- Panels
- Clefting disorders
- DLG1
Genes in panel
- ACTB 0
- ACTG1 0
- ALX1 2
- AMER1 0
- AMOTL1 2
- ANKRD11 0
- ARCN1 1
- ARHGAP29 1
- ARHGAP31 0
- ASXL1 0
- B3GLCT 0
- BCOR 0
- BMP2 0
- BMP4 1
- C2CD3 0
- C5orf42 0
- CC2D2A 0
- CDH1 1
- CDKN1C 0
- CHD7 0
- CHRNG 0
- CHST14 0
- CNTNAP1 1
- COL11A1 0
- COL11A2 0
- COL2A1 0
- COL9A1 0
- COLEC10 0
- COLEC11 0
- CREBBP 1
- CTCF 1
- CTNND1 1
- DHCR7 0
- DHODH 1
- DLL4 0
- DOCK6 0
- DVL1 0
- DVL3 0
- DYNC2H1 0
- DYNC2LI1 0
- EBP 0
- EDNRA 0
- EFNB1 1
- EFTUD2 0
- EIF2S3 0
- EIF3F 1
- EIF4A3 1
- EOGT 0
- EPG5 0
- ESCO2 1
- EYA1 0
- FAM20C 0
- FGD1 0
- FGFR1 0
- FGFR2 0
- FLNA 0
- FLNB 0
- FOXC2 0
- FOXE1 1
- FRAS1 0
- GDF11 2
- GJA1 0
- GLI2 1
- GLI3 0
- GNB1 1
- GPC3 0
- GRHL3 1
- HDAC8 0
- HNRNPK 1
- HYAL2 2
- HYLS1 0
- ICK 0
- IFT140 0
- IFT172 0
- IFT80 0
- IGF2 1
- IMPAD1 0
- INTS13 1
- IRF6 0
- KAT6A 0
- KAT6B 1
- KCNJ2 0
- KDM6A 0
- KIAA0586 0
- KIF1BP 0
- KIF7 0
- KMT2D 0
- MAP3K7 0
- MAPRE2 0
- MASP1 1
- MBTPS2 0
- MED12 2
- MEIS2 0
- MID1 0
- MKS1 0
- MSX1 0
- MYMK 1
- NECTIN1 1
- NEDD4L 0
- NEK1 1
- NIPBL 0
- NOTCH1 0
- OFD1 0
- PAX3 0
- PGAP3 1
- PGM1 2
- PHF8 2
- PIEZO2 0
- PIGN 0
- PIGV 0
- PLCB4 1
- POLR1A 1
- POLR1C 0
- POLR1D 0
- PORCN 0
- PPP1R13L 2
- PTCH1 0
- RAB34 1
- RBM10 1
- RIC1 1
- RIPK4 1
- ROR2 0
- RPL5 0
- RPS26 0
- RSPO2 1
- SALL4 0
- SATB2 1
- SCARF2 0
- SF3B2 1
- SF3B4 0
- SHH 0
- SIX1 0
- SIX3 0
- SKI 0
- SLC26A2 0
- SMAD3 0
- SMAD4 0
- SMARCA4 1
- SMC1A 0
- SMC3 0
- SMS 1
- SNRPB 0
- SON 0
- SOX9 0
- SPECC1L 0
- STAG2 1
- STAMBP 0
- TBX1 1
- TBX22 0
- TCOF1 0
- TCTN3 0
- TELO2 0
- TFAP2A 0
- TGDS 0
- TGFB3 0
- TGFBR1 0
- TGFBR2 0
- TMCO1 0
- TP63 0
- TRAPPC9 0
- TRIM37 0
- TRRAP 1
- TUBB 0
- TXNL4A 1
- USP9X 1
- WNT5A 0
- XYLT1 0
- YAP1 1
- ZC4H2 1
- ZEB2 1
- ZIC2 0
- ZIC3 0
- ZRSR2 2
- ZSWIM6 0
- ALX3 2
- ANKRD17 3
- ARHGEF38 1
- ARID1A 1
- ARID1B 1
- ATR 0
- AUTS2 1
- B3GALT6 0
- B4GALT7 1
- BUB1B 0
- CDC45 0
- CHD4 1
- COBLL1 1
- COL9A2 1
- COL9A3 1
- CRELD1 1
- DDX3X 0
- DDX59 0
- EDN1 1
- ESRP2 1
- FBRSL1 1
- FBXO11 1
- FGFR3 1
- FTO 0
- GATA3 0
- IFT52 0
- KAT5 1
- KDM1A 0
- KMT2A 1
- LMNA 0
- LRP6 1
- LRRC32 1
- MED13L 1
- MED25 0
- MEOX1 0
- MN1 1
- NOTCH2 1
- PHGDH 0
- PLCH1 1
- PLEKHA5 2
- PLEKHA7 1
- POGZ 1
- RARB 0
- RBPJ 0
- RPL11 1
- RPS28 1
- SCUBE3 1
- SEC23A 0
- SEPT9 1
- SHROOM3 1
- SMARCB1 1
- SMG9 0
- TBX15 0
- TTC21B 0
- UBE3B 1
- WDR19 0
- WDR34 0
- WDR35 0
- WDR60 0
- ZMPSTE24 0
- ACBD5 1
- AFDN 1
- ALG9 0
- ATRX 0
- B3GAT3 0
- CANT1 0
- CASK 0
- CHD1 1
- CHSY1 0
- CKAP2L 0
- DIS3L2 0
- DLG1 0
- DLX4 1
- DNMT3B 0
- FAM111A 0
- FANCL 0
- FOXP2 1
- FREM2 0
- FST 1
- GATA6 0
- GDF1 0
- GMNN 0
- GNAI3 1
- GRIP1 0
- HOXA2 1
- INTS1 1
- KANSL1 0
- KIF22 0
- LMX1B 0
- METTL23 0
- MYCN 1
- NBN 0
- NKX2-5 0
- NKX2-6 0
- NSDHL 0
- PGAP2 0
- PIGA 0
- PIGL 0
- PIK3R2 0
- POMT1 0
- POMT2 0
- PQBP1 0
- PSAT1 0
- PTDSS1 0
- RAI1 0
- RBM8A 0
- RPS17 0
- RPS19 0
- RYR1 1
- SEC24D 1
- SELENOI 1
- SIX5 1
- SMAD2 0
- SMOC1 0
- SOX2 0
- STIL 0
- STRA6 0
- STXBP1 0
- SUMO1 0
- TAF11 1
- TBX2 1
- TFAP2B 1
- TGFB2 0
- TOGARAM1 1
- TSR2 1
- TWIST2 0
- UQCC2 0
- VAX1 0
- WASHC5 0
- WNT3 0
- ZBTB24 1
- ZNF3 1
STRs in panel
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Clefting disorders
Gene: DLG1 Red List (low evidence)
DLG1 (discs large MAGUK scaffold protein 1)
EnsemblGeneIds (GRCh38): ENSG00000075711
EnsemblGeneIds (GRCh37): ENSG00000075711
OMIM: 601014, Gene2Phenotype
DLG1 is in 2 panels
EnsemblGeneIds (GRCh38): ENSG00000075711
EnsemblGeneIds (GRCh37): ENSG00000075711
OMIM: 601014, Gene2Phenotype
DLG1 is in 2 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- Literature
- Phenotypes
-
- Non-syndromic cleft lip with or without cleft palate
- OMIM
- 601014
- Clinvar variants
- Variants in DLG1
- Penetrance
- None
- Publications
-
- PMID: 28926086
- Panels with this gene
History Filter Activity
16 Sep 2020, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: DLG1 was added gene: DLG1 was added to Clefting_GEL. Sources: Literature,Expert Review Red Mode of inheritance for gene: DLG1 was set to Unknown Publications for gene: DLG1 were set to PMID: 28926086 Phenotypes for gene: DLG1 were set to Non-syndromic cleft lip with or without cleft palate