FSCN3 (fascin actin-bundling protein 3) - Rat Genome Database
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Gene: FSCN3 (fascin actin-bundling protein 3) Homo sapiens
Analyze
Symbol: FSCN3
Name: fascin actin-bundling protein 3
RGD ID: 1353847
HGNC Page HGNC
Description: Predicted to have actin filament binding activity. Predicted to be involved in actin filament bundle assembly; cell migration; and establishment or maintenance of cell polarity. Predicted to localize to several cellular components, including lamellipodium; microvillus; and ruffle; INTERACTS WITH benzo[a]pyrene; sodium arsenite; 1,2-dimethylhydrazine (ortholog).
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: fascin actin-bundling protein 3, testicular; fascin homolog 3, actin-bundling protein, testicular; fascin-3; testicular secretory protein Li 18; testis fascin
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 Ensembl7127,591,409 - 127,602,144 (+)EnsemblGRCh38hg38GRCh38
GRCh387127,593,736 - 127,602,144 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377127,233,790 - 127,242,198 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh377127,233,689 - 127,241,851 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367127,020,925 - 127,029,079 (+)NCBINCBI36hg18NCBI36
Build 347126,827,639 - 126,835,794NCBI
Celera7122,037,417 - 122,045,564 (+)NCBI
Cytogenetic Map7q32.1NCBI
HuRef7121,594,759 - 121,602,743 (+)NCBIHuRef
CHM1_17127,166,986 - 127,175,152 (+)NCBICHM1_1
CRA_TCAGchr7v27126,617,134 - 126,625,289 (+)NCBI
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
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
1. GOA_HUMAN data from the GO Consortium
2. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:10783262   PMID:11925108   PMID:12477932   PMID:12690205   PMID:15489334   PMID:17567994   PMID:21873635   PMID:28514442  


Genomics

Comparative Map Data
FSCN3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl7127,591,409 - 127,602,144 (+)EnsemblGRCh38hg38GRCh38
GRCh387127,593,736 - 127,602,144 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh377127,233,790 - 127,242,198 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh377127,233,689 - 127,241,851 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 367127,020,925 - 127,029,079 (+)NCBINCBI36hg18NCBI36
Build 347126,827,639 - 126,835,794NCBI
Celera7122,037,417 - 122,045,564 (+)NCBI
Cytogenetic Map7q32.1NCBI
HuRef7121,594,759 - 121,602,743 (+)NCBIHuRef
CHM1_17127,166,986 - 127,175,152 (+)NCBICHM1_1
CRA_TCAGchr7v27126,617,134 - 126,625,289 (+)NCBI
Fscn3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39628,427,869 - 28,438,621 (+)NCBIGRCm39mm39
GRCm38628,427,870 - 28,438,622 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl628,427,789 - 28,438,622 (+)EnsemblGRCm38mm10GRCm38
MGSCv37628,377,901 - 28,388,622 (+)NCBIGRCm37mm9NCBIm37
MGSCv36628,377,911 - 28,388,632 (+)NCBImm8
Celera628,434,941 - 28,445,662 (+)NCBICelera
Cytogenetic Map6A3.3NCBI
Fscn3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2457,042,797 - 57,052,224 (+)NCBI
Rnor_6.0 Ensembl455,720,010 - 55,729,457 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0455,719,976 - 55,729,442 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0455,467,449 - 55,476,891 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4455,298,103 - 55,307,523 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1455,548,259 - 55,557,678 (+)NCBI
Celera452,154,383 - 52,163,752 (+)NCBICelera
Cytogenetic Map4q22NCBI
Fscn3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554798,648,582 - 8,654,493 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554798,649,022 - 8,656,899 (+)NCBIChiLan1.0ChiLan1.0
FSCN3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.17132,244,268 - 132,252,312 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7132,244,268 - 132,250,913 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v07119,589,219 - 119,597,360 (+)NCBIMhudiblu_PPA_v0panPan3
FSCN3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl148,722,069 - 8,730,729 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.1148,719,857 - 8,730,881 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Fscn3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_00493647914,794,876 - 14,803,549 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FSCN3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1820,686,746 - 20,693,552 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11820,684,621 - 20,693,552 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21821,688,295 - 21,697,317 (-)NCBISscrofa10.2Sscrofa10.2susScr3
FSCN3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12196,407,983 - 96,416,313 (+)NCBI
ChlSab1.1 Ensembl2196,409,005 - 96,414,922 (+)Ensembl
Fscn3
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247838,345,467 - 8,356,973 (-)NCBI

Position Markers
AF047019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,234,015 - 127,234,383UniSTSGRCh37
Build 367127,021,251 - 127,021,619RGDNCBI36
Celera7122,037,743 - 122,038,104RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,595,085 - 121,595,275UniSTS
CRA_TCAGchr7v27126,617,460 - 126,617,821UniSTS
ECD03327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,240,060 - 127,240,859UniSTSGRCh37
Build 367127,027,296 - 127,028,095RGDNCBI36
Celera7122,043,781 - 122,044,580RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,600,952 - 121,601,751UniSTS
CRA_TCAGchr7v27126,623,498 - 126,624,297UniSTS
ECD04411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,234,383 - 127,235,148UniSTSGRCh37
Build 367127,021,619 - 127,022,384RGDNCBI36
Celera7122,038,104 - 122,038,869RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,595,275 - 121,596,040UniSTS
CRA_TCAGchr7v27126,617,821 - 126,618,586UniSTS
ECD05740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,235,190 - 127,235,918UniSTSGRCh37
Build 367127,022,426 - 127,023,154RGDNCBI36
Celera7122,038,911 - 122,039,639RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,596,082 - 121,596,810UniSTS
CRA_TCAGchr7v27126,618,628 - 126,619,356UniSTS
ECD08247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,235,988 - 127,236,648UniSTSGRCh37
Build 367127,023,224 - 127,023,884RGDNCBI36
Celera7122,039,709 - 122,040,369RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,596,880 - 121,597,540UniSTS
CRA_TCAGchr7v27126,619,426 - 126,620,086UniSTS
ECD11753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,241,283 - 127,241,846UniSTSGRCh37
Build 367127,028,519 - 127,029,082RGDNCBI36
Celera7122,045,004 - 122,045,567RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,602,175 - 121,602,738UniSTS
CRA_TCAGchr7v27126,624,721 - 126,625,284UniSTS
ECD12933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,232,963 - 127,233,494UniSTSGRCh37
Build 367127,020,199 - 127,020,730RGDNCBI36
Celera7122,036,691 - 122,037,222RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,594,033 - 121,594,564UniSTS
CRA_TCAGchr7v27126,616,408 - 126,616,939UniSTS
ECD14734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,233,611 - 127,234,214UniSTSGRCh37
GRCh377127,233,611 - 127,234,098UniSTSGRCh37
Build 367127,020,847 - 127,021,334RGDNCBI36
Celera7122,037,339 - 122,037,826RGD
Celera7122,037,339 - 122,037,942UniSTS
HuRef7121,594,681 - 121,595,168UniSTS
CRA_TCAGchr7v27126,617,056 - 126,617,659UniSTS
CRA_TCAGchr7v27126,617,056 - 126,617,543UniSTS
ECD15359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,238,248 - 127,238,720UniSTSGRCh37
Build 367127,025,484 - 127,025,956RGDNCBI36
Celera7122,041,969 - 122,042,441RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,599,140 - 121,599,612UniSTS
CRA_TCAGchr7v27126,621,686 - 126,622,158UniSTS
ECD18282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,239,337 - 127,239,703UniSTSGRCh37
Build 367127,026,573 - 127,026,939RGDNCBI36
Celera7122,043,058 - 122,043,424RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,600,229 - 121,600,595UniSTS
CRA_TCAGchr7v27126,622,775 - 126,623,141UniSTS
REN115674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,231,793 - 127,232,034UniSTSGRCh37
Build 367127,019,029 - 127,019,270RGDNCBI36
Celera7122,035,521 - 122,035,762RGD
HuRef7121,592,863 - 121,593,104UniSTS
CRA_TCAGchr7v27126,615,238 - 126,615,479UniSTS
REN115675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,231,957 - 127,232,195UniSTSGRCh37
Build 367127,019,193 - 127,019,431RGDNCBI36
Celera7122,035,685 - 122,035,923RGD
HuRef7121,593,027 - 121,593,265UniSTS
CRA_TCAGchr7v27126,615,402 - 126,615,640UniSTS
REN115676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,232,586 - 127,232,821UniSTSGRCh37
Build 367127,019,822 - 127,020,057RGDNCBI36
Celera7122,036,314 - 122,036,549RGD
HuRef7121,593,656 - 121,593,891UniSTS
CRA_TCAGchr7v27126,616,031 - 126,616,266UniSTS
REN115677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,232,812 - 127,233,080UniSTSGRCh37
Build 367127,020,048 - 127,020,316RGDNCBI36
Celera7122,036,540 - 122,036,808RGD
HuRef7121,593,882 - 121,594,150UniSTS
CRA_TCAGchr7v27126,616,257 - 126,616,525UniSTS
REN115678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,233,063 - 127,233,314UniSTSGRCh37
Build 367127,020,299 - 127,020,550RGDNCBI36
Celera7122,036,791 - 122,037,042RGD
HuRef7121,594,133 - 121,594,384UniSTS
CRA_TCAGchr7v27126,616,508 - 126,616,759UniSTS
REN115679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,233,284 - 127,233,531UniSTSGRCh37
Build 367127,020,520 - 127,020,767RGDNCBI36
Celera7122,037,012 - 122,037,259RGD
HuRef7121,594,354 - 121,594,601UniSTS
CRA_TCAGchr7v27126,616,729 - 126,616,976UniSTS
REN115680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,233,508 - 127,233,742UniSTSGRCh37
Build 367127,020,744 - 127,020,978RGDNCBI36
Celera7122,037,236 - 122,037,470RGD
HuRef7121,594,578 - 121,594,812UniSTS
CRA_TCAGchr7v27126,616,953 - 126,617,187UniSTS
REN115681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,233,696 - 127,233,943UniSTSGRCh37
Build 367127,020,932 - 127,021,179RGDNCBI36
Celera7122,037,424 - 122,037,671RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,594,766 - 121,595,013UniSTS
CRA_TCAGchr7v27126,617,141 - 126,617,388UniSTS
REN115682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,233,807 - 127,234,065UniSTSGRCh37
Build 367127,021,043 - 127,021,301RGDNCBI36
Celera7122,037,535 - 122,037,793RGD
HuRef7121,594,877 - 121,595,135UniSTS
CRA_TCAGchr7v27126,617,252 - 126,617,510UniSTS
REN115684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,234,273 - 127,234,538UniSTSGRCh37
GRCh377127,234,185 - 127,234,538UniSTSGRCh37
Build 367127,021,421 - 127,021,774RGDNCBI36
Celera7122,037,913 - 122,038,259RGD
Celera7122,038,001 - 122,038,259UniSTS
CRA_TCAGchr7v27126,617,630 - 126,617,976UniSTS
CRA_TCAGchr7v27126,617,718 - 126,617,976UniSTS
REN115685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,234,515 - 127,234,764UniSTSGRCh37
Build 367127,021,751 - 127,022,000RGDNCBI36
Celera7122,038,236 - 122,038,485RGD
HuRef7121,595,407 - 121,595,656UniSTS
CRA_TCAGchr7v27126,617,953 - 126,618,202UniSTS
REN115686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,234,760 - 127,234,998UniSTSGRCh37
Build 367127,021,996 - 127,022,234RGDNCBI36
Celera7122,038,481 - 122,038,719RGD
HuRef7121,595,652 - 121,595,890UniSTS
CRA_TCAGchr7v27126,618,198 - 126,618,436UniSTS
REN115687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,234,973 - 127,235,225UniSTSGRCh37
Build 367127,022,209 - 127,022,461RGDNCBI36
Celera7122,038,694 - 122,038,946RGD
HuRef7121,595,865 - 121,596,117UniSTS
CRA_TCAGchr7v27126,618,411 - 126,618,663UniSTS
REN115688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,235,202 - 127,235,454UniSTSGRCh37
Build 367127,022,438 - 127,022,690RGDNCBI36
Celera7122,038,923 - 122,039,175RGD
HuRef7121,596,094 - 121,596,346UniSTS
CRA_TCAGchr7v27126,618,640 - 126,618,892UniSTS
REN115689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,235,449 - 127,235,675UniSTSGRCh37
Build 367127,022,685 - 127,022,911RGDNCBI36
Celera7122,039,170 - 122,039,396RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,596,341 - 121,596,567UniSTS
CRA_TCAGchr7v27126,618,887 - 126,619,113UniSTS
REN115690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,235,655 - 127,235,923UniSTSGRCh37
Build 367127,022,891 - 127,023,159RGDNCBI36
Celera7122,039,376 - 122,039,644RGD
Cytogenetic Map7q31.3UniSTS
HuRef7121,596,547 - 121,596,815UniSTS
CRA_TCAGchr7v27126,619,093 - 126,619,361UniSTS
REN115691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,235,920 - 127,236,173UniSTSGRCh37
Build 367127,023,156 - 127,023,409RGDNCBI36
Celera7122,039,641 - 122,039,894RGD
HuRef7121,596,812 - 121,597,065UniSTS
CRA_TCAGchr7v27126,619,358 - 126,619,611UniSTS
REN115692  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,236,143 - 127,236,377UniSTSGRCh37
Build 367127,023,379 - 127,023,613RGDNCBI36
Celera7122,039,864 - 122,040,098RGD
HuRef7121,597,035 - 121,597,269UniSTS
CRA_TCAGchr7v27126,619,581 - 126,619,815UniSTS
REN115693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,236,354 - 127,236,602UniSTSGRCh37
Build 367127,023,590 - 127,023,838RGDNCBI36
Celera7122,040,075 - 122,040,323RGD
HuRef7121,597,246 - 121,597,494UniSTS
CRA_TCAGchr7v27126,619,792 - 126,620,040UniSTS
REN115694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,236,580 - 127,236,836UniSTSGRCh37
Build 367127,023,816 - 127,024,072RGDNCBI36
Celera7122,040,301 - 122,040,557RGD
HuRef7121,597,472 - 121,597,728UniSTS
CRA_TCAGchr7v27126,620,018 - 126,620,274UniSTS
REN115695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,236,817 - 127,237,060UniSTSGRCh37
Build 367127,024,053 - 127,024,296RGDNCBI36
Celera7122,040,538 - 122,040,781RGD
HuRef7121,597,709 - 121,597,952UniSTS
CRA_TCAGchr7v27126,620,255 - 126,620,498UniSTS
REN115696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,237,000 - 127,237,229UniSTSGRCh37
Build 367127,024,236 - 127,024,465RGDNCBI36
Celera7122,040,721 - 122,040,950RGD
HuRef7121,597,892 - 121,598,121UniSTS
CRA_TCAGchr7v27126,620,438 - 126,620,667UniSTS
REN115697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,237,190 - 127,237,442UniSTSGRCh37
Build 367127,024,426 - 127,024,678RGDNCBI36
Celera7122,040,911 - 122,041,163RGD
HuRef7121,598,082 - 121,598,334UniSTS
CRA_TCAGchr7v27126,620,628 - 126,620,880UniSTS
REN115698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,237,273 - 127,237,498UniSTSGRCh37
Build 367127,024,509 - 127,024,734RGDNCBI36
Celera7122,040,994 - 122,041,219RGD
HuRef7121,598,165 - 121,598,390UniSTS
CRA_TCAGchr7v27126,620,711 - 126,620,936UniSTS
REN115699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,237,822 - 127,238,050UniSTSGRCh37
Build 367127,025,058 - 127,025,286RGDNCBI36
Celera7122,041,543 - 122,041,771RGD
HuRef7121,598,714 - 121,598,942UniSTS
CRA_TCAGchr7v27126,621,260 - 126,621,488UniSTS
REN115700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,238,020 - 127,238,265UniSTSGRCh37
Build 367127,025,256 - 127,025,501RGDNCBI36
Celera7122,041,741 - 122,041,986RGD
HuRef7121,598,912 - 121,599,157UniSTS
CRA_TCAGchr7v27126,621,458 - 126,621,703UniSTS
REN115701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,238,248 - 127,238,491UniSTSGRCh37
Build 367127,025,484 - 127,025,727RGDNCBI36
Celera7122,041,969 - 122,042,212RGD
HuRef7121,599,140 - 121,599,383UniSTS
CRA_TCAGchr7v27126,621,686 - 126,621,929UniSTS
REN115702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,238,468 - 127,238,704UniSTSGRCh37
Build 367127,025,704 - 127,025,940RGDNCBI36
Celera7122,042,189 - 122,042,425RGD
HuRef7121,599,360 - 121,599,596UniSTS
CRA_TCAGchr7v27126,621,906 - 126,622,142UniSTS
REN115703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,238,624 - 127,238,850UniSTSGRCh37
Build 367127,025,860 - 127,026,086RGDNCBI36
Celera7122,042,345 - 122,042,571RGD
HuRef7121,599,516 - 121,599,742UniSTS
CRA_TCAGchr7v27126,622,062 - 126,622,288UniSTS
REN115704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,238,923 - 127,239,173UniSTSGRCh37
Build 367127,026,159 - 127,026,409RGDNCBI36
Celera7122,042,644 - 122,042,894RGD
HuRef7121,599,815 - 121,600,065UniSTS
CRA_TCAGchr7v27126,622,361 - 126,622,611UniSTS
REN115705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,239,152 - 127,239,396UniSTSGRCh37
Build 367127,026,388 - 127,026,632RGDNCBI36
Celera7122,042,873 - 122,043,117RGD
HuRef7121,600,044 - 121,600,288UniSTS
CRA_TCAGchr7v27126,622,590 - 126,622,834UniSTS
REN115706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,239,373 - 127,239,612UniSTSGRCh37
Build 367127,026,609 - 127,026,848RGDNCBI36
Celera7122,043,094 - 122,043,333RGD
HuRef7121,600,265 - 121,600,504UniSTS
CRA_TCAGchr7v27126,622,811 - 126,623,050UniSTS
REN115707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,239,484 - 127,239,710UniSTSGRCh37
Build 367127,026,720 - 127,026,946RGDNCBI36
Celera7122,043,205 - 122,043,431RGD
HuRef7121,600,376 - 121,600,602UniSTS
CRA_TCAGchr7v27126,622,922 - 126,623,148UniSTS
REN115708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,239,979 - 127,240,208UniSTSGRCh37
Build 367127,027,215 - 127,027,444RGDNCBI36
Celera7122,043,700 - 122,043,929RGD
HuRef7121,600,871 - 121,601,100UniSTS
CRA_TCAGchr7v27126,623,417 - 126,623,646UniSTS
REN115709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,240,196 - 127,240,432UniSTSGRCh37
Build 367127,027,432 - 127,027,668RGDNCBI36
Celera7122,043,917 - 122,044,153RGD
HuRef7121,601,088 - 121,601,324UniSTS
CRA_TCAGchr7v27126,623,634 - 126,623,870UniSTS
REN115710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,240,404 - 127,240,648UniSTSGRCh37
Build 367127,027,640 - 127,027,884RGDNCBI36
Celera7122,044,125 - 122,044,369RGD
HuRef7121,601,296 - 121,601,540UniSTS
CRA_TCAGchr7v27126,623,842 - 126,624,086UniSTS
REN115711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,240,645 - 127,240,902UniSTSGRCh37
Build 367127,027,881 - 127,028,138RGDNCBI36
Celera7122,044,366 - 122,044,623RGD
HuRef7121,601,537 - 121,601,794UniSTS
CRA_TCAGchr7v27126,624,083 - 126,624,340UniSTS
REN115712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,240,875 - 127,241,132UniSTSGRCh37
Build 367127,028,111 - 127,028,368RGDNCBI36
Celera7122,044,596 - 122,044,853RGD
HuRef7121,601,767 - 121,602,024UniSTS
CRA_TCAGchr7v27126,624,313 - 126,624,570UniSTS
REN115713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,241,120 - 127,241,353UniSTSGRCh37
Build 367127,028,356 - 127,028,589RGDNCBI36
Celera7122,044,841 - 122,045,074RGD
HuRef7121,602,012 - 121,602,245UniSTS
CRA_TCAGchr7v27126,624,558 - 126,624,791UniSTS
REN115714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,241,328 - 127,241,552UniSTSGRCh37
Build 367127,028,564 - 127,028,788RGDNCBI36
Celera7122,045,049 - 122,045,273RGD
HuRef7121,602,220 - 121,602,444UniSTS
CRA_TCAGchr7v27126,624,766 - 126,624,990UniSTS
REN115715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,241,539 - 127,241,769UniSTSGRCh37
Build 367127,028,775 - 127,029,005RGDNCBI36
Celera7122,045,260 - 122,045,490RGD
HuRef7121,602,431 - 121,602,661UniSTS
CRA_TCAGchr7v27126,624,977 - 126,625,207UniSTS
REN115716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,241,729 - 127,241,978UniSTSGRCh37
Build 367127,028,965 - 127,029,214RGDNCBI36
Celera7122,045,450 - 122,045,699RGD
HuRef7121,602,621 - 121,602,870UniSTS
CRA_TCAGchr7v27126,625,167 - 126,625,416UniSTS
REN115717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,241,888 - 127,242,124UniSTSGRCh37
Build 367127,029,124 - 127,029,360RGDNCBI36
Celera7122,045,609 - 122,045,845RGD
HuRef7121,602,780 - 121,603,016UniSTS
CRA_TCAGchr7v27126,625,326 - 126,625,562UniSTS
stSG613726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,231,741 - 127,233,123UniSTSGRCh37
Build 367127,018,977 - 127,020,359RGDNCBI36
Celera7122,035,469 - 122,036,851RGD
HuRef7121,592,811 - 121,594,193UniSTS
CRA_TCAGchr7v27126,615,186 - 126,616,568UniSTS
stSG613727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,233,104 - 127,234,544UniSTSGRCh37
Build 367127,020,340 - 127,021,780RGDNCBI36
Celera7122,036,832 - 122,038,265RGD
HuRef7121,594,174 - 121,595,436UniSTS
CRA_TCAGchr7v27126,616,549 - 126,617,982UniSTS
stSG613728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,234,525 - 127,235,784UniSTSGRCh37
Build 367127,021,761 - 127,023,020RGDNCBI36
Celera7122,038,246 - 122,039,505RGD
HuRef7121,595,417 - 121,596,676UniSTS
CRA_TCAGchr7v27126,617,963 - 126,619,222UniSTS
stSG613729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,235,653 - 127,236,660UniSTSGRCh37
Build 367127,022,889 - 127,023,896RGDNCBI36
Celera7122,039,374 - 122,040,381RGD
HuRef7121,596,545 - 121,597,552UniSTS
CRA_TCAGchr7v27126,619,091 - 126,620,098UniSTS
stSG613730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,238,276 - 127,239,356UniSTSGRCh37
Build 367127,025,512 - 127,026,592RGDNCBI36
Celera7122,041,997 - 122,043,077RGD
HuRef7121,599,168 - 121,600,248UniSTS
CRA_TCAGchr7v27126,621,714 - 126,622,794UniSTS
stSG613731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377127,239,456 - 127,240,483UniSTSGRCh37
Build 367127,026,692 - 127,027,719RGDNCBI36
Celera7122,043,177 - 122,044,204RGD
HuRef7121,600,348 - 121,601,375UniSTS
CRA_TCAGchr7v27126,622,894 - 126,623,921UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1180
Count of miRNA genes:748
Interacting mature miRNAs:895
Transcripts:ENST00000265825, ENST00000420086, ENST00000421705, ENST00000469242, ENST00000478328, ENST00000478821
Prediction methods:Microtar, 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 adipose tissue appendage entire extraembryonic component
High
Medium 1 1 1 1 361 2 1
Low 56 221 59 5 113 4 295 35 475 8 132 103 1 42 180
Below cutoff 2247 2547 1475 493 1480 340 3756 1838 2827 286 883 1388 160 1143 2383 4

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000265825   ⟹   ENSP00000265825
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7127,593,736 - 127,602,144 (+)Ensembl
RefSeq Acc Id: ENST00000421705   ⟹   ENSP00000402472
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7127,593,742 - 127,595,485 (+)Ensembl
RefSeq Acc Id: ENST00000469242
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7127,595,441 - 127,596,618 (+)Ensembl
RefSeq Acc Id: ENST00000478328
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7127,591,409 - 127,595,468 (+)Ensembl
RefSeq Acc Id: ENST00000478821   ⟹   ENSP00000473531
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl7127,593,728 - 127,596,330 (+)Ensembl
RefSeq Acc Id: NM_020369   ⟹   NP_065102
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,593,736 - 127,602,144 (+)NCBI
GRCh377127,233,689 - 127,241,851 (+)ENTREZGENE
Build 367127,020,925 - 127,029,079 (+)NCBI Archive
Celera7122,037,417 - 122,045,564 (+)RGD
HuRef7121,594,759 - 121,602,743 (+)ENTREZGENE
CHM1_17127,166,986 - 127,175,152 (+)NCBI
CRA_TCAGchr7v27126,617,134 - 126,625,289 (+)ENTREZGENE
Sequence:
Reference Sequences
RefSeq Acc Id: NP_065102   ⟸   NM_020369
- UniProtKB: Q9NQT6 (UniProtKB/Swiss-Prot),   A0A140VK18 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000473531   ⟸   ENST00000478821
RefSeq Acc Id: ENSP00000402472   ⟸   ENST00000421705
RefSeq Acc Id: ENSP00000265825   ⟸   ENST00000265825
Protein Domains
Fascin

Promoters
RGD ID:6805701
Promoter ID:HG_KWN:59594
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000059256,   OTTHUMT00000141969,   OTTHUMT00000141970,   OTTHUMT00000141975,   OTTHUMT00000141976,   UC010LLC.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367127,020,111 - 127,021,067 (-)MPROMDB
RGD ID:7211839
Promoter ID:EPDNEW_H11664
Type:initiation region
Name:FSCN3_1
Description:fascin actin-bundling protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11667  EPDNEW_H11668  EPDNEW_H11669  EPDNEW_H11670  EPDNEW_H11666  EPDNEW_H11671  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,588,447 - 127,588,507EPDNEW
RGD ID:7211849
Promoter ID:EPDNEW_H11666
Type:initiation region
Name:FSCN3_3
Description:fascin actin-bundling protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11664  EPDNEW_H11667  EPDNEW_H11668  EPDNEW_H11669  EPDNEW_H11670  EPDNEW_H11671  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,589,137 - 127,589,197EPDNEW
RGD ID:7211841
Promoter ID:EPDNEW_H11667
Type:initiation region
Name:FSCN3_2
Description:fascin actin-bundling protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11664  EPDNEW_H11668  EPDNEW_H11669  EPDNEW_H11670  EPDNEW_H11666  EPDNEW_H11671  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,589,596 - 127,589,656EPDNEW
RGD ID:7211843
Promoter ID:EPDNEW_H11668
Type:initiation region
Name:FSCN3_4
Description:fascin actin-bundling protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11664  EPDNEW_H11667  EPDNEW_H11669  EPDNEW_H11670  EPDNEW_H11666  EPDNEW_H11671  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,590,034 - 127,590,094EPDNEW
RGD ID:7211845
Promoter ID:EPDNEW_H11669
Type:initiation region
Name:FSCN3_7
Description:fascin actin-bundling protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11664  EPDNEW_H11667  EPDNEW_H11668  EPDNEW_H11670  EPDNEW_H11666  EPDNEW_H11671  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,591,018 - 127,591,078EPDNEW
RGD ID:7211847
Promoter ID:EPDNEW_H11670
Type:initiation region
Name:FSCN3_5
Description:fascin actin-bundling protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11664  EPDNEW_H11667  EPDNEW_H11668  EPDNEW_H11669  EPDNEW_H11666  EPDNEW_H11671  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,591,310 - 127,591,370EPDNEW
RGD ID:7211851
Promoter ID:EPDNEW_H11671
Type:initiation region
Name:FSCN3_6
Description:fascin actin-bundling protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11664  EPDNEW_H11667  EPDNEW_H11668  EPDNEW_H11669  EPDNEW_H11670  EPDNEW_H11666  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387127,593,659 - 127,593,719EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q31.33-32.3(chr7:126859732-132750936)x1 copy number loss See cases [RCV000054171] Chr7:126859732..132750936 [GRCh38]
Chr7:126499786..132435696 [GRCh37]
Chr7:126287022..132086236 [NCBI36]
Chr7:7q31.33-32.3
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3
pathogenic
GRCh38/hg38 7q31.32-32.1(chr7:123829366-127947731)x1 copy number loss See cases [RCV000137416] Chr7:123829366..127947731 [GRCh38]
Chr7:123469420..127587784 [GRCh37]
Chr7:123256656..127375020 [NCBI36]
Chr7:7q31.32-32.1
likely pathogenic
GRCh38/hg38 7q31.2-33(chr7:117326805-134790689)x1 copy number loss See cases [RCV000138226] Chr7:117326805..134790689 [GRCh38]
Chr7:116966859..134475440 [GRCh37]
Chr7:116754095..134125980 [NCBI36]
Chr7:7q31.2-33
pathogenic
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 copy number gain See cases [RCV000138847] Chr7:121863759..159335865 [GRCh38]
Chr7:121503813..159128555 [GRCh37]
Chr7:121291049..158821316 [NCBI36]
Chr7:7q31.32-36.3
pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 copy number gain See cases [RCV000141413] Chr7:115459015..159325817 [GRCh38]
Chr7:115099069..159118507 [GRCh37]
Chr7:114886305..158811268 [NCBI36]
Chr7:7q31.2-36.3
pathogenic
GRCh38/hg38 7q31.33-33(chr7:124170657-134163594)x1 copy number loss See cases [RCV000142552] Chr7:124170657..134163594 [GRCh38]
Chr7:123810711..133848346 [GRCh37]
Chr7:123597947..133498886 [NCBI36]
Chr7:7q31.33-33
pathogenic
GRCh38/hg38 7q31.32-32.1(chr7:122018122-128907727)x1 copy number loss See cases [RCV000142521] Chr7:122018122..128907727 [GRCh38]
Chr7:121658176..128547780 [GRCh37]
Chr7:121445412..128335016 [NCBI36]
Chr7:7q31.32-32.1
pathogenic
GRCh37/hg19 7q31.1-32.1(chr7:111613396-127897316)x1 copy number loss See cases [RCV000240177] Chr7:111613396..127897316 [GRCh37]
Chr7:7q31.1-32.1
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q32.1(chr7:127186082-127723736)x3 copy number gain See cases [RCV000512583] Chr7:127186082..127723736 [GRCh37]
Chr7:7q32.1
uncertain significance
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q31.32-32.2(chr7:121480906-129389003)x1 copy number loss not provided [RCV000847911] Chr7:121480906..129389003 [GRCh37]
Chr7:7q31.32-32.2
pathogenic
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3961 AgrOrtholog
COSMIC FSCN3 COSMIC
Ensembl Genes ENSG00000106328 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000265825 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000402472 UniProtKB/TrEMBL
  ENSP00000473531 UniProtKB/TrEMBL
Ensembl Transcript ENST00000265825 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000421705 UniProtKB/TrEMBL
  ENST00000478821 UniProtKB/TrEMBL
GTEx ENSG00000106328 GTEx
HGNC ID HGNC:3961 ENTREZGENE
Human Proteome Map FSCN3 Human Proteome Map
InterPro Actin-crosslinking UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Fascin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Fascin-domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Fascin_metazoans UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FSCN3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:29999 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 29999 ENTREZGENE
OMIM 615800 OMIM
PANTHER PTHR10551 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10551:SF1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Fascin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA28379 PharmGKB
PIRSF Fascin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50405 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A140VK18 ENTREZGENE, UniProtKB/TrEMBL
  F8WDZ8_HUMAN UniProtKB/TrEMBL
  FSCN3_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  R4GN86_HUMAN UniProtKB/TrEMBL
UniProt Secondary A4D0Z2 UniProtKB/Swiss-Prot
  A6NLL7 UniProtKB/Swiss-Prot
  B2RA62 UniProtKB/Swiss-Prot
  B4DU68 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-01 FSCN3  fascin actin-bundling protein 3    fascin actin-bundling protein 3, testicular  Symbol and/or name change 5135510 APPROVED
2014-02-11 FSCN3  fascin actin-bundling protein 3, testicular    fascin homolog 3, actin-bundling protein, testicular (Strongylocentrotus purpuratus)  Symbol and/or name change 5135510 APPROVED