BMAL1 (basic helix-loop-helix ARNT like 1) - Rat Genome Database

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Gene: BMAL1 (basic helix-loop-helix ARNT like 1) Homo sapiens
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Symbol: BMAL1
Name: basic helix-loop-helix ARNT like 1
RGD ID: 732520
HGNC Page HGNC:701
Description: Enables E-box binding activity; Hsp90 protein binding activity; and aryl hydrocarbon receptor binding activity. Involved in several processes, including positive regulation of circadian rhythm; regulation of macromolecule metabolic process; and response to redox state. Located in nucleoplasm. Part of CLOCK-BMAL transcription complex. Implicated in alcohol dependence and bipolar disorder.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ARNT-like protein 1, brain and muscle; ARNTL; ARNTL1; aryl hydrocarbon receptor nuclear translocator like; aryl hydrocarbon receptor nuclear translocator-like protein 1; basic helix-loop-helix ARNT-like protein 1; basic helix-loop-helix family member e5; basic-helix-loop-helix-PAS orphan MOP3; basic-helix-loop-helix-PAS protein MOP3; bHLH-PAS protein JAP3; bHLHe5; BMAL1c; brain and muscle ARNT-like 1; class E basic helix-loop-helix protein 5; JAP3; member of PAS protein 3; member of PAS superfamily 3; MGC47515; MOP3; mutant basic helix-loop-helix ARNT-like protein 1; PAS domain containing 3; PAS domain-containing protein 3; PASD3; testis tissue sperm-binding protein Li 50e; TIC
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
NCBI Annotation Information: Note: This gene has been reviewed for its involvement in coronavirus biology, and is involved in immune response or antiviral activity.
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381113,276,652 - 13,387,266 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1113,276,652 - 13,387,266 (+)EnsemblGRCh38hg38GRCh38
GRCh371113,298,199 - 13,408,813 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361113,255,901 - 13,365,389 (+)NCBINCBI36Build 36hg18NCBI36
Build 341113,255,925 - 13,365,386NCBI
Celera1113,425,472 - 13,534,997 (+)NCBICelera
Cytogenetic Map11p15.3NCBI
HuRef1112,979,421 - 13,089,003 (+)NCBIHuRef
CHM1_11113,298,302 - 13,407,784 (+)NCBICHM1_1
T2T-CHM13v2.01113,369,378 - 13,480,010 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
BMAL1Humanalcohol dependence susceptibilityIAGP 401976551DNA:SNP::(rs6486120) (human)RGD 
BMAL1Humanalcohol withdrawal syndrome severityIEP 401976556mRNA:decreased expression:peripheral blood mononuclear cells (human)RGD 
BMAL1Humanantidepressant type abuse  ISOBmal1 (Mus musculus)405866348mRNA:increased expression:hippocampal formation (mouse)RGD 
BMAL1Humanbipolar disorder sexual_dimorphismIAGP 405866353associated with Alcohol-related disorders and DNA:SNP::(rs11600996) (Human)RGD 
BMAL1HumanBrain Hypoxia-Ischemia  ISOBmal1 (Rattus norvegicus)10043348protein:increased expression:pineal glandRGD 
BMAL1Humancholestasis  ISOBmal1 (Rattus norvegicus)10043349mRNA:increased expression:cholangiocyteRGD 
BMAL1Humancocaine abuse  ISOBmal1 (Mus musculus)405866348mRNA:decreased expression:caudate-putamen (mouse)RGD 
BMAL1HumanExperimental Diabetes Mellitus  ISOBmal1 (Rattus norvegicus)2301030 RGD 
BMAL1HumanPremature Aging  ISOBmal1 (Mus musculus)10043345 RGD 
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BMAL1Humanintellectual disability  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Intellectual disabilityClinVar 
BMAL1Humanprimary ovarian insufficiency  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Premature ovarian failureClinVarPMID:25741868
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BMAL1HumanChemical and Drug Induced Liver Injury  EXP 11554173CTD Direct Evidence: therapeuticCTDPMID:36602574
BMAL1Humanchronic myeloid leukemia  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:16999817
BMAL1HumanFemale Infertility  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:20200203
BMAL1Humanhyperargininemia  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:27056296
BMAL1HumanMultiple Abnormalities  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:24652800
BMAL1HumanMyocardial Ischemia  EXP 11554173CTD Direct Evidence: marker/mechanismCTDPMID:16214533
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BMAL1Humandiabetes mellitus  ISSBmal1 (Mus musculus)13592920 MouseDO 

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BMAL1Human(+)-epicatechin-3-O-gallate multiple interactionsEXP 6480464[Gallic Acid co-treated with gallocatechol co-treated with epigallocatechin gallate co-treated with epicatechin gallate] affects the reaction [Hydrogen Peroxide affects the expression of BMAL1 mRNA] more ...CTDPMID:29061316
BMAL1Human(+)-schisandrin B multiple interactionsISOBmal1 (Rattus norvegicus)6480464schizandrin B inhibits the reaction [Carbon Tetrachloride results in increased expression of BMAL1 mRNA]CTDPMID:31150632
BMAL1Human(-)-epigallocatechin 3-gallate multiple interactionsEXP 6480464[Gallic Acid co-treated with gallocatechol co-treated with epigallocatechin gallate co-treated with epicatechin gallate] affects the reaction [Hydrogen Peroxide affects the expression of BMAL1 mRNA] more ...CTDPMID:22079256 and PMID:29061316
BMAL1Human(1->4)-beta-D-glucan multiple interactionsISOBmal1 (Mus musculus)6480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of ARNTL mRNACTDPMID:36331819
BMAL1Human1,2-dichloroethane increases expressionISOBmal1 (Mus musculus)6480464ethylene dichloride results in increased expression of BMAL1 mRNACTDPMID:28960355
BMAL1Human1,2-dimethylhydrazine increases expressionISOBmal1 (Mus musculus)64804641 and 2-Dimethylhydrazine results in increased expression of BMAL1 mRNACTDPMID:22206623
BMAL1Human1,2-dimethylhydrazine multiple interactionsISOBmal1 (Mus musculus)6480464Folic Acid inhibits the reaction [1 and 2-Dimethylhydrazine results in increased expression of BMAL1 mRNA]CTDPMID:22206623
BMAL1Human1,3-dichloropropan-2-ol multiple interactionsEXP 6480464BMAL1 protein inhibits the reaction [1 more ...CTDPMID:36805544
BMAL1Human1,3-dichloropropan-2-ol decreases expressionISOBmal1 (Mus musculus)64804641 and 3-dichloro-2-propanol results in decreased expression of BMAL1 proteinCTDPMID:36805544
BMAL1Human17beta-estradiol decreases expressionISOBmal1 (Rattus norvegicus)6480464Estradiol results in decreased expression of ARNTL mRNACTDPMID:32145629
BMAL1Human17beta-estradiol increases expressionISOBmal1 (Mus musculus)6480464Estradiol results in increased expression of BMAL1 mRNACTDPMID:39298647
BMAL1Human17beta-estradiol multiple interactionsISOBmal1 (Mus musculus)6480464[Polyphenols co-treated with Estradiol] results in decreased expression of BMAL1 mRNACTDPMID:30077407
BMAL1Human2,2',4,4',5,5'-hexachlorobiphenyl multiple interactionsISOBmal1 (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with 2 more ...CTDPMID:28433925 and PMID:32784060
BMAL1Human2,2',4,4'-Tetrabromodiphenyl ether affects expressionISOBmal1 (Mus musculus)64804642 more ...CTDPMID:30294300
BMAL1Human2,2',4,4'-Tetrabromodiphenyl ether multiple interactionsISOBmal1 (Mus musculus)6480464[Flame Retardants results in increased abundance of 2 more ...CTDPMID:38995820
BMAL1Human2,3',4,4',5-Pentachlorobiphenyl increases expressionISOBmal1 (Mus musculus)64804642 more ...CTDPMID:31388691
BMAL1Human2,3,7,8-tetrachlorodibenzodioxine increases expressionISOBmal1 (Rattus norvegicus)6480464Tetrachlorodibenzodioxin results in increased expression of BMAL1 mRNACTDPMID:21215274
BMAL1Human2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOBmal1 (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with 2 more ...CTDPMID:21182907 more ...
BMAL1Human2,3,7,8-tetrachlorodibenzodioxine affects expressionISOBmal1 (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of BMAL1 mRNA and Tetrachlorodibenzodioxin affects the expression of BMAL1 proteinCTDPMID:21182907 more ...
BMAL1Human2,3,7,8-tetrachlorodibenzodioxine increases expressionISOBmal1 (Mus musculus)6480464Tetrachlorodibenzodioxin results in increased expression of BMAL1 mRNACTDPMID:18487412

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Biological Process
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BMAL1Humanautophagy acts_upstream_of_or_withinISOMGI:21803619068941 PMID:26945058MGIPMID:26945058
BMAL1Humancircadian regulation of gene expression involved_inIDA 150520179 PMID:23229515 and PMID:24005054UniProtPMID:23229515 and PMID:24005054
BMAL1Humancircadian regulation of gene expression involved_inISSUniProtKB:Q9WTL8150520179 UniProtGO_REF:0000024
BMAL1Humancircadian rhythm  ISOBmal1 (Rattus norvegicus)9068941 RGDPMID:9735336 more ...
BMAL1Humancircadian rhythm acts_upstream_of_or_withinISOMGI:21803619068941 PMID:11163178 and PMID:26945058MGIPMID:11163178 and PMID:26945058
BMAL1Humancircadian rhythm acts_upstream_of_or_withinISOBmal1 (Mus musculus)9068941 PMID:12024206 more ...MGIPMID:12024206 more ...
BMAL1Humancircadian rhythm acts_upstream_of_or_withinISOBmal1 (Mus musculus)9068941 PMID:17264215MGIPMID:17264215
BMAL1Humancircadian rhythm involved_inIBAMGI:1096381 more ...150520179 GO_CentralGO_REF:0000033
BMAL1Humancircadian rhythm involved_inTAS 150520179 PMID:9616112PINCPMID:9616112
BMAL1Humanenergy homeostasis involved_inISSMGI:1096381150520179 UniProtGO_REF:0000024
BMAL1Humangene expression acts_upstream_of_or_withinISOMGI:21803619068941 PMID:26945058MGIPMID:26945058
BMAL1Humanmaternal process involved in parturition involved_inISOBmal1 (Mus musculus)9068941 PMID:22697126CACAOPMID:22697126
BMAL1Humannegative regulation of cold-induced thermogenesis involved_inISSUniProtKB:Q9WTL8150520179 PMID:25749863YuBioLabPMID:25749863
BMAL1Humannegative regulation of DNA-templated transcription involved_inISSUniProtKB:O08785150520179 UniProtGO_REF:0000024
BMAL1Humannegative regulation of fat cell differentiation involved_inISSUniProtKB:Q9WTL8150520179 UniProtGO_REF:0000024
BMAL1Humannegative regulation of nuclear receptor-mediated glucocorticoid signaling pathway involved_inISSUniProtKB:Q9WTL8150520179 UniProtGO_REF:0000024
BMAL1Humannegative regulation of TOR signaling involved_inISSUniProtKB:Q9WTL8150520179 UniProtGO_REF:0000024
BMAL1Humanoxidative stress-induced premature senescence involved_inISSUniProtKB:Q9WTL8150520179 UniProtGO_REF:0000024
BMAL1Humanpositive regulation of canonical Wnt signaling pathway involved_inISSUniProtKB:Q9WTL8150520179 UniProtGO_REF:0000024
BMAL1Humanpositive regulation of circadian rhythm involved_inIDA 150520179 PMID:23229515ComplexPortalPMID:23229515
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Cellular Component
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Original Reference(s)
BMAL1Humanaryl hydrocarbon receptor complex part_ofIBAPANTHER:PTN000548496 and UniProtKB:P27540150520179 GO_CentralGO_REF:0000033
BMAL1Humanchromatin located_inISAtfclass:1.2.5150520179 NTNU_SBGO_REF:0000113
BMAL1Humanchromatoid body located_inISSUniProtKB:Q9WTL8150520179 UniProtGO_REF:0000024
BMAL1HumanCLOCK-BMAL transcription complex part_ofIPI 150520179 PMID:23229515ComplexPortalPMID:23229515
BMAL1Humancytoplasm located_inIEAUniProtKB-SubCell:SL-0086150520179 UniProtGO_REF:0000044
BMAL1Humancytoplasm located_inIEAUniProtKB-KW:KW-0963150520179 UniProtGO_REF:0000043
BMAL1Humancytoplasm located_inIEAInterPro:IPR001067150520179 InterProGO_REF:0000002
BMAL1Humanintracellular membrane-bounded organelle located_inIDA 150520179 HPAGO_REF:0000052
BMAL1Humannuclear body located_inISOBmal1 (Mus musculus)9068941 PMID:18644859MGIPMID:18644859
BMAL1Humannucleoplasm located_inIDA 150520179 HPAGO_REF:0000052
BMAL1Humannucleoplasm located_inTAS 150520179 ReactomeReactome:R-HSA-5663124 more ...
BMAL1Humannucleus is_active_inISSMGI:1096381150520179 UniProtGO_REF:0000024
BMAL1Humannucleus is_active_inIBAFB:FBgn0002723 more ...150520179 GO_CentralGO_REF:0000033
BMAL1Humannucleus located_inIDA 150520179 PMID:23229515 and PMID:24005054UniProtPMID:23229515 and PMID:24005054
BMAL1Humannucleus located_inIEAInterPro:IPR001067150520179 InterProGO_REF:0000002
BMAL1Humannucleus located_inIEAUniProtKB-KW:KW-0539150520179 UniProtGO_REF:0000043
BMAL1Humannucleus located_inIEAUniProtKB-SubCell:SL-0191150520179 UniProtGO_REF:0000044
BMAL1HumanPML body located_inIEAUniProtKB-SubCell:SL-0465150520179 UniProtGO_REF:0000044
BMAL1Humantranscription regulator complex part_ofIEAInterPro:IPR001067150520179 InterProGO_REF:0000002
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Molecular Function
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BMAL1Humanaryl hydrocarbon receptor binding enablesIPIUniProtKB:P35869150520179 PMID:9079689BHF-UCLPMID:9079689
BMAL1HumanbHLH transcription factor binding enablesISOUniProtKB:O145039068941 PMID:15193144 and PMID:15560782BHF-UCLPMID:15193144 and PMID:15560782
BMAL1HumanbHLH transcription factor binding enablesISOUniProtKB:O14503 and UniProtKB:Q99PV59068941 PMID:12397359BHF-UCLPMID:12397359
BMAL1HumanDNA binding enablesIEAUniProtKB-KW:KW-0238150520179 UniProtGO_REF:0000043
BMAL1HumanDNA binding enablesIDA 150520179 PMID:11441146UniProtPMID:11441146
BMAL1HumanDNA-binding transcription activator activity, RNA polymerase II-specific enablesISOBmal1 (Mus musculus)9068941 PMID:15560782BHF-UCLPMID:15560782
BMAL1HumanDNA-binding transcription factor activity enablesIEAInterPro:IPR001067150520179 InterProGO_REF:0000002
BMAL1HumanDNA-binding transcription factor activity, RNA polymerase II-specific enablesIBAFB:FBgn0002723 more ...150520179 GO_CentralGO_REF:0000033
BMAL1HumanDNA-binding transcription factor activity, RNA polymerase II-specific enablesISSUniProtKB:Q9WTL8150520179 BHF-UCLGO_REF:0000024
BMAL1HumanDNA-binding transcription factor activity, RNA polymerase II-specific enablesISAtfclass:1.2.5150520179 NTNU_SBGO_REF:0000113
BMAL1HumanDNA-binding transcription factor binding enablesIPIUniProtKB:Q8IV76150520179 PMID:25936801GO_CentralPMID:25936801
BMAL1HumanE-box binding enablesIDA 150520179 PMID:12738229 and PMID:23785138UniProtPMID:12738229 and PMID:23785138
BMAL1HumanHsp90 protein binding enablesIDA 150520179 PMID:9079689BHF-UCLPMID:9079689
BMAL1Humanprotein binding enablesIPIUniProtKB:P41235150520179 PMID:30530698UniProtPMID:30530698
BMAL1Humanprotein binding enablesIPIUniProtKB:P49841 and UniProtKB:Q8TC59150520179 PMID:28903391UniProtPMID:28903391
BMAL1Humanprotein binding enablesIPIUniProtKB:Q93008150520179 PMID:29626158UniProtPMID:29626158
BMAL1Humanprotein binding enablesIPIUniProtKB:Q05086150520179 PMID:24728990UniProtPMID:24728990
BMAL1Humanprotein binding enablesIPIUniProtKB:O15516150520179 PMID:11018023 more ...IntActPMID:11018023 more ...
BMAL1Humanprotein binding enablesIPIUniProtKB:P29375150520179 PMID:21960634UniProtPMID:21960634
BMAL1Humanprotein binding enablesIPIUniProtKB:Q09472 and UniProtKB:Q92831150520179 PMID:14645221UniProtPMID:14645221
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Original Reference(s)
BMAL1HumanAddictive alcohol use susceptibilityIAGP 401976551DNA:SNP::(rs6486120) (human)RGD 
BMAL1HumanBipolar affective disorder susceptibilityIAGP 405866353DNA:SNP::(rs11600996) (Human)RGD 
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BMAL1HumanIntellectual disability  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Intellectual disabilityClinVar 
BMAL1HumanPremature ovarian insufficiency  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Premature ovarian failureClinVarPMID:25741868

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#
Reference Title
Reference Citation
1. Clock genes polymorphisms in male bipolar patients with comorbid alcohol abuse. Banach E, etal., J Affect Disord. 2018 Dec 1;241:142-146. doi: 10.1016/j.jad.2018.07.080. Epub 2018 Jul 31.
2. Mop3 is an essential component of the master circadian pacemaker in mammals. Bunger MK, etal., Cell 2000 Dec 22;103(7):1009-17.
3. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
4. Reduced expression of circadian clock genes in male alcoholic patients. Huang MC, etal., Alcohol Clin Exp Res. 2010 Nov;34(11):1899-904. doi: 10.1111/j.1530-0277.2010.01278.x. Epub 2010 Aug 24.
5. Early aging and age-related pathologies in mice deficient in BMAL1, the core componentof the circadian clock. Kondratov RV, etal., Genes Dev. 2006 Jul 15;20(14):1868-73.
6. Circadian clock gene polymorphisms in alcohol use disorders and alcohol consumption. Kovanen L, etal., Alcohol Alcohol. 2010 Jul-Aug;45(4):303-11. doi: 10.1093/alcalc/agq035. Epub 2010 Jun 16.
7. [Changes of biological clock protein in neonatal rats with hypoxic-ischemic brain damage]. Li YF, etal., Zhongguo Dang Dai Er Ke Za Zhi. 2013 Jan;15(1):62-6.
8. Increased melatonin synthesis in pineal glands of rats in streptozotocin induced type 1 diabetes. Peschke E, etal., J Pineal Res. 2008 Jul 1.
9. Melatonin inhibits cholangiocyte hyperplasia in cholestatic rats by interaction with MT1 but not MT2 melatonin receptors. Renzi A, etal., Am J Physiol Gastrointest Liver Physiol. 2011 Oct;301(4):G634-43. doi: 10.1152/ajpgi.00206.2011. Epub 2011 Jul 14.
10. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
11. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
12. Effect of fluoxetine and cocaine on the expression of clock genes in the mouse hippocampus and striatum. Uz T, etal., Neuroscience. 2005;134(4):1309-16. doi: 10.1016/j.neuroscience.2005.05.003.
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PMID:9079689   PMID:9144434   PMID:9576906   PMID:9616112   PMID:9704006   PMID:9989497   PMID:10531061   PMID:11018023   PMID:11439184   PMID:11441146   PMID:11875063   PMID:12397359  
PMID:12477932   PMID:12738229   PMID:12897057   PMID:14645221   PMID:14701732   PMID:14701734   PMID:14702039   PMID:14750904   PMID:15193144   PMID:16474406   PMID:16507006   PMID:16528748  
PMID:16628007   PMID:17274950   PMID:17457720   PMID:17728404   PMID:17994337   PMID:18228528   PMID:18411297   PMID:18430226   PMID:18517031   PMID:18587630   PMID:18662547   PMID:18663240  
PMID:19274049   PMID:19277210   PMID:19296127   PMID:19328558   PMID:19460752   PMID:19470168   PMID:19693801   PMID:19839995   PMID:19861541   PMID:19861640   PMID:19912323   PMID:19913121  
PMID:19922678   PMID:19934327   PMID:20072116   PMID:20093779   PMID:20174623   PMID:20180986   PMID:20211142   PMID:20222832   PMID:20368993   PMID:20446921   PMID:20551151   PMID:20628086  
PMID:20819778   PMID:20861012   PMID:21102462   PMID:21363938   PMID:21380491   PMID:21411511   PMID:21628546   PMID:21799909   PMID:21873635   PMID:21960634   PMID:21966465   PMID:21990077  
PMID:22105622   PMID:22217103   PMID:22510946   PMID:22990020   PMID:23003921   PMID:23033538   PMID:23129285   PMID:23206673   PMID:23229515   PMID:23323702   PMID:23337503   PMID:23358160  
PMID:23395176   PMID:23449886   PMID:23503662   PMID:23546644   PMID:23555304   PMID:23563360   PMID:23584858   PMID:23602568   PMID:23606611   PMID:23785138   PMID:24005054   PMID:24103761  
PMID:24277452   PMID:24385426   PMID:24418196   PMID:24636202   PMID:24722188   PMID:24728990   PMID:25070164   PMID:25175925   PMID:25182847   PMID:25203321   PMID:25231870   PMID:25310406  
PMID:25352340   PMID:25416956   PMID:25480789   PMID:25660546   PMID:25741730   PMID:25749863   PMID:25756610   PMID:25798074   PMID:25799324   PMID:25936801   PMID:26134245   PMID:26164627  
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BMAL1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381113,276,652 - 13,387,266 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1113,276,652 - 13,387,266 (+)EnsemblGRCh38hg38GRCh38
GRCh371113,298,199 - 13,408,813 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361113,255,901 - 13,365,389 (+)NCBINCBI36Build 36hg18NCBI36
Build 341113,255,925 - 13,365,386NCBI
Celera1113,425,472 - 13,534,997 (+)NCBICelera
Cytogenetic Map11p15.3NCBI
HuRef1112,979,421 - 13,089,003 (+)NCBIHuRef
CHM1_11113,298,302 - 13,407,784 (+)NCBICHM1_1
T2T-CHM13v2.01113,369,378 - 13,480,010 (+)NCBIT2T-CHM13v2.0
Bmal1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397112,777,820 - 112,913,333 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7112,806,672 - 112,913,333 (+)EnsemblGRCm39 Ensembl
GRCm387113,178,471 - 113,314,126 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7113,207,465 - 113,314,126 (+)EnsemblGRCm38mm10GRCm38
MGSCv377120,350,979 - 120,457,636 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367112,998,646 - 113,105,303 (+)NCBIMGSCv36mm8
Celera7113,186,397 - 113,287,835 (+)NCBICelera
Cytogenetic Map7F1NCBI
cM Map759.17NCBI
Bmal1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81176,766,222 - 176,864,741 (+)NCBIGRCr8
mRatBN7.21167,331,756 - 167,430,235 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1167,331,633 - 167,430,231 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1175,666,810 - 175,765,622 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01182,852,900 - 182,951,712 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01175,548,108 - 175,646,871 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01178,039,002 - 178,137,469 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1178,039,063 - 178,137,465 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01185,007,527 - 185,105,413 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41171,062,181 - 171,162,426 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11171,251,951 - 171,282,040 (+)NCBI
Celera1165,202,275 - 165,299,946 (+)NCBICelera
Cytogenetic Map1q33NCBI
Bmal1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541428,684,226 - 28,748,360 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541428,652,663 - 28,748,360 (+)NCBIChiLan1.0ChiLan1.0
BMAL1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2915,716,032 - 15,825,471 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11115,678,367 - 15,788,400 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01113,436,580 - 13,547,135 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11113,163,028 - 13,240,376 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1113,163,028 - 13,240,376 (+)Ensemblpanpan1.1panPan2
ARNTL
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12136,254,235 - 36,323,915 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2136,290,070 - 36,323,622 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2135,726,263 - 35,827,668 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02137,105,577 - 37,207,038 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2137,105,604 - 37,207,069 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12136,364,101 - 36,465,527 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02136,540,532 - 36,641,924 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02136,829,310 - 36,930,753 (+)NCBIUU_Cfam_GSD_1.0
Bmal1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494749,133,675 - 49,231,340 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365285,164,481 - 5,239,128 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365285,167,611 - 5,239,128 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ARNTL
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl245,895,289 - 45,988,570 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1245,895,637 - 46,025,174 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2249,303,279 - 49,335,397 (-)NCBISscrofa10.2Sscrofa10.2susScr3
BMAL1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1151,430,670 - 51,540,344 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl151,431,180 - 51,462,674 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038149,016,016 - 149,124,776 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Bmal1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247665,317,635 - 5,391,645 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247665,295,120 - 5,391,645 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in BMAL1
62 total Variants

1 to 10 of 57 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13
pathogenic
NM_001030272.2(ARNTL):c.180-132C>T single nucleotide variant Malignant melanoma [RCV000069258] Chr11:13356923 [GRCh38]
Chr11:13378470 [GRCh37]
Chr11:13335046 [NCBI36]
Chr11:11p15.3
not provided
NM_001030272.2(ARNTL):c.-134-6526C>T single nucleotide variant Lung cancer [RCV000109850] Chr11:13343419 [GRCh38]
Chr11:13364966 [GRCh37]
Chr11:11p15.3
uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3
pathogenic
GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3 copy number gain See cases [RCV000133997] Chr11:446754..18904742 [GRCh38]
Chr11:446754..18926289 [GRCh37]
Chr11:436754..18882865 [NCBI36]
Chr11:11p15.5-15.1
pathogenic
GRCh38/hg38 11p15.4-15.2(chr11:9989516-16825806)x1 copy number loss See cases [RCV000136773] Chr11:9989516..16825806 [GRCh38]
Chr11:10011063..16847353 [GRCh37]
Chr11:9967639..16803929 [NCBI36]
Chr11:11p15.4-15.2
pathogenic
NM_001297719.2(BMAL1):c.18G>C (p.Met6Ile) single nucleotide variant Premature ovarian failure [RCV001270219] Chr11:13354326 [GRCh38]
Chr11:13375873 [GRCh37]
Chr11:11p15.3
uncertain significance
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
1 to 10 of 57 rows

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR142hsa-miR-142-3pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCRFunctional MTI21799909
MIR142hsa-miR-142-3pMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI22958478
MIR142hsa-miR-142-3pMirtarbaseexternal_infoMicroarrayFunctional MTI (Weak)17612493
MIR494hsa-miR-494-3pMirtarbaseexternal_infoLuciferase reporter assay//qRT-PCRFunctional MTI21799909
MIR155hsa-miR-155-5pMirtarbaseexternal_infoProteomicsFunctional MTI (Weak)20584899

Predicted Target Of
Summary Value
Count of predictions:4914
Count of miRNA genes:1096
Interacting mature miRNAs:1371
Transcripts:ENST00000361003, ENST00000389707, ENST00000389708, ENST00000396441, ENST00000401424, ENST00000403290, ENST00000403482, ENST00000403510, ENST00000472842, ENST00000480685, ENST00000482049, ENST00000485918, ENST00000497429, ENST00000524392, ENST00000527998, ENST00000529050, ENST00000529388, ENST00000529390, ENST00000529825, ENST00000530357, ENST00000531665, ENST00000533520, ENST00000534102, ENST00000534544
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 140 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
407055938GWAS704914_Hhematocrit QTL GWAS704914 (human)4e-17hematocrithematocrit (CMO:0000037)111331437913314380Human
597031570GWAS1127644_Hprogesterone measurement QTL GWAS1127644 (human)2e-08progesterone measurement111334173213341733Human
597146012GWAS1242086_Hosteoarthritis, knee QTL GWAS1242086 (human)8e-12osteoarthritis, knee111330743213307433Human
597336727GWAS1432801_HC-reactive protein measurement QTL GWAS1432801 (human)2e-39C-reactive protein measurementblood C-reactive protein level (CMO:0003160)111333997713339978Human
597086616GWAS1182690_Htype 2 diabetes mellitus QTL GWAS1182690 (human)1e-09type 2 diabetes mellitus111331916313319164Human
407001933GWAS650909_Hage at menarche QTL GWAS650909 (human)7e-20age at menarche111329389213293893Human
597155975GWAS1252049_Hsex hormone-binding globulin measurement QTL GWAS1252049 (human)2e-12sex hormone-binding globulin measurement111333945813339459Human
597035655GWAS1131729_Htriglyceride measurement QTL GWAS1131729 (human)3e-20triglyceride measurementblood triglyceride level (CMO:0000118)111333997713339978Human
597148547GWAS1244621_Heducational attainment QTL GWAS1244621 (human)0.0000004educational attainment111330759213307593Human
597148546GWAS1244620_Heducational attainment QTL GWAS1244620 (human)3e-08educational attainment111328238213282383Human

1 to 10 of 140 rows
D6S1560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37633,554,695 - 33,554,928UniSTSGRCh37
Build 36633,662,673 - 33,662,906RGDNCBI36
Celera635,109,074 - 35,109,307RGD
HuRef633,296,158 - 33,296,391UniSTS
HuRef1113,045,939 - 13,046,452UniSTS
HuRef11121,219,431 - 121,219,625UniSTS
Marshfield Genetic Map647.71RGD
Genethon Genetic Map647.6UniSTS
deCODE Assembly Map652.75UniSTS
Whitehead-YAC Contig Map6 UniSTS
D11S1794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371113,335,758 - 13,336,010UniSTSGRCh37
Build 361113,292,334 - 13,292,586RGDNCBI36
Celera1113,461,906 - 13,462,158RGD
Cytogenetic Map11p15UniSTS
HuRef1113,015,902 - 13,016,154UniSTS
Marshfield Genetic Map1119.86RGD
Marshfield Genetic Map1119.86UniSTS
Genethon Genetic Map1122.3UniSTS
TNG Radiation Hybrid Map116444.0UniSTS
deCODE Assembly Map1122.28UniSTS
Whitehead-YAC Contig Map11 UniSTS
RH119816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371113,399,099 - 13,399,232UniSTSGRCh37
Build 361113,355,675 - 13,355,808RGDNCBI36
Celera1113,525,277 - 13,525,410RGD
Cytogenetic Map11p15UniSTS
HuRef1113,079,283 - 13,079,416UniSTS
TNG Radiation Hybrid Map116470.0UniSTS
D11S4441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371113,360,410 - 13,360,605UniSTSGRCh37
Build 361113,316,986 - 13,317,181RGDNCBI36
Celera1113,486,581 - 13,486,776RGD
Cytogenetic Map11p15UniSTS
HuRef1113,040,578 - 13,040,773UniSTS
RH78096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371113,406,551 - 13,406,689UniSTSGRCh37
Build 361113,363,127 - 13,363,265RGDNCBI36
Celera1113,532,733 - 13,532,871RGD
Cytogenetic Map11p15UniSTS
HuRef1113,086,739 - 13,086,877UniSTS
GeneMap99-GB4 RH Map1156.65UniSTS
NCBI RH Map1163.0UniSTS
ARNTL_1824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371113,408,153 - 13,408,882UniSTSGRCh37
Build 361113,364,729 - 13,365,458RGDNCBI36
Celera1113,534,337 - 13,535,066RGD
HuRef1113,088,343 - 13,089,072UniSTS
WI-14129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371113,406,353 - 13,406,502UniSTSGRCh37
Build 361113,362,929 - 13,363,078RGDNCBI36
Celera1113,532,535 - 13,532,684RGD
Cytogenetic Map11p15UniSTS
HuRef1113,086,541 - 13,086,690UniSTS
GeneMap99-GB4 RH Map1152.99UniSTS
Whitehead-RH Map1150.6UniSTS
NCBI RH Map1160.7UniSTS
MARC_12777-12778:999891099:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371113,407,282 - 13,408,252UniSTSGRCh37
Celera1113,533,464 - 13,534,436UniSTS
HuRef1113,087,470 - 13,088,442UniSTS




adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2248 4973 1726 2351 6 624 1924 465 2269 7284 6450 53 3734 1 852 1744 1617 175 1


1 to 30 of 92 rows
RefSeq Transcripts NM_001030272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001030273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001297719 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001297722 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001297724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147785 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147787 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 30 of 92 rows

Ensembl Acc Id: ENST00000389707   ⟹   ENSP00000374357
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,798 - 13,387,266 (+)Ensembl
Ensembl Acc Id: ENST00000401424   ⟹   ENSP00000385915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,778 - 13,387,261 (+)Ensembl
Ensembl Acc Id: ENST00000403290   ⟹   ENSP00000384517
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,790 - 13,387,266 (+)Ensembl
Ensembl Acc Id: ENST00000403482   ⟹   ENSP00000385897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,356,878 - 13,387,266 (+)Ensembl
Ensembl Acc Id: ENST00000403510   ⟹   ENSP00000385581
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,790 - 13,387,262 (+)Ensembl
Ensembl Acc Id: ENST00000472842
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,375,679 - 13,387,263 (+)Ensembl
Ensembl Acc Id: ENST00000480685
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,829 - 13,356,929 (+)Ensembl
Ensembl Acc Id: ENST00000482049   ⟹   ENSP00000436721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,885 - 13,358,558 (+)Ensembl
Ensembl Acc Id: ENST00000485918
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,349,945 - 13,354,631 (+)Ensembl
Ensembl Acc Id: ENST00000497429
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,358,434 - 13,372,409 (+)Ensembl
Ensembl Acc Id: ENST00000524392   ⟹   ENSP00000436442
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,374,093 - 13,387,266 (+)Ensembl
Ensembl Acc Id: ENST00000527998   ⟹   ENSP00000433540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,639 - 13,358,440 (+)Ensembl
Ensembl Acc Id: ENST00000529050   ⟹   ENSP00000434044
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,276,652 - 13,354,377 (+)Ensembl
Ensembl Acc Id: ENST00000529388   ⟹   ENSP00000433571
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,752 - 13,387,263 (+)Ensembl
Ensembl Acc Id: ENST00000529390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,372,209 - 13,376,771 (+)Ensembl
Ensembl Acc Id: ENST00000529825   ⟹   ENSP00000434263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,794 - 13,358,481 (+)Ensembl
Ensembl Acc Id: ENST00000530357   ⟹   ENSP00000436313
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,815 - 13,365,592 (+)Ensembl
Ensembl Acc Id: ENST00000531665   ⟹   ENSP00000434781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,309,986 - 13,357,096 (+)Ensembl
Ensembl Acc Id: ENST00000533520   ⟹   ENSP00000431488
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,793 - 13,358,514 (+)Ensembl
Ensembl Acc Id: ENST00000534102
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,365,416 - 13,369,740 (+)Ensembl
Ensembl Acc Id: ENST00000534544   ⟹   ENSP00000431566
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,276,652 - 13,356,777 (+)Ensembl
Ensembl Acc Id: ENST00000673626   ⟹   ENSP00000500988
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,829 - 13,387,261 (+)Ensembl
Ensembl Acc Id: ENST00000673817   ⟹   ENSP00000501212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,830 - 13,387,262 (+)Ensembl
Ensembl Acc Id: ENST00000673834   ⟹   ENSP00000500983
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,829 - 13,387,180 (+)Ensembl
Ensembl Acc Id: ENST00000673868   ⟹   ENSP00000500968
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,360,348 - 13,387,261 (+)Ensembl
Ensembl Acc Id: ENST00000673888   ⟹   ENSP00000501059
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,878 - 13,387,262 (+)Ensembl
Ensembl Acc Id: ENST00000673892   ⟹   ENSP00000501106
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,842 - 13,387,263 (+)Ensembl
Ensembl Acc Id: ENST00000674108   ⟹   ENSP00000501035
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1113,277,798 - 13,387,266 (+)Ensembl
RefSeq Acc Id: NM_001030272   ⟹   NP_001025443
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
GRCh371113,299,325 - 13,408,813 (+)ENTREZGENE
Build 361113,255,901 - 13,365,389 (+)NCBI Archive
HuRef1112,979,421 - 13,089,003 (+)ENTREZGENE
CHM1_11113,298,251 - 13,407,784 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001030273   ⟹   NP_001025444
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
GRCh371113,299,325 - 13,408,813 (+)ENTREZGENE
Build 361113,255,901 - 13,365,389 (+)NCBI Archive
HuRef1112,979,421 - 13,089,003 (+)ENTREZGENE
CHM1_11113,298,251 - 13,407,784 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001178   ⟹   NP_001169
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
GRCh371113,299,325 - 13,408,813 (+)ENTREZGENE
Build 361113,255,901 - 13,365,389 (+)NCBI Archive
HuRef1112,979,421 - 13,089,003 (+)ENTREZGENE
CHM1_11113,298,251 - 13,407,784 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001297719   ⟹   NP_001284648
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
CHM1_11113,298,251 - 13,407,784 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001297722   ⟹   NP_001284651
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
CHM1_11113,298,251 - 13,407,784 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001297724   ⟹   NP_001284653
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
CHM1_11113,298,251 - 13,407,784 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351804   ⟹   NP_001338733
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,276,652 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,369,378 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351805   ⟹   NP_001338734
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351806   ⟹   NP_001338735
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351807   ⟹   NP_001338736
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351808   ⟹   NP_001338737
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351809   ⟹   NP_001338738
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351810   ⟹   NP_001338739
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351811   ⟹   NP_001338740
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351812   ⟹   NP_001338741
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351813   ⟹   NP_001338742
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351814   ⟹   NP_001338743
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351815   ⟹   NP_001338744
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351816   ⟹   NP_001338745
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351817   ⟹   NP_001338746
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351818   ⟹   NP_001338747
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351819   ⟹   NP_001338748
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351820   ⟹   NP_001338749
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351821   ⟹   NP_001338750
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351822   ⟹   NP_001338751
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351823   ⟹   NP_001338752
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001351824   ⟹   NP_001338753
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NR_147785
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NR_147786
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NR_147787
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NR_147788
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NR_147789
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NR_147790
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: NR_147791
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520105   ⟹   XP_011518407
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,276,652 - 13,387,266 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520107   ⟹   XP_011518409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,276,652 - 13,387,266 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011520109   ⟹   XP_011518411
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017017738   ⟹   XP_016873227
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,276,652 - 13,387,266 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017017739   ⟹   XP_016873228
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,276,652 - 13,387,266 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017017741   ⟹   XP_016873230
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024448522   ⟹   XP_024304290
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,354,530 - 13,387,266 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047426952   ⟹   XP_047282908
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
RefSeq Acc Id: XM_047426953   ⟹   XP_047282909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
RefSeq Acc Id: XM_047426954   ⟹   XP_047282910
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
RefSeq Acc Id: XM_047426955   ⟹   XP_047282911
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,387,266 (+)NCBI
RefSeq Acc Id: XM_047426956   ⟹   XP_047282912
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,318,572 - 13,387,266 (+)NCBI
RefSeq Acc Id: XM_047426957   ⟹   XP_047282913
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,276,652 - 13,381,245 (+)NCBI
RefSeq Acc Id: XM_047426958   ⟹   XP_047282914
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,276,652 - 13,369,756 (+)NCBI
RefSeq Acc Id: XM_054368794   ⟹   XP_054224769
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,369,378 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368795   ⟹   XP_054224770
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,369,378 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368796   ⟹   XP_054224771
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,369,378 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368797   ⟹   XP_054224772
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,369,378 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368798   ⟹   XP_054224773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368799   ⟹   XP_054224774
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368800   ⟹   XP_054224775
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368801   ⟹   XP_054224776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368802   ⟹   XP_054224777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368803   ⟹   XP_054224778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,370,517 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368804   ⟹   XP_054224779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,447,294 - 13,480,010 (+)NCBI
RefSeq Acc Id: XM_054368805   ⟹   XP_054224780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,369,378 - 13,471,166 (+)NCBI
RefSeq Acc Id: XM_054368806   ⟹   XP_054224781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01113,369,378 - 13,462,499 (+)NCBI
1 to 30 of 97 rows
Protein RefSeqs NP_001025443 (Get FASTA)   NCBI Sequence Viewer  
  NP_001025444 (Get FASTA)   NCBI Sequence Viewer  
  NP_001169 (Get FASTA)   NCBI Sequence Viewer  
  NP_001284648 (Get FASTA)   NCBI Sequence Viewer  
  NP_001284651 (Get FASTA)   NCBI Sequence Viewer  
  NP_001284653 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338733 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338734 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338735 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338736 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338737 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338738 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338739 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338740 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338741 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338742 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338743 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338744 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338745 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338746 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338747 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338748 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338749 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338750 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338751 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338752 (Get FASTA)   NCBI Sequence Viewer  
  NP_001338753 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518407 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518409 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518411 (Get FASTA)   NCBI Sequence Viewer  
1 to 30 of 97 rows
1 to 5 of 76 rows
1 to 5 of 76 rows
RefSeq Acc Id: NP_001169   ⟸   NM_001178
- Peptide Label: isoform a
- UniProtKB: A0A140VKD3 (UniProtKB/TrEMBL),   B2RCL8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001025444   ⟸   NM_001030273
- Peptide Label: isoform b
- UniProtKB: B2RCL8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001025443   ⟸   NM_001030272
- Peptide Label: isoform a
- UniProtKB: A0A140VKD3 (UniProtKB/TrEMBL),   B2RCL8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001284648   ⟸   NM_001297719
- Peptide Label: isoform c
- UniProtKB: Q99631 (UniProtKB/Swiss-Prot),   Q8IUT4 (UniProtKB/Swiss-Prot),   Q4G136 (UniProtKB/Swiss-Prot),   O00317 (UniProtKB/Swiss-Prot),   O00316 (UniProtKB/Swiss-Prot),   O00315 (UniProtKB/Swiss-Prot),   O00314 (UniProtKB/Swiss-Prot),   O00313 (UniProtKB/Swiss-Prot),   D3DQW6 (UniProtKB/Swiss-Prot),   B7WPG7 (UniProtKB/Swiss-Prot),   B5ME11 (UniProtKB/Swiss-Prot),   A8K645 (UniProtKB/Swiss-Prot),   A2I2N6 (UniProtKB/Swiss-Prot),   Q99649 (UniProtKB/Swiss-Prot),   O00327 (UniProtKB/Swiss-Prot),   B2RCL8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001284653   ⟸   NM_001297724
- Peptide Label: isoform d
- UniProtKB: B2RCL8 (UniProtKB/TrEMBL)
- Sequence:
bHLH   PAC   PAS

Name Modeler Protein Id AA Range Protein Structure
AF-O00327-F1-model_v2 AlphaFold O00327 1-626 view protein structure

RGD ID:6789136
Promoter ID:HG_KWN:12357
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:ENST00000361003,   ENST00000389708,   ENST00000396441,   NM_001030272,   NM_001030273,   OTTHUMT00000319170,   OTTHUMT00000319177,   OTTHUMT00000319178,   OTTHUMT00000319179,   UC001MKR.1,   UC001MKS.1,   UC001MKT.1,   UC001MKU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361113,255,456 - 13,256,152 (+)MPROMDB
RGD ID:7219695
Promoter ID:EPDNEW_H15594
Type:initiation region
Name:ARNTL_1
Description:aryl hydrocarbon receptor nuclear translocator like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381113,277,790 - 13,277,850EPDNEW


1 to 40 of 90 rows
Database
Acc Id
Source(s)
COSMIC BMAL1 COSMIC
Ensembl Genes ENSG00000133794 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000389707 ENTREZGENE
  ENST00000389707.8 UniProtKB/Swiss-Prot
  ENST00000401424 ENTREZGENE
  ENST00000401424.6 UniProtKB/Swiss-Prot
  ENST00000403290 ENTREZGENE
  ENST00000403290.6 UniProtKB/Swiss-Prot
  ENST00000403482 ENTREZGENE
  ENST00000403482.7 UniProtKB/Swiss-Prot
  ENST00000403510 ENTREZGENE
  ENST00000403510.8 UniProtKB/Swiss-Prot
  ENST00000529388 ENTREZGENE
  ENST00000529388.6 UniProtKB/Swiss-Prot
  ENST00000673626 ENTREZGENE
  ENST00000673817 ENTREZGENE
  ENST00000673892 ENTREZGENE
Gene3D-CATH 4.10.280.10 UniProtKB/Swiss-Prot
  PAS domain UniProtKB/Swiss-Prot
GTEx ENSG00000133794 GTEx
HGNC ID HGNC:701 ENTREZGENE
Human Proteome Map BMAL1 Human Proteome Map
InterPro bHLH_dom UniProtKB/Swiss-Prot
  Circadian_TF UniProtKB/Swiss-Prot
  HLH_DNA-bd_sf UniProtKB/Swiss-Prot
  Nuc_translocat UniProtKB/Swiss-Prot
  PAC UniProtKB/Swiss-Prot
  PAS UniProtKB/Swiss-Prot
  PAS-like_dom_sf UniProtKB/Swiss-Prot
  PAS_fold UniProtKB/Swiss-Prot
KEGG Report hsa:406 UniProtKB/Swiss-Prot
NCBI Gene 406 ENTREZGENE
OMIM 602550 OMIM
PANTHER CIRCADIAN PROTEIN CLOCK/ARNT/BMAL/PAS UniProtKB/Swiss-Prot
Pfam HLH UniProtKB/Swiss-Prot
  PAS UniProtKB/Swiss-Prot
  PAS_11 UniProtKB/Swiss-Prot
PharmGKB PA24996 PharmGKB
PRINTS NCTRNSLOCATR UniProtKB/Swiss-Prot
PROSITE BHLH UniProtKB/Swiss-Prot
1 to 40 of 90 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2022-07-25 BMAL1  basic helix-loop-helix ARNT like 1  ARNTL  aryl hydrocarbon receptor nuclear translocator like  Symbol and/or name change 19259463 PROVISIONAL
2015-12-01 ARNTL  aryl hydrocarbon receptor nuclear translocator like  ARNTL  aryl hydrocarbon receptor nuclear translocator-like  Symbol and/or name change 5135510 APPROVED