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DMPK and SMN1
Data Source:
BioGRID
(two hybrid)
DMPK
SMN1
Description
DM1 protein kinase
survival of motor neuron 1, telomeric
Image
GO Annotations
Cellular Component
Nuclear Outer Membrane
Endoplasmic Reticulum Membrane
Cytosol
Plasma Membrane
Integral Component Of Mitochondrial Outer Membrane
Nuclear Membrane
Sarcoplasmic Reticulum Membrane
Nucleus
Nucleoplasm
Cytoplasm
Cytosol
Cajal Body
Nuclear Body
Z Disc
Axon
SMN Complex
SMN-Sm Protein Complex
Cytoplasmic Ribonucleoprotein Granule
Neuron Projection
Perikaryon
Gemini Of Coiled Bodies
Molecular Function
Protein Serine/threonine Kinase Activity
Protein Binding
ATP Binding
Myosin Phosphatase Regulator Activity
Metal Ion Binding
Protein Serine Kinase Activity
Protein Threonine Kinase Activity
RNA Binding
Protein Binding
Identical Protein Binding
Biological Process
Regulation Of Sodium Ion Transport
Protein Phosphorylation
Cellular Calcium Ion Homeostasis
Nuclear Envelope Organization
Regulation Of Heart Contraction
Muscle Cell Apoptotic Process
Regulation Of Myotube Differentiation
Regulation Of Skeletal Muscle Contraction By Calcium Ion Signaling
Regulation Of Excitatory Postsynaptic Membrane Potential Involved In Skeletal Muscle Contraction
Peptidyl-serine Phosphorylation
Intracellular Signal Transduction
Regulation Of Phosphoprotein Phosphatase Activity
Regulation Of Synapse Structural Plasticity
Regulation Of Cardiac Conduction
Spliceosomal Complex Assembly
Spliceosomal SnRNP Assembly
DNA-templated Transcription, Termination
Nervous System Development
Import Into Nucleus
Pathways
Ion homeostasis
snRNP Assembly
Drugs
Bisindolylmaleimide VIII
Nusinersen
Diseases
Myotonic dystrophy (DM)
Spinal muscular atrophy (SMA), including: SMA type I (SMA1) / Werdning-Hoffman disease; SMA type II (SMA2); SMA type III (SMA3) / Kugeleberg-Welander disease; SMA type IV (SMA4); X-linked SMA 2 (SMAX2); X-linked distal SMA 3 (DSMAX); Distal SMA autosomal recessive type 4 (DSMA4); Congenital distal spinal muscular atrophy (SMAL); SMA proximal adult autosomal dominant (SMAPAD)
GWAS
Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) (
30940143
)
Interacting Genes
18 interacting genes:
ANXA7
ATN1
ATXN1
CELF1
FXYD1
GABARAP
GEMIN4
HOXA2
HSPB2
PIN1
PLN
PPP1R12A
RAC1
RAF1
RPS10
SMN1
TK1
UBQLN4
165 interacting genes:
A1BG
A2M
ACTB
ACTL6B
ADAMTS10
AGAP1
ANXA2
APLP1
ARFGAP1
ATP5F1B
ATP6V1A
BAG6
BCL2
BLOC1S6
BYSL
C9orf72
CARHSP1
CCDC90B
CENPB
CHTOP
COIL
COL4A2
COL4A5
COPS6
CPNE6
CRIP2
CSAD
DDAH2
DDX20
DHX9
DMPK
DOCK7
DUS2
DYNC1I1
EEF1A1
EEF1A2
EHHADH
EIF3G
EXT2
EZH2
FAM20C
FAM9B
FBL
FGB
FLAD1
FNDC11
FUBP1
GAPDH
GAR1
GDF9
GEMIN2
GEMIN5
GEMIN7
H3-4
HADHB
HMGXB3
HNRNPR
HNRNPU
HNRNPUL1
IGHM
ILF3
IMMT
INPP5K
IQUB
ITCH
JADE1
KDM1A
KIF5A
KLHL5
KMT2B
KPNB1
KRTAP19-6
KRTAP19-7
KRTAP21-2
KRTAP6-1
KRTAP6-2
LENG8
LRIF1
LSM1
LSM10
LSM11
LSM2
LSM3
LSM4
LSM5
LSM6
LSM7
MAGED1
MAST2
MED31
MKI67
MPP1
MRPL37
MSH2
NGFR
NKIRAS2
NMT2
NRN1
NTAQ1
OSTF1
PDE4DIP
PKM
PLXNA3
POLR1C
POLR2A
POP7
PPIG
PSME1
QARS1
RBBP4
RBBP6
RBFOX2
RBM48
REX1BD
RN7SL1
RNU1-1
RNU11
RNU2-1
RNU4-1
RPL13
RPS2
RXRA
SCARNA1
SDF4
SELENOW
SEMA5B
SETDB1
SMC5
SMN2
SNORA81
SNRPB
SNRPD1
SNRPD2
SNRPD3
SNRPE
SNU13
SNUPN
SP110
SPANXN2
STRAP
STXBP2
STXBP3
SULT1A3
SUMO3
SYNCRIP
TAF1C
TERC
TIAL1
TLE1
TMSB4X
TP53
TRMT2A
TUBA1A
TUBB3
UCHL1
UNC119
USP4
VPS28
WDR18
WDR73
WIZ
ZBTB16
ZNF431
ZRANB2
ZXDC
Entrez ID
1760
6606
HPRD ID
05645
02646
Ensembl ID
ENSG00000104936
ENSG00000172062
Uniprot IDs
B4DM55
B4DZE2
E5KR05
E5KR06
E5KR07
I6L989
Q09013
B4DP61
E7EQZ4
Q16637
PDB IDs
1WT6
2VD5
1G5V
1MHN
2LEH
4A4E
4A4G
4GLI
4QQ6
5XJL
5XJQ
5XJR
5XJS
5XJT
5XJU
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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