Incidental Mutation 'IGL02429:Vmn2r30'
ID293023
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r30
Ensembl Gene ENSMUSG00000070847
Gene Namevomeronasal 2, receptor 30
SynonymsV2r15
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02429
Quality Score
Status
Chromosome7
Chromosomal Location7311333-7337609 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 7334244 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Tyrosine at position 131 (C131Y)
Ref Sequence ENSEMBL: ENSMUSP00000134223 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072475] [ENSMUST00000174368] [ENSMUST00000210877]
Predicted Effect possibly damaging
Transcript: ENSMUST00000072475
AA Change: C131Y

PolyPhen 2 Score 0.552 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000072296
Gene: ENSMUSG00000070847
AA Change: C131Y

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 160 469 2.1e-25 PFAM
Pfam:NCD3G 512 565 8.1e-21 PFAM
Pfam:7tm_3 598 833 2.1e-55 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000174368
AA Change: C131Y

PolyPhen 2 Score 0.952 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000134223
Gene: ENSMUSG00000070847
AA Change: C131Y

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 155 468 1.5e-27 PFAM
Pfam:NCD3G 512 564 7.2e-16 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000210877
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acmsd A T 1: 127,759,716 D245V probably damaging Het
Adamts16 G A 13: 70,787,170 probably benign Het
Arhgap36 A G X: 49,494,706 D77G possibly damaging Het
Asap1 A T 15: 64,167,740 M187K probably damaging Het
Aspm T C 1: 139,479,810 V2145A probably benign Het
Casc4 A G 2: 121,911,987 T306A probably benign Het
Cd46 T C 1: 195,085,424 T110A probably benign Het
Chl1 T A 6: 103,664,809 probably benign Het
Clca3b A G 3: 144,828,135 L493S probably damaging Het
Col11a2 C T 17: 34,042,292 T72M probably damaging Het
Cyfip1 T A 7: 55,871,982 probably benign Het
Frmd4b T C 6: 97,325,429 probably benign Het
Glyr1 A G 16: 5,019,376 M397T probably benign Het
Gtf2a1l G T 17: 88,668,713 M1I probably null Het
Hdac4 A G 1: 92,012,695 L154P probably benign Het
Ints8 A T 4: 11,231,720 C422S probably damaging Het
Kng2 T A 16: 23,012,079 K160I probably damaging Het
Lrrc23 C A 6: 124,778,167 A136S probably damaging Het
Ltf T C 9: 111,026,125 I402T possibly damaging Het
Lyst G A 13: 13,660,956 C1741Y probably benign Het
Mfsd4a T C 1: 132,028,499 H509R probably benign Het
Mthfd1l A G 10: 4,089,334 K782E probably damaging Het
Mvb12b G A 2: 33,827,788 R114W probably damaging Het
Myh4 A T 11: 67,258,982 K1818* probably null Het
Myo1h C T 5: 114,359,738 probably benign Het
Ncapd3 T A 9: 27,089,302 S1402T probably benign Het
Nutm2 A G 13: 50,469,480 N71S probably benign Het
Oas1c C A 5: 120,802,068 M344I probably benign Het
Olfr978 T A 9: 39,993,842 F11I probably benign Het
Phldb1 A G 9: 44,700,950 L1019P probably damaging Het
Plxnc1 T C 10: 94,882,591 E494G probably benign Het
Pole T C 5: 110,299,800 I734T probably benign Het
Ppp1r3b T C 8: 35,384,615 S203P probably benign Het
Pth2r G T 1: 65,346,839 M240I probably benign Het
Ptprr T A 10: 116,273,767 F394I probably damaging Het
Rabgef1 T C 5: 130,210,488 S265P possibly damaging Het
Rbpjl A G 2: 164,413,895 D353G possibly damaging Het
Rfc3 A G 5: 151,651,131 Y8H probably benign Het
Rph3a A T 5: 120,980,124 probably null Het
Runx1t1 A T 4: 13,865,294 probably benign Het
Slc37a1 T A 17: 31,300,509 probably null Het
Slc38a10 T C 11: 120,134,888 probably benign Het
Slc38a6 T C 12: 73,350,568 V328A probably benign Het
Slf2 T C 19: 44,941,728 S415P probably benign Het
Spata17 C A 1: 187,140,434 R60L possibly damaging Het
Svil T A 18: 5,118,369 D2237E probably benign Het
Swap70 T A 7: 110,263,972 N169K probably benign Het
Tnfrsf11a A G 1: 105,827,718 D505G probably benign Het
Traf1 A G 2: 34,949,103 V70A probably benign Het
Traf3 T A 12: 111,243,465 V165E probably benign Het
Trpc5 T C X: 144,411,799 E570G probably damaging Het
Ubash3a A G 17: 31,241,305 N601S probably benign Het
Vmn2r43 T C 7: 8,255,552 I221V probably benign Het
Vmn2r97 T A 17: 18,930,334 V481E possibly damaging Het
Wisp3 T C 10: 39,154,993 N178S probably benign Het
Other mutations in Vmn2r30
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01797:Vmn2r30 APN 7 7334196 missense probably benign
IGL02114:Vmn2r30 APN 7 7337409 missense possibly damaging 0.62
IGL03214:Vmn2r30 APN 7 7334260 missense probably benign 0.00
R1723:Vmn2r30 UTSW 7 7334260 missense probably benign 0.00
R4472:Vmn2r30 UTSW 7 7317092 missense probably damaging 1.00
R5409:Vmn2r30 UTSW 7 7312548 missense probably damaging 1.00
R5979:Vmn2r30 UTSW 7 7312335 missense probably damaging 0.99
R6035:Vmn2r30 UTSW 7 7334351 missense probably benign 0.34
R6035:Vmn2r30 UTSW 7 7334351 missense probably benign 0.34
R6336:Vmn2r30 UTSW 7 7334308 missense probably benign 0.03
R6904:Vmn2r30 UTSW 7 7312548 missense probably damaging 1.00
V8831:Vmn2r30 UTSW 7 7334149 missense probably benign 0.00
Posted On2015-04-16