtccaattgtggtctacttatcaagttaggagtgctgactggtca cttgaagctttactctacaaatgggatatgaaatgtgtccacattcctcttgagtctttt gatgcagacaaagaagatatagcagaatctacccttccaggaagacatacagttgaaatg ctggtcatttcctttgcaaaggacagtctctga

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