Incidental Mutation 'R8163:Gpr25'
ID 633601
Institutional Source Beutler Lab
Gene Symbol Gpr25
Ensembl Gene ENSMUSG00000052759
Gene Name G protein-coupled receptor 25
Synonyms LOC383563
MMRRC Submission
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock # R8163 (G1)
Quality Score 225.009
Status Validated
Chromosome 1
Chromosomal Location 136259797-136260873 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 136259858 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 339 (D339G)
Ref Sequence ENSEMBL: ENSMUSP00000083583 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086395]
AlphaFold P0C5I1
Predicted Effect probably damaging
Transcript: ENSMUST00000086395
AA Change: D339G

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000083583
Gene: ENSMUSG00000052759
AA Change: D339G

DomainStartEndE-ValueType
Pfam:7tm_1 56 304 1.1e-40 PFAM
low complexity region 328 342 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.2%
Validation Efficiency 100% (53/53)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is intronless and encodes a member of the G-protein coupled receptor 1 family. G-protein coupled receptors are membrane proteins which activate signaling cascades as a response to extracellular stress. This gene has been linked to arterial stiffness. [provided by RefSeq, Nov 2012]
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930022D16Rik A G 11: 109,414,057 I11V unknown Het
Ago3 G T 4: 126,368,584 T391K probably benign Het
Asap1 A G 15: 64,092,050 W1100R probably damaging Het
Bbof1 T C 12: 84,426,762 S289P possibly damaging Het
Cd3d T C 9: 44,985,654 F109L probably benign Het
Cebpd A T 16: 15,887,977 E218V probably damaging Het
Cfl1 T C 19: 5,493,500 probably benign Het
Cpa2 A C 6: 30,564,351 I394L probably damaging Het
Ddx50 C A 10: 62,639,899 V348F possibly damaging Het
Dnajc28 G A 16: 91,616,907 R150* probably null Het
Echs1 A G 7: 140,112,444 V130A possibly damaging Het
Eif2s2 A G 2: 154,892,701 S2P probably benign Het
Fastk A G 5: 24,444,275 I38T probably benign Het
Fat3 G A 9: 15,959,759 R3779C probably damaging Het
Fat4 A T 3: 38,979,732 N2511I possibly damaging Het
Fbxw13 G A 9: 109,183,054 T315I probably benign Het
Fzd5 A T 1: 64,735,193 Y470N probably damaging Het
G530012D18Rik C G 1: 85,577,214 D113E unknown Het
Gm884 A T 11: 103,615,862 I1760K unknown Het
Igsf9b T A 9: 27,322,611 probably null Het
Il5 T A 11: 53,723,986 M125K possibly damaging Het
Iqub G A 6: 24,449,715 T717I probably benign Het
Katnb1 T C 8: 95,096,386 F403S probably damaging Het
Krt26 T C 11: 99,329,672 I451V probably benign Het
Krt88 T C 15: 101,453,508 L132P probably damaging Het
Kynu G T 2: 43,628,954 G245V probably damaging Het
Lap3 C T 5: 45,512,047 R513* probably null Het
Lin9 C T 1: 180,659,126 R126W probably damaging Het
Lrrtm2 C T 18: 35,213,724 R175H probably damaging Het
N4bp2l2 A G 5: 150,661,309 L60P probably damaging Het
Ncr1 T C 7: 4,340,829 F142S probably damaging Het
Nktr TAGAAG TAG 9: 121,750,863 probably benign Het
Olfr1443 A G 19: 12,680,188 I27V probably benign Het
Parp16 T A 9: 65,229,949 H152Q probably damaging Het
Plaa C G 4: 94,569,403 V777L probably benign Het
Prnp A G 2: 131,936,988 T187A probably benign Het
Pzp T G 6: 128,512,194 I485L probably benign Het
Rc3h1 T A 1: 160,955,059 Y703N probably damaging Het
Rngtt G A 4: 33,325,109 C110Y probably damaging Het
Rps10 G A 17: 27,634,111 R95C probably benign Het
Scn9a T A 2: 66,484,401 I1658F probably damaging Het
Sec16a A T 2: 26,416,421 W702R Het
Taf6 G T 5: 138,181,976 Q339K possibly damaging Het
Tbcd C T 11: 121,493,885 T315M probably benign Het
Tmem198 C T 1: 75,483,027 P209S possibly damaging Het
Vmn2r78 G A 7: 86,954,452 A613T probably damaging Het
Vps13c G A 9: 67,950,438 E2651K probably benign Het
Wdfy4 C T 14: 33,151,588 V255I Het
Zfhx3 A G 8: 108,949,293 D2325G probably damaging Het
Zfp36l2 T C 17: 84,187,123 N29D possibly damaging Het
Zfp692 T A 11: 58,310,373 probably null Het
Other mutations in Gpr25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03028:Gpr25 APN 1 136260812 missense probably benign 0.00
R1728:Gpr25 UTSW 1 136260710 missense probably benign
R1729:Gpr25 UTSW 1 136260710 missense probably benign
R1732:Gpr25 UTSW 1 136260128 missense probably benign 0.01
R1739:Gpr25 UTSW 1 136260710 missense probably benign
R1762:Gpr25 UTSW 1 136260710 missense probably benign
R1783:Gpr25 UTSW 1 136260710 missense probably benign
R1785:Gpr25 UTSW 1 136260710 missense probably benign
R1907:Gpr25 UTSW 1 136260800 missense probably benign 0.00
R2877:Gpr25 UTSW 1 136260815 missense possibly damaging 0.86
R3081:Gpr25 UTSW 1 136259885 missense possibly damaging 0.68
R5132:Gpr25 UTSW 1 136260365 missense probably damaging 1.00
R7133:Gpr25 UTSW 1 136260821 missense probably damaging 1.00
R8248:Gpr25 UTSW 1 136260677 missense probably benign 0.03
R9051:Gpr25 UTSW 1 136260288 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TTTGTGAGAACAGCCAGCC -3'
(R):5'- CATCATCTTCACCGTGGAGAGC -3'

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