18q21.2-q23CNV Type: Deletion
Largest CNV size: 28724903 bp
Statistics Box:
Number of Reports: 5
Number of Reports: 5
Summary Information
Deletions within this region were identified in two cases 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...
Deletion
Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies.
Deletion
Minor Reports
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
egle_16_DD/ID_discovery_cases
Patients assessed in the course of the Lithuanian-Swiss cooperation programme "Research and Development", the joint research project "Unique Genome Variants in Congenital Neurodevelopment Disorders: Origin, Genomic Mechanisms, Functional and Clinical Consequences" (UNIGENE)
66
All cases present with either syndromic or non-syndromic developmental delay/intellectual disability (DD/ID), ranging from mild to profound
N/A
N/A
23500000
1
0
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
28724903
2
0
2
miclea_22_DD/ID_discovery_cases
Patients presented in Clinical Emergency Hospital for Children Cluj-Napoca betwwen January 2015 and July 2017.
189
Diagnosis of global developmental delay (DD) or intellectual disability (ID) based on intelligence quotient evaluated by WISC-IV and developmental quotient evaluated by NEPSY.
Range, 1-18 yrs.
51.85% Male
28790809
0
1
1
sansovic_17_DD/ID/ASD_discovery_cases
Unrelated patients from Croatia referred to the Department of Medical Genetics and Reproductive Health, Children's Hospital Zagreb, University of Zagreb School of Medicine
337
Cases diagnosed by clinical geneticists or pediatricians to have developmental delay/intellectual disability (DD/ID), ASD, congenital anomalies, or a combination of those features
Mean, 7 years (range, 1 month-25 years)
N/A
25385000
1
0
1
sherman_21_ASD_discovery_cases
ASD probands from the Simons Simplex Collection (n=2,594) and the SPARK cohort (n=9,483) screened for mosaic CNVs (mCNVs)
12077
Cohort diagnosis of ASD
Range, 3-40+ yrs.
NA
28964635
1
0
1
Controls
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
egle_16_DD/ID_discovery_controls
CNVs from the Database of Genomic Variants (DGV)
N/A
Control
N/A
N/A
0
0
0
0
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
sherman_21_ASD_discovery_controls
Unaffected siblings of ASD probands from the Simons Simplex Collection (n=2,424) and the SPARK cohort (n=3,076) screened for mosaic CNVs (mCNVs)
5500
Control (unaffected siblings of ASD probands)
Range, 3-18 yrs.
NA
0
0
0
0
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
egle_16_DD/ID_discovery_cases
Lithuania
aCGH
Agilent 60K, Agilent 105K, or Agilent 1M
ADM-2
Feature Extraction 10.7.3.1, CytoGenomics 3.0.0.27 (Agilent)
FISH or RT-PCR
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
miclea_22_DD/ID_discovery_cases
Romania
Solid phase hybridization
Illumina Infinium OmniExpress-24 BeadChip
NA
Illumina GenomeStudio v.2.0.
None
sansovic_17_DD/ID/ASD_discovery_cases
Croatia
aCGH
Agilent SurePrint G3 Unrestricted CGH ISCA v2
Agilent Feature Extraction (v12.0), Agilent CytoGenomics (v3.0 and v4.0)
None
sherman_21_ASD_discovery_cases
NA
Solid phase hybridization
Illumina 1Mv1, Illumina 1Mv3, Illumina Omni2.5, Illumina Infinium Global Screening Array-24 v.1.0
MoChA
None
Controls
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
egle_16_DD/ID_discovery_controls
N/A
N/A
N/A
kaminsky_11_DD/ID/ASD_discovery_controls
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
sherman_21_ASD_discovery_controls
NA
Solid phase hybridization
Illumina 1Mv1, Illumina 1Mv3, Illumina Omni2.5, Illumina Infinium Global Screening Array-24 v.1.0
MoChA
None
Cases
Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
egle_16_DD/ID_discovery_cases-case7_1
14 mos.
F
Developmental delay
Minor facial anomalies, congenital heart disease, thickened nails
Developmental delay
56805961
80224243
23418283
GRCh38
Deletion
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004245
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
53637007
80252149
26615143
GRCh38
Deletion
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004492
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
51605752
80252149
28646398
GRCh38
Deletion
Yes
miclea_22_DD/ID_discovery_cases-case189
NA
NA
Developmental delay and intellectual disability
Global developmental delay, microcephaly, epilepsy, dysmorphic features
Intellectual disability
51340017
80130825
28790809
GRCh38
Duplication
No
sansovic_17_DD/ID/ASD_discovery_cases-case55
4 yrs.
M
Developmental delay/intellectual disability
Developmental delay/intellectual disability, Congenital anomalies, Dysmorphism
54957845
80252149
25294305
GRCh38
Deletion
No
sherman_21_ASD_discovery_cases-SPARK_SP0088291
47 yrs.
M
ASD
ASD proband from the SPARK cohort. SCQ summary score: NA. Mosaic cell fraction: 0.2726. CNV occurs on the maternal haplotype.
51288104
80252738
28964635
GRCh38
Deletion
No
Controls
No Control Data Available
Cases
Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
egle_16_DD/ID_discovery_cases-case7_1
FISH or RT-PCR
De novo
LINC02565,RNU6-737P,RNU6-742P,RSL24D1P11,LINC01897,HMGN1P30,MIR122HG,MIR122,MIR3591,SNORA108,RPL9P31,MRPL37P1,RNU6-219P,RNU2-69P,RAX,RPS26P54,GLUD1P4,PMAIP1,NFE2L3P1,RN7SL342P,SDCCAG3P1,SINHCAFP2,RNU6-567P,RPS3AP49,RNU4-17P,MC4R,MRPS5P4,CTBP2P3,HMGN1P31,RNU6-116P,RPL30P14,RPIAP1,RPL17P44,ACTBP9,RN7SL705P,RNU6-142P,ATP5MC1P6,SERPINB12,SERPINB4,SERPINB3,RPL12P39,PRPF19P1,RNU6-1037P,MIR5011,RPL31P9,DSEL,LINC01912,AKR1B10P2,RNU6-39P,SDHCP1,LINC01910,LARP7P3,RPS2P6,RN7SL795P,HNRNPA1P11,RNA5SP460,MIR548AV,RN7SL401P,RN7SL551P,FAUP1,LINC01922,LINC01893,LINC00683,ARL2BPP1,CCND3P2,RNU6-346P,RPL26P35,BDP1P,RNA5SP461,RNU6-655P,LINC01896,SLC25A6P4,WDR7-OT1,LINC-ROR,ST8SIA3,ONECUT2,FECH,NARS,LINC01926,OACYLP,SEC11C,GRP,CPLX4,LMAN1,LINC01544,ZCCHC2,KDSR,VPS4B,SERPINB5,SERPINB13,SERPINB7,SERPINB2,SERPINB10,SERPINB8,LINC01916,LINC01903,SOCS6,LINC01909,LIVAR,LINC01899,LINC02582,FBXO15,TIMM21,CYB5A,CNDP2,LINC00909,ZADH2,SMIM21,LINC01898,C18orf65,LINC01927,LINC01879,GALR1,SALL3,KCNG2,PQLC1,HSBP1L1,TXNL4A,RBFA,ADNP2,PARD6G-AS1,WDR7,BOD1L2,NEDD4L,ALPK2,ZNF532,CCBE1,CDH20,PIGN,RELCH,TNFRSF11A,BCL2,SERPINB11,LINC01924,LINC00305,LINC01538,CDH7,CDH19,TMX3,CCDC102B,DOK6,CD226,RTTN,GTSCR1,LINC01541,CBLN2,NETO1,C18orf63,CNDP1,ZNF407,TSHZ1,ZNF516,ZNF236-DT,ZNF236,MBP,LINC01029,ATP9B,NFATC1,RBFADN,PARD6G,ATP8B1,RNF152,PHLPP1,HMSD,LINC00908,CTDP1,MALT1
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004245
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
SNORA37,SNRPGP2,RPSAP57,MAP1LC3P,RNA5SP459,MIR4529,RPL21P126,LINC01415,LINC02565,RNU6-737P,RNU6-742P,RSL24D1P11,LINC01897,HMGN1P30,MIR122HG,MIR122,MIR3591,SNORA108,RPL9P31,MRPL37P1,RNU6-219P,RNU2-69P,RAX,RPS26P54,GLUD1P4,PMAIP1,NFE2L3P1,RN7SL342P,SDCCAG3P1,SINHCAFP2,RNU6-567P,RPS3AP49,RNU4-17P,MC4R,MRPS5P4,CTBP2P3,HMGN1P31,RNU6-116P,RPL30P14,RPIAP1,RPL17P44,ACTBP9,RN7SL705P,RNU6-142P,ATP5MC1P6,SERPINB12,SERPINB4,SERPINB3,RPL12P39,PRPF19P1,RNU6-1037P,MIR5011,RPL31P9,DSEL,LINC01912,AKR1B10P2,RNU6-39P,SDHCP1,LINC01910,LARP7P3,RPS2P6,RN7SL795P,HNRNPA1P11,RNA5SP460,MIR548AV,RN7SL401P,RN7SL551P,FAUP1,LINC01922,LINC01893,LINC00683,ARL2BPP1,CCND3P2,RNU6-346P,RPL26P35,BDP1P,RNA5SP461,RNU6-655P,LINC01896,SLC25A6P4,MBD2,POLI,STARD6,C18orf54,DYNAP,LINC01929,TCF4-AS1,TCF4-AS2,LINC01416,LINC01905,WDR7-OT1,LINC-ROR,ST8SIA3,ONECUT2,FECH,NARS,LINC01926,OACYLP,SEC11C,GRP,CPLX4,LMAN1,LINC01544,ZCCHC2,KDSR,VPS4B,SERPINB5,SERPINB13,SERPINB7,SERPINB2,SERPINB10,SERPINB8,LINC01916,LINC01903,SOCS6,LINC01909,LIVAR,LINC01899,LINC02582,FBXO15,TIMM21,CYB5A,CNDP2,LINC00909,ZADH2,SMIM21,LINC01898,C18orf65,LINC01927,LINC01879,GALR1,SALL3,KCNG2,PQLC1,HSBP1L1,TXNL4A,RBFA,ADNP2,PARD6G-AS1,RAB27B,CCDC68,LINC01539,WDR7,BOD1L2,NEDD4L,ALPK2,ZNF532,CCBE1,CDH20,PIGN,RELCH,TNFRSF11A,BCL2,SERPINB11,LINC01924,LINC00305,LINC01538,CDH7,CDH19,TMX3,CCDC102B,DOK6,CD226,RTTN,GTSCR1,LINC01541,CBLN2,NETO1,C18orf63,CNDP1,ZNF407,TSHZ1,ZNF516,ZNF236-DT,ZNF236,MBP,LINC01029,ATP9B,NFATC1,RBFADN,PARD6G,TCF4,TXNL1,ATP8B1,RNF152,PHLPP1,HMSD,LINC00908,CTDP1,MALT1
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004492
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
RSL24D1P9,RPS8P3,VN1R76P,MIR4528,RPL29P32,SNORA37,SNRPGP2,RPSAP57,MAP1LC3P,RNA5SP459,MIR4529,RPL21P126,LINC01415,LINC02565,RNU6-737P,RNU6-742P,RSL24D1P11,LINC01897,HMGN1P30,MIR122HG,MIR122,MIR3591,SNORA108,RPL9P31,MRPL37P1,RNU6-219P,RNU2-69P,RAX,RPS26P54,GLUD1P4,PMAIP1,NFE2L3P1,RN7SL342P,SDCCAG3P1,SINHCAFP2,RNU6-567P,RPS3AP49,RNU4-17P,MC4R,MRPS5P4,CTBP2P3,HMGN1P31,RNU6-116P,RPL30P14,RPIAP1,RPL17P44,ACTBP9,RN7SL705P,RNU6-142P,ATP5MC1P6,SERPINB12,SERPINB4,SERPINB3,RPL12P39,PRPF19P1,RNU6-1037P,MIR5011,RPL31P9,DSEL,LINC01912,AKR1B10P2,RNU6-39P,SDHCP1,LINC01910,LARP7P3,RPS2P6,RN7SL795P,HNRNPA1P11,RNA5SP460,MIR548AV,RN7SL401P,RN7SL551P,FAUP1,LINC01922,LINC01893,LINC00683,ARL2BPP1,CCND3P2,RNU6-346P,RPL26P35,BDP1P,RNA5SP461,RNU6-655P,LINC01896,SLC25A6P4,LINC01917,LINC01919,MBD2,POLI,STARD6,C18orf54,DYNAP,LINC01929,TCF4-AS1,TCF4-AS2,LINC01416,LINC01905,WDR7-OT1,LINC-ROR,ST8SIA3,ONECUT2,FECH,NARS,LINC01926,OACYLP,SEC11C,GRP,CPLX4,LMAN1,LINC01544,ZCCHC2,KDSR,VPS4B,SERPINB5,SERPINB13,SERPINB7,SERPINB2,SERPINB10,SERPINB8,LINC01916,LINC01903,SOCS6,LINC01909,LIVAR,LINC01899,LINC02582,FBXO15,TIMM21,CYB5A,CNDP2,LINC00909,ZADH2,SMIM21,LINC01898,C18orf65,LINC01927,LINC01879,GALR1,SALL3,KCNG2,PQLC1,HSBP1L1,TXNL4A,RBFA,ADNP2,PARD6G-AS1,RAB27B,CCDC68,LINC01539,WDR7,BOD1L2,NEDD4L,ALPK2,ZNF532,CCBE1,CDH20,PIGN,RELCH,TNFRSF11A,BCL2,SERPINB11,LINC01924,LINC00305,LINC01538,CDH7,CDH19,TMX3,CCDC102B,DOK6,CD226,RTTN,GTSCR1,LINC01541,CBLN2,NETO1,C18orf63,CNDP1,ZNF407,TSHZ1,ZNF516,ZNF236-DT,ZNF236,MBP,LINC01029,ATP9B,NFATC1,RBFADN,PARD6G,LINC01630,DCC,TCF4,TXNL1,ATP8B1,RNF152,PHLPP1,HMSD,LINC00908,CTDP1,MALT1
miclea_22_DD/ID_discovery_cases-case189
Unknown
CDH7,ACTBP9,BCL2,CYB5A,FECH,DCC,SALL3,CDH20,CDH19,ST8SIA3,RAX,TIMM21,ZCCHC2,TMX3,CNDP2,ZNF407,ZNF532,RELCH,RBFA,CCDC102B,SLC66A2,CCDC68,NETO1,CNDP1,DSEL,SERPINB12,SERPINB11,SEC11C,ALPK2,DIPK1C,CBLN2,CCBE1,FAUP1,STARD6,DOK6,RNF152,GTSCR1,C18orf54,FBXO15,LINC00305,CTBP2P3,GLUD1P4,GALR1,KDSR,GRP,DYNAP,RSL24D1P11,LINC01924,ZADH2,HMSD,SMIM21,BOD1L2,CPLX4,RPS2P6,MAP1LC3P,ATP9B,ENTR1P1,MRPS5P4,LINC01879,RPL29P32,LINC02864,OACYLP,LINC00683,ZNF407-AS1,RPSAP57,ARL2BPP1,RPS3AP49,LINC01538,ZNF516-DT,MIR122,HSBP1L1,RPIAP1,NFE2L3P1,RPL31P9,DSEL-AS1,AKR1B10P2,C18orf63,LINC01896,SINHCAFP2,SS18L2P2,SNORA37,HMGN1P31,BDP1P,RPL26P35,HNRNPA1P11,RPL30P14,RSL24D1P9,RPL17P44,SNRPGP2,NARS1,MBP,MTL3P,NFATC1,SERPINB2,MC4R,LMAN1,LINC01415,ZNF236-DT,RPS26P54,RPS8P3,HMGN1P30,FAM32DP,RPL21P126,RPL9P31,RPL12P39,LINC01630,VN1R76P,MRPL37P1,LINC01541,SLC25A6P4,LINC01898,NETO1-DT,RBFADN,SDHCP1,ATP5MC1P6,LINC02582,LINC01539,PRPF19P1,MIR4528,MIR4529,MIR3591,MIR5011,MIR548AV,RNU6-39P,LINC01544,RNA5SP459,LINC-ROR,RNA5SP461,RNA5SP460,LINC01029,LINC01910,ZNF516-AS1,LINC01416,LINC01929,LINC01927,LINC01922,MALT1-AS1,LINC01909,LINC01903,PMAIP1,SERPINB8,ATP8B1,RAB27B,SERPINB13,SERPINB10,SERPINB5,LINC01917,LINC01919,LINC01905,LINC01899,LIVAR,LINC02565,LINC01893,LINC01912,TCF4-AS1,LINC01926,RN7SL342P,SERPINB4,TCF4,SERPINB3,RN7SL795P,RNU6-567P,RNU6-219P,RNU6-142P,CCND3P2,TCF4-AS2,RN7SL551P,RNU6-655P,RNU4-17P,RN7SL401P,RNU6-116P,RNU6-737P,RNU6-742P,RNU6-1037P,RNU2-69P,SNORA108,LARP7P3,RN7SL705P,RNU6-346P,LINC01916,LINC01897,WDR7-OT1,MIR122HG,MBD2,SERPINB7,TNFRSF11A,ZNF236,CUPIN1P,KDSR-DT,ONECUT2,TSHZ1,VPS4B,ZNF516,CTDP1,SOCS6,TXNL1,CD226,MALT1,TXNL4A,ADNP2,POLI,NEDD4L,RTTN,PHLPP1,PIGN,KCNG2,WDR7
sansovic_17_DD/ID/ASD_discovery_cases-case55
De novo
RNA5SP459,MIR4529,RPL21P126,LINC01415,LINC02565,RNU6-737P,RNU6-742P,RSL24D1P11,LINC01897,HMGN1P30,MIR122HG,MIR122,MIR3591,SNORA108,RPL9P31,MRPL37P1,RNU6-219P,RNU2-69P,RAX,RPS26P54,GLUD1P4,PMAIP1,NFE2L3P1,RN7SL342P,SDCCAG3P1,SINHCAFP2,RNU6-567P,RPS3AP49,RNU4-17P,MC4R,MRPS5P4,CTBP2P3,HMGN1P31,RNU6-116P,RPL30P14,RPIAP1,RPL17P44,ACTBP9,RN7SL705P,RNU6-142P,ATP5MC1P6,SERPINB12,SERPINB4,SERPINB3,RPL12P39,PRPF19P1,RNU6-1037P,MIR5011,RPL31P9,DSEL,LINC01912,AKR1B10P2,RNU6-39P,SDHCP1,LINC01910,LARP7P3,RPS2P6,RN7SL795P,HNRNPA1P11,RNA5SP460,MIR548AV,RN7SL401P,RN7SL551P,FAUP1,LINC01922,LINC01893,LINC00683,ARL2BPP1,CCND3P2,RNU6-346P,RPL26P35,BDP1P,RNA5SP461,RNU6-655P,LINC01896,SLC25A6P4,LINC01929,TCF4-AS1,TCF4-AS2,LINC01416,LINC01905,WDR7-OT1,LINC-ROR,ST8SIA3,ONECUT2,FECH,NARS,LINC01926,OACYLP,SEC11C,GRP,CPLX4,LMAN1,LINC01544,ZCCHC2,KDSR,VPS4B,SERPINB5,SERPINB13,SERPINB7,SERPINB2,SERPINB10,SERPINB8,LINC01916,LINC01903,SOCS6,LINC01909,LIVAR,LINC01899,LINC02582,FBXO15,TIMM21,CYB5A,CNDP2,LINC00909,ZADH2,SMIM21,LINC01898,C18orf65,LINC01927,LINC01879,GALR1,SALL3,KCNG2,PQLC1,HSBP1L1,TXNL4A,RBFA,ADNP2,PARD6G-AS1,CCDC68,LINC01539,WDR7,BOD1L2,NEDD4L,ALPK2,ZNF532,CCBE1,CDH20,PIGN,RELCH,TNFRSF11A,BCL2,SERPINB11,LINC01924,LINC00305,LINC01538,CDH7,CDH19,TMX3,CCDC102B,DOK6,CD226,RTTN,GTSCR1,LINC01541,CBLN2,NETO1,C18orf63,CNDP1,ZNF407,TSHZ1,ZNF516,ZNF236-DT,ZNF236,MBP,LINC01029,ATP9B,NFATC1,RBFADN,PARD6G,TCF4,TXNL1,ATP8B1,RNF152,PHLPP1,HMSD,LINC00908,CTDP1,MALT1
sherman_21_ASD_discovery_cases-SPARK_SP0088291
BCL2,CDH7,ACTBP9,FECH,DCC,CYB5A,CDH19,CDH20,SALL3,TIMM21,ST8SIA3,RAX,ZCCHC2,CNDP2,ZNF407,TMX3,ZNF532,RELCH,RBFA,CCDC102B,SLC66A2,CCDC68,NETO1,SERPINB11,SEC11C,CNDP1,SERPINB12,PARD6G,DSEL,DIPK1C,ALPK2,FAUP1,CCBE1,STARD6,CBLN2,CTBP2P3,DOK6,LINC00305,GTSCR1,RNF152,C18orf54,FBXO15,GRP,GLUD1P4,KDSR,GALR1,HMSD,BOD1L2,RSL24D1P11,DYNAP,LINC01924,SMIM21,ZADH2,CPLX4,RPS2P6,ENTR1P1,MAP1LC3P,MRPS5P4,ATP9B,LINC02864,LINC01538,ARL2BPP1,LINC00683,RPSAP57,LINC01879,ZNF516-DT,RPL29P32,RPS3AP49,OACYLP,HSBP1L1,MIR122,RPIAP1,RPL31P9,NFE2L3P1,LINC01896,C18orf63,AKR1B10P2,HMGN1P31,BDP1P,SINHCAFP2,SNORA37,SS18L2P2,HNRNPA1P11,RPL26P35,RPL30P14,RSL24D1P9,RPL17P44,SNRPGP2,PARD6G-AS1,MBP,SERPINB2,NFATC1,LMAN1,MC4R,MTL3P,NARS1,LINC01415,ZNF236-DT,HMGN1P30,RPS26P54,RPS8P3,FAM32DP,RPL21P126,LINC01630,RPL9P31,RPL12P39,VN1R76P,MRPL37P1,SLC25A6P4,LINC01898,LINC01541,LINC02582,LINC01539,ATP5MC1P6,RBFADN,PRPF19P1,SDHCP1,MIR4528,MIR3591,MIR4529,MIR548AV,MIR5011,RNA5SP461,RNA5SP460,RNA5SP459,RNU6-39P,LINC01544,LINC-ROR,LINC01927,LINC01909,LINC01922,LINC01929,LINC01910,LINC01903,LINC01416,LINC01029,ATP8B1,SERPINB13,RAB27B,SERPINB5,SERPINB8,SERPINB10,PMAIP1,LINC01917,LINC01899,LIVAR,LINC01919,LINC01905,LINC01912,TCF4-AS1,LINC01893,LINC01926,LINC02565,RN7SL342P,TCF4,SERPINB3,SERPINB4,RN7SL795P,RNU6-219P,RNU6-655P,CCND3P2,RNU6-142P,RN7SL551P,RNU6-567P,TCF4-AS2,RNU6-116P,RN7SL401P,RNU4-17P,RN7SL705P,RNU6-742P,LARP7P3,RNU6-346P,RNU2-69P,RNU6-737P,RNU6-1037P,SNORA108,LINC01897,WDR7-OT1,LINC01916,MIR122HG,TNFRSF11A,ZNF236,MBD2,SERPINB7,CUPIN1P,TSHZ1,ZNF516,VPS4B,SOCS6,TXNL1,CTDP1,ONECUT2,ADNP2,CD226,POLI,MALT1,TXNL4A,KCNG2,NEDD4L,WDR7,PIGN,PHLPP1,RTTN
Controls
No Control Data Available
No Animal Model Data Available