Incidental Mutation 'IGL02224:Vmn2r113'
ID 285261
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r113
Ensembl Gene ENSMUSG00000092111
Gene Name vomeronasal 2, receptor 113
Synonyms EG434701
Accession Numbers
Essential gene? Probably non essential (E-score: 0.135) question?
Stock # IGL02224
Quality Score
Status
Chromosome 17
Chromosomal Location 23162158-23177788 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 23174960 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 524 (R524*)
Ref Sequence ENSEMBL: ENSMUSP00000127981 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170322]
AlphaFold E9PZA6
Predicted Effect probably null
Transcript: ENSMUST00000170322
AA Change: R524*
SMART Domains Protein: ENSMUSP00000127981
Gene: ENSMUSG00000092111
AA Change: R524*

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 146 470 9e-26 PFAM
Pfam:NCD3G 512 564 5.1e-21 PFAM
Pfam:7tm_3 595 832 5.7e-56 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c12 T A 13: 4,329,289 (GRCm39) T23S probably damaging Het
Alpk3 G A 7: 80,726,616 (GRCm39) probably benign Het
Atp8b3 A G 10: 80,361,810 (GRCm39) probably benign Het
Atr C T 9: 95,760,682 (GRCm39) R1051C probably damaging Het
B4galt2 T C 4: 117,734,110 (GRCm39) D309G probably benign Het
C130026L21Rik A G 5: 111,730,291 (GRCm39) noncoding transcript Het
Cadm3 A G 1: 173,165,628 (GRCm39) I344T possibly damaging Het
Cd101 T C 3: 100,924,318 (GRCm39) T370A probably benign Het
Col6a5 A T 9: 105,741,534 (GRCm39) S2462T probably damaging Het
Csf3r A T 4: 125,937,332 (GRCm39) N739Y probably benign Het
Ensa T C 3: 95,535,990 (GRCm39) S108P probably benign Het
Fancd2 T A 6: 113,545,281 (GRCm39) probably null Het
Fbp1 T A 13: 63,035,821 (GRCm39) T13S probably damaging Het
Flrt2 C A 12: 95,746,802 (GRCm39) T380K possibly damaging Het
Gpatch11 T C 17: 79,148,522 (GRCm39) probably benign Het
Hagh A G 17: 25,071,861 (GRCm39) D29G probably damaging Het
Hmmr T C 11: 40,600,831 (GRCm39) Q513R unknown Het
Hoxb8 T C 11: 96,173,981 (GRCm39) S65P probably benign Het
Il4ra T C 7: 125,169,271 (GRCm39) probably benign Het
Lbp A G 2: 158,148,669 (GRCm39) N27S probably damaging Het
Msh4 G A 3: 153,595,822 (GRCm39) T76I possibly damaging Het
Nfat5 T C 8: 108,071,447 (GRCm39) V281A probably benign Het
Or10ag53 C T 2: 87,082,821 (GRCm39) S180F probably benign Het
Or13c25 A T 4: 52,911,392 (GRCm39) V134D probably damaging Het
Or4p20 C T 2: 88,254,052 (GRCm39) probably null Het
Or5b106 T A 19: 13,123,120 (GRCm39) K301M probably damaging Het
Or5w16 T A 2: 87,576,757 (GRCm39) C72* probably null Het
Phf11b A T 14: 59,563,515 (GRCm39) probably benign Het
Pik3c2a A G 7: 115,962,575 (GRCm39) probably benign Het
Prdx1 T A 4: 116,549,064 (GRCm39) F66L probably damaging Het
Prss39 A G 1: 34,538,459 (GRCm39) H108R probably damaging Het
Spta1 C A 1: 174,045,255 (GRCm39) probably benign Het
Tmem87b A G 2: 128,676,127 (GRCm39) I297V possibly damaging Het
Vmn1r191 T C 13: 22,363,068 (GRCm39) R229G probably damaging Het
Washc2 T A 6: 116,197,530 (GRCm39) D254E possibly damaging Het
Zfp318 C T 17: 46,707,736 (GRCm39) R265* probably null Het
Zfp773 T C 7: 7,135,975 (GRCm39) H207R probably benign Het
Other mutations in Vmn2r113
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01318:Vmn2r113 APN 17 23,177,309 (GRCm39) missense probably benign 0.01
IGL01386:Vmn2r113 APN 17 23,175,024 (GRCm39) missense possibly damaging 0.94
IGL01743:Vmn2r113 APN 17 23,177,285 (GRCm39) missense probably benign 0.03
IGL02498:Vmn2r113 APN 17 23,177,349 (GRCm39) missense probably damaging 0.99
IGL02969:Vmn2r113 APN 17 23,177,591 (GRCm39) missense probably benign 0.13
IGL03010:Vmn2r113 APN 17 23,175,038 (GRCm39) missense possibly damaging 0.90
IGL03240:Vmn2r113 APN 17 23,174,931 (GRCm39) missense probably benign 0.19
R1853:Vmn2r113 UTSW 17 23,164,501 (GRCm39) missense probably benign
R2058:Vmn2r113 UTSW 17 23,177,223 (GRCm39) nonsense probably null
R3010:Vmn2r113 UTSW 17 23,177,105 (GRCm39) missense probably damaging 0.97
R4942:Vmn2r113 UTSW 17 23,177,321 (GRCm39) missense probably damaging 0.97
R5072:Vmn2r113 UTSW 17 23,177,329 (GRCm39) nonsense probably null
R5755:Vmn2r113 UTSW 17 23,176,955 (GRCm39) missense probably benign 0.00
R6513:Vmn2r113 UTSW 17 23,177,715 (GRCm39) missense probably damaging 0.99
R7164:Vmn2r113 UTSW 17 23,167,137 (GRCm39) missense probably benign
R7936:Vmn2r113 UTSW 17 23,176,917 (GRCm39) missense probably benign 0.05
R8087:Vmn2r113 UTSW 17 23,177,711 (GRCm39) missense possibly damaging 0.66
R8193:Vmn2r113 UTSW 17 23,164,501 (GRCm39) missense probably benign 0.06
R8196:Vmn2r113 UTSW 17 23,176,938 (GRCm39) missense probably damaging 0.99
R8414:Vmn2r113 UTSW 17 23,177,753 (GRCm39) nonsense probably null
R8490:Vmn2r113 UTSW 17 23,177,372 (GRCm39) missense probably benign 0.18
Posted On 2015-04-16