RGL3 (ral guanine nucleotide dissociation stimulator like 3) - Rat Genome Database

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Gene: RGL3 (ral guanine nucleotide dissociation stimulator like 3) Homo sapiens
Analyze
Symbol: RGL3
Name: ral guanine nucleotide dissociation stimulator like 3
RGD ID: 1320262
HGNC Page HGNC:30282
Description: Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in Ras protein signal transduction. Predicted to be located in cytosol. Predicted to be active in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ00153; FLJ32585; FLJ44275; MGC126805; MGC138163; ral guanine nucleotide dissociation stimulator-like 3; ralGDS-like 3; RalGEF-like protein 3, mouse homolog
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
GRCh381911,394,060 - 11,419,314 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1911,384,341 - 11,419,328 (-)EnsemblGRCh38hg38GRCh38
GRCh371911,504,736 - 11,529,990 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361911,366,001 - 11,391,004 (-)NCBINCBI36Build 36hg18NCBI36
Celera1911,399,604 - 11,424,860 (-)NCBICelera
Cytogenetic Map19p13.2NCBI
HuRef1911,080,677 - 11,105,452 (-)NCBIHuRef
CHM1_11911,505,738 - 11,530,962 (-)NCBICHM1_1
T2T-CHM13v2.01911,521,038 - 11,546,286 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytosol  (TAS)
plasma membrane  (IBA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:14702039   PMID:16344560   PMID:19913121   PMID:20628086   PMID:21873635   PMID:30021884   PMID:32296183   PMID:33961781   PMID:37704626  


Genomics

Comparative Map Data
RGL3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381911,394,060 - 11,419,314 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1911,384,341 - 11,419,328 (-)EnsemblGRCh38hg38GRCh38
GRCh371911,504,736 - 11,529,990 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361911,366,001 - 11,391,004 (-)NCBINCBI36Build 36hg18NCBI36
Celera1911,399,604 - 11,424,860 (-)NCBICelera
Cytogenetic Map19p13.2NCBI
HuRef1911,080,677 - 11,105,452 (-)NCBIHuRef
CHM1_11911,505,738 - 11,530,962 (-)NCBICHM1_1
T2T-CHM13v2.01911,521,038 - 11,546,286 (-)NCBIT2T-CHM13v2.0
Rgl3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39921,882,475 - 21,900,765 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl921,880,007 - 21,900,742 (-)EnsemblGRCm39 Ensembl
GRCm38921,971,179 - 21,989,468 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl921,968,711 - 21,989,446 (-)EnsemblGRCm38mm10GRCm38
MGSCv37921,775,971 - 21,793,897 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36921,721,929 - 21,739,855 (-)NCBIMGSCv36mm8
Celera919,240,955 - 19,259,141 (-)NCBICelera
Cytogenetic Map9A3NCBI
cM Map97.96NCBI
Ralgdsl3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8828,775,187 - 28,796,765 (-)NCBIGRCr8
mRatBN7.2820,500,846 - 20,520,471 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl820,500,846 - 20,520,471 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx824,530,248 - 24,549,942 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0822,827,385 - 22,847,085 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0820,730,436 - 20,750,013 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0822,980,727 - 23,000,881 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl822,979,181 - 23,000,485 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0823,035,212 - 23,055,282 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4821,072,473 - 21,092,569 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1821,072,486 - 21,092,659 (-)NCBI
Celera821,891,406 - 21,910,979 (-)NCBICelera
Cytogenetic Map8q13NCBI
Rgl3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554952,305,053 - 2,316,841 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554952,304,820 - 2,319,171 (-)NCBIChiLan1.0ChiLan1.0
RGL3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22016,305,568 - 16,333,233 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11915,307,114 - 15,332,659 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01910,932,016 - 10,966,701 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11911,652,354 - 11,674,443 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1911,652,700 - 11,685,293 (-)Ensemblpanpan1.1panPan2
RGL3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12049,926,916 - 49,942,013 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2049,925,185 - 49,942,130 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2049,798,045 - 49,813,150 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02050,445,230 - 50,460,344 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2050,445,290 - 50,460,440 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12049,655,510 - 49,670,638 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02050,081,655 - 50,097,001 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02050,324,843 - 50,339,959 (+)NCBIUU_Cfam_GSD_1.0
Rgl3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118208,863,481 - 208,877,061 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366591,478,805 - 1,491,085 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366591,477,645 - 1,491,170 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ODAD3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl270,073,067 - 70,087,796 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1270,073,061 - 70,087,990 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2270,359,229 - 70,373,200 (+)NCBISscrofa10.2Sscrofa10.2susScr3
RGL3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1610,320,348 - 10,348,188 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660749,542,176 - 9,567,218 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Rgl3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248283,194,473 - 3,206,239 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248283,192,885 - 3,207,617 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in RGL3
89 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.2-13.13(chr19:8831147-13331227)x3 copy number gain See cases [RCV000052908] Chr19:8831147..13331227 [GRCh38]
Chr19:8941823..13442041 [GRCh37]
Chr19:8802823..13303041 [NCBI36]
Chr19:19p13.2-13.13		 likely pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:10315258-14048994)x3 copy number gain See cases [RCV000052909] Chr19:10315258..14048994 [GRCh38]
Chr19:10425934..14159806 [GRCh37]
Chr19:10286934..14020806 [NCBI36]
Chr19:19p13.2-13.12		 pathogenic
GRCh38/hg38 19p13.2(chr19:11138895-11549951)x3 copy number gain See cases [RCV000054109] Chr19:11138895..11549951 [GRCh38]
Chr19:11249571..11660766 [GRCh37]
Chr19:11110571..11521766 [NCBI36]
Chr19:19p13.2		 uncertain significance
GRCh38/hg38 19p13.2-13.12(chr19:11227942-14532135)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053944]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053944]|See cases [RCV000053944] Chr19:11227942..14532135 [GRCh38]
Chr19:11338618..14642947 [GRCh37]
Chr19:11199618..14503947 [NCBI36]
Chr19:19p13.2-13.12		 pathogenic
NM_001035223.3(RGL3):c.1808G>A (p.Arg603Gln) single nucleotide variant Malignant melanoma [RCV000071928] Chr19:11397536 [GRCh38]
Chr19:11508212 [GRCh37]
Chr19:11369212 [NCBI36]
Chr19:19p13.2		 not provided
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:10319474-13777860)x1 copy number loss See cases [RCV000141568] Chr19:10319474..13777860 [GRCh38]
Chr19:10430150..13888674 [GRCh37]
Chr19:10291150..13749674 [NCBI36]
Chr19:19p13.2-13.13		 pathogenic
GRCh37/hg19 19p13.2-13.12(chr19:9678768-14853426) copy number gain See cases [RCV000446985] Chr19:9678768..14853426 [GRCh37]
Chr19:19p13.2-13.12		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
NM_001035223.4(RGL3):c.2105G>A (p.Arg702Gln) single nucleotide variant not specified [RCV004319970] Chr19:11394430 [GRCh38]
Chr19:11505106 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_001035223.4(RGL3):c.1650-13G>A single nucleotide variant not specified [RCV004326637] Chr19:11399964 [GRCh38]
Chr19:11510640 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1498C>T (p.Arg500Trp) single nucleotide variant not specified [RCV004307628] Chr19:11400284 [GRCh38]
Chr19:11510960 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
Single allele deletion not provided [RCV000844961] Chr19:10642984..12810067 [GRCh37]
Chr19:19p13.2		 not provided
NC_000019.9:g.(?_11277234)_(13249220_?)dup duplication not provided [RCV003105511] Chr19:11277234..13249220 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.953C>A (p.Pro318Gln) single nucleotide variant not specified [RCV004291958] Chr19:11406462 [GRCh38]
Chr19:11517138 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.2(chr19:11445773-12160664)x3 copy number gain not provided [RCV001007032] Chr19:11445773..12160664 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.2(chr19:10642984-12810067) copy number loss not provided [RCV001249213] Chr19:10642984..12810067 [GRCh37]
Chr19:19p13.2		 not provided
GRCh37/hg19 19p13.2(chr19:10957601-11672041)x1 copy number loss See cases [RCV001263055] Chr19:10957601..11672041 [GRCh37]
Chr19:19p13.2		 pathogenic
NM_001035223.4(RGL3):c.982A>C (p.Ile328Leu) single nucleotide variant not specified [RCV004293026] Chr19:11406433 [GRCh38]
Chr19:11517109 [GRCh37]
Chr19:19p13.2		 uncertain significance
NC_000019.9:g.(?_10828919)_(13482613_?)dup duplication Charcot-Marie-Tooth disease dominant intermediate B [RCV003109233]|Deficiency of alpha-mannosidase [RCV003109232]|Episodic ataxia type 2 [RCV003109234]|Glutaric aciduria, type 1 [RCV003122092] Chr19:10828919..13482613 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.2(chr19:9941033-11739567)x3 copy number gain not provided [RCV001834267] Chr19:9941033..11739567 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1712C>T (p.Pro571Leu) single nucleotide variant not specified [RCV004331813] Chr19:11399889 [GRCh38]
Chr19:11510565 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.533C>T (p.Ala178Val) single nucleotide variant not specified [RCV004294306] Chr19:11416041 [GRCh38]
Chr19:11526717 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.562G>A (p.Ala188Thr) single nucleotide variant not specified [RCV004314601] Chr19:11416012 [GRCh38]
Chr19:11526688 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.53G>A (p.Gly18Asp) single nucleotide variant not specified [RCV004136997] Chr19:11418765 [GRCh38]
Chr19:11529441 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1552C>T (p.Arg518Trp) single nucleotide variant not specified [RCV004104132] Chr19:11400230 [GRCh38]
Chr19:11510906 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1786G>A (p.Ala596Thr) single nucleotide variant not specified [RCV004118263] Chr19:11397558 [GRCh38]
Chr19:11508234 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.884T>C (p.Val295Ala) single nucleotide variant not specified [RCV004193371] Chr19:11406531 [GRCh38]
Chr19:11517207 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1177C>A (p.Leu393Ile) single nucleotide variant not specified [RCV004216211] Chr19:11405155 [GRCh38]
Chr19:11515831 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.2086C>T (p.Arg696Trp) single nucleotide variant not specified [RCV004180916] Chr19:11394449 [GRCh38]
Chr19:11505125 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1087G>A (p.Gly363Arg) single nucleotide variant not specified [RCV004165467] Chr19:11405336 [GRCh38]
Chr19:11516012 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.2006G>A (p.Gly669Glu) single nucleotide variant not specified [RCV004175194] Chr19:11397252 [GRCh38]
Chr19:11507928 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.866C>G (p.Pro289Arg) single nucleotide variant not specified [RCV004089989] Chr19:11406549 [GRCh38]
Chr19:11517225 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1126C>T (p.Leu376Phe) single nucleotide variant not specified [RCV004086890] Chr19:11405206 [GRCh38]
Chr19:11515882 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.808G>A (p.Glu270Lys) single nucleotide variant not specified [RCV004126105] Chr19:11406607 [GRCh38]
Chr19:11517283 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.23A>G (p.Glu8Gly) single nucleotide variant not specified [RCV004153987] Chr19:11419256 [GRCh38]
Chr19:11529932 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.2104C>T (p.Arg702Trp) single nucleotide variant not specified [RCV004242764] Chr19:11394431 [GRCh38]
Chr19:11505107 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.2071A>G (p.Arg691Gly) single nucleotide variant not specified [RCV004115868] Chr19:11394464 [GRCh38]
Chr19:11505140 [GRCh37]
Chr19:19p13.2		 likely benign
NM_001035223.4(RGL3):c.706C>T (p.Leu236Phe) single nucleotide variant not specified [RCV004097553] Chr19:11406796 [GRCh38]
Chr19:11517472 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.8G>T (p.Arg3Leu) single nucleotide variant not specified [RCV004195157] Chr19:11419271 [GRCh38]
Chr19:11529947 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1726C>A (p.Pro576Thr) single nucleotide variant not specified [RCV004120378] Chr19:11399875 [GRCh38]
Chr19:11510551 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1667C>G (p.Pro556Arg) single nucleotide variant not specified [RCV004132991] Chr19:11399934 [GRCh38]
Chr19:11510610 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1625G>C (p.Gly542Ala) single nucleotide variant not specified [RCV004203039] Chr19:11400064 [GRCh38]
Chr19:11510740 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1149G>C (p.Glu383Asp) single nucleotide variant not specified [RCV004209208] Chr19:11405183 [GRCh38]
Chr19:11515859 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.362C>T (p.Pro121Leu) single nucleotide variant not specified [RCV004162422] Chr19:11416845 [GRCh38]
Chr19:11527519 [GRCh37]
Chr19:19p13.2		 likely benign
NM_001035223.4(RGL3):c.907G>A (p.Gly303Ser) single nucleotide variant not specified [RCV004235108] Chr19:11406508 [GRCh38]
Chr19:11517184 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.391G>A (p.Ala131Thr) single nucleotide variant not specified [RCV004175838] Chr19:11416648 [GRCh38]
Chr19:11527322 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1895T>A (p.Ile632Asn) single nucleotide variant not specified [RCV004113114] Chr19:11397449 [GRCh38]
Chr19:11508125 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1855G>A (p.Val619Ile) single nucleotide variant not specified [RCV004092372] Chr19:11397489 [GRCh38]
Chr19:11508165 [GRCh37]
Chr19:19p13.2		 likely benign
NM_001035223.4(RGL3):c.356C>T (p.Pro119Leu) single nucleotide variant not specified [RCV004194084] Chr19:11416851 [GRCh38]
Chr19:11527525 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.781G>A (p.Glu261Lys) single nucleotide variant not specified [RCV004072748] Chr19:11406634 [GRCh38]
Chr19:11517310 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1201G>A (p.Gly401Arg) single nucleotide variant not specified [RCV004102689] Chr19:11402691 [GRCh38]
Chr19:11513367 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1366T>C (p.Trp456Arg) single nucleotide variant not specified [RCV004120443] Chr19:11402129 [GRCh38]
Chr19:11512805 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.179A>G (p.His60Arg) single nucleotide variant not specified [RCV004186620] Chr19:11417028 [GRCh38]
Chr19:11527702 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.968G>A (p.Arg323Gln) single nucleotide variant not specified [RCV004239261] Chr19:11406447 [GRCh38]
Chr19:11517123 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1927G>A (p.Val643Met) single nucleotide variant not specified [RCV004089897] Chr19:11397331 [GRCh38]
Chr19:11508007 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1430A>C (p.His477Pro) single nucleotide variant not specified [RCV004211399] Chr19:11402065 [GRCh38]
Chr19:11512741 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.866C>A (p.Pro289His) single nucleotide variant not specified [RCV004257690] Chr19:11406549 [GRCh38]
Chr19:11517225 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1727C>T (p.Pro576Leu) single nucleotide variant not specified [RCV004266788] Chr19:11399874 [GRCh38]
Chr19:11510550 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.657A>T (p.Gln219His) single nucleotide variant not specified [RCV004327081] Chr19:11406845 [GRCh38]
Chr19:11517521 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.299A>G (p.Tyr100Cys) single nucleotide variant not specified [RCV004337669] Chr19:11416908 [GRCh38]
Chr19:11527582 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.28G>C (p.Ala10Pro) single nucleotide variant not specified [RCV004343702] Chr19:11419251 [GRCh38]
Chr19:11529927 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1558A>G (p.Ser520Gly) single nucleotide variant not specified [RCV004360555] Chr19:11400224 [GRCh38]
Chr19:11510900 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1835C>T (p.Ser612Leu) single nucleotide variant not specified [RCV004336670] Chr19:11397509 [GRCh38]
Chr19:11508185 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.253G>A (p.Asp85Asn) single nucleotide variant not provided [RCV003406853] Chr19:11416954 [GRCh38]
Chr19:11527628 [GRCh37]
Chr19:19p13.2		 likely benign
GRCh37/hg19 19p13.2(chr19:10441330-13077352)x1 copy number loss not specified [RCV003986120] Chr19:10441330..13077352 [GRCh37]
Chr19:19p13.2		 pathogenic
NM_001035223.4(RGL3):c.1777C>T (p.Arg593Trp) single nucleotide variant not specified [RCV004448872] Chr19:11397567 [GRCh38]
Chr19:11508243 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.402T>A (p.Asp134Glu) single nucleotide variant not specified [RCV004448878] Chr19:11416637 [GRCh38]
Chr19:11527311 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1381C>T (p.Arg461Cys) single nucleotide variant not specified [RCV004448867] Chr19:11402114 [GRCh38]
Chr19:11512790 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.440T>G (p.Val147Gly) single nucleotide variant not specified [RCV004448879] Chr19:11416134 [GRCh38]
Chr19:11526810 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.502C>A (p.Leu168Met) single nucleotide variant not specified [RCV004448881] Chr19:11416072 [GRCh38]
Chr19:11526748 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1097G>A (p.Ser366Asn) single nucleotide variant not specified [RCV004448862] Chr19:11405326 [GRCh38]
Chr19:11516002 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1279T>G (p.Phe427Val) single nucleotide variant not specified [RCV004448865] Chr19:11402505 [GRCh38]
Chr19:11513181 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1679C>T (p.Pro560Leu) single nucleotide variant not specified [RCV004448870] Chr19:11399922 [GRCh38]
Chr19:11510598 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1823C>T (p.Ala608Val) single nucleotide variant not specified [RCV004448874] Chr19:11397521 [GRCh38]
Chr19:11508197 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.71G>A (p.Gly24Asp) single nucleotide variant not specified [RCV004448885] Chr19:11418747 [GRCh38]
Chr19:11529423 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1473C>A (p.Thr491=) single nucleotide variant not provided [RCV003884977] Chr19:11402022 [GRCh38]
Chr19:11512698 [GRCh37]
Chr19:19p13.2		 likely benign
NM_001035223.4(RGL3):c.1232G>A (p.Ser411Asn) single nucleotide variant not specified [RCV004448863] Chr19:11402660 [GRCh38]
Chr19:11513336 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1381C>G (p.Arg461Gly) single nucleotide variant not specified [RCV004448866] Chr19:11402114 [GRCh38]
Chr19:11512790 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1940C>G (p.Ala647Gly) single nucleotide variant not specified [RCV004448875] Chr19:11397318 [GRCh38]
Chr19:11507994 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.2054T>C (p.Met685Thr) single nucleotide variant not specified [RCV004448876] Chr19:11394481 [GRCh38]
Chr19:11505157 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.587T>C (p.Leu196Ser) single nucleotide variant not specified [RCV004448883] Chr19:11415987 [GRCh38]
Chr19:11526663 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.608A>T (p.Gln203Leu) single nucleotide variant not specified [RCV004448884] Chr19:11415966 [GRCh38]
Chr19:11526642 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.949G>A (p.Ala317Thr) single nucleotide variant not specified [RCV004448888] Chr19:11406466 [GRCh38]
Chr19:11517142 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1265C>G (p.Pro422Arg) single nucleotide variant not specified [RCV004448864] Chr19:11402519 [GRCh38]
Chr19:11513195 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1448C>G (p.Ala483Gly) single nucleotide variant not specified [RCV004448868] Chr19:11402047 [GRCh38]
Chr19:11512723 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1639C>G (p.Pro547Ala) single nucleotide variant not specified [RCV004448869] Chr19:11400050 [GRCh38]
Chr19:11510726 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1702G>C (p.Gly568Arg) single nucleotide variant not specified [RCV004448871] Chr19:11399899 [GRCh38]
Chr19:11510575 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1820C>T (p.Pro607Leu) single nucleotide variant not specified [RCV004448873] Chr19:11397524 [GRCh38]
Chr19:11508200 [GRCh37]
Chr19:19p13.2		 likely benign
NM_001035223.4(RGL3):c.479G>A (p.Arg160Gln) single nucleotide variant not specified [RCV004448880] Chr19:11416095 [GRCh38]
Chr19:11526771 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.775G>T (p.Asp259Tyr) single nucleotide variant not specified [RCV004448886] Chr19:11406727 [GRCh38]
Chr19:11517403 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.2089C>G (p.Arg697Gly) single nucleotide variant not specified [RCV004658378] Chr19:11394446 [GRCh38]
Chr19:11505122 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1024T>A (p.Ser342Thr) single nucleotide variant not specified [RCV004658379] Chr19:11405399 [GRCh38]
Chr19:11516075 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.98G>A (p.Arg33Gln) single nucleotide variant not specified [RCV004658381] Chr19:11418720 [GRCh38]
Chr19:11529396 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.244G>T (p.Val82Leu) single nucleotide variant not specified [RCV004658380] Chr19:11416963 [GRCh38]
Chr19:11527637 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.305C>G (p.Thr102Ser) single nucleotide variant not specified [RCV004671906] Chr19:11416902 [GRCh38]
Chr19:11527576 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1433C>T (p.Pro478Leu) single nucleotide variant not specified [RCV004671907] Chr19:11402062 [GRCh38]
Chr19:11512738 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.192C>G (p.Ser64Arg) single nucleotide variant not specified [RCV004671908] Chr19:11417015 [GRCh38]
Chr19:11527689 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.32T>C (p.Leu11Pro) single nucleotide variant not specified [RCV004671909] Chr19:11419247 [GRCh38]
Chr19:11529923 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001035223.4(RGL3):c.1255G>A (p.Gly419Ser) single nucleotide variant not specified [RCV004671910] Chr19:11402529 [GRCh38]
Chr19:11513205 [GRCh37]
Chr19:19p13.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5691
Count of miRNA genes:1127
Interacting mature miRNAs:1450
Transcripts:ENST00000380456, ENST00000393423, ENST00000453604, ENST00000561570, ENST00000561687, ENST00000562663, ENST00000563436, ENST00000563726, ENST00000565895, ENST00000566153, ENST00000566919, ENST00000567080, ENST00000567431, ENST00000568420, ENST00000568628, ENST00000569439, ENST00000589032
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407312196GWAS961172_HDiuretic use measurement QTL GWAS961172 (human)8e-13Diuretic use measurement191141608911416090Human
407000263GWAS649239_Hsystolic blood pressure QTL GWAS649239 (human)1e-62systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407400013GWAS1048989_Hsystolic blood pressure QTL GWAS1048989 (human)3e-46systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407389890GWAS1038866_Hdiastolic blood pressure QTL GWAS1038866 (human)5e-40diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407393859GWAS1042835_Hmean arterial pressure QTL GWAS1042835 (human)3e-17Calcium channel blocker use measurementmean arterial blood pressure (CMO:0000009)191141608911416090Human
407321162GWAS970138_Hmean arterial pressure QTL GWAS970138 (human)6e-10mean arterial pressuremean arterial blood pressure (CMO:0000009)191140215411402155Human
406897488GWAS546464_Hpulse pressure measurement QTL GWAS546464 (human)3e-08pulse pressure measurementpulse pressure (CMO:0000292)191141608911416090Human
407108562GWAS757538_Hcardiovascular disease QTL GWAS757538 (human)9e-42cardiovascular disease191141608911416090Human
407395664GWAS1044640_HDiuretic use measurement QTL GWAS1044640 (human)1e-11Diuretic use measurement191141608911416090Human
407389776GWAS1038752_Hsystolic blood pressure QTL GWAS1038752 (human)5e-33systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407331934GWAS980910_Hsystolic blood pressure QTL GWAS980910 (human)1e-09systolic blood pressuresystolic blood pressure (CMO:0000004)191140215411402155Human
407252319GWAS901295_Hdiastolic blood pressure QTL GWAS901295 (human)1e-17diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407417554GWAS1066530_Hpulse pressure measurement QTL GWAS1066530 (human)4e-20pulse pressure measurementpulse pressure (CMO:0000292)191141608911416090Human
407385426GWAS1034402_Hhypertension, pregnancy-induced QTL GWAS1034402 (human)5e-09hypertension, pregnancy-induced191141608911416090Human
407417555GWAS1066531_Hpulse pressure measurement QTL GWAS1066531 (human)0.000004pulse pressure measurementpulse pressure (CMO:0000292)191139750111397502Human
1643451SLIPL6_HSerum lipid level QTL 6 (human)2.190.0008Lipid level19116075902Human
406924259GWAS573235_Hsystolic blood pressure QTL GWAS573235 (human)3e-13systolic blood pressuresystolic blood pressure (CMO:0000004)191139592911395930Human
407383787GWAS1032763_Hsystolic blood pressure QTL GWAS1032763 (human)8e-40systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407109349GWAS758325_Hhypertension QTL GWAS758325 (human)8e-16hypertension191141608911416090Human
407084650GWAS733626_Hsystolic blood pressure QTL GWAS733626 (human)4e-36systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407329261GWAS978237_Hdiastolic blood pressure QTL GWAS978237 (human)3e-08diastolic blood pressurediastolic blood pressure (CMO:0000005)191140215411402155Human
407397477GWAS1046453_Hmean arterial pressure QTL GWAS1046453 (human)4e-48mean arterial pressuremean arterial blood pressure (CMO:0000009)191141608911416090Human
407252082GWAS901058_Hdiastolic blood pressure QTL GWAS901058 (human)5e-23diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407005431GWAS654407_Hmean corpuscular hemoglobin QTL GWAS654407 (human)1e-11mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)191139782911397830Human
406902901GWAS551877_Hsystolic blood pressure QTL GWAS551877 (human)2e-21systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
406960381GWAS609357_Hsystolic blood pressure QTL GWAS609357 (human)7e-09systolic blood pressuresystolic blood pressure (CMO:0000004)191141550611415507Human
1298476BP3_HBlood pressure QTL 3 (human)2.4Blood pressuresystolic19116075902Human
407397239GWAS1046215_HBeta blocking agent use measurement QTL GWAS1046215 (human)2e-14Beta blocking agent use measurement191141608911416090Human
407011330GWAS660306_Hhypertension QTL GWAS660306 (human)1e-14hypertension191141608911416090Human
407392648GWAS1041624_Hsystolic blood pressure QTL GWAS1041624 (human)9e-18systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407251204GWAS900180_Hsystolic blood pressure QTL GWAS900180 (human)4e-18systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407393163GWAS1042139_Hpreeclampsia QTL GWAS1042139 (human)2e-11preeclampsia191141608911416090Human
407101574GWAS750550_Hmean corpuscular hemoglobin QTL GWAS750550 (human)2e-11mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)191140073711400738Human
1581534BP76_HBlood pressure QTL 76 (human)20.001Blood pressurepulse pressure19116075902Human
1581535BP65_HBlood pressure QTL 65 (human)3.10.001Blood pressurepulse pressure19116075902Human
407179023GWAS827999_Hdiastolic blood pressure QTL GWAS827999 (human)1e-10diastolic blood pressurediastolic blood pressure (CMO:0000005)191139750111397502Human
1298499UAE1_HUrinary albumin excretion QTL 1 (human)2.730.0009Urinary albumin excretionurine albumin:creatinine ratio (ACR)19116075902Human
1300034BP50_HBlood pressure QTL 50 (human)2.10.00094Blood pressuresystolic191108946337089463Human
407414557GWAS1063533_Hdiastolic blood pressure QTL GWAS1063533 (human)6e-19diastolic blood pressurediastolic blood pressure (CMO:0000005)191139750111397502Human
407414558GWAS1063534_Hdiastolic blood pressure QTL GWAS1063534 (human)2e-102diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407314577GWAS963553_HCalcium channel blocker use measurement QTL GWAS963553 (human)1e-15Calcium channel blocker use measurement191141608911416090Human
407150099GWAS799075_Hhypertension QTL GWAS799075 (human)2e-08hypertension191141608911416090Human
406893849GWAS542825_Hdiastolic blood pressure QTL GWAS542825 (human)4e-22diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407393172GWAS1042148_Hpreeclampsia QTL GWAS1042148 (human)3e-10preeclampsia191141608911416090Human
407215392GWAS864368_Hcryptic phenotype measurement QTL GWAS864368 (human)1e-10cryptic phenotype measurement191141608911416090Human
407032612GWAS681588_Hpulse pressure measurement QTL GWAS681588 (human)0.0000006pulse pressure measurementpulse pressure (CMO:0000292)191141608911416090Human
407011626GWAS660602_Hdiastolic blood pressure QTL GWAS660602 (human)4e-28Agents acting on the renin-angiotensin system use measurementdiastolic blood pressure (CMO:0000005)191141608911416090Human
407395873GWAS1044849_Hcoronary artery disease QTL GWAS1044849 (human)6e-11coronary artery disease191141608911416090Human
407357101GWAS1006077_Hdiastolic blood pressure QTL GWAS1006077 (human)2e-38diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407235247GWAS884223_Hpreeclampsia, hypertension, pregnancy-induced QTL GWAS884223 (human)7e-13diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407036585GWAS685561_Hsystolic blood pressure QTL GWAS685561 (human)9e-27systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407178926GWAS827902_Hdiastolic blood pressure QTL GWAS827902 (human)4e-52diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407317035GWAS966011_HAgents acting on the renin-angiotensin system use measurement QTL GWAS966011 (human)1e-24Agents acting on the renin-angiotensin system use measurement191141608911416090Human
407285928GWAS934904_Hvaginal microbiome measurement QTL GWAS934904 (human)0.000004vaginal microbiome measurement191141710511417106Human
407012141GWAS661117_Hmean arterial pressure QTL GWAS661117 (human)7e-11mean arterial pressuremean arterial blood pressure (CMO:0000009)191141608911416090Human
407037741GWAS686717_Hdiastolic blood pressure QTL GWAS686717 (human)3e-32diastolic blood pressurediastolic blood pressure (CMO:0000005)191141608911416090Human
407043249GWAS692225_Hmean corpuscular volume QTL GWAS692225 (human)1e-09mean corpuscular volumemean corpuscular volume (CMO:0000038)191139782911397830Human
407395643GWAS1044619_Hpulse pressure measurement QTL GWAS1044619 (human)8e-18pulse pressure measurementpulse pressure (CMO:0000292)191141608911416090Human
407398323GWAS1047299_Hsystolic blood pressure QTL GWAS1047299 (human)6e-18systolic blood pressuresystolic blood pressure (CMO:0000004)191139750111397502Human
407312188GWAS961164_HBeta blocking agent use measurement QTL GWAS961164 (human)5e-12Beta blocking agent use measurement191141608911416090Human
2314591INSUL4_HInsulin level QTL 4 (human)3.80.000038Insulin levelfasting19116075902Human
407398325GWAS1047301_Hsystolic blood pressure QTL GWAS1047301 (human)6e-82systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407009084GWAS658060_Hsystolic blood pressure QTL GWAS658060 (human)1e-23systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human
407032637GWAS681613_Hhypertension QTL GWAS681613 (human)3e-15systolic blood pressuresystolic blood pressure (CMO:0000004)191141608911416090Human

Markers in Region
RH45126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371911,504,800 - 11,505,036UniSTSGRCh37
Build 361911,365,800 - 11,366,036RGDNCBI36
Celera1911,399,672 - 11,399,908RGD
Cytogenetic Map19p13.2UniSTS
HuRef1911,080,745 - 11,080,981UniSTS
GeneMap99-GB4 RH Map1971.07UniSTS
NCBI RH Map1987.9UniSTS
RH102074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371911,531,481 - 11,531,615UniSTSGRCh37
Build 361911,392,481 - 11,392,615RGDNCBI36
Celera1911,426,331 - 11,426,465RGD
Cytogenetic Map19p13.2UniSTS
HuRef1911,106,923 - 11,107,057UniSTS
GeneMap99-GB4 RH Map1971.07UniSTS
SHGC-110871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371911,516,026 - 11,516,156UniSTSGRCh37
Build 361911,377,026 - 11,377,156RGDNCBI36
Celera1911,410,895 - 11,411,025RGD
Cytogenetic Map19p13.2UniSTS
HuRef1911,091,442 - 11,091,572UniSTS
TNG Radiation Hybrid Map193891.0UniSTS
RGL3__5490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371911,504,608 - 11,505,170UniSTSGRCh37
Build 361911,365,608 - 11,366,170RGDNCBI36
Celera1911,399,480 - 11,400,042RGD
HuRef1911,080,553 - 11,081,115UniSTS
L17705  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21.3UniSTS
GDB:631802  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p35.3-p33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map3q21-q22UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.22-p11.21UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map2q21UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map20p11.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map2p24.1UniSTS
L17877  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map9q21.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map17q25.3UniSTS


Expression

RNA-SEQ Expression

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 2422 2788 2231 4942 1716 2323 5 619 1720 462 2262 7074 6254 39 3700 850 1736 1591 172 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001035223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001161616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC008481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC024575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC014426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC064475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC101756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC111958 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM992649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB184397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000380456   ⟹   ENSP00000369823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,394,060 - 11,419,314 (-)Ensembl
Ensembl Acc Id: ENST00000393423   ⟹   ENSP00000377075
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,394,325 - 11,419,328 (-)Ensembl
Ensembl Acc Id: ENST00000453604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,402,228 - 11,419,314 (-)Ensembl
Ensembl Acc Id: ENST00000561570
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,416,850 - 11,419,317 (-)Ensembl
Ensembl Acc Id: ENST00000561687
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,406,824 - 11,416,234 (-)Ensembl
Ensembl Acc Id: ENST00000562663   ⟹   ENSP00000454678
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,384,341 - 11,419,273 (-)Ensembl
Ensembl Acc Id: ENST00000563436
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,416,007 - 11,416,830 (-)Ensembl
Ensembl Acc Id: ENST00000563726   ⟹   ENSP00000455922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,384,512 - 11,419,310 (-)Ensembl
Ensembl Acc Id: ENST00000565895
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,405,212 - 11,406,943 (-)Ensembl
Ensembl Acc Id: ENST00000566153
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,394,056 - 11,411,270 (-)Ensembl
Ensembl Acc Id: ENST00000566919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,397,244 - 11,397,769 (-)Ensembl
Ensembl Acc Id: ENST00000567080   ⟹   ENSP00000456429
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,416,039 - 11,419,314 (-)Ensembl
Ensembl Acc Id: ENST00000567431   ⟹   ENSP00000464876
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,415,937 - 11,418,573 (-)Ensembl
Ensembl Acc Id: ENST00000568420
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,416,463 - 11,419,305 (-)Ensembl
Ensembl Acc Id: ENST00000568628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,394,064 - 11,397,546 (-)Ensembl
Ensembl Acc Id: ENST00000569439
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,406,736 - 11,419,317 (-)Ensembl
Ensembl Acc Id: ENST00000589032   ⟹   ENSP00000466669
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,402,078 - 11,406,602 (-)Ensembl
RefSeq Acc Id: NM_001035223   ⟹   NP_001030300
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381911,394,060 - 11,419,314 (-)NCBI
GRCh371911,504,732 - 11,530,018 (-)RGD
Build 361911,366,001 - 11,391,004 (-)NCBI Archive
Celera1911,399,604 - 11,424,860 (-)RGD
HuRef1911,080,677 - 11,105,452 (-)ENTREZGENE
CHM1_11911,505,738 - 11,530,962 (-)NCBI
T2T-CHM13v2.01911,521,038 - 11,546,286 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001161616   ⟹   NP_001155088
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381911,394,060 - 11,419,314 (-)NCBI
GRCh371911,504,732 - 11,530,018 (-)RGD
Celera1911,399,604 - 11,424,860 (-)RGD
HuRef1911,080,677 - 11,105,452 (-)ENTREZGENE
CHM1_11911,505,738 - 11,530,962 (-)NCBI
T2T-CHM13v2.01911,521,038 - 11,546,286 (-)NCBI
Sequence:
RefSeq Acc Id: NP_001030300   ⟸   NM_001035223
- Peptide Label: isoform 2
- UniProtKB: Q0P6G0 (UniProtKB/Swiss-Prot),   B7ZL22 (UniProtKB/Swiss-Prot),   B5ME84 (UniProtKB/Swiss-Prot),   Q3MIN7 (UniProtKB/Swiss-Prot),   A0A0A0MRX4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001155088   ⟸   NM_001161616
- Peptide Label: isoform 1
- Sequence:
Ensembl Acc Id: ENSP00000466669   ⟸   ENST00000589032
Ensembl Acc Id: ENSP00000454678   ⟸   ENST00000562663
Ensembl Acc Id: ENSP00000455922   ⟸   ENST00000563726
Ensembl Acc Id: ENSP00000377075   ⟸   ENST00000393423
Ensembl Acc Id: ENSP00000369823   ⟸   ENST00000380456
Ensembl Acc Id: ENSP00000456429   ⟸   ENST00000567080
Ensembl Acc Id: ENSP00000464876   ⟸   ENST00000567431
Protein Domains
N-terminal Ras-GEF   Ras-associating   Ras-GEF

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q3MIN7-F1-model_v2 AlphaFold Q3MIN7 1-710 view protein structure

Promoters
RGD ID:6795579
Promoter ID:HG_KWN:28915
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562
Transcripts:ENST00000222139,   UC002MRK.1,   UC002MRL.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361911,355,749 - 11,356,249 (-)MPROMDB
RGD ID:6795576
Promoter ID:HG_KWN:28919
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:ENST00000393423,   NM_001035223,   NM_001161616,   UC002MRM.1,   UC002MRN.1,   UC002MRQ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361911,390,576 - 11,391,076 (-)MPROMDB
RGD ID:7238599
Promoter ID:EPDNEW_H25046
Type:initiation region
Name:RGL3_1
Description:ral guanine nucleotide dissociation stimulator like 3
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
GRCh381911,419,314 - 11,419,374EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30282 AgrOrtholog
COSMIC RGL3 COSMIC
Ensembl Genes ENSG00000205517 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000380456 ENTREZGENE
  ENST00000380456.8 UniProtKB/Swiss-Prot
  ENST00000393423 ENTREZGENE
  ENST00000393423.7 UniProtKB/Swiss-Prot
  ENST00000562663.5 UniProtKB/TrEMBL
  ENST00000563726.5 UniProtKB/TrEMBL
  ENST00000567080.1 UniProtKB/TrEMBL
  ENST00000567431.5 UniProtKB/TrEMBL
  ENST00000589032.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.840.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Son of sevenless (SoS) protein Chain: S domain 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000205517 GTEx
HGNC ID HGNC:30282 ENTREZGENE
Human Proteome Map RGL3 Human Proteome Map
InterPro RA_dom UniProtKB/Swiss-Prot
  Ras-like_GEF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ras-like_Gua-exchang_fac_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ras_G-nucl-exch_fac_CS UniProtKB/Swiss-Prot
  Ras_GEF_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RASGEF_cat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RASGEF_cat_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGL3 UniProtKB/Swiss-Prot
  Ubiquitin-like_domsf UniProtKB/Swiss-Prot
KEGG Report hsa:57139 UniProtKB/Swiss-Prot
NCBI Gene 57139 ENTREZGENE
OMIM 616743 OMIM
PANTHER 1700018F24RIK PROTEIN-RELATED UniProtKB/TrEMBL
  1700018F24RIK PROTEIN-RELATED-RELATED UniProtKB/TrEMBL
  PTHR23113 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR23113:SF220 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam PF00788 UniProtKB/Swiss-Prot
  RasGEF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RasGEF_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134979213 PharmGKB
PROSITE PS50200 UniProtKB/Swiss-Prot
  RASGEF UniProtKB/Swiss-Prot
  RASGEF_CAT UniProtKB/Swiss-Prot
  RASGEF_NTER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART RasGEF UniProtKB/Swiss-Prot
  RasGEFN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SM00314 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48366 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF54236 UniProtKB/Swiss-Prot
UniProt A0A0A0MRX4 ENTREZGENE
  B5ME84 ENTREZGENE
  B7ZL22 ENTREZGENE
  H3BN42_HUMAN UniProtKB/TrEMBL
  H3BQS8_HUMAN UniProtKB/TrEMBL
  H3BRW0_HUMAN UniProtKB/TrEMBL
  K7EIS7_HUMAN UniProtKB/TrEMBL
  K7EMV7_HUMAN UniProtKB/TrEMBL
  Q0P6G0 ENTREZGENE
  Q3MIN7 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A0A0A0MRX4 UniProtKB/Swiss-Prot
  B5ME84 UniProtKB/Swiss-Prot
  B7ZL22 UniProtKB/Swiss-Prot
  Q0P6G0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-21 RGL3  ral guanine nucleotide dissociation stimulator like 3    ral guanine nucleotide dissociation stimulator-like 3  Symbol and/or name change 5135510 APPROVED