10q26.13-q26.3CNV Type: Deletion
Largest CNV size: 11269411 bp
Statistics Box:
Number of Reports: 6
Number of Reports: 6
Summary Information
Deletions within this region were found in three 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
Minor Reports
Title
Author, Year
Report Class
CNV Type
Large-scale discovery of novel genetic causes of developmental disorders.
Duplication
Routine Chromosomal Microarray Analysis is Necessary in Korean Patients With Unexplained Developmental Delay/Mental Retardation/Autism Spectrum Dis...
Deletion
The diagnostic yield of intellectual disability: combined whole genome low-coverage sequencing and medical exome sequencing
Deletion
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
digregorio_17_DD/ID_discovery_cases
Consecutive cases examined in the Medical Genetics Unit at the "Citta della Salte e della Scienza" University Hospital (Turin, Italy) from 2008 to 2014 (cases with CNVs are present in DECIPHER database)
1015
Cases diagnosed with idiopathic developmental delay and/or intellectual disability (DD/ID)
N/A
N/A
11000000
1
0
1
fitzgerald_14_ASD/DD/ID_discovery_cases
Children recruited through all 24 regional genetics services of the UK National Health Service and Republic of Ireland as part of the Deciphering Developmental Disorders Study
1133
Cases affected by severe, undiagnosed developmental disorders; most common phenotypes include developmental delay, intellectual disability, specific learning disability, autism, seizures, microcephaly, and dysmorphic features.
Median age, 5.5 years
N/A
12230124
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
11269411
3
0
3
maini_18_ASD/DD/ID_discovery_cases
Patients evaluated at the Clinical Genetics Unit of Arcispedale Santa Maria Nuova, AUSL-IRCCS of Reggio Emilia that were investigated through aCGH between 2005 and 2016
293
Cases presented with one or more neurodevelopmental disorders (NDD), multiple congenital anomalies (MCA), and/or dysmorphic features. Most frequent neurodevelopmental diagnoses include language delay (78.5%), intellectual disability (66.4%), motor delay (50.7%), and ASD (13.9%); dysmorphic features were also frequently observed (52.7%)
Mean age, 7 yrs. (range, 1 mo.-29 yrs.)
57.5% Male
10350000
1
1
2
shin_15_ASD/DD/ID_discovery_cases
Patients with normal karyotype referred for further genetic testing from March 2012-April 2014
96
34 cases with ASD, 54 cases with DD/ID, 8 cases with ASD and DD/ID
N/A
69.8% Male
10744000
1
0
1
wang_20_ID_discovery_cases
Patients recruited from the Department of Neurology, Affiliated Childrens Hospital of the Capital Institute of Pediatrics (Beijing, China) between Jan. 2016.01 and Dec. 2018.
95
All cases presented with intellectual disability (ID); 52 patients had ID with multiple congenital anomalies, and 14 patients had ID with autism spectrum disorder
Range, 1 yr. 1 mo.-16 yrs.
68.0% Male
8851245
1
0
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
digregorio_17_DD/ID_discovery_cases
Italian
aCGH
Agilent 60K (SurePrint G3 Human CGH Microarray 8x60K)
ADM-2
Agilent CGH Analytics software ver. 4.0.81
qPCR
fitzgerald_14_ASD/DD/ID_discovery_cases
UK and Ireland
aCGH, WES
Agilent 2x1M, Agilent Exome+
Cnsolidate, CoNVex
None
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
maini_18_ASD/DD/ID_discovery_cases
Italian
aCGH, array SNP
Multiple platforms, including Agilent and Affymetrix arrays (8x60K oligochips since 2012)
None
shin_15_ASD/DD/ID_discovery_cases
Korean
Array SNP
Affymetrix CytoScan 750K
Affymetrix ChAS v.2.1, Nexus Copy Number v.7.5 (BioDiscovery)
None
wang_20_ID_discovery_cases
Han Chinese
WGS
Illumina HiSeq 2000
Short Oligonucleotide Analysis Package (SOAP) v.2.21
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
digregorio_17_DD/ID_discovery_cases-DECIPHER_283660
N/A
M
Developmental delay/intellectual disability
122741466
133590967
10849502
GRCh38
Deletion
Yes
fitzgerald_14_ASD/DD/ID_discovery_cases-DECIPHER259550
N/A
F
Learning disability
Clinodactyly of the 5th finger; Specific learning disability; Joint hypermobility; Lumbar hyperlordosis; Gingival overgrowth
121391297
133567431
12176135
GRCh38
Duplication
No
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001027
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
122265252
133620674
11355423
GRCh38
Deletion
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001103
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
123307835
133620674
10312840
GRCh38
Deletion
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004312
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
123580320
133558988
9978669
GRCh38
Deletion
Yes
maini_18_ASD/DD/ID_discovery_cases-case55
7 mos.
F
Developmental delay
Birth history: born at 38 weeks gestation following a pregnancy marked by pre-perinatal distress. Developmental milestones: motor delay, language delay. Language and communication evaluation: language disorder N/A. Behavioral/psychiatric evaluation: no reported behavioral or psychiatric abnormalities. Epilepsy/abnormal EEG: positive for epilepsy and/or abnormal EEG. Additional medical history: congenital heart defects, cerebral malformations. Dysmorphic features: prominent forehead, upslanting palpebral fissures, small mouth, small, posteriorly rotated, and asymmetric ears with thick helices. Growth parameters: normal head circumference, short stature. Family history: negative for consanguineity, negative for familiarity, family history negative for NDDs.
Not reported
123275588
133591019
10315432
GRCh38
Deletion
No
maini_18_ASD/DD/ID_discovery_cases-case_unknown7
N/A
N/A
NDD/MCA/dysmorphic features
CNV was identified in an individual with one or more neurodevelopmental disorders (NDD), multiple congenital anomalies (MCA), and/or dysmorphic features (detailed clinical information was not available). CNV classified as pathogenic
124232055
133591019
9358965
GRCh38
Duplication
No
shin_15_ASD/DD/ID_discovery_cases-case6
2 yrs.
M
Developmental delay
Developmental delay
122922664
133612882
10690219
GRCh38
Deletion
No
wang_20_ID_discovery_cases-case6
3 yrs. 11 mos.
F
Intellectual disability
Small hands and feet, hypoplastic labia minora, hypotonia
Intellectual disability
124931431
133782675
8851245
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
digregorio_17_DD/ID_discovery_cases-DECIPHER_283660
qPCR
Maternal (translocation)
HMX3,HMX2,RPS26P39,YBX2P1,NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,OR6L1P,CUZD1,FAM24B,FAM24A,PSTK,IKZF5,ACADSB,BUB3,GPR26,CHST15,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,DMBT1P1,C10orf88,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,CPXM2,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
fitzgerald_14_ASD/DD/ID_discovery_cases-DECIPHER259550
De novo
Multiplex
Not segregated
RN7SKP167,RPS15AP5,RNU6-728P,MIR3941,ARMS2,HMX3,HMX2,RPS26P39,YBX2P1,NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,ATE1-AS1,NSMCE4A,HTRA1,DMBT1,C10orf120,CUZD1,FAM24B,FAM24A,PSTK,IKZF5,ACADSB,BUB3,GPR26,CHST15,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,FGFR2,ATE1,TACC2,BTBD16,PLEKHA1,DMBT1P1,C10orf88,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,CPXM2,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001027
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
RNU6-728P,MIR3941,ARMS2,HMX3,HMX2,RPS26P39,YBX2P1,NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,OR6L1P,HTRA1,DMBT1,C10orf120,CUZD1,FAM24B,FAM24A,PSTK,IKZF5,ACADSB,BUB3,GPR26,CHST15,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,BTBD16,PLEKHA1,DMBT1P1,C10orf88,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,CPXM2,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001103
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
YBX2P1,NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,OR6L1P,GPR26,CHST15,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,CPXM2,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00004312
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
YBX2P1,NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,GPR26,CHST15,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,CPXM2,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
maini_18_ASD/DD/ID_discovery_cases-case55
De novo
Simplex
Possibly segregated
YBX2P1,NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,OR6L1P,GPR26,CHST15,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,CPXM2,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
maini_18_ASD/DD/ID_discovery_cases-case_unknown7
De novo
Unknown
Unknown
NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,OR6L1P,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
shin_15_ASD/DD/ID_discovery_cases-case6
Unknown
Unknown
HMX3,HMX2,RPS26P39,YBX2P1,NKX1-2,RPS10P18,FAM53B-AS1,NPM1P31,MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MMP21,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,OR6L1P,PSTK,IKZF5,ACADSB,BUB3,GPR26,CHST15,OAT,ABRAXAS2,ZRANB1,TEX36,EDRF1,EDRF1-AS1,UROS,DHX32,LINC00601,NPS,MKI67,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,C10orf91,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,C10orf88,LHPP,FAM53B,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2,LINC01163,MGMT,EBF3,GLRX3,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,CPXM2,EEF1AKMT2,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
wang_20_ID_discovery_cases-case6
Unknown
Unknown
Unknown
MIR4296,MRPS21P6,RPS27P18,TEX36-AS1,ALDOAP2,MIR4484,RNU2-42P,GNG10P1,FANK1-AS1,RNA5SP328,SAR1AP2,FOXI2,BUB1P1,CLRN3,LINC02667,MIR4297,CTAGE7P,PPIAP32,MIR378C,TCERG1L-AS1,LINC01165,NKX6-2,LINC01167,RPL5P28,UTF1,VENTX,MIR202HG,MIR202,ZNF511,BANF1P2,FUOM,MIR3944,SPRN,OR7M1P,OR6L1P,FRG2B,RARRES2P2,AGGF1P2,CLUHP5,DUX4L28,DUX4L25,DUX4L24,DUX4L23,DUX4L22,DUX4L21,DUX4L20,DUX4L29,DUX4L10,DUX4L11,DUX4L12,DUX4L13,DUX4L14,DUX4L15,RPL23AP60,ZRANB1,TEX36,EDRF1-DT,EDRF1,EDRF1-AS1,MMP21,UROS,DHX32,LINC00601,NPS,MKI67,LINC02666,LINC01164,PPP2R2D,BNIP3,DPYSL4,LRRC27,PWWP2B,LINC02870,LINC01166,LINC01168,ADGRA1,ADGRA1-AS1,ADAM8,ZNF511-PRAP1,CALY,PRAP1,ECHS1,PAOX,MTG1,SCART1,CYP2E1,CTBP2,FANK1,ADAM12,C10orf90,DOCK1,INSYN2A,LINC01163,MGMT,EBF3,GLRX3,LINC02646,TCERG1L,STK32C,INPP5A,CFAP46,TUBGCP2,OR6L2P,SYCE1,PTPRE,C10orf143,JAKMIP3,KNDC1,BCCIP
Controls
No Control Data Available
No Animal Model Data Available