Incidental Mutation 'R7205:Adgrl2'
ID |
560497 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adgrl2
|
Ensembl Gene |
ENSMUSG00000028184 |
Gene Name |
adhesion G protein-coupled receptor L2 |
Synonyms |
Lphn2, Lphh1, Lec1 |
MMRRC Submission |
045283-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7205 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
148521219-148696191 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 148564585 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 332
(Y332N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000143626
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000106128]
[ENSMUST00000195988]
[ENSMUST00000196526]
[ENSMUST00000197567]
[ENSMUST00000198779]
[ENSMUST00000199059]
[ENSMUST00000199238]
[ENSMUST00000199750]
[ENSMUST00000200154]
[ENSMUST00000200543]
|
AlphaFold |
Q8JZZ7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000106128
AA Change: Y332N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000101734 Gene: ENSMUSG00000028184 AA Change: Y332N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
2.5e-26 |
PFAM |
OLF
|
142 |
398 |
5.22e-140 |
SMART |
HormR
|
469 |
534 |
3.14e-20 |
SMART |
Pfam:GAIN
|
537 |
764 |
1.3e-58 |
PFAM |
GPS
|
788 |
840 |
3.47e-25 |
SMART |
Pfam:7tm_2
|
848 |
1108 |
4.6e-69 |
PFAM |
Pfam:Latrophilin
|
1128 |
1487 |
6.4e-181 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000195988
AA Change: Y332N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000143444 Gene: ENSMUSG00000028184 AA Change: Y332N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
3.3e-23 |
PFAM |
OLF
|
142 |
398 |
3.3e-142 |
SMART |
HormR
|
469 |
534 |
2e-22 |
SMART |
GPS
|
788 |
840 |
2.1e-27 |
SMART |
Pfam:7tm_2
|
848 |
1099 |
8.1e-66 |
PFAM |
Pfam:Latrophilin
|
1119 |
1189 |
2.2e-28 |
PFAM |
Pfam:Latrophilin
|
1184 |
1435 |
5.5e-123 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000196526
AA Change: Y328N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000143788 Gene: ENSMUSG00000028184 AA Change: Y328N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
8.7e-24 |
PFAM |
OLF
|
138 |
394 |
3.4e-142 |
SMART |
HormR
|
465 |
530 |
2e-22 |
SMART |
Pfam:GAIN
|
533 |
747 |
1.1e-54 |
PFAM |
GPS
|
771 |
823 |
2.2e-27 |
SMART |
Pfam:7tm_2
|
831 |
1067 |
6.5e-68 |
PFAM |
Pfam:Latrophilin
|
1087 |
1158 |
9.9e-36 |
PFAM |
low complexity region
|
1163 |
1173 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000197567
AA Change: Y332N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000143626 Gene: ENSMUSG00000028184 AA Change: Y332N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
1.9e-26 |
PFAM |
OLF
|
142 |
398 |
5.22e-140 |
SMART |
HormR
|
469 |
534 |
3.14e-20 |
SMART |
Pfam:GAIN
|
537 |
764 |
1.1e-58 |
PFAM |
GPS
|
788 |
840 |
3.47e-25 |
SMART |
Pfam:7tm_2
|
848 |
1108 |
6.4e-69 |
PFAM |
Pfam:Latrophilin
|
1128 |
1487 |
2.8e-181 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000198779
AA Change: Y332N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000142347 Gene: ENSMUSG00000028184 AA Change: Y332N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
3.4e-23 |
PFAM |
OLF
|
142 |
398 |
3.3e-142 |
SMART |
HormR
|
469 |
534 |
2e-22 |
SMART |
GPS
|
788 |
840 |
2.1e-27 |
SMART |
Pfam:7tm_2
|
848 |
1084 |
1.8e-66 |
PFAM |
Pfam:Latrophilin
|
1104 |
1452 |
7e-174 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000199059
AA Change: Y332N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000143150 Gene: ENSMUSG00000028184 AA Change: Y332N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
3.4e-23 |
PFAM |
OLF
|
142 |
398 |
3.3e-142 |
SMART |
HormR
|
469 |
534 |
2e-22 |
SMART |
GPS
|
788 |
840 |
2.1e-27 |
SMART |
Pfam:7tm_2
|
848 |
1099 |
8.3e-66 |
PFAM |
Pfam:Latrophilin
|
1119 |
1467 |
7.1e-174 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000199238
AA Change: Y332N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000142405 Gene: ENSMUSG00000028184 AA Change: Y332N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
3.4e-23 |
PFAM |
OLF
|
142 |
398 |
3.3e-142 |
SMART |
HormR
|
469 |
534 |
2e-22 |
SMART |
GPS
|
788 |
840 |
2.1e-27 |
SMART |
Pfam:7tm_2
|
848 |
1099 |
8.4e-66 |
PFAM |
Pfam:Latrophilin
|
1119 |
1478 |
1.6e-187 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000199750
AA Change: Y332N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000143320 Gene: ENSMUSG00000028184 AA Change: Y332N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
3.1e-23 |
PFAM |
OLF
|
142 |
398 |
3.3e-142 |
SMART |
HormR
|
403 |
468 |
1.9e-22 |
SMART |
GPS
|
709 |
761 |
2.1e-27 |
SMART |
Pfam:7tm_2
|
769 |
1005 |
1.6e-66 |
PFAM |
Pfam:Latrophilin
|
1025 |
1095 |
2e-28 |
PFAM |
Pfam:Latrophilin
|
1090 |
1341 |
4.9e-123 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000200154
AA Change: Y328N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000142865 Gene: ENSMUSG00000028184 AA Change: Y328N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
2.5e-23 |
PFAM |
OLF
|
138 |
394 |
3.3e-142 |
SMART |
HormR
|
465 |
530 |
2e-22 |
SMART |
GPS
|
771 |
823 |
2.1e-27 |
SMART |
Pfam:7tm_2
|
831 |
1067 |
1.2e-66 |
PFAM |
Pfam:Latrophilin
|
1087 |
1123 |
2.2e-4 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000200543
AA Change: Y328N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000142336 Gene: ENSMUSG00000028184 AA Change: Y328N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Gal_Lectin
|
49 |
129 |
3.2e-23 |
PFAM |
OLF
|
138 |
394 |
3.3e-142 |
SMART |
HormR
|
465 |
530 |
2e-22 |
SMART |
GPS
|
771 |
823 |
2.1e-27 |
SMART |
Pfam:7tm_2
|
831 |
1067 |
1.7e-66 |
PFAM |
Pfam:Latrophilin
|
1087 |
1157 |
2.1e-28 |
PFAM |
Pfam:Latrophilin
|
1152 |
1403 |
5.3e-123 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
97% (99/102) |
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. The encoded protein participates in the regulation of exocytosis. The proprotein is thought to be further cleaved within a cysteine-rich G-protein-coupled receptor proteolysis site into two chains that are non-covalently bound at the cell membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] PHENOTYPE: Homozygous null mice die prenatally at fetal stages. Heterozygous mice exhibit decreased locomotor activity in an open field test. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
T |
7: 119,993,587 (GRCm39) |
K1269M |
possibly damaging |
Het |
Adgrv1 |
C |
T |
13: 81,627,777 (GRCm39) |
V3695I |
probably benign |
Het |
Aldh1l1 |
A |
T |
6: 90,575,257 (GRCm39) |
Y848F |
probably damaging |
Het |
Ambra1 |
T |
C |
2: 91,598,103 (GRCm39) |
V88A |
possibly damaging |
Het |
Ankrd12 |
C |
T |
17: 66,292,160 (GRCm39) |
R1091Q |
probably damaging |
Het |
Apob |
T |
G |
12: 8,055,087 (GRCm39) |
V1362G |
probably damaging |
Het |
Arhgap17 |
A |
G |
7: 122,905,661 (GRCm39) |
L328P |
probably damaging |
Het |
Arhgap27 |
A |
C |
11: 103,235,367 (GRCm39) |
V9G |
probably benign |
Het |
Arhgap33 |
A |
T |
7: 30,232,434 (GRCm39) |
D34E |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,873,259 (GRCm39) |
D14G |
probably benign |
Het |
Atf6b |
T |
C |
17: 34,872,703 (GRCm39) |
Y575H |
probably damaging |
Het |
Bcl2l2 |
T |
G |
14: 55,122,058 (GRCm39) |
S74A |
probably benign |
Het |
Begain |
T |
C |
12: 109,004,794 (GRCm39) |
T73A |
possibly damaging |
Het |
Bicdl1 |
C |
T |
5: 115,808,340 (GRCm39) |
R264Q |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,914,588 (GRCm39) |
D701G |
probably benign |
Het |
Cd200r4 |
G |
T |
16: 44,653,529 (GRCm39) |
V146L |
probably damaging |
Het |
Cd226 |
G |
A |
18: 89,265,322 (GRCm39) |
C200Y |
probably damaging |
Het |
Cdcp3 |
T |
C |
7: 130,879,352 (GRCm39) |
|
probably null |
Het |
Cdhr18 |
T |
C |
14: 13,866,032 (GRCm38) |
T286A |
|
Het |
Cdk12 |
A |
G |
11: 98,115,451 (GRCm39) |
N864S |
unknown |
Het |
Cfhr4 |
A |
T |
1: 139,680,788 (GRCm39) |
Y243* |
probably null |
Het |
Clcnkb |
A |
T |
4: 141,135,946 (GRCm39) |
L413Q |
probably damaging |
Het |
Cldn10 |
T |
C |
14: 119,099,255 (GRCm39) |
V123A |
possibly damaging |
Het |
Cnn1 |
T |
A |
9: 22,017,078 (GRCm39) |
|
probably null |
Het |
Cpa5 |
C |
A |
6: 30,630,829 (GRCm39) |
Q364K |
probably benign |
Het |
Cstdc5 |
T |
C |
16: 36,187,809 (GRCm39) |
I19V |
probably benign |
Het |
Ddx11 |
A |
G |
17: 66,437,766 (GRCm39) |
E164G |
probably benign |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Drc7 |
T |
A |
8: 95,804,549 (GRCm39) |
Y855N |
probably damaging |
Het |
Fam20b |
C |
A |
1: 156,529,968 (GRCm39) |
|
probably null |
Het |
Fip1l1 |
T |
A |
5: 74,748,736 (GRCm39) |
|
probably null |
Het |
Flt4 |
A |
G |
11: 49,525,125 (GRCm39) |
D657G |
probably null |
Het |
Fmo3 |
T |
A |
1: 162,781,857 (GRCm39) |
T499S |
possibly damaging |
Het |
Fyco1 |
C |
T |
9: 123,651,491 (GRCm39) |
G1190S |
probably benign |
Het |
Galnt17 |
C |
A |
5: 131,335,590 (GRCm39) |
|
probably benign |
Het |
Ggcx |
T |
C |
6: 72,404,987 (GRCm39) |
I465T |
probably damaging |
Het |
Gm7361 |
T |
A |
5: 26,466,116 (GRCm39) |
N159K |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,695,663 (GRCm39) |
N54S |
unknown |
Het |
Grin2c |
G |
A |
11: 115,141,876 (GRCm39) |
P848S |
probably damaging |
Het |
Grina |
T |
C |
15: 76,133,287 (GRCm39) |
V285A |
probably damaging |
Het |
Gtpbp6 |
A |
G |
5: 110,252,478 (GRCm39) |
L381P |
probably damaging |
Het |
Herc2 |
G |
T |
7: 55,832,388 (GRCm39) |
G3028V |
probably damaging |
Het |
Ibsp |
A |
T |
5: 104,458,297 (GRCm39) |
Y278F |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,184,433 (GRCm39) |
L846* |
probably null |
Het |
Kif17 |
A |
G |
4: 138,021,077 (GRCm39) |
K849E |
probably benign |
Het |
Krt77 |
G |
A |
15: 101,777,806 (GRCm39) |
P83L |
probably benign |
Het |
Ky |
T |
G |
9: 102,419,491 (GRCm39) |
D499E |
probably damaging |
Het |
Lrp3 |
A |
T |
7: 34,902,051 (GRCm39) |
M610K |
probably damaging |
Het |
Lrrfip1 |
T |
A |
1: 91,019,338 (GRCm39) |
D156E |
probably benign |
Het |
Map6 |
C |
A |
7: 98,918,257 (GRCm39) |
H343Q |
probably benign |
Het |
Micu2 |
G |
T |
14: 58,191,606 (GRCm39) |
D148E |
probably benign |
Het |
Mks1 |
T |
A |
11: 87,747,428 (GRCm39) |
S153T |
probably benign |
Het |
Msantd5f3 |
A |
G |
4: 73,573,157 (GRCm39) |
Y132C |
probably damaging |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
Myh9 |
T |
C |
15: 77,667,672 (GRCm39) |
K587R |
probably benign |
Het |
Neb |
T |
C |
2: 52,086,368 (GRCm39) |
Y5478C |
probably damaging |
Het |
Nelfe |
G |
A |
17: 35,069,912 (GRCm39) |
|
probably null |
Het |
Nps |
T |
A |
7: 134,870,510 (GRCm39) |
L11I |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,394,283 (GRCm39) |
D731V |
probably damaging |
Het |
Nup50 |
A |
G |
15: 84,817,859 (GRCm39) |
T93A |
probably benign |
Het |
Nup98 |
A |
T |
7: 101,844,248 (GRCm39) |
F29Y |
unknown |
Het |
Oprd1 |
A |
G |
4: 131,841,112 (GRCm39) |
I282T |
probably damaging |
Het |
Or4c103 |
T |
C |
2: 88,513,767 (GRCm39) |
H103R |
possibly damaging |
Het |
Or5p50 |
T |
C |
7: 107,421,782 (GRCm39) |
N298S |
probably benign |
Het |
Or6b3 |
A |
T |
1: 92,439,573 (GRCm39) |
M59K |
probably benign |
Het |
Or6d12 |
A |
G |
6: 116,492,936 (GRCm39) |
Y66C |
probably damaging |
Het |
Osbp2 |
T |
C |
11: 3,662,134 (GRCm39) |
I240V |
probably damaging |
Het |
Otub2 |
C |
A |
12: 103,359,163 (GRCm39) |
P84Q |
probably benign |
Het |
Parp9 |
A |
T |
16: 35,777,360 (GRCm39) |
I435F |
probably benign |
Het |
Pcdh18 |
C |
T |
3: 49,709,923 (GRCm39) |
R464H |
probably benign |
Het |
Pcsk6 |
G |
T |
7: 65,675,156 (GRCm39) |
|
probably null |
Het |
Ptgs2 |
G |
A |
1: 149,978,512 (GRCm39) |
R208Q |
probably benign |
Het |
Rab11b |
G |
A |
17: 33,968,841 (GRCm39) |
R51C |
probably damaging |
Het |
Rad1 |
A |
G |
15: 10,493,343 (GRCm39) |
I257V |
probably benign |
Het |
Rbms3 |
C |
T |
9: 116,415,085 (GRCm39) |
|
probably null |
Het |
Rxfp2 |
A |
T |
5: 149,983,364 (GRCm39) |
I300L |
probably benign |
Het |
Rxfp2 |
C |
A |
5: 149,983,368 (GRCm39) |
T301K |
probably benign |
Het |
Sars2 |
G |
T |
7: 28,443,733 (GRCm39) |
A112S |
probably benign |
Het |
Scn10a |
T |
C |
9: 119,442,616 (GRCm39) |
D1543G |
probably damaging |
Het |
Serpinb1b |
A |
G |
13: 33,271,406 (GRCm39) |
H59R |
probably benign |
Het |
Sgsm2 |
T |
A |
11: 74,745,319 (GRCm39) |
D661V |
possibly damaging |
Het |
Smad6 |
C |
A |
9: 63,927,688 (GRCm39) |
V207L |
probably damaging |
Het |
Son |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCAGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,183 (GRCm39) |
|
probably benign |
Het |
Spata31h1 |
A |
T |
10: 82,125,161 (GRCm39) |
D2616E |
probably benign |
Het |
Tenm2 |
C |
T |
11: 35,939,956 (GRCm39) |
R1390Q |
probably damaging |
Het |
Tmem132a |
T |
A |
19: 10,844,295 (GRCm39) |
Q101L |
probably damaging |
Het |
Tmem151a |
A |
G |
19: 5,132,801 (GRCm39) |
V135A |
probably damaging |
Het |
Trappc10 |
T |
C |
10: 78,046,262 (GRCm39) |
K443E |
probably damaging |
Het |
Trrap |
A |
T |
5: 144,779,517 (GRCm39) |
N3161I |
possibly damaging |
Het |
Tspan32 |
G |
T |
7: 142,558,863 (GRCm39) |
R6L |
possibly damaging |
Het |
Tut7 |
C |
G |
13: 59,936,364 (GRCm39) |
D1246H |
probably damaging |
Het |
Ugt2a2 |
T |
C |
5: 87,608,468 (GRCm39) |
D457G |
possibly damaging |
Het |
Ulk2 |
A |
T |
11: 61,725,657 (GRCm39) |
S140T |
possibly damaging |
Het |
Upf1 |
C |
T |
8: 70,792,695 (GRCm39) |
A338T |
possibly damaging |
Het |
Usp43 |
C |
T |
11: 67,774,110 (GRCm39) |
R460Q |
probably null |
Het |
Uxs1 |
A |
G |
1: 43,856,118 (GRCm39) |
|
probably benign |
Het |
Vmn1r59 |
A |
G |
7: 5,457,725 (GRCm39) |
C12R |
probably damaging |
Het |
Wdr64 |
A |
G |
1: 175,617,499 (GRCm39) |
D693G |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,920,839 (GRCm39) |
|
probably null |
Het |
Wnt2 |
G |
T |
6: 18,028,046 (GRCm39) |
R63S |
probably benign |
Het |
Zfp418 |
A |
T |
7: 7,184,562 (GRCm39) |
Q175L |
probably benign |
Het |
|
Other mutations in Adgrl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00426:Adgrl2
|
APN |
3 |
148,571,244 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00572:Adgrl2
|
APN |
3 |
148,532,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01624:Adgrl2
|
APN |
3 |
148,542,163 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01796:Adgrl2
|
APN |
3 |
148,564,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02380:Adgrl2
|
APN |
3 |
148,534,125 (GRCm39) |
nonsense |
probably null |
|
IGL02468:Adgrl2
|
APN |
3 |
148,596,116 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Adgrl2
|
APN |
3 |
148,532,161 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02869:Adgrl2
|
APN |
3 |
148,596,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03248:Adgrl2
|
APN |
3 |
148,523,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03343:Adgrl2
|
APN |
3 |
148,565,016 (GRCm39) |
missense |
probably damaging |
0.98 |
P0157:Adgrl2
|
UTSW |
3 |
148,564,699 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Adgrl2
|
UTSW |
3 |
148,522,934 (GRCm39) |
missense |
|
|
PIT4544001:Adgrl2
|
UTSW |
3 |
148,596,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R0165:Adgrl2
|
UTSW |
3 |
148,558,499 (GRCm39) |
splice site |
probably benign |
|
R0242:Adgrl2
|
UTSW |
3 |
148,544,821 (GRCm39) |
splice site |
probably null |
|
R0242:Adgrl2
|
UTSW |
3 |
148,544,821 (GRCm39) |
splice site |
probably null |
|
R0344:Adgrl2
|
UTSW |
3 |
148,571,231 (GRCm39) |
splice site |
probably null |
|
R0488:Adgrl2
|
UTSW |
3 |
148,552,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Adgrl2
|
UTSW |
3 |
148,564,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Adgrl2
|
UTSW |
3 |
148,544,880 (GRCm39) |
missense |
probably damaging |
0.98 |
R0674:Adgrl2
|
UTSW |
3 |
148,543,315 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1401:Adgrl2
|
UTSW |
3 |
148,528,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R1543:Adgrl2
|
UTSW |
3 |
148,564,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R1575:Adgrl2
|
UTSW |
3 |
148,558,398 (GRCm39) |
missense |
probably benign |
0.17 |
R1645:Adgrl2
|
UTSW |
3 |
148,571,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Adgrl2
|
UTSW |
3 |
148,558,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Adgrl2
|
UTSW |
3 |
148,522,880 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2014:Adgrl2
|
UTSW |
3 |
148,532,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Adgrl2
|
UTSW |
3 |
148,596,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R2131:Adgrl2
|
UTSW |
3 |
148,596,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R2400:Adgrl2
|
UTSW |
3 |
148,557,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R2997:Adgrl2
|
UTSW |
3 |
148,523,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R3161:Adgrl2
|
UTSW |
3 |
148,523,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R3416:Adgrl2
|
UTSW |
3 |
148,564,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R3417:Adgrl2
|
UTSW |
3 |
148,564,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R3551:Adgrl2
|
UTSW |
3 |
148,564,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R3760:Adgrl2
|
UTSW |
3 |
148,522,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Adgrl2
|
UTSW |
3 |
148,544,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Adgrl2
|
UTSW |
3 |
148,564,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R4911:Adgrl2
|
UTSW |
3 |
148,596,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R4945:Adgrl2
|
UTSW |
3 |
148,528,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R5313:Adgrl2
|
UTSW |
3 |
148,529,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Adgrl2
|
UTSW |
3 |
148,523,480 (GRCm39) |
missense |
probably benign |
0.01 |
R5540:Adgrl2
|
UTSW |
3 |
148,543,198 (GRCm39) |
critical splice donor site |
probably null |
|
R5583:Adgrl2
|
UTSW |
3 |
148,564,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Adgrl2
|
UTSW |
3 |
148,564,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Adgrl2
|
UTSW |
3 |
148,528,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R6197:Adgrl2
|
UTSW |
3 |
148,564,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6284:Adgrl2
|
UTSW |
3 |
148,532,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R6877:Adgrl2
|
UTSW |
3 |
148,522,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7048:Adgrl2
|
UTSW |
3 |
148,552,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Adgrl2
|
UTSW |
3 |
148,552,506 (GRCm39) |
missense |
probably benign |
0.00 |
R7348:Adgrl2
|
UTSW |
3 |
148,523,402 (GRCm39) |
missense |
|
|
R7382:Adgrl2
|
UTSW |
3 |
148,522,919 (GRCm39) |
missense |
|
|
R7486:Adgrl2
|
UTSW |
3 |
148,523,330 (GRCm39) |
missense |
|
|
R7498:Adgrl2
|
UTSW |
3 |
148,564,852 (GRCm39) |
nonsense |
probably null |
|
R7644:Adgrl2
|
UTSW |
3 |
148,544,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7690:Adgrl2
|
UTSW |
3 |
148,522,934 (GRCm39) |
missense |
|
|
R7742:Adgrl2
|
UTSW |
3 |
148,542,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R7745:Adgrl2
|
UTSW |
3 |
148,542,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R8291:Adgrl2
|
UTSW |
3 |
148,556,554 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8326:Adgrl2
|
UTSW |
3 |
148,533,190 (GRCm39) |
missense |
|
|
R8343:Adgrl2
|
UTSW |
3 |
148,552,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R8344:Adgrl2
|
UTSW |
3 |
148,565,161 (GRCm39) |
missense |
probably damaging |
0.98 |
R8487:Adgrl2
|
UTSW |
3 |
148,565,122 (GRCm39) |
missense |
probably benign |
0.06 |
R8748:Adgrl2
|
UTSW |
3 |
148,532,026 (GRCm39) |
missense |
|
|
R8769:Adgrl2
|
UTSW |
3 |
148,522,917 (GRCm39) |
missense |
|
|
R8804:Adgrl2
|
UTSW |
3 |
148,552,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Adgrl2
|
UTSW |
3 |
148,558,163 (GRCm39) |
intron |
probably benign |
|
R8943:Adgrl2
|
UTSW |
3 |
148,534,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R8977:Adgrl2
|
UTSW |
3 |
148,660,223 (GRCm39) |
missense |
probably null |
|
R9030:Adgrl2
|
UTSW |
3 |
148,544,761 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9105:Adgrl2
|
UTSW |
3 |
148,543,289 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9427:Adgrl2
|
UTSW |
3 |
148,526,068 (GRCm39) |
missense |
|
|
R9471:Adgrl2
|
UTSW |
3 |
148,558,365 (GRCm39) |
missense |
probably benign |
|
R9646:Adgrl2
|
UTSW |
3 |
148,544,926 (GRCm39) |
missense |
probably damaging |
0.96 |
R9742:Adgrl2
|
UTSW |
3 |
148,541,986 (GRCm39) |
critical splice donor site |
probably null |
|
RF007:Adgrl2
|
UTSW |
3 |
148,544,884 (GRCm39) |
missense |
probably damaging |
1.00 |
X0009:Adgrl2
|
UTSW |
3 |
148,558,290 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Adgrl2
|
UTSW |
3 |
148,571,230 (GRCm39) |
splice site |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- AGCAAGTATTCTTACCTTGGGC -3'
(R):5'- ATGAGAACGGCTTATGGGTC -3'
Sequencing Primer
(F):5'- ACTCCAGGGAATACCGTAAAATG -3'
(R):5'- TCATTTATGCCACGGAGCAG -3'
|
Posted On |
2019-06-26 |