VGLL4 (vestigial like family member 4) - Rat Genome Database

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Gene: VGLL4 (vestigial like family member 4) Homo sapiens
Analyze
Symbol: VGLL4
Name: vestigial like family member 4
RGD ID: 1323223
HGNC Page HGNC:28966
Description: Predicted to enable transcription coactivator binding activity. Involved in negative regulation of Wnt signaling pathway; negative regulation of cell growth; and negative regulation of hippo signaling. Predicted to be located in nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: KIAA0121; transcription cofactor vestigial-like protein 4; vestigial like 4; Vestigial-like 4; vestigial-like family member 4; VGL-4
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38311,556,067 - 11,721,815 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl311,556,069 - 11,771,350 (-)EnsemblGRCh38hg38GRCh38
GRCh37311,597,541 - 11,762,013 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36311,572,544 - 11,737,037 (-)NCBINCBI36Build 36hg18NCBI36
Build 34311,572,543 - 11,737,037NCBI
Celera311,532,949 - 11,697,489 (-)NCBICelera
Cytogenetic Map3p25.3-p25.2NCBI
HuRef311,531,091 - 11,695,667 (-)NCBIHuRef
CHM1_1311,547,671 - 11,712,219 (-)NCBICHM1_1
T2T-CHM13v2.0311,551,371 - 11,717,542 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VGLL4HumanNeurodevelopmental Disorders  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Neurodevelopmental disorderClinVarPMID:25741868

1 to 20 of 101 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VGLL4Human(1->4)-beta-D-glucan multiple interactionsISOVgll4 (Mus musculus)6480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of VGLL4 mRNACTDPMID:36331819
VGLL4Human17alpha-ethynylestradiol affects expressionISOVgll4 (Mus musculus)6480464Ethinyl Estradiol affects the expression of VGLL4 mRNACTDPMID:17555576
VGLL4Human17alpha-ethynylestradiol multiple interactionsISOVgll4 (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of VGLL4 mRNACTDPMID:17942748
VGLL4Human17alpha-ethynylestradiol increases expressionISOVgll4 (Mus musculus)6480464Ethinyl Estradiol results in increased expression of VGLL4 mRNACTDPMID:17942748
VGLL4Human2,2',4,4'-Tetrabromodiphenyl ether increases expressionISOVgll4 (Rattus norvegicus)64804642 more ...CTDPMID:27291303
VGLL4Human2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOVgll4 (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of VGLL4 mRNACTDPMID:17942748
VGLL4Human2,3,7,8-tetrachlorodibenzodioxine affects expressionISOVgll4 (Rattus norvegicus)6480464Tetrachlorodibenzodioxin affects the expression of VGLL4 mRNACTDPMID:34747641
VGLL4Human2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOVgll4 (Mus musculus)6480464Tetrachlorodibenzodioxin results in decreased expression of VGLL4 mRNACTDPMID:26290441
VGLL4Human2,3,7,8-tetrachlorodibenzodioxine affects expressionISOVgll4 (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of VGLL4 mRNACTDPMID:21570461
VGLL4Human2-methylcholine affects expressionEXP 6480464beta-methylcholine affects the expression of VGLL4 mRNACTDPMID:21179406
VGLL4Human3-isobutyl-1-methyl-7H-xanthine multiple interactionsEXP 6480464[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of VGLL4 mRNACTDPMID:28628672
VGLL4Human4,4'-diaminodiphenylmethane decreases expressionISOVgll4 (Mus musculus)64804644 and 4'-diaminodiphenylmethane results in decreased expression of VGLL4 mRNACTDPMID:18648102
VGLL4Human4,4'-sulfonyldiphenol multiple interactionsEXP 6480464[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in increased expression of VGLL4 mRNACTDPMID:28628672
VGLL4Human4,4'-sulfonyldiphenol affects methylationISOVgll4 (Mus musculus)6480464bisphenol S affects the methylation of VGLL4 geneCTDPMID:31683443
VGLL4Human4,4'-sulfonyldiphenol decreases methylationISOVgll4 (Mus musculus)6480464bisphenol S results in decreased methylation of VGLL4 exonCTDPMID:33297965
VGLL4Human4-hydroxyphenyl retinamide increases expressionISOVgll4 (Mus musculus)6480464Fenretinide results in increased expression of VGLL4 mRNACTDPMID:28973697
VGLL4Humanaflatoxin B1 increases methylationEXP 6480464Aflatoxin B1 results in increased methylation of VGLL4 gene and Aflatoxin B1 results in increased methylation of VGLL4 intronCTDPMID:27153756 and PMID:30157460
VGLL4HumanAflatoxin B2 alpha increases methylationEXP 6480464aflatoxin B2 results in increased methylation of VGLL4 intronCTDPMID:30157460
VGLL4Humanamphetamine decreases expressionISOVgll4 (Rattus norvegicus)6480464Amphetamine results in decreased expression of VGLL4 mRNACTDPMID:30779732
VGLL4Humanantimycin A decreases expressionEXP 6480464Antimycin A results in decreased expression of VGLL4 mRNACTDPMID:33512557

1 to 20 of 101 rows

Biological Process
1 to 9 of 9 rows

  
1 to 9 of 9 rows

Cellular Component

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
VGLL4Humannucleus located_inISSUniProtKB:Q80V24150520179 UniProtGO_REF:0000024
VGLL4Humannucleus located_inIEAUniProtKB-KW:KW-0539150520179 UniProtGO_REF:0000043
VGLL4Humannucleus located_inIEAUniProtKB-SubCell:SL-0191150520179 UniProtGO_REF:0000044

Molecular Function

  


#
Reference Title
Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
PMID:8590280   PMID:8889548   PMID:12477932   PMID:14702039   PMID:15140898   PMID:15489334   PMID:16344560   PMID:18029348   PMID:19240061   PMID:19322201   PMID:20379614   PMID:20702774  
PMID:21044950   PMID:21079607   PMID:21839727   PMID:21873635   PMID:22094256   PMID:23319000   PMID:23765749   PMID:24068947   PMID:24458094   PMID:24525233   PMID:24983835   PMID:25352025  
PMID:25429064   PMID:25701461   PMID:26186194   PMID:26460480   PMID:26760575   PMID:26972000   PMID:28042509   PMID:28051067   PMID:28514442   PMID:28611215   PMID:28733631   PMID:28739871  
PMID:29117863   PMID:29512748   PMID:29513927   PMID:29882479   PMID:30396996   PMID:31559693   PMID:31748508   PMID:32296183   PMID:33141998   PMID:33506898   PMID:33961781   PMID:34004031  
PMID:34075638   PMID:34396425   PMID:35140242   PMID:35563538   PMID:36657637   PMID:38334954  



VGLL4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38311,556,067 - 11,721,815 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl311,556,069 - 11,771,350 (-)EnsemblGRCh38hg38GRCh38
GRCh37311,597,541 - 11,762,013 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36311,572,544 - 11,737,037 (-)NCBINCBI36Build 36hg18NCBI36
Build 34311,572,543 - 11,737,037NCBI
Celera311,532,949 - 11,697,489 (-)NCBICelera
Cytogenetic Map3p25.3-p25.2NCBI
HuRef311,531,091 - 11,695,667 (-)NCBIHuRef
CHM1_1311,547,671 - 11,712,219 (-)NCBICHM1_1
T2T-CHM13v2.0311,551,371 - 11,717,542 (-)NCBIT2T-CHM13v2.0
Vgll4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm396114,836,850 - 114,946,932 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl6114,837,589 - 114,946,955 (-)EnsemblGRCm39 Ensembl
GRCm386114,860,621 - 114,970,007 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl6114,860,628 - 114,969,994 (-)EnsemblGRCm38mm10GRCm38
MGSCv376114,812,108 - 114,871,770 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv366114,827,709 - 114,887,371 (-)NCBIMGSCv36mm8
Celera6116,699,571 - 116,759,386 (-)NCBICelera
Cytogenetic Map6E3NCBI
cM Map653.07NCBI
Vgll4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr84149,598,151 - 149,711,186 (-)NCBIGRCr8
mRatBN7.24147,925,630 - 148,038,519 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl4147,927,034 - 148,038,471 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx4154,151,173 - 154,264,033 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.04149,934,223 - 150,047,087 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.04148,558,058 - 148,670,911 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.04146,778,556 - 146,890,063 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4146,779,276 - 146,839,397 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04210,069,578 - 210,129,654 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44150,995,533 - 151,055,736 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.14151,240,377 - 151,300,577 (-)NCBI
Celera4136,824,155 - 136,883,668 (-)NCBICelera
Cytogenetic Map4q42NCBI
Vgll4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542914,303,682 - 14,400,743 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495542914,301,509 - 14,413,163 (-)NCBIChiLan1.0ChiLan1.0
VGLL4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2211,549,922 - 11,715,904 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1311,554,683 - 11,719,713 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0311,489,805 - 11,654,507 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1311,834,746 - 11,999,783 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl311,834,746 - 11,981,877 (-)Ensemblpanpan1.1panPan2
VGLL4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1206,751,951 - 6,915,650 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl206,751,801 - 6,913,201 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha206,788,411 - 6,951,089 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0206,781,024 - 6,944,924 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl206,780,872 - 6,973,869 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1206,498,117 - 6,661,200 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0206,854,645 - 7,017,774 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0206,825,251 - 6,988,564 (+)NCBIUU_Cfam_GSD_1.0
Vgll4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494216,971,272 - 17,120,226 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366021,815,313 - 1,936,031 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366021,789,479 - 1,938,440 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
VGLL4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1367,698,083 - 67,872,486 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11367,698,082 - 67,873,119 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21374,916,759 - 74,947,883 (-)NCBISscrofa10.2Sscrofa10.2susScr3
VGLL4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12247,572,345 - 47,734,089 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2247,574,828 - 47,658,057 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666041118,782,175 - 118,944,113 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Vgll4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624943113,215 - 232,216 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in VGLL4
51 total Variants

1 to 10 of 81 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
GRCh38/hg38 3p25.3-25.2(chr3:8581778-12015238)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051480]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051480]|See cases [RCV000051480] Chr3:8581778..12015238 [GRCh38]
Chr3:8623464..12056738 [GRCh37]
Chr3:8598464..12031738 [NCBI36]
Chr3:3p25.3-25.2
pathogenic
GRCh38/hg38 3p25.3-25.2(chr3:10019780-12251358)x1 copy number loss See cases [RCV000051506] Chr3:10019780..12251358 [GRCh38]
Chr3:10061464..12292857 [GRCh37]
Chr3:10036464..12267857 [NCBI36]
Chr3:3p25.3-25.2
pathogenic
GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3 copy number gain See cases [RCV000051097] Chr3:52266..37148076 [GRCh38]
Chr3:93949..37189567 [GRCh37]
Chr3:68949..37164571 [NCBI36]
Chr3:3p26.3-22.2
pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:52066-20280127)x3 copy number gain See cases [RCV000051690] Chr3:52066..20280127 [GRCh38]
Chr3:93749..20321619 [GRCh37]
Chr3:68749..20296623 [NCBI36]
Chr3:3p26.3-24.3
pathogenic
GRCh38/hg38 3p26.3-24.1(chr3:52266-29248782)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051718]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051718]|See cases [RCV000051718] Chr3:52266..29248782 [GRCh38]
Chr3:93949..29290273 [GRCh37]
Chr3:68949..29265277 [NCBI36]
Chr3:3p26.3-24.1
pathogenic
GRCh38/hg38 3p26.3-24.3(chr3:63843-19510600)x3 copy number gain See cases [RCV000051719] Chr3:63843..19510600 [GRCh38]
Chr3:105526..19552092 [GRCh37]
Chr3:80526..19527096 [NCBI36]
Chr3:3p26.3-24.3
pathogenic
GRCh38/hg38 3p25.3-22.2(chr3:11463328-38919543)x3 copy number gain See cases [RCV000051720] Chr3:11463328..38919543 [GRCh38]
Chr3:11504802..38961034 [GRCh37]
Chr3:11479802..38936038 [NCBI36]
Chr3:3p25.3-22.2
pathogenic
GRCh38/hg38 3p25.3-25.2(chr3:9394874-11690612)x1 copy number loss See cases [RCV000137433] Chr3:9394874..11690612 [GRCh38]
Chr3:9436558..11732086 [GRCh37]
Chr3:9411558..11707086 [NCBI36]
Chr3:3p25.3-25.2
pathogenic
GRCh38/hg38 3p26.1-25.2(chr3:7975734-12636917)x3 copy number gain See cases [RCV000137309] Chr3:7975734..12636917 [GRCh38]
Chr3:8017421..12678416 [GRCh37]
Chr3:7992421..12653416 [NCBI36]
Chr3:3p26.1-25.2
likely pathogenic
GRCh38/hg38 3p26.3-25.2(chr3:32241-12681483)x1 copy number loss See cases [RCV000138143] Chr3:32241..12681483 [GRCh38]
Chr3:73914..12722982 [GRCh37]
Chr3:48914..12697982 [NCBI36]
Chr3:3p26.3-25.2
pathogenic
1 to 10 of 81 rows

Predicted Target Of
Summary Value
Count of predictions:5843
Count of miRNA genes:1229
Interacting mature miRNAs:1574
Transcripts:ENST00000273038, ENST00000404339, ENST00000413604, ENST00000417206, ENST00000417466, ENST00000418000, ENST00000419541, ENST00000424529, ENST00000424709, ENST00000426568, ENST00000430365, ENST00000437722, ENST00000445411, ENST00000451674, ENST00000458499, ENST00000463387, ENST00000480288
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.


1 to 10 of 55 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
407023043GWAS672019_HHVA measurement QTL GWAS672019 (human)0.000002HVA measurement31158394011583941Human
597210905GWAS1306979_Hbirth weight, parental genotype effect measurement QTL GWAS1306979 (human)3e-08birth weight, parental genotype effect measurementneonatal body weight (CMO:0002079)31159503411595035Human
597134998GWAS1231072_Hdiastolic blood pressure QTL GWAS1231072 (human)6e-09diastolic blood pressurediastolic blood pressure (CMO:0000005)31163595311635954Human
596954134GWAS1073653_Hbody mass index QTL GWAS1073653 (human)1e-10body mass index31158794611587947Human
597317144GWAS1413218_Hbody surface area QTL GWAS1413218 (human)3e-09body surface area31158877811588779Human
597105683GWAS1201757_Hcortex volume change measurement, age at assessment QTL GWAS1201757 (human)0.000004cortex volume change measurement, age at assessment31162799711627998Human
597280669GWAS1376743_HBMI-adjusted hip circumference QTL GWAS1376743 (human)2e-09BMI-adjusted hip circumferencehip circumference (CMO:0000014)31166026011660261Human
597280668GWAS1376742_HBMI-adjusted hip circumference QTL GWAS1376742 (human)4e-10BMI-adjusted hip circumferencehip circumference (CMO:0000014)31156772411567725Human
597238815GWAS1334889_Happendicular lean mass QTL GWAS1334889 (human)6e-13appendicular lean mass31158877811588779Human
406894539GWAS543515_HHVA measurement, 5-HIAA measurement QTL GWAS543515 (human)0.000008HVA measurement, 5-HIAA measurementcervical spinal cord 5-HIAA level (CMO:0003127)31158394011583941Human

1 to 10 of 55 rows
D3S3714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,668,640 - 11,668,792UniSTSGRCh37
Build 36311,643,640 - 11,643,792RGDNCBI36
Celera311,603,945 - 11,604,097RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,602,119 - 11,602,271UniSTS
Marshfield Genetic Map336.65RGD
Marshfield Genetic Map336.65UniSTS
Genethon Genetic Map330.4UniSTS
deCODE Assembly Map330.16UniSTS
Whitehead-YAC Contig Map3 UniSTS
D3S3680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,726,147 - 11,726,272UniSTSGRCh37
Build 36311,701,147 - 11,701,272RGDNCBI36
Celera311,661,430 - 11,661,555RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,659,594 - 11,659,721UniSTS
Marshfield Genetic Map336.1RGD
Marshfield Genetic Map336.1UniSTS
Genethon Genetic Map330.4UniSTS
deCODE Assembly Map330.13UniSTS
Stanford-G3 RH Map3522.0UniSTS
Whitehead-YAC Contig Map3 UniSTS
NCBI RH Map3138.4UniSTS
GeneMap99-G3 RH Map3522.0UniSTS
RH15949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,597,593 - 11,597,730UniSTSGRCh37
Build 36311,572,593 - 11,572,730RGDNCBI36
Celera311,532,998 - 11,533,135RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,531,140 - 11,531,277UniSTS
GeneMap99-GB4 RH Map350.67UniSTS
NCBI RH Map3166.8UniSTS
SHGC-76714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,738,901 - 11,739,043UniSTSGRCh37
Build 36311,713,901 - 11,714,043RGDNCBI36
Celera311,674,186 - 11,674,328RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,672,353 - 11,672,495UniSTS
GeneMap99-GB4 RH Map352.69UniSTS
NCBI RH Map3162.3UniSTS
RH25345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,597,726 - 11,597,968UniSTSGRCh37
Build 36311,572,726 - 11,572,968RGDNCBI36
Celera311,533,131 - 11,533,373RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,531,273 - 11,531,515UniSTS
SHGC-144750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,603,851 - 11,604,172UniSTSGRCh37
Build 36311,578,851 - 11,579,172RGDNCBI36
Celera311,539,257 - 11,539,578RGD
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map3p25.3UniSTS
HuRef311,537,399 - 11,537,720UniSTS
TNG Radiation Hybrid Map37007.0UniSTS
SHGC-76706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,598,868 - 11,598,998UniSTSGRCh37
Build 36311,573,868 - 11,573,998RGDNCBI36
Celera311,534,273 - 11,534,403RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,532,415 - 11,532,545UniSTS
TNG Radiation Hybrid Map36990.0UniSTS
GeneMap99-GB4 RH Map350.67UniSTS
NCBI RH Map3165.6UniSTS
SHGC-76717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,599,342 - 11,599,524UniSTSGRCh37
Build 36311,574,342 - 11,574,524RGDNCBI36
Celera311,534,747 - 11,534,929RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,532,889 - 11,533,071UniSTS
TNG Radiation Hybrid Map37002.0UniSTS
GeneMap99-GB4 RH Map352.79UniSTS
NCBI RH Map3132.9UniSTS
RH36277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,704,043 - 11,704,142UniSTSGRCh37
Build 36311,679,043 - 11,679,142RGDNCBI36
Celera311,639,328 - 11,639,427RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,637,494 - 11,637,593UniSTS
GeneMap99-GB4 RH Map357.32UniSTS
NCBI RH Map3142.6UniSTS
D3S3828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,597,586 - 11,597,693UniSTSGRCh37
Build 36311,572,586 - 11,572,693RGDNCBI36
Celera311,532,991 - 11,533,098RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,531,133 - 11,531,240UniSTS
Whitehead-YAC Contig Map3 UniSTS
RH48202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37311,697,826 - 11,697,955UniSTSGRCh37
Build 36311,672,826 - 11,672,955RGDNCBI36
Celera311,633,109 - 11,633,238RGD
Cytogenetic Map3p25.3UniSTS
HuRef311,631,275 - 11,631,404UniSTS
GeneMap99-GB4 RH Map350.85UniSTS
NCBI RH Map3164.5UniSTS




adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2251 4971 1725 2351 5 622 1951 465 2269 7303 6469 53 3732 852 1744 1617 174 1


1 to 30 of 59 rows
RefSeq Transcripts NM_001128219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001128220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001128221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001284390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001284391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014667 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011534269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017007542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453836 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047449263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054348507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC022001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC090939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI809612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 30 of 59 rows

Ensembl Acc Id: ENST00000273038   ⟹   ENSP00000273038
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,556,070 - 11,720,746 (-)Ensembl
Ensembl Acc Id: ENST00000413604   ⟹   ENSP00000404624
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,558,069 - 11,604,581 (-)Ensembl
Ensembl Acc Id: ENST00000414047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,720,456 - 11,724,979 (-)Ensembl
Ensembl Acc Id: ENST00000417206   ⟹   ENSP00000391932
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,564,766 - 11,719,638 (-)Ensembl
Ensembl Acc Id: ENST00000417466   ⟹   ENSP00000411670
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,564,848 - 11,719,619 (-)Ensembl
Ensembl Acc Id: ENST00000418000   ⟹   ENSP00000394439
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,559,332 - 11,719,594 (-)Ensembl
Ensembl Acc Id: ENST00000419541   ⟹   ENSP00000395557
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,564,892 - 11,710,537 (-)Ensembl
Ensembl Acc Id: ENST00000424529   ⟹   ENSP00000402878
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,558,470 - 11,568,924 (-)Ensembl
Ensembl Acc Id: ENST00000424709   ⟹   ENSP00000391554
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,564,852 - 11,612,667 (-)Ensembl
Ensembl Acc Id: ENST00000426568   ⟹   ENSP00000413030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,558,476 - 11,720,722 (-)Ensembl
Ensembl Acc Id: ENST00000430365   ⟹   ENSP00000404251
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,556,069 - 11,643,915 (-)Ensembl
Ensembl Acc Id: ENST00000437722   ⟹   ENSP00000393100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,564,915 - 11,610,504 (-)Ensembl
Ensembl Acc Id: ENST00000445411   ⟹   ENSP00000412923
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,558,758 - 11,720,729 (-)Ensembl
Ensembl Acc Id: ENST00000451674   ⟹   ENSP00000416615
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,558,343 - 11,582,391 (-)Ensembl
Ensembl Acc Id: ENST00000458499   ⟹   ENSP00000394123
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,559,351 - 11,627,406 (-)Ensembl
Ensembl Acc Id: ENST00000463387
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,699,546 - 11,720,460 (-)Ensembl
Ensembl Acc Id: ENST00000480288
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,601,992 - 11,633,671 (-)Ensembl
Ensembl Acc Id: ENST00000623028   ⟹   ENSP00000485472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,601,910 - 11,771,350 (-)Ensembl
Ensembl Acc Id: ENST00000638314   ⟹   ENSP00000492281
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl311,702,696 - 11,703,034 (-)Ensembl
RefSeq Acc Id: NM_001128219   ⟹   NP_001121691
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,643,915 (-)NCBI
GRCh37311,597,543 - 11,762,220 (-)NCBI
Celera311,532,949 - 11,697,489 (-)RGD
HuRef311,531,088 - 11,695,689 (-)NCBI
CHM1_1311,547,668 - 11,634,617 (-)NCBI
T2T-CHM13v2.0311,551,373 - 11,639,661 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001128220   ⟹   NP_001121692
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,582,356 (-)NCBI
GRCh37311,597,543 - 11,762,220 (-)NCBI
Celera311,532,949 - 11,697,489 (-)RGD
HuRef311,531,088 - 11,695,689 (-)NCBI
CHM1_1311,547,668 - 11,573,975 (-)NCBI
T2T-CHM13v2.0311,551,373 - 11,577,605 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001128221   ⟹   NP_001121693
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,568,798 (-)NCBI
GRCh37311,597,543 - 11,762,220 (-)NCBI
Celera311,532,949 - 11,697,489 (-)RGD
HuRef311,531,088 - 11,695,689 (-)NCBI
CHM1_1311,547,668 - 11,560,526 (-)NCBI
T2T-CHM13v2.0311,551,373 - 11,564,104 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001284390   ⟹   NP_001271319
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,720,539 (-)NCBI
HuRef311,531,088 - 11,695,689 (-)NCBI
CHM1_1311,547,668 - 11,712,241 (-)NCBI
T2T-CHM13v2.0311,551,373 - 11,716,266 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001284391   ⟹   NP_001271320
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,067 - 11,604,581 (-)NCBI
HuRef311,531,088 - 11,695,689 (-)NCBI
CHM1_1311,547,668 - 11,599,132 (-)NCBI
T2T-CHM13v2.0311,551,371 - 11,600,403 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014667   ⟹   NP_055482
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,720,539 (-)NCBI
GRCh37311,597,543 - 11,762,220 (-)NCBI
Build 36311,572,544 - 11,737,037 (-)NCBI Archive
Celera311,532,949 - 11,697,489 (-)RGD
HuRef311,531,088 - 11,695,689 (-)NCBI
CHM1_1311,547,668 - 11,712,241 (-)NCBI
T2T-CHM13v2.0311,551,373 - 11,716,266 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011534269   ⟹   XP_011532571
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,067 - 11,610,370 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024453835   ⟹   XP_024309603
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,067 - 11,719,529 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024453836   ⟹   XP_024309604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,067 - 11,710,814 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024453837   ⟹   XP_024309605
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,719,529 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047449259   ⟹   XP_047305215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,067 - 11,721,815 (-)NCBI
RefSeq Acc Id: XM_047449260   ⟹   XP_047305216
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,067 - 11,702,998 (-)NCBI
RefSeq Acc Id: XM_047449261   ⟹   XP_047305217
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,067 - 11,633,421 (-)NCBI
RefSeq Acc Id: XM_047449262   ⟹   XP_047305218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,721,815 (-)NCBI
RefSeq Acc Id: XM_047449263   ⟹   XP_047305219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,556,069 - 11,643,915 (-)NCBI
RefSeq Acc Id: XM_054348499   ⟹   XP_054204474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,371 - 11,717,542 (-)NCBI
RefSeq Acc Id: XM_054348500   ⟹   XP_054204475
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,371 - 11,698,729 (-)NCBI
RefSeq Acc Id: XM_054348501   ⟹   XP_054204476
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,371 - 11,715,394 (-)NCBI
RefSeq Acc Id: XM_054348502   ⟹   XP_054204477
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,371 - 11,706,534 (-)NCBI
RefSeq Acc Id: XM_054348503   ⟹   XP_054204478
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,371 - 11,629,168 (-)NCBI
RefSeq Acc Id: XM_054348504   ⟹   XP_054204479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,373 - 11,717,542 (-)NCBI
RefSeq Acc Id: XM_054348505   ⟹   XP_054204480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,373 - 11,639,661 (-)NCBI
RefSeq Acc Id: XM_054348506   ⟹   XP_054204481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,373 - 11,715,275 (-)NCBI
RefSeq Acc Id: XM_054348507   ⟹   XP_054204482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0311,551,371 - 11,606,131 (-)NCBI
1 to 30 of 56 rows
Protein RefSeqs NP_001121691 (Get FASTA)   NCBI Sequence Viewer  
  NP_001121692 (Get FASTA)   NCBI Sequence Viewer  
  NP_001121693 (Get FASTA)   NCBI Sequence Viewer  
  NP_001271319 (Get FASTA)   NCBI Sequence Viewer  
  NP_001271320 (Get FASTA)   NCBI Sequence Viewer  
  NP_055482 (Get FASTA)   NCBI Sequence Viewer  
  XP_011532571 (Get FASTA)   NCBI Sequence Viewer  
  XP_024309603 (Get FASTA)   NCBI Sequence Viewer  
  XP_024309604 (Get FASTA)   NCBI Sequence Viewer  
  XP_024309605 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305215 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305216 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305217 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305218 (Get FASTA)   NCBI Sequence Viewer  
  XP_047305219 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204474 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204475 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204476 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204477 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204478 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204479 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204480 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204481 (Get FASTA)   NCBI Sequence Viewer  
  XP_054204482 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH01514 (Get FASTA)   NCBI Sequence Viewer  
  AAH03038 (Get FASTA)   NCBI Sequence Viewer  
  ABD48891 (Get FASTA)   NCBI Sequence Viewer  
  ABD48892 (Get FASTA)   NCBI Sequence Viewer  
  ABD48893 (Get FASTA)   NCBI Sequence Viewer  
  ABD48894 (Get FASTA)   NCBI Sequence Viewer  
1 to 30 of 56 rows
1 to 5 of 40 rows
1 to 5 of 40 rows
RefSeq Acc Id: NP_055482   ⟸   NM_014667
- Peptide Label: isoform b
- UniProtKB: Q9BQ78 (UniProtKB/Swiss-Prot),   Q7L5V0 (UniProtKB/Swiss-Prot),   Q14135 (UniProtKB/Swiss-Prot),   J3KN68 (UniProtKB/Swiss-Prot),   G5E9M7 (UniProtKB/Swiss-Prot),   B4DTS7 (UniProtKB/Swiss-Prot),   A0A075B6E4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001121691   ⟸   NM_001128219
- Peptide Label: isoform a
- Sequence:
RefSeq Acc Id: NP_001121692   ⟸   NM_001128220
- Peptide Label: isoform c
- UniProtKB: Q0H0I7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001121693   ⟸   NM_001128221
- Peptide Label: isoform d
- UniProtKB: Q0H0I7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001271319   ⟸   NM_001284390
- Peptide Label: isoform e
- UniProtKB: A0A0A6YYI5 (UniProtKB/TrEMBL)
- Sequence:

Name Modeler Protein Id AA Range Protein Structure
AF-Q14135-F1-model_v2 AlphaFold Q14135 1-290 view protein structure

RGD ID:6863590
Promoter ID:EPDNEW_H4960
Type:initiation region
Name:VGLL4_1
Description:vestigial like family member 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4961  EPDNEW_H4962  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,582,356 - 11,582,416EPDNEW
RGD ID:6801930
Promoter ID:HG_KWN:43750
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:NM_001128221,   OTTHUMT00000339146
Position:
Human AssemblyChrPosition (strand)Source
Build 36311,584,961 - 11,586,012 (-)MPROMDB
RGD ID:6801927
Promoter ID:HG_KWN:43751
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000339140
Position:
Human AssemblyChrPosition (strand)Source
Build 36311,598,421 - 11,598,921 (-)MPROMDB
RGD ID:6812445
Promoter ID:HG_ACW:52861
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:VGLL4.LAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 36311,618,156 - 11,618,656 (-)MPROMDB
RGD ID:6801926
Promoter ID:HG_KWN:43752
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000339139
Position:
Human AssemblyChrPosition (strand)Source
Build 36311,620,466 - 11,620,966 (-)MPROMDB
RGD ID:6801924
Promoter ID:HG_KWN:43757
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:NM_001128219
Position:
Human AssemblyChrPosition (strand)Source
Build 36311,660,099 - 11,660,599 (-)MPROMDB
RGD ID:6863592
Promoter ID:EPDNEW_H4961
Type:initiation region
Name:VGLL4_3
Description:vestigial like family member 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4960  EPDNEW_H4962  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,720,539 - 11,720,599EPDNEW
RGD ID:6863594
Promoter ID:EPDNEW_H4962
Type:initiation region
Name:VGLL4_2
Description:vestigial like family member 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H4960  EPDNEW_H4961  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38311,720,746 - 11,720,806EPDNEW
RGD ID:6801931
Promoter ID:HG_KWN:43759
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_2Hour,   HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000339231,   OTTHUMT00000339232,   OTTHUMT00000339233
Position:
Human AssemblyChrPosition (strand)Source
Build 36311,735,906 - 11,736,502 (-)MPROMDB
RGD ID:6801929
Promoter ID:HG_KWN:43761
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_014667,   OTTHUMT00000339147,   OTTHUMT00000339230,   UC003BWG.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36311,736,844 - 11,737,344 (-)MPROMDB


1 to 40 of 55 rows
Database
Acc Id
Source(s)
COSMIC VGLL4 COSMIC
Ensembl Genes ENSG00000144560 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000273038 ENTREZGENE
  ENST00000273038.7 UniProtKB/Swiss-Prot
  ENST00000413604 ENTREZGENE
  ENST00000418000 ENTREZGENE
  ENST00000424529 ENTREZGENE
  ENST00000424529.6 UniProtKB/Swiss-Prot
  ENST00000426568 ENTREZGENE
  ENST00000430365 ENTREZGENE
  ENST00000430365.7 UniProtKB/Swiss-Prot
  ENST00000451674 ENTREZGENE
  ENST00000451674.6 UniProtKB/Swiss-Prot
GTEx ENSG00000144560 GTEx
HGNC ID HGNC:28966 ENTREZGENE
Human Proteome Map VGLL4 Human Proteome Map
InterPro TDU_repeat UniProtKB/Swiss-Prot
  VGLL4 UniProtKB/Swiss-Prot
KEGG Report hsa:9686 UniProtKB/Swiss-Prot
NCBI Gene 9686 ENTREZGENE
OMIM 618692 OMIM
PANTHER PTHR17604 UniProtKB/Swiss-Prot
  TRANSCRIPTION COFACTOR VESTIGIAL-LIKE PROTEIN 4 UniProtKB/Swiss-Prot
Pfam VGLL4 UniProtKB/Swiss-Prot
PharmGKB PA128394553 PharmGKB
SMART TDU UniProtKB/Swiss-Prot
UniProt A0A024R2F0 ENTREZGENE
  A0A075B6E4 ENTREZGENE
  A0A096LP98_HUMAN UniProtKB/TrEMBL
  A0A0A6YYI5 ENTREZGENE, UniProtKB/TrEMBL
  A0A9K3Y712 ENTREZGENE
  B4DTS7 ENTREZGENE
  C9JBN2_HUMAN UniProtKB/TrEMBL
  C9JX59_HUMAN UniProtKB/TrEMBL
  E7EQU6 ENTREZGENE, UniProtKB/TrEMBL
  E7ERW0 ENTREZGENE, UniProtKB/TrEMBL
  E7EUJ2_HUMAN UniProtKB/TrEMBL
  E7EWF5_HUMAN UniProtKB/TrEMBL
  F8W708_HUMAN UniProtKB/TrEMBL
  F8WBN7_HUMAN UniProtKB/TrEMBL
1 to 40 of 55 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-01 VGLL4  vestigial like family member 4    vestigial-like family member 4  Symbol and/or name change 5135510 APPROVED
2014-03-05 VGLL4  vestigial-like family member 4    vestigial like 4 (Drosophila)  Symbol and/or name change 5135510 APPROVED