SRD5A3-AS1 (SRD5A3 antisense RNA 1) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: SRD5A3-AS1 (SRD5A3 antisense RNA 1) Homo sapiens
Analyze
Symbol: SRD5A3-AS1
Name: SRD5A3 antisense RNA 1
RGD ID: 6766521
HGNC Page HGNC:44138
Description: ASSOCIATED WITH Abnormality of the nervous system; congenital disorder of glycosylation; congenital disorder of glycosylation Iq; INTERACTS WITH bisphenol A; rotenone
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38455,366,601 - 55,385,580 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl455,363,971 - 55,395,847 (-)EnsemblGRCh38hg38GRCh38
GRCh37456,232,768 - 56,251,747 (-)NCBIGRCh37GRCh37hg19GRCh37
Celera453,734,596 - 53,753,573 (-)NCBICelera
Cytogenetic Map4q12NCBI
HuRef452,181,770 - 52,200,698 (-)NCBIHuRef
CHM1_1456,267,930 - 56,286,901 (-)NCBICHM1_1
T2T-CHM13v2.0458,854,739 - 58,873,724 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
bisphenol A  (EXP)
rotenone  (EXP)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
Additional References at PubMed
PMID:12477932  


Genomics

Variants

.
Variants in SRD5A3-AS1
106 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_024592.5(SRD5A3):c.603G>A (p.Trp201Ter) single nucleotide variant Congenital disorder of glycosylation [RCV000851210]|Inborn genetic diseases [RCV000623571]|SRD5A3-congenital disorder of glycosylation [RCV000779444]|not provided [RCV000178363] Chr4:55367628 [GRCh38]
Chr4:56233795 [GRCh37]
Chr4:4q12		 pathogenic|likely pathogenic|uncertain significance
GRCh38/hg38 4q12-13.2(chr4:51831622-66991489)x3 copy number gain See cases [RCV000051771] Chr4:51831622..66991489 [GRCh38]
Chr4:52697788..67857207 [GRCh37]
Chr4:52392545..67539802 [NCBI36]
Chr4:4q12-13.2		 pathogenic
GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3 copy number gain See cases [RCV000051772] Chr4:51831622..97505618 [GRCh38]
Chr4:52697788..98426769 [GRCh37]
Chr4:52392545..98645792 [NCBI36]
Chr4:4q12-22.3		 pathogenic
GRCh38/hg38 4q12-13.1(chr4:51899860-59984479)x3 copy number gain See cases [RCV000051773] Chr4:51899860..59984479 [GRCh38]
Chr4:52766026..60850197 [GRCh37]
Chr4:52460783..60532792 [NCBI36]
Chr4:4q12-13.1		 pathogenic
GRCh38/hg38 4p13-q13.1(chr4:44356201-62245882)x3 copy number gain See cases [RCV000050683] Chr4:44356201..62245882 [GRCh38]
Chr4:44358218..63111600 [GRCh37]
Chr4:44052975..62794195 [NCBI36]
Chr4:4p13-q13.1		 pathogenic
GRCh38/hg38 4q12-13.1(chr4:52639018-59984479)x1 copy number loss See cases [RCV000053265] Chr4:52639018..59984479 [GRCh38]
Chr4:53505185..60850197 [GRCh37]
Chr4:53199942..60532792 [NCBI36]
Chr4:4q12-13.1		 pathogenic
GRCh38/hg38 4q12-13.1(chr4:54198601-62270115)x1 copy number loss See cases [RCV000053266] Chr4:54198601..62270115 [GRCh38]
Chr4:55064768..63135833 [GRCh37]
Chr4:54759525..62818428 [NCBI36]
Chr4:4q12-13.1		 pathogenic
NM_024592.5(SRD5A3):c.744T>G (p.Phe248Leu) single nucleotide variant not provided [RCV000254750] Chr4:55369878 [GRCh38]
Chr4:56236045 [GRCh37]
Chr4:4q12		 likely pathogenic
NM_024592.5(SRD5A3):c.*341CA[20] microsatellite Congenital disorder of glycosylation [RCV000261815] Chr4:55370432..55370433 [GRCh38]
Chr4:56236599..56236600 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.*2063G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000263698] Chr4:55372154 [GRCh38]
Chr4:56238321 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.566A>C (p.Tyr189Ser) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000872899]|not provided [RCV001705093]|not specified [RCV000192865] Chr4:55367591 [GRCh38]
Chr4:56233758 [GRCh37]
Chr4:4q12		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_024592.5(SRD5A3):c.*2915A>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000268034] Chr4:55373006 [GRCh38]
Chr4:56239173 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*321C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000276891]|not provided [RCV001613153] Chr4:55370412 [GRCh38]
Chr4:56236579 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.*2112G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000267558] Chr4:55372203 [GRCh38]
Chr4:56238370 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*1601G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000314399] Chr4:55371692 [GRCh38]
Chr4:56237859 [GRCh37]
Chr4:4q12		 benign|uncertain significance
NM_024592.5(SRD5A3):c.*546G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000376255] Chr4:55370637 [GRCh38]
Chr4:56236804 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.*2589G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000335842] Chr4:55372680 [GRCh38]
Chr4:56238847 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.*2005T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000356067] Chr4:55372096 [GRCh38]
Chr4:56238263 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.*1329T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000400935] Chr4:55371420 [GRCh38]
Chr4:56237587 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*879C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000380494] Chr4:55370970 [GRCh38]
Chr4:56237137 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.*104T>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000403365] Chr4:55370195 [GRCh38]
Chr4:56236362 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*991C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000288439] Chr4:55371082 [GRCh38]
Chr4:56237249 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2984A>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000304410] Chr4:55373075 [GRCh38]
Chr4:56239242 [GRCh37]
Chr4:4q12		 likely benign|uncertain significance
NM_024592.5(SRD5A3):c.*2090G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000321231] Chr4:55372181 [GRCh38]
Chr4:56238348 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.925C>G (p.His309Asp) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001081196]|not provided [RCV000513911]|not specified [RCV000437013] Chr4:55370059 [GRCh38]
Chr4:56236226 [GRCh37]
Chr4:4q12		 benign|likely benign|uncertain significance
NM_024592.5(SRD5A3):c.*1859C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000408351] Chr4:55371950 [GRCh38]
Chr4:56238117 [GRCh37]
Chr4:4q12		 benign|uncertain significance
NM_024592.5(SRD5A3):c.*1504A>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000291604] Chr4:55371595 [GRCh38]
Chr4:56237762 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*854G>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000323486] Chr4:55370945 [GRCh38]
Chr4:56237112 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2870A>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000362659] Chr4:55372961 [GRCh38]
Chr4:56239128 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2858del deletion Congenital disorder of glycosylation [RCV000307927] Chr4:55372936 [GRCh38]
Chr4:56239103 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2368G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000293555] Chr4:55372459 [GRCh38]
Chr4:56238626 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.*92G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000365998] Chr4:55370183 [GRCh38]
Chr4:56236350 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2437G>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000389114] Chr4:55372528 [GRCh38]
Chr4:56238695 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*70C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000308866]|not provided [RCV001534996] Chr4:55370161 [GRCh38]
Chr4:56236328 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.*1069G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000345775] Chr4:55371160 [GRCh38]
Chr4:56237327 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.*311ACCGAAAA[1] microsatellite Congenital disorder of glycosylation [RCV000369292]|not provided [RCV001613152] Chr4:55370401..55370408 [GRCh38]
Chr4:56236568..56236575 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.*1518C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000348824] Chr4:55371609 [GRCh38]
Chr4:56237776 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*261A>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000312230] Chr4:55370352 [GRCh38]
Chr4:56236519 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*1706G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000371247] Chr4:55371797 [GRCh38]
Chr4:56237964 [GRCh37]
Chr4:4q12		 benign|likely benign
NM_024592.5(SRD5A3):c.*2430C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000350912] Chr4:55372521 [GRCh38]
Chr4:56238688 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*341CA[24] microsatellite Congenital disorder of glycosylation [RCV000354338] Chr4:55370431..55370432 [GRCh38]
Chr4:56236598..56236599 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2560A>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000278410] Chr4:55372651 [GRCh38]
Chr4:56238818 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*340_*341del deletion Congenital disorder of glycosylation [RCV000315605] Chr4:55370431..55370432 [GRCh38]
Chr4:56236598..56236599 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2193G>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000381854] Chr4:55372284 [GRCh38]
Chr4:56238451 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2844del deletion Congenital disorder of glycosylation [RCV000347701] Chr4:55372935 [GRCh38]
Chr4:56239102 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2277del deletion Congenital disorder of glycosylation [RCV000385444] Chr4:55372368 [GRCh38]
Chr4:56238535 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*341CA[18] microsatellite Congenital disorder of glycosylation [RCV000319227] Chr4:55370432..55370437 [GRCh38]
Chr4:56236599..56236604 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*707G>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000284845] Chr4:55370798 [GRCh38]
Chr4:56236965 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*1567T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000391920] Chr4:55371658 [GRCh38]
Chr4:56237825 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*1935C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000298930] Chr4:55372026 [GRCh38]
Chr4:56238193 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2134G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000324958] Chr4:55372225 [GRCh38]
Chr4:56238392 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2804C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000393541] Chr4:55372895 [GRCh38]
Chr4:56239062 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2858dup duplication Congenital disorder of glycosylation [RCV000393549] Chr4:55372935..55372936 [GRCh38]
Chr4:56239102..56239103 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2844_*2845del deletion Congenital disorder of glycosylation [RCV000311572] Chr4:55372934..55372935 [GRCh38]
Chr4:56239101..56239102 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2227G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000290028] Chr4:55372318 [GRCh38]
Chr4:56238485 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2111G>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000359956] Chr4:55372202 [GRCh38]
Chr4:56238369 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2256C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000328681] Chr4:55372347 [GRCh38]
Chr4:56238514 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.672C>T (p.Leu224=) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000648110]|not provided [RCV001698232] Chr4:55367697 [GRCh38]
Chr4:56233864 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.*6C>T single nucleotide variant not specified [RCV000434081] Chr4:55370097 [GRCh38]
Chr4:56236264 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.758C>T (p.Ser253Phe) single nucleotide variant not provided [RCV003312605] Chr4:55369892 [GRCh38]
Chr4:56236059 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.682A>C (p.Arg228=) single nucleotide variant not provided [RCV000924610] Chr4:55367707 [GRCh38]
Chr4:56233874 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.821A>G (p.Asn274Ser) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001062116] Chr4:55369955 [GRCh38]
Chr4:56236122 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.951_955del (p.Phe318fs) deletion Inborn genetic diseases [RCV002535656]|Low-set ears [RCV001270115]|SRD5A3-congenital disorder of glycosylation [RCV000779445]|SRD5A3-congenital disorder of glycosylation [RCV002507348]|not provided [RCV001528813] Chr4:55370081..55370085 [GRCh38]
Chr4:56236248..56236252 [GRCh37]
Chr4:4q12		 conflicting interpretations of pathogenicity|uncertain significance
NM_024592.5(SRD5A3):c.695C>A (p.Ala232Glu) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV000809499] Chr4:55367720 [GRCh38]
Chr4:56233887 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.698-139T>C single nucleotide variant not provided [RCV000835609] Chr4:55369693 [GRCh38]
Chr4:56235860 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.837A>G (p.Leu279=) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002539418]|SRD5A3-related condition [RCV003968158] Chr4:55369971 [GRCh38]
Chr4:56236138 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.698-68C>G single nucleotide variant not provided [RCV000835613] Chr4:55369764 [GRCh38]
Chr4:56235931 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.*2950T>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001151492] Chr4:55373041 [GRCh38]
Chr4:56239208 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2637T>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001150725] Chr4:55372728 [GRCh38]
Chr4:56238895 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2641G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001150726] Chr4:55372732 [GRCh38]
Chr4:56238899 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*275G>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001146298]|not provided [RCV001577181] Chr4:55370366 [GRCh38]
Chr4:56236533 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.*621C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001149098] Chr4:55370712 [GRCh38]
Chr4:56236879 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.921G>C (p.Pro307=) single nucleotide variant Congenital disorder of glycosylation [RCV000851213] Chr4:55370055 [GRCh38]
Chr4:56236222 [GRCh37]
Chr4:4q12		 likely pathogenic
NM_024592.5(SRD5A3):c.*2306C>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001149220] Chr4:55372397 [GRCh38]
Chr4:56238564 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*590C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001146299] Chr4:55370681 [GRCh38]
Chr4:56236848 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*873A>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001149101] Chr4:55370964 [GRCh38]
Chr4:56237131 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*968C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001149102] Chr4:55371059 [GRCh38]
Chr4:56237226 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.617G>T (p.Gly206Val) single nucleotide variant not provided [RCV001560513] Chr4:55367642 [GRCh38]
Chr4:56233809 [GRCh37]
Chr4:4q12		 likely pathogenic
NM_024592.5(SRD5A3):c.563-203T>G single nucleotide variant not provided [RCV001670324] Chr4:55367385 [GRCh38]
Chr4:56233552 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.934G>C (p.Ala312Pro) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001144404] Chr4:55370068 [GRCh38]
Chr4:56236235 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2022A>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001144518] Chr4:55372113 [GRCh38]
Chr4:56238280 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2120T>G single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001146445] Chr4:55372211 [GRCh38]
Chr4:56238378 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2248G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001146446] Chr4:55372339 [GRCh38]
Chr4:56238506 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*812T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001149100] Chr4:55370903 [GRCh38]
Chr4:56237070 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2437G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001149221] Chr4:55372528 [GRCh38]
Chr4:56238695 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.698-96A>G single nucleotide variant not provided [RCV001556918] Chr4:55369736 [GRCh38]
Chr4:56235903 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.697+225G>A single nucleotide variant not provided [RCV001717574] Chr4:55367947 [GRCh38]
Chr4:56234114 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.698-237G>T single nucleotide variant not provided [RCV001546531] Chr4:55369595 [GRCh38]
Chr4:56235762 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.563-331T>C single nucleotide variant not provided [RCV001591987] Chr4:55367257 [GRCh38]
Chr4:56233424 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.802G>A (p.Val268Ile) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001144403] Chr4:55369936 [GRCh38]
Chr4:56236103 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.673G>A (p.Gly225Ser) single nucleotide variant Inborn genetic diseases [RCV004032734]|SRD5A3-congenital disorder of glycosylation [RCV001144402] Chr4:55367698 [GRCh38]
Chr4:56233865 [GRCh37]
Chr4:4q12		 likely benign|uncertain significance
NM_024592.5(SRD5A3):c.*1624G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001144516] Chr4:55371715 [GRCh38]
Chr4:56237882 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2884C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001150727] Chr4:55372975 [GRCh38]
Chr4:56239142 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2983T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001154515] Chr4:55373074 [GRCh38]
Chr4:56239241 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.698-86_698-85del deletion not provided [RCV001713417] Chr4:55369731..55369732 [GRCh38]
Chr4:56235898..56235899 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.645_670del (p.His216fs) deletion not provided [RCV001585608] Chr4:55367669..55367694 [GRCh38]
Chr4:56233836..56233861 [GRCh37]
Chr4:4q12		 likely pathogenic
NM_024592.5(SRD5A3):c.*622C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001149099] Chr4:55370713 [GRCh38]
Chr4:56236880 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*2950T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001150728] Chr4:55373041 [GRCh38]
Chr4:56239208 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*594C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001146300] Chr4:55370685 [GRCh38]
Chr4:56236852 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*1665G>A single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001144517] Chr4:55371756 [GRCh38]
Chr4:56237923 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.*242T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001146297] Chr4:55370333 [GRCh38]
Chr4:56236500 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.911T>C (p.Val304Ala) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001321716]|SRD5A3-congenital disorder of glycosylation [RCV002476508] Chr4:55370045 [GRCh38]
Chr4:56236212 [GRCh37]
Chr4:4q12		 uncertain significance
GRCh38/hg38 4q12-21.1(chr4:51891814-76009719)x1 copy number loss Piebaldism [RCV001420508] Chr4:51891814..76009719 [GRCh38]
Chr4:4q12-21.1		 pathogenic
NM_024592.5(SRD5A3):c.698-85del deletion not provided [RCV001613815] Chr4:55369731 [GRCh38]
Chr4:56235898 [GRCh37]
Chr4:4q12		 benign
NM_024592.5(SRD5A3):c.698-8C>T single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001505939] Chr4:55369824 [GRCh38]
Chr4:56235991 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.825A>C (p.Leu275Phe) single nucleotide variant not provided [RCV001760957] Chr4:55369959 [GRCh38]
Chr4:56236126 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.851T>G (p.Val284Gly) single nucleotide variant not provided [RCV001767146] Chr4:55369985 [GRCh38]
Chr4:56236152 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.869T>C (p.Leu290Pro) single nucleotide variant not provided [RCV001761328] Chr4:55370003 [GRCh38]
Chr4:56236170 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.698-1G>A single nucleotide variant Abnormality of the nervous system [RCV001814567] Chr4:55369831 [GRCh38]
Chr4:56235998 [GRCh37]
Chr4:4q12		 likely pathogenic
NM_024592.5(SRD5A3):c.633C>G (p.Ile211Met) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001986712] Chr4:55367658 [GRCh38]
Chr4:56233825 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.613C>T (p.Leu205Phe) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV001944665] Chr4:55367638 [GRCh38]
Chr4:56233805 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.920C>T (p.Pro307Leu) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002029172] Chr4:55370054 [GRCh38]
Chr4:56236221 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.942A>G (p.Leu314=) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002199962] Chr4:55370076 [GRCh38]
Chr4:56236243 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.697+1G>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002246742] Chr4:55367723 [GRCh38]
Chr4:56233890 [GRCh37]
Chr4:4q12		 pathogenic|conflicting interpretations of pathogenicity
NM_024592.5(SRD5A3):c.627G>A (p.Met209Ile) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002908323] Chr4:55367652 [GRCh38]
Chr4:56233819 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.686A>G (p.Lys229Arg) single nucleotide variant Inborn genetic diseases [RCV002707825] Chr4:55367711 [GRCh38]
Chr4:56233878 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.598C>T (p.Arg200Trp) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002637856] Chr4:55367623 [GRCh38]
Chr4:56233790 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.789C>T (p.Tyr263=) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002572418] Chr4:55369923 [GRCh38]
Chr4:56236090 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.751G>C (p.Val251Leu) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002833208] Chr4:55369885 [GRCh38]
Chr4:56236052 [GRCh37]
Chr4:4q12		 uncertain significance
NM_024592.5(SRD5A3):c.697+13T>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002939157] Chr4:55367735 [GRCh38]
Chr4:56233902 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.586T>C (p.Leu196=) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002628323] Chr4:55367611 [GRCh38]
Chr4:56233778 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.927T>C (p.His309=) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV002654335] Chr4:55370061 [GRCh38]
Chr4:56236228 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.810T>A (p.Phe270Leu) single nucleotide variant Inborn genetic diseases [RCV003202936] Chr4:55369944 [GRCh38]
Chr4:56236111 [GRCh37]
Chr4:4q12		 uncertain significance
GRCh38/hg38 4p16.3-q12(chr4:85624-57073230)x3 copy number gain Neurodevelopmental disorder [RCV003327613] Chr4:85624..57073230 [GRCh38]
Chr4:4p16.3-q12		 pathogenic
NM_024592.5(SRD5A3):c.918C>T (p.Tyr306=) single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV003527267] Chr4:55370052 [GRCh38]
Chr4:56236219 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.563-16A>C single nucleotide variant SRD5A3-congenital disorder of glycosylation [RCV003640288] Chr4:55367572 [GRCh38]
Chr4:56233739 [GRCh37]
Chr4:4q12		 likely benign
NM_024592.5(SRD5A3):c.720C>T (p.His240=) single nucleotide variant SRD5A3-related condition [RCV003902295] Chr4:55369854 [GRCh38]
Chr4:56236021 [GRCh37]
Chr4:4q12		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2696
Count of miRNA genes:696
Interacting mature miRNAs:791
Transcripts:ENST00000433175, ENST00000510637, ENST00000591915, ENST00000592823, ENST00000595103, ENST00000595734, ENST00000596289, ENST00000596312, ENST00000598819, ENST00000598906, ENST00000599135, ENST00000601433, ENST00000608086, ENST00000608136, ENST00000608265, ENST00000608558, ENST00000609051, ENST00000609487, ENST00000609500, ENST00000609573, ENST00000609580, ENST00000609700
Prediction methods:Microtar, Miranda, Rnahybrid
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
SHGC-142651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37456,235,985 - 56,236,294UniSTSGRCh37
Build 36455,930,742 - 55,931,051RGDNCBI36
Celera453,737,813 - 53,738,122RGD
Cytogenetic Map4q12UniSTS
HuRef452,184,951 - 52,185,260UniSTS
SHGC-59633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371159,666,604 - 59,666,823UniSTSGRCh37
GRCh37456,236,252 - 56,236,473UniSTSGRCh37
Build 36455,931,009 - 55,931,230RGDNCBI36
Celera453,738,080 - 53,738,301RGD
Celera1157,029,356 - 57,029,575UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map11q12.1UniSTS
HuRef452,185,218 - 52,185,439UniSTS
HuRef1156,014,002 - 56,014,221UniSTS
GeneMap99-GB4 RH Map4334.02UniSTS
Whitehead-RH Map4411.1UniSTS
NCBI RH Map4583.0UniSTS
SHGC-67770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371159,666,618 - 59,666,755UniSTSGRCh37
GRCh37456,236,266 - 56,236,403UniSTSGRCh37
Build 36455,931,023 - 55,931,160RGDNCBI36
Celera453,738,094 - 53,738,231RGD
Celera1157,029,370 - 57,029,507UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map11q12.1UniSTS
HuRef1156,014,016 - 56,014,153UniSTS
HuRef452,185,232 - 52,185,369UniSTS
GeneMap99-GB4 RH Map4345.85UniSTS
SHGC-68214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37456,238,166 - 56,238,315UniSTSGRCh37
Build 36455,932,923 - 55,933,072RGDNCBI36
Celera453,739,992 - 53,740,141RGD
Cytogenetic Map4q12UniSTS
HuRef452,187,130 - 52,187,279UniSTS
GeneMap99-GB4 RH Map4334.23UniSTS
NCBI RH Map4582.2UniSTS
GDB:631802  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p35.3-p33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map3q21-q22UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.22-p11.21UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map2q21UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map20p11.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map2p24.1UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 171
Low 1145 1236 446 80 500 45 2574 735 2706 176 965 952 38 877 1574 1
Below cutoff 1282 1715 1267 532 1388 409 1780 1458 1002 242 312 655 132 327 1214 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NR_037969 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC064824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC069200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC034006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ574699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MW803800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MW803801 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MW803802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988181 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988183 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988185 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000433175
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,363,971 - 55,383,396 (-)Ensembl
RefSeq Acc Id: ENST00000510637
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,601 - 55,385,580 (-)Ensembl
RefSeq Acc Id: ENST00000591915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,377,607 - 55,387,443 (-)Ensembl
RefSeq Acc Id: ENST00000592823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,374,875 - 55,395,842 (-)Ensembl
RefSeq Acc Id: ENST00000595103
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,954 - 55,385,625 (-)Ensembl
RefSeq Acc Id: ENST00000595734
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,954 - 55,385,666 (-)Ensembl
RefSeq Acc Id: ENST00000596289
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,954 - 55,385,300 (-)Ensembl
RefSeq Acc Id: ENST00000596312
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,954 - 55,381,893 (-)Ensembl
RefSeq Acc Id: ENST00000598819
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,387,321 - 55,395,830 (-)Ensembl
RefSeq Acc Id: ENST00000598906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,954 - 55,383,882 (-)Ensembl
RefSeq Acc Id: ENST00000599135
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,377,607 - 55,395,842 (-)Ensembl
RefSeq Acc Id: ENST00000601433
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,382,538 - 55,395,837 (-)Ensembl
RefSeq Acc Id: ENST00000608086
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,375,972 (-)Ensembl
RefSeq Acc Id: ENST00000608136
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,386,778 - 55,395,847 (-)Ensembl
RefSeq Acc Id: ENST00000608265
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,385,608 (-)Ensembl
RefSeq Acc Id: ENST00000608558
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,383,805 (-)Ensembl
RefSeq Acc Id: ENST00000609051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,385,608 (-)Ensembl
RefSeq Acc Id: ENST00000609487
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,385,615 (-)Ensembl
RefSeq Acc Id: ENST00000609500
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,380,892 (-)Ensembl
RefSeq Acc Id: ENST00000609573
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,017 - 55,385,585 (-)Ensembl
RefSeq Acc Id: ENST00000609580
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,386,406 (-)Ensembl
RefSeq Acc Id: ENST00000609700
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,012 - 55,383,450 (-)Ensembl
RefSeq Acc Id: ENST00000610396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,954 - 55,386,687 (-)Ensembl
RefSeq Acc Id: ENST00000613794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,382,663 (-)Ensembl
RefSeq Acc Id: ENST00000619203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,374,924 - 55,386,892 (-)Ensembl
RefSeq Acc Id: ENST00000619685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,367,010 - 55,375,188 (-)Ensembl
RefSeq Acc Id: ENST00000619912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,954 - 55,382,642 (-)Ensembl
RefSeq Acc Id: ENST00000666009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl455,366,601 - 55,385,606 (-)Ensembl
RefSeq Acc Id: NR_037969
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38455,366,601 - 55,385,580 (-)NCBI
GRCh37456,232,768 - 56,251,747 (-)NCBI
HuRef452,181,770 - 52,200,698 (-)NCBI
CHM1_1456,267,930 - 56,286,901 (-)NCBI
T2T-CHM13v2.0458,854,739 - 58,873,724 (-)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
COSMIC SRD5A3-AS1 COSMIC
Ensembl Genes ENSG00000249700 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000510637 ENTREZGENE
GTEx ENSG00000249700 GTEx
HGNC ID HGNC:44138 ENTREZGENE
Human Proteome Map SRD5A3-AS1 Human Proteome Map
NCBI Gene SRD5A3-AS1 ENTREZGENE
RNAcentral URS000075B6E1 RNACentral


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2012-08-21 SRD5A3-AS1  SRD5A3 antisense RNA 1  SRD5A3-AS1  SRD5A3 antisense RNA 1 (non-protein coding)  Symbol and/or name change 5135510 APPROVED