Incidental Mutation 'R8344:Adgrl2'
ID |
645074 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adgrl2
|
Ensembl Gene |
ENSMUSG00000028184 |
Gene Name |
adhesion G protein-coupled receptor L2 |
Synonyms |
Lphn2, Lphh1, Lec1 |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R8344 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
3 |
Chromosomal Location |
148521219-148696191 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 148565161 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Serine
at position 140
(C140S)
|
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: C140S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000101734 Gene: ENSMUSG00000028184 AA Change: C140S
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: C140S
PolyPhen 2
Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000143444 Gene: ENSMUSG00000028184 AA Change: C140S
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: C136S
PolyPhen 2
Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000143788 Gene: ENSMUSG00000028184 AA Change: C136S
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: C140S
PolyPhen 2
Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000143626 Gene: ENSMUSG00000028184 AA Change: C140S
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: C140S
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000142347 Gene: ENSMUSG00000028184 AA Change: C140S
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: C140S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000143150 Gene: ENSMUSG00000028184 AA Change: C140S
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: C140S
PolyPhen 2
Score 0.980 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000142405 Gene: ENSMUSG00000028184 AA Change: C140S
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: C140S
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000143320 Gene: ENSMUSG00000028184 AA Change: C140S
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: C136S
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000142865 Gene: ENSMUSG00000028184 AA Change: C136S
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: C136S
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000142336 Gene: ENSMUSG00000028184 AA Change: C136S
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: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
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. 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: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
A |
T |
19: 31,888,519 (GRCm39) |
Y83F |
possibly damaging |
Het |
Adgre1 |
C |
G |
17: 57,715,459 (GRCm39) |
Q260E |
probably benign |
Het |
Adgrf4 |
T |
A |
17: 42,977,799 (GRCm39) |
M515L |
probably benign |
Het |
Ago3 |
T |
A |
4: 126,270,721 (GRCm39) |
K258* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,003,002 (GRCm39) |
E573V |
possibly damaging |
Het |
Atxn7l3b |
T |
A |
10: 112,764,567 (GRCm39) |
I21F |
possibly damaging |
Het |
Bckdha |
C |
T |
7: 25,330,872 (GRCm39) |
R298H |
probably damaging |
Het |
Cacng3 |
A |
C |
7: 122,367,569 (GRCm39) |
I150L |
possibly damaging |
Het |
Ccdc18 |
A |
T |
5: 108,309,369 (GRCm39) |
K321N |
possibly damaging |
Het |
Ccl11 |
A |
T |
11: 81,952,568 (GRCm39) |
K47M |
possibly damaging |
Het |
Cdkn2a |
T |
C |
4: 89,194,987 (GRCm39) |
I142M |
probably benign |
Het |
Cfap65 |
C |
T |
1: 74,967,203 (GRCm39) |
G249R |
probably benign |
Het |
Chrna1 |
C |
A |
2: 73,400,953 (GRCm39) |
E192D |
probably benign |
Het |
Clasp1 |
A |
G |
1: 118,431,629 (GRCm39) |
N420D |
probably damaging |
Het |
Clca3a2 |
T |
A |
3: 144,511,703 (GRCm39) |
|
probably null |
Het |
Cntn2 |
T |
C |
1: 132,449,512 (GRCm39) |
Y643C |
probably damaging |
Het |
Dcun1d1 |
G |
A |
3: 35,951,703 (GRCm39) |
H204Y |
probably benign |
Het |
Dlg2 |
A |
T |
7: 92,087,222 (GRCm39) |
Q767L |
possibly damaging |
Het |
Dnah11 |
A |
G |
12: 118,049,466 (GRCm39) |
S1653P |
probably benign |
Het |
Dvl3 |
T |
A |
16: 20,342,513 (GRCm39) |
|
probably null |
Het |
Egf |
T |
C |
3: 129,548,592 (GRCm39) |
T8A |
unknown |
Het |
Eln |
G |
T |
5: 134,757,246 (GRCm39) |
T219K |
unknown |
Het |
Evc |
T |
C |
5: 37,471,872 (GRCm39) |
D536G |
possibly damaging |
Het |
Fbxo3 |
A |
G |
2: 103,881,553 (GRCm39) |
E295G |
possibly damaging |
Het |
Gp2 |
C |
T |
7: 119,042,010 (GRCm39) |
C505Y |
probably benign |
Het |
Gpr37 |
A |
G |
6: 25,669,530 (GRCm39) |
F438S |
probably damaging |
Het |
Gsk3b |
T |
C |
16: 38,011,987 (GRCm39) |
S236P |
probably benign |
Het |
Kdm5d |
A |
G |
Y: 942,477 (GRCm39) |
T1381A |
probably benign |
Het |
Klhl12 |
T |
C |
1: 134,413,460 (GRCm39) |
I315T |
possibly damaging |
Het |
Ltb |
T |
A |
17: 35,414,169 (GRCm39) |
N102K |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,420,649 (GRCm39) |
T202A |
probably benign |
Het |
Macf1 |
C |
A |
4: 123,278,476 (GRCm39) |
D5993Y |
probably damaging |
Het |
Mak |
T |
A |
13: 41,199,679 (GRCm39) |
D320V |
probably benign |
Het |
Map2 |
G |
A |
1: 66,460,872 (GRCm39) |
R1556H |
probably damaging |
Het |
Mgat4d |
G |
T |
8: 84,094,762 (GRCm39) |
M266I |
probably benign |
Het |
Mmp24 |
G |
T |
2: 155,652,223 (GRCm39) |
R310S |
possibly damaging |
Het |
Myh6 |
A |
T |
14: 55,190,891 (GRCm39) |
L928Q |
probably damaging |
Het |
Npnt |
A |
G |
3: 132,614,217 (GRCm39) |
L179P |
probably damaging |
Het |
Or2f1b |
A |
G |
6: 42,739,499 (GRCm39) |
N171S |
probably benign |
Het |
Or4c11c |
A |
G |
2: 88,661,727 (GRCm39) |
I89V |
probably benign |
Het |
Or8g55 |
T |
G |
9: 39,785,231 (GRCm39) |
F220C |
probably benign |
Het |
Parp4 |
A |
T |
14: 56,886,186 (GRCm39) |
Y1755F |
unknown |
Het |
Phactr1 |
A |
G |
13: 42,863,297 (GRCm39) |
E74G |
possibly damaging |
Het |
Pira12 |
T |
A |
7: 3,899,954 (GRCm39) |
E216V |
possibly damaging |
Het |
Plcg1 |
G |
A |
2: 160,589,816 (GRCm39) |
M113I |
probably benign |
Het |
Plekhh2 |
T |
G |
17: 84,879,189 (GRCm39) |
S638A |
possibly damaging |
Het |
Ppp2r3d |
T |
A |
9: 101,088,985 (GRCm39) |
H446L |
probably benign |
Het |
Prkcg |
G |
T |
7: 3,378,686 (GRCm39) |
D644Y |
probably damaging |
Het |
Rbbp8nl |
G |
T |
2: 179,921,506 (GRCm39) |
R293S |
probably benign |
Het |
Rbl2 |
A |
T |
8: 91,842,387 (GRCm39) |
H1057L |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,387,819 (GRCm39) |
H1076L |
possibly damaging |
Het |
Scn11a |
A |
C |
9: 119,611,036 (GRCm39) |
D938E |
probably benign |
Het |
Sec24b |
T |
C |
3: 129,798,650 (GRCm39) |
D573G |
probably damaging |
Het |
Serpinf1 |
T |
G |
11: 75,306,397 (GRCm39) |
Q147P |
unknown |
Het |
Skint6 |
C |
T |
4: 113,093,642 (GRCm39) |
G167D |
probably damaging |
Het |
Slc15a5 |
A |
G |
6: 138,056,898 (GRCm39) |
F6S |
probably damaging |
Het |
Smc2 |
T |
A |
4: 52,449,376 (GRCm39) |
I179K |
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,677,073 (GRCm39) |
K57R |
possibly damaging |
Het |
Smpdl3b |
T |
A |
4: 132,473,990 (GRCm39) |
H25L |
probably damaging |
Het |
Srpk1 |
T |
C |
17: 28,839,398 (GRCm39) |
D35G |
unknown |
Het |
Strn |
A |
G |
17: 78,980,076 (GRCm39) |
V324A |
probably damaging |
Het |
Sult6b2 |
T |
C |
6: 142,736,022 (GRCm39) |
K191E |
probably benign |
Het |
Tmem168 |
A |
G |
6: 13,583,324 (GRCm39) |
I519T |
probably benign |
Het |
Tmem41a |
T |
C |
16: 21,756,784 (GRCm39) |
T112A |
probably benign |
Het |
Tmem67 |
A |
G |
4: 12,058,576 (GRCm39) |
I507T |
probably benign |
Het |
Tns1 |
T |
C |
1: 74,024,201 (GRCm39) |
E454G |
probably damaging |
Het |
Trim26 |
C |
A |
17: 37,168,602 (GRCm39) |
D422E |
unknown |
Het |
Triobp |
C |
A |
15: 78,842,475 (GRCm39) |
R58S |
possibly damaging |
Het |
Trp53 |
T |
C |
11: 69,478,409 (GRCm39) |
F106S |
probably damaging |
Het |
Tshz3 |
C |
A |
7: 36,470,962 (GRCm39) |
Q984K |
probably damaging |
Het |
Ttll3 |
A |
G |
6: 113,371,959 (GRCm39) |
E73G |
probably damaging |
Het |
Vmn1r194 |
A |
G |
13: 22,429,247 (GRCm39) |
N288S |
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 |
R7205:Adgrl2
|
UTSW |
3 |
148,564,585 (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 |
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'- CTGGCGGCTGTTTTGAAAATC -3'
(R):5'- TGTGAAAATAAAGGCCAGCCAC -3'
Sequencing Primer
(F):5'- GCGGCTGTTTTGAAAATCTTCTAAAG -3'
(R):5'- GGGTAAAATGGACTTTCCTCT -3'
|
Posted On |
2020-09-02 |