416 genes and genomic entities tagged
“watchlist”
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416 genes and genomic entities
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- AARS
- ADAM22
- ADD1
- ADPRHL2
- AIFM1
- AJAP1
- AKT1
- AMBRA1
- AMTN
- ANGPT1
- AP2S1
- AP3B2
- AQP1
- ARAP3
- ARCN1
- ARHGAP35
- ARHGEF40
- ARL3
- ARX
- ATAD3A
- ATN1_CAG
- ATP11A
- ATP5A1
- ATP6AP1
- ATP6AP2
- ATPAF2
- ATXN1_CAG
- ATXN2L
- ATXN3_CAG
- B3GNT2
- B9D1
- BACE2
- BCORL1
- BCS1L
- BHLHE22
- BLOC1S1
- BMP2
- BORCS8
- BRD4
- CACNA1E
- CACNA2D1
- CACNB2
- CAPN15
- CAPNS1
- CAPRIN1
- CASK
- CCDC186
- CCDC32
- CCDC88C
- CDC40
- CDK5RAP2
- CDKN1A
- CDKN2B
- CDKN2C
- CDON
- CDX2
- CELSR3
- CHD5
- CHP1
- CHRM1
- CLIC2
- CLPP
- CNP
- CNTN1
- COASY
- COCH
- COL4A3
- COLGALT1
- COPB1
- COQ9
- COX16
- CPA1
- CRBN
- CRELD1
- CRMP1
- CST3
- CSTB_CCCCGCCCCGCG
- CTGF
- CYP27A1
- CYS1
- DACT1
- DALRD3
- DCC
- DCHS1
- DCHS2
- DDX59
- DEAF1
- DENND3
- DHCR24
- DHCR7
- DHX16
- DIAPH1
- DLAT
- DLG1
- DLL1
- DNAH5
- DNAH6
- DONSON
- DPM1
- DPM3
- DPT
- DTNA
- DYNC1I2
- EBP
- ECE1
- EEF1B2
- EIF2S3
- EIF4ENIF1
- ELK1
- EMG1
- EN1
- EOMES
- EPB41L1
- EPHA7
- EPHB4
- ERGIC3
- ERMARD
- ESR2
- EXOC3L2
- EXOC7
- FAAH2
- FAM120C
- FAM136A
- FARSA
- FAT2
- FAT4
- FBXO11
- FBXW7
- FCGR2A
- FCGR3A
- FDFT1
- FGF14_TTC
- FGF23
- FICD
- FILIP1
- FOXD2
- FRY
- FRYL
- FTO
- FXN_GAA
- GALM
- GAS2L2
- GATA1
- GDF6
- GDNF
- GFRA1
- GIMAP5
- GLIS2
- GLS
- GMNN
- GNAL
- GPKOW
- GREM1
- GSPT2
- GTPBP3
- GYG1
- HAX1
- HCCS
- HDAC6
- HEATR3
- HEATR5B
- HIRA
- HIST1H4J
- HNRNPD
- HOXA1
- HS2ST1
- HSCB
- HSPD1
- HTT
- ICK
- IFIH1
- IFT81
- IGF2
- IGSF10
- IL17RA
- IL27RA
- IPO8
- IQSEC1
- ISCA-37423-Gain
- ISPD
- ITGB4
- ITPR1
- IVNS1ABP
- JAG1
- JAKMIP1
- JMJD1C
- KATNB1
- KCNK4
- KCNN3
- KDM1A
- KDM3B
- KHDC3L
- KHDRBS1
- KIF14
- KIF3B
- KIF5B
- KIF7
- KITLG
- KMT2C
- KRT83
- LAMC2
- LARGE1
- LAS1L
- LAT
- LEFTY2
- LIG3
- LINGO1
- LIPT2
- LMAN2L
- LMNB1
- LNPK
- LSM7
- LSR
- LZTFL1
- MACC1
- MAFB
- MAGEL2
- MANBA
- MAPK10
- MARS
- MAST1
- MED13L
- MED17
- MIR17HG
- MITF
- MMP15
- MRE11
- MSH5
- MT-ND6
- MTMR14
- MYBPC3
- MYCN
- MYH10
- MYH14
- MYLPF
- MYOD1
- NAA15
- NAXD
- NCAPD2
- NCAPH
- NCLN
- NDUFAF1
- NDUFAF4
- NDUFS7
- NDUFV2
- NEFL
- NEK1
- NFIB
- NKX2-1
- NLRP2
- NMNAT1
- NOP56_GGCCTG
- NOS3
- NOTCH3
- NPC1
- NRCAM
- NRG1
- NUAK2
- NUP62
- NUP88
- NUP98
- NXN
- P4HB
- PAK2
- PAM16
- PANK4
- PARP6
- PAX8
- PBX1
- PCGF2
- PDCD6IP
- PDSS1
- PEX11A
- PEX5
- PGRMC1
- PHC1
- PI4KA
- PIGS
- PIGV
- PISD
- PLEKHM1
- PLK4
- PLXNA2
- PLXNB2
- PNLIP
- POLR2C
- POLR3H
- POLR3K
- PPP1R12A
- PPP1R13L
- PPP1R35
- PPP2R2B_CAG
- PRDM13
- PRKACB
- PRKCB
- PRRT2
- PSPH
- PTCH2
- PTF1A
- PTPMT1
- PTPN13
- PTPN14
- PTPRJ
- PYGM
- RAD51C
- RAP1B
- RAX
- RHBDF1
- RHEB
- RIC1
- RIPOR2
- RMI1
- RNPC3
- ROBO1
- RORC
- RPL15
- RPL26
- RPS15
- RPS23
- RPS27A
- RPS29
- SART3
- SCN5A
- SCYL2
- SEC24D
- SEC31A
- SEC61B
- SEMA3C
- SEMA3D
- SHH
- SHROOM3
- SHROOM4
- SIK3
- SIPA1L3
- SLC17A9
- SLC25A42
- SLC26A6
- SLC30A5
- SLC35A1
- SLC35A3
- SLC45A1
- SLC6A6
- SLC9A7
- SMARCAD1
- SMARCD2
- SMG9
- SNAI2
- SNX27
- SOBP
- SPINT2
- SPTBN2
- SPTBN4
- SPTLC1
- SRGAP3
- SRP54
- SRP72
- STX3
- SUCLG1
- SUFU
- SVIL
- SYT2
- TAF13
- TARS
- TBATA
- TBC1D20
- TBCB
- TBCE
- TBP_CAG
- TBX1
- TCF12
- TCIRG1
- TCTN1
- TERT
- TET3
- TFAP2A
- TKFC
- TKT
- TMEM132E
- TMPRSS9
- TNK2
- TOGARAM1
- TRAF7
- TRAPPC10
- TREX1
- TRIP13
- TSEN15
- TSEN34
- TSFM
- TSPAN8
- TUBA8
- TUBB
- TUBGCP4
- TWIST2
- UCP2
- UFC1
- UQCC3
- UQCRC1
- VAMP1
- VCL
- VLDLR
- VWA8
- WDR11
- WDR81
- WFS1
- WNK3
- WNT2B
- WNT9B
- WSB2
- YARS
- YIF1B
- ZAP70
- ZBTB11
- ZCCHC8
- ZNF141
- ZNF668
- ZSWIM6
Tagged
- adult-onset
- age-specific-variation
- Autism Spectrum Disorder
- chimeric-gene
- cnv
- condition_removed
- curated_removed
- curated-variant-list
- current
- currently-ngs-unreportable
- dd_review
- deletions
- de novo
- digenic
- disputed
- dominant-negative
- drug-dosing
- drug-toxicity
- early-onset
- ensembl_ids_known_missing
- founder-effect
- gene-checked
- gene-duplication
- gene-therapy-trial
- internal_inclusion_list_only
- locus-type-immunoglobulin-gene
- locus-type-phenotype-only
- locus-type-pseudogene
- locus-type-rna-long-non-coding
- locus-type-rna-micro
- locus-type-rna-misc
- locus-type-rna-ribosomal
- locus-type-rna-small-nuclear
- locus-type-rna-transfer
- locus-type-rna-vault
- locus-type-small-nucleolar
- locus-type-T-cell-receptor-gene
- locus-type-unknown
- microdeletion
- microduplication
- missense
- monogenic-polygenic
- mosaicism
- multifactorial
- new-gene-name
- ngs-false-positive-region
- NGS Not Validated
- non-coding-known-pathogenic
- nucleotide-repeat-expansion
- pathogenic-synonymous
- pharmacogenetics
- polygenic
- prognosis
- promoter
- Pseudoautosomal region 1
- Pseudoautosomal region 2
- Q1_26_demote_amber
- Q1_26_demote_red
- Q1_26_expert_review
- Q1_26_MOI
- Q1_26_NHS_review
- Q1_26_promote_green
- Q2_26_demote_amber
- Q2_26_demote_red
- Q2_26_expert_review
- Q2_26_MOI
- Q2_26_NHS_review
- Q2_26_promote_green
- Q3_25_demote_red
- Q3_25_expert_review
- Q3_25_MOI
- Q3_25_NHS_review
- Q3_25_promote_green
- Q4_25_demote_amber
- Q4_25_demote_red
- Q4_25_expert_review
- Q4_25_MOI
- Q4_25_NHS_review
- Q4_25_promote_green
- recurrent-variant
- refuted
- regulatory-region
- Skewed X-inactivation
- somatic
- special_caller_only
- special_consideration
- STR
- structural-variant
- sva
- technical-limitations
- to_be_confirmed_NHSE
- treatable
- watchlist
- watchlist_moi
- x-linked-over-dominance
- y-chromosome