Genes in panel
- ACE 0
- ACTG2 0
- ACTN4 0
- ADAMTS9 0
- AGT 0
- AGTR1 0
- AGXT 0
- AHI1 0
- ALMS1 0
- AMN 0
- ANKS6 0
- ANOS1 0
- AP2S1 0
- APOA1 0
- APOE 0
- APRT 0
- AQP2 0
- ARHGDIA 0
- ARL13B 0
- ARL6 0
- ATP1A1 0
- ATP6V0A4 0
- ATP6V1B1 0
- AVPR2 0
- B9D2 0
- BBS1 0
- BBS10 0
- BBS12 0
- BBS2 0
- BBS4 0
- BBS5 0
- BBS7 0
- BBS9 0
- BCS1L 0
- BMP4 0
- BNC2 0
- BSND 0
- C3 0
- CA2 0
- CACNA1D 0
- CACNA1H 0
- CASR 0
- CC2D2A 0
- CD151 0
- CD46 0
- CDC73 0
- CENPF 0
- CEP104 0
- CEP164 0
- CEP290 0
- CEP41 0
- CEP55 0
- CEP83 0
- CFB 0
- CFH 0
- CFHR1 0
- CFHR2 0
- CFHR3 0
- CFHR5 0
- CFI 0
- CHD1L 0
- CHD7 0
- CHRNA3 0
- CLCN2 0
- CLCN5 0
- CLCNKA 0
- CLCNKB 0
- CLDN10 0
- CLDN16 0
- CLDN19 0
- CNNM2 0
- COL4A1 0
- COL4A3 0
- COL4A4 0
- COL4A5 0
- COQ2 0
- COQ6 0
- COQ8B 0
- CPT2 0
- CRB2 0
- CSPP1 0
- CTNS 0
- CTU2 0
- CUBN 0
- CUL3 0
- CYP11B1 0
- CYP11B2 0
- CYP17A1 0
- CYP21A2 0
- CYP24A1 0
- CYP27B1 0
- CYP2R1 0
- DDX59 0
- DGKE 0
- DHCR7 0
- DLC1 0
- DMP1 0
- DNAJB11 0
- DSTYK 0
- DYNC2H1 0
- DZIP1L 0
- EGF 0
- EGFR 0
- EMP2 0
- ENPP1 0
- EXOC3L2 0
- EYA1 0
- FAH 0
- FAM111A 0
- FAM20A 0
- FAM58A 0
- FAN1 0
- FAT1 0
- FGA 0
- FGF23 0
- FN1 0
- FRAS1 0
- FREM1 0
- FREM2 0
- FXYD2 0
- GALNT3 0
- GANAB 0
- GATA3 0
- GATM 0
- GLA 0
- GLI3 0
- GNA11 0
- GPC3 0
- GREB1L 0
- GRHPR 0
- GRIP1 0
- GSN 0
- HAAO 0
- HNF1B 0
- HNF4A 0
- HOGA1 0
- HOXA13 0
- HPRT1 0
- HPSE2 0
- HSD11B2 0
- HSD17B4 0
- HYLS1 0
- IFT122 0
- IFT140 0
- IFT172 0
- IFT27 0
- IFT43 0
- INF2 0
- INPP5E 0
- INVS 0
- IQCB1 0
- ITGA3 0
- ITGA8 0
- ITSN1 0
- JAG1 0
- KANK2 0
- KCNA1 0
- KCNJ1 0
- KCNJ10 0
- KCNJ5 0
- KDM6A 0
- KIAA0556 1
- KIAA0586 0
- KIAA0753 0
- KIF14 0
- KIF7 0
- KL 0
- KLHL3 0
- KMT2D 0
- KYNU 0
- LAGE3 0
- LAMB2 0
- LCAT 0
- LIFR 0
- LMX1B 0
- LRIG2 0
- LRP4 0
- LYZ 0
- LZTFL1 0
- MAGED2 0
- MAGI2 0
- MAPKBP1 0
- MKKS 0
- MKS1 0
- MMACHC 0
- MUC1 0
- MUT 0
- MYH9 0
- MYO1E 0
- MYOCD 0
- NADSYN1 0
- NEK1 0
- NEK8 0
- NIPBL 0
- NLRP3 0
- NOTCH2 0
- NPHP1 0
- NPHP3 0
- NPHP4 0
- NPHS1 0
- NPHS2 0
- NR3C1 0
- NR3C2 0
- NUP107 0
- NUP133 0
- NUP85 0
- NUP93 0
- OCRL 0
- OFD1 0
- OSGEP 0
- PAX2 0
- PBX1 0
- PCBD1 0
- PDE3A 0
- PDSS2 0
- PHEX 0
- PKD1 0
- PKD2 0
- PKHD1 0
- PLCE1 0
- PODXL 0
- PRKCSH 0
- PTH1R 0
- PTPRO 0
- REN 0
- RET 0
- RMND1 0
- ROBO2 0
- ROR2 0
- RPGRIP1L 0
- RRM2B 0
- SALL1 0
- SALL4 0
- SARS2 0
- SBDS 0
- SCARB2 0
- SCNN1A 0
- SCNN1B 0
- SCNN1G 0
- SDCCAG8 0
- SEC61A1 0
- SGPL1 0
- SIX1 0
- SIX5 0
- SLC12A1 0
- SLC12A3 0
- SLC22A12 0
- SLC26A1 0
- SLC2A2 0
- SLC2A9 0
- SLC34A1 0
- SLC34A3 0
- SLC3A1 0
- SLC4A1 0
- SLC4A4 0
- SLC5A2 0
- SLC7A7 0
- SLC7A9 0
- SLC9A3R1 0
- SLIT2 0
- SMARCAL1 0
- STRA6 0
- STRADA 0
- STX16 0
- TBC1D1 0
- TBC1D8B 0
- TBX18 0
- TCTN1 0
- TCTN2 0
- TCTN3 0
- TFAP2A 0
- TMEM107 0
- TMEM138 0
- TMEM216 0
- TMEM231 0
- TMEM237 0
- TMEM67 0
- TNS2 0
- TP53RK 0
- TPRKB 0
- TRAF3IP1 0
- TRAP1 0
- TRPC6 0
- TRPM6 0
- TSC1 0
- TSC2 0
- TTC21B 0
- TTC8 0
- TXNDC15 0
- UMOD 0
- VDR 0
- VHL 0
- VIPAS39 0
- VPS33B 0
- WDPCP 0
- WDR19 0
- WDR35 0
- WDR60 1
- WDR73 0
- WNK1 0
- WNK4 0
- WNT5A 0
- WT1 0
- XDH 0
- ZIC3 0
- ADAMTS13 0
- ADCY10 0
- ANLN 0
- BBIP1 0
- CD2AP 0
- CEP120 0
- COQ7 0
- DCDC2 0
- FGF20 0
- GLIS2 0
- IFT74 0
- LAMA5 0
- SOX11 0
- SRGAP1 0
- THBD 0
- APOL1 0
- ARHGAP24 0
- ATXN10 0
- B9D1 0
- BICC1 0
- BMP7 0
- C2CD3 0
- C5orf42 0
- CBWD1 0
- CCDC28B 0
- CDC5L 0
- CDX2 0
- COL4A2 0
- COQ8A 0
- COQ9 0
- DACT1 0
- EHHADH 0
- EVC 0
- EVC2 0
- EZH2 0
- FGF10 0
- FGF8 0
- FGFR1 0
- FGFR2 0
- FGFR3 0
- FOXC1 0
- FOXC2 0
- HOXA4 0
- HOXB6 0
- ICK 0
- IFT57 0
- IFT81 0
- ITGB4 0
- KANK1 0
- KANK4 0
- LMNA 0
- NUP160 0
- NUP205 0
- NUP37 0
- PDE6D 0
- POC1B 0
- SCLT1 0
- SEC63 0
- SEMA3A 0
- SIX2 0
- SLC41A1 0
- SOX17 0
- TNXB 0
- TRIM32 0
- UPK3A 0
- VTN 0
- WDR34 1
- XPNPEP3 0
- XPO5 0
- ZNF423 0
STRs in panel
Prev
Next
Regions in panel
Prev
Next
This Panel is marked as Deleted
Kidneyome_SuperPanel_VCGS
Gene: VTN Red List (low evidence)
VTN (vitronectin)
EnsemblGeneIds (GRCh38): ENSG00000109072
EnsemblGeneIds (GRCh37): ENSG00000109072
OMIM: 193190, Gene2Phenotype
VTN is in 1 panel
EnsemblGeneIds (GRCh38): ENSG00000109072
EnsemblGeneIds (GRCh37): ENSG00000109072
OMIM: 193190, Gene2Phenotype
VTN is in 1 panel
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Red
- Victorian Clinical Genetics Services
- Phenotypes
-
- Atypical haemolytic uraemic syndrome
- OMIM
- 193190
- Clinvar variants
- Variants in VTN
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
28 Jan 2020, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Eleanor Williams (Genomics England Curator)gene: VTN was added gene: VTN was added to Kidneyome_SuperPanel_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Red Mode of inheritance for gene: VTN was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: VTN were set to 30377230 Phenotypes for gene: VTN were set to Atypical haemolytic uraemic syndrome