8q23.3-q24.3CNV Type: Duplication
Largest CNV size: 31589017 bp
Statistics Box:
Number of Reports: 4
Number of Reports: 4
Summary Information
Rare singleton duplication within this region was found in a case from a study of 15,749 individuals from the International Standards for Cytogenomic Arrays (ISCA) consortium with unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome (Kaminsky et al., 2011).
Additional Locus Information
References
Major Reports
Title
Author, Year
Report Class
CNV Type
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Duplication
Minor Reports
Title
Author, Year
Report Class
CNV Type
Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch Caribbean
Duplication
Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort
Duplication
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
akter_24_ASD/ADHD/DD/ID_discovery_cases
Individuals clinically diagnosed with one or more neurodevelopmental disorders (NDDs) by neurologists from July 2019 to December 2022 from multiple tertiary hospitals across Bangladesh.
576
Cases presented with one or more neurodevelopmental disorders; specific diagnoses of ASD, ADHD, and intellectual disability were made by clinical specialists and complemented by formal assessments, such as ADOS-2 and DSM-5, where appropriate.
98.26% under 18 years of age
67.71% Male
30623748
0
1
1
kaminsky_11_DD/ID/ASD_discovery_cases
Cases from the International Standards for Cytogenomic Arrays (ISCA) consortium
15749
Unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome
NA
NA
31589017
0
1
1
streata_22_ASD/DD/ID_discovery_cases
Patients evaluated for global developmental delay and/or intellectual disability in pediatric, child neurology, or medical genetics departments throughout Romania who were referred to the Regional Centre for Medical Genetics for genetic testing between 2015 and 2022.
371
All cases presented with global developmental delay (DD) and/or intellectual disability (ID); a subset of cases also presented with autism spectrum disorder (ASD).
Range, 6 mos.-40 yrs. (median age, 5.5 yrs.)
63.07% Male
29064281
0
1
1
verberne_22_ASD/DD/ID_discovery_cases
Patients in the Dutch Caribbean referred to a visiting Dutch clinical geneticist between November 2011 and November 2019 by local pediatricians for a clinical genetic evaluation at the outpatient pediatric clinics of the Curacao Medical Center, Dr. Horacio E. Oduber Hospital (Aruba), Fundashon Mariadal (Bonaire), and St. Maarten Medical Center.
331
Common reasons for referral included developmental delay (DD) and/or intellectual disability (ID) (39%), with or without other anomalies, and congenital anomalies (24%); a subset of individuals also presented with autism spectrum disorder (ASD) and/or seizures.
Range, 0-18.7 yrs. (median age 3.95 yrs.)
NA
30759425
0
1
1
Controls
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
kaminsky_11_DD/ID/ASD_discovery_controls
Controls from the International Standards for Cytogenomic Arrays (ISCA) consortium
10118
Controls
NA
NA
NA
NA
NA
NA
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
akter_24_ASD/ADHD/DD/ID_discovery_cases
Bangladesh
CMA
Illumina Global Screening Array-24+ v3.0
Illumina CNVPartition 3.2.1 plug-in of GenomeStudio
kaminsky_11_DD/ID/ASD_discovery_cases
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
FISH, qPCR, MLPA, aCGH, standard G-banded chromosome analysis
streata_22_ASD/DD/ID_discovery_cases
Romania
aCGH
Agilent SurePrint G3 ISCA v.2 8x60K, Agilent 4x180K, OGT CytoSure ISCA v.2 8x60K
NA
Agilent CytoGenomics, OGT CytoSure Interpret
CMA, karyotyping, and/or MLPA
verberne_22_ASD/DD/ID_discovery_cases
Dutch Caribbean
CMA
NA
NA
NA
None
Controls
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
kaminsky_11_DD/ID/ASD_discovery_controls
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
Cases
Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
akter_24_ASD/ADHD/DD/ID_discovery_cases-case48
9.7 yrs.
F
Developmental delay and seizures
Developmental milestones: delayed speech and language development (HP:0000750). Motor and musculoskeletal evaluation: spasticity (HP:0001257). Behavioral/psychiatric evaluation: atypical behavior (HP:0000708). Epilepsy/seizures: seizure (HP:0001250). Growth parameters: head circumference 47 cm, height 113 cm, weight 20.5 kg.
114429340
145053087
30623748
GRCh38
Duplication
No
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000257
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
113580402
145054634
31474233
GRCh38
Duplication
Yes
streata_22_ASD/DD/ID_discovery_cases-case328
NA
M
Developmental delay and intellectual disability
Global developmental delay, speech and/or language delay or impairment, facial dysmorphism.
Mild/moderate intellectual disability
115990501
145054781
29064281
GRCh38
Duplication
Yes
verberne_22_ASD/DD/ID_discovery_cases-case129
NA
M
Agenesis of the corpus callosum, hypotonia, facial dysmorphism
114308604
145068028
30759425
GRCh38
Duplication
No
Controls
No Control Data Available
Cases
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
akter_24_ASD/ADHD/DD/ID_discovery_cases-case48
Unknown
ADGRB1,ANXA13,ADCY8,CYP11B2,EEF1D,EXT1,CYP11B1,CYC1,AGO2,MTBP,OPLAH,PHF20L1,CPSF1,VPS28,HGH1,ATAD2,THEM6,CYHR1,ASAP1,COMMD5,FAM135B,CYRIB,MRPL13,KCNK9,CHRAC1,LY6K,EXOSC4,TRMT12,SLC39A4,NTAQ1,GSDMC,ZNF250,SLURP1,SLC45A4,ZFAT,C8orf33,LYNX1,PYCR3,SLC52A2,DEPTOR,DERL1,GSDMD,DSCC1,ZNF696,RHPN1-AS1,SCRT1,UTP23,MAF1,TRAPPC9,TATDN1,ZNF34,EPPK1,MAPRE1P1,ARHGAP39,SHARPIN,NAPRT,TIGD5,C8orf76,HPYR1,TBC1D31,FAM83A,ZNF251,KIFC2,PARP10,MED30,PPP1R16A,MFSD3,FBXO32,MAL2,TOP1MT,RHPN1,LYPD2,ZNF572,TMEM71,CCDC26,FAM91A1,ST13P6,LINC00964,TSNARE1,ADCK5,FER1L6-AS2,TMEM65,LRATD2,COL22A1,SLC30A8,HAS2,GLI4,GRINA,HSF1,GPR20,GML,GPT,MAPK15,TMEM249,LINC01591,ZNF252P,FAM83H,GPIHBP1,NSMCE2,ZNF517,WDR97,NRBP2,LINC02878,ZNF252P-AS1,KLHL38,TMED10P1,LINC02904,ZFP41,ZNF707,PEG13,MRPS36P3,SPATC1,CYCSP23,SMPD5,CDK5P1,IMPDH1P6,RPL32P20,MAFA,MROH5,C8orf82,LRRC24,FER1L6-AS1,AARD,SAMD12,SLURP2,MIR30B,MIR30D,RPS26P35,ZFAT-AS1,MIR151A,SCX,IQANK1,SAMD12-AS1,MROH6,LINC00051,ARF1P3,HAS2-AS1,LINC02912,TSSK5P,RPL23AP56,RAD21-AS1,CASC8,MROH1,MIR661,MIR548D1,FER1L6,MIR937,LINC01300,OC90,MIR939,CDC42P3,MTRF1LP2,LINC00861,KNOP1P5,CCDC166,MRS2P1,LY6E,KCNQ3,LY6H,TONSL,CCN3,MYC,NDUFB9,TNFRSF11B,LY6E-DT,FAM83A-AS1,UBA52P5,CASC11,RPS10P16,ZNHIT1P1,RPL35AP19,LNCOC1,TONSL-AS1,AK3P2,PTCSC1,MIR1207,MIR1208,MIR1204,MIR1234,MIR1302-7,MIR1205,MIR1206,HMGB1P19,RFPL4AP5,NCAPGP1,HNRNPA1P38,MIR3610,MIR548AA1,MIR3686,MIR4662B,ZHX1-C8orf76,MIR4663,MIR4664,C8orf17,MIR4472-1,MIR4662A,ASAP1-IT2,MINCR,LINC00536,RNA5SP277,RNA5SP276,RNA5SP278,MTND2P7,MIR5194,PCAT1,DUTP2,CCAT2,SOD1P3,MROH4P,DENND3-AS1,RNF139-DT,LINC00824,PRNCR1,ENPP2,RAD21,RPL8,PLEC,POU5F1B,PVT1,PTK2,LY6L,MIR6844,MIR6845,MIR6847,MIR6848,MIR7112,MIR6893,MIR548AZ,MIR6850,MIR6846,MIR7848,MIR6849,ERICD,CASC19,MAFA-AS1,LINC01151,LINC02855,MAL2-AS1,SMILR,SQLE-DT,RN7SKP206,RN7SKP175,WASHC5-AS1,RNU7-181P,RN7SL329P,RN7SL396P,RN7SKP155,SLA,GFUS,TAF2,COL14A1,TG,SNTB1,TRPS1,ST3GAL1,SQLE,ZYXP1,RNU6-875P,RNU6-442P,RNU1-35P,RNU6-628P,RNU6-756P,RN7SL826P,RN7SKP226,RN7SL395P,RN7SL228P,RNU6-144P,RNU6-869P,RN7SL260P,RNU6-220P,RNU11-4P,RNU6-1255P,RN7SKP153,RNVU1-32,RNU6-12P,MTCO1P49,RNU4-25P,CARS1P2,LINC02055,LYNX1-SLURP2,CCN4,EIF3H,ZNF16,ZNF7,LY6D,GPAA1,PSCA,JRK,FOXH1,DGAT1,ST3GAL1-DT,TRIB1,ZNF623,WASHC5,LRRC14,MTSS1,HHLA1,RECQL4,ZHX2,ZHX1,PTP4A3,RNF139,NDRG1,DENND3,PUF60,KHDRBS3,COLEC10,BOP1,EFR3A,DNAAF11,ZC3H3,ARC,FBXL6,SCRIB
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000257
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
De novo
Unknown
Unknown
CARSP2,RNA5SP276,RAD21-AS1,MIR3610,AARD,RN7SL228P,RN7SL826P,RPS10P16,RPS26P35,RNU6-12P,MIR548AZ,CYCSP23,RN7SKP153,RN7SL396P,RNA5SP277,NCAPGP1,RPL35AP19,MRPS36P3,CDK5P1,HMGB1P19,FAM83A-AS1,MIR4663,UBA52P5,RNU6-628P,RNU6-875P,MIR548AA1,MIR548D1,DUTP2,IMPDH1P6,RN7SKP155,ARF1P3,RNU6-756P,MIR6844,MIR4662B,MIR4662A,RN7SL329P,RNU6-442P,SOD1P3,KNOP1P5,RFPL4AP5,RNU6-869P,FAM84B,RNU11-4P,MYC,MIR1204,TMEM75,MIR1205,RNU1-106P,MIR1206,RNU4-25P,MIR1207,MIR1208,RN7SKP226,RN7SKP206,MIR3686,MTRF1LP2,RNU7-181P,MIR5194,RNU6-1255P,ASAP1-IT2,MIR7848,ST13P6,MTND2P7,MTCO1P49,ZFAT-AS1,MIR30B,MIR30D,RPL23AP56,MAPRE1P1,RNU1-35P,RNU6-144P,ZYXP1,C8orf17,CHRAC1,ERICD,MIR151A,RNA5SP278,LINC01300,MIR1302-7,MIR4472-1,LINC00051,RN7SL260P,ARC,THEM6,SLURP1,LYPD2,SLURP2,LYNX1,ZNHIT1P1,CYP11B1,CDC42P3,LY6E,AK3P2,LY6H,GPIHBP1,GLI4,MINCR,RNU6-220P,RHPN1-AS1,MAFA-AS1,RN7SKP175,MROH6,NAPRT,TIGD5,TSTA3,BREA2,CCDC166,FAM83H,MIR4664,MIR937,MIR6845,MIR661,GRINA,SMPD5,OPLAH,MIR6846,EXOSC4,MIR6847,GPAA1,SHARPIN,MAF1,HGH1,TSSK5P,MIR7112,SCX,MIR6848,SCRT1,TMEM249,FBXL6,MIR939,MIR1234,MIR6849,SLC39A4,MIR6893,TONSL-AS1,MFSD3,RECQL4,C8orf82,RPL8,MIR6850,TMED10P1,ZNF252P-AS1,RAD21,MED30,TNFRSF11B,MAL2,MAL2-AS1,DSCC1,MRPL13,DERL1,C8orf76,ZHX1-C8orf76,ZHX1,FBXO32,KLHL38,FAM91A1,TMEM65,TRMT12,RNF139-AS1,RNF139,NDUFB9,ZNF572,SQLE,LINC00861,PRNCR1,CASC11,OC90,HHLA1,TMEM71,NCRNA00250,KCNK9,PEG13,AGO2,GPR20,MROH5,HNRNPA1P38,MROH4P,JRK,PSCA,LY6K,LNCOC1,LYNX1-SLURP2,LY6D,CYP11B2,C8orf31,LY6L,ZNF696,TOP1MT,RHPN1,MAFA,GSDMD,EEF1D,PYCR3,ZNF707,MAPK15,SCRIB,PUF60,NRBP2,EPPK1,PARP10,SPATC1,CYC1,WDR97,BOP1,DGAT1,SLC52A2,ADCK5,CPSF1,VPS28,CYHR1,KIFC2,FOXH1,PPP1R16A,GPT,LRRC14,LRRC24,ZNF251,ZNF34,RN7SL395P,ZNF517,COMMD5,ZNF250,ZNF16,ZNF252P,C8orf33,TRPS1,LINC00536,EIF3H,UTP23,SLC30A8,EXT1,SAMD12-AS1,COLEC10,ENPP2,TAF2,DEPTOR,COL14A1,MTBP,HAS2-AS1,SMILR,ZHX2,TBC1D31,FAM83A,ATAD2,WDYHV1,FER1L6,FER1L6-AS1,FER1L6-AS2,TATDN1,MTSS1,LINC00964,WASHC5,WASHC5-AS1,NSMCE2,TRIB1,CASC19,CASC8,POU5F1B,CCAT2,LINC00824,GSDMC,FAM49B,ASAP1,ADCY8,EFR3A,KCNQ3,HPYR1,LRRC6,PHF20L1,TG,SLA,NDRG1,ST3GAL1,ZFAT,KHDRBS3,COL22A1,TRAPPC9,PTK2,DENND3,SLC45A4,PTP4A3,TSNARE1,ADGRB1,GML,LY6E-DT,ZFP41,ZC3H3,IQANK1,PLEC,MROH1,HSF1,TONSL,ARHGAP39,ZNF7,SAMD12,SNTB1,HAS2,LINC01151,ANXA13,PCAT1,PVT1,CCDC26,LINC01591,LINC02055,FAM135B,ZNF623
streata_22_ASD/DD/ID_discovery_cases-case328
CMA, karyotyping, and/or MLPA
De novo
ADGRB1,ANXA13,ADCY8,CYP11B2,EEF1D,EXT1,CYP11B1,CYC1,AGO2,MTBP,OPLAH,PHF20L1,CPSF1,VPS28,HGH1,ATAD2,THEM6,CYHR1,ASAP1,COMMD5,FAM135B,CYRIB,MRPL13,KCNK9,CHRAC1,LY6K,EXOSC4,TRMT12,SLC39A4,NTAQ1,GSDMC,ZNF250,SLURP1,SLC45A4,ZFAT,C8orf33,LYNX1,PYCR3,SLC52A2,DEPTOR,DERL1,GSDMD,DSCC1,ZNF696,RHPN1-AS1,SCRT1,UTP23,MAF1,TRAPPC9,TATDN1,ZNF34,EPPK1,MAPRE1P1,ARHGAP39,SHARPIN,NAPRT,TIGD5,C8orf76,HPYR1,TBC1D31,FAM83A,ZNF251,KIFC2,PARP10,MED30,PPP1R16A,MFSD3,FBXO32,MAL2,TOP1MT,RHPN1,LYPD2,ZNF572,TMEM71,CCDC26,FAM91A1,ST13P6,LINC00964,TSNARE1,ADCK5,FER1L6-AS2,TMEM65,LRATD2,COL22A1,SLC30A8,HAS2,GLI4,GRINA,HSF1,GPR20,GML,GPT,MAPK15,TMEM249,LINC01591,ZNF252P,FAM83H,GPIHBP1,NSMCE2,ZNF517,WDR97,NRBP2,LINC02878,ZNF252P-AS1,KLHL38,TMED10P1,LINC02904,ZFP41,ZNF707,PEG13,MRPS36P3,SPATC1,CYCSP23,SMPD5,CDK5P1,IMPDH1P6,RPL32P20,MAFA,MROH5,C8orf82,LRRC24,FER1L6-AS1,AARD,SAMD12,SLURP2,MIR30B,MIR30D,RPS26P35,ZFAT-AS1,MIR151A,SCX,IQANK1,SAMD12-AS1,MROH6,LINC00051,ARF1P3,HAS2-AS1,LINC02912,TSSK5P,RPL23AP56,RAD21-AS1,CASC8,MROH1,MIR661,MIR548D1,FER1L6,MIR937,LINC01300,OC90,MIR939,CDC42P3,MTRF1LP2,LINC00861,KNOP1P5,CCDC166,MRS2P1,LY6E,KCNQ3,LY6H,TONSL,CCN3,MYC,NDUFB9,TNFRSF11B,LY6E-DT,FAM83A-AS1,UBA52P5,CASC11,RPS10P16,ZNHIT1P1,RPL35AP19,LNCOC1,TONSL-AS1,AK3P2,PTCSC1,MIR1207,MIR1208,MIR1204,MIR1234,MIR1302-7,MIR1205,MIR1206,HMGB1P19,RFPL4AP5,NCAPGP1,HNRNPA1P38,MIR3610,MIR548AA1,MIR3686,MIR4662B,ZHX1-C8orf76,MIR4663,MIR4664,C8orf17,MIR4472-1,MIR4662A,ASAP1-IT2,MINCR,LINC00536,RNA5SP277,RNA5SP276,RNA5SP278,MTND2P7,MIR5194,PCAT1,DUTP2,CCAT2,SOD1P3,MROH4P,DENND3-AS1,RNF139-DT,LINC00824,PRNCR1,ENPP2,RAD21,RPL8,PLEC,POU5F1B,PVT1,PTK2,LY6L,MIR6844,MIR6845,MIR6847,MIR6848,MIR7112,MIR6893,MIR548AZ,MIR6850,MIR6846,MIR7848,MIR6849,ERICD,CASC19,MAFA-AS1,LINC01151,LINC02855,MAL2-AS1,SMILR,SQLE-DT,RN7SKP206,RN7SKP175,WASHC5-AS1,RNU7-181P,RN7SL329P,RN7SL396P,RN7SKP155,SLA,GFUS,TAF2,COL14A1,TG,SNTB1,ST3GAL1,SQLE,ZYXP1,RNU6-875P,RNU6-442P,RNU1-35P,RNU6-628P,RNU6-756P,RN7SL826P,RN7SKP226,RN7SL395P,RN7SL228P,RNU6-144P,RNU6-869P,RN7SL260P,RNU6-220P,RNU11-4P,RNU6-1255P,RN7SKP153,RNVU1-32,RNU6-12P,MTCO1P49,RNU4-25P,LINC02055,LYNX1-SLURP2,CCN4,EIF3H,ZNF16,ZNF7,LY6D,GPAA1,PSCA,JRK,FOXH1,DGAT1,ST3GAL1-DT,TRIB1,ZNF623,WASHC5,LRRC14,MTSS1,HHLA1,RECQL4,ZHX2,ZHX1,PTP4A3,RNF139,NDRG1,DENND3,PUF60,KHDRBS3,COLEC10,BOP1,EFR3A,DNAAF11,ZC3H3,ARC,FBXL6,SCRIB
verberne_22_ASD/DD/ID_discovery_cases-case129
De novo
ADGRB1,ANXA13,ADCY8,CYP11B2,EEF1D,EXT1,CYP11B1,CYC1,AGO2,MTBP,OPLAH,PHF20L1,CPSF1,VPS28,HGH1,ATAD2,THEM6,CYHR1,ASAP1,COMMD5,FAM135B,CYRIB,MRPL13,KCNK9,CHRAC1,LY6K,EXOSC4,TRMT12,SLC39A4,NTAQ1,GSDMC,ZNF250,SLURP1,SLC45A4,ZFAT,C8orf33,LYNX1,PYCR3,SLC52A2,DEPTOR,DERL1,GSDMD,DSCC1,ZNF696,RHPN1-AS1,SCRT1,UTP23,MAF1,TRAPPC9,TATDN1,ZNF34,EPPK1,MAPRE1P1,ARHGAP39,SHARPIN,NAPRT,TIGD5,C8orf76,HPYR1,TBC1D31,FAM83A,ZNF251,KIFC2,PARP10,MED30,PPP1R16A,MFSD3,FBXO32,MAL2,TOP1MT,RHPN1,LYPD2,ZNF572,TMEM71,CCDC26,FAM91A1,ST13P6,LINC00964,TSNARE1,ADCK5,FER1L6-AS2,TMEM65,LRATD2,COL22A1,SLC30A8,HAS2,GLI4,GRINA,HSF1,GPR20,GML,GPT,MAPK15,TMEM249,LINC01591,ZNF252P,FAM83H,GPIHBP1,NSMCE2,ZNF517,WDR97,NRBP2,LINC02878,ZNF252P-AS1,KLHL38,TMED10P1,LINC02904,ZFP41,ZNF707,PEG13,MRPS36P3,SPATC1,CYCSP23,SMPD5,CDK5P1,IMPDH1P6,RPL32P20,MAFA,MROH5,C8orf82,LRRC24,FER1L6-AS1,AARD,SAMD12,SLURP2,MIR30B,MIR30D,RPS26P35,ZFAT-AS1,MIR151A,SCX,IQANK1,SAMD12-AS1,MROH6,LINC00051,ARF1P3,HAS2-AS1,LINC02912,TSSK5P,RPL23AP56,RAD21-AS1,CASC8,MROH1,MIR661,MIR548D1,FER1L6,MIR937,LINC01300,OC90,MIR939,CDC42P3,MTRF1LP2,LINC00861,KNOP1P5,CCDC166,MRS2P1,LY6E,KCNQ3,LY6H,TONSL,CCN3,MYC,NDUFB9,TNFRSF11B,LY6E-DT,FAM83A-AS1,UBA52P5,CASC11,RPS10P16,ZNHIT1P1,RPL35AP19,LNCOC1,TONSL-AS1,AK3P2,PTCSC1,MIR1207,MIR1208,MIR1204,MIR1234,MIR1302-7,MIR1205,MIR1206,HMGB1P19,RFPL4AP5,NCAPGP1,HNRNPA1P38,MIR3610,MIR548AA1,MIR3686,MIR4662B,ZHX1-C8orf76,MIR4663,MIR4664,C8orf17,MIR4472-1,MIR4662A,ASAP1-IT2,MINCR,LINC00536,RNA5SP277,RNA5SP276,RNA5SP278,MTND2P7,MIR5194,PCAT1,DUTP2,CCAT2,SOD1P3,MROH4P,DENND3-AS1,RNF139-DT,LINC00824,PRNCR1,ENPP2,RAD21,RPL8,PLEC,POU5F1B,PVT1,PTK2,LY6L,MIR6844,MIR6845,MIR6847,MIR6848,MIR7112,MIR6893,MIR548AZ,MIR6850,MIR6846,MIR7848,MIR6849,ERICD,CASC19,MAFA-AS1,LINC01151,LINC02855,MAL2-AS1,SMILR,SQLE-DT,RN7SKP206,RN7SKP175,WASHC5-AS1,RNU7-181P,RN7SL329P,RN7SL396P,RN7SKP155,SLA,GFUS,TAF2,COL14A1,TG,SNTB1,TRPS1,ST3GAL1,SQLE,ZYXP1,RNU6-875P,RNU6-442P,RNU1-35P,RNU6-628P,RNU6-756P,RN7SL826P,RN7SKP226,RN7SL395P,RN7SL228P,RNU6-144P,RNU6-869P,RN7SL260P,RNU6-220P,RNU11-4P,RNU6-1255P,RN7SKP153,RNVU1-32,RNU6-12P,MTCO1P49,RNU4-25P,CARS1P2,LINC02055,LYNX1-SLURP2,CCN4,EIF3H,ZNF16,ZNF7,LY6D,GPAA1,PSCA,JRK,FOXH1,DGAT1,ST3GAL1-DT,TRIB1,ZNF623,WASHC5,LRRC14,MTSS1,HHLA1,RECQL4,ZHX2,ZHX1,PTP4A3,RNF139,NDRG1,DENND3,PUF60,KHDRBS3,COLEC10,BOP1,EFR3A,DNAAF11,ZC3H3,ARC,FBXL6,SCRIB
Controls
No Control Data Available
No Animal Model Data Available