Homo sapiens (human): 10771
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Entry
10771 CDS
T01001
Symbol
ZMYND11, BRAM1, BS69, MRD30
Name
(RefSeq) zinc finger MYND-type containing 11
KO
K23218
zinc finger MYND domain-containing protein 11
Organism
hsa
Homo sapiens (human)
Disease
H00773
Autosomal dominant intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
10771 (ZMYND11)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
Other histone modification proteins
10771 (ZMYND11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ZMYND11_CC
MYND_ZMYND11_ZMYD8
PWWP
Bromodomain
SAMD1_WH
zf-MYND
PHD
DUF1002
vRNAP_dom
Motif
Other DBs
NCBI-GeneID:
10771
NCBI-ProteinID:
NP_001357026
OMIM:
608668
HGNC:
16966
Ensembl:
ENSG00000015171
UniProt:
Q15326
Structure
PDB
PDBj
LinkDB
All DBs
Position
10:130088..254637
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AA seq
602 aa
AA seq
DB search
MARLTKRRQADTKAIQHLWAAIEIIRNQKQIANIDRITKYMSRVHGMHPKETTRQLSLAV
KDGLIVETLTVGCKGSKAGIEQEGYWLPGDEIDWETENHDWYCFECHLPGEVLICDLCFR
VYHSKCLSDEFRLRDSSSPWQCPVCRSIKKKNTNKQEMGTYLRFIVSRMKERAIDLNKKG
KDNKHPMYRRLVHSAVDVPTIQEKVNEGKYRSYEEFKADAQLLLHNTVIFYGADSEQADI
ARMLYKDTCHELDELQLCKNCFYLSNARPDNWFCYPCIPNHELVWAKMKGFGFWPAKVMQ
KEDNQVDVRFFGHHHQRAWIPSENIQDITVNIHRLHVKRSMGWKKACDELELHQRFLREG
RFWKSKNEDRGEEEAESSISSTSNEQLKVTQEPRAKKGRRNQSVEPKKEEPEPETEAVSS
SQEIPTMPQPIEKVSVSTQTKKLSASSPRMLHRSTQTTNDGVCQSMCHDKYTKIFNDFKD
RMKSDHKRETERVVREALEKLRSEMEEEKRQAVNKAVANMQGEMDRKCKQVKEKCKEEFV
EEIKKLATQHKQLISQTKKKQWCYNCEEEAMYHCCWNTSYCSIKCQQEHWHAEHKRTCRR
KR
NT seq
1809 nt
NT seq
+upstream
nt +downstream
nt
atggcacgtttaacaaaaagacgacaggcggatacaaaagctatccagcatctttgggca
gccattgagattatacggaaccagaagcagattgccaacattgaccgtattacaaagtat
atgtctcgagtccacggtatgcaccctaaagagaccacccgtcagctgagcttagctgtg
aaagatggtcttattgtcgaaactctaacagtgggctgcaaaggttcaaaagctggtatt
gaacaagaaggatattggttgccaggagatgagattgactgggaaacagaaaatcatgac
tggtattgttttgaatgccatttgcctggagaggtgttgatatgtgacctgtgttttcgt
gtgtatcattccaagtgtttgtctgatgagttcaggcttagagacagcagtagtccctgg
cagtgcccagtttgcaggagcattaagaagaagaatacaaacaaacaggagatgggcaca
tacctcagattcattgtctcccgcatgaaggagagggctatagatcttaataaaaagggg
aaggacaataaacacccgatgtacaggaggctggtgcactcagctgtggacgttcccacc
attcaagagaaagtgaatgaagggaaataccgaagttatgaagagttcaaagctgatgcc
caattgcttctccacaataccgtgattttctatggagcagacagtgagcaagctgacatt
gcgaggatgctatataaagacacatgtcatgagctggatgaactgcagctttgcaagaat
tgcttttacttgtcaaatgctcgtcctgacaactggttctgttatccttgtatacctaat
catgagctggtttgggctaaaatgaaaggttttgggttttggccagccaaagtcatgcag
aaagaagacaatcaagtcgacgttcgcttctttggccaccaccaccagagggcctggatt
ccttctgaaaacattcaagatatcacagtcaacattcatcggctgcacgtgaagcgcagt
atgggttggaaaaaggcctgtgatgagctggagctgcatcagcgtttcctacgagaaggg
agattttggaaatctaagaatgaggaccgaggtgaggaagaggcagaatccagtatctcc
tccaccagtaatgagcagctaaaggtcactcaagaaccaagagcaaagaaaggacgacgt
aatcaaagtgtggagcccaaaaaggaagaaccagagcctgaaacagaagcagtaagttct
agccaggaaatacccacgatgcctcagcccatcgaaaaagtctccgtgtcaactcagaca
aagaagttaagtgcctcttcaccaagaatgctgcatcggagcacccagaccacaaacgac
ggcgtgtgtcagagcatgtgccatgacaaatacaccaagatcttcaatgacttcaaagac
cggatgaagtcggaccacaagcgggagacagagcgtgttgtccgagaagctctggagaag
ctgcgttctgaaatggaagaagaaaagagacaagctgtaaataaagctgtagccaacatg
cagggtgagatggacagaaaatgtaagcaagtaaaggaaaagtgtaaggaagaatttgta
gaagaaatcaagaagctggcaacacagcacaagcaactgatttctcagaccaagaagaag
cagtggtgctacaactgtgaggaggaggccatgtaccactgctgctggaacacatcctac
tgctccatcaagtgccagcaggagcactggcacgcggagcacaagcgcacctgccgccgg
aaaagatga
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