Incidental Mutation 'R4398:Gpr20'
ID 325604
Institutional Source Beutler Lab
Gene Symbol Gpr20
Ensembl Gene ENSMUSG00000045281
Gene Name G protein-coupled receptor 20
Synonyms A430106B11Rik
MMRRC Submission 041130-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4398 (G1)
Quality Score 191
Status Validated
Chromosome 15
Chromosomal Location 73566453-73579354 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 73568125 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 88 (T88I)
Ref Sequence ENSEMBL: ENSMUSP00000063910 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000064166]
AlphaFold Q8BYC4
Predicted Effect probably benign
Transcript: ENSMUST00000064166
AA Change: T88I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000063910
Gene: ENSMUSG00000045281
AA Change: T88I

DomainStartEndE-ValueType
Pfam:7tm_1 68 296 7.7e-32 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.7%
Validation Efficiency 96% (53/55)
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts20 C A 15: 94,231,576 (GRCm39) R871L possibly damaging Het
Adcy5 G A 16: 35,089,363 (GRCm39) C520Y probably damaging Het
AI661453 G A 17: 47,779,042 (GRCm39) probably benign Het
Bptf T C 11: 107,001,670 (GRCm39) K481E probably damaging Het
Cnot10 T A 9: 114,460,949 (GRCm39) K74* probably null Het
Ctc1 C T 11: 68,913,697 (GRCm39) P200S probably damaging Het
Dact1 T C 12: 71,363,959 (GRCm39) Y210H probably damaging Het
Dbn1 T C 13: 55,623,194 (GRCm39) T430A probably benign Het
Dmd A C X: 82,765,624 (GRCm39) T657P probably benign Het
Efnb2 C T 8: 8,670,832 (GRCm39) R256H possibly damaging Het
Eif4a1 T C 11: 69,560,070 (GRCm39) I116M possibly damaging Het
F730035P03Rik A T 7: 99,429,475 (GRCm39) noncoding transcript Het
Fbn1 C T 2: 125,239,701 (GRCm39) V329I probably benign Het
Herc1 T G 9: 66,386,735 (GRCm39) V3783G probably benign Het
Khdc1a A G 1: 21,420,617 (GRCm39) D79G possibly damaging Het
Klk1b16 A T 7: 43,790,851 (GRCm39) I218F probably damaging Het
Malrd1 C T 2: 16,155,594 (GRCm39) T2001I unknown Het
Mia3 A G 1: 183,111,733 (GRCm39) S556P probably damaging Het
Myo3a T A 2: 22,467,854 (GRCm39) D369E probably benign Het
Nelfa T C 5: 34,058,623 (GRCm39) D279G possibly damaging Het
Ntrk3 A T 7: 77,900,517 (GRCm39) C607* probably null Het
Or13a20 T C 7: 140,232,741 (GRCm39) V283A possibly damaging Het
Pclo A T 5: 14,825,380 (GRCm39) Q1371L probably damaging Het
Pdzd2 A T 15: 12,376,061 (GRCm39) V1358E probably benign Het
Pgr T C 9: 8,903,750 (GRCm39) probably null Het
Prag1 A G 8: 36,570,809 (GRCm39) D464G probably damaging Het
Prickle4 A G 17: 48,001,456 (GRCm39) probably benign Het
Prim2 A G 1: 33,551,192 (GRCm39) Y309H probably damaging Het
Prkaa1 A G 15: 5,206,642 (GRCm39) Q464R possibly damaging Het
Rab36 G A 10: 74,880,328 (GRCm39) V63I probably damaging Het
Rint1 T A 5: 23,999,445 (GRCm39) I78K possibly damaging Het
Rnf130 T A 11: 49,962,205 (GRCm39) F217Y probably benign Het
Smad7 T C 18: 75,527,234 (GRCm39) V360A probably damaging Het
Sp110 A C 1: 85,505,050 (GRCm39) F434C probably benign Het
Stag1 A G 9: 100,838,659 (GRCm39) probably benign Het
Tlr12 T A 4: 128,509,988 (GRCm39) D754V probably benign Het
Tmf1 G A 6: 97,155,857 (GRCm39) P43L probably damaging Het
Togaram1 A G 12: 65,027,630 (GRCm39) N873S probably benign Het
Tsn C T 1: 118,238,799 (GRCm39) probably benign Het
Ubn1 A G 16: 4,882,289 (GRCm39) K250R probably damaging Het
Vmn1r25 A T 6: 57,955,812 (GRCm39) V159D probably damaging Het
Vmn2r89 T C 14: 51,689,551 (GRCm39) L18P probably damaging Het
Vps8 T G 16: 21,323,216 (GRCm39) N689K probably damaging Het
Ythdc1 T A 5: 86,963,513 (GRCm39) D30E possibly damaging Het
Ythdc1 G T 5: 86,983,679 (GRCm39) probably benign Het
Zfp407 G A 18: 84,580,856 (GRCm39) Q86* probably null Het
Zfp521 C T 18: 13,979,601 (GRCm39) E271K probably benign Het
Other mutations in Gpr20
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01759:Gpr20 APN 15 73,568,269 (GRCm39) missense probably damaging 1.00
IGL02312:Gpr20 APN 15 73,568,275 (GRCm39) missense probably benign 0.00
I1329:Gpr20 UTSW 15 73,567,612 (GRCm39) missense probably damaging 1.00
R1188:Gpr20 UTSW 15 73,567,617 (GRCm39) missense probably damaging 1.00
R1604:Gpr20 UTSW 15 73,567,853 (GRCm39) missense probably damaging 0.98
R1687:Gpr20 UTSW 15 73,567,751 (GRCm39) missense probably benign 0.21
R4436:Gpr20 UTSW 15 73,567,649 (GRCm39) missense probably benign 0.06
R4505:Gpr20 UTSW 15 73,568,321 (GRCm39) missense probably benign 0.03
R4615:Gpr20 UTSW 15 73,567,585 (GRCm39) missense probably benign
R4616:Gpr20 UTSW 15 73,567,585 (GRCm39) missense probably benign
R4617:Gpr20 UTSW 15 73,567,585 (GRCm39) missense probably benign
R4618:Gpr20 UTSW 15 73,567,585 (GRCm39) missense probably benign
R6120:Gpr20 UTSW 15 73,567,853 (GRCm39) missense probably damaging 0.98
R7224:Gpr20 UTSW 15 73,567,981 (GRCm39) missense probably damaging 1.00
R8313:Gpr20 UTSW 15 73,568,161 (GRCm39) missense probably damaging 1.00
R9525:Gpr20 UTSW 15 73,567,681 (GRCm39) missense probably benign 0.31
Predicted Primers PCR Primer
(F):5'- AAAGATGCACACGGCCTTGG -3'
(R):5'- AGATGCCCCTGTTCCATCAC -3'

Sequencing Primer
(F):5'- TTGCACAATGGCCAGGTAGC -3'
(R):5'- ACTTTGCCCGGCTGGATGAG -3'
Posted On 2015-07-06