Download interactions: TXT MITAB-2.5
Interaction | Interactor | Experiments | Homologs | Category | Interaction Score |
Confidence |
---|---|---|---|---|---|---|
UBR1
E3 ubiquitin-protein ligase UBR1 |
1 |
4 |
Small-scale |
0.512 | High |
|
Q9VFG4
pyruvate kinase |
1 |
1 |
High-throughput |
0.484 | High |
|
UBIQP
Polyubiquitin [Cleaved into: Ubiquitin] |
1 |
5 |
Small-scale |
0.481 | High |
|
HSP7D
Heat shock 70 kDa protein cognate 4 |
1 |
3 |
Small-scale |
0.479 | High |
|
Q7YU15
Klarsicht, isoform B |
1 |
0 |
Small-scale |
0.460 | High |
|
Q9VIB5
Carboxylic ester hydrolase |
1 |
0 |
Small-scale |
0.460 | High |
|
LDAH
Lipid droplet-associated hydrolase |
1 |
0 |
Small-scale |
0.460 | High |
|
PYRG
CTP synthase |
1 |
0 |
High-throughput |
0.458 | High |
|
P91634
PI-3 kinase |
1 |
2 |
High-throughput |
0.445 | High |
|
MICAL
[F-actin]-monooxygenase Mical |
1 |
1 |
High-throughput |
0.445 | High |
|
Q8IRJ0
Tyrosine-protein phosphatase |
1 |
1 |
High-throughput |
0.445 | High |
|
LARP
La-related protein 1 |
1 |
1 |
High-throughput |
0.445 | High |
|
Q9VD23
Pyruvate kinase |
1 |
1 |
High-throughput |
0.445 | High |
|
Q9W0L7
ubiquitinyl hydrolase 1 |
1 |
1 |
High-throughput |
0.445 | High |
|
FUTSC
Microtubule-associated protein futsch |
1 |
1 |
High-throughput |
0.445 | High |
|
A1Z871
CAP, isoform B |
1 |
1 |
High-throughput |
0.442 | High |
|
PSC
Polycomb group protein Psc |
1 |
1 |
High-throughput |
0.442 | High |
|
Q9W418
GH17761p |
1 |
5 |
Small-scale |
0.439 | High |
|
R9PY16
Ubiquitin-like domain-containing protein |
1 |
5 |
Small-scale |
0.439 | High |
|
O61380
Eukaryotic translation initiation factor 4G1, isoform A |
1 |
0 |
High-throughput |
0.426 | High |
|
CHDM
Chromodomain-helicase-DNA-binding protein Mi-2 homolog |
1 |
0 |
High-throughput |
0.426 | High |
|
BICD
Protein bicaudal D |
1 |
0 |
High-throughput |
0.426 | High |
|
DDX17
ATP-dependent RNA helicase p62 |
1 |
0 |
High-throughput |
0.426 | High |
|
MLE
Dosage compensation regulator mle |
1 |
0 |
High-throughput |
0.426 | High |
|
PSB1
Proteasome subunit beta type-1 |
1 |
0 |
High-throughput |
0.426 | High |
|
KAPR2
cAMP-dependent protein kinase type II regulatory subunit |
1 |
0 |
High-throughput |
0.426 | High |
|
Q0E993
Valine--tRNA ligase |
1 |
0 |
High-throughput |
0.426 | High |
|
SODE
Extracellular superoxide dismutase [Cu-Zn] |
1 |
0 |
High-throughput |
0.426 | High |
|
Q7JUF2
Diego, isoform A |
1 |
0 |
High-throughput |
0.426 | High |
|
Q7KN85
ATP-citrate synthase |
1 |
0 |
High-throughput |
0.426 | High |
|
Q7KTW9
Asparagine synthetase [glutamine-hydrolyzing] |
1 |
0 |
High-throughput |
0.426 | High |
|
RNZ
Ribonuclease Z, mitochondrial |
1 |
0 |
High-throughput |
0.426 | High |
|
Q9V405
26S proteasome regulatory complex subunit p48A |
1 |
0 |
High-throughput |
0.426 | High |
|
Q9VDJ9
non-specific serine/threonine protein kinase |
1 |
0 |
High-throughput |
0.426 | High |
|
TPC10
Trafficking protein particle complex subunit 10 |
1 |
0 |
High-throughput |
0.426 | High |
|
Q9VH61
asparaginase |
1 |
0 |
High-throughput |
0.426 | High |
|
UBP36
Ubiquitin carboxyl-terminal hydrolase 36 |
1 |
0 |
High-throughput |
0.426 | High |
|
PGM
Phosphoglucomutase |
1 |
0 |
High-throughput |
0.426 | High |
|
Q9W1H8
acetyl-CoA C-acyltransferase |
1 |
0 |
High-throughput |
0.426 | High |
|
Q9W2S2
Autophagy-related 8a, isoform A |
1 |
0 |
High-throughput |
0.426 | High |
|
Q9W4J4
GM14292p |
1 |
0 |
High-throughput |
0.426 | High |
|
A1Z8W9
Gartenzwerg, isoform A |
1 |
1 |
High-throughput |
0.407 | High |
|
AXO
Axotactin |
1 |
1 |
High-throughput |
0.407 | High |
|
VINC
Vinculin |
1 |
2 |
High-throughput |
0.407 | High |
|
O76894
EG:56G7.1 protein |
1 |
2 |
High-throughput |
0.407 | High |
|
CTNA
Catenin alpha |
1 |
1 |
High-throughput |
0.407 | High |
|
Q494M1
DNA topoisomerase I |
1 |
2 |
High-throughput |
0.407 | High |
|
Q59DY1
IP21282p |
1 |
1 |
High-throughput |
0.407 | High |
|
Q5U156
RE01954p |
1 |
1 |
High-throughput |
0.407 | High |
|
Q6NQY9
RNA helicase |
1 |
1 |
High-throughput |
0.407 | High |
|
Q7KSF4
Cheerio, isoform G |
1 |
1 |
High-throughput |
0.407 | High |
|
Q7KU89
Puratrophin-1-like, isoform A |
1 |
1 |
High-throughput |
0.407 | High |
|
Q7KUL1
Dally-like, isoform C |
1 |
1 |
High-throughput |
0.407 | High |
|
Q7KVD1
Trio, isoform A |
1 |
1 |
High-throughput |
0.407 | High |
|
Q8IMT4
CHK kinase-like domain-containing protein |
1 |
1 |
High-throughput |
0.407 | High |
|
Q8IPP9
Trichohyalin |
1 |
1 |
High-throughput |
0.407 | High |
|
Q8IQK2
Guanylate cyclase |
1 |
1 |
High-throughput |
0.407 | High |
|
Q8MLR6
Pickpocket 3 |
1 |
1 |
High-throughput |
0.407 | High |
|
Q8T0D3
Dek, isoform B |
1 |
1 |
High-throughput |
0.407 | High |
|
Q95SM8
GH13859p |
1 |
1 |
High-throughput |
0.407 | High |
|
ASP
Protein abnormal spindle |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VDE3
LD08669p |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9VF02
Helicase 89B, isoform B |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VKI0
CENP-meta, isoform C |
1 |
1 |
High-throughput |
0.407 | High |
|
WDR82
WD repeat-containing protein 82 |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9VM32
Anion exchange protein |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VMS2
Nuclear receptor coactivator 6, isoform C |
1 |
1 |
High-throughput |
0.407 | High |
|
NPFR
Neuropeptide F receptor |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VRM6
Lethal |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9VS00
Cilia- and flagella-associated protein 52 |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9VSL8
Rhea, isoform B |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VU79
Guanylate cyclase |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VVK7
Nucleobindin 1 |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VX46
Pickpocket 23, isoform A |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9VX86
Peptidase M14 carboxypeptidase A domain-containing protein |
1 |
1 |
High-throughput |
0.407 | High |
|
NU153
Nuclear pore complex protein Nup153 |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9VYP5
Uncharacterized protein, isoform B |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9W0B8
Coatomer subunit alpha |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9W117
ubiquitinyl hydrolase 1 |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9W1M7
Phosphatidylinositol 3-kinase catalytic subunit type 3 |
1 |
2 |
High-throughput |
0.407 | High |
|
Q9W3B8
LP09875p |
1 |
3 |
High-throughput |
0.407 | High |
|
Q9W4I4
Helix loop helix protein 4C, isoform A |
1 |
1 |
High-throughput |
0.407 | High |
|
Q9W4X4
1-phosphatidylinositol 4-kinase |
1 |
2 |
High-throughput |
0.407 | High |
|
A1Z823
PRA1 family protein |
1 |
0 |
High-throughput |
0.282 | High |
|
MERH
Moesin/ezrin/radixin homolog 2 |
1 |
0 |
High-throughput |
0.282 | High |
|
Q8T452
AT16729p |
1 |
0 |
High-throughput |
0.253 | Low |
|
Q9V3A7
Structural maintenance of chromosomes protein |
1 |
0 |
High-throughput |
0.253 | Low |
|
Q9VCH4
Myoblast city |
1 |
0 |
High-throughput |
0.253 | Low |
|
Q9VIK0
Alpha-methylacyl-CoA racemase, isoform A |
1 |
0 |
High-throughput |
0.253 | Low |
|
Q9VXN3
LD07988p |
1 |
0 |
High-throughput |
0.253 | Low |
|
Q9W1T1
Large ribosomal subunit protein eL22 |
1 |
0 |
High-throughput |
0.253 | Low |
|
Q9W2G9
Acyl-coenzyme A oxidase |
1 |
0 |
High-throughput |
0.253 | Low |
|
A1Z934
Enoyl-CoA hydratase, mitochondrial |
1 |
0 |
High-throughput |
0.232 | Low |
|
A1Z9J3
Short stop, isoform H |
1 |
0 |
High-throughput |
0.232 | Low |
|
JV
Protein javelin |
1 |
0 |
High-throughput |
0.232 | Low |
|
VILYA
RING finger protein vilya |
1 |
0 |
High-throughput |
0.232 | Low |
|
SIM
Protein single-minded |
1 |
0 |
High-throughput |
0.232 | Low |
|
LAMB1
Laminin subunit beta-1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
ESM5
Enhancer of split m5 protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
FER
Tyrosine-protein kinase Fer |
1 |
0 |
High-throughput |
0.232 | Low |
|
RG84C
GTPase-activating protein RacGAP84C |
1 |
0 |
High-throughput |
0.232 | Low |
|
DIA
Protein diaphanous |
1 |
0 |
High-throughput |
0.232 | Low |
|
CCNE
G1/S-specific cyclin-E |
1 |
0 |
High-throughput |
0.232 | Low |
|
G39AB
Gustatory and pheromone receptor 39a, isoform C |
1 |
0 |
High-throughput |
0.232 | Low |
|
SC5A6
Putative sodium-dependent multivitamin transporter |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q1RKS3
IP06621p |
1 |
0 |
High-throughput |
0.232 | Low |
|
SMG
Protein Smaug |
1 |
0 |
High-throughput |
0.232 | Low |
|
MY31D
Unconventional myosin ID |
1 |
0 |
High-throughput |
0.232 | Low |
|
FLII
Protein flightless-1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
MAN2
Alpha-mannosidase 2 |
1 |
0 |
High-throughput |
0.232 | Low |
|
CAZ
RNA-binding protein cabeza |
1 |
0 |
High-throughput |
0.232 | Low |
|
OCTB2
Octopamine receptor beta-2R |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q5U0V7
phosphoinositide 5-phosphatase |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q7K012
Brahma associated protein 55kD |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q7K3Q3
Regulatory protein zeste |
1 |
0 |
High-throughput |
0.232 | Low |
|
DGT5
Augmin complex subunit dgt5 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q7KT67
Spermatogenesis-associated protein 17 |
1 |
0 |
High-throughput |
0.232 | Low |
|
GCNA
Germ cell nuclear acidic protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
MMD4
Modifier of mdg4 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8I0F1
AT27831p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8IMK8
Protein TsetseEP domain-containing protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8IMN4
FI23135p1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8INL4
IP12394p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8INU2
Dynamin associated protein 160, isoform B |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8INY3
FI02050p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8IP19
Dachshund, isoform B |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8IPB8
Ionotropic receptor 31a, isoform D |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8IQI2
Uncharacterized protein, isoform E |
1 |
0 |
High-throughput |
0.232 | Low |
|
LIMK1
LIM domain kinase 1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
ANKL2
Ankyrin repeat and LEM domain-containing protein 2 homolog |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8MRN4
GH12664p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q8T5S8
procollagen-proline 4-dioxygenase |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q961C4
LD23619p |
1 |
0 |
High-throughput |
0.232 | Low |
|
STEL8
Stellate orphon protein at 12D |
1 |
0 |
High-throughput |
0.232 | Low |
|
VATH
V-type proton ATPase subunit H |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9V406
Activator protein 4 |
1 |
0 |
High-throughput |
0.232 | Low |
|
PLXB
Plexin-B |
1 |
0 |
High-throughput |
0.232 | Low |
|
CP6T3
Probable cytochrome P450 6t3 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9V9X0
FI18240p1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VAK7
F-box involved in polyQ pathogenesis, isoform A |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VB71
Cilia- and flagella-associated protein 58 central coiled coil domain-containing protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
SAMC
S-adenosylmethionine mitochondrial carrier protein homolog |
1 |
0 |
High-throughput |
0.232 | Low |
|
GR93C
Putative gustatory receptor 93c |
1 |
0 |
High-throughput |
0.232 | Low |
|
TOTB
Protein Turandot B |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VEF1
Uncharacterized protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
NRM
Nurim homolog |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VEK7
Cellular repressor of E1A-stimulated genes, isoform A |
1 |
0 |
High-throughput |
0.232 | Low |
|
ATD3A
ATPase family AAA domain-containing protein 3A homolog |
1 |
0 |
High-throughput |
0.232 | Low |
|
SAP18
Histone deacetylase complex subunit SAP18 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VFA8
Uncharacterized protein, isoform D |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VFC7
Mf5 protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VFE7
Nuclear pore protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VFJ1
rRNA biogenesis protein RRP36 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VFN7
GEO07678p1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
CLCN2
Chloride channel protein 2 |
1 |
0 |
High-throughput |
0.232 | Low |
|
NINAG
Neither inactivation nor afterpotential protein G |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VGR1
GRIP and coiled-coil domain containing 88 kDa |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VH66
FI18258p1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VHL6
FI03639p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VJJ8
LD30602p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VLK1
U3 small nucleolar ribonucleoprotein protein MPP10 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VM62
LD34181p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VMJ2
RT07854p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VNW6
Delta-1-pyrroline-5-carboxylate synthase [Includes: Glutamate 5-kinase |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VNX0
Uncharacterized protein, isoform A |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VPC7
CCDC66 domain-containing protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
PUS10
Putative tRNA pseudouridine synthase Pus10 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VQG6
Rab-like protein 3 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VQU3
LD22655p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VS57
RE14391p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VSW6
FI03822p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VTS6
Antisocial isoform 2 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VU88
AT31531p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VU89
RE10861p |
1 |
0 |
High-throughput |
0.232 | Low |
|
GARS
Glycine--tRNA ligase |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VUR2
LD31322p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VUY2
Ig-like domain-containing protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VV40
Golgin 104 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VVC6
Ephexin, isoform D |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VVH6
Uncharacterized protein |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VW36
Male sterile |
1 |
0 |
High-throughput |
0.232 | Low |
|
LSDA
Possible lysine-specific histone demethylase 1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VXK9
RH04127p |
1 |
0 |
High-throughput |
0.232 | Low |
|
TMA16
Translation machinery-associated protein 16 homolog |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VYC7
GH11189p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VYW4
LD04461p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9VYY7
Heterochromatin protein 5, isoform B |
1 |
0 |
High-throughput |
0.232 | Low |
|
CF298
Cilia- and flagella-associated protein 298 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W0R0
Cell division cycle 5, isoform A |
1 |
0 |
High-throughput |
0.232 | Low |
|
ICE1
Little elongation complex subunit 1 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W2C9
Lysyl oxidase-like 2 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W2W9
HL08167p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W3J6
FI06457p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W3N8
non-specific serine/threonine protein kinase |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W3Z4
GH18625p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W499
60S ribosomal protein L35 |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W4Y0
RE44620p |
1 |
0 |
High-throughput |
0.232 | Low |
|
Q9W4Y3
Terribly reduced optic lobes, isoform AT |
1 |
0 |
High-throughput |
0.232 | Low |
Service provided by Combinatics, Japan
Last updated: 15 Jul 2024