KEGG   Homo sapiens (human): 4990
Entry
4990              CDS       T01001                                 
Symbol
SIX6, MCOPCT2, ODRMD, OPTX2, Six9
Name
(RefSeq) SIX homeobox 6
  KO
K19473  homeobox protein SIX3/6
Organism
hsa  Homo sapiens (human)
Disease
H02231  Optic disc anomalies with retinal and/or macular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4990 (SIX6)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain SINE
    4990 (SIX6)
SSDB
Motif
Pfam: SIX1_SD Homeodomain Homeobox_KN FAM199X HTH_3
Other DBs
NCBI-GeneID: 4990
NCBI-ProteinID: NP_031400
OMIM: 606326
HGNC: 10892
Ensembl: ENSG00000184302
UniProt: O95475 Q6P051
Position
14:60509146..60512850
AA seq 246 aa
MFQLPILNFSPQQVAGVCETLEESGDVERLGRFLWSLPVAPAACEALNKNESVLRARAIV
AFHGGNYRELYHILENHKFTKESHAKLQALWLEAHYQEAEKLRGRPLGPVDKYRVRKKFP
LPRTIWDGEQKTHCFKERTRHLLREWYLQDPYPNPSKKRELAQATGLTPTQVGNWFKNRR
QRDRAAAAKNRLQQQVLSQGSGRALRAEGDGTPEVLGVATSPAASLSSKAATSAISITSS
DSECDI
NT seq 741 nt   +upstreamnt  +downstreamnt
atgttccagctgcccatcttgaatttcagcccccagcaagtggccggggtatgtgagacc
ctggaagagagcggcgatgtggagcgcctgggtcgcttcctctggtcgctgcccgtggcc
cctgcggcctgcgaggccctcaacaagaatgagtcggtgctacgcgcacgagccatcgtg
gcctttcacggtggcaactaccgcgagctctatcatatcctggaaaaccacaagttcacc
aaggagtcgcacgccaagctgcaggcgctgtggcttgaagcacactaccaggaggctgag
aagctgcgtggaagacccctgggacctgtggacaagtaccgagtaaggaagaagttcccg
ctgccgcgcaccatttgggacggcgaacagaagacacactgcttcaaggagcgcacgcgg
cacctgctacgcgagtggtacctgcaggatccataccctaaccccagcaaaaaacgtgag
ctcgcccaggcaaccggactgacccctacgcaggtgggcaactggttcaaaaaccgccga
caaagggaccgagcggctgcagccaagaacagactccagcagcaggtcctgtcacagggt
tccgggcgggcactacgggcggagggcgacggcacgccagaggtgctgggcgtcgccacc
agcccggccgccagtctatccagcaaggcggccacttcagccatctccatcacgtccagc
gacagcgagtgcgacatctga

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