117 genes and genomic entities tagged
“Q3_25_promote_green”
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117 genes and genomic entities
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- ACOX2
- ADSSL1
- AIFM1
- ANXA11
- AP1B1
- ARHGAP19
- ARSG
- ATAD3A
- BRSK1
- CASQ1
- CCT6A
- CD2AP
- CDK5
- CDK9
- CMPK2
- COX18
- CPOX
- CRNKL1
- CTGF
- CYP2U1
- DHX38
- DISP1
- DPP9
- DST
- DYRK1A
- EFEMP1
- ELFN1
- ERCC1
- EXOSC8
- FBXL4
- FGF4
- FICD
- FLII
- FLVCR1
- FRMD7
- GLA
- GPKOW
- GUK1
- HAVCR2
- HEATR5B
- HGF
- HSD11B2
- IFNAR1
- INPP4A
- IRF1
- ISCA-37446-Loss
- ISCA-37448-Loss
- ISCA-37498-Loss
- ISCA-46296-Loss
- ISCA-46300-Loss
- ISL1
- ITCH
- KCND3
- KDF1
- KDM1A
- KIAA0391
- KIAA0556
- KLHL24
- LAMC3
- LINC01081
- LINC01082
- LSS
- MC4R
- MED12L
- MED16
- MSH3
- MT-TK
- MTO1
- NAXD
- NF1
- NFIA
- NOTCH3
- NR6A1
- OGDHL
- PAX6
- PDE12
- PDE1B
- PKD2
- PLD1
- POC5
- POT1
- PPOX
- PTBP1
- PTRH2
- RBFOX2
- RCC1
- RNU4-2
- RNU5B-1
- RNU6-1
- RNU6-2
- RNU6-8
- RNU6-9
- RPL3L
- RREB1
- SF1
- SGCG
- SLC30A2
- SLC39A4
- SLC46A1
- SOD1
- SPG11
- SPTLC1
- SPTLC2
- TANGO2
- TDP1
- TMEFF1
- TMEM167A
- TNR
- TTC19
- UBR5
- UGGT1
- UNC13A
- UNC45A
- UPF1
- VIPAS39
- VSX2
- WARS
Tagged
- adult-onset
- age-specific-variation
- Autism Spectrum Disorder
- chimeric-gene
- cnv
- condition_removed
- curated_removed
- curated-variant-list
- currently-ngs-unreportable
- currently-not-available-via-GLH-non-WGS-testing
- dd_review
- deletions
- de novo
- digenic
- disputed
- dominant-negative
- drug-dosing
- drug-toxicity
- early-onset
- ensembl_ids_known_missing
- for-review
- founder-effect
- gene
- gene-checked
- gene-duplication
- gene-therapy-trial
- internal_inclusion_list_only
- loc
- 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
- nested STR
- new
- 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_25_ demote_red
- Q1_25_ expert_review
- Q1_25_ MOI
- Q1_25_ NHS_review
- Q1_25_ promote_green
- Q1_26_demote_amber
- Q1_26_demote_red
- Q1_26_expert_review
- Q1_26_MOI
- Q1_26_NHS_review
- Q1_26_promote_green
- Q2_25_ demote_amber
- Q2_25_ demote_red
- Q2_25_expert_review
- Q2_25_ MOI
- Q2_25_ NHS_review
- Q2_25_ phenotype
- Q2_25_ promote_green
- Q3_24_demote_red
- Q3_24_expert_review
- Q3_24_MOI
- Q3_24_NHS_review
- Q3_24_promote_green
- Q3_25_demote_amber
- Q3_25_demote_red
- Q3_25_expert_review
- Q3_25_MOI
- Q3_25_NHS_review
- Q3_25_promote_green
- Q4_24_demote_red
- Q4_24_expert_review
- Q4_24_MOI
- Q4_24_NHS_review
- Q4_24_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
- spec
- 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