Incidental Mutation 'IGL02947:Vmn1r4'
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ID364764
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r4
Ensembl Gene ENSMUSG00000071893
Gene Namevomeronasal 1 receptor 4
SynonymsC230065D10Rik, V1rc21
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.053) question?
Stock #IGL02947
Quality Score
Status
Chromosome6
Chromosomal Location56924015-56958100 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 56957246 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Serine at position 245 (F245S)
Ref Sequence ENSEMBL: ENSMUSP00000153919 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096612] [ENSMUST00000176838] [ENSMUST00000227073]
Predicted Effect probably benign
Transcript: ENSMUST00000096612
AA Change: F245S

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000094369
Gene: ENSMUSG00000071893
AA Change: F245S

DomainStartEndE-ValueType
Pfam:V1R 28 293 3.8e-58 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000176838
AA Change: F245S

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000135323
Gene: ENSMUSG00000071893
AA Change: F245S

DomainStartEndE-ValueType
Pfam:V1R 28 293 3.8e-58 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000227073
AA Change: F245S

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001L19Rik T A 13: 68,611,193 F95L probably benign Het
Aasdh A G 5: 76,902,110 V13A probably benign Het
Atp8b5 T A 4: 43,305,774 I106K possibly damaging Het
Cdh15 T C 8: 122,865,372 S633P probably benign Het
Celsr3 A G 9: 108,845,935 T228A probably benign Het
Chrng A G 1: 87,209,884 probably null Het
Coprs T C 8: 13,885,782 E79G probably damaging Het
Cpb2 A C 14: 75,283,318 Y391S probably damaging Het
Cyp2j8 A T 4: 96,470,578 I368N probably damaging Het
Ddah1 T C 3: 145,759,087 F76L probably benign Het
Eif2ak4 A G 2: 118,431,033 T573A probably benign Het
Exoc6b T A 6: 84,858,429 M375L probably benign Het
Fasn T C 11: 120,815,676 E994G probably damaging Het
Fem1a T A 17: 56,258,640 C578S probably benign Het
Garnl3 A G 2: 33,046,594 S188P probably damaging Het
Gpn3 T C 5: 122,378,488 V60A possibly damaging Het
Hnrnpr A G 4: 136,316,379 D59G probably damaging Het
Hydin A T 8: 110,418,462 E815V probably damaging Het
Itga9 C T 9: 118,658,533 T228M probably damaging Het
Kpna7 T C 5: 144,994,074 I320M probably damaging Het
Lnpep T C 17: 17,570,972 T437A probably damaging Het
Ltf C T 9: 111,038,947 T48I probably benign Het
Masp1 T G 16: 23,494,726 D153A probably damaging Het
Mcpt9 T A 14: 56,026,916 R241* probably null Het
Msantd4 T A 9: 4,384,787 S171T probably damaging Het
Nos1 G A 5: 117,943,317 V1229M probably damaging Het
Npc1l1 A G 11: 6,229,246 S55P probably benign Het
Oc90 T C 15: 65,888,134 K212R probably benign Het
Olfr1095 C T 2: 86,850,786 R304K probably benign Het
Olfr446 A G 6: 42,927,896 I222V probably benign Het
Olfr771 C A 10: 129,160,570 C138F probably damaging Het
Prr12 T A 7: 45,048,556 Q645L unknown Het
Psmd9 A G 5: 123,246,215 I145V probably benign Het
Rbks T C 5: 31,660,063 I121V probably benign Het
Rnase2b A T 14: 51,162,807 Y115F probably damaging Het
Sarnp A G 10: 128,839,854 E78G probably benign Het
Sltm A G 9: 70,591,664 S1007G probably benign Het
Spata31d1c T A 13: 65,034,945 Y100* probably null Het
Srrm2 T C 17: 23,810,746 S222P probably benign Het
Sult3a1 G A 10: 33,864,050 R35Q possibly damaging Het
Tfap4 T C 16: 4,551,360 D132G probably damaging Het
Tmem53 C T 4: 117,268,088 Q111* probably null Het
Togaram1 T A 12: 65,021,500 V1709D probably damaging Het
Trpm3 A T 19: 22,901,119 D628V probably damaging Het
Ttn T A 2: 76,714,494 K31009* probably null Het
Vldlr A G 19: 27,239,720 I58V probably benign Het
Vrtn T A 12: 84,648,484 S3T probably damaging Het
Vwa7 A G 17: 35,023,500 probably null Het
Wrnip1 T A 13: 32,822,070 Y632N probably damaging Het
Other mutations in Vmn1r4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02532:Vmn1r4 APN 6 56957150 missense possibly damaging 0.85
IGL02709:Vmn1r4 APN 6 56956539 nonsense probably null
R0436:Vmn1r4 UTSW 6 56956962 missense probably damaging 1.00
R0518:Vmn1r4 UTSW 6 56956898 missense probably benign
R1639:Vmn1r4 UTSW 6 56957075 missense probably damaging 0.99
R1667:Vmn1r4 UTSW 6 56956753 missense probably damaging 0.98
R1776:Vmn1r4 UTSW 6 56957038 missense probably benign 0.00
R1976:Vmn1r4 UTSW 6 56956738 missense probably damaging 1.00
R3746:Vmn1r4 UTSW 6 56957131 missense probably damaging 0.98
R4724:Vmn1r4 UTSW 6 56957364 missense probably benign 0.04
R4814:Vmn1r4 UTSW 6 56956730 missense possibly damaging 0.60
R5709:Vmn1r4 UTSW 6 56956619 missense probably benign 0.22
R6468:Vmn1r4 UTSW 6 56956867 missense probably benign 0.00
R6963:Vmn1r4 UTSW 6 56956784 missense probably damaging 0.99
R7385:Vmn1r4 UTSW 6 56956736 missense probably damaging 1.00
R7953:Vmn1r4 UTSW 6 56956530 missense probably benign 0.38
R8138:Vmn1r4 UTSW 6 56957406 makesense probably null
Z1088:Vmn1r4 UTSW 6 56957065 missense possibly damaging 0.94
Posted On2015-12-18