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11q24.2-q25CNV Type: Deletion


Largest CNV size: 10078000 bp

Statistics Box:
Number of Reports: 6



Summary Information

Summary statement in development

Additional Locus Information

Genome browsers

USCS Symbol             NCBI Symbol

Decipher

            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
Functional impact of global rare copy number variation in autism spectrum disorders.
Deletion
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders.
Deletion
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Deletion-Duplication
Performance of case-control rare copy number variation annotation in classification of autism.
Deletion

Minor Reports

Title
Author, Year
Report Class
CNV Type
Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia.
Deletion

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 akshoomoff_14_ASD_discovery_cases
 17 patients with Jacobsen syndrome (11q terminal deletion disorder), prospectively recruited from the 11q Research and Resource Group; and 3 additional patients with atypical distal 11q deletions
 20
 Diagnosis of ASD assessed using ADOS (n=18) or ADI-R (n=2). Cognitive abilities in cases assessed using the Bayley Scales of Infant and Toddler Development, Third Edition; the Differential Ability Scales; the Wechsler Intelligence Scale for Children, Fourth Edition; or the Wechsler Adult Intelligence Scale, Fourth Edition.
 Range, 3.8-21.9 yrs.
 20.0% Male
 10900000
 5
 0
 5
 engchuan_15_ASD_discovery_cases
 Samples from the Autism Genome Project (AGP)
 1892
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 N/A
 85.78% Male
 5426435
 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
 10841977
 3
 1
 4
 pinto_10_ASD_discovery_cases
 Autism Genome Project (AGP) consortium patient cohort from families with at least two ASD individuals
 996
 ASD (ADI-R and ADOS): strict, broad, or spectrum ASD
 
 
 5426436
 1
 0
 1
 rosenfeld_10_ASD_discovery_cases
 Samples submitted between 3/2004 and 7/2008 that had ASD as indication for study (Signature Genomic Labs, Spokane, WA)
 1461
 ASD
 
 
 10035758
 1
 0
 1
 wang_10_ASD_discovery_cases
 ASD patients recruited from Centers for Autism in Zagreb, Rijeka, and Split (Croatia)
 103
 ASD (according to DSM-IV criteria)
 Mean, 21.5 10.3
 78.6% Male
 10078000
 1
 0
 1

Controls

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 engchuan_15_ASD_discovery_controls
 Platform-matched controls from three large studies: SAGE (Study of Addiction Genetics and Environment), Ontario Colorectal Cancer study, and HABC (Health Aging and Body Composition)
 2342
 Controls; subjects had no previous psychiatric history
 N/A
 46.67% Male
 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
 wang_10_ASD_discovery_controls
 Healthy blood donors with no history of mental illness, behavioral disorders, or substance abuse
 203
 Controls
 Mean, 32.5 8.06
 71.9% Male
 10078000
 0
 0
 0

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 akshoomoff_14_ASD_discovery_cases
  N/A
 aCGH
  Signature Genomics custom-designed OS V2.0
 
 
 None
 engchuan_15_ASD_discovery_cases
  Caucasian
 Solid phase hybridization
  Illumina 1M
 
 
 Yes
 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
 pinto_10_ASD_discovery_cases
  European
 Solid phase hybridization
  Illumina Infinium 1M SNP microarray
 QuantiSNP, iPattern
 
 qPCR, long-range PCR (LR-PCR), MLPA, FISH, aCGH (Agilent 1M), array SNP (Affymetrix 500K)
 rosenfeld_10_ASD_discovery_cases
 
 aCGH
  BACs aCGH, whole-genome oligo-aCGH
 
 
 FISH
 wang_10_ASD_discovery_cases
  Croatian
 Solid phase hybridization
  Illumina HumanHap550 BeadChip
 PennCNV
 BeadStudio
 None

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  engchuan_15_ASD_discovery_controls
  Caucasian
  Solid phase hybridization
  Illumina 1M
 
 
  None
  kaminsky_11_DD/ID/ASD_discovery_controls
  NA
  aCGH
  Agilent 44K, Agilent 105K
 
  Feature Extraction, DNA Analytics
 
  wang_10_ASD_discovery_controls
  Croatian
  Solid phase hybridization
  Illumina HumanHap550 BeadChip
  PennCNV
  BeadStudio
  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
  akshoomoff_14_ASD_discovery_cases-patient1
 15.9 yrs.
 F
 Jacobsen syndrome
 Research diagnosis: non-spectrum. ADOS classification: non-spectrum. SCQ score above cutoff: yes.
 IQ estimate: 36 (test given: Differential Ability Scales). VABS-II composite score: 54.
 127019075
 135006516 (approximate endpoint)
  7900000
 Unknown
 Deletion
 No
  akshoomoff_14_ASD_discovery_cases-patient2
 4.0 yrs.
 F
 ASD and Jacobsen syndrome
 Research diagnosis: ASD. ADOS classification: autism. SCQ score above cutoff: no.
 IQ estimate: 69 (test given: Differential Ability Scales, Preschool Version). VABS-II composite score: 82.
 126205251
 135006516 (approximate endpoint)
  8700000
 Unknown
 Deletion
 No
  akshoomoff_14_ASD_discovery_cases-patient3
 13.7 yrs.
 F
 Jacobsen syndrome
 Research diagnosis: non-spectrum. ADOS classification: non-spectrum. SCQ score above cutoff: no.
 IQ estimate: 40 (test given: Wechsler Intelligence Scale for Children-Fourth Edition). VABS-II composite score: 67.
 124943082
 135006516 (approximate endpoint)
  10000000
 Unknown
 Deletion
 No
  akshoomoff_14_ASD_discovery_cases-patient4
 5.8 yrs.
 M
 ASD and Jacobsen syndrome
 Research diagnosis: ASD. ADOS classification: autism. SCQ score above cutoff: yes.
 IQ estimate: 45 (test given: Differential Ability Scales, Preschool Version). VABS-II composite score: 71.
 123939888
 135006516 (approximate endpoint)
  10900000
 Unknown
 Deletion
 No
  akshoomoff_14_ASD_discovery_cases-patient5
 4.0 yrs.
 M
 ASD and Jacobsen syndrome
 Research diagnosis: ASD. ADOS classification: autism. SCQ score above cutoff: yes.
 IQ estimate: 49 (test given: Differential Ability Scales, Preschool Version). VABS-II composite score: 78.
 124210383
 135006516 (approximate endpoint)
  10700000
 Unknown
 Deletion
 No
  engchuan_15_ASD_discovery_cases-case6240_4
 N/A
 N/A
 ASD
 Diagnosis of ASD based on Autism Diagnostic Observation Schedule (ADOS) and Autism Diagnostic Interview-Revised (ADI-R)
 
 127258834
 132685269
  5426436
 GRCh38
 Deletion
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000848
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 127604660
 134998454
  7393795
 GRCh38
 Deletion
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000865
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 124155723
 134998513
  10842791
 GRCh38
 Deletion
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001110
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 126445805
 134998513
  8552709
 GRCh38
 Duplication
 Yes
  kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00002222
 NA
 NA
 Developmental delay/intellectual disability/ASD
 Clinical profile NA
 Cognitive profile NA
 126433740
 135040246
  8606507
 GRCh38
 Deletion
 Yes
  pinto_10_ASD_discovery_cases-case6240_4
 NA
 M
 Autism
 Language delay, macrocephaly, automutilations, minor dysmorphic facial features (low ears flat nose and nasal bridge high forehead), normal neurological exam; brain MRI: white mader abnormalities; chromosome 11q deletion syndrome (Jacobsen syndrome)
 Mild MR
 127258834
 132685269
  5426436
 GRCh38
 Deletion
 Yes
  rosenfeld_10_ASD_discovery_cases-case25653
 NA
 NA
 ASD
 NA
 NA
 124395610
 134431368
  10035758
 Unknown
 Deletion
 Yes
  wang_10_ASD_discovery_cases-AC0052
 26
 F
 ASD
 NA
 NA
 124992618
 135070522
  10077905
 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
 akshoomoff_14_ASD_discovery_cases-patient1
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 akshoomoff_14_ASD_discovery_cases-patient2
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 akshoomoff_14_ASD_discovery_cases-patient3
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 akshoomoff_14_ASD_discovery_cases-patient4
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: VWA5A,OR8G2,OR8G1,OR8G5,OR8D1,OR8D2,OR8B2,OR8B3,OR8B4,OR8B8,OR8B12,OR8A1,PANX3,TBRG1,SIAE,SPA17,NRGN,VSIG2,ESAM,MSANTD2,ROBO3,ROBO4,HEPACAM,HEPN1,CCDC15,SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 akshoomoff_14_ASD_discovery_cases-patient5
 
 
 Unknown
 Unknown
 Unknown
 Estimated gene content: OR8B2,OR8B3,OR8B4,OR8B8,OR8B12,OR8A1,PANX3,TBRG1,SIAE,SPA17,NRGN,VSIG2,ESAM,MSANTD2,ROBO3,ROBO4,HEPACAM,HEPN1,CCDC15,SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,C11orf44,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 engchuan_15_ASD_discovery_cases-case6240_4
 
 
 De novo
 
 
 RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,ARHGAP32,NTM,OPCML
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000848
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000865
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001110
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00002222
 FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
 
 Unknown
 Unknown
 Unknown
 MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 
 pinto_10_ASD_discovery_cases-case6240_4
 qPCR
 
 De novo
 Simplex
 NA
 RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,ARHGAP32,NTM,OPCML
 
 rosenfeld_10_ASD_discovery_cases-case25653
 FISH
 
 Unknown
 Unknown
 Unknown
 CCDC15,SLC37A2,TMEM218,PKNOX2,FEZ1,EI24,STT3A,CHEK1,ACRV1,PATE1,PATE2,PATE3,PATE4,HYLS1,PUS3,DDX25,CDON,RPUSD4,FAM118B,SRPR,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3,ETS1,FLI1,KCNJ1,KCNJ5,C11orf45,TP53AIP1,ARHGAP32,BARX2,TMEM45B,NFRKB,PRDM10,APLP2,ST14,ZBTB44,ADAMTS8,ADAMTS15,SNX19,NTM,OPCML,SPATA19,IGSF9B,JAM3,NCAPD3,VPS26B,THYN1,ACAD8,GLB1L3,GLB1L2,B3GAT1
 
 wang_10_ASD_discovery_cases-AC0052
 
 
 Unknown
 NA
 NA
 PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,KIRREL3,ARHGAP32,NTM,OPCML,NCAPD3
 

Controls

No Control Data Available
No Animal Model Data Available
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