KEGG   Homo sapiens (human): 4618
Entry
4618              CDS       T01001                                 
Symbol
MYF6, CNM3, MRF4, bHLHc4, myf-6
Name
(RefSeq) myogenic factor 6
  KO
K18485  myogenic factor 6
Organism
hsa  Homo sapiens (human)
Disease
H00700  Centronuclear myopathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4618 (MYF6)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Basic helix-loop-helix (bHLH)
   Myogenic transcription factors
    4618 (MYF6)
SSDB
Motif
Pfam: Basic HLH Myf5 HMG_box_2
Other DBs
NCBI-GeneID: 4618
NCBI-ProteinID: NP_002460
OMIM: 159991
HGNC: 7566
Ensembl: ENSG00000111046
UniProt: P23409
LinkDB
Position
12:80707634..80709474
AA seq 242 aa
MMMDLFETGSYFFYLDGENVTLQPLEVAEGSPLYPGSDGTLSPCQDQMPPEAGSDSSGEE
HVLAPPGLQPPHCPGQCLIWACKTCKRKSAPTDRRKAATLRERRRLKKINEAFEALKRRT
VANPNQRLPKVEILRSAISYIERLQDLLHRLDQQEKMQELGVDPFSYRPKQENLEGADFL
RTCSSQWPSVSDHSRGLVITAKEGGASIDSSASSSLRCLSSIVDSISSEERKLPCVEEVV
EK
NT seq 729 nt   +upstreamnt  +downstreamnt
atgatgatggacctttttgaaactggctcctatttcttctacttggatggggaaaatgtt
actctgcagccattagaagtggcagaaggctctcctttgtatccagggagtgatggtacc
ttgtccccctgccaggaccaaatgcccccggaagcggggagcgacagcagcggagaggaa
catgtcctggcgcccccgggcctgcagcctccacactgccccggccagtgtctgatctgg
gcttgcaagacctgcaagagaaaatctgcccccactgaccggcgaaaagccgccaccctg
cgcgaaaggaggaggctaaagaaaatcaacgaggccttcgaggcactgaagcggcgaact
gtggccaaccccaaccagaggctgcccaaggtggagattctgcggagcgccatcagctat
attgagcggctgcaggacctgctgcaccggctggatcagcaggagaagatgcaggagctg
ggggtggaccccttcagctacagacccaaacaagaaaatcttgagggtgcggatttcctg
cgcacctgcagctcccagtggccaagtgtttccgatcattccagggggctcgtgataacg
gctaaggaaggaggagcaagtattgattcgtcagcctcgagtagccttcgatgcctttct
tccatcgtggacagtatttcctcggaggaacgcaaactcccctgcgtggaggaagtggtg
gagaagtaa

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