Incidental Mutation 'IGL00819:Vmn1r204'
ID14786
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r204
Ensembl Gene ENSMUSG00000094637
Gene Namevomeronasal 1 receptor 204
SynonymsGm11301
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.091) question?
Stock #IGL00819
Quality Score
Status
Chromosome13
Chromosomal Location22553198-22558200 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 22556947 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Stop codon at position 249 (Y249*)
Ref Sequence ENSEMBL: ENSMUSP00000154519 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091728] [ENSMUST00000228195]
Predicted Effect probably null
Transcript: ENSMUST00000091728
AA Change: Y249*
SMART Domains Protein: ENSMUSP00000089321
Gene: ENSMUSG00000094637
AA Change: Y249*

DomainStartEndE-ValueType
Pfam:TAS2R 3 293 8.4e-8 PFAM
Pfam:V1R 35 297 1.2e-40 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000228195
AA Change: Y249*
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankrd35 A T 3: 96,683,034 probably null Het
Apaf1 G T 10: 90,997,340 probably null Het
Ash1l T A 3: 89,007,736 V1891E possibly damaging Het
Atm A G 9: 53,518,531 S402P probably damaging Het
Camk2g C T 14: 20,737,330 G500S probably damaging Het
Ccdc150 T A 1: 54,263,573 N117K probably damaging Het
Ccl7 A G 11: 82,046,575 N45S probably benign Het
Dnah2 A T 11: 69,473,350 probably null Het
Efcab6 A G 15: 84,018,642 I169T probably benign Het
Exo1 T C 1: 175,896,237 V383A probably benign Het
Fbxl2 A G 9: 113,983,979 probably benign Het
Fryl A T 5: 73,148,108 V106D possibly damaging Het
Fsip1 C A 2: 118,249,912 R121L possibly damaging Het
Igsf9 T C 1: 172,496,636 S789P probably benign Het
Klf7 T C 1: 64,042,317 D284G possibly damaging Het
Mbtd1 A G 11: 93,931,811 probably null Het
Mef2c A T 13: 83,625,380 D125V probably damaging Het
Nectin4 T C 1: 171,384,686 L284S probably damaging Het
Numa1 G T 7: 101,992,710 G122W possibly damaging Het
Pcbd1 A C 10: 61,092,140 E27A probably benign Het
Pclo A G 5: 14,858,846 N5056S unknown Het
Pelp1 G A 11: 70,394,618 P808L unknown Het
Ppp1r12a T C 10: 108,240,821 S304P probably damaging Het
Ppp1r7 T A 1: 93,346,256 D51E probably benign Het
Rassf6 T C 5: 90,604,071 K308E probably benign Het
Rel A T 11: 23,743,029 F335I probably benign Het
Scnn1g A G 7: 121,740,437 E153G probably benign Het
Slc2a5 T C 4: 150,125,656 Y33H probably damaging Het
Slit2 G A 5: 47,989,151 E95K possibly damaging Het
Tpra1 T A 6: 88,909,336 Y65* probably null Het
Trip12 C T 1: 84,754,272 G994S probably damaging Het
Trnt1 T A 6: 106,776,222 Y195* probably null Het
Ttn A G 2: 76,743,050 I17506T probably damaging Het
Ubr4 C T 4: 139,476,282 T4761I possibly damaging Het
Zfp212 C T 6: 47,931,322 P412S probably damaging Het
Zhx1 A G 15: 58,054,694 V52A probably benign Het
Zpbp2 A T 11: 98,557,592 H245L probably damaging Het
Other mutations in Vmn1r204
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01349:Vmn1r204 APN 13 22556334 missense probably damaging 0.99
IGL02653:Vmn1r204 APN 13 22556630 missense probably benign 0.34
R0029:Vmn1r204 UTSW 13 22556418 missense probably benign 0.12
R0078:Vmn1r204 UTSW 13 22556209 missense probably benign 0.01
R0562:Vmn1r204 UTSW 13 22556678 missense probably benign 0.00
R1124:Vmn1r204 UTSW 13 22557039 missense possibly damaging 0.76
R1521:Vmn1r204 UTSW 13 22557078 missense probably benign 0.30
R1544:Vmn1r204 UTSW 13 22556295 missense probably benign 0.13
R2238:Vmn1r204 UTSW 13 22556823 missense probably benign 0.01
R2418:Vmn1r204 UTSW 13 22556250 missense probably damaging 1.00
R2419:Vmn1r204 UTSW 13 22556250 missense probably damaging 1.00
R3944:Vmn1r204 UTSW 13 22556844 missense probably benign 0.02
R4675:Vmn1r204 UTSW 13 22556792 missense probably damaging 1.00
R4782:Vmn1r204 UTSW 13 22556697 missense probably benign 0.03
R4985:Vmn1r204 UTSW 13 22557060 missense probably damaging 1.00
R5219:Vmn1r204 UTSW 13 22556899 missense probably damaging 1.00
R5268:Vmn1r204 UTSW 13 22556742 missense probably damaging 1.00
R6652:Vmn1r204 UTSW 13 22556403 missense probably damaging 0.99
R6943:Vmn1r204 UTSW 13 22556304 missense probably benign 0.00
R7264:Vmn1r204 UTSW 13 22556997 missense probably benign 0.23
R7299:Vmn1r204 UTSW 13 22556805 missense probably damaging 1.00
R7301:Vmn1r204 UTSW 13 22556805 missense probably damaging 1.00
R7593:Vmn1r204 UTSW 13 22556584 nonsense probably null
R7872:Vmn1r204 UTSW 13 22556234 missense probably benign 0.00
R7955:Vmn1r204 UTSW 13 22556234 missense probably benign 0.00
Posted On2012-12-06