Incidental Mutation 'R0498:Adgrf2'
ID 40634
Institutional Source Beutler Lab
Gene Symbol Adgrf2
Ensembl Gene ENSMUSG00000057899
Gene Name adhesion G protein-coupled receptor F2
Synonyms PGR20, Gpr111
MMRRC Submission 038694-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0498 (G1)
Quality Score 217
Status Validated
Chromosome 17
Chromosomal Location 43007021-43053070 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 43025206 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000109244 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113614]
AlphaFold E9Q4J9
Predicted Effect probably benign
Transcript: ENSMUST00000113614
SMART Domains Protein: ENSMUSP00000109244
Gene: ENSMUSG00000057899

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
GPS 325 376 2.05e-4 SMART
Pfam:7tm_2 378 625 4.1e-29 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 96.9%
  • 20x: 94.4%
Validation Efficiency 100% (68/68)
MGI Phenotype PHENOTYPE: Mice homozygous for a reporter allele exhibit normal viability and fertility. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930433I11Rik A T 7: 40,642,718 (GRCm39) D220V probably benign Het
Aldh18a1 A G 19: 40,562,716 (GRCm39) V219A probably benign Het
Anapc10 A G 8: 80,501,610 (GRCm39) D126G probably benign Het
Ap1m2 T C 9: 21,207,129 (GRCm39) *426W probably null Het
Arhgap21 A G 2: 20,867,928 (GRCm39) I865T probably damaging Het
Armc8 A G 9: 99,379,345 (GRCm39) V527A probably damaging Het
Asic5 A T 3: 81,913,778 (GRCm39) probably benign Het
Baz2b A C 2: 59,732,340 (GRCm39) probably benign Het
Bpifa5 T C 2: 154,009,169 (GRCm39) V237A probably damaging Het
Brip1 T A 11: 86,088,745 (GRCm39) K52I possibly damaging Het
Cacna1g T C 11: 94,350,685 (GRCm39) I387V probably damaging Het
Cbr4 A G 8: 61,948,107 (GRCm39) I135V probably benign Het
Ccdc66 C T 14: 27,222,197 (GRCm39) probably null Het
Cubn G A 2: 13,449,078 (GRCm39) T999M probably damaging Het
Dnai3 G T 3: 145,787,119 (GRCm39) D305E possibly damaging Het
Dpp8 C T 9: 64,953,077 (GRCm39) probably benign Het
Dsg1b T C 18: 20,542,390 (GRCm39) S966P possibly damaging Het
Erp27 T C 6: 136,896,862 (GRCm39) probably benign Het
Fat4 A T 3: 39,034,786 (GRCm39) I2813L probably benign Het
Fhod1 G A 8: 106,056,488 (GRCm39) R1101C probably damaging Het
Hoxc9 T C 15: 102,892,359 (GRCm39) S191P probably damaging Het
Izumo4 T C 10: 80,540,030 (GRCm39) probably null Het
Kalrn C T 16: 33,875,261 (GRCm39) D104N possibly damaging Het
Kank4 A T 4: 98,667,873 (GRCm39) D191E probably benign Het
Kbtbd11 A G 8: 15,077,605 (GRCm39) E68G probably benign Het
Kdr C T 5: 76,119,798 (GRCm39) V654I probably benign Het
Klra1 A T 6: 130,349,782 (GRCm39) probably null Het
Kmt2e T A 5: 23,683,970 (GRCm39) Y373* probably null Het
Lepr A T 4: 101,602,889 (GRCm39) M226L probably benign Het
Lrp1b T A 2: 41,348,417 (GRCm39) I800F probably benign Het
Lta4h T C 10: 93,307,833 (GRCm39) probably benign Het
Map3k7 T C 4: 31,974,814 (GRCm39) probably benign Het
Map4k4 G A 1: 40,029,338 (GRCm39) R371Q probably benign Het
Mgat4f A G 1: 134,318,610 (GRCm39) I461V possibly damaging Het
Mme A G 3: 63,253,487 (GRCm39) I444V probably damaging Het
Mms19 C T 19: 41,938,212 (GRCm39) R582Q possibly damaging Het
Mtss1 A G 15: 58,817,286 (GRCm39) S502P probably damaging Het
Myo3a G T 2: 22,467,441 (GRCm39) A232S possibly damaging Het
Nwd2 G T 5: 63,963,686 (GRCm39) W1090L probably damaging Het
Or4k15 A C 14: 50,364,750 (GRCm39) T239P probably damaging Het
Or8b12 G A 9: 37,657,550 (GRCm39) G40E probably damaging Het
Pcm1 G A 8: 41,746,806 (GRCm39) S1335N probably benign Het
Pdzph1 A G 17: 59,280,825 (GRCm39) F486L probably benign Het
Piezo2 T C 18: 63,235,245 (GRCm39) K552R possibly damaging Het
Plekhs1 T A 19: 56,469,536 (GRCm39) probably null Het
Pprc1 C T 19: 46,060,007 (GRCm39) Q1514* probably null Het
Ralgapa1 T C 12: 55,736,576 (GRCm39) T1831A possibly damaging Het
Rnpep G T 1: 135,193,090 (GRCm39) D455E probably damaging Het
Rpgrip1 T A 14: 52,368,771 (GRCm39) probably benign Het
Saxo1 A T 4: 86,397,133 (GRCm39) M135K possibly damaging Het
Serpina12 T C 12: 104,002,048 (GRCm39) T223A probably damaging Het
Serpinb3a A G 1: 106,974,880 (GRCm39) F218L probably damaging Het
Serpinb9f T G 13: 33,509,990 (GRCm39) probably benign Het
Spata33 A G 8: 123,948,662 (GRCm39) D98G probably benign Het
Stard13 T A 5: 150,975,942 (GRCm39) Y742F probably damaging Het
Tecta A G 9: 42,288,910 (GRCm39) Y552H probably damaging Het
Tie1 A T 4: 118,336,358 (GRCm39) probably benign Het
Tmem161a A G 8: 70,633,623 (GRCm39) T254A probably benign Het
Tmem30a G T 9: 79,681,376 (GRCm39) Y264* probably null Het
Tmem87a A T 2: 120,224,946 (GRCm39) I105K probably benign Het
Tnrc6b A T 15: 80,742,920 (GRCm39) D51V probably damaging Het
Trgc3 T A 13: 19,445,262 (GRCm39) M70K probably damaging Het
Trpc4 T C 3: 54,198,632 (GRCm39) F519L probably damaging Het
Ttn T C 2: 76,539,925 (GRCm39) T26027A probably damaging Het
Vmn1r198 A C 13: 22,539,144 (GRCm39) H121P probably damaging Het
Vps33a A G 5: 123,709,024 (GRCm39) F64L probably benign Het
Zfp1008 T C 13: 62,755,201 (GRCm39) N39S probably damaging Het
Zfp994 A T 17: 22,419,882 (GRCm39) C356S probably damaging Het
Other mutations in Adgrf2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00885:Adgrf2 APN 17 43,025,206 (GRCm39) splice site probably benign
IGL01089:Adgrf2 APN 17 43,021,049 (GRCm39) missense probably damaging 1.00
IGL01601:Adgrf2 APN 17 43,020,940 (GRCm39) missense probably benign
IGL01765:Adgrf2 APN 17 43,030,426 (GRCm39) missense probably benign 0.06
IGL02946:Adgrf2 APN 17 43,021,384 (GRCm39) missense probably damaging 1.00
R0720:Adgrf2 UTSW 17 43,024,063 (GRCm39) missense probably damaging 1.00
R0831:Adgrf2 UTSW 17 43,021,334 (GRCm39) missense probably damaging 0.96
R1664:Adgrf2 UTSW 17 43,025,305 (GRCm39) missense possibly damaging 0.92
R2008:Adgrf2 UTSW 17 43,021,013 (GRCm39) missense probably damaging 0.96
R2306:Adgrf2 UTSW 17 43,024,010 (GRCm39) missense possibly damaging 0.92
R2519:Adgrf2 UTSW 17 43,021,298 (GRCm39) missense probably damaging 1.00
R3713:Adgrf2 UTSW 17 43,023,979 (GRCm39) missense probably damaging 1.00
R3736:Adgrf2 UTSW 17 43,021,903 (GRCm39) missense probably benign 0.32
R4272:Adgrf2 UTSW 17 43,021,013 (GRCm39) missense probably damaging 0.99
R4273:Adgrf2 UTSW 17 43,021,013 (GRCm39) missense probably damaging 0.99
R4422:Adgrf2 UTSW 17 43,024,046 (GRCm39) missense probably benign
R4732:Adgrf2 UTSW 17 43,021,645 (GRCm39) missense probably damaging 1.00
R4733:Adgrf2 UTSW 17 43,021,645 (GRCm39) missense probably damaging 1.00
R4906:Adgrf2 UTSW 17 43,022,084 (GRCm39) missense probably benign
R5053:Adgrf2 UTSW 17 43,021,334 (GRCm39) missense probably damaging 0.96
R5078:Adgrf2 UTSW 17 43,021,877 (GRCm39) missense probably damaging 1.00
R5089:Adgrf2 UTSW 17 43,020,988 (GRCm39) missense probably benign 0.00
R5147:Adgrf2 UTSW 17 43,021,574 (GRCm39) missense probably damaging 0.99
R5953:Adgrf2 UTSW 17 43,021,229 (GRCm39) missense probably damaging 1.00
R5968:Adgrf2 UTSW 17 43,026,063 (GRCm39) critical splice donor site probably null
R6791:Adgrf2 UTSW 17 43,021,774 (GRCm39) missense probably benign 0.02
R7138:Adgrf2 UTSW 17 43,021,874 (GRCm39) missense probably damaging 1.00
R7612:Adgrf2 UTSW 17 43,025,271 (GRCm39) missense possibly damaging 0.68
R7670:Adgrf2 UTSW 17 43,022,263 (GRCm39) missense probably damaging 1.00
R8291:Adgrf2 UTSW 17 43,021,451 (GRCm39) missense probably damaging 1.00
R8418:Adgrf2 UTSW 17 43,021,477 (GRCm39) missense probably benign 0.01
R8510:Adgrf2 UTSW 17 43,030,431 (GRCm39) nonsense probably null
R9736:Adgrf2 UTSW 17 43,022,212 (GRCm39) missense probably benign 0.42
X0061:Adgrf2 UTSW 17 43,023,965 (GRCm39) missense probably benign 0.37
X0067:Adgrf2 UTSW 17 43,021,559 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGCCCAAATGACCAGGCTCTTAC -3'
(R):5'- CACCTTACTGACTGGCAGATGCAG -3'

Sequencing Primer
(F):5'- AGGCTCTTACATGCCTGC -3'
(R):5'- TGGCAGATGCAGCCATGAC -3'
Posted On 2013-05-23