Incidental Mutation 'R5663:Adgra3'
ID 444193
Institutional Source Beutler Lab
Gene Symbol Adgra3
Ensembl Gene ENSMUSG00000029090
Gene Name adhesion G protein-coupled receptor A3
Synonyms Tem5-like, 3830613O22Rik, Gpr125
MMRRC Submission 043306-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5663 (G1)
Quality Score 225
Status Not validated
Chromosome 5
Chromosomal Location 50117293-50216338 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 50156627 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Aspartic acid at position 368 (N368D)
Ref Sequence ENSEMBL: ENSMUSP00000030971 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030971]
AlphaFold Q7TT36
Predicted Effect probably benign
Transcript: ENSMUST00000030971
AA Change: N368D

PolyPhen 2 Score 0.143 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000030971
Gene: ENSMUSG00000029090
AA Change: N368D

DomainStartEndE-ValueType
signal peptide 1 27 N/A INTRINSIC
low complexity region 36 48 N/A INTRINSIC
LRR 68 92 1.71e1 SMART
LRR_TYP 93 116 2.27e-4 SMART
LRR_TYP 117 140 4.11e-2 SMART
LRR_TYP 141 164 3.89e-3 SMART
LRRCT 176 225 5.24e-5 SMART
IG 238 331 8.26e-5 SMART
GPS 686 738 4.81e-3 SMART
Pfam:7tm_2 746 1031 1.6e-16 PFAM
low complexity region 1251 1262 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198818
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.6%
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 G protein-coupled receptor superfamily. This membrane protein may play a role in tumor angiogenesis through its interaction with the human homolog of the Drosophila disc large tumor suppressor gene. This gene is mapped to a candidate region of chromosome 4 which may be associated with bipolar disorder and schizophrenia. [provided by RefSeq, Oct 2012]
PHENOTYPE: Homozygous mutant mice are fertile and grossly normal. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agfg1 T A 1: 82,871,173 (GRCm39) S444R probably damaging Het
Arhgap44 A T 11: 64,915,117 (GRCm39) F384I probably damaging Het
Atp8b2 T C 3: 89,849,101 (GRCm39) N1078D probably benign Het
Bcan G A 3: 87,902,920 (GRCm39) T286I probably damaging Het
Cacna1d A G 14: 29,845,297 (GRCm39) L624P probably damaging Het
Ccn5 G A 2: 163,667,173 (GRCm39) R58Q probably damaging Het
Cimip1 C T 2: 173,369,690 (GRCm39) P68L probably damaging Het
Dnah7c C A 1: 46,574,308 (GRCm39) F994L probably damaging Het
Dpp6 A G 5: 27,254,620 (GRCm39) I12V possibly damaging Het
Edil3 A G 13: 89,190,627 (GRCm39) I101M probably damaging Het
Elapor1 T C 3: 108,399,399 (GRCm39) T64A probably benign Het
Farp2 T C 1: 93,497,735 (GRCm39) V255A probably damaging Het
Fhip1a T C 3: 85,579,740 (GRCm39) T822A probably benign Het
Fzr1 A G 10: 81,206,360 (GRCm39) S137P probably benign Het
H2-Eb2 T C 17: 34,552,382 (GRCm39) F76L possibly damaging Het
Helb A G 10: 119,941,698 (GRCm39) I330T possibly damaging Het
Il18rap T A 1: 40,570,717 (GRCm39) C220S probably damaging Het
Kdm4c T C 4: 74,317,585 (GRCm39) V966A probably damaging Het
Kdm5b T C 1: 134,558,373 (GRCm39) V1460A probably benign Het
Kif15 T A 9: 122,820,916 (GRCm39) probably null Het
Liat1 A G 11: 75,891,047 (GRCm39) K54E probably damaging Het
Lrrc37 A G 11: 103,503,949 (GRCm39) V497A probably benign Het
Masp1 T C 16: 23,271,688 (GRCm39) E621G possibly damaging Het
Mier1 T A 4: 103,007,739 (GRCm39) S285T probably damaging Het
Mroh6 A G 15: 75,760,437 (GRCm39) S46P probably benign Het
Myo1h A T 5: 114,472,155 (GRCm39) Q395L probably damaging Het
Ndufb5 T C 3: 32,801,898 (GRCm39) I86T possibly damaging Het
Nelfb T A 2: 25,093,501 (GRCm39) E417V probably benign Het
Nfkb1 T G 3: 135,309,612 (GRCm39) D494A possibly damaging Het
Nid1 G A 13: 13,647,419 (GRCm39) C395Y probably damaging Het
Nr4a3 G T 4: 48,055,931 (GRCm39) R319I probably damaging Het
Or2ag13 T A 7: 106,472,877 (GRCm39) T192S probably benign Het
Or4e1 A T 14: 52,701,052 (GRCm39) I138K probably benign Het
Or6f2 G A 7: 139,756,234 (GRCm39) C67Y probably damaging Het
Paqr5 A G 9: 61,876,144 (GRCm39) V130A probably benign Het
Phlpp2 G A 8: 110,630,976 (GRCm39) V207I probably benign Het
Pik3ca C T 3: 32,516,928 (GRCm39) T1052M probably damaging Het
Pikfyve T C 1: 65,255,187 (GRCm39) Y347H probably benign Het
Ptprz1 A G 6: 23,035,142 (GRCm39) H1964R probably damaging Het
Rassf7 C T 7: 140,797,003 (GRCm39) T72I probably damaging Het
Rfx3 A G 19: 27,771,017 (GRCm39) F603S probably damaging Het
Slc27a4 T A 2: 29,702,382 (GRCm39) V477D probably damaging Het
Slc9a3 A C 13: 74,311,831 (GRCm39) D593A probably damaging Het
Smyd1 A G 6: 71,216,705 (GRCm39) I14T probably benign Het
Sox6 T A 7: 115,149,289 (GRCm39) I404L probably benign Het
Tas2r121 G A 6: 132,677,520 (GRCm39) H151Y probably benign Het
Tgfb1 C T 7: 25,393,706 (GRCm39) T192M possibly damaging Het
Ubr4 T C 4: 139,155,894 (GRCm39) Y2240H possibly damaging Het
Whrn T A 4: 63,336,685 (GRCm39) N626Y probably damaging Het
Xrra1 T A 7: 99,535,250 (GRCm39) I185N probably damaging Het
Zfp94 G A 7: 24,002,252 (GRCm39) R397W probably damaging Het
Other mutations in Adgra3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00777:Adgra3 APN 5 50,183,100 (GRCm39) missense probably damaging 1.00
IGL00848:Adgra3 APN 5 50,159,291 (GRCm39) missense probably damaging 1.00
IGL01455:Adgra3 APN 5 50,144,899 (GRCm39) nonsense probably null
IGL01665:Adgra3 APN 5 50,164,272 (GRCm39) missense possibly damaging 0.64
IGL02151:Adgra3 APN 5 50,136,484 (GRCm39) missense probably benign
IGL02239:Adgra3 APN 5 50,118,054 (GRCm39) missense probably damaging 1.00
IGL02351:Adgra3 APN 5 50,215,900 (GRCm39) missense probably benign 0.19
IGL02358:Adgra3 APN 5 50,215,900 (GRCm39) missense probably benign 0.19
IGL02938:Adgra3 APN 5 50,118,659 (GRCm39) missense probably benign 0.01
IGL03028:Adgra3 APN 5 50,174,194 (GRCm39) missense probably benign 0.30
aperture UTSW 5 50,156,487 (GRCm39) nonsense probably null
saltatory UTSW 5 50,117,901 (GRCm39) missense probably benign 0.09
ANU74:Adgra3 UTSW 5 50,118,380 (GRCm39) missense probably benign 0.16
R0041:Adgra3 UTSW 5 50,117,901 (GRCm39) missense probably benign 0.09
R0041:Adgra3 UTSW 5 50,117,901 (GRCm39) missense probably benign 0.09
R0121:Adgra3 UTSW 5 50,183,128 (GRCm39) splice site probably benign
R0125:Adgra3 UTSW 5 50,159,194 (GRCm39) splice site probably benign
R0137:Adgra3 UTSW 5 50,121,182 (GRCm39) splice site probably benign
R0415:Adgra3 UTSW 5 50,119,099 (GRCm39) splice site probably benign
R0479:Adgra3 UTSW 5 50,147,607 (GRCm39) missense probably benign 0.00
R0505:Adgra3 UTSW 5 50,166,676 (GRCm39) critical splice donor site probably null
R0831:Adgra3 UTSW 5 50,128,144 (GRCm39) missense probably damaging 1.00
R0883:Adgra3 UTSW 5 50,118,065 (GRCm39) missense probably damaging 1.00
R0920:Adgra3 UTSW 5 50,118,503 (GRCm39) missense probably benign 0.19
R1139:Adgra3 UTSW 5 50,119,097 (GRCm39) splice site probably null
R1211:Adgra3 UTSW 5 50,164,218 (GRCm39) missense possibly damaging 0.88
R1370:Adgra3 UTSW 5 50,118,129 (GRCm39) missense possibly damaging 0.56
R1530:Adgra3 UTSW 5 50,118,479 (GRCm39) missense probably benign 0.00
R1703:Adgra3 UTSW 5 50,164,117 (GRCm39) missense probably benign 0.00
R1782:Adgra3 UTSW 5 50,129,404 (GRCm39) missense probably benign 0.02
R1843:Adgra3 UTSW 5 50,118,834 (GRCm39) missense probably damaging 1.00
R2157:Adgra3 UTSW 5 50,159,283 (GRCm39) missense possibly damaging 0.87
R2281:Adgra3 UTSW 5 50,159,222 (GRCm39) missense probably benign 0.04
R2385:Adgra3 UTSW 5 50,136,908 (GRCm39) missense possibly damaging 0.95
R2426:Adgra3 UTSW 5 50,166,791 (GRCm39) missense possibly damaging 0.61
R3084:Adgra3 UTSW 5 50,170,733 (GRCm39) critical splice donor site probably null
R3086:Adgra3 UTSW 5 50,170,733 (GRCm39) critical splice donor site probably null
R3409:Adgra3 UTSW 5 50,159,272 (GRCm39) missense probably damaging 1.00
R3410:Adgra3 UTSW 5 50,159,272 (GRCm39) missense probably damaging 1.00
R3411:Adgra3 UTSW 5 50,159,272 (GRCm39) missense probably damaging 1.00
R4301:Adgra3 UTSW 5 50,118,420 (GRCm39) missense possibly damaging 0.94
R4360:Adgra3 UTSW 5 50,147,552 (GRCm39) missense possibly damaging 0.92
R4475:Adgra3 UTSW 5 50,159,240 (GRCm39) missense probably damaging 1.00
R4569:Adgra3 UTSW 5 50,117,905 (GRCm39) missense probably damaging 1.00
R4607:Adgra3 UTSW 5 50,128,081 (GRCm39) missense probably damaging 0.98
R4667:Adgra3 UTSW 5 50,136,298 (GRCm39) missense possibly damaging 0.94
R4671:Adgra3 UTSW 5 50,136,710 (GRCm39) missense probably damaging 1.00
R4886:Adgra3 UTSW 5 50,156,537 (GRCm39) missense probably benign 0.07
R5197:Adgra3 UTSW 5 50,118,096 (GRCm39) missense probably benign 0.01
R5208:Adgra3 UTSW 5 50,168,857 (GRCm39) missense probably damaging 0.99
R5313:Adgra3 UTSW 5 50,118,651 (GRCm39) missense probably benign 0.24
R5435:Adgra3 UTSW 5 50,147,468 (GRCm39) missense probably damaging 0.99
R6038:Adgra3 UTSW 5 50,156,487 (GRCm39) nonsense probably null
R6038:Adgra3 UTSW 5 50,156,487 (GRCm39) nonsense probably null
R6064:Adgra3 UTSW 5 50,117,667 (GRCm39) missense probably damaging 0.97
R6259:Adgra3 UTSW 5 50,156,483 (GRCm39) missense possibly damaging 0.63
R6272:Adgra3 UTSW 5 50,166,791 (GRCm39) missense possibly damaging 0.61
R6293:Adgra3 UTSW 5 50,118,189 (GRCm39) missense probably benign 0.21
R6296:Adgra3 UTSW 5 50,118,189 (GRCm39) missense probably benign 0.21
R6297:Adgra3 UTSW 5 50,118,189 (GRCm39) missense probably benign 0.21
R6352:Adgra3 UTSW 5 50,147,592 (GRCm39) missense probably benign 0.01
R6352:Adgra3 UTSW 5 50,136,478 (GRCm39) missense probably benign
R6989:Adgra3 UTSW 5 50,164,226 (GRCm39) missense probably damaging 1.00
R7026:Adgra3 UTSW 5 50,118,083 (GRCm39) missense probably benign
R7147:Adgra3 UTSW 5 50,118,587 (GRCm39) missense probably damaging 1.00
R7206:Adgra3 UTSW 5 50,164,238 (GRCm39) missense probably damaging 1.00
R7381:Adgra3 UTSW 5 50,216,116 (GRCm39) start codon destroyed probably null
R7508:Adgra3 UTSW 5 50,174,209 (GRCm39) missense probably benign 0.10
R7538:Adgra3 UTSW 5 50,118,792 (GRCm39) missense probably benign 0.01
R7579:Adgra3 UTSW 5 50,144,977 (GRCm39) missense probably benign
R7951:Adgra3 UTSW 5 50,121,126 (GRCm39) missense probably damaging 1.00
R8269:Adgra3 UTSW 5 50,121,079 (GRCm39) missense probably damaging 0.98
R8458:Adgra3 UTSW 5 50,145,013 (GRCm39) missense probably damaging 0.99
R8486:Adgra3 UTSW 5 50,147,621 (GRCm39) missense probably damaging 0.98
R8912:Adgra3 UTSW 5 50,118,273 (GRCm39) missense possibly damaging 0.61
R8955:Adgra3 UTSW 5 50,118,731 (GRCm39) missense probably benign 0.05
R9108:Adgra3 UTSW 5 50,136,295 (GRCm39) missense probably damaging 1.00
R9112:Adgra3 UTSW 5 50,118,395 (GRCm39) missense probably damaging 1.00
R9191:Adgra3 UTSW 5 50,145,006 (GRCm39) missense possibly damaging 0.88
R9267:Adgra3 UTSW 5 50,155,618 (GRCm39) missense possibly damaging 0.87
R9312:Adgra3 UTSW 5 50,117,900 (GRCm39) missense probably damaging 1.00
R9537:Adgra3 UTSW 5 50,118,207 (GRCm39) missense possibly damaging 0.82
R9614:Adgra3 UTSW 5 50,164,250 (GRCm39) missense probably damaging 1.00
RF005:Adgra3 UTSW 5 50,170,729 (GRCm39) splice site probably null
RF024:Adgra3 UTSW 5 50,170,729 (GRCm39) splice site probably null
RF036:Adgra3 UTSW 5 50,215,983 (GRCm39) small deletion probably benign
X0065:Adgra3 UTSW 5 50,129,304 (GRCm39) missense probably benign
Z1187:Adgra3 UTSW 5 50,136,421 (GRCm39) missense probably damaging 1.00
Z1192:Adgra3 UTSW 5 50,156,623 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GCATAACTCAAGTGAATCAGAATGTCC -3'
(R):5'- TGCATCCATATATCCATGGGAAC -3'

Sequencing Primer
(F):5'- CTCAAGTGAATCAGAATGTCCTATAG -3'
(R):5'- CCCTCAGGTTGTGTATGTGTG -3'
Posted On 2016-11-09