- Panels
- Arthrogryposis
- EXOSC9
Genes in panel
- ACTA1 4
- ACTC1 1
- ADAMTS10 1
- ADAMTS15 2
- ADCY6 4
- ADGRG6 1
- ALG3 2
- ANTXR2 1
- ASCC1 2
- ASXL1 2
- ATP1A2 3
- B3GALNT2 3
- B4GAT1 3
- BICD2 3
- CACNA1E 2
- CHAT 1
- CHRNA1 1
- CHRNB1 1
- CHRND 1
- CHRNE 1
- CHRNG 1
- CHST14 1
- CNTNAP1 1
- COASY 4
- COL12A1 2
- COL25A1 2
- COL6A1 4
- COL6A2 2
- COL6A3 2
- COLQ 1
- CRLF1 1
- DAG1 2
- DHCR24 2
- DNM2 2
- DOK7 1
- DPAGT1 3
- DST 3
- DYNC1H1 2
- EBP 3
- ECEL1 2
- ERBB3 4
- ERCC1 4
- ERCC5 4
- ERCC6 1
- ERCC8 1
- ERGIC1 3
- EXOSC3 1
- FAM20C 1
- FBN2 3
- FGFR2 2
- FGFR3 2
- FILIP1 4
- FKBP10 1
- FKRP 2
- FKTN 2
- FLNA 3
- FLNB 1
- FLNC 4
- GBA 2
- GBE1 1
- GLDN 1
- GLE1 2
- GMPPB 2
- HSPG2 1
- IRF6 1
- ISPD 3
- KAT6B 1
- KCNK3 2
- KIAA1109 1
- KIDINS220 3
- KIF21A 4
- KLHL40 1
- KLHL41 1
- KLHL7 1
- LAMA2 2
- LARGE1 3
- LGI3 2
- LGI4 1
- LMOD3 1
- LMX1B 4
- MAGEL2 2
- MED12 4
- MET 3
- MTM1 1
- MUSK 1
- MYBPC1 2
- MYH3 5
- MYH8 1
- MYMK 1
- NALCN 1
- NEB 1
- NEK9 4
- ORAI1 2
- PEX1 1
- PEX10 1
- PEX11B 1
- PEX12 1
- PEX13 1
- PEX14 1
- PEX16 1
- PEX19 0
- PEX2 1
- PEX26 1
- PEX3 1
- PEX5 1
- PEX6 3
- PEX7 1
- PFKM 1
- PIEZO2 3
- PIP5K1C 5
- PLOD1 1
- PLOD2 1
- POMGNT1 2
- POMGNT2 3
- POMK 2
- POMT1 2
- POMT2 2
- POR 1
- PRG4 1
- RAPSN 1
- RIPK4 1
- RYR1 2
- SCARF2 1
- SCN1A 3
- SCN4A 4
- SELENON 6
- SKI 1
- SLC18A3 4
- SLC29A3 3
- SLC35A3 4
- SLC5A7 1
- SLC6A9 4
- SMAD3 2
- SMAD4 1
- SMN1 3
- SMPD4 2
- STAC3 2
- STIM1 3
- SYNE1 5
- TGFB2 1
- TGFB3 1
- TGFBR1 1
- TGFBR2 1
- TMEM5 4
- TNNI2 2
- TNNT1 1
- TNNT3 2
- TOR1A 2
- TOR1AIP1 4
- TPM2 3
- TPM3 1
- TRPV4 1
- TSEN54 1
- TTN 3
- UBA1 1
- VAMP1 1
- VIPAS39 2
- VPS33B 2
- ZC4H2 2
- ZMPSTE24 1
- AGRN 2
- ATAD1 2
- BORCS5 1
- CIAO1 2
- CNTN1 4
- DDR2 1
- DPM2 2
- MYLPF 4
- MYOD1 2
- NRDC 1
- NUP88 2
- SCYL2 2
- SENP7 1
- SVIL 3
- TRIP4 5
- ABHD5 1
- ACADM 1
- ACADS 0
- ACADVL 0
- ADSL 0
- AGL 0
- AIMP1 0
- ALG14 0
- ALG2 1
- ANO5 2
- ANXA3 1
- ATP2A1 1
- BAG3 1
- BIN1 1
- C12orf65 2
- CAMLG 1
- CAPN3 0
- CAV3 0
- CCDC47 2
- CCDC78 0
- CEP55 1
- CFL2 1
- CHCHD10 0
- CHKB 2
- CHMP1A 1
- CLCF1 0
- COL4A1 2
- COL4A2 1
- COL9A3 0
- CPT2 1
- CRYAB 1
- CTDP1 1
- CUL4B 0
- DES 1
- DMD 2
- DMPK 2
- DNAJB6 1
- DOLK 2
- DPM1 2
- DPM3 1
- DUX4 2
- DYSF 2
- EGR2 0
- EMD 3
- ETFA 1
- ETFB 1
- ETFDH 1
- EXOSC9 1
- FAM111B 1
- FHL1 1
- FKBP14 1
- GAA 1
- GARS 2
- GDAP1 1
- GFER 1
- GFM2 1
- GFPT1 1
- GNE 1
- GRN 1
- HADH 1
- HADHA 1
- HADHB 1
- HNRNPA1 1
- HRAS 1
- IBA57 1
- IGHMBP2 1
- ISCU 1
- ISLR2 2
- ITGA7 2
- KBTBD13 1
- KIF26B 2
- KIF5C 1
- L1CAM 2
- LAMP2 1
- LDB3 1
- LMNA 3
- LPIN1 1
- MATR3 1
- MEGF10 1
- MFN2 1
- MICU1 2
- MPZ 1
- MTMR1 1
- MT-TL1 1
- MYF6 1
- MYH14 1
- MYH2 3
- MYH7 4
- MYL1 4
- MYO9A 1
- MYOT 1
- NEFL 1
- PABPN1 3
- PI4KA 1
- PIGS 1
- PLEC 2
- PNPLA2 1
- POLG 1
- PSD3 1
- PUS1 1
- PYGM 1
- RBCK1 1
- RRM2B 1
- SGCA 1
- SGCB 1
- SGCD 1
- SGCG 1
- SIL1 1
- SLC22A5 1
- SLC25A4 1
- SLC25A42 1
- SLC52A3 1
- SMCHD1 3
- STIM2 1
- SYNE2 3
- SYT2 1
- TBCD 3
- TCAP 2
- TIA1 1
- TK2 1
- TMEM43 2
- TRIM32 0
- TSEN2 1
- TSEN34 1
- UNC50 1
- UTRN 0
- VCP 1
- VPS8 1
- YARS2 1
- ZNF335 1
STRs in panel
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Regions in panel
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Arthrogryposis
Gene: EXOSC9 Red List (low evidence)
EXOSC9 (exosome component 9)
EnsemblGeneIds (GRCh38): ENSG00000123737
EnsemblGeneIds (GRCh37): ENSG00000123737
OMIM: 606180, Gene2Phenotype
EXOSC9 is in 4 panels
EnsemblGeneIds (GRCh38): ENSG00000123737
EnsemblGeneIds (GRCh37): ENSG00000123737
OMIM: 606180, Gene2Phenotype
EXOSC9 is in 4 panels
1 review
Rebecca Foulger (Genomics England curator)
I don't know
Added to Arthrogryposis panel as suggested by Zerin Hyder (Genomics England Clinical Team).Created: 26 Nov 2019, 3:16 p.m. | Last Modified: 26 Nov 2019, 3:16 p.m.
Panel Version: 2.64
Created: 26 Nov 2019, 3:16 p.m.
Last Modified: 26 Nov 2019, 3:16 p.m.
Panel version: 2.64
Last Modified: 26 Nov 2019, 3:16 p.m.
Panel version: 2.64
Details
- Sources
-
- Expert Review Red
- OMIM
- 606180
- Clinvar variants
- Variants in EXOSC9
- Penetrance
- None
- Panels with this gene
History Filter Activity
26 Nov 2019, Gel status: 1
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: EXOSC9 was added gene: EXOSC9 was added to Arthrogryposis. Sources: Expert Review Red Mode of inheritance for gene: EXOSC9 was set to