Incidental Mutation 'R8188:Adgrf5'
ID 635002
Institutional Source Beutler Lab
Gene Symbol Adgrf5
Ensembl Gene ENSMUSG00000056492
Gene Name adhesion G protein-coupled receptor F5
Synonyms 8430401C09Rik, Gpr116
MMRRC Submission 067611-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8188 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 43671342-43770448 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 43741503 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Tyrosine at position 380 (C380Y)
Ref Sequence ENSEMBL: ENSMUSP00000109229 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113599]
AlphaFold G5E8Q8
Predicted Effect probably damaging
Transcript: ENSMUST00000113599
AA Change: C380Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000109229
Gene: ENSMUSG00000056492
AA Change: C380Y

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Blast:EGF 118 161 8e-14 BLAST
Pfam:SEA 165 263 9.2e-14 PFAM
IG 276 366 1.54e-4 SMART
Blast:IG_like 374 464 2e-31 BLAST
IG 475 561 1.04e-1 SMART
low complexity region 815 823 N/A INTRINSIC
GPS 949 1004 6.49e-16 SMART
Pfam:7tm_2 1011 1264 1.2e-35 PFAM
low complexity region 1328 1347 N/A INTRINSIC
Meta Mutation Damage Score 0.4469 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
Validation Efficiency 100% (56/56)
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit premature death, decreased body weight and respiratory distress associated with pulmonary alveolar proteinosis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aco1 C G 4: 40,180,284 (GRCm39) A395G probably benign Het
Astn2 T C 4: 65,977,418 (GRCm39) T422A unknown Het
Baz1b G T 5: 135,233,916 (GRCm39) V148F probably benign Het
Bicd1 A C 6: 149,451,854 (GRCm39) S823R probably damaging Het
Bltp3b C T 10: 89,647,928 (GRCm39) T1330M possibly damaging Het
Blvra A C 2: 126,937,047 (GRCm39) S167R probably damaging Het
Camsap2 G T 1: 136,225,132 (GRCm39) probably null Het
Card14 T C 11: 119,228,623 (GRCm39) S650P probably damaging Het
Ccdc121rt2 A G 5: 112,597,993 (GRCm39) D180G possibly damaging Het
Cdh2 A G 18: 16,781,593 (GRCm39) I166T probably damaging Het
Cdnf T C 2: 3,514,228 (GRCm39) V22A probably benign Het
Cfhr4 T A 1: 139,625,868 (GRCm39) I869F probably damaging Het
Chd2 T A 7: 73,079,504 (GRCm39) K1799* probably null Het
Col20a1 G A 2: 180,658,126 (GRCm39) probably null Het
Cyp4a31 T C 4: 115,426,943 (GRCm39) I182T probably benign Het
Dap3 A T 3: 88,843,543 (GRCm39) F25L probably benign Het
Dcc T A 18: 71,943,928 (GRCm39) Y241F probably benign Het
Ddx46 A G 13: 55,814,029 (GRCm39) I662V possibly damaging Het
Dzip3 T C 16: 48,772,499 (GRCm39) D390G probably damaging Het
Eif1 A G 11: 100,211,624 (GRCm39) D55G probably benign Het
Exosc5 T A 7: 25,358,790 (GRCm39) S44T probably damaging Het
Fat2 A G 11: 55,163,997 (GRCm39) V3086A probably damaging Het
Fcamr T A 1: 130,730,665 (GRCm39) probably null Het
Gcg T C 2: 62,309,004 (GRCm39) D50G probably damaging Het
Gm7298 A G 6: 121,763,537 (GRCm39) probably null Het
Hfe A G 13: 23,892,175 (GRCm39) V63A probably damaging Het
Hoxd11 T A 2: 74,514,298 (GRCm39) I276N probably damaging Het
Htt T C 5: 34,919,287 (GRCm39) S13P probably benign Het
Il12a T A 3: 68,598,872 (GRCm39) C18S unknown Het
Itk G T 11: 46,222,776 (GRCm39) Y564* probably null Het
Lrrc46 A T 11: 96,931,705 (GRCm39) L39Q probably damaging Het
Myom3 T A 4: 135,507,231 (GRCm39) L537Q probably damaging Het
Nrap A C 19: 56,325,010 (GRCm39) Y1234* probably null Het
Or51q1 T C 7: 103,628,743 (GRCm39) S121P probably damaging Het
Or8b9 A T 9: 37,766,407 (GRCm39) M98L probably benign Het
Parn T C 16: 13,359,020 (GRCm39) D574G probably benign Het
Pbrm1 A G 14: 30,789,773 (GRCm39) I807V probably damaging Het
Pclo T A 5: 14,725,193 (GRCm39) S1350R unknown Het
Pira13 T C 7: 3,826,126 (GRCm39) H289R unknown Het
Plaa T C 4: 94,474,586 (GRCm39) Q272R probably damaging Het
Rfx6 T A 10: 51,594,292 (GRCm39) I174N probably benign Het
Ripk2 T A 4: 16,139,218 (GRCm39) K226N probably damaging Het
Scgb1b2 T C 7: 30,990,946 (GRCm39) D54G possibly damaging Het
Slc45a4 T C 15: 73,456,383 (GRCm39) Y599C probably benign Het
Slc7a13 T C 4: 19,819,082 (GRCm39) V94A probably benign Het
Slc7a8 A G 14: 54,972,579 (GRCm39) F281L probably benign Het
Slco4c1 T A 1: 96,772,261 (GRCm39) T243S probably damaging Het
Smim30 C T 6: 13,870,541 (GRCm39) G57E probably damaging Het
Stat5b A G 11: 100,692,262 (GRCm39) I174T probably damaging Het
Styk1 C A 6: 131,281,848 (GRCm39) V257L probably benign Het
Tmem268 T C 4: 63,498,209 (GRCm39) F210L probably damaging Het
Ugt2b35 T A 5: 87,149,302 (GRCm39) S184R probably damaging Het
Vps50 T A 6: 3,562,297 (GRCm39) L464* probably null Het
Zfhx2 A T 14: 55,301,898 (GRCm39) S2029T probably benign Het
Zfp235 T A 7: 23,841,296 (GRCm39) F572I probably damaging Het
Zfp280d T C 9: 72,267,615 (GRCm39) I766T probably benign Het
Zfr T G 15: 12,171,904 (GRCm39) C933W probably damaging Het
Other mutations in Adgrf5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00501:Adgrf5 APN 17 43,760,806 (GRCm39) missense possibly damaging 0.79
IGL00590:Adgrf5 APN 17 43,764,038 (GRCm39) missense probably damaging 1.00
IGL01128:Adgrf5 APN 17 43,733,400 (GRCm39) missense possibly damaging 0.95
IGL01131:Adgrf5 APN 17 43,733,400 (GRCm39) missense possibly damaging 0.95
IGL01132:Adgrf5 APN 17 43,733,400 (GRCm39) missense possibly damaging 0.95
IGL01392:Adgrf5 APN 17 43,760,903 (GRCm39) missense probably benign 0.00
IGL01475:Adgrf5 APN 17 43,761,245 (GRCm39) missense probably benign 0.00
IGL01614:Adgrf5 APN 17 43,735,362 (GRCm39) missense possibly damaging 0.53
IGL01654:Adgrf5 APN 17 43,762,061 (GRCm39) missense possibly damaging 0.89
IGL02053:Adgrf5 APN 17 43,761,058 (GRCm39) missense possibly damaging 0.47
IGL02175:Adgrf5 APN 17 43,761,901 (GRCm39) missense probably damaging 1.00
IGL02416:Adgrf5 APN 17 43,755,871 (GRCm39) splice site probably null
IGL02525:Adgrf5 APN 17 43,760,854 (GRCm39) missense probably damaging 1.00
IGL03035:Adgrf5 APN 17 43,741,518 (GRCm39) missense possibly damaging 0.80
duct_tape UTSW 17 43,756,006 (GRCm39) missense probably benign 0.04
Flypaper UTSW 17 43,733,552 (GRCm39) splice site probably benign
goop UTSW 17 43,752,860 (GRCm39) missense probably damaging 0.99
Heaped UTSW 17 43,757,927 (GRCm39) missense possibly damaging 0.93
la_brea UTSW 17 43,763,214 (GRCm39) critical splice donor site probably null
Motel UTSW 17 43,761,271 (GRCm39) missense probably damaging 1.00
noel UTSW 17 43,741,503 (GRCm39) missense probably damaging 1.00
Schmutzfinger UTSW 17 43,735,709 (GRCm39) nonsense probably null
sticky UTSW 17 43,748,462 (GRCm39) missense probably damaging 0.98
sweetie UTSW 17 43,761,874 (GRCm39) missense probably damaging 0.96
PIT4812001:Adgrf5 UTSW 17 43,761,260 (GRCm39) missense probably damaging 1.00
R0699:Adgrf5 UTSW 17 43,733,552 (GRCm39) splice site probably null
R0972:Adgrf5 UTSW 17 43,761,874 (GRCm39) missense probably damaging 0.96
R1521:Adgrf5 UTSW 17 43,741,443 (GRCm39) missense probably benign 0.03
R1523:Adgrf5 UTSW 17 43,761,044 (GRCm39) missense probably benign 0.00
R1758:Adgrf5 UTSW 17 43,735,484 (GRCm39) critical splice donor site probably null
R1767:Adgrf5 UTSW 17 43,761,455 (GRCm39) missense possibly damaging 0.87
R1799:Adgrf5 UTSW 17 43,750,958 (GRCm39) missense probably damaging 0.98
R1800:Adgrf5 UTSW 17 43,761,973 (GRCm39) missense probably damaging 1.00
R1888:Adgrf5 UTSW 17 43,737,896 (GRCm39) splice site probably null
R1888:Adgrf5 UTSW 17 43,737,896 (GRCm39) splice site probably null
R2057:Adgrf5 UTSW 17 43,739,477 (GRCm39) missense possibly damaging 0.88
R2058:Adgrf5 UTSW 17 43,739,477 (GRCm39) missense possibly damaging 0.88
R2059:Adgrf5 UTSW 17 43,739,477 (GRCm39) missense possibly damaging 0.88
R2410:Adgrf5 UTSW 17 43,766,157 (GRCm39) missense probably benign 0.11
R2568:Adgrf5 UTSW 17 43,748,562 (GRCm39) missense probably damaging 1.00
R2847:Adgrf5 UTSW 17 43,733,531 (GRCm39) missense possibly damaging 0.69
R2848:Adgrf5 UTSW 17 43,733,531 (GRCm39) missense possibly damaging 0.69
R3800:Adgrf5 UTSW 17 43,757,951 (GRCm39) splice site probably benign
R3856:Adgrf5 UTSW 17 43,757,927 (GRCm39) missense possibly damaging 0.93
R4021:Adgrf5 UTSW 17 43,741,605 (GRCm39) splice site probably benign
R4075:Adgrf5 UTSW 17 43,761,086 (GRCm39) missense probably damaging 1.00
R4366:Adgrf5 UTSW 17 43,752,860 (GRCm39) missense probably damaging 0.99
R4409:Adgrf5 UTSW 17 43,752,738 (GRCm39) missense probably damaging 1.00
R4570:Adgrf5 UTSW 17 43,756,006 (GRCm39) missense probably benign 0.04
R4616:Adgrf5 UTSW 17 43,763,331 (GRCm39) missense probably benign 0.38
R4623:Adgrf5 UTSW 17 43,761,874 (GRCm39) missense probably benign 0.16
R4645:Adgrf5 UTSW 17 43,748,416 (GRCm39) missense probably damaging 1.00
R5211:Adgrf5 UTSW 17 43,733,511 (GRCm39) missense probably benign 0.32
R5268:Adgrf5 UTSW 17 43,761,890 (GRCm39) missense probably damaging 1.00
R5280:Adgrf5 UTSW 17 43,737,225 (GRCm39) missense probably damaging 1.00
R5326:Adgrf5 UTSW 17 43,750,965 (GRCm39) missense probably damaging 0.98
R5762:Adgrf5 UTSW 17 43,741,586 (GRCm39) missense probably null 0.16
R5856:Adgrf5 UTSW 17 43,757,011 (GRCm39) missense probably benign 0.09
R6007:Adgrf5 UTSW 17 43,748,462 (GRCm39) missense probably damaging 0.98
R6153:Adgrf5 UTSW 17 43,761,974 (GRCm39) missense possibly damaging 0.96
R6451:Adgrf5 UTSW 17 43,735,709 (GRCm39) nonsense probably null
R6535:Adgrf5 UTSW 17 43,750,920 (GRCm39) missense probably benign 0.05
R6536:Adgrf5 UTSW 17 43,733,552 (GRCm39) splice site probably benign
R6602:Adgrf5 UTSW 17 43,761,195 (GRCm39) missense probably benign 0.32
R6882:Adgrf5 UTSW 17 43,761,271 (GRCm39) missense probably damaging 1.00
R6992:Adgrf5 UTSW 17 43,763,214 (GRCm39) critical splice donor site probably null
R7137:Adgrf5 UTSW 17 43,761,788 (GRCm39) missense probably damaging 1.00
R7170:Adgrf5 UTSW 17 43,757,029 (GRCm39) missense possibly damaging 0.92
R7313:Adgrf5 UTSW 17 43,763,368 (GRCm39) critical splice donor site probably null
R7313:Adgrf5 UTSW 17 43,755,974 (GRCm39) missense probably benign 0.01
R7331:Adgrf5 UTSW 17 43,748,484 (GRCm39) missense probably damaging 0.99
R7346:Adgrf5 UTSW 17 43,762,070 (GRCm39) missense probably damaging 1.00
R7350:Adgrf5 UTSW 17 43,739,335 (GRCm39) critical splice acceptor site probably null
R7667:Adgrf5 UTSW 17 43,756,930 (GRCm39) missense probably benign 0.01
R7717:Adgrf5 UTSW 17 43,761,644 (GRCm39) missense probably damaging 1.00
R7731:Adgrf5 UTSW 17 43,761,451 (GRCm39) missense probably damaging 1.00
R7877:Adgrf5 UTSW 17 43,752,729 (GRCm39) missense possibly damaging 0.63
R7950:Adgrf5 UTSW 17 43,762,048 (GRCm39) missense probably damaging 0.99
R7988:Adgrf5 UTSW 17 43,750,704 (GRCm39) intron probably benign
R8219:Adgrf5 UTSW 17 43,760,750 (GRCm39) missense probably benign 0.13
R8284:Adgrf5 UTSW 17 43,766,161 (GRCm39) missense unknown
R8460:Adgrf5 UTSW 17 43,750,699 (GRCm39) intron probably benign
R8504:Adgrf5 UTSW 17 43,757,840 (GRCm39) missense probably benign 0.01
R8751:Adgrf5 UTSW 17 43,748,574 (GRCm39) missense possibly damaging 0.80
R8852:Adgrf5 UTSW 17 43,763,989 (GRCm39) missense possibly damaging 0.82
R9196:Adgrf5 UTSW 17 43,755,995 (GRCm39) missense possibly damaging 0.94
R9418:Adgrf5 UTSW 17 43,737,864 (GRCm39) missense probably benign 0.00
R9671:Adgrf5 UTSW 17 43,760,795 (GRCm39) missense probably damaging 1.00
R9734:Adgrf5 UTSW 17 43,763,199 (GRCm39) missense probably damaging 1.00
R9756:Adgrf5 UTSW 17 43,761,137 (GRCm39) missense probably benign 0.01
R9765:Adgrf5 UTSW 17 43,748,491 (GRCm39) missense probably damaging 1.00
X0017:Adgrf5 UTSW 17 43,737,936 (GRCm39) missense probably damaging 1.00
Z1177:Adgrf5 UTSW 17 43,755,944 (GRCm39) missense probably benign 0.00
Z1191:Adgrf5 UTSW 17 43,755,926 (GRCm39) missense probably benign 0.17
Predicted Primers PCR Primer
(F):5'- TGTCAAGTCGCAGATGCCAC -3'
(R):5'- GCATCAGAACTAGTGGTTTGGG -3'

Sequencing Primer
(F):5'- CGGCACATGAAACGAGGCTC -3'
(R):5'- GTTTTCATGGTCCAGAATAAACACC -3'
Posted On 2020-07-13