Gene Name |
heterogeneous nuclear ribonucleoprotein U-like 1 |
survival of motor neuron 1, telomeric |
Image |
No pdb structure |
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Gene Ontology Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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Protein-Protein Interactions |
46 interactors:
BRD7
C14orf1
CRMP1
DZIP3
EP300
ERG
EWSR1
GIT2
HNRNPF
HNRNPH2
HNRNPH3
IL7R
ITCH
MAPK1IP1L
MARS
MED31
NEDD4
NXF1
NXF2
NXF3
PIAS4
PPIL1
PRMT1
PRMT2
PRPF40A
RBM22
RBM4
RBM4B
ROPN1
RPA1
RPA2
SF1
SF3B4
SMN1
SMN2
SNRPB2
SNRPC
SORBS3
SRSF9
TGM2
TLX3
TP53
TP53BP2
VPS37C
WWP2
ZNF207
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136 interactors:
A1BG
A2M
ACTB
ACTL6B
ADAMTS10
AGAP1
APLP1
ARFGAP1
ATP5B
ATP6V1A
BAG6
BCL2
C19orf60
CARHSP1
CCDC90B
CENPB
COIL
COL4A2
COL4A5
COPS6
CPNE6
CRIP2
CSAD
DDAH2
DDX20
DHX9
DMPK
DOCK7
DUS2
DYNC1I1
EEF1A1
EIF3G
EXT2
EZH2
FAM20C
FBL
FGB
FLAD1
FUBP1
GAPDH
GAR1
GDF9
GEMIN2
GEMIN5
GEMIN7
HADHB
HIST3H3
HMGXB3
HNRNPR
HNRNPU
HNRNPUL1
IGHM
ILF3
IMMT
INPP5K
JADE1
KDM1A
KIF5A
KLHL5
KMT2B
KPNB1
LENG8
LRIF1
LSM1
LSM10
LSM11
LSM2
LSM3
LSM4
LSM5
LSM6
LSM7
MAST2
MED31
MKI67
MPP1
MRPL37
MSH2
NGFR
NKIRAS2
NMT2
OSTF1
PDE4DIP
PKM
PLXNA3
POLR2A
POP7
PSME1
QARS
RBBP4
RBBP6
RBFOX2
RBM48
RN7SL1
RNU1-1
RNU2-1
RPL13
RPS2
RXRA
SDF4
SEMA5B
SETDB1
SMC5
SMN2
SNRPB
SNRPD1
SNRPD2
SNRPD3
SNRPE
SNUPN
SP110
STRAP
STXBP2
STXBP3
SULT1A3
SUMO3
SYNCRIP
TAF1C
TIAL1
TLE1
TMSB4X
TP53
TRMT2A
TUBA1A
TUBB3
UCHL1
UNC119
USP4
WDR18
WDR73
WDYHV1
WIZ
ZBTB16
ZNF431
ZRANB2
ZXDC
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Entrez ID |
11100 |
6606 |
HPRD ID |
10428 |
02646 |
Ensembl ID |
ENSG00000105323
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ENSG00000172062
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Uniprot IDs |
B7Z4B8
Q9BUJ2
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B4DP61
Q16637
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PDB IDs |
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1G5V
1MHN
2LEH
3S6N
4A4E
4A4G
4GLI
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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atrophy
centromeric
compensate
copies
copy
degeneration
deletions
detectable
display
donor
easily
exon
fails
fatal
harbor
hindering
homozygous
infant
intragenic
italian
modifier
muscular
null
predictable
sma
smn2
splice
unusually
weakness
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Tagcloud (Difference) ? |
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atrophy
centromeric
compensate
copies
copy
degeneration
deletions
detectable
display
donor
easily
exon
fails
fatal
harbor
hindering
homozygous
infant
intragenic
italian
modifier
muscular
null
predictable
sma
smn2
splice
unusually
weakness
|
Tagcloud (Intersection) ? |
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