Incidental Mutation 'R5455:Adgrf1'
ID 432738
Institutional Source Beutler Lab
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 # R5455 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 43581220-43635628 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 43632034 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 null
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
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.7%
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ascc3 T C 10: 50,725,679 (GRCm39) V2134A probably benign Het
Cct6b T G 11: 82,645,943 (GRCm39) I80L probably benign Het
Cfap20dc A T 14: 8,536,516 (GRCm38) probably null Het
Crebbp C A 16: 3,903,831 (GRCm39) V1765L probably benign Het
Cul9 C T 17: 46,821,772 (GRCm39) probably null Het
Cyp2c40 A G 19: 39,792,236 (GRCm39) I236T possibly damaging Het
Dbndd2 C A 2: 164,332,113 (GRCm39) T112K possibly damaging Het
Dmrtc2 A C 7: 24,571,916 (GRCm39) S4R probably benign Het
Dnah6 C T 6: 73,052,717 (GRCm39) V2988I probably benign Het
Dnajb12 GC G 10: 59,728,574 (GRCm39) probably null Het
Ercc3 T C 18: 32,400,262 (GRCm39) S705P possibly damaging Het
Gm10306 T G 4: 94,445,077 (GRCm39) probably benign Het
H2-Q6 T C 17: 35,643,860 (GRCm39) L3P unknown Het
Kcnn4 T C 7: 24,076,978 (GRCm39) S176P probably damaging Het
Maml2 T A 9: 13,617,039 (GRCm39) Y128* probably null Het
Map2 G A 1: 66,438,550 (GRCm39) E25K probably damaging Het
Morc2b T A 17: 33,357,584 (GRCm39) M63L probably benign Het
Mthfd1 A G 12: 76,348,062 (GRCm39) I569V probably benign Het
Myh8 G A 11: 67,192,244 (GRCm39) R1399H possibly damaging Het
Nop2 T C 6: 125,117,606 (GRCm39) I424T probably benign Het
Olfm5 T C 7: 103,803,669 (GRCm39) R265G probably damaging Het
Opalin T C 19: 41,058,392 (GRCm39) T14A probably benign Het
Or10j7 A G 1: 173,011,818 (GRCm39) F61S probably damaging Het
Or7a36 C T 10: 78,820,371 (GRCm39) S249F possibly damaging Het
Pced1b C A 15: 97,282,274 (GRCm39) S104R probably benign Het
Pdia2 T G 17: 26,416,137 (GRCm39) Q310P probably null Het
Ppil6 A G 10: 41,374,541 (GRCm39) T141A probably benign Het
Prrc2b A G 2: 32,111,355 (GRCm39) probably null Het
Stxbp5 A G 10: 9,684,252 (GRCm39) S573P probably benign Het
Synpo2l C A 14: 20,712,360 (GRCm39) A87S probably damaging Het
Tor1b GGACG GG 2: 30,846,957 (GRCm39) probably benign Het
Vmn1r89 A T 7: 12,954,194 (GRCm39) H121L probably benign Het
Vmn2r99 T A 17: 19,614,408 (GRCm39) C709* probably null Het
Vstm4 A G 14: 32,585,835 (GRCm39) H134R possibly damaging Het
Zan C T 5: 137,452,262 (GRCm39) C1569Y unknown Het
Zdhhc13 A G 7: 48,455,323 (GRCm39) T122A possibly damaging Het
Zpbp2 G T 11: 98,448,429 (GRCm39) V249L probably benign 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
IGL03296:Adgrf1 APN 17 43,632,044 (GRCm39) splice site probably benign
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
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
Predicted Primers PCR Primer
(F):5'- TGGTTTCATCTGTAGCGCTC -3'
(R):5'- AGAGGTGCTCAGATGCATGC -3'

Sequencing Primer
(F):5'- TTCCAGGGCAGTCAAAGC -3'
(R):5'- AGATGCATGCCCAGCAGGTAC -3'
Posted On 2016-10-06