Homo sapiens (human): 4204
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Entry
4204 CDS
T01001
Symbol
MECP2, AUTSX3, MRX16, MRX79, MRXS13, MRXSL, PPMX, RS, RTS, RTT
Name
(RefSeq) methyl-CpG binding protein 2
KO
K11588
methyl CpG binding protein 2
Organism
hsa
Homo sapiens (human)
Disease
H00440
Rett syndrome
H00658
X-linked syndromic intellectual developmental disorder
H01211
MECP2-related severe neonatal encephalopathy
H02111
Autism
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
4204 (MECP2)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Heterochromatin formation proteins
MBPs (metylated DNA binding proteins)
4204 (MECP2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MBD
Motif
Other DBs
NCBI-GeneID:
4204
NCBI-ProteinID:
NP_004983
OMIM:
300005
HGNC:
6990
Ensembl:
ENSG00000169057
UniProt:
P51608
D3YJ43
Q59FJ6
Structure
PDB
PDBj
LinkDB
All DBs
Position
X:complement(154021573..154097717)
Genome browser
AA seq
486 aa
AA seq
DB search
MVAGMLGLREEKSEDQDLQGLKDKPLKFKKVKKDKKEEKEGKHEPVQPSAHHSAEPAEAG
KAETSEGSGSAPAVPEASASPKQRRSIIRDRGPMYDDPTLPEGWTRKLKQRKSGRSAGKY
DVYLINPQGKAFRSKVELIAYFEKVGDTSLDPNDFDFTVTGRGSPSRREQKPPKKPKSPK
APGTGRGRGRPKGSGTTRPKAATSEGVQVKRVLEKSPGKLLVKMPFQTSPGGKAEGGGAT
TSTQVMVIKRPGRKRKAEADPQAIPKKRGRKPGSVVAAAAAEAKKKAVKESSIRSVQETV
LPIKKRKTRETVSIEVKEVVKPLLVSTLGEKSGKGLKTCKSPGRKSKESSPKGRSSSASS
PPKKEHHHHHHHSESPKAPVPLLPPLPPPPPEPESSEDPTSPPEPQDLSSSVCKEEKMPR
GGSLESDGCPKEPAKTQPAVATAATAAEKYKHRGEGERKDIVSSSMPRPNREEPVDSRTP
VTERVS
NT seq
1461 nt
NT seq
+upstream
nt +downstream
nt
atggtagctgggatgttagggctcagggaagaaaagtcagaagaccaggacctccagggc
ctcaaggacaaacccctcaagtttaaaaaggtgaagaaagataagaaagaagagaaagag
ggcaagcatgagcccgtgcagccatcagcccaccactctgctgagcccgcagaggcaggc
aaagcagagacatcagaagggtcaggctccgccccggctgtgccggaagcttctgcctcc
cccaaacagcggcgctccatcatccgtgaccggggacccatgtatgatgaccccaccctg
cctgaaggctggacacggaagcttaagcaaaggaaatctggccgctctgctgggaagtat
gatgtgtatttgatcaatccccagggaaaagcctttcgctctaaagtggagttgattgcg
tacttcgaaaaggtaggcgacacatccctggaccctaatgattttgacttcacggtaact
gggagagggagcccctcccggcgagagcagaaaccacctaagaagcccaaatctcccaaa
gctccaggaactggcagaggccggggacgccccaaagggagcggcaccacgagacccaag
gcggccacgtcagagggtgtgcaggtgaaaagggtcctggagaaaagtcctgggaagctc
cttgtcaagatgccttttcaaacttcgccagggggcaaggctgaggggggtggggccacc
acatccacccaggtcatggtgatcaaacgccccggcaggaagcgaaaagctgaggccgac
cctcaggccattcccaagaaacggggccgaaagccggggagtgtggtggcagccgctgcc
gccgaggccaaaaagaaagccgtgaaggagtcttctatccgatctgtgcaggagaccgta
ctccccatcaagaagcgcaagacccgggagacggtcagcatcgaggtcaaggaagtggtg
aagcccctgctggtgtccaccctcggtgagaagagcgggaaaggactgaagacctgtaag
agccctgggcggaaaagcaaggagagcagccccaaggggcgcagcagcagcgcctcctca
ccccccaagaaggagcaccaccaccatcaccaccactcagagtccccaaaggcccccgtg
ccactgctcccacccctgcccccacctccacctgagcccgagagctccgaggaccccacc
agcccccctgagccccaggacttgagcagcagcgtctgcaaagaggagaagatgcccaga
ggaggctcactggagagcgacggctgccccaaggagccagctaagactcagcccgcggtt
gccaccgccgccacggccgcagaaaagtacaaacaccgaggggagggagagcgcaaagac
attgtttcatcctccatgccaaggccaaacagagaggagcctgtggacagccggacgccc
gtgaccgagagagttagctga
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