FUBP1 (far upstream element binding protein 1) - Rat Genome Database

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Gene: FUBP1 (far upstream element binding protein 1) Homo sapiens
Analyze
Symbol: FUBP1
Name: far upstream element binding protein 1
RGD ID: 1344155
HGNC Page HGNC
Description: Enables RNA binding activity. Involved in positive regulation of gene expression. Located in nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: DNA helicase V; far upstream element (FUSE) binding protein 1; far upstream element binding protein; far upstream element-binding protein 1; FBP; FUBP; FUSE binding protein 1; FUSE-binding protein 1; hDH V
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl177,944,055 - 77,979,110 (-)EnsemblGRCh38hg38GRCh38
GRCh38177,944,055 - 77,979,435 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37178,409,740 - 78,444,756 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36178,186,179 - 78,217,365 (-)NCBINCBI36hg18NCBI36
Build 34178,126,110 - 78,156,735NCBI
Celera176,652,669 - 76,683,855 (-)NCBI
Cytogenetic Map1p31.1NCBI
HuRef176,545,210 - 76,576,401 (-)NCBIHuRef
CHM1_1178,529,931 - 78,561,136 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dibromophenyl 2,4,5-tribromophenyl ether  (ISO)
2,4-dinitrotoluene  (ISO)
2-hydroxypropanoic acid  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-sulfonyldiphenol  (EXP)
4-hydroxynon-2-enal  (EXP)
4-hydroxyphenyl retinamide  (ISO)
acrylamide  (EXP)
aflatoxin B1  (ISO)
all-trans-retinoic acid  (EXP)
amphetamine  (ISO)
aristolochic acid  (EXP)
Aroclor 1254  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
bisphenol A  (EXP,ISO)
bleomycin A2  (ISO)
carbamazepine  (EXP)
carbon nanotube  (ISO)
choline  (ISO)
cisplatin  (EXP,ISO)
clofibrate  (ISO)
cobalt dichloride  (EXP)
cocaine  (ISO)
copper(II) chloride  (ISO)
cyclosporin A  (EXP)
dexamethasone  (EXP)
diallyl trisulfide  (EXP)
diarsenic trioxide  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
enzyme inhibitor  (EXP)
finasteride  (ISO)
flutamide  (ISO)
folic acid  (ISO)
geraniol  (EXP)
hexadecanoic acid  (EXP)
hyaluronic acid  (ISO)
hydrogen peroxide  (ISO)
indometacin  (EXP)
ivermectin  (EXP)
ketamine  (ISO)
L-methionine  (ISO)
lead(0)  (EXP)
lead(2+)  (EXP)
leflunomide  (EXP)
miconazole  (ISO)
N-methyl-4-phenylpyridinium  (EXP)
nickel atom  (EXP)
ochratoxin A  (EXP)
oxaliplatin  (ISO)
paracetamol  (EXP,ISO)
pentachlorophenol  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (ISO)
quinoline  (EXP)
rac-lactic acid  (EXP)
SB 431542  (EXP)
silicon dioxide  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (EXP)
sodium dichromate  (ISO)
succimer  (ISO)
sunitinib  (EXP)
T-2 toxin  (ISO)
tamoxifen  (ISO)
tanespimycin  (EXP)
tert-butyl hydroperoxide  (EXP)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
topotecan  (ISO)
trichostatin A  (EXP)
Triptolide  (ISO)
triptonide  (ISO)
troglitazone  (ISO)
valproic acid  (EXP)
vinclozolin  (ISO)
vincristine  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IBA)
nucleoplasm  (IDA)
nucleus  (IBA,IDA,ISO)
synapse  (ISO)

Molecular Function

References

Additional References at PubMed
PMID:8125259   PMID:10734235   PMID:10882074   PMID:11003644   PMID:11071946   PMID:11222755   PMID:11239393   PMID:11875576   PMID:12176931   PMID:12477932   PMID:12819782   PMID:15146197  
PMID:15302935   PMID:15489334   PMID:15502847   PMID:15592455   PMID:16159877   PMID:16169070   PMID:16289162   PMID:16344560   PMID:16628215   PMID:16672220   PMID:16712791   PMID:16964243  
PMID:17353931   PMID:17676665   PMID:18029348   PMID:19003864   PMID:19015535   PMID:19087307   PMID:19165527   PMID:19219071   PMID:19299420   PMID:19322201   PMID:19585652   PMID:19637194  
PMID:19738201   PMID:19928837   PMID:20348541   PMID:20420426   PMID:20467437   PMID:20802533   PMID:21145461   PMID:21285945   PMID:21319273   PMID:21367899   PMID:21779003   PMID:21817013  
PMID:21855647   PMID:21873635   PMID:21988832   PMID:22304920   PMID:22588899   PMID:22623428   PMID:22658674   PMID:22681889   PMID:22863883   PMID:22869205   PMID:22926519   PMID:22939629  
PMID:23463506   PMID:23818605   PMID:24030748   PMID:24117486   PMID:24189637   PMID:24192769   PMID:24347226   PMID:24457600   PMID:24711643   PMID:24798327   PMID:24966911   PMID:25796446  
PMID:25921289   PMID:25963833   PMID:25995247   PMID:26177862   PMID:26209609   PMID:26344197   PMID:26490982   PMID:26496610   PMID:26545048   PMID:26641092   PMID:26901106   PMID:26949251  
PMID:27157613   PMID:27197155   PMID:27599538   PMID:27609421   PMID:28076379   PMID:28225217   PMID:28302793   PMID:28533407   PMID:28611215   PMID:28667493   PMID:28780352   PMID:28977470  
PMID:29031818   PMID:29117863   PMID:29128334   PMID:29395067   PMID:29467282   PMID:29507755   PMID:29509190   PMID:29656893   PMID:29743362   PMID:29791485   PMID:29997244   PMID:30301530  
PMID:30463901   PMID:30500954   PMID:30585729   PMID:30635626   PMID:30653565   PMID:30711629   PMID:30737378   PMID:30778852   PMID:30890647   PMID:30948266   PMID:31046837   PMID:31300519  
PMID:31343991   PMID:31511046   PMID:31553912   PMID:31570706   PMID:31586073   PMID:31587040   PMID:32129710   PMID:32203420   PMID:32296183   PMID:32414810   PMID:32416067   PMID:32433053  
PMID:32481602   PMID:32555178   PMID:32626933   PMID:32877691   PMID:33476628   PMID:33649780   PMID:33954195   PMID:33961781   PMID:34079125   PMID:34274028  


Genomics

Comparative Map Data
FUBP1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl177,944,055 - 77,979,110 (-)EnsemblGRCh38hg38GRCh38
GRCh38177,944,055 - 77,979,435 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37178,409,740 - 78,444,756 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36178,186,179 - 78,217,365 (-)NCBINCBI36hg18NCBI36
Build 34178,126,110 - 78,156,735NCBI
Celera176,652,669 - 76,683,855 (-)NCBI
Cytogenetic Map1p31.1NCBI
HuRef176,545,210 - 76,576,401 (-)NCBIHuRef
CHM1_1178,529,931 - 78,561,136 (-)NCBICHM1_1
Fubp1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm393151,916,059 - 151,942,467 (+)NCBIGRCm39mm39
GRCm39 Ensembl3151,916,059 - 151,942,463 (+)Ensembl
GRCm383152,210,422 - 152,236,830 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl3152,210,422 - 152,236,826 (+)EnsemblGRCm38mm10GRCm38
MGSCv373151,873,422 - 151,899,794 (+)NCBIGRCm37mm9NCBIm37
MGSCv363152,147,907 - 152,174,212 (+)NCBImm8
Celera3158,688,293 - 158,714,689 (+)NCBICelera
Cytogenetic Map3H3NCBI
cM Map377.05NCBI
Fubp1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.22241,159,481 - 241,186,591 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl2241,159,512 - 241,186,602 (+)Ensembl
Rnor_6.02257,425,676 - 257,452,745 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2257,425,679 - 257,449,568 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02276,102,238 - 276,129,492 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42250,749,095 - 250,777,521 (+)NCBIRGSC3.4rn4RGSC3.4
Celera2233,094,240 - 233,117,161 (+)NCBICelera
Cytogenetic Map2q45NCBI
Fubp1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542315,245,610 - 15,278,628 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495542315,245,645 - 15,278,628 (+)NCBIChiLan1.0ChiLan1.0
FUBP1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1179,244,892 - 79,280,448 (-)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v0177,162,675 - 77,198,486 (-)NCBIMhudiblu_PPA_v0panPan3
FUBP1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1668,923,215 - 68,963,766 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha671,580,919 - 71,621,261 (+)NCBI
ROS_Cfam_1.0669,508,282 - 69,548,642 (+)NCBI
UMICH_Zoey_3.1669,015,218 - 69,054,818 (+)NCBI
UNSW_CanFamBas_1.0668,959,769 - 69,000,118 (+)NCBI
UU_Cfam_GSD_1.0669,446,187 - 69,486,514 (+)NCBI
Fubp1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505889,218,777 - 89,250,519 (-)NCBI
SpeTri2.0NW_0049365714,729,135 - 4,760,943 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FUBP1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6135,281,521 - 135,318,714 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16135,281,474 - 135,319,055 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.26125,463,226 - 125,500,521 (+)NCBISscrofa10.2Sscrofa10.2susScr3
FUBP1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12055,194,681 - 55,233,666 (+)NCBIChlSab1.1chlSab2
ChlSab1.12055,194,681 - 55,233,666 (+)NCBIChlSab1.1chlSab2
ChlSab1.12055,194,681 - 55,233,666 (+)NCBIChlSab1.1chlSab2
ChlSab1.12055,194,681 - 55,233,666 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl2055,194,743 - 55,230,277 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366603362,279,926 - 62,320,345 (-)NCBIVero_WHO_p1.0
Fubp1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474219,279,544 - 19,313,139 (+)NCBIHetGla_female_1.0hetGla2

Position Markers
SHGC-75049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,413,052 - 78,413,155UniSTSGRCh37
Build 36178,185,640 - 78,185,743RGDNCBI36
Celera176,652,130 - 76,652,233RGD
Cytogenetic Map1p31.1UniSTS
HuRef176,544,671 - 76,544,774UniSTS
TNG Radiation Hybrid Map144812.0UniSTS
GeneMap99-GB4 RH Map1216.0UniSTS
NCBI RH Map1518.0UniSTS
D1S257E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,413,059 - 78,413,155UniSTSGRCh37
Build 36178,185,647 - 78,185,743RGDNCBI36
Celera176,652,137 - 76,652,233RGD
Cytogenetic Map1p31.1UniSTS
HuRef176,544,678 - 76,544,774UniSTS
Whitehead-YAC Contig Map1 UniSTS
AL034068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,423,029 - 78,423,182UniSTSGRCh37
Build 36178,195,617 - 78,195,770RGDNCBI36
Celera176,662,107 - 76,662,260RGD
Cytogenetic Map1p31.1UniSTS
HuRef176,554,648 - 76,554,801UniSTS
SHGC-155233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,420,265 - 78,420,561UniSTSGRCh37
Build 36178,192,853 - 78,193,149RGDNCBI36
Celera176,659,343 - 76,659,639RGD
Cytogenetic Map1p31.1UniSTS
HuRef176,551,884 - 76,552,180UniSTS
TNG Radiation Hybrid Map144846.0UniSTS
SHGC-75042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,418,135 - 78,418,271UniSTSGRCh37
Build 36178,190,723 - 78,190,859RGDNCBI36
Celera176,657,213 - 76,657,349RGD
Cytogenetic Map1p31.1UniSTS
HuRef176,549,754 - 76,549,890UniSTS
TNG Radiation Hybrid Map144840.0UniSTS
GeneMap99-GB4 RH Map1209.19UniSTS
NCBI RH Map1518.0UniSTS
SHGC-75032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,423,860 - 78,424,021UniSTSGRCh37
Build 36178,196,448 - 78,196,609RGDNCBI36
Celera176,662,938 - 76,663,099RGD
Cytogenetic Map1p31.1UniSTS
HuRef176,555,479 - 76,555,640UniSTS
TNG Radiation Hybrid Map144852.0UniSTS
GeneMap99-GB4 RH Map1193.94UniSTS
FUBP1_2823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,414,046 - 78,414,559UniSTSGRCh37
Build 36178,186,634 - 78,187,147RGDNCBI36
Celera176,653,124 - 76,653,637RGD
HuRef176,545,665 - 76,546,178UniSTS
FUBP1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37178,414,109 - 78,414,263UniSTSGRCh37
Celera176,653,187 - 76,653,341UniSTS
HuRef176,545,728 - 76,545,882UniSTS
D1S3413  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1p31.1UniSTS
Whitehead-YAC Contig Map1 UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1126
Count of miRNA genes:521
Interacting mature miRNAs:569
Transcripts:ENST00000294623, ENST00000370767, ENST00000370768, ENST00000421641, ENST00000436586, ENST00000470287, ENST00000474632, ENST00000480673, ENST00000483894, ENST00000487684, ENST00000488814, ENST00000489495, ENST00000492405, ENST00000492724
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2428 2286 1538 442 1414 284 4291 1994 2950 394 1444 1605 171 1204 2728 4
Low 11 704 188 182 537 181 65 203 783 25 13 8 4 1 60 1 2
Below cutoff 1 3 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_033243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001303433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001376057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_130152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_146540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_164756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011542391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011542392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011542393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017002739 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017002740 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017002743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001737524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_946790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_946791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209366 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC096948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303568 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL049951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL532525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW295160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC010083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ649331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ934904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX538272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB133133 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN291186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA113820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ900935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510733 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY569017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U05040 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000294623   ⟹   ENSP00000294623
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,946,482 - 77,979,087 (-)Ensembl
RefSeq Acc Id: ENST00000370767   ⟹   ENSP00000359803
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,948,405 - 77,979,092 (-)Ensembl
RefSeq Acc Id: ENST00000370768   ⟹   ENSP00000359804
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,979,072 (-)Ensembl
RefSeq Acc Id: ENST00000421641   ⟹   ENSP00000402630
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,965,069 - 77,979,110 (-)Ensembl
RefSeq Acc Id: ENST00000470287
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,955,255 - 77,960,785 (-)Ensembl
RefSeq Acc Id: ENST00000474632
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,947,692 (-)Ensembl
RefSeq Acc Id: ENST00000480673
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,946,576 (-)Ensembl
RefSeq Acc Id: ENST00000483894
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,945,895 (-)Ensembl
RefSeq Acc Id: ENST00000487684
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,948,970 - 77,955,458 (-)Ensembl
RefSeq Acc Id: ENST00000488814
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,949,267 (-)Ensembl
RefSeq Acc Id: ENST00000489495
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,948,333 (-)Ensembl
RefSeq Acc Id: ENST00000492405
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,955,282 (-)Ensembl
RefSeq Acc Id: ENST00000492724
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl177,944,055 - 77,955,339 (-)Ensembl
RefSeq Acc Id: NM_001303433   ⟹   NP_001290362
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
CHM1_1178,530,427 - 78,561,248 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001376055   ⟹   NP_001362984
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
RefSeq Acc Id: NM_001376056   ⟹   NP_001362985
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
RefSeq Acc Id: NM_001376057   ⟹   NP_001362986
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
RefSeq Acc Id: NM_003902   ⟹   NP_003893
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
GRCh37178,409,740 - 78,444,839 (-)NCBI
Build 36178,186,179 - 78,217,365 (-)NCBI Archive
HuRef176,545,210 - 76,576,401 (-)ENTREZGENE
CHM1_1178,530,427 - 78,561,248 (-)NCBI
Sequence:
RefSeq Acc Id: NR_130152
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,946,482 - 77,979,072 (-)NCBI
CHM1_1178,528,507 - 78,561,248 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146539
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146540
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
Sequence:
RefSeq Acc Id: NR_164755
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
RefSeq Acc Id: NR_164756
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,072 (-)NCBI
RefSeq Acc Id: XM_011542391   ⟹   XP_011540693
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011542392   ⟹   XP_011540694
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,110 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011542393   ⟹   XP_011540695
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,076 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017002739   ⟹   XP_016858228
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,435 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017002740   ⟹   XP_016858229
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017002743   ⟹   XP_016858232
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,130 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737514
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737515
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737516
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737517
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737518
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737519
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737520
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,110 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001737521
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,205 (-)NCBI
Sequence:
RefSeq Acc Id: XR_946790
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,114 (-)NCBI
Sequence:
RefSeq Acc Id: XR_946791
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,944,055 - 77,979,205 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_003893   ⟸   NM_003902
- Peptide Label: isoform 2
- UniProtKB: Q96AE4 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001290362   ⟸   NM_001303433
- Peptide Label: isoform 1
- UniProtKB: Q96AE4 (UniProtKB/Swiss-Prot),   B4DT31 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011540694   ⟸   XM_011542392
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011540693   ⟸   XM_011542391
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011540695   ⟸   XM_011542393
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016858228   ⟸   XM_017002739
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016858232   ⟸   XM_017002743
- Peptide Label: isoform X7
- UniProtKB: Q96AE4 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016858229   ⟸   XM_017002740
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: NP_001362985   ⟸   NM_001376056
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001362986   ⟸   NM_001376057
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001362984   ⟸   NM_001376055
- Peptide Label: isoform 3
RefSeq Acc Id: ENSP00000359803   ⟸   ENST00000370767
RefSeq Acc Id: ENSP00000359804   ⟸   ENST00000370768
RefSeq Acc Id: ENSP00000294623   ⟸   ENST00000294623
RefSeq Acc Id: ENSP00000402630   ⟸   ENST00000421641
Protein Domains
KH

Promoters
RGD ID:6855962
Promoter ID:EPDNEW_H1146
Type:initiation region
Name:FUBP1_1
Description:far upstream element binding protein 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,979,064 - 77,979,124EPDNEW
RGD ID:6785613
Promoter ID:HG_KWN:3354
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000098141
Position:
Human AssemblyChrPosition (strand)Source
Build 36178,183,611 - 78,184,111 (-)MPROMDB
RGD ID:6785612
Promoter ID:HG_KWN:3355
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000098137,   OTTHUMT00000098140,   OTTHUMT00000098142
Position:
Human AssemblyChrPosition (strand)Source
Build 36178,185,551 - 78,187,382 (-)MPROMDB
RGD ID:6785610
Promoter ID:HG_KWN:3356
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000098136
Position:
Human AssemblyChrPosition (strand)Source
Build 36178,187,461 - 78,188,512 (-)MPROMDB
RGD ID:6785611
Promoter ID:HG_KWN:3357
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000098138,   OTTHUMT00000098139,   OTTHUMT00000098143
Position:
Human AssemblyChrPosition (strand)Source
Build 36178,193,461 - 78,193,961 (-)MPROMDB
RGD ID:6785614
Promoter ID:HG_KWN:3358
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:OTTHUMT00000098144
Position:
Human AssemblyChrPosition (strand)Source
Build 36178,198,606 - 78,199,612 (-)MPROMDB
RGD ID:6785098
Promoter ID:HG_KWN:3359
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000294623,   ENST00000370767,   ENST00000370773,   ENST00000394922,   NM_003902,   OTTHUMT00000098135,   OTTHUMT00000098622,   OTTHUMT00000098623,   OTTHUMT00000098624,   OTTHUMT00000098630,   UC001DIH.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36178,216,191 - 78,217,622 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p31.1-13.3(chr1:72661709-107456880)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]|See cases [RCV000051825] Chr1:72661709..107456880 [GRCh38]
Chr1:73127392..107999502 [GRCh37]
Chr1:72899980..107801025 [NCBI36]
Chr1:1p31.1-13.3
pathogenic
NM_003902.5(FUBP1):c.243A>C (p.Gln81His) single nucleotide variant not specified [RCV000121142] Chr1:77968172 [GRCh38]
Chr1:78433856 [GRCh37]
Chr1:1p31.1
not provided
NM_003902.5(FUBP1):c.538G>T (p.Gly180Cys) single nucleotide variant not specified [RCV000121143] Chr1:77965167 [GRCh38]
Chr1:78430851 [GRCh37]
Chr1:1p31.1
not provided
NM_003902.5(FUBP1):c.56G>A (p.Gly19Asp) single nucleotide variant not specified [RCV000121137] Chr1:77978949 [GRCh38]
Chr1:78444633 [GRCh37]
Chr1:1p31.1
not provided
NM_003902.5(FUBP1):c.992G>A (p.Arg331Gln) single nucleotide variant not specified [RCV000121138] Chr1:77964111 [GRCh38]
Chr1:78429796 [GRCh37]
Chr1:1p31.1
not provided
NM_003902.5(FUBP1):c.1429C>T (p.Pro477Ser) single nucleotide variant not specified [RCV000121139] Chr1:77960411 [GRCh38]
Chr1:78426096 [GRCh37]
Chr1:1p31.1
not provided
NM_003902.5(FUBP1):c.1588A>G (p.Thr530Ala) single nucleotide variant not specified [RCV000121140] Chr1:77956689 [GRCh38]
Chr1:78422374 [GRCh37]
Chr1:1p31.1
not provided
NM_003902.5(FUBP1):c.1801A>G (p.Thr601Ala) single nucleotide variant not specified [RCV000121141] Chr1:77949280 [GRCh38]
Chr1:78414965 [GRCh37]
Chr1:1p31.1
not provided
GRCh38/hg38 1p32.1-22.3(chr1:58819605-86098611)x1 copy number loss See cases [RCV000136913] Chr1:58819605..86098611 [GRCh38]
Chr1:59285277..86564294 [GRCh37]
Chr1:59057865..86336882 [NCBI36]
Chr1:1p32.1-22.3
pathogenic
GRCh38/hg38 1p31.1-22.2(chr1:76419302-88628464)x1 copy number loss See cases [RCV000138957] Chr1:76419302..88628464 [GRCh38]
Chr1:76884987..89094147 [GRCh37]
Chr1:76657575..88866735 [NCBI36]
Chr1:1p31.1-22.2
pathogenic
GRCh38/hg38 1p31.1(chr1:77777821-79122486)x1 copy number loss See cases [RCV000140751] Chr1:77777821..79122486 [GRCh38]
Chr1:78243506..79588171 [GRCh37]
Chr1:78016094..79360759 [NCBI36]
Chr1:1p31.1
uncertain significance
NM_003902.5(FUBP1):c.1611G>A (p.Trp537Ter) single nucleotide variant Ductal breast carcinoma [RCV000207329] Chr1:77956666 [GRCh38]
Chr1:78422351 [GRCh37]
Chr1:1p31.1
uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12
likely benign
NM_003902.5(FUBP1):c.1042-8C>G single nucleotide variant not specified [RCV000454438] Chr1:77963723 [GRCh38]
Chr1:78429408 [GRCh37]
Chr1:1p31.1
benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p31.1-22.1(chr1:72044544-92505091)x1 copy number loss See cases [RCV000510161] Chr1:72044544..92505091 [GRCh37]
Chr1:1p31.1-22.1
pathogenic
GRCh37/hg19 1p31.3-22.3(chr1:64321264-88153669)x1 copy number loss See cases [RCV000511392] Chr1:64321264..88153669 [GRCh37]
Chr1:1p31.3-22.3
pathogenic|uncertain significance
GRCh37/hg19 1p31.1(chr1:74848936-80324850)x3 copy number gain See cases [RCV000510973] Chr1:74848936..80324850 [GRCh37]
Chr1:1p31.1
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p31.3-31.1(chr1:61351024-79583933)x1 copy number loss See cases [RCV000512152] Chr1:61351024..79583933 [GRCh37]
Chr1:1p31.3-31.1
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_001303433.1(FUBP1):c.1266C>T (p.Ser422=) single nucleotide variant not provided [RCV000964814] Chr1:77962911 [GRCh38]
Chr1:78428596 [GRCh37]
Chr1:1p31.1
benign
NM_003902.5(FUBP1):c.54T>C (p.Gly18=) single nucleotide variant not provided [RCV000958459] Chr1:77978951 [GRCh38]
Chr1:78444635 [GRCh37]
Chr1:1p31.1
benign
GRCh37/hg19 1p31.1(chr1:78186240-81611776)x3 copy number gain not provided [RCV000846841] Chr1:78186240..81611776 [GRCh37]
Chr1:1p31.1
uncertain significance
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1
uncertain significance
Single allele deletion not provided [RCV000844927] Chr1:66085524..88429789 [GRCh37]
Chr1:1p31.3-22.2
not provided
GRCh37/hg19 1p31.1(chr1:78186240-81611776)x3 copy number gain not provided [RCV000847217] Chr1:78186240..81611776 [GRCh37]
Chr1:1p31.1
uncertain significance
GRCh37/hg19 1p31.1(chr1:78257937-79159519)x3 copy number gain not provided [RCV001005117] Chr1:78257937..79159519 [GRCh37]
Chr1:1p31.1
uncertain significance
GRCh37/hg19 1p31.3-22.3(chr1:67851233-86101340)x1 copy number loss not provided [RCV000846441] Chr1:67851233..86101340 [GRCh37]
Chr1:1p31.3-22.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:4004 AgrOrtholog
COSMIC FUBP1 COSMIC
Ensembl Genes ENSG00000162613 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000294623 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000359803 UniProtKB/TrEMBL
  ENSP00000359804 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000402630 UniProtKB/TrEMBL
Ensembl Transcript ENST00000294623 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000370767 UniProtKB/TrEMBL
  ENST00000370768 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000421641 UniProtKB/TrEMBL
Gene3D-CATH 3.30.1370.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000162613 GTEx
HGNC ID HGNC:4004 ENTREZGENE
Human Proteome Map FUBP1 Human Proteome Map
InterPro FUBP_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KH_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KH_dom_type_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KH_dom_type_1_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8880 UniProtKB/Swiss-Prot
NCBI Gene 8880 ENTREZGENE
OMIM 603444 OMIM
Pfam DUF1897 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KH_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA28420 PharmGKB
PROSITE KH_TYPE_1 UniProtKB/Swiss-Prot
SMART SM00322 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF54791 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1Z1G4M2_HUMAN UniProtKB/TrEMBL
  A0A384MDX9_HUMAN UniProtKB/TrEMBL
  B4DT31 ENTREZGENE, UniProtKB/TrEMBL
  C9JSZ1_HUMAN UniProtKB/TrEMBL
  E9PEB5_HUMAN UniProtKB/TrEMBL
  FUBP1_HUMAN UniProtKB/Swiss-Prot
  Q6PJY1_HUMAN UniProtKB/TrEMBL
  Q96AE4 ENTREZGENE
UniProt Secondary E9PCF5 UniProtKB/TrEMBL
  Q12828 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-10 FUBP1  far upstream element binding protein 1  FUBP1  far upstream element (FUSE) binding protein 1  Symbol and/or name change 5135510 APPROVED