Incidental Mutation 'R0633:Lpar5'
ID 58067
Institutional Source Beutler Lab
Gene Symbol Lpar5
Ensembl Gene ENSMUSG00000067714
Gene Name lysophosphatidic acid receptor 5
Synonyms LPA5, LOC381810, Gpr92, GPR93
MMRRC Submission 038822-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.079) question?
Stock # R0633 (G1)
Quality Score 222
Status Not validated
Chromosome 6
Chromosomal Location 125067920-125082472 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to C at 125081991 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Serine at position 225 (Y225S)
Ref Sequence ENSEMBL: ENSMUSP00000132511 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088292] [ENSMUST00000140346] [ENSMUST00000171989]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000088292
AA Change: Y225S

PolyPhen 2 Score 0.255 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000085630
Gene: ENSMUSG00000067714
AA Change: Y225S

low complexity region 15 27 N/A INTRINSIC
Pfam:7tm_1 55 313 7.4e-40 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000140346
SMART Domains Protein: ENSMUSP00000119904
Gene: ENSMUSG00000067714

low complexity region 15 27 N/A INTRINSIC
Pfam:7tm_1 55 164 1.5e-30 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000171989
AA Change: Y225S

PolyPhen 2 Score 0.255 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000132511
Gene: ENSMUSG00000067714
AA Change: Y225S

low complexity region 15 27 N/A INTRINSIC
Pfam:7tm_1 55 313 1.1e-48 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203956
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.4%
  • 20x: 94.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the rhodopsin class of G protein-coupled transmembrane receptors. This protein transmits extracellular signals from lysophosphatidic acid to cells through heterotrimeric G proteins and mediates numerous cellular processes. Many G protein receptors serve as targets for pharmaceutical drugs. Transcript variants of this gene have been described.[provided by RefSeq, Dec 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit resistance to neuropathic pain and myelin sheath alterations. Mice homozygous for a different targeted allele exhibit decreased nociception sensitivity, decreased anxiety-related response and enhanced coordination and spatial learning. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921530L21Rik T G 14: 95,881,943 (GRCm38) N45K probably damaging Het
Adamts8 A T 9: 30,943,511 (GRCm38) R18S probably damaging Het
Adgb G A 10: 10,391,729 (GRCm38) A923V probably benign Het
Aldh1a3 A G 7: 66,400,222 (GRCm38) V416A probably damaging Het
Alox5 C T 6: 116,420,384 (GRCm38) G280R probably damaging Het
Anapc5 A T 5: 122,800,632 (GRCm38) Y360N probably damaging Het
Apbb1 C T 7: 105,558,963 (GRCm38) V685I probably damaging Het
Apc2 C A 10: 80,307,455 (GRCm38) A463E probably damaging Het
Arhgap21 C T 2: 20,855,387 (GRCm38) W1170* probably null Het
Atat1 G A 17: 35,901,423 (GRCm38) R305C probably damaging Het
Brd8dc A G 18: 34,586,266 (GRCm38) V167A possibly damaging Het
Cars2 T C 8: 11,550,511 (GRCm38) D56G probably benign Het
Cdc42bpb T C 12: 111,345,555 (GRCm38) I108V probably damaging Het
Cftr T A 6: 18,305,980 (GRCm38) I1255K probably damaging Het
Ckap5 T C 2: 91,550,743 (GRCm38) L148P probably damaging Het
Cntn4 A G 6: 106,679,248 (GRCm38) probably null Het
Cpe G A 8: 64,609,203 (GRCm38) P273L probably damaging Het
Cpsf7 A G 19: 10,531,782 (GRCm38) D19G probably benign Het
Ddx25 C A 9: 35,545,972 (GRCm38) R349L probably damaging Het
Depdc7 T C 2: 104,722,881 (GRCm38) D446G probably benign Het
Det1 T A 7: 78,843,935 (GRCm38) N107I probably benign Het
Dock6 A T 9: 21,844,417 (GRCm38) D170E probably benign Het
Dvl1 C T 4: 155,858,295 (GRCm38) L673F probably damaging Het
Gucy1b1 A T 3: 82,045,460 (GRCm38) I222K probably benign Het
Hfm1 T C 5: 106,917,601 (GRCm38) T71A possibly damaging Het
Ikzf1 A G 11: 11,769,223 (GRCm38) E310G probably damaging Het
Impg1 T C 9: 80,394,155 (GRCm38) E163G possibly damaging Het
Itpr2 G T 6: 146,374,456 (GRCm38) H426Q probably damaging Het
Itpripl2 C T 7: 118,490,256 (GRCm38) G360D probably benign Het
Kif14 C T 1: 136,527,305 (GRCm38) R1572C probably damaging Het
L3mbtl3 A T 10: 26,302,685 (GRCm38) H568Q unknown Het
Lgi2 A G 5: 52,554,460 (GRCm38) Y173H probably damaging Het
Lpin3 A G 2: 160,903,974 (GRCm38) H675R probably damaging Het
Lrp2 C A 2: 69,448,120 (GRCm38) G3963V probably damaging Het
Man1a2 G T 3: 100,684,575 (GRCm38) D13E possibly damaging Het
Map1a T C 2: 121,308,014 (GRCm38) V2753A probably damaging Het
Mitf C A 6: 98,003,904 (GRCm38) N97K probably damaging Het
Msh2 A G 17: 87,672,810 (GRCm38) probably null Het
Msr1 T C 8: 39,620,000 (GRCm38) E170G probably damaging Het
Myrip C A 9: 120,388,236 (GRCm38) R79S probably damaging Het
Nek10 G A 14: 14,857,782 (GRCm38) probably null Het
Neto1 C T 18: 86,404,729 (GRCm38) R104* probably null Het
Nom1 A C 5: 29,451,100 (GRCm38) K821T probably damaging Het
Nrxn1 A G 17: 90,704,181 (GRCm38) V340A probably damaging Het
Nxpe4 A T 9: 48,396,597 (GRCm38) I334F probably benign Het
Or1e23 A G 11: 73,516,927 (GRCm38) S91P probably benign Het
Or2ag1 T C 7: 106,713,977 (GRCm38) K235E probably benign Het
Or4a74 T C 2: 89,609,374 (GRCm38) M243V probably benign Het
Or5al7 T A 2: 86,162,091 (GRCm38) N286I probably damaging Het
Or5b124 T C 19: 13,633,336 (GRCm38) V75A probably damaging Het
Or8k27 C T 2: 86,445,129 (GRCm38) M284I probably benign Het
Padi4 A G 4: 140,757,585 (GRCm38) S322P probably damaging Het
Peli3 A G 19: 4,941,782 (GRCm38) Y44H probably damaging Het
Prdm4 A G 10: 85,907,903 (GRCm38) S163P probably damaging Het
Prom2 T C 2: 127,539,525 (GRCm38) D227G probably benign Het
Ptgfr C T 3: 151,801,763 (GRCm38) R321H probably benign Het
Resf1 A T 6: 149,325,701 (GRCm38) I82L probably benign Het
Rgs3 G A 4: 62,625,906 (GRCm38) R136H probably damaging Het
Rgsl1 T G 1: 153,844,107 (GRCm38) N3T possibly damaging Het
Rif1 T C 2: 52,112,563 (GRCm38) S2010P probably benign Het
Rngtt T C 4: 33,368,690 (GRCm38) F408L probably damaging Het
Rtn3 T G 19: 7,457,593 (GRCm38) T326P probably benign Het
Slc18b1 A C 10: 23,806,038 (GRCm38) M167L probably benign Het
Slc22a26 A G 19: 7,788,210 (GRCm38) probably null Het
Slitrk6 T C 14: 110,751,885 (GRCm38) D130G probably damaging Het
Snap47 A G 11: 59,428,613 (GRCm38) V233A probably benign Het
Sumf1 A C 6: 108,144,671 (GRCm38) Y158D probably damaging Het
Tbc1d15 A T 10: 115,220,310 (GRCm38) H252Q probably benign Het
Thsd7b T C 1: 130,188,526 (GRCm38) S1339P possibly damaging Het
Tmem45a2 T C 16: 57,049,414 (GRCm38) I56V probably benign Het
Ttc21b A G 2: 66,236,233 (GRCm38) S359P probably benign Het
Ttc27 T C 17: 74,729,977 (GRCm38) I215T probably benign Het
Ttn C T 2: 76,724,195 (GRCm38) V30759I possibly damaging Het
Vdac3 T C 8: 22,580,388 (GRCm38) N168S probably damaging Het
Wdr7 T C 18: 63,865,300 (GRCm38) V1106A probably benign Het
Wrap73 T A 4: 154,142,491 (GRCm38) F16Y probably damaging Het
Zfat C A 15: 68,180,803 (GRCm38) D381Y probably damaging Het
Other mutations in Lpar5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01719:Lpar5 APN 6 125,082,006 (GRCm38) missense possibly damaging 0.94
IGL01830:Lpar5 APN 6 125,081,822 (GRCm38) missense probably benign 0.01
IGL01975:Lpar5 APN 6 125,081,787 (GRCm38) missense probably damaging 0.99
IGL02021:Lpar5 APN 6 125,081,992 (GRCm38) nonsense probably null
IGL02718:Lpar5 APN 6 125,082,244 (GRCm38) missense probably damaging 1.00
IGL03027:Lpar5 APN 6 125,082,240 (GRCm38) missense probably damaging 1.00
IGL03300:Lpar5 APN 6 125,082,240 (GRCm38) missense probably damaging 1.00
F5770:Lpar5 UTSW 6 125,081,727 (GRCm38) missense possibly damaging 0.88
R1639:Lpar5 UTSW 6 125,081,601 (GRCm38) missense probably damaging 1.00
R1822:Lpar5 UTSW 6 125,081,415 (GRCm38) missense possibly damaging 0.76
R2227:Lpar5 UTSW 6 125,081,135 (GRCm38) critical splice acceptor site probably null
R4019:Lpar5 UTSW 6 125,081,675 (GRCm38) missense probably damaging 1.00
R4288:Lpar5 UTSW 6 125,081,864 (GRCm38) missense probably benign 0.00
R4705:Lpar5 UTSW 6 125,082,207 (GRCm38) missense possibly damaging 0.64
R4787:Lpar5 UTSW 6 125,082,498 (GRCm38) splice site probably null
R5027:Lpar5 UTSW 6 125,082,147 (GRCm38) missense possibly damaging 0.69
R6114:Lpar5 UTSW 6 125,081,676 (GRCm38) missense probably damaging 1.00
R7197:Lpar5 UTSW 6 125,082,384 (GRCm38) missense probably benign 0.00
R7779:Lpar5 UTSW 6 125,082,244 (GRCm38) missense probably damaging 1.00
R8193:Lpar5 UTSW 6 125,081,339 (GRCm38) missense probably benign
R8264:Lpar5 UTSW 6 125,081,502 (GRCm38) missense probably damaging 1.00
R9460:Lpar5 UTSW 6 125,081,271 (GRCm38) start gained probably benign
R9628:Lpar5 UTSW 6 125,081,985 (GRCm38) missense probably damaging 0.96
V7580:Lpar5 UTSW 6 125,081,727 (GRCm38) missense possibly damaging 0.88
V7581:Lpar5 UTSW 6 125,081,727 (GRCm38) missense possibly damaging 0.88
V7582:Lpar5 UTSW 6 125,081,727 (GRCm38) missense possibly damaging 0.88
Z1176:Lpar5 UTSW 6 125,082,072 (GRCm38) missense probably damaging 1.00
Z1176:Lpar5 UTSW 6 125,081,379 (GRCm38) missense possibly damaging 0.92
Z1177:Lpar5 UTSW 6 125,082,018 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2013-07-11