Incidental Mutation 'IGL01611:Gpr157'
ID 92098
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gpr157
Ensembl Gene ENSMUSG00000047875
Gene Name G protein-coupled receptor 157
Synonyms F730108M23Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01611
Quality Score
Status
Chromosome 4
Chromosomal Location 150171960-150190457 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 150186094 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 219 (S219P)
Ref Sequence ENSEMBL: ENSMUSP00000092020 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094451]
AlphaFold Q8C206
Predicted Effect possibly damaging
Transcript: ENSMUST00000094451
AA Change: S219P

PolyPhen 2 Score 0.589 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000092020
Gene: ENSMUSG00000047875
AA Change: S219P

DomainStartEndE-ValueType
Pfam:Dicty_CAR 11 205 4.1e-12 PFAM
Pfam:Frizzled 14 250 2e-8 PFAM
Pfam:7tm_2 14 274 2e-15 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930447C04Rik A G 12: 72,954,644 (GRCm39) L209S possibly damaging Het
Abcc2 G T 19: 43,815,068 (GRCm39) V1152F probably damaging Het
Adam9 C T 8: 25,457,212 (GRCm39) V639I probably benign Het
Cdc6 A G 11: 98,805,989 (GRCm39) I388V probably benign Het
Chrm5 C T 2: 112,310,651 (GRCm39) W155* probably null Het
Chrna9 A G 5: 66,128,287 (GRCm39) D161G probably damaging Het
Det1 A G 7: 78,477,702 (GRCm39) V541A possibly damaging Het
Efhc1 G T 1: 21,060,911 (GRCm39) *649L probably null Het
Ehbp1 C T 11: 22,122,883 (GRCm39) V146M probably damaging Het
Enam A C 5: 88,651,608 (GRCm39) D1039A probably damaging Het
Fam20b A T 1: 156,530,035 (GRCm39) V133E probably benign Het
Frem2 T A 3: 53,563,130 (GRCm39) Q459L probably benign Het
Gapdhs C T 7: 30,429,866 (GRCm39) probably benign Het
Gm3404 T A 5: 146,465,157 (GRCm39) V299D possibly damaging Het
Gorasp2 C A 2: 70,519,604 (GRCm39) H310N possibly damaging Het
Gpt2 T A 8: 86,246,167 (GRCm39) C375* probably null Het
Gtf2h3 T C 5: 124,733,748 (GRCm39) S274P probably damaging Het
Hmg20b C T 10: 81,183,309 (GRCm39) V83M probably benign Het
Igf2r G T 17: 12,944,302 (GRCm39) Y400* probably null Het
Ipo9 A T 1: 135,314,431 (GRCm39) W942R possibly damaging Het
Iqch T C 9: 63,403,519 (GRCm39) probably null Het
Kcnh3 T C 15: 99,127,383 (GRCm39) L393P probably benign Het
Kcnk12 T A 17: 88,104,495 (GRCm39) I130L probably benign Het
Lcorl T C 5: 45,904,434 (GRCm39) T205A probably damaging Het
Lpar6 G T 14: 73,476,878 (GRCm39) A280S probably damaging Het
Mgarp A T 3: 51,296,570 (GRCm39) V152E probably damaging Het
Pard3b A G 1: 62,677,021 (GRCm39) D1184G probably damaging Het
Pcnt A G 10: 76,272,258 (GRCm39) probably null Het
Pde6b A G 5: 108,551,262 (GRCm39) N182S possibly damaging Het
Pom121 T C 5: 135,412,526 (GRCm39) K516E unknown Het
Psmg2 G A 18: 67,786,293 (GRCm39) V218I probably benign Het
Ptpn18 T C 1: 34,498,898 (GRCm39) probably benign Het
Rapgef5 C T 12: 117,717,154 (GRCm39) probably benign Het
Ryr2 A G 13: 11,606,202 (GRCm39) L4460S possibly damaging Het
Sema6b T C 17: 56,436,969 (GRCm39) probably null Het
Serpinb6d T A 13: 33,850,375 (GRCm39) C67* probably null Het
Sorbs2 T G 8: 46,248,381 (GRCm39) V510G probably null Het
Spic T A 10: 88,511,864 (GRCm39) I131F possibly damaging Het
Spire2 T C 8: 124,086,137 (GRCm39) S290P probably damaging Het
Tas2r117 C T 6: 132,780,447 (GRCm39) S195F probably benign Het
Tas2r117 T C 6: 132,780,450 (GRCm39) V196A probably damaging Het
Tff1 C T 17: 31,381,703 (GRCm39) G58D probably damaging Het
Tmprss11g T C 5: 86,638,640 (GRCm39) T283A probably benign Het
Toporsl T A 4: 52,610,794 (GRCm39) L229H probably damaging Het
Vmn2r80 G A 10: 79,007,488 (GRCm39) G488D probably damaging Het
Vps54 T A 11: 21,261,082 (GRCm39) V583D probably damaging Het
Vwa1 T C 4: 155,855,255 (GRCm39) E286G possibly damaging Het
Vwde A T 6: 13,219,977 (GRCm39) I58N probably damaging Het
Zbtb11 T C 16: 55,800,973 (GRCm39) V109A probably damaging Het
Zfp319 C T 8: 96,055,540 (GRCm39) R221Q probably benign Het
Other mutations in Gpr157
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02233:Gpr157 APN 4 150,186,184 (GRCm39) missense possibly damaging 0.63
R2912:Gpr157 UTSW 4 150,183,222 (GRCm39) missense probably benign 0.08
R2913:Gpr157 UTSW 4 150,183,222 (GRCm39) missense probably benign 0.08
R4721:Gpr157 UTSW 4 150,183,420 (GRCm39) missense probably benign 0.01
R4840:Gpr157 UTSW 4 150,186,823 (GRCm39) missense probably benign 0.00
R5089:Gpr157 UTSW 4 150,186,750 (GRCm39) missense possibly damaging 0.89
R5322:Gpr157 UTSW 4 150,183,309 (GRCm39) missense probably benign
R5445:Gpr157 UTSW 4 150,186,825 (GRCm39) missense probably benign 0.00
R6210:Gpr157 UTSW 4 150,186,055 (GRCm39) missense probably damaging 1.00
R7252:Gpr157 UTSW 4 150,183,331 (GRCm39) missense probably benign 0.01
R8246:Gpr157 UTSW 4 150,186,753 (GRCm39) missense possibly damaging 0.80
R8274:Gpr157 UTSW 4 150,172,500 (GRCm39) missense probably damaging 1.00
Posted On 2013-12-09