Incidental Mutation 'IGL02272:Vmn2r24'
ID 287172
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r24
Ensembl Gene ENSMUSG00000072780
Gene Name vomeronasal 2, receptor 24
Synonyms EG243628
Accession Numbers
Essential gene? Probably non essential (E-score: 0.055) question?
Stock # IGL02272
Quality Score
Status
Chromosome 6
Chromosomal Location 123755930-123793239 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 123763843 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Isoleucine at position 240 (N240I)
Ref Sequence ENSEMBL: ENSMUSP00000074602 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075095]
AlphaFold D3YUI0
Predicted Effect possibly damaging
Transcript: ENSMUST00000075095
AA Change: N240I

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000074602
Gene: ENSMUSG00000072780
AA Change: N240I

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:ANF_receptor 82 469 1.6e-32 PFAM
Pfam:NCD3G 518 571 1.1e-22 PFAM
Pfam:7tm_3 602 839 1.1e-54 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre1 T A 17: 57,757,021 (GRCm39) C759* probably null Het
Adgrg6 T A 10: 14,344,573 (GRCm39) M127L probably damaging Het
Anxa9 A G 3: 95,213,205 (GRCm39) V47A probably benign Het
Arhgef12 T A 9: 42,912,748 (GRCm39) D483V probably damaging Het
Arrdc3 C A 13: 81,039,769 (GRCm39) probably benign Het
Ccdc169 A G 3: 55,058,169 (GRCm39) E67G probably damaging Het
Ccdc191 T A 16: 43,780,385 (GRCm39) V731D possibly damaging Het
Cdh3 G T 8: 107,274,468 (GRCm39) probably null Het
Cntnap1 G A 11: 101,069,142 (GRCm39) V199M probably damaging Het
Cntnap3 A T 13: 64,905,225 (GRCm39) V852E probably damaging Het
Csmd1 A T 8: 16,249,907 (GRCm39) S1024T probably damaging Het
Cyp3a25 T C 5: 145,930,075 (GRCm39) probably benign Het
Dusp6 T A 10: 99,101,881 (GRCm39) V289D probably damaging Het
Ecpas A T 4: 58,811,731 (GRCm39) N1439K probably benign Het
Epha6 C T 16: 59,639,300 (GRCm39) R858Q probably damaging Het
Flrt2 T A 12: 95,746,478 (GRCm39) F272Y probably damaging Het
Gbf1 T A 19: 46,258,242 (GRCm39) W846R probably damaging Het
Gtpbp2 T A 17: 46,475,707 (GRCm39) V152E probably benign Het
Hmces A G 6: 87,894,837 (GRCm39) probably null Het
Hsph1 A G 5: 149,540,995 (GRCm39) S852P probably benign Het
Kat6b A C 14: 21,676,846 (GRCm39) K394Q probably damaging Het
Kdr G A 5: 76,122,500 (GRCm39) T475I probably benign Het
Klhl25 A G 7: 75,516,368 (GRCm39) T425A probably benign Het
Klk1b8 T A 7: 43,602,217 (GRCm39) C50S probably damaging Het
Kri1 T C 9: 21,187,464 (GRCm39) Y343C probably damaging Het
Lamb1 T C 12: 31,355,768 (GRCm39) S953P probably benign Het
Lpin1 A G 12: 16,597,601 (GRCm39) V681A probably damaging Het
Lpin3 A G 2: 160,743,581 (GRCm39) T508A probably benign Het
Moxd1 T A 10: 24,158,598 (GRCm39) Y417* probably null Het
Mthfd1l T G 10: 3,991,812 (GRCm39) I588S probably damaging Het
Myo5c C A 9: 75,173,442 (GRCm39) N543K possibly damaging Het
Myo9a T A 9: 59,791,883 (GRCm39) probably benign Het
Nme8 T C 13: 19,842,996 (GRCm39) Y393C probably damaging Het
Nr2e1 T G 10: 42,443,975 (GRCm39) N249T probably damaging Het
Pex11g A G 8: 3,515,898 (GRCm39) V45A probably benign Het
Pkhd1 C A 1: 20,279,484 (GRCm39) G2945W probably damaging Het
Plxnd1 A G 6: 115,970,589 (GRCm39) F393S probably damaging Het
Ppp3cc A G 14: 70,473,938 (GRCm39) V353A probably damaging Het
Prss16 T A 13: 22,187,205 (GRCm39) Q455L probably damaging Het
Ptpn6 A T 6: 124,698,171 (GRCm39) V524E probably damaging Het
Rap1gap A G 4: 137,443,877 (GRCm39) Y163C probably damaging Het
Rnf31 C T 14: 55,836,239 (GRCm39) L598F probably damaging Het
Sardh T G 2: 27,115,003 (GRCm39) D550A probably benign Het
Serpinc1 T G 1: 160,827,562 (GRCm39) I387S probably damaging Het
Sh3d19 A T 3: 86,028,474 (GRCm39) D650V probably benign Het
Sipa1l2 T A 8: 126,218,750 (GRCm39) T196S probably damaging Het
Slc25a46 T C 18: 31,716,621 (GRCm39) T294A probably benign Het
Srrm2 T C 17: 24,034,756 (GRCm39) probably benign Het
Steap2 T A 5: 5,727,612 (GRCm39) N241I probably benign Het
Tcaf3 T C 6: 42,573,594 (GRCm39) Y206C probably damaging Het
Tmem259 T A 10: 79,814,297 (GRCm39) Q322L probably damaging Het
Tnni2 C A 7: 141,997,166 (GRCm39) Q52K possibly damaging Het
Ttn A G 2: 76,565,372 (GRCm39) V28285A possibly damaging Het
Uba7 T A 9: 107,853,352 (GRCm39) S99R probably benign Het
Ubxn2b A T 4: 6,216,071 (GRCm39) K331N probably damaging Het
Usp50 G A 2: 126,611,864 (GRCm39) T232I probably damaging Het
Vmn2r116 G A 17: 23,604,973 (GRCm39) M95I probably benign Het
Vmn2r116 T A 17: 23,604,978 (GRCm39) L97Q probably damaging Het
Vmn2r72 T C 7: 85,399,901 (GRCm39) R383G probably benign Het
Other mutations in Vmn2r24
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00954:Vmn2r24 APN 6 123,792,596 (GRCm39) missense probably damaging 1.00
IGL01382:Vmn2r24 APN 6 123,763,938 (GRCm39) missense possibly damaging 0.62
IGL01592:Vmn2r24 APN 6 123,764,445 (GRCm39) missense probably benign 0.30
IGL01754:Vmn2r24 APN 6 123,781,120 (GRCm39) missense probably damaging 1.00
IGL01939:Vmn2r24 APN 6 123,764,404 (GRCm39) missense probably benign
IGL02140:Vmn2r24 APN 6 123,757,631 (GRCm39) missense probably damaging 0.98
IGL02568:Vmn2r24 APN 6 123,792,812 (GRCm39) missense probably benign 0.36
IGL02748:Vmn2r24 APN 6 123,793,057 (GRCm39) missense possibly damaging 0.90
IGL03022:Vmn2r24 APN 6 123,755,967 (GRCm39) missense probably damaging 0.99
IGL03343:Vmn2r24 APN 6 123,793,070 (GRCm39) missense probably damaging 1.00
R0357:Vmn2r24 UTSW 6 123,792,369 (GRCm39) frame shift probably null
R0453:Vmn2r24 UTSW 6 123,757,350 (GRCm39) critical splice acceptor site probably null
R0538:Vmn2r24 UTSW 6 123,793,012 (GRCm39) missense probably benign 0.32
R0607:Vmn2r24 UTSW 6 123,763,893 (GRCm39) missense probably benign
R1381:Vmn2r24 UTSW 6 123,763,692 (GRCm39) missense probably damaging 1.00
R1589:Vmn2r24 UTSW 6 123,783,479 (GRCm39) splice site probably benign
R1848:Vmn2r24 UTSW 6 123,793,183 (GRCm39) missense probably damaging 1.00
R2035:Vmn2r24 UTSW 6 123,793,019 (GRCm39) missense probably damaging 1.00
R2077:Vmn2r24 UTSW 6 123,792,358 (GRCm39) missense probably damaging 1.00
R2122:Vmn2r24 UTSW 6 123,792,353 (GRCm39) missense possibly damaging 0.81
R2145:Vmn2r24 UTSW 6 123,755,972 (GRCm39) missense probably benign
R2483:Vmn2r24 UTSW 6 123,792,997 (GRCm39) missense probably damaging 1.00
R2512:Vmn2r24 UTSW 6 123,763,985 (GRCm39) missense probably benign 0.01
R3001:Vmn2r24 UTSW 6 123,781,231 (GRCm39) missense probably benign 0.00
R3002:Vmn2r24 UTSW 6 123,781,231 (GRCm39) missense probably benign 0.00
R3236:Vmn2r24 UTSW 6 123,755,984 (GRCm39) nonsense probably null
R3623:Vmn2r24 UTSW 6 123,792,997 (GRCm39) missense probably damaging 1.00
R3624:Vmn2r24 UTSW 6 123,792,997 (GRCm39) missense probably damaging 1.00
R3835:Vmn2r24 UTSW 6 123,764,412 (GRCm39) missense probably benign 0.33
R4074:Vmn2r24 UTSW 6 123,764,374 (GRCm39) missense possibly damaging 0.92
R4075:Vmn2r24 UTSW 6 123,764,374 (GRCm39) missense possibly damaging 0.92
R4812:Vmn2r24 UTSW 6 123,756,144 (GRCm39) missense probably benign 0.00
R4825:Vmn2r24 UTSW 6 123,792,739 (GRCm39) missense probably benign 0.02
R5351:Vmn2r24 UTSW 6 123,793,223 (GRCm39) missense possibly damaging 0.80
R5665:Vmn2r24 UTSW 6 123,763,938 (GRCm39) missense possibly damaging 0.62
R5790:Vmn2r24 UTSW 6 123,792,499 (GRCm39) missense probably benign
R5808:Vmn2r24 UTSW 6 123,792,597 (GRCm39) nonsense probably null
R5879:Vmn2r24 UTSW 6 123,764,226 (GRCm39) missense possibly damaging 0.89
R5923:Vmn2r24 UTSW 6 123,792,751 (GRCm39) missense probably damaging 0.96
R5969:Vmn2r24 UTSW 6 123,755,981 (GRCm39) missense probably benign 0.00
R6050:Vmn2r24 UTSW 6 123,792,691 (GRCm39) missense probably damaging 1.00
R6171:Vmn2r24 UTSW 6 123,764,205 (GRCm39) missense probably damaging 0.98
R6174:Vmn2r24 UTSW 6 123,793,236 (GRCm39) missense probably benign 0.00
R6356:Vmn2r24 UTSW 6 123,783,368 (GRCm39) missense possibly damaging 0.93
R6562:Vmn2r24 UTSW 6 123,757,386 (GRCm39) missense probably benign 0.01
R6563:Vmn2r24 UTSW 6 123,781,137 (GRCm39) missense possibly damaging 0.86
R6584:Vmn2r24 UTSW 6 123,792,764 (GRCm39) missense possibly damaging 0.53
R6630:Vmn2r24 UTSW 6 123,763,981 (GRCm39) missense probably benign 0.00
R6803:Vmn2r24 UTSW 6 123,755,960 (GRCm39) missense possibly damaging 0.64
R6864:Vmn2r24 UTSW 6 123,756,117 (GRCm39) missense possibly damaging 0.89
R7252:Vmn2r24 UTSW 6 123,764,191 (GRCm39) missense possibly damaging 0.90
R7369:Vmn2r24 UTSW 6 123,792,638 (GRCm39) missense probably damaging 0.99
R7646:Vmn2r24 UTSW 6 123,793,169 (GRCm39) missense probably benign 0.20
R7799:Vmn2r24 UTSW 6 123,757,422 (GRCm39) missense probably benign 0.00
R7803:Vmn2r24 UTSW 6 123,757,438 (GRCm39) missense probably benign 0.00
R7959:Vmn2r24 UTSW 6 123,755,949 (GRCm39) missense possibly damaging 0.86
R8215:Vmn2r24 UTSW 6 123,756,077 (GRCm39) missense probably benign 0.10
R8796:Vmn2r24 UTSW 6 123,757,500 (GRCm39) missense probably benign
R9172:Vmn2r24 UTSW 6 123,783,432 (GRCm39) missense probably damaging 1.00
R9300:Vmn2r24 UTSW 6 123,793,030 (GRCm39) missense possibly damaging 0.46
R9369:Vmn2r24 UTSW 6 123,792,357 (GRCm39) missense probably damaging 1.00
R9375:Vmn2r24 UTSW 6 123,792,542 (GRCm39) missense probably damaging 1.00
R9523:Vmn2r24 UTSW 6 123,763,950 (GRCm39) missense possibly damaging 0.89
R9546:Vmn2r24 UTSW 6 123,764,266 (GRCm39) missense probably damaging 0.98
RF006:Vmn2r24 UTSW 6 123,783,378 (GRCm39) missense probably damaging 1.00
RF016:Vmn2r24 UTSW 6 123,781,174 (GRCm39) missense probably benign 0.04
X0023:Vmn2r24 UTSW 6 123,764,359 (GRCm39) missense probably damaging 0.99
Z1088:Vmn2r24 UTSW 6 123,781,155 (GRCm39) missense probably benign 0.00
Z1177:Vmn2r24 UTSW 6 123,763,719 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16