SMN1 |
HNRNPR |
||
---|---|---|---|
Gene Name | survival of motor neuron 1, telomeric | heterogeneous nuclear ribonucleoprotein R | |
Image | |||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 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 | 9 interactors: BMPR2 FARSA HIST3H3 IL7R KHDRBS2 PRMT1 RPL26 SMN1 TAB1 | |
Entrez ID | 6606 | 10236 | |
HPRD ID | 02646 | 06228 | |
Ensembl ID | ENSG00000172062 | ENSG00000125944 | |
Uniprot IDs | B4DP61 Q16637 | B4DT28 E7ETM7 O43390 Q0VGD6 Q6MZS5 S4R3J4 | |
PDB IDs | 1G5V 1MHN 2LEH 3S6N 4A4E 4A4G 4GLI | 2DK2 | |
Enriched GO Terms of Interacting Partners? |
|
||
Tagcloud ? | 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
|
absent
alleles
aml
atlas
australasian
bank
box
conjunction
enrichment
epigenetic
frequently
hypermethylation
leukemic
marks
matr3
promoter
sf3a1
sf3b1
silence
silico
somatic
splicing
srsf2
suppressing
u2af1
u937
ybx3
zfr
zrsr2
|
|
Tagcloud (Difference) ? | 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
|
absent
alleles
aml
atlas
australasian
bank
box
conjunction
enrichment
epigenetic
frequently
hypermethylation
leukemic
marks
matr3
promoter
sf3a1
sf3b1
silence
silico
somatic
splicing
srsf2
suppressing
u2af1
u937
ybx3
zfr
zrsr2
|
|
Tagcloud (Intersection) ? |