Incidental Mutation 'R5664:Vmn2r76'
ID 444265
Institutional Source Beutler Lab
Gene Symbol Vmn2r76
Ensembl Gene ENSMUSG00000091239
Gene Name vomeronasal 2, receptor 76
Synonyms
MMRRC Submission 043307-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.166) question?
Stock # R5664 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 85874414-85895409 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 85895202 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000127309 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165771]
AlphaFold E9Q3F5
Predicted Effect probably null
Transcript: ENSMUST00000165771
SMART Domains Protein: ENSMUSP00000127309
Gene: ENSMUSG00000091239

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 78 470 1.2e-29 PFAM
low complexity region 476 489 N/A INTRINSIC
Pfam:NCD3G 513 565 3.7e-22 PFAM
Pfam:7tm_3 598 833 1.4e-52 PFAM
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610030E20Rik T A 6: 72,325,977 (GRCm39) probably null Het
9430015G10Rik T A 4: 156,208,016 (GRCm39) L112H probably damaging Het
Acaca T C 11: 84,134,210 (GRCm39) L441P probably damaging Het
Ank3 G A 10: 69,838,395 (GRCm39) R1566K possibly damaging Het
Arsj A T 3: 126,232,306 (GRCm39) I351F probably damaging Het
Atp6v1b2 A G 8: 69,560,272 (GRCm39) T373A probably damaging Het
Atr C A 9: 95,787,866 (GRCm39) N1486K probably benign Het
Avl9 T C 6: 56,730,824 (GRCm39) S583P probably damaging Het
Bptf A T 11: 106,964,525 (GRCm39) D1493E probably benign Het
Brme1 A T 8: 84,893,288 (GRCm39) I152F probably benign Het
C2cd2l T C 9: 44,225,069 (GRCm39) E548G probably damaging Het
Capn3 G A 2: 120,307,506 (GRCm39) R15Q probably benign Het
Ccl3 A G 11: 83,540,039 (GRCm39) F22S probably benign Het
Clcf1 T C 19: 4,272,150 (GRCm39) F69S probably damaging Het
Col13a1 T C 10: 61,686,895 (GRCm39) E170G probably damaging Het
Dhx29 T A 13: 113,083,413 (GRCm39) F489L probably damaging Het
Dhx8 A T 11: 101,631,577 (GRCm39) N390I probably damaging Het
Dkk1 T A 19: 30,526,189 (GRCm39) Y135F probably benign Het
Edil3 G T 13: 89,467,832 (GRCm39) V446F probably damaging Het
Epha5 T A 5: 84,479,725 (GRCm39) E93V probably damaging Het
Epsti1 C T 14: 78,201,104 (GRCm39) T196I possibly damaging Het
Fras1 T C 5: 96,876,394 (GRCm39) S2376P possibly damaging Het
Frem2 A G 3: 53,559,911 (GRCm39) V1532A probably benign Het
Fsip2 T A 2: 82,818,439 (GRCm39) M4724K probably benign Het
Gcat T A 15: 78,927,273 (GRCm39) L238Q probably damaging Het
Gimap6 T C 6: 48,679,209 (GRCm39) K276E probably benign Het
Gjb5 T A 4: 127,249,722 (GRCm39) I141F probably benign Het
Glt6d1 T C 2: 25,704,192 (GRCm39) I7V probably benign Het
Gtf2h5 G A 17: 6,134,799 (GRCm39) G30R probably damaging Het
Herc6 C A 6: 57,595,669 (GRCm39) T449K probably benign Het
Hpn A T 7: 30,798,687 (GRCm39) Y132N probably damaging Het
Hpx A T 7: 105,244,355 (GRCm39) M190K probably benign Het
Inf2 A G 12: 112,578,162 (GRCm39) H1151R unknown Het
Krt74 A G 15: 101,669,014 (GRCm39) noncoding transcript Het
Loxl3 G A 6: 83,026,863 (GRCm39) S564N probably benign Het
Map7 T A 10: 20,143,105 (GRCm39) V418E unknown Het
Mrpl37 T C 4: 106,921,588 (GRCm39) N214D probably benign Het
Mthfr T C 4: 148,139,923 (GRCm39) Y656H probably damaging Het
Myo9b A G 8: 71,812,526 (GRCm39) D2099G probably benign Het
Nktr T A 9: 121,578,483 (GRCm39) C825* probably null Het
Nomo1 A G 7: 45,725,581 (GRCm39) E1029G probably benign Het
Nup133 T C 8: 124,633,020 (GRCm39) D1037G probably benign Het
Or4b12 A G 2: 90,095,959 (GRCm39) F272L probably damaging Het
Or5w22 T C 2: 87,363,178 (GRCm39) L267P probably benign Het
Pcdhb14 T A 18: 37,582,049 (GRCm39) V385D possibly damaging Het
Pik3c2g T C 6: 139,682,733 (GRCm39) L38P probably damaging Het
Pkd1 A T 17: 24,788,345 (GRCm39) D701V probably damaging Het
Pnpla6 A G 8: 3,587,478 (GRCm39) T1070A probably damaging Het
Ppl T C 16: 4,923,919 (GRCm39) D185G probably benign Het
Prp2rt C A 13: 97,235,629 (GRCm39) L39F probably damaging Het
Prss1l C T 6: 41,371,605 (GRCm39) P17L probably benign Het
Prune1 A T 3: 95,165,489 (GRCm39) L261Q probably damaging Het
Qser1 A T 2: 104,608,541 (GRCm39) L1444I probably damaging Het
Serpina6 A C 12: 103,620,726 (GRCm39) C8G probably damaging Het
Sla2 A T 2: 156,716,919 (GRCm39) D180E probably benign Het
Slc4a4 C T 5: 89,176,103 (GRCm39) L25F probably damaging Het
Snhg16 A T 11: 116,563,490 (GRCm39) T27S possibly damaging Het
Tbx3 A G 5: 119,816,796 (GRCm39) K311R possibly damaging Het
Tdpoz6 A G 3: 93,599,994 (GRCm39) F125S probably benign Het
Thbs2 A T 17: 14,910,099 (GRCm39) C167S probably damaging Het
Trak1 T A 9: 121,301,373 (GRCm39) C710S possibly damaging Het
Tsks G A 7: 44,603,208 (GRCm39) E337K probably damaging Het
Vcpip1 A G 1: 9,816,604 (GRCm39) I593T probably damaging Het
Vmn2r118 A G 17: 55,899,765 (GRCm39) I713T possibly damaging Het
Vmn2r23 C T 6: 123,690,033 (GRCm39) T303M probably damaging Het
Vmn2r68 A T 7: 84,882,978 (GRCm39) M258K probably benign Het
Wap A G 11: 6,588,609 (GRCm39) I5T possibly damaging Het
Zfp235 A C 7: 23,841,576 (GRCm39) H665P probably damaging Het
Other mutations in Vmn2r76
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00969:Vmn2r76 APN 7 85,877,925 (GRCm39) missense probably benign
IGL01374:Vmn2r76 APN 7 85,874,857 (GRCm39) missense probably benign 0.02
IGL01419:Vmn2r76 APN 7 85,874,910 (GRCm39) missense probably benign 0.32
IGL01627:Vmn2r76 APN 7 85,874,871 (GRCm39) missense probably damaging 1.00
IGL01730:Vmn2r76 APN 7 85,879,406 (GRCm39) missense probably benign 0.02
IGL01957:Vmn2r76 APN 7 85,877,925 (GRCm39) missense probably benign
IGL02214:Vmn2r76 APN 7 85,879,138 (GRCm39) missense probably benign 0.07
IGL02489:Vmn2r76 APN 7 85,878,071 (GRCm39) missense probably benign 0.41
IGL02543:Vmn2r76 APN 7 85,879,356 (GRCm39) missense probably benign 0.06
IGL02579:Vmn2r76 APN 7 85,877,961 (GRCm39) nonsense probably null
IGL02598:Vmn2r76 APN 7 85,877,879 (GRCm39) missense probably benign 0.05
IGL02720:Vmn2r76 APN 7 85,874,914 (GRCm39) missense probably benign 0.35
IGL02745:Vmn2r76 APN 7 85,879,495 (GRCm39) missense probably benign 0.06
IGL03393:Vmn2r76 APN 7 85,879,034 (GRCm39) missense probably benign 0.01
R0483:Vmn2r76 UTSW 7 85,874,959 (GRCm39) missense probably damaging 1.00
R0513:Vmn2r76 UTSW 7 85,877,987 (GRCm39) missense probably benign 0.01
R0528:Vmn2r76 UTSW 7 85,879,506 (GRCm39) missense possibly damaging 0.80
R0601:Vmn2r76 UTSW 7 85,875,323 (GRCm39) critical splice acceptor site probably null
R0662:Vmn2r76 UTSW 7 85,879,578 (GRCm39) missense probably benign 0.39
R0883:Vmn2r76 UTSW 7 85,877,904 (GRCm39) missense probably benign 0.00
R1532:Vmn2r76 UTSW 7 85,879,454 (GRCm39) missense probably benign 0.02
R1694:Vmn2r76 UTSW 7 85,879,356 (GRCm39) missense probably benign 0.06
R1696:Vmn2r76 UTSW 7 85,880,464 (GRCm39) missense possibly damaging 0.56
R2135:Vmn2r76 UTSW 7 85,880,219 (GRCm39) missense probably benign 0.02
R2151:Vmn2r76 UTSW 7 85,879,692 (GRCm39) missense probably benign
R2181:Vmn2r76 UTSW 7 85,874,743 (GRCm39) missense probably benign 0.00
R2268:Vmn2r76 UTSW 7 85,879,707 (GRCm39) missense probably benign 0.03
R2877:Vmn2r76 UTSW 7 85,875,201 (GRCm39) missense probably benign 0.00
R3155:Vmn2r76 UTSW 7 85,874,959 (GRCm39) missense probably damaging 1.00
R3746:Vmn2r76 UTSW 7 85,874,763 (GRCm39) missense probably benign 0.11
R3799:Vmn2r76 UTSW 7 85,875,244 (GRCm39) missense probably benign 0.00
R3825:Vmn2r76 UTSW 7 85,880,415 (GRCm39) missense probably benign 0.10
R4058:Vmn2r76 UTSW 7 85,879,508 (GRCm39) missense probably benign 0.00
R4237:Vmn2r76 UTSW 7 85,879,740 (GRCm39) missense probably benign 0.00
R4404:Vmn2r76 UTSW 7 85,877,511 (GRCm39) missense probably benign 0.16
R4796:Vmn2r76 UTSW 7 85,879,652 (GRCm39) missense possibly damaging 0.95
R4838:Vmn2r76 UTSW 7 85,874,733 (GRCm39) missense probably damaging 1.00
R5175:Vmn2r76 UTSW 7 85,877,915 (GRCm39) missense probably benign 0.00
R5268:Vmn2r76 UTSW 7 85,875,267 (GRCm39) missense probably damaging 1.00
R5381:Vmn2r76 UTSW 7 85,874,496 (GRCm39) missense probably damaging 1.00
R5531:Vmn2r76 UTSW 7 85,874,657 (GRCm39) missense probably damaging 1.00
R5566:Vmn2r76 UTSW 7 85,875,286 (GRCm39) missense probably damaging 1.00
R5646:Vmn2r76 UTSW 7 85,875,261 (GRCm39) missense probably damaging 0.98
R5818:Vmn2r76 UTSW 7 85,879,142 (GRCm39) missense probably benign 0.00
R6093:Vmn2r76 UTSW 7 85,877,469 (GRCm39) nonsense probably null
R6651:Vmn2r76 UTSW 7 85,878,059 (GRCm39) missense possibly damaging 0.64
R6741:Vmn2r76 UTSW 7 85,879,560 (GRCm39) missense probably benign
R6750:Vmn2r76 UTSW 7 85,875,114 (GRCm39) missense probably damaging 1.00
R7082:Vmn2r76 UTSW 7 85,874,440 (GRCm39) missense probably benign 0.01
R7136:Vmn2r76 UTSW 7 85,877,975 (GRCm39) missense probably benign 0.06
R7524:Vmn2r76 UTSW 7 85,879,374 (GRCm39) missense probably benign 0.00
R7524:Vmn2r76 UTSW 7 85,874,577 (GRCm39) missense probably benign 0.22
R7611:Vmn2r76 UTSW 7 85,879,388 (GRCm39) missense probably benign 0.04
R7833:Vmn2r76 UTSW 7 85,877,892 (GRCm39) missense probably benign
R8002:Vmn2r76 UTSW 7 85,879,271 (GRCm39) missense probably benign 0.05
R8021:Vmn2r76 UTSW 7 85,874,958 (GRCm39) missense probably damaging 1.00
R8023:Vmn2r76 UTSW 7 85,879,028 (GRCm39) missense probably benign 0.00
R8250:Vmn2r76 UTSW 7 85,875,231 (GRCm39) missense possibly damaging 0.82
R8428:Vmn2r76 UTSW 7 85,874,479 (GRCm39) missense possibly damaging 0.63
R8874:Vmn2r76 UTSW 7 85,877,999 (GRCm39) missense probably damaging 1.00
R9139:Vmn2r76 UTSW 7 85,879,170 (GRCm39) missense probably benign 0.02
R9357:Vmn2r76 UTSW 7 85,880,428 (GRCm39) missense probably benign 0.43
Z1176:Vmn2r76 UTSW 7 85,895,271 (GRCm39) missense probably benign 0.39
Predicted Primers PCR Primer
(F):5'- AATTGGTGTTACTCTAGGACCATG -3'
(R):5'- TTGGTCTTAAAGGCTTCCATGC -3'

Sequencing Primer
(F):5'- GTGTTACTCTAGGACCATGATAAAAC -3'
(R):5'- AAAGGCTTCCATGCTTTTCTG -3'
Posted On 2016-11-09