Yp11.31-q11.223CNV Type: Duplication
Largest CNV size: 20199212 bp
Statistics Box:
Number of Reports: 2
Number of Reports: 2
Summary Information
Duplications involving 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...
Duplication
Minor Reports
Title
Author, Year
Report Class
CNV Type
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Duplication
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
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
20199212
0
3
3
yuen_17_ASD_discovery_cases
ASD genomes (1745 ASD probands, 879 ASD-affected siblings, 1 ASD-affected father, and 1 ASD-affected grandfather) from AGRE (n=730), the AGRE; Autism Treatment Network cohort (n=192) ,the ASD: Genomes to Outcomes Study cohort (n=1421), the Baby Siblings Research Consortium (n=43), the Baby Siblings Research Consortium; The Autism Simplex Collection cohort (n=6), the Infant Sibling Study (n=62), th
2626
ASD diagnosis of research quality when meeting criteria on one (n=437) or both (n=1361) of the diagnostic measures ADI-R and ADOS; clinical diagnosis of ASD (n=819) when given by expert clinician according to DSM-IV or DSM-5
N/A
78.71% Male
21251999
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
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
yuen_17_ASD_discovery_cases
N/A
WGS
Complete Genomics, Illumina HiSeq 2000, HiSeq X
None (CNV validation not available, CNV not detected by validation method, or CNV not detected by WGS but was detected by validation methodology)
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
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000930
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
2786811
22358529
19571719
GRCh38
Duplication
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001156
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
2786811
22358529
19571719
GRCh38
Duplication
Yes
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001967
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
2787210
22302412
19515203
GRCh38
Duplication
Yes
yuen_17_ASD_discovery_cases-caseAU071203
N/A
N/A
ASD
Case cohort: AGRE. Clinical description: N/A
2781460
21739542
18958083
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
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00000930
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
SRY,RNASEH2CP1,TOMM22P2,NAP1L1P2,EEF1A1P41,AGPAT5P1,PRRC2CP1,TGIF2LY,USP12PY,RNF19BPY,RNU6-303P,SERBP1P2,RNU2-57P,VDAC1P6,EIF4A1P2,KRT18P10,SNX3P1Y,RPL26P37,DLGAP5P1,TTTY23B,TSPY2,TSPY11P,TSPY19P,LINC00280,TTTY21B,SRIP3,GOT2P5,AMELY,ATP5PFP1,GPR143P,RN7SKP282,RNU6-941P,RNU6-521P,RBMY2HP,TSPY12P,TTTY12,ZNF92P1Y,BPY2DP,ZNF736P7Y,ZNF736P9Y,TSPY24P,ZNF736P6Y,MTND6P1,MTCYBP1,MTND1P1,MTND2P3,TRIM60P3Y,ZNF736P10Y,LINC00279,TTTY19,OFD1P3Y,CDY3P,USP9YP22,ELOCP4,TTTY20,TSPY8,TSPY7P,FAM197Y6,TSPY3,FAM197Y5,TSPY1,FAM197Y4,TSPY9P,TSPY6P,TSPY10,FAM197Y1,TSPY15P,TSPY25P,TSPY16P,TTTY8,TTTY7B,TTTY21,TTTY22,RBMY2NP,TSPY18P,TSPY13P,TTTY23,RBMY2OP,TSPY20P,TSPY5P,RNA5SP518,RNA5SP519,DUX4L31,PCMTD1P1,RNA5-8SP6,C2orf27AP1,ANKRD20A6P,SNX18P1Y,DUX4L16,DUX4L17,DUX4L18,DUX4L19,PABPC1P5,ACTR3BP1,MTND1P12,RCC2P1,ASS1P6,RPS24P1,RN7SL702P,FAM8A4P,ARSEP1,SHROOM2P1,CDY4P,DPPA2P1,PSMA6P1,TMSB4Y,VCY,VCY1B,PNPLA4P1,AGKP1,MED13P1,CYCSP46,RNU6-109P,RNU6-184P,SURF6P1,ELOCP35,TUBB1P2,RNA5SP520,RNA5SP521,CLUHP1,CDY5P,ACTG1P2,USP9YP23,USP9YP27,RNU1-128P,TRAPPC2P3,OFD1P1Y,ELOCP6,CDY2B,CDY6P,USP9YP7,USP9YP6,CDY7P,USP9YP32,CDY2A,ELOCP12,TRAPPC2P8,USP9YP15,RNU1-95P,USP9YP16,XKRY2,ACTG1P11,ELOCP26,CDY9P,TAF9P2,RNA5SP522,RNA5SP523,TUBB1P1,ELOCP13,RNU1-48P,USP9YP5,XKRYP1,PRYP5,ELOCP7,USP9YP1,GPM6BP1,TTTY9B,RAB9AP4,TRAPPC2P7,GPM6BP2,USP9YP2,ELOCP14,PRYP6,XKRYP2,USP9YP10,USP9YP28,RNU1-41P,MTCYBP2,ZNF839P1,CD24P4,RNU6-255P,GAPDHP19,RCC2P2,ZNF885P,KDM5DP1,HSFY4P,GAPDHP17,TMEM167AP1,TOMM22P1,NEFLP1,PRORY,RBMY2TP,FAM197Y10,TSPY14P,ELOCP5,CDY10P,USP9YP3,USP9YP8,CDY11P,OFD1P16Y,RBMY2AP,HSFY5P,CDY12P,ELOCP15,TTTY6B,RBMY1F,RBMY1KP,TSPY22P,ZFY,ZFY-AS1,UBE2V1P3,FAM197Y9,RBMY2GP,TTTY1B,TTTY7,TTTY8B,TSPY17P,TTTY16,ZNF736P8Y,RBMY2JP,RBMY2KP,TTTY18,TTTY11,USP9YP4,RBMY1A3P,TSPY4,FAM197Y8,FAM197Y7,FAM197Y3,FAM197Y2,RBMY3AP,TTTY2,TTTY1,RBMY2QP,CDC27P2,SLC9B1P1,MXRA5Y,ARSFP1,ARSDP1,GYG2P1,MED14P1,TTTY15,DDX3Y,CASKP1,SFPQP1,TAB3P1,NLGN4Y-AS1,PUDPP1,STSP1,FAM41AY1,TAF9P1,PRYP1,XKRY,USP9YP34,CDY8P,PRYP2,CLUHP2,FAM41AY2,OFD1P4Y,HSFY1,OFD1P6Y,OFD1P7Y,BCORP1,TXLNGY,KDM5D,ZNF886P,TTTY10,TBL1YP1,RPS4Y2,RBMY2EP,RBMY1B,RBMY1A1,TTTY13,RBMY1E,OFD1P8Y,USP9YP17,PRY2,TSPY23P,RBMY2UP,TTTY5,RBMY2FP,TTTY25P,RPS4Y1,HSFY3P,LINC00278,TTTY2B,TBL1Y,RFTN1P1,XGY1,USP9Y,UTY,ANOS2P,FAM224B,OFD1P2Y,FAM224A,USP9YP14,OFD1P5Y,HSFY2,EIF1AY,RBMY1HP,RBMY1D,PCDH11Y,PRKY,NLGN4Y,TTTY14
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001156
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
SRY,RNASEH2CP1,TOMM22P2,NAP1L1P2,EEF1A1P41,AGPAT5P1,PRRC2CP1,TGIF2LY,USP12PY,RNF19BPY,RNU6-303P,SERBP1P2,RNU2-57P,VDAC1P6,EIF4A1P2,KRT18P10,SNX3P1Y,RPL26P37,DLGAP5P1,TTTY23B,TSPY2,TSPY11P,TSPY19P,LINC00280,TTTY21B,SRIP3,GOT2P5,AMELY,ATP5PFP1,GPR143P,RN7SKP282,RNU6-941P,RNU6-521P,RBMY2HP,TSPY12P,TTTY12,ZNF92P1Y,BPY2DP,ZNF736P7Y,ZNF736P9Y,TSPY24P,ZNF736P6Y,MTND6P1,MTCYBP1,MTND1P1,MTND2P3,TRIM60P3Y,ZNF736P10Y,LINC00279,TTTY19,OFD1P3Y,CDY3P,USP9YP22,ELOCP4,TTTY20,TSPY8,TSPY7P,FAM197Y6,TSPY3,FAM197Y5,TSPY1,FAM197Y4,TSPY9P,TSPY6P,TSPY10,FAM197Y1,TSPY15P,TSPY25P,TSPY16P,TTTY8,TTTY7B,TTTY21,TTTY22,RBMY2NP,TSPY18P,TSPY13P,TTTY23,RBMY2OP,TSPY20P,TSPY5P,RNA5SP518,RNA5SP519,DUX4L31,PCMTD1P1,RNA5-8SP6,C2orf27AP1,ANKRD20A6P,SNX18P1Y,DUX4L16,DUX4L17,DUX4L18,DUX4L19,PABPC1P5,ACTR3BP1,MTND1P12,RCC2P1,ASS1P6,RPS24P1,RN7SL702P,FAM8A4P,ARSEP1,SHROOM2P1,CDY4P,DPPA2P1,PSMA6P1,TMSB4Y,VCY,VCY1B,PNPLA4P1,AGKP1,MED13P1,CYCSP46,RNU6-109P,RNU6-184P,SURF6P1,ELOCP35,TUBB1P2,RNA5SP520,RNA5SP521,CLUHP1,CDY5P,ACTG1P2,USP9YP23,USP9YP27,RNU1-128P,TRAPPC2P3,OFD1P1Y,ELOCP6,CDY2B,CDY6P,USP9YP7,USP9YP6,CDY7P,USP9YP32,CDY2A,ELOCP12,TRAPPC2P8,USP9YP15,RNU1-95P,USP9YP16,XKRY2,ACTG1P11,ELOCP26,CDY9P,TAF9P2,RNA5SP522,RNA5SP523,TUBB1P1,ELOCP13,RNU1-48P,USP9YP5,XKRYP1,PRYP5,ELOCP7,USP9YP1,GPM6BP1,TTTY9B,RAB9AP4,TRAPPC2P7,GPM6BP2,USP9YP2,ELOCP14,PRYP6,XKRYP2,USP9YP10,USP9YP28,RNU1-41P,MTCYBP2,ZNF839P1,CD24P4,RNU6-255P,GAPDHP19,RCC2P2,ZNF885P,KDM5DP1,HSFY4P,GAPDHP17,TMEM167AP1,TOMM22P1,NEFLP1,PRORY,RBMY2TP,FAM197Y10,TSPY14P,ELOCP5,CDY10P,USP9YP3,USP9YP8,CDY11P,OFD1P16Y,RBMY2AP,HSFY5P,CDY12P,ELOCP15,TTTY6B,RBMY1F,RBMY1KP,TSPY22P,ZFY,ZFY-AS1,UBE2V1P3,FAM197Y9,RBMY2GP,TTTY1B,TTTY7,TTTY8B,TSPY17P,TTTY16,ZNF736P8Y,RBMY2JP,RBMY2KP,TTTY18,TTTY11,USP9YP4,RBMY1A3P,TSPY4,FAM197Y8,FAM197Y7,FAM197Y3,FAM197Y2,RBMY3AP,TTTY2,TTTY1,RBMY2QP,CDC27P2,SLC9B1P1,MXRA5Y,ARSFP1,ARSDP1,GYG2P1,MED14P1,TTTY15,DDX3Y,CASKP1,SFPQP1,TAB3P1,NLGN4Y-AS1,PUDPP1,STSP1,FAM41AY1,TAF9P1,PRYP1,XKRY,USP9YP34,CDY8P,PRYP2,CLUHP2,FAM41AY2,OFD1P4Y,HSFY1,OFD1P6Y,OFD1P7Y,BCORP1,TXLNGY,KDM5D,ZNF886P,TTTY10,TBL1YP1,RPS4Y2,RBMY2EP,RBMY1B,RBMY1A1,TTTY13,RBMY1E,OFD1P8Y,USP9YP17,PRY2,TSPY23P,RBMY2UP,TTTY5,RBMY2FP,TTTY25P,RPS4Y1,HSFY3P,LINC00278,TTTY2B,TBL1Y,RFTN1P1,XGY1,USP9Y,UTY,ANOS2P,FAM224B,OFD1P2Y,FAM224A,USP9YP14,OFD1P5Y,HSFY2,EIF1AY,RBMY1HP,RBMY1D,PCDH11Y,PRKY,NLGN4Y,TTTY14
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00001967
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
SRY,RNASEH2CP1,TOMM22P2,NAP1L1P2,EEF1A1P41,AGPAT5P1,PRRC2CP1,TGIF2LY,USP12PY,RNF19BPY,RNU6-303P,SERBP1P2,RNU2-57P,VDAC1P6,EIF4A1P2,KRT18P10,SNX3P1Y,RPL26P37,DLGAP5P1,TTTY23B,TSPY2,TSPY11P,TSPY19P,LINC00280,TTTY21B,SRIP3,GOT2P5,AMELY,ATP5PFP1,GPR143P,RN7SKP282,RNU6-941P,RNU6-521P,RBMY2HP,TSPY12P,TTTY12,ZNF92P1Y,BPY2DP,ZNF736P7Y,ZNF736P9Y,TSPY24P,ZNF736P6Y,MTND6P1,MTCYBP1,MTND1P1,MTND2P3,TRIM60P3Y,ZNF736P10Y,LINC00279,TTTY19,OFD1P3Y,CDY3P,USP9YP22,ELOCP4,TTTY20,TSPY8,TSPY7P,FAM197Y6,TSPY3,FAM197Y5,TSPY1,FAM197Y4,TSPY9P,TSPY6P,TSPY10,FAM197Y1,TSPY15P,TSPY25P,TSPY16P,TTTY8,TTTY7B,TTTY21,TTTY22,RBMY2NP,TSPY18P,TSPY13P,TTTY23,RBMY2OP,TSPY20P,TSPY5P,RNA5SP518,RNA5SP519,DUX4L31,PCMTD1P1,RNA5-8SP6,C2orf27AP1,ANKRD20A6P,SNX18P1Y,DUX4L16,DUX4L17,DUX4L18,DUX4L19,PABPC1P5,ACTR3BP1,MTND1P12,RCC2P1,ASS1P6,RPS24P1,RN7SL702P,FAM8A4P,ARSEP1,SHROOM2P1,CDY4P,DPPA2P1,PSMA6P1,TMSB4Y,VCY,VCY1B,PNPLA4P1,AGKP1,MED13P1,CYCSP46,RNU6-109P,RNU6-184P,SURF6P1,ELOCP35,TUBB1P2,RNA5SP520,RNA5SP521,CLUHP1,CDY5P,ACTG1P2,USP9YP23,USP9YP27,RNU1-128P,TRAPPC2P3,OFD1P1Y,ELOCP6,CDY2B,CDY6P,USP9YP7,USP9YP6,CDY7P,USP9YP32,CDY2A,ELOCP12,TRAPPC2P8,USP9YP15,RNU1-95P,USP9YP16,XKRY2,ACTG1P11,ELOCP26,CDY9P,TAF9P2,RNA5SP522,RNA5SP523,TUBB1P1,ELOCP13,RNU1-48P,USP9YP5,XKRYP1,PRYP5,ELOCP7,USP9YP1,GPM6BP1,TTTY9B,RAB9AP4,TRAPPC2P7,GPM6BP2,USP9YP2,ELOCP14,PRYP6,XKRYP2,USP9YP10,USP9YP28,RNU1-41P,MTCYBP2,ZNF839P1,CD24P4,RNU6-255P,GAPDHP19,RCC2P2,ZNF885P,KDM5DP1,HSFY4P,GAPDHP17,TMEM167AP1,TOMM22P1,NEFLP1,PRORY,RBMY2TP,FAM197Y10,TSPY14P,ELOCP5,CDY10P,USP9YP3,USP9YP8,CDY11P,OFD1P16Y,RBMY2AP,HSFY5P,CDY12P,ELOCP15,TTTY6B,RBMY1F,RBMY1KP,ZFY,ZFY-AS1,UBE2V1P3,FAM197Y9,RBMY2GP,TTTY1B,TTTY7,TTTY8B,TSPY17P,TTTY16,ZNF736P8Y,RBMY2JP,RBMY2KP,TTTY18,TTTY11,USP9YP4,RBMY1A3P,TSPY4,FAM197Y8,FAM197Y7,FAM197Y3,FAM197Y2,RBMY3AP,TTTY2,TTTY1,RBMY2QP,CDC27P2,SLC9B1P1,MXRA5Y,ARSFP1,ARSDP1,GYG2P1,MED14P1,TTTY15,DDX3Y,CASKP1,SFPQP1,TAB3P1,NLGN4Y-AS1,PUDPP1,STSP1,FAM41AY1,TAF9P1,PRYP1,XKRY,USP9YP34,CDY8P,PRYP2,CLUHP2,FAM41AY2,OFD1P4Y,HSFY1,OFD1P6Y,OFD1P7Y,BCORP1,TXLNGY,KDM5D,ZNF886P,TTTY10,TBL1YP1,RPS4Y2,RBMY2EP,RBMY1B,RBMY1A1,TTTY13,RBMY1E,OFD1P8Y,USP9YP17,PRY2,TSPY23P,RBMY2UP,TTTY5,RPS4Y1,HSFY3P,LINC00278,TTTY2B,TBL1Y,RFTN1P1,XGY1,USP9Y,UTY,ANOS2P,FAM224B,OFD1P2Y,FAM224A,USP9YP14,OFD1P5Y,HSFY2,EIF1AY,RBMY1HP,RBMY1D,PCDH11Y,PRKY,NLGN4Y,TTTY14
yuen_17_ASD_discovery_cases-caseAU071203
Not available
De novo
Multiplex
Not segregated
RNU6-1334P,SRY,RNASEH2CP1,TOMM22P2,NAP1L1P2,EEF1A1P41,AGPAT5P1,PRRC2CP1,TGIF2LY,USP12PY,RNF19BPY,RNU6-303P,SERBP1P2,RNU2-57P,VDAC1P6,EIF4A1P2,KRT18P10,SNX3P1Y,RPL26P37,DLGAP5P1,TTTY23B,TSPY2,TSPY11P,TSPY19P,LINC00280,TTTY21B,SRIP3,GOT2P5,AMELY,ATP5PFP1,GPR143P,RN7SKP282,RNU6-941P,RNU6-521P,RBMY2HP,TSPY12P,TTTY12,ZNF92P1Y,BPY2DP,ZNF736P7Y,ZNF736P9Y,TSPY24P,ZNF736P6Y,MTND6P1,MTCYBP1,MTND1P1,MTND2P3,TRIM60P3Y,ZNF736P10Y,LINC00279,TTTY19,OFD1P3Y,CDY3P,USP9YP22,ELOCP4,TTTY20,TSPY8,TSPY7P,FAM197Y6,TSPY3,FAM197Y5,TSPY1,FAM197Y4,TSPY9P,TSPY6P,TSPY10,FAM197Y1,TSPY15P,TSPY25P,TSPY16P,TTTY8,TTTY7B,TTTY21,TTTY22,RBMY2NP,TSPY18P,TSPY13P,TTTY23,RBMY2OP,TSPY20P,TSPY5P,RNA5SP518,RNA5SP519,DUX4L31,PCMTD1P1,RNA5-8SP6,C2orf27AP1,ANKRD20A6P,SNX18P1Y,DUX4L16,DUX4L17,DUX4L18,DUX4L19,PABPC1P5,ACTR3BP1,MTND1P12,RCC2P1,ASS1P6,RPS24P1,RN7SL702P,FAM8A4P,ARSEP1,SHROOM2P1,CDY4P,DPPA2P1,PSMA6P1,TMSB4Y,VCY,VCY1B,PNPLA4P1,AGKP1,MED13P1,CYCSP46,RNU6-109P,RNU6-184P,SURF6P1,ELOCP35,TUBB1P2,RNA5SP520,RNA5SP521,CLUHP1,CDY5P,ACTG1P2,USP9YP23,USP9YP27,RNU1-128P,TRAPPC2P3,OFD1P1Y,ELOCP6,CDY2B,CDY6P,USP9YP7,USP9YP6,CDY7P,USP9YP32,CDY2A,ELOCP12,TRAPPC2P8,USP9YP15,RNU1-95P,USP9YP16,XKRY2,ACTG1P11,ELOCP26,CDY9P,TAF9P2,RNA5SP522,RNA5SP523,TUBB1P1,ELOCP13,RNU1-48P,USP9YP5,XKRYP1,PRYP5,ELOCP7,USP9YP1,GPM6BP1,TTTY9B,RAB9AP4,TRAPPC2P7,GPM6BP2,USP9YP2,ELOCP14,PRYP6,XKRYP2,USP9YP10,USP9YP28,RNU1-41P,MTCYBP2,ZNF839P1,CD24P4,RNU6-255P,GAPDHP19,RCC2P2,ZNF885P,KDM5DP1,HSFY4P,GAPDHP17,TMEM167AP1,TOMM22P1,NEFLP1,PRORY,RBMY2TP,FAM197Y10,TSPY14P,ELOCP5,CDY10P,USP9YP3,USP9YP8,CDY11P,ZFY,ZFY-AS1,UBE2V1P3,FAM197Y9,RBMY2GP,TTTY1B,TTTY7,TTTY8B,TSPY17P,TTTY16,ZNF736P8Y,RBMY2JP,RBMY2KP,TTTY18,TTTY11,USP9YP4,RBMY1A3P,TSPY4,FAM197Y8,FAM197Y7,FAM197Y3,FAM197Y2,RBMY3AP,TTTY2,TTTY1,RBMY2QP,CDC27P2,SLC9B1P1,MXRA5Y,ARSFP1,ARSDP1,GYG2P1,MED14P1,TTTY15,DDX3Y,CASKP1,SFPQP1,TAB3P1,NLGN4Y-AS1,PUDPP1,STSP1,FAM41AY1,TAF9P1,PRYP1,XKRY,USP9YP34,CDY8P,PRYP2,CLUHP2,FAM41AY2,OFD1P4Y,HSFY1,OFD1P6Y,OFD1P7Y,BCORP1,TXLNGY,KDM5D,ZNF886P,TTTY10,TBL1YP1,RPS4Y2,RBMY2EP,RBMY1B,RBMY1A1,TTTY13,RPS4Y1,HSFY3P,LINC00278,TTTY2B,TBL1Y,RFTN1P1,XGY1,USP9Y,UTY,ANOS2P,FAM224B,OFD1P2Y,FAM224A,USP9YP14,OFD1P5Y,HSFY2,EIF1AY,RBMY1HP,PCDH11Y,PRKY,NLGN4Y,TTTY14
Controls
No Control Data Available
No Animal Model Data Available