DISC1 (DISC1 scaffold protein) - Rat Genome Database

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Gene: DISC1 (DISC1 scaffold protein) Homo sapiens
Analyze
Symbol: DISC1
Name: DISC1 scaffold protein
RGD ID: 736704
HGNC Page HGNC:2888
Description: Enables identical protein binding activity. Involved in several processes, including neuron migration; positive regulation of Wnt signaling pathway; and positive regulation of neuroblast proliferation. Acts upstream of or within non-motile cilium assembly. Located in several cellular components, including ciliary base; cytoskeleton; and mitochondrion. Is active in several cellular components, including GABA-ergic synapse; glutamatergic synapse; and postsynaptic density. Implicated in autism spectrum disorder (multiple); bipolar disorder; chronic fatigue syndrome; major depressive disorder; and psychotic disorder (multiple). Biomarker of major depressive disorder; schizophrenia; and substance-related disorder.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: C1orf136; disrupted in schizophrenia 1; disrupted in schizophrenia 1 protein; FLJ13381; FLJ21640; FLJ25311; FLJ41105; KIAA0457; Putative uncharacterized protein C1orf136; SCZD9
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
GRCh381231,626,790 - 232,041,272 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1231,626,790 - 232,041,272 (+)EnsemblGRCh38hg38GRCh38
GRCh371231,762,536 - 232,177,018 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361229,829,184 - 230,243,641 (+)NCBINCBI36Build 36hg18NCBI36
Build 341228,069,295 - 228,483,607NCBI
Celera1205,027,310 - 205,445,842 (+)NCBICelera
Cytogenetic Map1q42.2NCBI
HuRef1202,246,109 - 202,664,353 (+)NCBIHuRef
CHM1_11233,036,406 - 233,450,761 (+)NCBICHM1_1
T2T-CHM13v2.01231,009,996 - 231,426,811 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. A functional polymorphism in the disrupted-in schizophrenia 1 gene is associated with chronic fatigue syndrome. Fukuda S, etal., Life Sci. 2010 May 8;86(19-20):722-5. Epub 2010 Mar 20.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling. Hashimoto R, etal., Hum Mol Genet. 2006 Oct 15;15(20):3024-33. Epub 2006 Sep 7.
4. DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder. Hennah W, etal., Mol Psychiatry. 2009 Sep;14(9):865-73. Epub 2008 Mar 4.
5. Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder. Hodgkinson CA, etal., Am J Hum Genet. 2004 Nov;75(5):862-72. Epub 2004 Sep 22.
6. Association of DISC1 gene with schizophrenia in families from two distinct French and Algerian populations. Lepagnol-Bestel AM, etal., Psychiatr Genet. 2010 Dec;20(6):298-303.
7. Disruption of two novel genes by a translocation co-segregating with schizophrenia. Millar JK, etal., Hum Mol Genet. 2000 May 22;9(9):1415-23.
8. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
9. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
10. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
11. A form of DISC1 enriched in nucleus: altered subcellular distribution in orbitofrontal cortex in psychosis and substance/alcohol abuse. Sawamura N, etal., Proc Natl Acad Sci U S A. 2005 Jan 25;102(4):1187-92. Epub 2005 Jan 18.
12. Limited association between Disrupted in Schizophrenia 1 (DISC1) gene and bipolar disorder in the Chinese population. Xiao Y, etal., Psychiatr Genet. 2011 Feb;21(1):42-6.
13. Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study. Zheng F, etal., Behav Brain Funct. 2011 May 15;7:14.
Additional References at PubMed
PMID:9455484   PMID:10945471   PMID:11443544   PMID:11468279   PMID:12477932   PMID:12506198   PMID:12573262   PMID:12812986   PMID:12874605   PMID:14532331   PMID:14623284   PMID:14702039  
PMID:14962739   PMID:15094396   PMID:15121183   PMID:15184103   PMID:15342131   PMID:15478311   PMID:15728732   PMID:15797709   PMID:15838535   PMID:15939883   PMID:15940305   PMID:16039834  
PMID:16054297   PMID:16056147   PMID:16103888   PMID:16209927   PMID:16243297   PMID:16275808   PMID:16293762   PMID:16389590   PMID:16510495   PMID:16524593   PMID:16710414   PMID:16736468  
PMID:16814263   PMID:16843095   PMID:16936715   PMID:16936759   PMID:16997000   PMID:17006672   PMID:17035248   PMID:17043677   PMID:17055463   PMID:17117617   PMID:17185386   PMID:17286247  
PMID:17389905   PMID:17579608   PMID:17673452   PMID:17823207   PMID:17912248   PMID:17997036   PMID:18075479   PMID:18078707   PMID:18164685   PMID:18180429   PMID:18198266   PMID:18270998  
PMID:18395819   PMID:18400883   PMID:18469341   PMID:18474207   PMID:18497105   PMID:18583979   PMID:18620078   PMID:18762586   PMID:18800054   PMID:18818052   PMID:18955030   PMID:18983980  
PMID:19046394   PMID:19077115   PMID:19086053   PMID:19118814   PMID:19188535   PMID:19191256   PMID:19251251   PMID:19255581   PMID:19300510   PMID:19303846   PMID:19304459   PMID:19328558  
PMID:19352214   PMID:19367581   PMID:19414483   PMID:19451621   PMID:19455170   PMID:19502360   PMID:19548263   PMID:19583211   PMID:19586833   PMID:19632097   PMID:19693267   PMID:19782967  
PMID:19805229   PMID:19913623   PMID:19944766   PMID:20048751   PMID:20084519   PMID:20168324   PMID:20212127   PMID:20339536   PMID:20351714   PMID:20360304   PMID:20379614   PMID:20398908  
PMID:20531374   PMID:20531939   PMID:20574532   PMID:20602615   PMID:20628343   PMID:20666147   PMID:20691427   PMID:20850505   PMID:20880836   PMID:20956536   PMID:21041608   PMID:21079610  
PMID:21091867   PMID:21149852   PMID:21256178   PMID:21298101   PMID:21315744   PMID:21358711   PMID:21368031   PMID:21376542   PMID:21445958   PMID:21471969   PMID:21483430   PMID:21483435  
PMID:21605958   PMID:21642004   PMID:21659360   PMID:21739582   PMID:21853134   PMID:21873635   PMID:21878470   PMID:21998303   PMID:22015021   PMID:22095064   PMID:22099458   PMID:22099459  
PMID:22153077   PMID:22228767   PMID:22291444   PMID:22337479   PMID:22363459   PMID:22385968   PMID:22422769   PMID:22434823   PMID:22472875   PMID:22516458   PMID:22547224   PMID:22558309  
PMID:22659396   PMID:22693340   PMID:22798627   PMID:22801410   PMID:22815203   PMID:22832604   PMID:22869032   PMID:22901592   PMID:23011268   PMID:23140672   PMID:23233134   PMID:23253390  
PMID:23283688   PMID:23347445   PMID:23379509   PMID:23389941   PMID:23481583   PMID:23497821   PMID:23581481   PMID:23602339   PMID:23637159   PMID:23732877   PMID:23832957   PMID:23855403  
PMID:23921125   PMID:24013095   PMID:24090488   PMID:24092329   PMID:24146131   PMID:24169524   PMID:24219803   PMID:24289909   PMID:24474471   PMID:24722188   PMID:24770450   PMID:24908665  
PMID:24909300   PMID:24934694   PMID:24940743   PMID:25012417   PMID:25016072   PMID:25043320   PMID:25092219   PMID:25218871   PMID:25433637   PMID:25533973   PMID:25620115   PMID:25635053  
PMID:25705664   PMID:25821909   PMID:26062786   PMID:26078884   PMID:26162659   PMID:26186194   PMID:26206934   PMID:26209938   PMID:26299970   PMID:26315603   PMID:26443054   PMID:26475744  
PMID:26546129   PMID:26553875   PMID:26615762   PMID:26945459   PMID:26997180   PMID:27023224   PMID:27026592   PMID:27052956   PMID:27121900   PMID:27236031   PMID:27333658   PMID:27346367  
PMID:27354230   PMID:27369464   PMID:27466199   PMID:27595595   PMID:27852062   PMID:28249940   PMID:28263187   PMID:28472294   PMID:28514442   PMID:28630456   PMID:28727686   PMID:28946750  
PMID:28981898   PMID:29031911   PMID:29100974   PMID:29103808   PMID:29107702   PMID:29324815   PMID:29410289   PMID:29643329   PMID:29643356   PMID:29676528   PMID:29845934   PMID:29945223  
PMID:29961565   PMID:29987050   PMID:30118782   PMID:30252773   PMID:30286368   PMID:30397826   PMID:30410030   PMID:30488644   PMID:30561706   PMID:30599263   PMID:30976040   PMID:31106784  
PMID:31264367   PMID:31398428   PMID:31413325   PMID:31444471   PMID:31916893   PMID:32296183   PMID:32482796   PMID:32493513   PMID:32707033   PMID:33008326   PMID:33253521   PMID:33550790  
PMID:33961781   PMID:34369648   PMID:34728620   PMID:34981809   PMID:35044719   PMID:35165396   PMID:35361701   PMID:35367090   PMID:35461978   PMID:35509820   PMID:35513527   PMID:35944360  
PMID:36215168   PMID:36397361   PMID:36538041   PMID:36858606   PMID:37668563  


Genomics

Comparative Map Data
DISC1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381231,626,790 - 232,041,272 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1231,626,790 - 232,041,272 (+)EnsemblGRCh38hg38GRCh38
GRCh371231,762,536 - 232,177,018 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361229,829,184 - 230,243,641 (+)NCBINCBI36Build 36hg18NCBI36
Build 341228,069,295 - 228,483,607NCBI
Celera1205,027,310 - 205,445,842 (+)NCBICelera
Cytogenetic Map1q42.2NCBI
HuRef1202,246,109 - 202,664,353 (+)NCBIHuRef
CHM1_11233,036,406 - 233,450,761 (+)NCBICHM1_1
T2T-CHM13v2.01231,009,996 - 231,426,811 (+)NCBIT2T-CHM13v2.0
Disc1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398125,773,928 - 125,991,882 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl8125,780,934 - 125,988,597 (+)EnsemblGRCm39 Ensembl
GRCm388125,048,767 - 125,265,143 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8125,054,195 - 125,261,858 (+)EnsemblGRCm38mm10GRCm38
MGSCv378127,578,095 - 127,785,051 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv368127,940,285 - 128,148,274 (+)NCBIMGSCv36mm8
Celera8129,364,004 - 129,569,546 (+)NCBICelera
Cytogenetic Map8E2NCBI
cM Map873.26NCBI
Disc1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81969,911,548 - 70,120,970 (+)NCBIGRCr8
mRatBN7.21953,014,201 - 53,223,617 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1953,014,616 - 53,219,778 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1959,798,589 - 60,006,037 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01960,649,615 - 60,856,157 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01962,725,049 - 62,932,128 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01957,818,838 - 58,069,992 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1957,820,260 - 58,066,152 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01968,529,791 - 68,641,620 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.01968,711,386 - 68,769,050 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41955,265,116 - 55,449,375 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11955,270,004 - 55,427,798 (+)NCBI
Celera1952,376,528 - 52,580,211 (+)NCBICelera
Cytogenetic Map19q12NCBI
Disc1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554926,953,389 - 7,239,328 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554926,946,528 - 7,239,328 (-)NCBIChiLan1.0ChiLan1.0
DISC1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2117,161,052 - 17,575,242 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1117,356,795 - 17,771,144 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01207,180,513 - 207,594,684 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11212,320,582 - 212,616,406 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1212,265,520 - 212,612,079 (+)Ensemblpanpan1.1panPan2
DISC1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.147,524,336 - 7,825,143 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl47,524,397 - 7,822,558 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha47,518,316 - 7,865,131 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.047,547,601 - 7,896,939 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl47,547,642 - 7,897,205 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.147,555,426 - 7,902,062 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.047,676,276 - 8,023,319 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.047,902,898 - 8,249,898 (-)NCBIUU_Cfam_GSD_1.0
Disc1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934442,878,559 - 43,045,852 (-)NCBIHiC_Itri_2
SpeTri2.0NW_00493648419,151,752 - 19,237,435 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
DISC1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1458,606,464 - 58,963,563 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11458,606,441 - 58,963,954 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21463,056,095 - 63,124,157 (-)NCBISscrofa10.2Sscrofa10.2susScr3
DISC1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12568,886,451 - 69,274,774 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2568,946,430 - 69,263,198 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605570,799,188 - 71,196,506 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Disc1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462477517,831,272 - 18,165,668 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462477517,820,590 - 18,165,640 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in DISC1
92 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
DISC1, HAPLOTYPE, HEP3 variation Schizophrenia 9 [RCV001844007] Chr1:1q42.1 pathogenic|risk factor
NM_018662.2(DISC1):c.1981+19568T>A single nucleotide variant Lung cancer [RCV000090589] Chr1:231838085 [GRCh38]
Chr1:231973831 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.2(DISC1):c.1982-16641A>T single nucleotide variant Lung cancer [RCV000090590] Chr1:231942187 [GRCh38]
Chr1:232077933 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh38/hg38 1q32.3-44(chr1:214023812-248918469)x3 copy number gain See cases [RCV000050981] Chr1:214023812..248918469 [GRCh38]
Chr1:214197155..249212668 [GRCh37]
Chr1:212263778..247179291 [NCBI36]
Chr1:1q32.3-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223347693-248918469)x3 copy number gain See cases [RCV000050581] Chr1:223347693..248918469 [GRCh38]
Chr1:223521035..249212668 [GRCh37]
Chr1:221587658..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q42.13-44(chr1:230106271-243677283)x1 copy number loss See cases [RCV000051082] Chr1:230106271..243677283 [GRCh38]
Chr1:230242018..243840585 [GRCh37]
Chr1:228308641..241907208 [NCBI36]
Chr1:1q42.13-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:221902539-248918469)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051875]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051875]|See cases [RCV000051875] Chr1:221902539..248918469 [GRCh38]
Chr1:222075881..249212668 [GRCh37]
Chr1:220142504..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223828500-248891309)x3 copy number gain See cases [RCV000051878] Chr1:223828500..248891309 [GRCh38]
Chr1:224016202..249185508 [GRCh37]
Chr1:222082825..247152131 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223887780-248891309)x3 copy number gain See cases [RCV000051880] Chr1:223887780..248891309 [GRCh38]
Chr1:224075482..249185508 [GRCh37]
Chr1:222142105..247152131 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3 copy number gain See cases [RCV000051861] Chr1:209646207..248931113 [GRCh38]
Chr1:209819552..249225312 [GRCh37]
Chr1:207886175..247191935 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh38/hg38 1q42.11-44(chr1:224096488-248918469)x3 copy number gain See cases [RCV000051882] Chr1:224096488..248918469 [GRCh38]
Chr1:224284190..249212668 [GRCh37]
Chr1:222350813..247179291 [NCBI36]
Chr1:1q42.11-44		 pathogenic
GRCh38/hg38 1q42.2(chr1:231950293-232057038)x1 copy number loss See cases [RCV000053216] Chr1:231950293..232057038 [GRCh38]
Chr1:232086039..232192784 [GRCh37]
Chr1:230152662..230259407 [NCBI36]
Chr1:1q42.2		 uncertain significance
NM_018662.2(DISC1):c.270G>A (p.Ser90=) single nucleotide variant Malignant melanoma [RCV000060108] Chr1:231694028 [GRCh38]
Chr1:231829774 [GRCh37]
Chr1:229896397 [NCBI36]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.54G>A (p.Val18=) single nucleotide variant not provided [RCV000084633] Chr1:231626921 [GRCh38]
Chr1:231762667 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.340A>T (p.Thr114Ser) single nucleotide variant not provided [RCV000084634] Chr1:231694098 [GRCh38]
Chr1:231829844 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.472G>A (p.Ala158Thr) single nucleotide variant not provided [RCV000084635] Chr1:231694230 [GRCh38]
Chr1:231829976 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.768C>T (p.His256=) single nucleotide variant not provided [RCV000084636] Chr1:231694526 [GRCh38]
Chr1:231830272 [GRCh37]
Chr1:1q42.2		 likely benign|not provided
NM_018662.3(DISC1):c.791G>A (p.Arg264Gln) single nucleotide variant not provided [RCV000084637] Chr1:231694549 [GRCh38]
Chr1:231830295 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.841G>A (p.Ala281Thr) single nucleotide variant not provided [RCV000084638] Chr1:231694599 [GRCh38]
Chr1:231830345 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1286C>G (p.Thr429Ser) single nucleotide variant not provided [RCV000084639] Chr1:231767157 [GRCh38]
Chr1:231902903 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1291A>G (p.Thr431Ala) single nucleotide variant not provided [RCV000084640] Chr1:231767162 [GRCh38]
Chr1:231902908 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1363C>T (p.Arg455Ter) single nucleotide variant not provided [RCV000084641] Chr1:231767234 [GRCh38]
Chr1:231902980 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1401A>G (p.Lys467=) single nucleotide variant not provided [RCV000084642] Chr1:231770837 [GRCh38]
Chr1:231906583 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1518A>G (p.Pro506=) single nucleotide variant not provided [RCV000084643] Chr1:231770954 [GRCh38]
Chr1:231906700 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1718C>T (p.Thr573Ile) single nucleotide variant not provided [RCV000084644] Chr1:231800136 [GRCh38]
Chr1:231935882 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1729A>G (p.Lys577Glu) single nucleotide variant not provided [RCV000084645] Chr1:231800147 [GRCh38]
Chr1:231935893 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1819C>T (p.Leu607Phe) single nucleotide variant not provided [RCV000084646] Chr1:231818355 [GRCh38]
Chr1:231954101 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.2063G>A (p.Gly688Glu) single nucleotide variant Inborn genetic diseases [RCV002514506]|not provided [RCV000084647] Chr1:232008805 [GRCh38]
Chr1:232144551 [GRCh37]
Chr1:1q42.2		 uncertain significance|not provided
NM_018662.3(DISC1):c.2157G>A (p.Glu719=) single nucleotide variant not provided [RCV000084648] Chr1:232008899 [GRCh38]
Chr1:232144645 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.2215G>A (p.Glu739Lys) single nucleotide variant not provided [RCV000084649] Chr1:232008957 [GRCh38]
Chr1:232144703 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.2221A>G (p.Lys741Glu) single nucleotide variant not provided [RCV000084650] Chr1:232008963 [GRCh38]
Chr1:232144709 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.2295T>A (p.Gly765=) single nucleotide variant DISC1-related condition [RCV003964954]|not provided [RCV000084651] Chr1:232009037 [GRCh38]
Chr1:232144783 [GRCh37]
Chr1:1q42.2		 likely benign|not provided
NM_018662.3(DISC1):c.2543G>A (p.Gly848Asp) single nucleotide variant not provided [RCV000084652] Chr1:232036809 [GRCh38]
Chr1:232172555 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.2550C>T (p.His850=) single nucleotide variant not provided [RCV000084653] Chr1:232036816 [GRCh38]
Chr1:232172562 [GRCh37]
Chr1:1q42.2		 not provided
GRCh38/hg38 1q32.2-44(chr1:209963625-248918469)x3 copy number gain See cases [RCV000134979] Chr1:209963625..248918469 [GRCh38]
Chr1:210136970..249212668 [GRCh37]
Chr1:208203593..247179291 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223815147-248918469)x3 copy number gain See cases [RCV000135839] Chr1:223815147..248918469 [GRCh38]
Chr1:224002849..249212668 [GRCh37]
Chr1:222069472..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q42.12-42.2(chr1:226185124-232872488)x1 copy number loss See cases [RCV000135796] Chr1:226185124..232872488 [GRCh38]
Chr1:226372825..233008234 [GRCh37]
Chr1:224439448..231074857 [NCBI36]
Chr1:1q42.12-42.2		 pathogenic
GRCh38/hg38 1q42.13-44(chr1:229022909-248918469)x3 copy number gain See cases [RCV000136666] Chr1:229022909..248918469 [GRCh38]
Chr1:229158656..249212668 [GRCh37]
Chr1:227225279..247179291 [NCBI36]
Chr1:1q42.13-44		 pathogenic
GRCh38/hg38 1q42.2(chr1:231432777-231696534)x1 copy number loss See cases [RCV000137604] Chr1:231432777..231696534 [GRCh38]
Chr1:231568523..231832280 [GRCh37]
Chr1:229635146..229898903 [NCBI36]
Chr1:1q42.2		 likely pathogenic
GRCh38/hg38 1q42.11-44(chr1:224022862-248918469)x3 copy number gain See cases [RCV000137769] Chr1:224022862..248918469 [GRCh38]
Chr1:224210564..249212668 [GRCh37]
Chr1:222277187..247179291 [NCBI36]
Chr1:1q42.11-44		 pathogenic
GRCh38/hg38 1q42.2(chr1:231613920-231678234)x3 copy number gain See cases [RCV000138574] Chr1:231613920..231678234 [GRCh38]
Chr1:231749666..231813980 [GRCh37]
Chr1:229816289..229880603 [NCBI36]
Chr1:1q42.2		 likely benign
GRCh38/hg38 1q42.2(chr1:231579387-231678175)x3 copy number gain See cases [RCV000141201] Chr1:231579387..231678175 [GRCh38]
Chr1:231715133..231813921 [GRCh37]
Chr1:229781756..229880544 [NCBI36]
Chr1:1q42.2		 benign|likely benign|conflicting data from submitters
GRCh38/hg38 1q42.12-44(chr1:225438480-248787200)x3 copy number gain See cases [RCV000142448] Chr1:225438480..248787200 [GRCh38]
Chr1:225626182..249060210 [GRCh37]
Chr1:223692805..247048022 [NCBI36]
Chr1:1q42.12-44		 pathogenic
GRCh38/hg38 1q32.2-44(chr1:207346642-248930485)x3 copy number gain See cases [RCV000143727] Chr1:207346642..248930485 [GRCh38]
Chr1:207519987..249224684 [GRCh37]
Chr1:205586610..247191307 [NCBI36]
Chr1:1q32.2-44		 pathogenic
NC_000001.11:g.231573658_231727458dup duplication Normal pregnancy [RCV000161194] Chr1:231573658..231727458 [GRCh38]
Chr1:231709404..231863204 [GRCh37]
Chr1:1q42.2		 not provided
NM_001164556.1(DISC1):c.-53210_67+50454dup duplication Gestational diabetes mellitus uncontrolled [RCV000161195] Chr1:231573658..231677388 [GRCh38]
Chr1:231709404..231813134 [GRCh37]
Chr1:1q42.2		 not provided
NM_001164556.1(DISC1):c.-51125_67+50454dup duplication Gestational diabetes mellitus uncontrolled [RCV000161196] Chr1:231575743..231677388 [GRCh38]
Chr1:231711489..231813134 [GRCh37]
Chr1:1q42.2		 not provided
NM_018662.3(DISC1):c.1017C>G (p.Asp339Glu) single nucleotide variant Inborn genetic diseases [RCV003246566] Chr1:231694775 [GRCh38]
Chr1:231830521 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3 copy number gain See cases [RCV000449172] Chr1:195483439..249213000 [GRCh37]
Chr1:1q31.3-44		 pathogenic
GRCh37/hg19 1q41-44(chr1:214697099-249224684)x3 copy number gain See cases [RCV000449210] Chr1:214697099..249224684 [GRCh37]
Chr1:1q41-44		 pathogenic
GRCh37/hg19 1q42.2-44(chr1:231670870-249213000)x3 copy number gain See cases [RCV000447654] Chr1:231670870..249213000 [GRCh37]
Chr1:1q42.2-44		 pathogenic
GRCh37/hg19 1q42.2(chr1:231710352-231813921)x3 copy number gain See cases [RCV000448163] Chr1:231710352..231813921 [GRCh37]
Chr1:1q42.2		 benign
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q42.11-44(chr1:224105294-249224684)x3 copy number gain See cases [RCV000510981] Chr1:224105294..249224684 [GRCh37]
Chr1:1q42.11-44		 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_018662.3(DISC1):c.1249C>T (p.Arg417Cys) single nucleotide variant Inborn genetic diseases [RCV003245751] Chr1:231750057 [GRCh38]
Chr1:231885803 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q41-44(chr1:218252551-249224684)x3 copy number gain not provided [RCV000684700] Chr1:218252551..249224684 [GRCh37]
Chr1:1q41-44		 pathogenic
GRCh37/hg19 1q42.13-44(chr1:228529973-249181598)x3 copy number gain not provided [RCV000684707] Chr1:228529973..249181598 [GRCh37]
Chr1:1q42.13-44		 pathogenic
GRCh37/hg19 1q42.2(chr1:231713096-231816223)x3 copy number gain not provided [RCV000684708] Chr1:231713096..231816223 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.2(chr1:231828116-231928554)x1 copy number loss not provided [RCV000684709] Chr1:231828116..231928554 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.2(chr1:231908346-231943836)x1 copy number loss not provided [RCV000684710] Chr1:231908346..231943836 [GRCh37]
Chr1:1q42.2		 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
NC_000001.11:g.(?_231740970)_(231949671_?)del deletion Autism [RCV000754141] Chr1:231740970..231949671 [GRCh38]
Chr1:1q42.2		 likely pathogenic
GRCh37/hg19 1q42.2(chr1:231709404-231813134)x3 copy number gain not provided [RCV000749391] Chr1:231709404..231813134 [GRCh37]
Chr1:1q42.2		 benign
GRCh37/hg19 1q42.2(chr1:231711622-231813134)x3 copy number gain not provided [RCV000749392] Chr1:231711622..231813134 [GRCh37]
Chr1:1q42.2		 benign
GRCh37/hg19 1q42.2(chr1:232074973-232121222)x3 copy number gain not provided [RCV000749393] Chr1:232074973..232121222 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.1295C>T (p.Pro432Leu) single nucleotide variant DISC1-related condition [RCV003933307]|not provided [RCV000951053] Chr1:231767166 [GRCh38]
Chr1:231902912 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1634+7C>G single nucleotide variant not provided [RCV000923408] Chr1:231771077 [GRCh38]
Chr1:231906823 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1347C>T (p.His449=) single nucleotide variant DISC1-related condition [RCV003958216]|not provided [RCV000905342] Chr1:231767218 [GRCh38]
Chr1:231902964 [GRCh37]
Chr1:1q42.2		 benign|likely benign
NM_018662.3(DISC1):c.1356C>T (p.Ile452=) single nucleotide variant DISC1-related condition [RCV003960781]|not provided [RCV000966786] Chr1:231767227 [GRCh38]
Chr1:231902973 [GRCh37]
Chr1:1q42.2		 benign|likely benign
NM_018662.3(DISC1):c.196C>T (p.Arg66Trp) single nucleotide variant DISC1-related condition [RCV003905939]|not provided [RCV000967942] Chr1:231693954 [GRCh38]
Chr1:231829700 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.211G>T (p.Val71Leu) single nucleotide variant DISC1-related condition [RCV003958307]|not provided [RCV000910269] Chr1:231693969 [GRCh38]
Chr1:231829715 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.990C>T (p.Leu330=) single nucleotide variant not provided [RCV000927994] Chr1:231694748 [GRCh38]
Chr1:231830494 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1034G>A (p.Arg345Gln) single nucleotide variant not provided [RCV000885120] Chr1:231694792 [GRCh38]
Chr1:231830538 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.2251G>C (p.Glu751Gln) single nucleotide variant DISC1-related condition [RCV003915822]|not provided [RCV000953168] Chr1:232008993 [GRCh38]
Chr1:232144739 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.988C>T (p.Leu330Phe) single nucleotide variant DISC1-related condition [RCV003920604]|not provided [RCV000884165] Chr1:231694746 [GRCh38]
Chr1:231830492 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.1756C>G (p.Pro586Ala) single nucleotide variant not provided [RCV000968873] Chr1:231800174 [GRCh38]
Chr1:231935920 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.954C>T (p.Ser318=) single nucleotide variant not provided [RCV000902167] Chr1:231694712 [GRCh38]
Chr1:231830458 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.555C>T (p.Asn185=) single nucleotide variant DISC1-related condition [RCV003975664]|not provided [RCV000894305] Chr1:231694313 [GRCh38]
Chr1:231830059 [GRCh37]
Chr1:1q42.2		 benign|likely benign
NM_018662.3(DISC1):c.508C>T (p.Arg170Cys) single nucleotide variant DISC1-related condition [RCV003970847]|not provided [RCV000964494] Chr1:231694266 [GRCh38]
Chr1:231830012 [GRCh37]
Chr1:1q42.2		 benign
GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3 copy number gain not provided [RCV000845852] Chr1:182388773..249111240 [GRCh37]
Chr1:1q25.3-44		 pathogenic
GRCh37/hg19 1q42.2(chr1:232073695-232138020)x3 copy number gain not provided [RCV000849439] Chr1:232073695..232138020 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q41-43(chr1:219916966-239004378)x3 copy number gain not provided [RCV001005175] Chr1:219916966..239004378 [GRCh37]
Chr1:1q41-43		 pathogenic
GRCh37/hg19 1q42.2(chr1:232067056-232204833)x3 copy number gain not provided [RCV001005192] Chr1:232067056..232204833 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.13-43(chr1:228832737-240993877)x3 copy number gain not provided [RCV001005187] Chr1:228832737..240993877 [GRCh37]
Chr1:1q42.13-43		 pathogenic
NM_018662.3(DISC1):c.163G>A (p.Gly55Arg) single nucleotide variant Inborn genetic diseases [RCV003239971] Chr1:231693921 [GRCh38]
Chr1:231829667 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.479G>T (p.Trp160Leu) single nucleotide variant DISC1-related condition [RCV003940574]|not provided [RCV000887163] Chr1:231694237 [GRCh38]
Chr1:231829983 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.2547C>T (p.Val849=) single nucleotide variant not provided [RCV000907753] Chr1:232036813 [GRCh38]
Chr1:232172559 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1591G>C (p.Gly531Arg) single nucleotide variant not provided [RCV000892049] Chr1:231771027 [GRCh38]
Chr1:231906773 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.1668A>G (p.Ser556=) single nucleotide variant not provided [RCV000929959] Chr1:231795275 [GRCh38]
Chr1:231931021 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.2368T>C (p.Leu790=) single nucleotide variant not provided [RCV000912599] Chr1:232026495 [GRCh38]
Chr1:232162241 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.2505G>A (p.Ala835=) single nucleotide variant not provided [RCV000911604] Chr1:232036771 [GRCh38]
Chr1:232172517 [GRCh37]
Chr1:1q42.2		 likely benign
GRCh37/hg19 1q42.2(chr1:231788026-232045506)x3 copy number gain not provided [RCV001005191] Chr1:231788026..232045506 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q41-42.2(chr1:223653722-234591807)x1 copy number loss not provided [RCV001005180] Chr1:223653722..234591807 [GRCh37]
Chr1:1q41-42.2		 pathogenic
GRCh37/hg19 1q42.2-43(chr1:231407943-237289859)x1 copy number loss not provided [RCV001537901] Chr1:231407943..237289859 [GRCh37]
Chr1:1q42.2-43		 pathogenic
GRCh37/hg19 1q32.1-44(chr1:204045948-249218992)x3 copy number gain See cases [RCV001007407] Chr1:204045948..249218992 [GRCh37]
Chr1:1q32.1-44		 pathogenic
GRCh37/hg19 1q42.2(chr1:231763761-232045506)x3 copy number gain not provided [RCV001005190] Chr1:231763761..232045506 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q32.2-44(chr1:210152794-249218992)x3 copy number gain See cases [RCV001194578] Chr1:210152794..249218992 [GRCh37]
Chr1:1q32.2-44		 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
NM_018662.3(DISC1):c.1453C>T (p.Gln485Ter) single nucleotide variant not specified [RCV002247140] Chr1:231770889 [GRCh38]
Chr1:231906635 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.2(chr1:231908212-232027911)x1 copy number loss not provided [RCV001832873] Chr1:231908212..232027911 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.12-42.2(chr1:226131690-231908227) copy number loss not specified [RCV002052878] Chr1:226131690..231908227 [GRCh37]
Chr1:1q42.12-42.2		 likely pathogenic
GRCh37/hg19 1q42.2(chr1:231922558-231943836)x1 copy number loss not provided [RCV001829113] Chr1:231922558..231943836 [GRCh37]
Chr1:1q42.2		 uncertain significance
NC_000001.10:g.(?_229567246)_(232172577_?)dup duplication Actin accumulation myopathy [RCV003120751]|not provided [RCV001943051] Chr1:229567246..232172577 [GRCh37]
Chr1:1q42.13-42.2		 uncertain significance|no classifications from unflagged records
NM_018662.3(DISC1):c.109C>T (p.Arg37Trp) single nucleotide variant not specified [RCV002247139] Chr1:231693867 [GRCh38]
Chr1:231829613 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3 copy number gain See cases [RCV002287837] Chr1:197867914..249224684 [GRCh37]
Chr1:1q31.3-44		 pathogenic
GRCh37/hg19 1q42.2(chr1:231639484-232061279)x3 copy number gain not provided [RCV002474927] Chr1:231639484..232061279 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.2(chr1:231859872-231966836)x1 copy number loss not provided [RCV002472912] Chr1:231859872..231966836 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.2(chr1:231949332-233142053)x1 copy number loss not provided [RCV002472892] Chr1:231949332..233142053 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.404C>T (p.Pro135Leu) single nucleotide variant Inborn genetic diseases [RCV002682646] Chr1:231694162 [GRCh38]
Chr1:231829908 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1006G>C (p.Val336Leu) single nucleotide variant Inborn genetic diseases [RCV002859572] Chr1:231694764 [GRCh38]
Chr1:231830510 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.457T>C (p.Ser153Pro) single nucleotide variant Inborn genetic diseases [RCV002733916] Chr1:231694215 [GRCh38]
Chr1:231829961 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.13-43(chr1:227992928-236659905)x3 copy number gain not provided [RCV002475638] Chr1:227992928..236659905 [GRCh37]
Chr1:1q42.13-43		 likely pathogenic
NM_018662.3(DISC1):c.379A>G (p.Arg127Gly) single nucleotide variant Inborn genetic diseases [RCV002753781] Chr1:231694137 [GRCh38]
Chr1:231829883 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.161T>G (p.Ile54Ser) single nucleotide variant Inborn genetic diseases [RCV002841051] Chr1:231693919 [GRCh38]
Chr1:231829665 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1946T>C (p.Leu649Pro) single nucleotide variant Inborn genetic diseases [RCV002879984] Chr1:231818482 [GRCh38]
Chr1:231954228 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.767A>G (p.His256Arg) single nucleotide variant Inborn genetic diseases [RCV002777053] Chr1:231694525 [GRCh38]
Chr1:231830271 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q41-44(chr1:223972939-249224684)x3 copy number gain not provided [RCV002475745] Chr1:223972939..249224684 [GRCh37]
Chr1:1q41-44		 pathogenic
NM_018662.3(DISC1):c.1036A>G (p.Arg346Gly) single nucleotide variant Inborn genetic diseases [RCV002760121] Chr1:231694794 [GRCh38]
Chr1:231830540 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.2252A>C (p.Glu751Ala) single nucleotide variant Inborn genetic diseases [RCV002978896] Chr1:232008994 [GRCh38]
Chr1:232144740 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1988G>A (p.Ser663Asn) single nucleotide variant Inborn genetic diseases [RCV002926141] Chr1:231958834 [GRCh38]
Chr1:232094580 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1252C>T (p.Arg418Cys) single nucleotide variant Inborn genetic diseases [RCV002887158] Chr1:231750060 [GRCh38]
Chr1:231885806 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1816G>C (p.Asp606His) single nucleotide variant Inborn genetic diseases [RCV002844377] Chr1:231818352 [GRCh38]
Chr1:231954098 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.950G>A (p.Ser317Asn) single nucleotide variant Inborn genetic diseases [RCV002926006] Chr1:231694708 [GRCh38]
Chr1:231830454 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.220G>A (p.Glu74Lys) single nucleotide variant Inborn genetic diseases [RCV002661422] Chr1:231693978 [GRCh38]
Chr1:231829724 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1724G>A (p.Arg575Lys) single nucleotide variant Inborn genetic diseases [RCV002798281] Chr1:231800142 [GRCh38]
Chr1:231935888 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1123A>T (p.Thr375Ser) single nucleotide variant Inborn genetic diseases [RCV002924597] Chr1:231749931 [GRCh38]
Chr1:231885677 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.641G>A (p.Arg214Gln) single nucleotide variant Inborn genetic diseases [RCV002701954] Chr1:231694399 [GRCh38]
Chr1:231830145 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.329C>T (p.Ser110Phe) single nucleotide variant Inborn genetic diseases [RCV002930705] Chr1:231694087 [GRCh38]
Chr1:231829833 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.11-43(chr1:224230307-243181599)x3 copy number gain not provided [RCV002509019] Chr1:224230307..243181599 [GRCh37]
Chr1:1q42.11-43		 not provided
NM_018662.3(DISC1):c.887A>G (p.Asp296Gly) single nucleotide variant Inborn genetic diseases [RCV002669872] Chr1:231694645 [GRCh38]
Chr1:231830391 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1516C>T (p.Pro506Ser) single nucleotide variant Inborn genetic diseases [RCV002768864] Chr1:231770952 [GRCh38]
Chr1:231906698 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1877G>A (p.Ser626Asn) single nucleotide variant Inborn genetic diseases [RCV002936492] Chr1:231818413 [GRCh38]
Chr1:231954159 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1249C>A (p.Arg417Ser) single nucleotide variant Inborn genetic diseases [RCV002897953] Chr1:231750057 [GRCh38]
Chr1:231885803 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1033C>T (p.Arg345Trp) single nucleotide variant Inborn genetic diseases [RCV003211466] Chr1:231694791 [GRCh38]
Chr1:231830537 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1619C>G (p.Pro540Arg) single nucleotide variant Inborn genetic diseases [RCV003201597] Chr1:231771055 [GRCh38]
Chr1:231906801 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.511G>A (p.Val171Ile) single nucleotide variant Inborn genetic diseases [RCV003263009] Chr1:231694269 [GRCh38]
Chr1:231830015 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1718C>A (p.Thr573Asn) single nucleotide variant Inborn genetic diseases [RCV003263520] Chr1:231800136 [GRCh38]
Chr1:231935882 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh38/hg38 1q42.13-44(chr1:230178121-243646135)x1 copy number loss Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 [RCV003327728] Chr1:230178121..243646135 [GRCh38]
Chr1:1q42.13-44		 pathogenic
NM_018662.3(DISC1):c.1015G>A (p.Asp339Asn) single nucleotide variant Inborn genetic diseases [RCV003371761] Chr1:231694773 [GRCh38]
Chr1:231830519 [GRCh37]
Chr1:1q42.2		 uncertain significance
GRCh37/hg19 1q42.13-43(chr1:230231959-238032346)x1 copy number loss not provided [RCV003484077] Chr1:230231959..238032346 [GRCh37]
Chr1:1q42.13-43		 pathogenic
GRCh37/hg19 1q42.13-44(chr1:229373250-249206595)x3 copy number gain not provided [RCV003484052] Chr1:229373250..249206595 [GRCh37]
Chr1:1q42.13-44		 pathogenic
GRCh37/hg19 1q42.2(chr1:231917141-231943836)x1 copy number loss not provided [RCV003484100] Chr1:231917141..231943836 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1361G>T (p.Arg454Ile) single nucleotide variant DISC1-related condition [RCV003400221] Chr1:231767232 [GRCh38]
Chr1:231902978 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.691C>T (p.Pro231Ser) single nucleotide variant DISC1-related condition [RCV003404661] Chr1:231694449 [GRCh38]
Chr1:231830195 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.2319C>T (p.Ile773=) single nucleotide variant DISC1-related condition [RCV003404212] Chr1:232026446 [GRCh38]
Chr1:232162192 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.560G>A (p.Cys187Tyr) single nucleotide variant DISC1-related condition [RCV003414585] Chr1:231694318 [GRCh38]
Chr1:231830064 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1493A>C (p.Gln498Pro) single nucleotide variant DISC1-related condition [RCV003414146] Chr1:231770929 [GRCh38]
Chr1:231906675 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1012C>T (p.Arg338Trp) single nucleotide variant not provided [RCV003490687] Chr1:231694770 [GRCh38]
Chr1:231830516 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.615dup (p.Phe206fs) duplication not provided [RCV003490686] Chr1:231694371..231694372 [GRCh38]
Chr1:231830117..231830118 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.1982-9T>C single nucleotide variant DISC1-related condition [RCV003911531] Chr1:231958819 [GRCh38]
Chr1:232094565 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.690A>G (p.Pro230=) single nucleotide variant DISC1-related condition [RCV003977221] Chr1:231694448 [GRCh38]
Chr1:231830194 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.2502G>A (p.Glu834=) single nucleotide variant DISC1-related condition [RCV003924441] Chr1:232036768 [GRCh38]
Chr1:232172514 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.342C>A (p.Thr114=) single nucleotide variant DISC1-related condition [RCV003957163] Chr1:231694100 [GRCh38]
Chr1:231829846 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.67+4G>A single nucleotide variant DISC1-related condition [RCV003959387] Chr1:231626938 [GRCh38]
Chr1:231762684 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1358C>T (p.Thr453Met) single nucleotide variant DISC1-related condition [RCV003931555] Chr1:231767229 [GRCh38]
Chr1:231902975 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.1219C>T (p.His407Tyr) single nucleotide variant DISC1-related condition [RCV003913882] Chr1:231750027 [GRCh38]
Chr1:231885773 [GRCh37]
Chr1:1q42.2		 uncertain significance
NM_018662.3(DISC1):c.347C>T (p.Ala116Val) single nucleotide variant DISC1-related condition [RCV003909296] Chr1:231694105 [GRCh38]
Chr1:231829851 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.42C>T (p.Gly14=) single nucleotide variant DISC1-related condition [RCV003959197] Chr1:231626909 [GRCh38]
Chr1:231762655 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.2172C>T (p.Asp724=) single nucleotide variant DISC1-related condition [RCV003902022] Chr1:232008914 [GRCh38]
Chr1:232144660 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.2263C>T (p.His755Tyr) single nucleotide variant DISC1-related condition [RCV003931395] Chr1:232009005 [GRCh38]
Chr1:232144751 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.1393C>T (p.Leu465=) single nucleotide variant DISC1-related condition [RCV003974456] Chr1:231767264 [GRCh38]
Chr1:231903010 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.1981+48069C>G single nucleotide variant DISC1-related condition [RCV003982200] Chr1:231866586 [GRCh38]
Chr1:232002332 [GRCh37]
Chr1:1q42.2		 benign
NM_018662.3(DISC1):c.38C>G (p.Ala13Gly) single nucleotide variant DISC1-related condition [RCV003972208] Chr1:231626905 [GRCh38]
Chr1:231762651 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1117+18828G>A single nucleotide variant DISC1-related condition [RCV003921552] Chr1:231720852 [GRCh38]
Chr1:231856598 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1977C>T (p.Ala659=) single nucleotide variant DISC1-related condition [RCV003896797] Chr1:231818513 [GRCh38]
Chr1:231954259 [GRCh37]
Chr1:1q42.2		 likely benign
NM_018662.3(DISC1):c.1634+13T>G single nucleotide variant DISC1-related condition [RCV003917368] Chr1:231771083 [GRCh38]
Chr1:231906829 [GRCh37]
Chr1:1q42.2		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:10993
Count of miRNA genes:1472
Interacting mature miRNAs:1986
Transcripts:ENST00000295051, ENST00000317586, ENST00000366632, ENST00000366633, ENST00000366636, ENST00000366637, ENST00000422590, ENST00000427560, ENST00000439617, ENST00000468399, ENST00000535944, ENST00000535983, ENST00000537876, ENST00000539444, ENST00000602281, ENST00000602600, ENST00000602700, ENST00000602713, ENST00000602822, ENST00000602873
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
D1S2709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,030,439 - 232,030,635UniSTSGRCh37
Build 361230,097,062 - 230,097,258RGDNCBI36
Celera1205,299,252 - 205,299,448RGD
Cytogenetic Map1q42.1UniSTS
Marshfield Genetic Map1247.23RGD
Marshfield Genetic Map1247.23UniSTS
Genethon Genetic Map1251.2UniSTS
deCODE Assembly Map1235.37UniSTS
D1S3462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,950,516 - 231,950,776UniSTSGRCh37
Build 361230,017,139 - 230,017,399RGDNCBI36
Celera1205,219,352 - 205,219,609RGD
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map1q42.1UniSTS
HuRef1202,437,654 - 202,437,911UniSTS
Marshfield Genetic Map1247.23UniSTS
Marshfield Genetic Map1247.23RGD
deCODE Assembly Map1235.37UniSTS
D1S2191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,176,556 - 232,176,844UniSTSGRCh37
Build 361230,243,179 - 230,243,467RGDNCBI36
Celera1205,445,380 - 205,445,668RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,663,891 - 202,664,179UniSTS
TNG Radiation Hybrid Map1117030.0UniSTS
GeneMap99-GB4 RH Map1738.98UniSTS
GeneMap99-GB4 RH Map1738.37UniSTS
Whitehead-RH Map1909.0UniSTS
Whitehead-YAC Contig Map1 UniSTS
NCBI RH Map12035.6UniSTS
RH93065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,945,853 - 231,945,984UniSTSGRCh37
Build 361230,012,476 - 230,012,607RGDNCBI36
Celera1205,214,689 - 205,214,820RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,432,991 - 202,433,122UniSTS
GeneMap99-GB4 RH Map1737.43UniSTS
AL034131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,012,124 - 232,012,304UniSTSGRCh37
Build 361230,078,747 - 230,078,927RGDNCBI36
Celera1205,280,951 - 205,281,131RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,499,182 - 202,499,362UniSTS
AL034292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,848,803 - 231,848,934UniSTSGRCh37
Build 361229,915,426 - 229,915,557RGDNCBI36
Celera1205,113,554 - 205,113,685RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,332,304 - 202,332,435UniSTS
RH121953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,002,293 - 232,002,433UniSTSGRCh37
Build 361230,068,916 - 230,069,056RGDNCBI36
Celera1205,271,120 - 205,271,260RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,489,423 - 202,489,563UniSTS
TNG Radiation Hybrid Map1115398.0UniSTS
RH122687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,029,427 - 232,029,751UniSTSGRCh37
Build 361230,096,050 - 230,096,374RGDNCBI36
Celera1205,298,240 - 205,298,564RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,516,471 - 202,516,795UniSTS
TNG Radiation Hybrid Map1115417.0UniSTS
G60191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,158,458 - 232,158,743UniSTSGRCh37
Build 361230,225,081 - 230,225,366RGDNCBI36
Celera1205,427,286 - 205,427,571RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,645,799 - 202,646,084UniSTS
TNG Radiation Hybrid Map1116980.0UniSTS
D3S587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37310,723,594 - 10,723,833UniSTSGRCh37
Build 36310,698,594 - 10,698,833RGDNCBI36
Celera310,659,049 - 10,659,288RGD
HuRef310,658,339 - 10,658,578UniSTS
D1S2517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,176,622 - 232,176,740UniSTSGRCh37
Build 361230,243,245 - 230,243,363RGDNCBI36
Celera1205,445,446 - 205,445,564RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,663,957 - 202,664,075UniSTS
SHGC-110351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,108,407 - 232,108,680UniSTSGRCh37
Build 361230,175,030 - 230,175,303RGDNCBI36
Celera1205,377,230 - 205,377,503RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,595,835 - 202,596,108UniSTS
TNG Radiation Hybrid Map1117009.0UniSTS
SHGC-144606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,011,170 - 232,011,448UniSTSGRCh37
Build 361230,077,793 - 230,078,071RGDNCBI36
Celera1205,279,997 - 205,280,275RGD
Cytogenetic Map1q42.1UniSTS
TNG Radiation Hybrid Map1115398.0UniSTS
G65049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,762,291 - 231,762,485UniSTSGRCh37
Build 361229,828,914 - 229,829,108RGDNCBI36
Celera1205,027,032 - 205,027,234RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,245,829 - 202,246,033UniSTS
SHGC-154930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,857,976 - 231,858,287UniSTSGRCh37
Build 361229,924,599 - 229,924,910RGDNCBI36
Celera1205,122,726 - 205,123,037RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,341,476 - 202,341,787UniSTS
TNG Radiation Hybrid Map1115704.0UniSTS
fb76e10.y1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,933,678 - 231,933,887UniSTSGRCh37
Build 361230,000,301 - 230,000,510RGDNCBI36
Celera1205,198,434 - 205,198,643RGD
Celera2182,824,691 - 182,824,876UniSTS
HuRef2181,089,101 - 181,089,283UniSTS
HuRef1202,416,809 - 202,417,032UniSTS
SHGC-76529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,002,219 - 232,002,353UniSTSGRCh37
Build 361230,068,842 - 230,068,976RGDNCBI36
Celera1205,271,046 - 205,271,180RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,489,349 - 202,489,483UniSTS
TNG Radiation Hybrid Map1115398.0UniSTS
GeneMap99-GB4 RH Map1738.98UniSTS
NCBI RH Map12035.6UniSTS
AL009787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,823,211 - 231,823,397UniSTSGRCh37
Build 361229,889,834 - 229,890,020RGDNCBI36
Celera1205,087,962 - 205,088,148RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,306,712 - 202,306,898UniSTS
SGC32126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,103,501 - 232,103,633UniSTSGRCh37
Build 361230,170,124 - 230,170,256RGDNCBI36
Celera1205,372,326 - 205,372,458RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,590,926 - 202,591,058UniSTS
GeneMap99-GB4 RH Map1738.67UniSTS
GeneMap99-GB4 RH Map1738.75UniSTS
Whitehead-RH Map1909.0UniSTS
NCBI RH Map12035.9UniSTS
AL009602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,844,758 - 231,844,943UniSTSGRCh37
Build 361229,911,381 - 229,911,566RGDNCBI36
Celera1205,109,509 - 205,109,694RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,328,259 - 202,328,444UniSTS
D1S1624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,950,584 - 231,950,776UniSTSGRCh37
Build 361230,017,207 - 230,017,399RGDNCBI36
Celera1205,219,420 - 205,219,609RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,437,722 - 202,437,911UniSTS
D1S1621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371231,950,604 - 231,950,776UniSTSGRCh37
Build 361230,017,227 - 230,017,399RGDNCBI36
Celera1205,219,440 - 205,219,609RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,437,742 - 202,437,911UniSTS
Whitehead-YAC Contig Map1 UniSTS
SHGC-76522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371232,103,470 - 232,103,602UniSTSGRCh37
Build 361230,170,093 - 230,170,225RGDNCBI36
Celera1205,372,295 - 205,372,427RGD
Cytogenetic Map1q42.1UniSTS
HuRef1202,590,895 - 202,591,027UniSTS
TNG Radiation Hybrid Map1117014.0UniSTS
GeneMap99-GB4 RH Map1737.43UniSTS
NCBI RH Map12035.3UniSTS
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
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
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
D3S587  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16q23.2UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1 7 2 17 75 1 71 2 5 6 63
Low 2260 2748 1408 320 1418 166 3730 1766 3566 300 1394 1533 162 1 1203 2244 5 2
Below cutoff 155 234 313 301 393 296 548 425 95 113 53 64 12 1 481

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_011681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001012957 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001012958 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001012959 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164537 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164538 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164550 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164553 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164554 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB007926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF222980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF222982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF222983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF222987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI075754 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ506177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ506178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK025293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096457 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL049973 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL161743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL359543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL445200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL450284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL626763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL751364 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC038954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC142622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC151225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804174 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804175 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804176 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804177 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804181 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804195 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804196 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ804216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KJ534822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000295051   ⟹   ENSP00000295051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,819,244 (+)Ensembl
RefSeq Acc Id: ENST00000317586   ⟹   ENSP00000320784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,724,074 (+)Ensembl
RefSeq Acc Id: ENST00000366632   ⟹   ENSP00000355592
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,855,380 (+)Ensembl
RefSeq Acc Id: ENST00000366633   ⟹   ENSP00000355593
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,855,380 (+)Ensembl
RefSeq Acc Id: ENST00000366636   ⟹   ENSP00000355596
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,866,712 (+)Ensembl
RefSeq Acc Id: ENST00000366637   ⟹   ENSP00000355597
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 232,041,127 (+)Ensembl
RefSeq Acc Id: ENST00000422590   ⟹   ENSP00000415147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,837 - 232,009,654 (+)Ensembl
RefSeq Acc Id: ENST00000427560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,818,905 - 232,009,022 (+)Ensembl
RefSeq Acc Id: ENST00000439617   ⟹   ENSP00000403888
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,790 - 232,041,272 (+)Ensembl
RefSeq Acc Id: ENST00000468399
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,629,390 - 231,702,661 (+)Ensembl
RefSeq Acc Id: ENST00000535944   ⟹   ENSP00000441193
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,819,244 (+)Ensembl
RefSeq Acc Id: ENST00000535983   ⟹   ENSP00000443996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 232,009,255 (+)Ensembl
RefSeq Acc Id: ENST00000537876   ⟹   ENSP00000440909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,866,685 (+)Ensembl
RefSeq Acc Id: ENST00000539444   ⟹   ENSP00000440953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,819,244 (+)Ensembl
RefSeq Acc Id: ENST00000602281   ⟹   ENSP00000473425
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,819,244 (+)Ensembl
RefSeq Acc Id: ENST00000602600
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,684,752 - 231,693,935 (+)Ensembl
RefSeq Acc Id: ENST00000602700   ⟹   ENSP00000473417
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,819,244 (+)Ensembl
RefSeq Acc Id: ENST00000602713   ⟹   ENSP00000473261
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,855,380 (+)Ensembl
RefSeq Acc Id: ENST00000602822   ⟹   ENSP00000473586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,819,244 (+)Ensembl
RefSeq Acc Id: ENST00000602873   ⟹   ENSP00000473386
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,819,244 (+)Ensembl
RefSeq Acc Id: ENST00000620189   ⟹   ENSP00000482174
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 232,041,268 (+)Ensembl
RefSeq Acc Id: ENST00000622252   ⟹   ENSP00000481791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 232,041,270 (+)Ensembl
RefSeq Acc Id: ENST00000628350   ⟹   ENSP00000487190
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1231,626,815 - 231,959,503 (+)Ensembl
RefSeq Acc Id: NM_001012957   ⟹   NP_001012975
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 232,041,272 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
Build 361229,829,184 - 230,243,641 (+)NCBI Archive
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,450,761 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,426,811 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001012958   ⟹   NP_001012976
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,724,074 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
Build 361229,829,184 - 229,926,443 (+)NCBI Archive
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,133,660 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,107,255 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001012959   ⟹   NP_001012977
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,866,708 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
Build 361229,829,184 - 230,069,077 (+)NCBI Archive
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,276,298 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,252,245 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164537   ⟹   NP_001158009
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 232,041,272 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,450,761 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,426,811 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164538   ⟹   NP_001158010
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 232,009,654 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,419,146 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,395,196 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164539   ⟹   NP_001158011
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,855,380 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,265,000 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,240,918 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164540   ⟹   NP_001158012
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 232,041,272 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,450,761 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,426,811 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164541   ⟹   NP_001158013
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 232,009,654 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,419,146 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,395,196 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164542   ⟹   NP_001158014
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,959,503 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,369,099 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,345,039 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164544   ⟹   NP_001158016
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,819,207 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,228,867 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,204,737 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164545   ⟹   NP_001158017
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,819,207 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,228,867 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,204,737 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164546   ⟹   NP_001158018
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,959,503 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,369,099 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,345,039 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164547   ⟹   NP_001158019
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 232,009,654 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,419,146 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,395,196 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164548   ⟹   NP_001158020
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,819,207 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,228,867 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,204,737 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164549   ⟹   NP_001158021
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,771,662 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,181,294 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,154,769 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164550   ⟹   NP_001158022
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,724,074 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,133,660 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,107,255 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164551   ⟹   NP_001158023
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,750,619 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,160,258 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,133,791 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164552   ⟹   NP_001158024
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,724,074 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,133,660 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,107,255 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164553   ⟹   NP_001158025
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,724,074 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,133,660 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,107,255 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164554   ⟹   NP_001158026
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,702,661 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,112,150 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,085,864 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164555   ⟹   NP_001158027
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,750,619 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,160,258 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,133,791 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001164556   ⟹   NP_001158028
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 231,819,207 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,228,867 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,204,737 (+)NCBI
Sequence:
RefSeq Acc Id: NM_018662   ⟹   NP_061132
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,790 - 232,041,272 (+)NCBI
GRCh371231,762,561 - 232,177,018 (+)ENTREZGENE
Build 361229,829,184 - 230,243,641 (+)NCBI Archive
HuRef1202,246,109 - 202,664,353 (+)ENTREZGENE
CHM1_11233,036,406 - 233,450,761 (+)NCBI
T2T-CHM13v2.01231,009,996 - 231,426,811 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001012975 (Get FASTA)   NCBI Sequence Viewer  
  NP_001012976 (Get FASTA)   NCBI Sequence Viewer  
  NP_001012977 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158009 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158010 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158011 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158012 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158013 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158014 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158016 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158017 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158018 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158019 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158020 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158021 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158022 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158023 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158024 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158025 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158026 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158027 (Get FASTA)   NCBI Sequence Viewer  
  NP_001158028 (Get FASTA)   NCBI Sequence Viewer  
  NP_061132 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF73874 (Get FASTA)   NCBI Sequence Viewer  
  AAF73877 (Get FASTA)   NCBI Sequence Viewer  
  AAF73889 (Get FASTA)   NCBI Sequence Viewer  
  AAI51226 (Get FASTA)   NCBI Sequence Viewer  
  ACR40040 (Get FASTA)   NCBI Sequence Viewer  
  ACR40041 (Get FASTA)   NCBI Sequence Viewer  
  ACR40042 (Get FASTA)   NCBI Sequence Viewer  
  ACR40043 (Get FASTA)   NCBI Sequence Viewer  
  ACR40044 (Get FASTA)   NCBI Sequence Viewer  
  ACR40045 (Get FASTA)   NCBI Sequence Viewer  
  ACR40046 (Get FASTA)   NCBI Sequence Viewer  
  ACR40047 (Get FASTA)   NCBI Sequence Viewer  
  ACR40048 (Get FASTA)   NCBI Sequence Viewer  
  ACR40049 (Get FASTA)   NCBI Sequence Viewer  
  ACR40050 (Get FASTA)   NCBI Sequence Viewer  
  ACR40051 (Get FASTA)   NCBI Sequence Viewer  
  ACR40052 (Get FASTA)   NCBI Sequence Viewer  
  ACR40053 (Get FASTA)   NCBI Sequence Viewer  
  ACR40054 (Get FASTA)   NCBI Sequence Viewer  
  ACR40055 (Get FASTA)   NCBI Sequence Viewer  
  ACR40056 (Get FASTA)   NCBI Sequence Viewer  
  ACR40057 (Get FASTA)   NCBI Sequence Viewer  
  ACR40058 (Get FASTA)   NCBI Sequence Viewer  
  ACR40059 (Get FASTA)   NCBI Sequence Viewer  
  ACR40060 (Get FASTA)   NCBI Sequence Viewer  
  ACR40061 (Get FASTA)   NCBI Sequence Viewer  
  ACR40062 (Get FASTA)   NCBI Sequence Viewer  
  ACR40063 (Get FASTA)   NCBI Sequence Viewer  
  ACR40064 (Get FASTA)   NCBI Sequence Viewer  
  ACR40065 (Get FASTA)   NCBI Sequence Viewer  
  ACR40066 (Get FASTA)   NCBI Sequence Viewer  
  ACR40067 (Get FASTA)   NCBI Sequence Viewer  
  ACR40068 (Get FASTA)   NCBI Sequence Viewer  
  ACR40069 (Get FASTA)   NCBI Sequence Viewer  
  ACR40070 (Get FASTA)   NCBI Sequence Viewer  
  ACR40071 (Get FASTA)   NCBI Sequence Viewer  
  ACR40072 (Get FASTA)   NCBI Sequence Viewer  
  ACR40073 (Get FASTA)   NCBI Sequence Viewer  
  ACR40074 (Get FASTA)   NCBI Sequence Viewer  
  ACR40075 (Get FASTA)   NCBI Sequence Viewer  
  ACR40076 (Get FASTA)   NCBI Sequence Viewer  
  ACR40077 (Get FASTA)   NCBI Sequence Viewer  
  ACR40078 (Get FASTA)   NCBI Sequence Viewer  
  ACR40079 (Get FASTA)   NCBI Sequence Viewer  
  ACR40080 (Get FASTA)   NCBI Sequence Viewer  
  ACR40081 (Get FASTA)   NCBI Sequence Viewer  
  ACR40082 (Get FASTA)   NCBI Sequence Viewer  
  AHW56462 (Get FASTA)   NCBI Sequence Viewer  
  BAA32302 (Get FASTA)   NCBI Sequence Viewer  
  CAD44628 (Get FASTA)   NCBI Sequence Viewer  
  CAD44631 (Get FASTA)   NCBI Sequence Viewer  
  EAW69966 (Get FASTA)   NCBI Sequence Viewer  
  EAW69967 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000295051
  ENSP00000295051.7
  ENSP00000320784
  ENSP00000320784.4
  ENSP00000355592
  ENSP00000355592.2
  ENSP00000355593
  ENSP00000355593.3
  ENSP00000355596
  ENSP00000355596.4
  ENSP00000355597
  ENSP00000355597.6
  ENSP00000403888
  ENSP00000403888.4
  ENSP00000415147.2
  ENSP00000440909.2
  ENSP00000440953
  ENSP00000440953.1
  ENSP00000441193.1
  ENSP00000443996
  ENSP00000443996.1
  ENSP00000473261.1
  ENSP00000473386
  ENSP00000473386.1
  ENSP00000473417
  ENSP00000473417.1
  ENSP00000473425
  ENSP00000473425.1
  ENSP00000473586.1
  ENSP00000481791
  ENSP00000481791.1
  ENSP00000487190
  ENSP00000487190.1
GenBank Protein Q9NRI5 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001158009   ⟸   NM_001164537
- Peptide Label: isoform a
- UniProtKB: C4P096 (UniProtKB/TrEMBL),   A7E2W8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_061132   ⟸   NM_018662
- Peptide Label: isoform L
- UniProtKB: Q9NRI3 (UniProtKB/Swiss-Prot),   Q9BX19 (UniProtKB/Swiss-Prot),   Q8IXJ1 (UniProtKB/Swiss-Prot),   Q8IXJ0 (UniProtKB/Swiss-Prot),   Q5VT45 (UniProtKB/Swiss-Prot),   Q5VT44 (UniProtKB/Swiss-Prot),   O75045 (UniProtKB/Swiss-Prot),   C9J6D0 (UniProtKB/Swiss-Prot),   C4P0C1 (UniProtKB/Swiss-Prot),   C4P0B6 (UniProtKB/Swiss-Prot),   C4P0B3 (UniProtKB/Swiss-Prot),   C4P0A3 (UniProtKB/Swiss-Prot),   C4P0A1 (UniProtKB/Swiss-Prot),   C4P095 (UniProtKB/Swiss-Prot),   C4P091 (UniProtKB/Swiss-Prot),   A6NLH2 (UniProtKB/Swiss-Prot),   Q9NRI4 (UniProtKB/Swiss-Prot),   Q9NRI5 (UniProtKB/Swiss-Prot),   A7E2W8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001012975   ⟸   NM_001012957
- Peptide Label: isoform Lv
- UniProtKB: A7E2W8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158012   ⟸   NM_001164540
- Peptide Label: isoform d
- UniProtKB: C4P094 (UniProtKB/TrEMBL),   A7E2W8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158010   ⟸   NM_001164538
- Peptide Label: isoform b
- UniProtKB: C4P098 (UniProtKB/TrEMBL),   A7E2W8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158013   ⟸   NM_001164541
- Peptide Label: isoform e
- UniProtKB: C4P0B1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158019   ⟸   NM_001164547
- Peptide Label: isoform i
- UniProtKB: C4P093 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158014   ⟸   NM_001164542
- Peptide Label: isoform f
- UniProtKB: C4P0A4 (UniProtKB/TrEMBL),   C4P0B1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158018   ⟸   NM_001164546
- Peptide Label: isoform i
- UniProtKB: C4P093 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001012977   ⟸   NM_001012959
- Peptide Label: isoform S
- UniProtKB: C4P0B1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158011   ⟸   NM_001164539
- Peptide Label: isoform c
- UniProtKB: Q9NRI5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001158016   ⟸   NM_001164544
- Peptide Label: isoform g
- UniProtKB: C4P0B1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158017   ⟸   NM_001164545
- Peptide Label: isoform h
- UniProtKB: C4P093 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158020   ⟸   NM_001164548
- Peptide Label: isoform k
- UniProtKB: C4P0A5 (UniProtKB/TrEMBL),   C4P093 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158028   ⟸   NM_001164556
- Peptide Label: isoform t
- UniProtKB: Q9NRI5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001158021   ⟸   NM_001164549
- Peptide Label: isoform l
- UniProtKB: C4P0C4 (UniProtKB/TrEMBL),   C4P093 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158023   ⟸   NM_001164551
- Peptide Label: isoform n
- UniProtKB: C4P0C8 (UniProtKB/TrEMBL),   C4P0A0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158027   ⟸   NM_001164555
- Peptide Label: isoform r
- UniProtKB: C4P0C7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158024   ⟸   NM_001164552
- Peptide Label: isoform o
- UniProtKB: C4P0D1 (UniProtKB/TrEMBL),   C4P092 (UniProtKB/TrEMBL),   Q5T406 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158022   ⟸   NM_001164550
- Peptide Label: isoform m
- UniProtKB: C4P0D2 (UniProtKB/TrEMBL),   C4P0A9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158025   ⟸   NM_001164553
- Peptide Label: isoform p
- UniProtKB: C4P0D0 (UniProtKB/TrEMBL),   C4P0A9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001012976   ⟸   NM_001012958
- Peptide Label: isoform Es
- UniProtKB: C4P0C7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001158026   ⟸   NM_001164554
- Peptide Label: isoform q
- UniProtKB: C4P0D3 (UniProtKB/TrEMBL),   C4P0A9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000482174   ⟸   ENST00000620189
RefSeq Acc Id: ENSP00000403888   ⟸   ENST00000439617
RefSeq Acc Id: ENSP00000481791   ⟸   ENST00000622252
RefSeq Acc Id: ENSP00000295051   ⟸   ENST00000295051
RefSeq Acc Id: ENSP00000441193   ⟸   ENST00000535944
RefSeq Acc Id: ENSP00000443996   ⟸   ENST00000535983
RefSeq Acc Id: ENSP00000487190   ⟸   ENST00000628350
RefSeq Acc Id: ENSP00000440909   ⟸   ENST00000537876
RefSeq Acc Id: ENSP00000355596   ⟸   ENST00000366636
RefSeq Acc Id: ENSP00000355597   ⟸   ENST00000366637
RefSeq Acc Id: ENSP00000355592   ⟸   ENST00000366632
RefSeq Acc Id: ENSP00000355593   ⟸   ENST00000366633
RefSeq Acc Id: ENSP00000473386   ⟸   ENST00000602873
RefSeq Acc Id: ENSP00000473586   ⟸   ENST00000602822
RefSeq Acc Id: ENSP00000473261   ⟸   ENST00000602713
RefSeq Acc Id: ENSP00000473417   ⟸   ENST00000602700
RefSeq Acc Id: ENSP00000473425   ⟸   ENST00000602281
RefSeq Acc Id: ENSP00000440953   ⟸   ENST00000539444
RefSeq Acc Id: ENSP00000320784   ⟸   ENST00000317586
RefSeq Acc Id: ENSP00000415147   ⟸   ENST00000422590

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NRI5-F1-model_v2 AlphaFold Q9NRI5 1-854 view protein structure

Promoters
RGD ID:6785856
Promoter ID:HG_KWN:7827
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   Lymphoblastoid,   NB4
Transcripts:ENST00000366633,   ENST00000366637,   NM_001012957,   NM_001012958,   NM_001164537,   NM_001164538,   NM_001164539,   NM_001164540,   NM_001164541,   NM_001164542,   NM_001164544,   NM_001164545,   NM_001164546,   NM_001164547,   NM_001164548,   NM_001164549,   NM_001164550,   NM_001164551,   NM_001164552,   NM_001164553,   NM_001164554,   NM_001164555,   NM_001164556,   NM_018662,   OTTHUMT00000092351,   OTTHUMT00000092356,   UC009XFR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361229,828,921 - 229,829,421 (+)MPROMDB
RGD ID:6785037
Promoter ID:HG_KWN:7828
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:ENST00000366638,   OTTHUMT00000092353,   UC001HVB.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361229,831,506 - 229,832,006 (+)MPROMDB
RGD ID:6859282
Promoter ID:EPDNEW_H2805
Type:initiation region
Name:DISC1_4
Description:disrupted in schizophrenia 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2806  EPDNEW_H2807  EPDNEW_H2808  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,680 - 231,626,740EPDNEW
RGD ID:6859284
Promoter ID:EPDNEW_H2806
Type:initiation region
Name:DISC1_1
Description:disrupted in schizophrenia 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2805  EPDNEW_H2807  EPDNEW_H2808  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,626,801 - 231,626,861EPDNEW
RGD ID:6859286
Promoter ID:EPDNEW_H2807
Type:initiation region
Name:DISC1_3
Description:disrupted in schizophrenia 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2805  EPDNEW_H2806  EPDNEW_H2808  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,694,680 - 231,694,740EPDNEW
RGD ID:6859288
Promoter ID:EPDNEW_H2808
Type:single initiation site
Name:DISC1_2
Description:disrupted in schizophrenia 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H2805  EPDNEW_H2806  EPDNEW_H2807  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381231,774,733 - 231,774,793EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:2888 AgrOrtholog
COSMIC DISC1 COSMIC
Ensembl Genes ENSG00000162946 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000295051 ENTREZGENE
  ENST00000295051.11 UniProtKB/TrEMBL
  ENST00000317586 ENTREZGENE
  ENST00000317586.8 UniProtKB/Swiss-Prot
  ENST00000366632 ENTREZGENE
  ENST00000366632.6 UniProtKB/TrEMBL
  ENST00000366633 ENTREZGENE
  ENST00000366633.7 UniProtKB/Swiss-Prot
  ENST00000366636 ENTREZGENE
  ENST00000366636.8 UniProtKB/Swiss-Prot
  ENST00000366637 ENTREZGENE
  ENST00000366637.8 UniProtKB/Swiss-Prot
  ENST00000422590.6 UniProtKB/TrEMBL
  ENST00000439617 ENTREZGENE
  ENST00000439617.8 UniProtKB/Swiss-Prot
  ENST00000535944.5 UniProtKB/TrEMBL
  ENST00000535983 ENTREZGENE
  ENST00000535983.5 UniProtKB/Swiss-Prot
  ENST00000537876.5 UniProtKB/TrEMBL
  ENST00000539444 ENTREZGENE
  ENST00000539444.5 UniProtKB/Swiss-Prot
  ENST00000602281 ENTREZGENE
  ENST00000602281.5 UniProtKB/Swiss-Prot
  ENST00000602700 ENTREZGENE
  ENST00000602700.5 UniProtKB/Swiss-Prot
  ENST00000602713.5 UniProtKB/Swiss-Prot
  ENST00000602822.5 UniProtKB/Swiss-Prot
  ENST00000602873 ENTREZGENE
  ENST00000602873.5 UniProtKB/Swiss-Prot
  ENST00000622252 ENTREZGENE
  ENST00000622252.4 UniProtKB/TrEMBL
  ENST00000628350 ENTREZGENE
  ENST00000628350.2 UniProtKB/Swiss-Prot
GTEx ENSG00000162946 GTEx
HGNC ID HGNC:2888 ENTREZGENE
Human Proteome Map DISC1 Human Proteome Map
InterPro DISC1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:27185 UniProtKB/Swiss-Prot
NCBI Gene 27185 ENTREZGENE
OMIM 605210 OMIM
PANTHER DISRUPTED IN SCHIZOPHRENIA 1 PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR14332 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27342 PharmGKB
PRINTS F138DOMAIN UniProtKB/TrEMBL
Superfamily-SCOP Prefoldin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6NLH2 ENTREZGENE
  A7E2W8 ENTREZGENE, UniProtKB/TrEMBL
  C4P091 ENTREZGENE
  C4P092 ENTREZGENE, UniProtKB/TrEMBL
  C4P093 ENTREZGENE, UniProtKB/TrEMBL
  C4P094 ENTREZGENE, UniProtKB/TrEMBL
  C4P095 ENTREZGENE
  C4P096 ENTREZGENE, UniProtKB/TrEMBL
  C4P098 ENTREZGENE, UniProtKB/TrEMBL
  C4P0A0 ENTREZGENE, UniProtKB/TrEMBL
  C4P0A1 ENTREZGENE
  C4P0A3 ENTREZGENE
  C4P0A4 ENTREZGENE, UniProtKB/TrEMBL
  C4P0A5 ENTREZGENE, UniProtKB/TrEMBL
  C4P0A9 ENTREZGENE, UniProtKB/TrEMBL
  C4P0B0_HUMAN UniProtKB/TrEMBL
  C4P0B1 ENTREZGENE, UniProtKB/TrEMBL
  C4P0B2_HUMAN UniProtKB/TrEMBL
  C4P0B3 ENTREZGENE
  C4P0B6 ENTREZGENE
  C4P0C1 ENTREZGENE
  C4P0C4 ENTREZGENE, UniProtKB/TrEMBL
  C4P0C7 ENTREZGENE, UniProtKB/TrEMBL
  C4P0C8 ENTREZGENE, UniProtKB/TrEMBL
  C4P0D0 ENTREZGENE, UniProtKB/TrEMBL
  C4P0D1 ENTREZGENE, UniProtKB/TrEMBL
  C4P0D2 ENTREZGENE, UniProtKB/TrEMBL
  C4P0D3 ENTREZGENE, UniProtKB/TrEMBL
  C9J6D0 ENTREZGENE
  DISC1_HUMAN UniProtKB/Swiss-Prot
  H0Y7U2_HUMAN UniProtKB/TrEMBL
  O75045 ENTREZGENE
  Q5T406 ENTREZGENE
  Q5VT44 ENTREZGENE
  Q5VT45 ENTREZGENE
  Q8IXJ0 ENTREZGENE
  Q8IXJ1 ENTREZGENE
  Q9BX19 ENTREZGENE
  Q9NRI3 ENTREZGENE
  Q9NRI4 ENTREZGENE
  Q9NRI5 ENTREZGENE
  X5DQV8_HUMAN UniProtKB/TrEMBL
UniProt Secondary A6NLH2 UniProtKB/Swiss-Prot
  C4P091 UniProtKB/Swiss-Prot
  C4P095 UniProtKB/Swiss-Prot
  C4P0A1 UniProtKB/Swiss-Prot
  C4P0A3 UniProtKB/Swiss-Prot
  C4P0B3 UniProtKB/Swiss-Prot
  C4P0B6 UniProtKB/Swiss-Prot
  C4P0C1 UniProtKB/Swiss-Prot
  C9J6D0 UniProtKB/Swiss-Prot
  O75045 UniProtKB/Swiss-Prot
  Q5T406 UniProtKB/TrEMBL
  Q5VT44 UniProtKB/Swiss-Prot
  Q5VT45 UniProtKB/Swiss-Prot
  Q8IXJ0 UniProtKB/Swiss-Prot
  Q8IXJ1 UniProtKB/Swiss-Prot
  Q9BX19 UniProtKB/Swiss-Prot
  Q9NRI3 UniProtKB/Swiss-Prot
  Q9NRI4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-03-06 DISC1  DISC1 scaffold protein  DISC1  disrupted in schizophrenia 1  Symbol and/or name change 5135510 APPROVED