RGSL1 (regulator of G protein signaling like 1) - Rat Genome Database

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Gene: RGSL1 (regulator of G protein signaling like 1) Homo sapiens
Analyze
Symbol: RGSL1
Name: regulator of G protein signaling like 1
RGD ID: 1353178
HGNC Page HGNC:18636
Description: Predicted to be located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp434E169; regulator of G-protein signaling like 1; regulator of G-protein signaling like 2; regulator of G-protein signaling protein-like; RGSL; RGSL2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381182,447,877 - 182,560,597 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1182,409,192 - 182,560,599 (+)EnsemblGRCh38hg38GRCh38
GRCh371182,419,281 - 182,529,732 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361180,685,910 - 180,796,355 (+)NCBINCBI36Build 36hg18NCBI36
Build 341179,189,074 - 179,261,389NCBI
Celera1155,530,353 - 155,640,967 (+)NCBICelera
Cytogenetic Map1q25.3NCBI
HuRef1153,655,619 - 153,766,201 (+)NCBIHuRef
CHM1_11183,842,215 - 183,953,173 (+)NCBICHM1_1
T2T-CHM13v2.01181,807,450 - 181,920,071 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
membrane  (IEA)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Identification of 9 novel transcripts and two RGSL genes within the hereditary prostate cancer region (HPC1) at 1q25. Silva AP, etal., Gene 2003 May 22;310:49-57.
Additional References at PubMed
PMID:11181995   PMID:11230166   PMID:12477932   PMID:12651916   PMID:14702039   PMID:15489334   PMID:16344560   PMID:16710414   PMID:18521847   PMID:20574532   PMID:21135262   PMID:21145461  
PMID:23248035   PMID:25969425   PMID:29987050   PMID:30021884   PMID:32513696   PMID:35831314  


Genomics

Comparative Map Data
RGSL1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381182,447,877 - 182,560,597 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1182,409,192 - 182,560,599 (+)EnsemblGRCh38hg38GRCh38
GRCh371182,419,281 - 182,529,732 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361180,685,910 - 180,796,355 (+)NCBINCBI36Build 36hg18NCBI36
Build 341179,189,074 - 179,261,389NCBI
Celera1155,530,353 - 155,640,967 (+)NCBICelera
Cytogenetic Map1q25.3NCBI
HuRef1153,655,619 - 153,766,201 (+)NCBIHuRef
CHM1_11183,842,215 - 183,953,173 (+)NCBICHM1_1
T2T-CHM13v2.01181,807,450 - 181,920,071 (+)NCBIT2T-CHM13v2.0
Rgsl1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391153,653,675 - 153,723,087 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1153,655,127 - 153,719,888 (-)EnsemblGRCm39 Ensembl
GRCm381153,777,929 - 153,847,341 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1153,779,381 - 153,844,142 (-)EnsemblGRCm38mm10GRCm38
MGSCv371155,632,253 - 155,691,266 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361155,541,606 - 155,570,376 (-)NCBIMGSCv36mm8
Celera1156,217,506 - 156,277,296 (-)NCBICelera
Cytogenetic Map1G3NCBI
cM Map165.43NCBI
Rgsl1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81368,465,558 - 68,520,306 (-)NCBIGRCr8
mRatBN7.21365,915,052 - 65,969,846 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1365,915,097 - 65,968,954 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.01371,206,268 - 71,276,799 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1371,209,560 - 71,276,497 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01376,187,588 - 76,196,173 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.01376,212,538 - 76,237,869 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41368,841,128 - 68,903,102 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1365,814,443 - 65,867,784 (-)NCBICelera
Cytogenetic Map13q21NCBI
Rgsl1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540621,332,926 - 21,390,893 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495540621,274,546 - 21,395,534 (+)NCBIChiLan1.0ChiLan1.0
RGSL1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2167,168,661 - 67,280,517 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1166,852,198 - 66,964,064 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01157,967,552 - 158,079,341 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11161,619,801 - 161,731,137 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1161,619,801 - 161,730,852 (+)Ensemblpanpan1.1panPan2
RGSL1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1715,739,709 - 15,985,528 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl715,740,928 - 15,872,257 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha715,322,784 - 15,570,962 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0715,469,152 - 15,713,309 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl715,471,398 - 15,604,074 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1715,377,147 - 15,625,594 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0715,485,814 - 15,733,640 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0715,617,114 - 15,862,790 (+)NCBIUU_Cfam_GSD_1.0
Rgsl1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934489,337,768 - 89,385,059 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364817,190,346 - 7,221,180 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364817,190,038 - 7,231,768 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RGSL1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl9123,814,171 - 123,879,496 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.19123,763,417 - 123,879,100 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.29135,968,686 - 136,080,671 (+)NCBISscrofa10.2Sscrofa10.2susScr3
RGSL1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12546,813,422 - 46,921,057 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2546,819,410 - 46,915,475 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605548,031,591 - 48,137,281 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in RGSL1
56 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q25.1-31.1(chr1:175035040-186042595)x1 copy number loss See cases [RCV000051221] Chr1:175035040..186042595 [GRCh38]
Chr1:175004176..186011727 [GRCh37]
Chr1:173270799..184278350 [NCBI36]
Chr1:1q25.1-31.1		 pathogenic
GRCh38/hg38 1q25.2-32.1(chr1:179032905-199724897)x1 copy number loss See cases [RCV000053948] Chr1:179032905..199724897 [GRCh38]
Chr1:179002040..199694025 [GRCh37]
Chr1:177268663..197960648 [NCBI36]
Chr1:1q25.2-32.1		 pathogenic
GRCh38/hg38 1q25.3-31.1(chr1:182137726-186931125)x1 copy number loss See cases [RCV000053949] Chr1:182137726..186931125 [GRCh38]
Chr1:182106861..186900257 [GRCh37]
Chr1:180373484..185166880 [NCBI36]
Chr1:1q25.3-31.1		 pathogenic
NM_001137669.1(RGSL1):c.89C>T (p.Ser30Phe) single nucleotide variant Malignant melanoma [RCV000064368] Chr1:182454033 [GRCh38]
Chr1:182423168 [GRCh37]
Chr1:180689791 [NCBI36]
Chr1:1q25.3		 not provided
NM_001137669.1(RGSL1):c.1143G>A (p.Gly381=) single nucleotide variant Malignant melanoma [RCV000064369] Chr1:182474254 [GRCh38]
Chr1:182443389 [GRCh37]
Chr1:180710012 [NCBI36]
Chr1:1q25.3		 not provided
NM_001137669.1(RGSL1):c.1392G>A (p.Val464=) single nucleotide variant Malignant melanoma [RCV000064370] Chr1:182474503 [GRCh38]
Chr1:182443638 [GRCh37]
Chr1:180710261 [NCBI36]
Chr1:1q25.3		 not provided
NM_001137669.1(RGSL1):c.191T>G (p.Leu64Ter) single nucleotide variant Lung cancer [RCV000090079] Chr1:182460023 [GRCh38]
Chr1:182429158 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.1(RGSL1):c.1431+5566A>G single nucleotide variant Lung cancer [RCV000090080] Chr1:182480108 [GRCh38]
Chr1:182449243 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.1(RGSL1):c.2365-125A>G single nucleotide variant Lung cancer [RCV000090081] Chr1:182532537 [GRCh38]
Chr1:182501672 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh38/hg38 1q25.2-31.3(chr1:176595962-196301688)x1 copy number loss See cases [RCV000134144] Chr1:176595962..196301688 [GRCh38]
Chr1:176565098..196270818 [GRCh37]
Chr1:174831721..194537441 [NCBI36]
Chr1:1q25.2-31.3		 pathogenic
GRCh38/hg38 1q24.3-31.1(chr1:171039975-186875957)x3 copy number gain See cases [RCV000134876] Chr1:171039975..186875957 [GRCh38]
Chr1:171009116..186845089 [GRCh37]
Chr1:169275740..185111712 [NCBI36]
Chr1:1q24.3-31.1		 pathogenic
GRCh38/hg38 1q24.3-31.2(chr1:170929720-191065409)x1 copy number loss See cases [RCV000142369] Chr1:170929720..191065409 [GRCh38]
Chr1:170898861..191034539 [GRCh37]
Chr1:169165485..189301162 [NCBI36]
Chr1:1q24.3-31.2		 pathogenic
GRCh38/hg38 1q24.2-31.1(chr1:170036068-187555148)x1 copy number loss See cases [RCV000143688] Chr1:170036068..187555148 [GRCh38]
Chr1:170005209..187524280 [GRCh37]
Chr1:168271833..185790903 [NCBI36]
Chr1:1q24.2-31.1		 pathogenic
GRCh37/hg19 1q25.3-31.2(chr1:181572003-191524283)x1 copy number loss See cases [RCV000240242] Chr1:181572003..191524283 [GRCh37]
Chr1:1q25.3-31.2		 pathogenic
GRCh37/hg19 1q23.3-25.3(chr1:161676893-184071723)x1 copy number loss See cases [RCV000447098] Chr1:161676893..184071723 [GRCh37]
Chr1:1q23.3-25.3		 pathogenic
GRCh37/hg19 1q25.2-32.1(chr1:179413479-201764737)x1 copy number loss See cases [RCV000445748] Chr1:179413479..201764737 [GRCh37]
Chr1:1q25.2-32.1		 pathogenic
GRCh37/hg19 1q25.2-25.3(chr1:179564752-183850820)x1 copy number loss See cases [RCV000448646] Chr1:179564752..183850820 [GRCh37]
Chr1:1q25.2-25.3		 pathogenic
GRCh37/hg19 1q25.2-32.1(chr1:179073386-200192265)x1 copy number loss See cases [RCV000448809] Chr1:179073386..200192265 [GRCh37]
Chr1:1q25.2-32.1		 pathogenic
GRCh37/hg19 1q25.3(chr1:180830413-183981164)x3 copy number gain See cases [RCV000448160] Chr1:180830413..183981164 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1q24.3-31.3(chr1:171990029-195086758)x1 copy number loss See cases [RCV000448686] Chr1:171990029..195086758 [GRCh37]
Chr1:1q24.3-31.3		 pathogenic
GRCh37/hg19 1q25.2-32.1(chr1:179011314-199022759)x1 copy number loss See cases [RCV000512128] Chr1:179011314..199022759 [GRCh37]
Chr1:1q25.2-32.1		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
NM_001137669.2(RGSL1):c.2624T>C (p.Val875Ala) single nucleotide variant Inborn genetic diseases [RCV003280612] Chr1:182540376 [GRCh38]
Chr1:182509511 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.583T>C (p.Tyr195His) single nucleotide variant Inborn genetic diseases [RCV003291202] Chr1:182473694 [GRCh38]
Chr1:182442829 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1q25.1-25.3(chr1:173138799-185129406)x3 copy number gain See cases [RCV000512520] Chr1:173138799..185129406 [GRCh37]
Chr1:1q25.1-25.3		 likely pathogenic
GRCh37/hg19 1q25.3(chr1:182175044-182472426)x1 copy number loss not provided [RCV000684677] Chr1:182175044..182472426 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q25.1-31.1(chr1:173131908-187406532)x1 copy number loss not provided [RCV000736735] Chr1:173131908..187406532 [GRCh37]
Chr1:1q25.1-31.1		 pathogenic
GRCh37/hg19 1q25.3(chr1:181863430-183148056)x1 copy number loss not provided [RCV000762696] Chr1:181863430..183148056 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.3216C>T (p.Ile1072=) single nucleotide variant not provided [RCV000919725] Chr1:182556042 [GRCh38]
Chr1:182525177 [GRCh37]
Chr1:1q25.3		 likely benign
NM_001137669.2(RGSL1):c.3131C>T (p.Ser1044Phe) single nucleotide variant Inborn genetic diseases [RCV003244841] Chr1:182554627 [GRCh38]
Chr1:182523762 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1708T>C (p.Phe570Leu) single nucleotide variant Inborn genetic diseases [RCV003247419] Chr1:182489193 [GRCh38]
Chr1:182458328 [GRCh37]
Chr1:1q25.3		 uncertain significance
NC_000001.10:g.172652343_183538289del10885947 deletion 1q24q25 microdeletion syndrome [RCV000785662] Chr1:172652343..183538289 [GRCh37]
Chr1:1q24.3-25.3		 pathogenic
GRCh37/hg19 1q25.3(chr1:180586428-183178629)x3 copy number gain not provided [RCV001005158] Chr1:180586428..183178629 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3 copy number gain not provided [RCV000845852] Chr1:182388773..249111240 [GRCh37]
Chr1:1q25.3-44		 pathogenic
NM_001137669.2(RGSL1):c.3035C>T (p.Ser1012Leu) single nucleotide variant Inborn genetic diseases [RCV003274534] Chr1:182551201 [GRCh38]
Chr1:182520336 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1q25.2-32.1(chr1:177551193-199599056)x1 copy number loss not provided [RCV001005157] Chr1:177551193..199599056 [GRCh37]
Chr1:1q25.2-32.1		 pathogenic
GRCh37/hg19 1q25.1-25.3(chr1:173162501-182702252)x3 copy number gain not provided [RCV001258487] Chr1:173162501..182702252 [GRCh37]
Chr1:1q25.1-25.3		 pathogenic
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44		 uncertain significance
GRCh37/hg19 1q24.3-31.3(chr1:171990029-195086758) copy number loss not specified [RCV002053736] Chr1:171990029..195086758 [GRCh37]
Chr1:1q24.3-31.3		 pathogenic
GRCh37/hg19 1q25.2-32.1(chr1:179413479-201764737) copy number loss not specified [RCV002053780] Chr1:179413479..201764737 [GRCh37]
Chr1:1q25.2-32.1		 pathogenic
GRCh37/hg19 1q25.3(chr1:180830413-183981164) copy number gain not specified [RCV002053802] Chr1:180830413..183981164 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1q25.2-32.1(chr1:179073386-200192265) copy number loss not specified [RCV002053769] Chr1:179073386..200192265 [GRCh37]
Chr1:1q25.2-32.1		 pathogenic
GRCh37/hg19 1q25.2-31.1(chr1:178522021-190322133)x1 copy number loss not provided [RCV001836604] Chr1:178522021..190322133 [GRCh37]
Chr1:1q25.2-31.1		 pathogenic
NC_000001.10:g.(?_179520308)_(183559464_?)dup duplication Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 [RCV002014062] Chr1:179520308..183559464 [GRCh37]
Chr1:1q25.2-25.3		 uncertain significance
GRCh37/hg19 1q25.3(chr1:182443031-182609230)x1 copy number loss not provided [RCV002472741] Chr1:182443031..182609230 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1q25.2-31.2(chr1:179727182-192260142)x1 copy number loss not provided [RCV002473949] Chr1:179727182..192260142 [GRCh37]
Chr1:1q25.2-31.2		 pathogenic
GRCh37/hg19 1q25.3(chr1:182442865-182609349)x1 copy number loss not provided [RCV002475783] Chr1:182442865..182609349 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.512G>A (p.Arg171Lys) single nucleotide variant Inborn genetic diseases [RCV002754057] Chr1:182473623 [GRCh38]
Chr1:182442758 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2713C>T (p.Arg905Trp) single nucleotide variant Inborn genetic diseases [RCV002733657] Chr1:182548360 [GRCh38]
Chr1:182517495 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.993A>C (p.Glu331Asp) single nucleotide variant Inborn genetic diseases [RCV002840775] Chr1:182474104 [GRCh38]
Chr1:182443239 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1300G>A (p.Glu434Lys) single nucleotide variant Inborn genetic diseases [RCV002773782] Chr1:182474411 [GRCh38]
Chr1:182443546 [GRCh37]
Chr1:1q25.3		 uncertain significance
GRCh37/hg19 1q25.3-32.3(chr1:181453460-213107248)x3 copy number gain not provided [RCV002475637] Chr1:181453460..213107248 [GRCh37]
Chr1:1q25.3-32.3		 pathogenic
NM_001137669.2(RGSL1):c.412A>G (p.Thr138Ala) single nucleotide variant Inborn genetic diseases [RCV002690032] Chr1:182472506 [GRCh38]
Chr1:182441641 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2929A>G (p.Lys977Glu) single nucleotide variant Inborn genetic diseases [RCV002981378] Chr1:182548820 [GRCh38]
Chr1:182517955 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1387G>T (p.Asp463Tyr) single nucleotide variant Inborn genetic diseases [RCV002737392] Chr1:182474498 [GRCh38]
Chr1:182443633 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1322T>G (p.Ile441Ser) single nucleotide variant Inborn genetic diseases [RCV002868455] Chr1:182474433 [GRCh38]
Chr1:182443568 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.179A>G (p.Lys60Arg) single nucleotide variant Inborn genetic diseases [RCV002980519] Chr1:182460011 [GRCh38]
Chr1:182429146 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1062G>T (p.Lys354Asn) single nucleotide variant Inborn genetic diseases [RCV002759491] Chr1:182474173 [GRCh38]
Chr1:182443308 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1858A>T (p.Thr620Ser) single nucleotide variant Inborn genetic diseases [RCV002799693] Chr1:182522036 [GRCh38]
Chr1:182491171 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2912T>A (p.Val971Asp) single nucleotide variant Inborn genetic diseases [RCV002821269] Chr1:182548803 [GRCh38]
Chr1:182517938 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.622T>C (p.Cys208Arg) single nucleotide variant Inborn genetic diseases [RCV002661690] Chr1:182473733 [GRCh38]
Chr1:182442868 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2195C>T (p.Thr732Ile) single nucleotide variant Inborn genetic diseases [RCV002661005] Chr1:182530313 [GRCh38]
Chr1:182499448 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.362A>G (p.Asp121Gly) single nucleotide variant Inborn genetic diseases [RCV002846033] Chr1:182472456 [GRCh38]
Chr1:182441591 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1273C>T (p.Arg425Cys) single nucleotide variant Inborn genetic diseases [RCV002978518] Chr1:182474384 [GRCh38]
Chr1:182443519 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.946A>C (p.Lys316Gln) single nucleotide variant Inborn genetic diseases [RCV002742650] Chr1:182474057 [GRCh38]
Chr1:182443192 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2516C>T (p.Thr839Ile) single nucleotide variant Inborn genetic diseases [RCV002699043] Chr1:182540268 [GRCh38]
Chr1:182509403 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1733C>T (p.Ser578Phe) single nucleotide variant Inborn genetic diseases [RCV002964870] Chr1:182493037 [GRCh38]
Chr1:182462172 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2462A>G (p.Tyr821Cys) single nucleotide variant Inborn genetic diseases [RCV002652294] Chr1:182532759 [GRCh38]
Chr1:182501894 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.564C>A (p.Ser188Arg) single nucleotide variant Inborn genetic diseases [RCV002748123] Chr1:182473675 [GRCh38]
Chr1:182442810 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2032G>A (p.Val678Ile) single nucleotide variant Inborn genetic diseases [RCV002832544] Chr1:182527679 [GRCh38]
Chr1:182496814 [GRCh37]
Chr1:1q25.3		 likely benign
NM_001137669.2(RGSL1):c.2731G>T (p.Asp911Tyr) single nucleotide variant Inborn genetic diseases [RCV002988126] Chr1:182548378 [GRCh38]
Chr1:182517513 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2391C>A (p.Ser797Arg) single nucleotide variant Inborn genetic diseases [RCV002668409] Chr1:182532688 [GRCh38]
Chr1:182501823 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1372C>A (p.Leu458Ile) single nucleotide variant Inborn genetic diseases [RCV002674882] Chr1:182474483 [GRCh38]
Chr1:182443618 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.3163G>A (p.Val1055Met) single nucleotide variant Inborn genetic diseases [RCV002747890] Chr1:182554659 [GRCh38]
Chr1:182523794 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2176C>T (p.Arg726Cys) single nucleotide variant Inborn genetic diseases [RCV002656444] Chr1:182530294 [GRCh38]
Chr1:182499429 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1147C>A (p.Pro383Thr) single nucleotide variant Inborn genetic diseases [RCV002723373] Chr1:182474258 [GRCh38]
Chr1:182443393 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.188G>C (p.Gly63Ala) single nucleotide variant Inborn genetic diseases [RCV002677736] Chr1:182460020 [GRCh38]
Chr1:182429155 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2333A>G (p.Lys778Arg) single nucleotide variant Inborn genetic diseases [RCV003193761] Chr1:182530879 [GRCh38]
Chr1:182500014 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1593G>C (p.Glu531Asp) single nucleotide variant Inborn genetic diseases [RCV003180584] Chr1:182489078 [GRCh38]
Chr1:182458213 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.536A>G (p.Gln179Arg) single nucleotide variant Inborn genetic diseases [RCV003205777] Chr1:182473647 [GRCh38]
Chr1:182442782 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.964A>G (p.Asn322Asp) single nucleotide variant Inborn genetic diseases [RCV003194250] Chr1:182474075 [GRCh38]
Chr1:182443210 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1220A>G (p.Gln407Arg) single nucleotide variant Inborn genetic diseases [RCV003202463] Chr1:182474331 [GRCh38]
Chr1:182443466 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.215G>A (p.Arg72Gln) single nucleotide variant Inborn genetic diseases [RCV003183692] Chr1:182460047 [GRCh38]
Chr1:182429182 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2167G>A (p.Ala723Thr) single nucleotide variant Inborn genetic diseases [RCV003192841] Chr1:182530285 [GRCh38]
Chr1:182499420 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.1957A>G (p.Thr653Ala) single nucleotide variant Inborn genetic diseases [RCV003196662] Chr1:182527604 [GRCh38]
Chr1:182496739 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.2515A>G (p.Thr839Ala) single nucleotide variant Inborn genetic diseases [RCV003286669] Chr1:182540267 [GRCh38]
Chr1:182509402 [GRCh37]
Chr1:1q25.3		 uncertain significance
NM_001137669.2(RGSL1):c.8G>A (p.Ser3Asn) single nucleotide variant Inborn genetic diseases [RCV003361207] Chr1:182450173 [GRCh38]
Chr1:182419308 [GRCh37]
Chr1:1q25.3		 likely benign
NM_001137669.2(RGSL1):c.735G>A (p.Arg245=) single nucleotide variant not provided [RCV003421260] Chr1:182473846 [GRCh38]
Chr1:182442981 [GRCh37]
Chr1:1q25.3		 likely benign
GRCh37/hg19 1q25.1-25.3(chr1:173162501-182702252)x3 copy number gain not specified [RCV003986506] Chr1:173162501..182702252 [GRCh37]
Chr1:1q25.1-25.3		 pathogenic
GRCh37/hg19 1q24.2-31.1(chr1:167994071-187711459)x1 copy number loss not specified [RCV003987250] Chr1:167994071..187711459 [GRCh37]
Chr1:1q24.2-31.1		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2843
Count of miRNA genes:1040
Interacting mature miRNAs:1245
Transcripts:ENST00000294854, ENST00000367561, ENST00000415960, ENST00000416676, ENST00000422241, ENST00000426890, ENST00000427189, ENST00000436031, ENST00000437548, ENST00000443996, ENST00000444367, ENST00000447374, ENST00000456971, ENST00000542961
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.

Markers in Region
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
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Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
RH124538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371182,452,228 - 182,453,503UniSTSGRCh37
Celera1155,563,325 - 155,564,600UniSTS
HuRef1153,688,596 - 153,689,871UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage
High
Medium 270
Low 1 1 17 15 9 15 3 3 2 106 5 1 2
Below cutoff 985 1243 715 300 723 226 1892 874 1871 64 464 597 74 642 1309

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001137669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001366934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011509504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001196 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017001197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446727 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336377 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336378 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054336385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF508902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF510428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL138776 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL139344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC121032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC121033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC142944 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB097250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000294854   ⟹   ENSP00000457748
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,146 - 182,560,597 (+)Ensembl
RefSeq Acc Id: ENST00000367561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,122 - 182,488,748 (+)Ensembl
RefSeq Acc Id: ENST00000415960   ⟹   ENSP00000454954
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,474,522 - 182,560,599 (+)Ensembl
RefSeq Acc Id: ENST00000416676   ⟹   ENSP00000458086
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,149 - 182,489,061 (+)Ensembl
RefSeq Acc Id: ENST00000422241   ⟹   ENSP00000456332
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,144 - 182,489,108 (+)Ensembl
RefSeq Acc Id: ENST00000426890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,121 - 182,472,400 (+)Ensembl
RefSeq Acc Id: ENST00000427189
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,133 - 182,460,127 (+)Ensembl
RefSeq Acc Id: ENST00000436031
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,492,955 - 182,560,593 (+)Ensembl
RefSeq Acc Id: ENST00000437548   ⟹   ENSP00000454969
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,453,384 - 182,472,487 (+)Ensembl
RefSeq Acc Id: ENST00000443996   ⟹   ENSP00000457491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,146 - 182,560,558 (+)Ensembl
RefSeq Acc Id: ENST00000444367
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,453,970 - 182,472,605 (+)Ensembl
RefSeq Acc Id: ENST00000447374   ⟹   ENSP00000454981
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,453,382 - 182,471,375 (+)Ensembl
RefSeq Acc Id: ENST00000456971
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,507,201 - 182,540,421 (+)Ensembl
RefSeq Acc Id: ENST00000634342
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,556,136 - 182,560,597 (+)Ensembl
RefSeq Acc Id: ENST00000634626   ⟹   ENSP00000489498
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,447,891 - 182,471,381 (+)Ensembl
RefSeq Acc Id: ENST00000634679   ⟹   ENSP00000489502
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,409,194 - 182,473,968 (+)Ensembl
RefSeq Acc Id: ENST00000634723   ⟹   ENSP00000489611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,447,886 - 182,472,408 (+)Ensembl
RefSeq Acc Id: ENST00000634758   ⟹   ENSP00000488942
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,409,192 - 182,473,886 (+)Ensembl
RefSeq Acc Id: ENST00000634801   ⟹   ENSP00000489508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,553,470 - 182,560,593 (+)Ensembl
RefSeq Acc Id: ENST00000635407   ⟹   ENSP00000489421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,450,158 - 182,471,377 (+)Ensembl
RefSeq Acc Id: ENST00000635539
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,447,891 - 182,460,121 (+)Ensembl
RefSeq Acc Id: ENST00000648414   ⟹   ENSP00000497245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1182,488,285 - 182,560,593 (+)Ensembl
RefSeq Acc Id: NM_001137669   ⟹   NP_001131141
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,560,597 (+)NCBI
GRCh371182,419,256 - 182,529,732 (+)RGD
GRCh371182,419,256 - 182,529,732 (+)NCBI
Celera1155,530,353 - 155,640,967 (+)RGD
HuRef1153,655,619 - 153,766,201 (+)ENTREZGENE
CHM1_11183,842,215 - 183,953,173 (+)NCBI
T2T-CHM13v2.01181,809,719 - 181,920,071 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001366934   ⟹   NP_001353863
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,560,597 (+)NCBI
T2T-CHM13v2.01181,809,719 - 181,920,071 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509494   ⟹   XP_011507796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,551,141 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011509500   ⟹   XP_011507802
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,532,747 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017001188   ⟹   XP_016856677
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,560,597 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017001189   ⟹   XP_016856678
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,560,597 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017001190   ⟹   XP_016856679
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,452,718 - 182,560,597 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017001191   ⟹   XP_016856680
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,448,323 - 182,560,597 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017001192   ⟹   XP_016856681
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,449,198 - 182,560,597 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017001193   ⟹   XP_016856682
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,447,877 - 182,560,597 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017001196   ⟹   XP_016856685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,460,062 - 182,560,597 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047419632   ⟹   XP_047275588
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,460,044 - 182,560,597 (+)NCBI
RefSeq Acc Id: XM_047419638   ⟹   XP_047275594
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,553,541 (+)NCBI
RefSeq Acc Id: XM_047419640   ⟹   XP_047275596
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,472,468 - 182,560,597 (+)NCBI
RefSeq Acc Id: XM_047419642   ⟹   XP_047275598
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,488,331 - 182,560,597 (+)NCBI
RefSeq Acc Id: XM_054336373   ⟹   XP_054192348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,809,719 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336374   ⟹   XP_054192349
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,809,719 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336375   ⟹   XP_054192350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,812,291 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336376   ⟹   XP_054192351
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,807,896 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336377   ⟹   XP_054192352
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,808,771 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336378   ⟹   XP_054192353
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,807,450 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336379   ⟹   XP_054192354
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,809,719 - 181,910,619 (+)NCBI
RefSeq Acc Id: XM_054336380   ⟹   XP_054192355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,819,617 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336381   ⟹   XP_054192356
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,809,719 - 181,913,015 (+)NCBI
RefSeq Acc Id: XM_054336382   ⟹   XP_054192357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,809,719 - 181,892,224 (+)NCBI
RefSeq Acc Id: XM_054336383   ⟹   XP_054192358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,832,040 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336384   ⟹   XP_054192359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,819,635 - 181,920,071 (+)NCBI
RefSeq Acc Id: XM_054336385   ⟹   XP_054192360
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01181,847,903 - 181,920,071 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001131141 (Get FASTA)   NCBI Sequence Viewer  
  NP_001353863 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507796 (Get FASTA)   NCBI Sequence Viewer  
  XP_011507802 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856677 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856678 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856679 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856680 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856681 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856682 (Get FASTA)   NCBI Sequence Viewer  
  XP_016856685 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275588 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275594 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275596 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275598 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192348 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192349 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192350 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192351 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192352 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192353 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192354 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192355 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192356 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192357 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192358 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192359 (Get FASTA)   NCBI Sequence Viewer  
  XP_054192360 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein A5PLK6 (Get FASTA)   NCBI Sequence Viewer  
  AAI42945 (Get FASTA)   NCBI Sequence Viewer  
  AAP30864 (Get FASTA)   NCBI Sequence Viewer  
  BAC87300 (Get FASTA)   NCBI Sequence Viewer  
  BAH13800 (Get FASTA)   NCBI Sequence Viewer  
  CAB66836 (Get FASTA)   NCBI Sequence Viewer  
  EAW91125 (Get FASTA)   NCBI Sequence Viewer  
  EAW91126 (Get FASTA)   NCBI Sequence Viewer  
  EAW91127 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000454954.2
  ENSP00000454969.1
  ENSP00000454981.1
  ENSP00000456332.1
  ENSP00000457491
  ENSP00000457491.1
  ENSP00000457748
  ENSP00000457748.1
  ENSP00000458086.1
  ENSP00000488942.1
  ENSP00000489421.1
  ENSP00000489498.1
  ENSP00000489502.1
  ENSP00000489508.1
  ENSP00000489611.1
  ENSP00000497245.1
Reference Protein Sequences
RefSeq Acc Id: NP_001131141   ⟸   NM_001137669
- Peptide Label: isoform 1
- UniProtKB: Q86UV0 (UniProtKB/Swiss-Prot),   Q6ZRL0 (UniProtKB/Swiss-Prot),   Q0VAJ5 (UniProtKB/Swiss-Prot),   Q0VAJ4 (UniProtKB/Swiss-Prot),   A6PVM3 (UniProtKB/Swiss-Prot),   A6PVM2 (UniProtKB/Swiss-Prot),   A2A2Z0 (UniProtKB/Swiss-Prot),   Q9H084 (UniProtKB/Swiss-Prot),   A5PLK6 (UniProtKB/Swiss-Prot),   B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507796   ⟸   XM_011509494
- Peptide Label: isoform X3
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011507802   ⟸   XM_011509500
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016856682   ⟸   XM_017001193
- Peptide Label: isoform X2
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856680   ⟸   XM_017001191
- Peptide Label: isoform X2
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856681   ⟸   XM_017001192
- Peptide Label: isoform X2
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856678   ⟸   XM_017001189
- Peptide Label: isoform X2
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856677   ⟸   XM_017001188
- Peptide Label: isoform X1
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856679   ⟸   XM_017001190
- Peptide Label: isoform X2
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016856685   ⟸   XM_017001196
- Peptide Label: isoform X7
- UniProtKB: A5PLK6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001353863   ⟸   NM_001366934
- Peptide Label: isoform 2
- UniProtKB: B7Z814 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000497245   ⟸   ENST00000648414
RefSeq Acc Id: ENSP00000489508   ⟸   ENST00000634801
RefSeq Acc Id: ENSP00000489611   ⟸   ENST00000634723
RefSeq Acc Id: ENSP00000488942   ⟸   ENST00000634758
RefSeq Acc Id: ENSP00000489502   ⟸   ENST00000634679
RefSeq Acc Id: ENSP00000489498   ⟸   ENST00000634626
RefSeq Acc Id: ENSP00000489421   ⟸   ENST00000635407
RefSeq Acc Id: ENSP00000457748   ⟸   ENST00000294854
RefSeq Acc Id: ENSP00000454954   ⟸   ENST00000415960
RefSeq Acc Id: ENSP00000458086   ⟸   ENST00000416676
RefSeq Acc Id: ENSP00000457491   ⟸   ENST00000443996
RefSeq Acc Id: ENSP00000454981   ⟸   ENST00000447374
RefSeq Acc Id: ENSP00000456332   ⟸   ENST00000422241
RefSeq Acc Id: ENSP00000454969   ⟸   ENST00000437548
RefSeq Acc Id: XP_047275594   ⟸   XM_047419638
- Peptide Label: isoform X5
- UniProtKB: H3BU64 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047275588   ⟸   XM_047419632
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047275596   ⟸   XM_047419640
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047275598   ⟸   XM_047419642
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054192353   ⟸   XM_054336378
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054192351   ⟸   XM_054336376
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054192352   ⟸   XM_054336377
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054192349   ⟸   XM_054336374
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054192348   ⟸   XM_054336373
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054192356   ⟸   XM_054336381
- Peptide Label: isoform X5
- UniProtKB: H3BU64 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054192354   ⟸   XM_054336379
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054192357   ⟸   XM_054336382
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054192350   ⟸   XM_054336375
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054192355   ⟸   XM_054336380
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054192359   ⟸   XM_054336384
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054192358   ⟸   XM_054336383
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054192360   ⟸   XM_054336385
- Peptide Label: isoform X8
Protein Domains
RGS

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A5PLK6-F1-model_v2 AlphaFold A5PLK6 1-1076 view protein structure

Promoters
RGD ID:6858310
Promoter ID:EPDNEW_H2320
Type:multiple initiation site
Name:RGSL1_1
Description:regulator of G protein signaling like 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381182,450,146 - 182,450,206EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:18636 AgrOrtholog
COSMIC RGSL1 COSMIC
Ensembl Genes ENSG00000121446 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000294854 ENTREZGENE
  ENST00000294854.13 UniProtKB/Swiss-Prot
  ENST00000415960.6 UniProtKB/TrEMBL
  ENST00000416676.5 UniProtKB/TrEMBL
  ENST00000422241.2 UniProtKB/TrEMBL
  ENST00000437548.5 UniProtKB/TrEMBL
  ENST00000443996 ENTREZGENE
  ENST00000443996.6 UniProtKB/TrEMBL
  ENST00000447374.5 UniProtKB/TrEMBL
  ENST00000634626.1 UniProtKB/TrEMBL
  ENST00000634679.1 UniProtKB/TrEMBL
  ENST00000634723.1 UniProtKB/TrEMBL
  ENST00000634758.1 UniProtKB/TrEMBL
  ENST00000634801.1 UniProtKB/TrEMBL
  ENST00000635407.1 UniProtKB/TrEMBL
  ENST00000648414.1 UniProtKB/TrEMBL
Gene3D-CATH 1.10.167.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000121446 GTEx
HGNC ID HGNC:18636 ENTREZGENE
Human Proteome Map RGSL1 Human Proteome Map
InterPro RGS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RGS_subdomain_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:353299 UniProtKB/Swiss-Prot
NCBI Gene 353299 ENTREZGENE
OMIM 611012 OMIM
  611013 OMIM
PANTHER REGULATOR OF G-PROTEIN SIGNALING PROTEIN-LIKE UniProtKB/Swiss-Prot
  REGULATOR OF G-PROTEIN SIGNALING PROTEIN-LIKE UniProtKB/Swiss-Prot
  REGULATOR OF G-PROTEIN SIGNALING PROTEIN-LIKE UniProtKB/TrEMBL
  REGULATOR OF G-PROTEIN SIGNALING PROTEIN-LIKE UniProtKB/TrEMBL
Pfam RGS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134870196 PharmGKB
PROSITE RGS UniProtKB/TrEMBL
Superfamily-SCOP SSF48097 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0U1RQD8_HUMAN UniProtKB/TrEMBL
  A0A0U1RRA3_HUMAN UniProtKB/TrEMBL
  A0A0U1RRF3_HUMAN UniProtKB/TrEMBL
  A0A0U1RRF6_HUMAN UniProtKB/TrEMBL
  A0A0U1RRG0_HUMAN UniProtKB/TrEMBL
  A0A0U1RRN0_HUMAN UniProtKB/TrEMBL
  A0A3B3ISC9_HUMAN UniProtKB/TrEMBL
  A2A2Z0 ENTREZGENE
  A5PLK6 ENTREZGENE
  A6PVM2 ENTREZGENE
  A6PVM3 ENTREZGENE
  B7Z814 ENTREZGENE, UniProtKB/TrEMBL
  H3BNQ0_HUMAN UniProtKB/TrEMBL
  H3BNR3_HUMAN UniProtKB/TrEMBL
  H3BNS3_HUMAN UniProtKB/TrEMBL
  H3BRN5_HUMAN UniProtKB/TrEMBL
  H3BU64 ENTREZGENE, UniProtKB/TrEMBL
  H3BVE8_HUMAN UniProtKB/TrEMBL
  Q0VAJ4 ENTREZGENE
  Q0VAJ5 ENTREZGENE
  Q6ZRL0 ENTREZGENE
  Q86UV0 ENTREZGENE
  Q9H084 ENTREZGENE
  RGSL_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A2A2Z0 UniProtKB/Swiss-Prot
  A6PVM2 UniProtKB/Swiss-Prot
  A6PVM3 UniProtKB/Swiss-Prot
  Q0VAJ4 UniProtKB/Swiss-Prot
  Q0VAJ5 UniProtKB/Swiss-Prot
  Q6ZRL0 UniProtKB/Swiss-Prot
  Q86UV0 UniProtKB/Swiss-Prot
  Q9H084 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-04-18 RGSL1  regulator of G protein signaling like 1    regulator of G-protein signaling like 1  Symbol and/or name change 5135510 APPROVED
2016-02-25 RGSL1  regulator of G-protein signaling like 1  RGSL2  regulator of G-protein signaling like 2  Data merged from RGD:1353853 737654 PROVISIONAL