Incidental Mutation 'R2939:Vmn2r55'
ID 264572
Institutional Source Beutler Lab
Gene Symbol Vmn2r55
Ensembl Gene ENSMUSG00000091045
Gene Name vomeronasal 2, receptor 55
Synonyms
MMRRC Submission 040516-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.098) question?
Stock # R2939 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 12385633-12422855 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 12385832 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 716 (L716P)
Ref Sequence ENSEMBL: ENSMUSP00000133483 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000172743]
AlphaFold A0A3B2W3J6
Predicted Effect probably damaging
Transcript: ENSMUST00000172743
AA Change: L716P

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000133483
Gene: ENSMUSG00000091045
AA Change: L716P

DomainStartEndE-ValueType
Pfam:ANF_receptor 5 397 3.4e-57 PFAM
Pfam:7tm_3 525 762 3.7e-54 PFAM
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.6%
Validation Efficiency 98% (62/63)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actl11 T C 9: 107,808,409 (GRCm39) Y911H possibly damaging Het
Arhgef26 A C 3: 62,288,331 (GRCm39) K467T possibly damaging Het
Armcx6 A T X: 133,650,625 (GRCm39) W69R probably damaging Het
Asl T C 5: 130,042,245 (GRCm39) Y277C probably damaging Het
Atm T C 9: 53,406,011 (GRCm39) Y1219C probably damaging Het
Azin2 C T 4: 128,828,397 (GRCm39) C270Y probably benign Het
Brsk1 A T 7: 4,711,139 (GRCm39) I545F possibly damaging Het
Carm1 C A 9: 21,490,692 (GRCm39) probably null Het
Cfap410 A G 10: 77,817,507 (GRCm39) N78S probably benign Het
Cfap69 G A 5: 5,694,432 (GRCm39) A143V probably damaging Het
Cldn14 T C 16: 93,716,192 (GRCm39) K218R probably damaging Het
Col5a3 T C 9: 20,706,954 (GRCm39) K714R unknown Het
Crybg2 A G 4: 133,809,745 (GRCm39) H1517R possibly damaging Het
Dagla A C 19: 10,233,728 (GRCm39) F382C probably damaging Het
Dixdc1 G A 9: 50,622,259 (GRCm39) A25V probably damaging Het
Dock6 A G 9: 21,750,496 (GRCm39) F473L possibly damaging Het
Eif5 T C 12: 111,506,713 (GRCm39) C102R probably damaging Het
Faiml A G 9: 99,114,527 (GRCm39) C121R probably damaging Het
Fhdc1 A G 3: 84,364,577 (GRCm39) V223A possibly damaging Het
Garin4 T C 1: 190,896,103 (GRCm39) D180G possibly damaging Het
Gpatch8 A G 11: 102,399,010 (GRCm39) V74A unknown Het
Haghl A G 17: 26,004,060 (GRCm39) V8A possibly damaging Het
Ksr1 A G 11: 78,936,007 (GRCm39) probably null Het
Lama5 A C 2: 179,840,747 (GRCm39) Y584D probably damaging Het
Lgi4 C T 7: 30,767,253 (GRCm39) R427* probably null Het
Lrriq1 T A 10: 102,980,750 (GRCm39) S1462C probably damaging Het
Map3k4 C T 17: 12,480,157 (GRCm39) E682K probably damaging Het
Myo9b G A 8: 71,786,981 (GRCm39) R721Q probably benign Het
Nherf1 C T 11: 115,071,270 (GRCm39) R335C probably damaging Het
Nmnat2 C A 1: 152,950,474 (GRCm39) S53Y probably damaging Het
Or8b12i C A 9: 20,082,061 (GRCm39) G269W probably benign Het
Or8g34 G A 9: 39,373,226 (GRCm39) M166I probably benign Het
Pcsk7 C T 9: 45,827,322 (GRCm39) A363V probably damaging Het
Pdrg1 C T 2: 152,854,355 (GRCm39) G62R probably damaging Het
Pdzd7 A G 19: 45,033,862 (GRCm39) I74T possibly damaging Het
Plcb4 T C 2: 135,781,123 (GRCm39) probably benign Het
Pramel28 A G 4: 143,693,247 (GRCm39) V77A probably benign Het
Rnf25 A G 1: 74,635,047 (GRCm39) V135A possibly damaging Het
Rph3a A G 5: 121,118,212 (GRCm39) probably benign Het
Rsf1 CG CGACGGCGGTG 7: 97,229,115 (GRCm39) probably benign Het
Senp6 G A 9: 80,051,124 (GRCm39) A1134T probably benign Het
Slc1a6 G T 10: 78,650,448 (GRCm39) *562L probably null Het
Slc26a6 G A 9: 108,734,236 (GRCm39) V206I probably benign Het
Slc45a3 A G 1: 131,905,637 (GRCm39) E206G probably damaging Het
Smc1a T A X: 150,816,695 (GRCm39) Y516N probably damaging Het
Smpd3 A G 8: 106,984,039 (GRCm39) V560A probably benign Het
Spata31g1 A G 4: 42,972,946 (GRCm39) K760E probably benign Het
Ssc4d T C 5: 135,994,578 (GRCm39) T51A possibly damaging Het
Suco A G 1: 161,676,220 (GRCm39) I386T probably damaging Het
Tecta A T 9: 42,289,290 (GRCm39) M425K possibly damaging Het
Tmprss11e G A 5: 86,869,266 (GRCm39) R96W probably damaging Het
Trim63 T C 4: 134,050,308 (GRCm39) probably benign Het
Trpv1 A G 11: 73,145,675 (GRCm39) K403R probably damaging Het
Ttc39d A G 17: 80,524,982 (GRCm39) Y547C probably damaging Het
Unc79 C T 12: 102,957,684 (GRCm39) T33I probably damaging Het
Usp47 G A 7: 111,681,743 (GRCm39) S518N probably damaging Het
Vmn2r22 T A 6: 123,614,594 (GRCm39) D332V probably damaging Het
Zfp558 T C 9: 18,367,924 (GRCm39) N288S possibly damaging Het
Other mutations in Vmn2r55
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02684:Vmn2r55 APN 7 12,404,887 (GRCm39) missense probably damaging 1.00
IGL03035:Vmn2r55 APN 7 12,404,743 (GRCm39) missense probably benign 0.01
IGL03115:Vmn2r55 APN 7 12,404,558 (GRCm39) missense probably damaging 1.00
IGL03251:Vmn2r55 APN 7 12,405,120 (GRCm39) splice site probably benign
R0140:Vmn2r55 UTSW 7 12,402,104 (GRCm39) missense possibly damaging 0.58
R0511:Vmn2r55 UTSW 7 12,404,945 (GRCm39) missense possibly damaging 0.88
R1281:Vmn2r55 UTSW 7 12,404,825 (GRCm39) missense probably benign 0.02
R1564:Vmn2r55 UTSW 7 12,418,678 (GRCm39) missense probably damaging 1.00
R1602:Vmn2r55 UTSW 7 12,386,571 (GRCm39) missense probably damaging 1.00
R1785:Vmn2r55 UTSW 7 12,402,111 (GRCm39) missense probably damaging 0.98
R2993:Vmn2r55 UTSW 7 12,418,882 (GRCm39) missense probably damaging 1.00
R3151:Vmn2r55 UTSW 7 12,404,634 (GRCm39) missense probably benign 0.06
R4272:Vmn2r55 UTSW 7 12,402,106 (GRCm39) missense probably benign 0.38
R4589:Vmn2r55 UTSW 7 12,404,822 (GRCm39) missense probably damaging 0.99
R4624:Vmn2r55 UTSW 7 12,404,627 (GRCm39) missense possibly damaging 0.83
R4965:Vmn2r55 UTSW 7 12,404,478 (GRCm39) missense possibly damaging 0.91
R5294:Vmn2r55 UTSW 7 12,385,791 (GRCm39) missense probably damaging 1.00
R5364:Vmn2r55 UTSW 7 12,404,830 (GRCm39) missense possibly damaging 0.51
R5395:Vmn2r55 UTSW 7 12,385,874 (GRCm39) missense probably damaging 1.00
R5401:Vmn2r55 UTSW 7 12,385,871 (GRCm39) missense probably benign
R5701:Vmn2r55 UTSW 7 12,404,492 (GRCm39) missense probably benign 0.00
R5771:Vmn2r55 UTSW 7 12,404,959 (GRCm39) missense probably damaging 1.00
R5846:Vmn2r55 UTSW 7 12,404,492 (GRCm39) missense probably benign 0.05
R6148:Vmn2r55 UTSW 7 12,402,069 (GRCm39) missense probably benign 0.01
R6159:Vmn2r55 UTSW 7 12,385,698 (GRCm39) missense probably damaging 1.00
R6541:Vmn2r55 UTSW 7 12,404,939 (GRCm39) missense probably damaging 1.00
R7286:Vmn2r55 UTSW 7 12,386,000 (GRCm39) missense probably damaging 0.99
R7483:Vmn2r55 UTSW 7 12,404,755 (GRCm39) missense probably benign 0.00
R8269:Vmn2r55 UTSW 7 12,404,585 (GRCm39) missense possibly damaging 0.86
R8749:Vmn2r55 UTSW 7 12,385,796 (GRCm39) missense probably damaging 1.00
R8914:Vmn2r55 UTSW 7 12,405,024 (GRCm39) missense probably benign 0.09
R9049:Vmn2r55 UTSW 7 12,418,908 (GRCm39) missense probably damaging 1.00
R9175:Vmn2r55 UTSW 7 12,385,793 (GRCm39) missense possibly damaging 0.67
R9344:Vmn2r55 UTSW 7 12,385,782 (GRCm39) nonsense probably null
R9498:Vmn2r55 UTSW 7 12,404,812 (GRCm39) missense probably damaging 1.00
R9715:Vmn2r55 UTSW 7 12,402,061 (GRCm39) missense probably damaging 1.00
Z1177:Vmn2r55 UTSW 7 12,405,106 (GRCm39) missense possibly damaging 0.91
Z1177:Vmn2r55 UTSW 7 12,385,764 (GRCm39) missense possibly damaging 0.83
Predicted Primers PCR Primer
(F):5'- CTTCTGTGGAGCATCTAACTCTGTC -3'
(R):5'- AGCCCCAGCACATTGTCATC -3'

Sequencing Primer
(F):5'- GCCTTGCTTTAGCCAGGAAG -3'
(R):5'- TGTCATCCAATGCCATGATGG -3'
Posted On 2015-02-05