Incidental Mutation 'R5385:Adgrl3'
ID |
425061 |
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 |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5385 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
81167985-81972980 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to G
at 81874648 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Aspartic acid
at position 1050
(Y1050D)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112823
(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 |
probably damaging
Transcript: ENSMUST00000036068
AA Change: Y1050D
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000045342 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000072521
AA Change: Y1050D
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000072336 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000117253
AA Change: Y982D
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000112470 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000117407
AA Change: Y1050D
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000112388 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 |
probably damaging
Transcript: ENSMUST00000117985
AA Change: Y982D
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000113950 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000118034
AA Change: Y982D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000113534 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 |
probably damaging
Transcript: ENSMUST00000118078
AA Change: Y982D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000112731 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 |
probably damaging
Transcript: ENSMUST00000118442
AA Change: Y1050D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000113836 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000119385
AA Change: Y1050D
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000113243 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000119788
AA Change: Y1050D
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000114067 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 |
probably damaging
Transcript: ENSMUST00000120128
AA Change: Y982D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000113208 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000120144
AA Change: Y982D
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000113619 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 |
probably damaging
Transcript: ENSMUST00000120292
AA Change: Y982D
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000112548 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000120445
AA Change: Y1050D
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000113249 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000120673
AA Change: Y1050D
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000113482 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000121641
AA Change: Y1050D
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000113694 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000121707
AA Change: Y1050D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000112823 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000122037
AA Change: Y982D
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000113374 Gene: ENSMUSG00000037605 AA Change: Y982D
Domain | Start | End | E-Value | Type |
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 |
unknown
Transcript: ENSMUST00000124117
AA Change: Y394D
|
SMART Domains |
Protein: ENSMUSP00000118882 Gene: ENSMUSG00000037605 AA Change: Y394D
Domain | Start | End | E-Value | Type |
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 damaging
Transcript: ENSMUST00000122356
AA Change: Y1050D
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000113600 Gene: ENSMUSG00000037605 AA Change: Y1050D
Domain | Start | End | E-Value | Type |
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 |
noncoding transcript
Transcript: ENSMUST00000153264
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000201055
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000132375
|
SMART Domains |
Protein: ENSMUSP00000117211 Gene: ENSMUSG00000037605
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.7%
|
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 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: 129 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17a |
T |
C |
10: 80,421,446 (GRCm39) |
T175A |
probably benign |
Het |
Adam23 |
A |
G |
1: 63,590,970 (GRCm39) |
D479G |
possibly damaging |
Het |
Ago4 |
A |
G |
4: 126,411,349 (GRCm39) |
I103T |
probably benign |
Het |
Ajuba |
T |
C |
14: 54,807,855 (GRCm39) |
Y459C |
probably damaging |
Het |
Aldh7a1 |
T |
A |
18: 56,667,325 (GRCm39) |
N316Y |
possibly damaging |
Het |
Alyref2 |
A |
G |
1: 171,331,271 (GRCm39) |
N16S |
probably benign |
Het |
Ankhd1 |
A |
G |
18: 36,724,548 (GRCm39) |
E402G |
probably damaging |
Het |
Ankrd36 |
A |
G |
11: 5,639,340 (GRCm39) |
|
probably benign |
Het |
Ap2b1 |
T |
C |
11: 83,233,427 (GRCm39) |
V480A |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,235,848 (GRCm39) |
R741G |
probably benign |
Het |
Canx |
A |
G |
11: 50,192,639 (GRCm39) |
L325P |
probably damaging |
Het |
Ccpg1 |
G |
A |
9: 72,920,326 (GRCm39) |
S647N |
probably benign |
Het |
Cdc37l1 |
T |
G |
19: 28,989,343 (GRCm39) |
S267A |
possibly damaging |
Het |
Cert1 |
A |
G |
13: 96,765,575 (GRCm39) |
T447A |
possibly damaging |
Het |
Ces1f |
A |
T |
8: 93,992,388 (GRCm39) |
C354* |
probably null |
Het |
Cpne1 |
A |
T |
2: 155,916,284 (GRCm39) |
V350D |
probably damaging |
Het |
Ctdsp2 |
A |
G |
10: 126,832,326 (GRCm39) |
T262A |
probably benign |
Het |
Cypt4 |
A |
G |
9: 24,536,596 (GRCm39) |
K29E |
possibly damaging |
Het |
Dlg2 |
T |
C |
7: 91,737,784 (GRCm39) |
V422A |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,286,041 (GRCm39) |
S2715P |
probably benign |
Het |
Dnah3 |
T |
A |
7: 119,524,126 (GRCm39) |
K3953N |
probably damaging |
Het |
Dnmt1 |
A |
G |
9: 20,829,776 (GRCm39) |
V647A |
probably damaging |
Het |
Duox2 |
A |
G |
2: 122,125,617 (GRCm39) |
V330A |
probably benign |
Het |
Dusp8 |
T |
A |
7: 141,643,730 (GRCm39) |
Q61L |
possibly damaging |
Het |
Dync2h1 |
T |
C |
9: 7,016,791 (GRCm39) |
D3573G |
probably damaging |
Het |
Ears2 |
G |
C |
7: 121,643,600 (GRCm39) |
T426S |
probably benign |
Het |
Ext1 |
C |
A |
15: 52,939,213 (GRCm39) |
W612L |
probably damaging |
Het |
Fam91a1 |
G |
A |
15: 58,320,243 (GRCm39) |
S645N |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,833,971 (GRCm39) |
L4207Q |
possibly damaging |
Het |
Fbxo38 |
A |
G |
18: 62,674,042 (GRCm39) |
M13T |
probably benign |
Het |
Fbxo48 |
G |
T |
11: 16,904,329 (GRCm39) |
L160F |
possibly damaging |
Het |
Fer1l4 |
G |
A |
2: 155,879,286 (GRCm39) |
Q906* |
probably null |
Het |
Fpr2 |
C |
A |
17: 18,113,309 (GRCm39) |
H102N |
probably benign |
Het |
Gm10134 |
T |
A |
2: 28,396,372 (GRCm39) |
|
probably benign |
Het |
Gpr107 |
A |
G |
2: 31,104,263 (GRCm39) |
T523A |
probably benign |
Het |
Grin3a |
G |
A |
4: 49,719,313 (GRCm39) |
P811L |
probably damaging |
Het |
Hivep1 |
A |
T |
13: 42,317,871 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
A |
G |
2: 31,350,333 (GRCm39) |
T5077A |
probably benign |
Het |
Hpse |
C |
T |
5: 100,856,590 (GRCm39) |
W136* |
probably null |
Het |
Ifitm3 |
T |
C |
7: 140,590,554 (GRCm39) |
N2S |
probably benign |
Het |
Ifnar2 |
T |
A |
16: 91,201,086 (GRCm39) |
D442E |
possibly damaging |
Het |
Jade1 |
T |
A |
3: 41,546,137 (GRCm39) |
I54N |
probably damaging |
Het |
Jag1 |
A |
T |
2: 136,937,464 (GRCm39) |
H303Q |
possibly damaging |
Het |
Kcnh4 |
T |
C |
11: 100,643,076 (GRCm39) |
D397G |
probably damaging |
Het |
Kcnj1 |
A |
G |
9: 32,308,019 (GRCm39) |
R148G |
probably damaging |
Het |
Lct |
T |
G |
1: 128,239,354 (GRCm39) |
K277N |
possibly damaging |
Het |
Loxl3 |
A |
G |
6: 83,027,593 (GRCm39) |
M712V |
probably damaging |
Het |
Ly75 |
A |
G |
2: 60,133,985 (GRCm39) |
C1547R |
probably damaging |
Het |
Marcks |
A |
G |
10: 37,014,453 (GRCm39) |
S27P |
probably damaging |
Het |
Mef2c |
A |
G |
13: 83,810,532 (GRCm39) |
T347A |
probably benign |
Het |
Mmp3 |
C |
T |
9: 7,451,759 (GRCm39) |
R366* |
probably null |
Het |
Mrgprx2 |
T |
C |
7: 48,132,753 (GRCm39) |
T22A |
probably benign |
Het |
Msc |
C |
A |
1: 14,825,644 (GRCm39) |
R110L |
probably damaging |
Het |
Mtcl3 |
A |
G |
10: 29,072,766 (GRCm39) |
D686G |
probably benign |
Het |
Myh11 |
A |
T |
16: 14,025,872 (GRCm39) |
V1366D |
possibly damaging |
Het |
Ncf1 |
A |
G |
5: 134,250,659 (GRCm39) |
L373P |
probably damaging |
Het |
Neb |
A |
T |
2: 52,079,873 (GRCm39) |
I85N |
probably damaging |
Het |
Nfkb1 |
A |
G |
3: 135,318,303 (GRCm39) |
V310A |
possibly damaging |
Het |
Nop2 |
T |
C |
6: 125,121,324 (GRCm39) |
V702A |
probably benign |
Het |
Nudt12 |
A |
G |
17: 59,310,434 (GRCm39) |
W390R |
probably damaging |
Het |
Or10ag53 |
C |
T |
2: 87,082,827 (GRCm39) |
P182L |
probably benign |
Het |
Or10v9 |
T |
A |
19: 11,832,541 (GRCm39) |
I259F |
probably damaging |
Het |
Or11g24 |
T |
A |
14: 50,662,846 (GRCm39) |
V290E |
possibly damaging |
Het |
Or1af1 |
G |
T |
2: 37,109,599 (GRCm39) |
A33S |
possibly damaging |
Het |
Or51e1 |
T |
C |
7: 102,358,553 (GRCm39) |
L29P |
probably damaging |
Het |
Or6c208 |
A |
G |
10: 129,223,633 (GRCm39) |
I44V |
probably benign |
Het |
Or6n2 |
A |
T |
1: 173,897,036 (GRCm39) |
K57N |
probably benign |
Het |
Or8a1b |
A |
T |
9: 37,623,317 (GRCm39) |
V86E |
probably damaging |
Het |
Or8c11 |
A |
T |
9: 38,289,281 (GRCm39) |
I29F |
probably benign |
Het |
Or8g2b |
A |
G |
9: 39,751,126 (GRCm39) |
Y132C |
possibly damaging |
Het |
Otub2 |
G |
A |
12: 103,359,055 (GRCm39) |
|
probably benign |
Het |
Pck2 |
A |
G |
14: 55,782,688 (GRCm39) |
E339G |
probably damaging |
Het |
Pdcd7 |
G |
A |
9: 65,265,974 (GRCm39) |
W477* |
probably null |
Het |
Pdpk1 |
G |
A |
17: 24,317,114 (GRCm39) |
Q250* |
probably null |
Het |
Pigb |
T |
A |
9: 72,946,827 (GRCm39) |
H16L |
probably benign |
Het |
Pitpnm1 |
T |
C |
19: 4,153,435 (GRCm39) |
F197S |
probably damaging |
Het |
Plekhh2 |
T |
C |
17: 84,864,894 (GRCm39) |
V94A |
probably benign |
Het |
Pnpla7 |
C |
A |
2: 24,931,031 (GRCm39) |
P882Q |
probably damaging |
Het |
Pold2 |
A |
G |
11: 5,826,760 (GRCm39) |
L58P |
probably damaging |
Het |
Pomt1 |
C |
G |
2: 32,134,311 (GRCm39) |
Y277* |
probably null |
Het |
Prex2 |
A |
G |
1: 11,210,204 (GRCm39) |
D548G |
probably damaging |
Het |
Prkra |
T |
G |
2: 76,469,622 (GRCm39) |
T146P |
probably damaging |
Het |
Prss51 |
T |
A |
14: 64,334,543 (GRCm39) |
V108E |
probably damaging |
Het |
Rai2 |
A |
G |
X: 160,561,636 (GRCm39) |
N363S |
probably benign |
Het |
Ranbp17 |
A |
T |
11: 33,169,241 (GRCm39) |
V991D |
possibly damaging |
Het |
Riox2 |
T |
A |
16: 59,306,979 (GRCm39) |
M290K |
probably benign |
Het |
Rnpepl1 |
T |
A |
1: 92,844,914 (GRCm39) |
L402Q |
probably damaging |
Het |
S1pr2 |
T |
C |
9: 20,878,890 (GRCm39) |
T313A |
probably benign |
Het |
Sesn2 |
A |
G |
4: 132,226,575 (GRCm39) |
I173T |
probably damaging |
Het |
Setx |
T |
G |
2: 29,024,045 (GRCm39) |
|
probably null |
Het |
Sfi1 |
ACA |
ACATCTTCCCAAAGCCAGTCA |
11: 3,103,382 (GRCm39) |
|
probably benign |
Het |
Sgsm3 |
T |
C |
15: 80,892,200 (GRCm39) |
V256A |
probably benign |
Het |
Shroom4 |
T |
A |
X: 6,497,523 (GRCm39) |
C894* |
probably null |
Het |
Slc13a5 |
T |
A |
11: 72,149,903 (GRCm39) |
E159D |
probably benign |
Het |
Slc16a7 |
A |
G |
10: 125,130,473 (GRCm39) |
Y71H |
possibly damaging |
Het |
Slc28a2b |
C |
A |
2: 122,353,259 (GRCm39) |
L480I |
probably benign |
Het |
Slc4a7 |
T |
C |
14: 14,773,345 (GRCm38) |
F772L |
possibly damaging |
Het |
Snapc4 |
A |
G |
2: 26,264,515 (GRCm39) |
S275P |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,968,580 (GRCm39) |
T558A |
possibly damaging |
Het |
Sspo |
C |
T |
6: 48,439,187 (GRCm39) |
P1612S |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,531,111 (GRCm39) |
E2456G |
probably damaging |
Het |
Stx1b |
A |
T |
7: 127,414,575 (GRCm39) |
D16E |
probably benign |
Het |
Supv3l1 |
A |
T |
10: 62,266,375 (GRCm39) |
N600K |
possibly damaging |
Het |
Syne1 |
C |
T |
10: 4,991,494 (GRCm39) |
V557I |
probably benign |
Het |
Tanc2 |
T |
A |
11: 105,667,672 (GRCm39) |
D84E |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,105,774 (GRCm39) |
L82Q |
probably damaging |
Het |
Tfip11 |
T |
C |
5: 112,479,086 (GRCm39) |
|
probably null |
Het |
Thtpa |
G |
T |
14: 55,333,290 (GRCm39) |
R125L |
probably damaging |
Het |
Tm9sf1 |
C |
T |
14: 55,880,301 (GRCm39) |
G32D |
possibly damaging |
Het |
Tmcc3 |
A |
T |
10: 94,415,015 (GRCm39) |
N239I |
probably damaging |
Het |
Tpd52 |
A |
T |
3: 8,996,255 (GRCm39) |
|
probably null |
Het |
Traf6 |
T |
A |
2: 101,515,100 (GRCm39) |
C85* |
probably null |
Het |
Trim68 |
T |
G |
7: 102,327,990 (GRCm39) |
D321A |
probably damaging |
Het |
Trmt6 |
C |
A |
2: 132,650,703 (GRCm39) |
A302S |
probably benign |
Het |
Ttbk1 |
T |
C |
17: 46,758,558 (GRCm39) |
D692G |
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,133,985 (GRCm39) |
W1067R |
probably damaging |
Het |
Ttc6 |
T |
A |
12: 57,689,821 (GRCm39) |
|
probably null |
Het |
Tut7 |
A |
T |
13: 59,937,660 (GRCm39) |
|
probably null |
Het |
Txnrd2 |
T |
G |
16: 18,296,442 (GRCm39) |
I468S |
probably damaging |
Het |
Ube2b |
A |
T |
11: 51,879,471 (GRCm39) |
Y100N |
probably damaging |
Het |
Ucn3 |
A |
T |
13: 3,991,474 (GRCm39) |
F59L |
probably benign |
Het |
Uggt1 |
A |
G |
1: 36,223,493 (GRCm39) |
Y599H |
probably damaging |
Het |
Ulk3 |
T |
A |
9: 57,498,023 (GRCm39) |
I108N |
possibly damaging |
Het |
Vav3 |
A |
G |
3: 109,434,791 (GRCm39) |
M441V |
possibly damaging |
Het |
Vmn2r1 |
T |
A |
3: 64,008,819 (GRCm39) |
D499E |
possibly damaging |
Het |
Vmn2r118 |
C |
T |
17: 55,918,565 (GRCm39) |
G109D |
probably benign |
Het |
Vmn2r5 |
T |
A |
3: 64,416,931 (GRCm39) |
M76L |
probably benign |
Het |
Vwa3a |
A |
G |
7: 120,389,365 (GRCm39) |
K68E |
possibly damaging |
Het |
Zmiz1 |
A |
T |
14: 25,650,237 (GRCm39) |
Y459F |
probably damaging |
Het |
|
Other mutations in Adgrl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |
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 |
R7877:Adgrl3
|
UTSW |
5 |
81,842,467 (GRCm39) |
missense |
probably benign |
0.30 |
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'- TTATTCGGAAACTGAAGCCTGG -3'
(R):5'- ACATTGAATCACACTCTCAGTTGC -3'
Sequencing Primer
(F):5'- GAAACTGAAGCCTGGGTTCATTTTTC -3'
(R):5'- CTGCTGTGAGGGTAAATCCACATC -3'
|
Posted On |
2016-08-04 |