Incidental Mutation 'IGL03296:Adgrf1'
ID 416100
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Adgrf1
Ensembl Gene ENSMUSG00000041293
Gene Name adhesion G protein-coupled receptor F1
Synonyms 5031409J19Rik, Gpr110
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03296
Quality Score
Status
Chromosome 17
Chromosomal Location 43581220-43635628 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 43632044 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000049380 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047399]
AlphaFold Q8VEC3
Predicted Effect probably benign
Transcript: ENSMUST00000047399
SMART Domains Protein: ENSMUSP00000049380
Gene: ENSMUSG00000041293

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
low complexity region 59 83 N/A INTRINSIC
Pfam:SEA 150 238 3.7e-10 PFAM
low complexity region 341 363 N/A INTRINSIC
GPS 528 576 5.56e-15 SMART
Pfam:7tm_2 580 832 2.1e-38 PFAM
Coding Region Coverage
Validation Efficiency
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: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef26 A G 3: 62,330,926 (GRCm39) T547A probably damaging Het
Cdc14a T A 3: 116,090,807 (GRCm39) H375L probably benign Het
Ddx43 T C 9: 78,306,380 (GRCm39) probably null Het
Dennd6a T C 14: 26,338,115 (GRCm39) probably null Het
Dock4 A T 12: 40,783,256 (GRCm39) E730V possibly damaging Het
Gpr55 A G 1: 85,868,753 (GRCm39) L276S probably damaging Het
Grid1 T C 14: 35,302,524 (GRCm39) F930L possibly damaging Het
Inf2 C T 12: 112,570,642 (GRCm39) Q394* probably null Het
Ints11 T C 4: 155,969,780 (GRCm39) probably null Het
Kcnd2 T C 6: 21,714,208 (GRCm39) V397A probably damaging Het
Lmntd1 A G 6: 145,359,203 (GRCm39) F316L probably benign Het
Loxl4 A T 19: 42,587,262 (GRCm39) probably benign Het
Lrrc37a C T 11: 103,388,499 (GRCm39) E2309K unknown Het
Lyl1 C T 8: 85,429,300 (GRCm39) P3L possibly damaging Het
Mindy4 T C 6: 55,274,738 (GRCm39) probably null Het
Mybpc2 A T 7: 44,156,308 (GRCm39) I835N probably damaging Het
Myo5a T C 9: 75,023,484 (GRCm39) I15T probably damaging Het
Nfkb2 A T 19: 46,298,367 (GRCm39) D557V probably damaging Het
Or11g27 A T 14: 50,771,402 (GRCm39) I178L possibly damaging Het
Pdk3 T C X: 92,875,503 (GRCm39) Y19C probably damaging Het
Pdpr G T 8: 111,841,430 (GRCm39) V221F probably damaging Het
Rab6a T C 7: 100,283,931 (GRCm39) Y128H probably benign Het
Rars1 A T 11: 35,707,523 (GRCm39) Y429* probably null Het
Rsl24d1 T C 9: 73,025,229 (GRCm39) probably null Het
Slc7a9 T C 7: 35,151,852 (GRCm39) F49S probably damaging Het
St14 C T 9: 31,020,008 (GRCm39) E34K probably damaging Het
Tcp10b A G 17: 13,292,443 (GRCm39) T289A probably damaging Het
Tenm2 T C 11: 35,942,852 (GRCm39) probably null Het
Tshz3 A T 7: 36,470,761 (GRCm39) T917S probably damaging Het
Vrtn T A 12: 84,695,622 (GRCm39) I124N probably damaging Het
Vwa8 A G 14: 79,420,540 (GRCm39) E1747G probably damaging Het
Wdr33 A T 18: 31,960,444 (GRCm39) Q36L probably benign Het
Xpo5 C T 17: 46,532,320 (GRCm39) R452* probably null Het
Zdhhc8 A T 16: 18,044,587 (GRCm39) L311Q possibly damaging Het
Other mutations in Adgrf1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01343:Adgrf1 APN 17 43,624,086 (GRCm39) missense probably null 0.92
IGL01359:Adgrf1 APN 17 43,621,577 (GRCm39) missense probably damaging 0.99
IGL02131:Adgrf1 APN 17 43,614,638 (GRCm39) missense probably damaging 0.99
IGL02692:Adgrf1 APN 17 43,614,669 (GRCm39) missense probably damaging 1.00
IGL02891:Adgrf1 APN 17 43,622,052 (GRCm39) missense probably damaging 0.96
IGL03027:Adgrf1 APN 17 43,607,605 (GRCm39) missense probably damaging 1.00
R0211:Adgrf1 UTSW 17 43,607,581 (GRCm39) missense probably damaging 1.00
R0211:Adgrf1 UTSW 17 43,607,581 (GRCm39) missense probably damaging 1.00
R0389:Adgrf1 UTSW 17 43,614,679 (GRCm39) critical splice donor site probably null
R0488:Adgrf1 UTSW 17 43,621,302 (GRCm39) missense probably damaging 0.99
R1591:Adgrf1 UTSW 17 43,621,872 (GRCm39) missense probably damaging 1.00
R1817:Adgrf1 UTSW 17 43,620,924 (GRCm39) missense probably benign 0.01
R1819:Adgrf1 UTSW 17 43,620,924 (GRCm39) missense probably benign 0.01
R2009:Adgrf1 UTSW 17 43,632,112 (GRCm39) nonsense probably null
R2032:Adgrf1 UTSW 17 43,622,166 (GRCm39) missense probably damaging 1.00
R2140:Adgrf1 UTSW 17 43,611,693 (GRCm39) missense probably damaging 0.99
R3953:Adgrf1 UTSW 17 43,621,098 (GRCm39) missense probably benign 0.08
R4679:Adgrf1 UTSW 17 43,621,384 (GRCm39) missense probably damaging 1.00
R4775:Adgrf1 UTSW 17 43,622,054 (GRCm39) missense probably damaging 1.00
R4858:Adgrf1 UTSW 17 43,614,563 (GRCm39) missense probably damaging 1.00
R4894:Adgrf1 UTSW 17 43,609,975 (GRCm39) nonsense probably null
R4895:Adgrf1 UTSW 17 43,621,511 (GRCm39) missense probably benign 0.33
R4935:Adgrf1 UTSW 17 43,606,130 (GRCm39) missense probably benign 0.00
R5027:Adgrf1 UTSW 17 43,614,638 (GRCm39) missense probably damaging 0.99
R5373:Adgrf1 UTSW 17 43,601,896 (GRCm39) start gained probably benign
R5374:Adgrf1 UTSW 17 43,601,896 (GRCm39) start gained probably benign
R5455:Adgrf1 UTSW 17 43,632,034 (GRCm39) splice site probably null
R5579:Adgrf1 UTSW 17 43,621,955 (GRCm39) missense probably damaging 1.00
R5985:Adgrf1 UTSW 17 43,604,146 (GRCm39) missense probably benign 0.00
R6038:Adgrf1 UTSW 17 43,606,100 (GRCm39) missense probably benign 0.00
R6038:Adgrf1 UTSW 17 43,606,100 (GRCm39) missense probably benign 0.00
R6160:Adgrf1 UTSW 17 43,621,578 (GRCm39) missense probably damaging 1.00
R6227:Adgrf1 UTSW 17 43,621,164 (GRCm39) missense probably benign 0.05
R6500:Adgrf1 UTSW 17 43,621,263 (GRCm39) missense probably damaging 1.00
R7066:Adgrf1 UTSW 17 43,621,151 (GRCm39) missense probably benign 0.05
R7099:Adgrf1 UTSW 17 43,621,493 (GRCm39) missense probably benign 0.00
R7561:Adgrf1 UTSW 17 43,622,000 (GRCm39) missense possibly damaging 0.94
R8359:Adgrf1 UTSW 17 43,621,286 (GRCm39) missense probably damaging 0.99
R8480:Adgrf1 UTSW 17 43,606,055 (GRCm39) missense probably benign 0.08
R8543:Adgrf1 UTSW 17 43,624,097 (GRCm39) missense probably null 0.99
R9023:Adgrf1 UTSW 17 43,614,651 (GRCm39) missense possibly damaging 0.53
R9074:Adgrf1 UTSW 17 43,601,879 (GRCm39) start gained probably benign
R9207:Adgrf1 UTSW 17 43,621,164 (GRCm39) missense probably benign 0.05
R9232:Adgrf1 UTSW 17 43,621,295 (GRCm39) missense probably benign 0.07
R9425:Adgrf1 UTSW 17 43,621,274 (GRCm39) missense possibly damaging 0.84
R9526:Adgrf1 UTSW 17 43,616,237 (GRCm39) missense possibly damaging 0.95
R9697:Adgrf1 UTSW 17 43,625,362 (GRCm39) missense possibly damaging 0.71
R9711:Adgrf1 UTSW 17 43,621,580 (GRCm39) missense possibly damaging 0.81
Z1177:Adgrf1 UTSW 17 43,621,038 (GRCm39) missense probably benign 0.14
Posted On 2016-08-02