Incidental Mutation 'R7877:Adgrl3'
ID 608488
Institutional Source Beutler Lab
Gene Symbol Adgrl3
Ensembl Gene ENSMUSG00000037605
Gene Name adhesion G protein-coupled receptor L3
Synonyms lectomedin 3, D130075K09Rik, 5430402I23Rik, Lphn3, LEC3
MMRRC Submission 045929-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7877 (G1)
Quality Score 225.009
Status Not validated
Chromosome 5
Chromosomal Location 81167985-81972980 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 81842467 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 865 (E865G)
Ref Sequence ENSEMBL: ENSMUSP00000112470 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036068] [ENSMUST00000072521] [ENSMUST00000117253] [ENSMUST00000117407] [ENSMUST00000117985] [ENSMUST00000118034] [ENSMUST00000118078] [ENSMUST00000118442] [ENSMUST00000119385] [ENSMUST00000119788] [ENSMUST00000120128] [ENSMUST00000120144] [ENSMUST00000120292] [ENSMUST00000120445] [ENSMUST00000120673] [ENSMUST00000121641] [ENSMUST00000121707] [ENSMUST00000122037] [ENSMUST00000122356] [ENSMUST00000132375]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000036068
AA Change: E933G

PolyPhen 2 Score 0.660 (Sensitivity: 0.86; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000045342
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 6.6e-27 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 1.1e-7 PFAM
Pfam:DUF3497 627 857 2.2e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1187 4.4e-72 PFAM
Pfam:Latrophilin 1206 1276 2.4e-30 PFAM
Pfam:Latrophilin 1272 1543 3.2e-113 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000072521
AA Change: E933G

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000072336
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 5.9e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 4.3e-8 PFAM
Pfam:GAIN 630 856 1.2e-58 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1187 2.5e-73 PFAM
Pfam:Latrophilin 1207 1274 4e-34 PFAM
Pfam:Latrophilin 1272 1543 5e-89 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000117253
AA Change: E865G

PolyPhen 2 Score 0.304 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000112470
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 1e-26 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 4.5e-8 PFAM
Pfam:DUF3497 559 789 1.2e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1110 5e-73 PFAM
Pfam:Latrophilin 1129 1265 7.5e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000117407
AA Change: E933G

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000112388
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 2.4e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 6e-8 PFAM
Pfam:DUF3497 627 857 2.6e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1178 7.7e-73 PFAM
Pfam:Latrophilin 1197 1321 1.8e-61 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000117985
AA Change: E865G

PolyPhen 2 Score 0.693 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000113950
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 1.3e-26 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 5.5e-8 PFAM
Pfam:DUF3497 559 789 1.6e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1119 1.7e-72 PFAM
Pfam:Latrophilin 1138 1512 6.8e-178 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000118034
AA Change: E865G

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000113534
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 1.2e-26 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 5.5e-8 PFAM
Pfam:DUF3497 559 789 1.6e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1110 6.6e-73 PFAM
Pfam:Latrophilin 1129 1503 6.7e-178 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000118078
AA Change: E865G

PolyPhen 2 Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000112731
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 9.7e-27 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 4.3e-8 PFAM
Pfam:DUF3497 559 789 1.2e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1110 4.8e-73 PFAM
Pfam:Latrophilin 1129 1201 2.6e-30 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000118442
AA Change: E933G

PolyPhen 2 Score 0.880 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000113836
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 1e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 4.7e-8 PFAM
Pfam:DUF3497 627 857 1.3e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1187 1.4e-72 PFAM
Pfam:Latrophilin 1206 1278 2.8e-30 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000119385
AA Change: E933G

PolyPhen 2 Score 0.101 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000113243
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 1e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 4.6e-8 PFAM
Pfam:DUF3497 627 857 1.3e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1178 5.2e-73 PFAM
Pfam:Latrophilin 1197 1269 2.7e-30 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000119788
AA Change: E933G

PolyPhen 2 Score 0.444 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000114067
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 1.3e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 5.7e-8 PFAM
Pfam:DUF3497 627 857 1.7e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1187 1.8e-72 PFAM
Pfam:Latrophilin 1206 1279 3.6e-31 PFAM
Pfam:Latrophilin 1273 1550 4.5e-113 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000120128
AA Change: E865G

PolyPhen 2 Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000113208
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 9.8e-27 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 4.4e-8 PFAM
Pfam:DUF3497 559 789 1.2e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1119 1.3e-72 PFAM
Pfam:Latrophilin 1138 1210 2.6e-30 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000120144
AA Change: E865G

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000113619
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 1e-26 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 4.5e-8 PFAM
Pfam:DUF3497 559 789 1.3e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1110 5.1e-73 PFAM
Pfam:Latrophilin 1129 1253 8.4e-62 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000120292
AA Change: E865G

PolyPhen 2 Score 0.880 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000112548
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 1e-26 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 4.5e-8 PFAM
Pfam:DUF3497 559 789 1.3e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1119 1.3e-72 PFAM
Pfam:Latrophilin 1138 1262 8.5e-62 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000120445
AA Change: E933G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000113249
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 2.2e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 2.8e-8 PFAM
Pfam:GAIN 630 856 5.1e-59 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1187 1.4e-73 PFAM
Pfam:Latrophilin 1207 1328 8e-64 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000120673
AA Change: E933G

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000113482
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 2.7e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 3.3e-8 PFAM
Pfam:GAIN 630 856 6.4e-59 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1187 1.8e-73 PFAM
Pfam:Latrophilin 1207 1580 1.4e-158 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000121641
AA Change: E933G

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000113694
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 1.3e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 5.8e-8 PFAM
Pfam:DUF3497 627 857 1.7e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1178 7e-73 PFAM
Pfam:Latrophilin 1197 1571 7.3e-178 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000121707
AA Change: E933G

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000112823
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 1.3e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 5.6e-8 PFAM
Pfam:DUF3497 627 857 1.7e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1178 6.8e-73 PFAM
Pfam:Latrophilin 1197 1267 6.4e-30 PFAM
Pfam:Latrophilin 1263 1534 8.7e-113 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000122037
AA Change: E865G

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000113374
Gene: ENSMUSG00000037605
AA Change: E865G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:Gal_Lectin 43 123 1.2e-26 PFAM
OLF 137 393 2.71e-170 SMART
low complexity region 426 448 N/A INTRINSIC
Pfam:HRM 495 553 5.3e-8 PFAM
Pfam:DUF3497 559 789 1.5e-84 PFAM
GPS 814 866 3.72e-25 SMART
Pfam:7tm_2 874 1110 6.3e-73 PFAM
Pfam:Latrophilin 1129 1199 4.4e-30 PFAM
Pfam:Latrophilin 1194 1460 1.3e-112 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000122356
AA Change: E933G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000113600
Gene: ENSMUSG00000037605
AA Change: E933G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 62 87 N/A INTRINSIC
Pfam:Gal_Lectin 111 191 2.8e-26 PFAM
OLF 205 461 2.71e-170 SMART
low complexity region 494 516 N/A INTRINSIC
Pfam:HRM 563 621 7e-8 PFAM
Pfam:DUF3497 627 857 3.1e-84 PFAM
GPS 882 934 3.72e-25 SMART
Pfam:7tm_2 942 1178 9.3e-73 PFAM
Pfam:Latrophilin 1197 1267 9e-30 PFAM
Pfam:Latrophilin 1262 1528 2.8e-112 PFAM
Predicted Effect
SMART Domains Protein: ENSMUSP00000118882
Gene: ENSMUSG00000037605
AA Change: E277G

DomainStartEndE-ValueType
Pfam:GAIN 2 201 1.8e-51 PFAM
GPS 227 279 3.72e-25 SMART
Pfam:7tm_2 287 523 9.1e-75 PFAM
Pfam:Latrophilin 543 610 7.2e-35 PFAM
Pfam:Latrophilin 607 873 1.8e-89 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000132375
SMART Domains Protein: ENSMUSP00000117211
Gene: ENSMUSG00000037605

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
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 latrophilin subfamily of G-protein coupled receptors (GPCR). Latrophilins may function in both cell adhesion and signal transduction. In experiments with non-human species, endogenous proteolytic cleavage within a cysteine-rich GPS (G-protein-coupled-receptor proteolysis site) domain resulted in two subunits (a large extracellular N-terminal cell adhesion subunit and a subunit with substantial similarity to the secretin/calcitonin family of GPCRs) being non-covalently bound at the cell membrane. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a gene trap allele exhibit increased dopamine and serotonine levels in the dorsal striatum, hyperactivity, increased stereotypic behavior and enhanced hyperactivity in response to cocaine. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700010I14Rik G A 17: 9,220,665 (GRCm39) C388Y probably damaging Het
4930522L14Rik G A 5: 109,884,230 (GRCm39) H543Y probably damaging Het
Abca1 A T 4: 53,046,135 (GRCm39) V1711E possibly damaging Het
Abca3 A T 17: 24,602,997 (GRCm39) K531* probably null Het
Adgrf5 A T 17: 43,752,729 (GRCm39) D557V possibly damaging Het
Adprhl1 T A 8: 13,275,316 (GRCm39) R481* probably null Het
Afap1l1 T A 18: 61,879,853 (GRCm39) D339V probably damaging Het
Atp9b T A 18: 80,890,412 (GRCm39) H309L Het
Baiap3 A G 17: 25,470,112 (GRCm39) V122A probably damaging Het
Btg4 T C 9: 51,029,240 (GRCm39) S142P probably benign Het
C1ra G A 6: 124,494,684 (GRCm39) E316K probably benign Het
Ccng2 C G 5: 93,421,202 (GRCm39) S237R probably benign Het
Cdca2 T A 14: 67,914,665 (GRCm39) T865S probably benign Het
Cdk12 A G 11: 98,131,661 (GRCm39) Y964C unknown Het
Cenpo A T 12: 4,264,573 (GRCm39) F273Y probably damaging Het
Cfap96 T A 8: 46,423,436 (GRCm39) K92M probably damaging Het
Chac1 T A 2: 119,183,987 (GRCm39) D196E probably damaging Het
Clec4n T C 6: 123,209,063 (GRCm39) F43L probably benign Het
Colgalt1 T A 8: 72,074,508 (GRCm39) C407S probably damaging Het
Csnk1g1 T A 9: 65,906,830 (GRCm39) probably null Het
Cyp2b23 T A 7: 26,385,851 (GRCm39) E2V probably damaging Het
Cyp51 T A 5: 4,152,929 (GRCm39) K91M probably damaging Het
Cyria A C 12: 12,414,798 (GRCm39) Y263S probably benign Het
Dnah8 G T 17: 30,882,348 (GRCm39) G640V probably benign Het
Dnajc2 G T 5: 21,965,637 (GRCm39) S505R possibly damaging Het
Fam124b A T 1: 80,191,053 (GRCm39) L110H probably damaging Het
Fem1b T A 9: 62,703,844 (GRCm39) Y472F probably benign Het
Frem1 A G 4: 82,932,049 (GRCm39) probably null Het
Gabrg1 A T 5: 70,973,415 (GRCm39) D46E probably damaging Het
Gbp4 T C 5: 105,266,161 (GRCm39) K627E probably benign Het
Glis1 A G 4: 107,491,900 (GRCm39) D776G probably damaging Het
Gm4847 A G 1: 166,467,575 (GRCm39) V207A possibly damaging Het
Gm7298 T A 6: 121,759,741 (GRCm39) Y1213* probably null Het
Gm8229 T A 14: 44,604,033 (GRCm39) L74* probably null Het
Hc A T 2: 34,887,411 (GRCm39) Y1364* probably null Het
Hnrnpa2b1 A T 6: 51,443,302 (GRCm39) S186R unknown Het
Hrh4 A G 18: 13,155,582 (GRCm39) I374V possibly damaging Het
Ighmbp2 A G 19: 3,311,490 (GRCm39) L975P probably damaging Het
Intu G A 3: 40,654,222 (GRCm39) V905I probably benign Het
Large1 T A 8: 73,843,071 (GRCm39) R151W probably damaging Het
Limd2 G A 11: 106,050,004 (GRCm39) T24M probably benign Het
Med16 A T 10: 79,734,206 (GRCm39) C569* probably null Het
Mettl1 T G 10: 126,880,390 (GRCm39) V104G possibly damaging Het
Mgat4c A G 10: 102,220,900 (GRCm39) T61A probably benign Het
Mrps31 T A 8: 22,914,367 (GRCm39) Y238N probably benign Het
Mrs2 T C 13: 25,181,113 (GRCm39) E236G probably damaging Het
Muc5ac G C 7: 141,363,040 (GRCm39) G2117A unknown Het
Noxred1 G A 12: 87,271,761 (GRCm39) A136V probably benign Het
Obscn T A 11: 59,024,588 (GRCm39) D484V probably damaging Het
Picalm C A 7: 89,779,876 (GRCm39) H32Q probably benign Het
Pik3r5 G A 11: 68,381,431 (GRCm39) G206R probably damaging Het
Plekhh2 G A 17: 84,882,434 (GRCm39) C680Y probably benign Het
Plxna1 A G 6: 89,300,241 (GRCm39) F1614S probably damaging Het
Ppip5k1 T C 2: 121,147,235 (GRCm39) M1129V probably benign Het
Prp2 C T 6: 132,572,928 (GRCm39) T7I unknown Het
Rrbp1 A T 2: 143,789,815 (GRCm39) probably benign Het
Sdhaf3 C T 6: 7,038,855 (GRCm39) T59M probably benign Het
Slc17a6 T A 7: 51,275,253 (GRCm39) I104N probably benign Het
Slc35c1 A T 2: 92,289,402 (GRCm39) W48R probably damaging Het
Slc5a4b A T 10: 75,910,886 (GRCm39) C317S probably damaging Het
Smim13 G T 13: 41,403,650 (GRCm39) probably benign Het
Snrpg T C 6: 86,355,761 (GRCm39) V76A probably benign Het
Sntb2 C T 8: 107,738,164 (GRCm39) T509I probably benign Het
Sptbn1 T C 11: 30,079,601 (GRCm39) D1276G possibly damaging Het
Sptbn2 A G 19: 4,794,290 (GRCm39) E1498G possibly damaging Het
Stau1 T A 2: 166,792,787 (GRCm39) N393Y possibly damaging Het
Tars2 A T 3: 95,653,401 (GRCm39) S500T probably damaging Het
Tbc1d23 A T 16: 56,993,488 (GRCm39) D559E probably benign Het
Trav14-2 T C 14: 53,878,508 (GRCm39) Y64H possibly damaging Het
Trpm3 A C 19: 22,882,148 (GRCm39) E838D probably benign Het
Vmn1r23 G A 6: 57,903,541 (GRCm39) A79V probably benign Het
Vmn1r48 G T 6: 90,013,431 (GRCm39) N131K probably benign Het
Vmn2r18 A T 5: 151,508,437 (GRCm39) M229K probably damaging Het
Zbtb4 G A 11: 69,666,863 (GRCm39) R56K probably benign Het
Zfp616 G T 11: 73,975,188 (GRCm39) G486W probably damaging Het
Zkscan8 A T 13: 21,704,580 (GRCm39) F453Y possibly damaging Het
Other mutations in Adgrl3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00391:Adgrl3 APN 5 81,872,071 (GRCm39) missense probably damaging 0.99
IGL00596:Adgrl3 APN 5 81,794,314 (GRCm39) missense probably benign 0.01
IGL00766:Adgrl3 APN 5 81,942,415 (GRCm39) missense probably damaging 1.00
IGL00787:Adgrl3 APN 5 81,841,401 (GRCm39) missense probably damaging 1.00
IGL00917:Adgrl3 APN 5 81,841,421 (GRCm39) missense possibly damaging 0.93
IGL01155:Adgrl3 APN 5 81,708,740 (GRCm39) missense probably benign 0.39
IGL01348:Adgrl3 APN 5 81,874,570 (GRCm39) missense probably damaging 1.00
IGL01401:Adgrl3 APN 5 81,836,516 (GRCm39) missense possibly damaging 0.94
IGL01443:Adgrl3 APN 5 81,613,134 (GRCm39) missense probably damaging 1.00
IGL01532:Adgrl3 APN 5 81,842,416 (GRCm39) missense probably damaging 1.00
IGL01779:Adgrl3 APN 5 81,535,717 (GRCm39) missense probably damaging 1.00
IGL01920:Adgrl3 APN 5 81,613,143 (GRCm39) missense probably damaging 1.00
IGL02065:Adgrl3 APN 5 81,660,064 (GRCm39) missense probably damaging 1.00
IGL02365:Adgrl3 APN 5 81,660,428 (GRCm39) missense probably damaging 1.00
IGL02879:Adgrl3 APN 5 81,659,966 (GRCm39) missense probably damaging 1.00
R0010:Adgrl3 UTSW 5 81,940,250 (GRCm39) missense possibly damaging 0.58
R0077:Adgrl3 UTSW 5 81,919,532 (GRCm39) splice site probably benign
R0103:Adgrl3 UTSW 5 81,940,194 (GRCm39) intron probably benign
R0138:Adgrl3 UTSW 5 81,841,454 (GRCm39) missense probably damaging 1.00
R0149:Adgrl3 UTSW 5 81,908,544 (GRCm39) missense probably damaging 1.00
R0349:Adgrl3 UTSW 5 81,919,491 (GRCm39) missense probably damaging 1.00
R0361:Adgrl3 UTSW 5 81,908,544 (GRCm39) missense probably damaging 1.00
R0522:Adgrl3 UTSW 5 81,874,648 (GRCm39) missense possibly damaging 0.91
R0610:Adgrl3 UTSW 5 81,841,563 (GRCm39) splice site probably benign
R0658:Adgrl3 UTSW 5 81,796,560 (GRCm39) missense probably benign 0.18
R0671:Adgrl3 UTSW 5 81,708,752 (GRCm39) missense probably benign 0.45
R0679:Adgrl3 UTSW 5 81,942,824 (GRCm39) missense probably damaging 1.00
R1413:Adgrl3 UTSW 5 81,841,366 (GRCm39) missense probably damaging 1.00
R1444:Adgrl3 UTSW 5 81,660,200 (GRCm39) missense probably damaging 1.00
R1574:Adgrl3 UTSW 5 81,935,296 (GRCm39) missense probably damaging 1.00
R1574:Adgrl3 UTSW 5 81,935,296 (GRCm39) missense probably damaging 1.00
R1738:Adgrl3 UTSW 5 81,535,826 (GRCm39) missense probably damaging 0.99
R1744:Adgrl3 UTSW 5 81,942,267 (GRCm39) missense probably damaging 1.00
R1803:Adgrl3 UTSW 5 81,919,464 (GRCm39) nonsense probably null
R1891:Adgrl3 UTSW 5 81,659,891 (GRCm39) missense probably damaging 1.00
R1988:Adgrl3 UTSW 5 81,836,414 (GRCm39) missense probably damaging 1.00
R2126:Adgrl3 UTSW 5 81,660,383 (GRCm39) missense probably damaging 1.00
R2136:Adgrl3 UTSW 5 81,660,101 (GRCm39) missense probably damaging 1.00
R2171:Adgrl3 UTSW 5 81,660,362 (GRCm39) nonsense probably null
R2891:Adgrl3 UTSW 5 81,841,366 (GRCm39) missense probably damaging 1.00
R3508:Adgrl3 UTSW 5 81,872,103 (GRCm39) missense probably damaging 1.00
R3732:Adgrl3 UTSW 5 81,942,793 (GRCm39) missense probably benign 0.05
R3732:Adgrl3 UTSW 5 81,942,793 (GRCm39) missense probably benign 0.05
R3733:Adgrl3 UTSW 5 81,942,793 (GRCm39) missense probably benign 0.05
R3982:Adgrl3 UTSW 5 81,842,373 (GRCm39) missense possibly damaging 0.95
R4085:Adgrl3 UTSW 5 81,660,391 (GRCm39) missense probably benign 0.02
R4462:Adgrl3 UTSW 5 81,836,357 (GRCm39) missense probably damaging 1.00
R4725:Adgrl3 UTSW 5 81,914,052 (GRCm39) missense possibly damaging 0.67
R4726:Adgrl3 UTSW 5 81,794,425 (GRCm39) missense possibly damaging 0.61
R4781:Adgrl3 UTSW 5 81,908,571 (GRCm39) missense probably damaging 1.00
R4837:Adgrl3 UTSW 5 81,914,081 (GRCm39) missense probably benign 0.07
R4841:Adgrl3 UTSW 5 81,942,118 (GRCm39) missense possibly damaging 0.53
R4883:Adgrl3 UTSW 5 81,837,493 (GRCm39) missense probably damaging 1.00
R4921:Adgrl3 UTSW 5 81,659,957 (GRCm39) missense probably damaging 1.00
R4945:Adgrl3 UTSW 5 81,659,895 (GRCm39) missense probably damaging 1.00
R5055:Adgrl3 UTSW 5 81,794,398 (GRCm39) missense possibly damaging 0.48
R5313:Adgrl3 UTSW 5 81,874,516 (GRCm39) missense probably damaging 1.00
R5385:Adgrl3 UTSW 5 81,874,648 (GRCm39) missense probably damaging 1.00
R5447:Adgrl3 UTSW 5 81,613,188 (GRCm39) intron probably benign
R5482:Adgrl3 UTSW 5 81,942,360 (GRCm39) missense probably damaging 1.00
R5586:Adgrl3 UTSW 5 81,871,994 (GRCm39) missense probably damaging 0.99
R5637:Adgrl3 UTSW 5 81,841,391 (GRCm39) missense probably damaging 1.00
R5919:Adgrl3 UTSW 5 81,794,417 (GRCm39) missense probably benign 0.00
R6090:Adgrl3 UTSW 5 81,660,173 (GRCm39) missense probably damaging 1.00
R6093:Adgrl3 UTSW 5 81,794,369 (GRCm39) missense probably benign 0.42
R6107:Adgrl3 UTSW 5 81,836,410 (GRCm39) missense probably damaging 0.97
R6245:Adgrl3 UTSW 5 81,836,403 (GRCm39) missense probably benign 0.01
R6426:Adgrl3 UTSW 5 81,874,717 (GRCm39) missense probably damaging 1.00
R6440:Adgrl3 UTSW 5 81,942,341 (GRCm39) nonsense probably null
R6516:Adgrl3 UTSW 5 81,613,119 (GRCm39) missense probably damaging 1.00
R6527:Adgrl3 UTSW 5 81,935,364 (GRCm39) missense probably damaging 0.99
R6622:Adgrl3 UTSW 5 81,942,606 (GRCm39) missense probably benign 0.34
R6842:Adgrl3 UTSW 5 81,888,927 (GRCm39) missense probably damaging 1.00
R6902:Adgrl3 UTSW 5 81,837,434 (GRCm39) missense probably damaging 1.00
R6921:Adgrl3 UTSW 5 81,796,560 (GRCm39) missense probably damaging 0.99
R7201:Adgrl3 UTSW 5 81,872,069 (GRCm39) missense probably damaging 1.00
R7207:Adgrl3 UTSW 5 81,457,874 (GRCm39) start codon destroyed probably null 0.33
R7215:Adgrl3 UTSW 5 81,841,397 (GRCm39) missense probably damaging 1.00
R7376:Adgrl3 UTSW 5 81,942,597 (GRCm39) missense probably damaging 1.00
R7441:Adgrl3 UTSW 5 81,871,987 (GRCm39) missense possibly damaging 0.70
R7582:Adgrl3 UTSW 5 81,841,523 (GRCm39) missense probably damaging 0.99
R7682:Adgrl3 UTSW 5 81,942,407 (GRCm39) missense probably damaging 0.97
R7863:Adgrl3 UTSW 5 81,660,596 (GRCm39) missense probably damaging 1.00
R8051:Adgrl3 UTSW 5 81,613,113 (GRCm39) missense probably damaging 1.00
R8237:Adgrl3 UTSW 5 81,935,408 (GRCm39) frame shift probably null
R8390:Adgrl3 UTSW 5 81,914,057 (GRCm39) missense probably damaging 1.00
R8392:Adgrl3 UTSW 5 81,794,397 (GRCm39) missense probably benign 0.01
R8475:Adgrl3 UTSW 5 81,871,976 (GRCm39) missense probably benign 0.31
R8478:Adgrl3 UTSW 5 81,942,348 (GRCm39) missense possibly damaging 0.87
R8550:Adgrl3 UTSW 5 81,942,599 (GRCm39) missense possibly damaging 0.79
R8685:Adgrl3 UTSW 5 81,874,708 (GRCm39) missense possibly damaging 0.91
R8792:Adgrl3 UTSW 5 81,836,522 (GRCm39) missense probably damaging 0.99
R8851:Adgrl3 UTSW 5 81,613,119 (GRCm39) missense probably damaging 1.00
R8868:Adgrl3 UTSW 5 81,794,451 (GRCm39) missense probably benign
R8889:Adgrl3 UTSW 5 81,874,516 (GRCm39) missense probably damaging 1.00
R8892:Adgrl3 UTSW 5 81,874,516 (GRCm39) missense probably damaging 1.00
R8942:Adgrl3 UTSW 5 81,796,568 (GRCm39) missense probably benign 0.09
R9023:Adgrl3 UTSW 5 81,613,065 (GRCm39) missense probably damaging 0.99
R9089:Adgrl3 UTSW 5 81,808,291 (GRCm39) missense possibly damaging 0.77
R9100:Adgrl3 UTSW 5 81,842,299 (GRCm39) missense possibly damaging 0.85
R9104:Adgrl3 UTSW 5 81,457,912 (GRCm39) missense probably benign 0.00
R9172:Adgrl3 UTSW 5 81,922,251 (GRCm39) missense probably benign 0.01
R9284:Adgrl3 UTSW 5 81,657,568 (GRCm39) splice site probably benign
R9286:Adgrl3 UTSW 5 81,794,413 (GRCm39) missense probably benign
R9644:Adgrl3 UTSW 5 81,872,036 (GRCm39) missense probably damaging 0.99
R9689:Adgrl3 UTSW 5 81,942,780 (GRCm39) missense probably damaging 0.98
R9757:Adgrl3 UTSW 5 81,613,086 (GRCm39) missense probably benign 0.07
R9795:Adgrl3 UTSW 5 81,837,421 (GRCm39) missense probably damaging 1.00
Z1088:Adgrl3 UTSW 5 81,660,005 (GRCm39) missense probably damaging 1.00
Z1088:Adgrl3 UTSW 5 81,477,729 (GRCm39) missense probably benign 0.33
Predicted Primers PCR Primer
(F):5'- TTCCACCATAGCAGTCAGAAG -3'
(R):5'- TTGTCTAAATTGAAATCAGGGAGGC -3'

Sequencing Primer
(F):5'- TAGCAGTCAGAAGAAAATTTCAACC -3'
(R):5'- AGGTGAATTTATTGAGCAAACTCTG -3'
Posted On 2019-12-20