- Panels
- Cerebral Palsy
- TENM1
Genes in panel
- ACADM 2
- ACTB 1
- ADAR 2
- ADAT3 1
- ADCY5 1
- ADD3 1
- ADNP 1
- AHDC1 2
- ALDH3A2 1
- ALS2 1
- AMPD2 1
- AP4B1 1
- AP4E1 1
- AP4M1 2
- AP4S1 1
- ARG1 1
- ARID2 2
- ARX 1
- ASXL1 1
- ASXL3 2
- ATL1 2
- ATM 1
- ATP1A3 2
- ATP7A 1
- ATP8A2 1
- ATRX 1
- AUTS2 2
- BCAP31 1
- BCL11A 2
- CACNA1A 3
- CACNA1G 1
- CAMTA1 1
- CASK 1
- CHD8 1
- CLTC 1
- COL4A1 3
- COL4A2 2
- CREBBP 2
- CSMD1 1
- CTNNA2 1
- CTNNB1 2
- CYP2U1 2
- DDC 2
- DDHD2 1
- DDX3X 1
- DOCK6 1
- DYNC1H1 1
- DYRK1A 2
- EARS2 1
- ECHS1 1
- ELOVL1 2
- ELP2 1
- ERCC8 2
- ESAM 1
- EXOSC3 1
- FAR1 1
- FARS2 1
- FBXO31 2
- FH 1
- FOXG1 1
- GCDH 2
- GCH1 1
- GNAO1 2
- GNB1 2
- GRIN1 1
- GRIN2B 1
- HECW2 2
- HPDL 3
- HPRT1 2
- IFIH1 1
- IRF2BPL 1
- ITPR1 2
- KAT6A 2
- KCNB1 2
- KCNC3 1
- KCNQ2 2
- KCNT1 2
- KDM5C 2
- KIDINS220 3
- KIF1A 2
- KMT2A 2
- KMT2B 3
- L1CAM 2
- MAP2K1 1
- MCOLN1 1
- MECP2 2
- MEF2C 2
- MINPP1 1
- MOCS2 1
- MSL3 1
- MT-TL1 2
- NAA10 1
- NDUFAF2 1
- NGLY1 1
- NKX2-1 1
- NSRP1 2
- NT5C2 1
- PAFAH1B1 1
- PAK3 2
- PANK2 2
- PCDH12 1
- PCYT2 1
- PDHA1 2
- PDHX 1
- PHIP 1
- PIGA 2
- PIGN 1
- PLA2G6 2
- PLP1 2
- POMGNT1 1
- PROC 2
- PRUNE1 1
- PURA 1
- RAB3GAP1 1
- RARS2 1
- RNASEH2A 1
- RNASEH2B 1
- RNASEH2C 1
- SACS 1
- SAMHD1 1
- SATB2 1
- SCN1A 1
- SCN2A 1
- SCN8A 2
- SEPSECS 1
- SLC16A2 1
- SLC2A1 1
- SLC5A6 1
- SLITRK2 1
- SPAST 3
- SPATA5 2
- SPATA5L1 2
- SPG11 1
- SPR 1
- SPTAN1 2
- SPTBN2 2
- ST3GAL5 1
- STAMBP 1
- STXBP1 1
- SUOX 1
- SYNGAP1 2
- TAF1 2
- TCF4 3
- TH 2
- TMX2 2
- TNR 1
- TRAPPC9 1
- TREX1 1
- TUBA1A 2
- TUBB2A 1
- TUBB2B 3
- TUBB3 1
- TUBB4A 2
- UBE3A 2
- VPS13D 1
- WDR26 1
- WDR45 1
- WWOX 1
- ZC4H2 1
- ZEB2 2
- ZSWIM6 1
- AGAP1 2
- ALK 1
- ARSA 1
- B4GALNT1 1
- BRAF 1
- BRAT1 1
- CACNA1D 1
- CDKL5 2
- CHD7 1
- CTBP1 2
- DHPS 1
- DHX32 1
- EEF1A2 2
- FRRS1L 3
- GABRB2 1
- GALC 1
- GSX2 1
- HCFC1 1
- HUWE1 2
- IQSEC2 3
- MAPK8IP3 1
- MAST1 1
- MCCC2 1
- MED12 1
- MMACHC 1
- MOCS1 2
- NALCN 1
- NDUFA12 1
- NFIX 1
- PIK3R2 1
- PNPLA6 1
- POGZ 1
- POLA1 1
- POLG 1
- PTPN11 2
- PTPN23 1
- REPS2 1
- RHOB 1
- RNU7-1 1
- SETD2 1
- SHANK3 2
- SLC13A5 1
- SLC1A2 1
- SMARCB1 2
- SNX14 1
- SON 2
- SYNE1 3
- TANGO2 2
- TEP1 2
- THOC2 2
- TSC1 1
- ZDHHC9 1
- ABCD1 1
- ABHD16A 1
- ACAD9 1
- AKT3 2
- ALDH7A1 1
- ARHGEF9 1
- ARID1B 1
- ARMC9 1
- ASL 1
- ASPA 1
- ATP1A2 1
- ATP6V1A 1
- ATP7B 1
- ATR 1
- BSCL2 1
- CACNA1B 1
- CAMK2B 1
- CAMK2G 1
- CCDC22 1
- CEP290 1
- CHCHD10 1
- CHD3 1
- CHD4 1
- CLCN4 2
- CLCN7 1
- CLN6 1
- COL6A3 1
- COQ4 1
- CTCF 1
- CUL3 1
- CYFIP2 1
- DCC 1
- DDX59 1
- DHCR7 1
- DIAPH1 1
- DLG4 1
- DNM2 1
- DNMT3A 1
- DUOX2 1
- EBF3 1
- EBP 1
- EHMT1 1
- EPG5 1
- ERLIN2 1
- EZH2 1
- FAM126A 1
- FAM20C 1
- FGD1 1
- FGFR1 1
- FLNA 2
- FUS 1
- GABBR2 1
- GABRB1 1
- GAD1 1
- GAMT 1
- GATAD2B 1
- GBA 1
- GFAP 1
- GRIN2A 1
- HIVEP2 1
- HPCA 1
- HSPD1 1
- IREB2 1
- KANK1 1
- KAT6B 1
- KCNH1 1
- KCNK9 1
- KCNQ3 1
- KCNQ5 1
- KDM3B 1
- KDM7A 1
- KIAA1109 1
- KIF14 1
- KIF5C 1
- KMT2D 1
- LAMA1 1
- LRP2 1
- LZTR1 1
- MACF1 1
- MAOB 1
- MBD5 1
- MED13L 1
- MFN2 3
- MLC1 1
- MUT 1
- MYH2 1
- MYO9A 1
- NEFL 1
- NEXMIF 1
- NFE2L2 1
- NFIB 1
- NOTCH1 1
- NR2F1 1
- NSD1 1
- NSD2 1
- OPHN1 1
- PACS1 1
- PCDH19 1
- PCLO 1
- PDE10A 1
- PGAP2 1
- PHF6 1
- PHKA2 1
- PIDD1 1
- PIK3CA 1
- PMM2 1
- POLR2A 1
- PPM1D 1
- PQBP1 1
- PUM1 1
- RARB 1
- ROGDI 1
- RTN4IP1 1
- RTTN 1
- SETBP1 1
- SGCE 1
- SIK1 1
- SLC25A12 1
- SLC35A2 1
- SLC6A5 1
- SMARCA2 1
- SMARCA4 1
- SMC1A 1
- SMC3 1
- SMG8 1
- SOX10 1
- SOX2 1
- TANC2 1
- TBCD 1
- TBCK 1
- TBR1 1
- TBX6 1
- TENM1 1
- TGM6 1
- TOR1A 1
- TRIO 1
- TRIP12 1
- TRPM3 1
- TSC2 1
- TSEN54 1
- TSHR 1
- TUBG1 1
- VPS13B 1
- VPS53 1
- WDR62 1
- ZBTB18 1
- ZIC2 1
- ZMYM2 1
- TRIT1 1
- ZMYND11 1
STRs in panel
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Regions in panel
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Cerebral Palsy
Gene: TENM1 Red List (low evidence)
TENM1 (teneurin transmembrane protein 1)
EnsemblGeneIds (GRCh38): ENSG00000009694
EnsemblGeneIds (GRCh37): ENSG00000009694
OMIM: 300588, Gene2Phenotype
TENM1 is in 3 panels
EnsemblGeneIds (GRCh38): ENSG00000009694
EnsemblGeneIds (GRCh37): ENSG00000009694
OMIM: 300588, Gene2Phenotype
TENM1 is in 3 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Red List (low evidence)
Single family reported, no functional evidence.Created: 21 Nov 2019, 9:40 a.m. | Last Modified: 21 Nov 2019, 9:40 a.m.
Panel Version: 0.0
Publications
Created: 21 Nov 2019, 9:40 a.m.
Last Modified: 21 Nov 2019, 9:40 a.m.
Panel version: 0.0
Last Modified: 21 Nov 2019, 9:40 a.m.
Panel version: 0.0
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- Victorian Clinical Genetics Services
- OMIM
- 300588
- Clinvar variants
- Variants in TENM1
- Penetrance
- None
- Panels with this gene
History Filter Activity
21 Nov 2019, Gel status: 1
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tenm1 has been classified as Red List (Low Evidence).
21 Nov 2019, Gel status: 1
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tenm1 has been classified as Red List (Low Evidence).
17 Nov 2019, Gel status: 3
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: TENM1 was added gene: TENM1 was added to Cerebral Palsy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: TENM1 was set to Unknown