Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atm |
T |
C |
9: 53,443,033 (GRCm39) |
T77A |
probably benign |
Het |
Brd8 |
T |
C |
18: 34,741,537 (GRCm39) |
M311V |
possibly damaging |
Het |
Cand2 |
T |
A |
6: 115,774,948 (GRCm39) |
I1052N |
probably damaging |
Het |
Ccdc121 |
G |
A |
5: 31,645,435 (GRCm39) |
R396Q |
probably benign |
Het |
Ceacam16 |
T |
A |
7: 19,592,531 (GRCm39) |
M126L |
probably benign |
Het |
Chd3 |
TGCTGCCGCTGCCGC |
TGCTGCCGCTGCCGCTGCCGC |
11: 69,253,013 (GRCm39) |
|
probably benign |
Het |
Cln8 |
C |
T |
8: 14,944,842 (GRCm39) |
T52I |
probably damaging |
Het |
Cops2 |
C |
A |
2: 125,682,400 (GRCm39) |
D194Y |
probably damaging |
Het |
Csf1 |
C |
T |
3: 107,656,483 (GRCm39) |
V71M |
probably damaging |
Het |
Dip2b |
T |
C |
15: 100,058,372 (GRCm39) |
F183S |
probably damaging |
Het |
Ears2 |
T |
A |
7: 121,643,832 (GRCm39) |
K375N |
probably benign |
Het |
Fbn1 |
C |
A |
2: 125,185,981 (GRCm39) |
G1596C |
probably damaging |
Het |
Fscn2 |
A |
T |
11: 120,258,546 (GRCm39) |
D390V |
possibly damaging |
Het |
Gm42669 |
A |
T |
5: 107,656,079 (GRCm39) |
I781F |
possibly damaging |
Het |
Gprin1 |
G |
T |
13: 54,885,871 (GRCm39) |
P801Q |
probably damaging |
Het |
Hira |
C |
A |
16: 18,765,150 (GRCm39) |
S609R |
probably damaging |
Het |
Htt |
G |
T |
5: 35,033,292 (GRCm39) |
K1853N |
probably benign |
Het |
Kif2c |
T |
C |
4: 117,035,437 (GRCm39) |
I4V |
probably benign |
Het |
Marveld2 |
A |
G |
13: 100,748,447 (GRCm39) |
Y211H |
probably damaging |
Het |
Myd88 |
G |
A |
9: 119,167,175 (GRCm39) |
|
probably null |
Het |
Nup153 |
A |
T |
13: 46,840,706 (GRCm39) |
N967K |
possibly damaging |
Het |
Or4a76 |
A |
C |
2: 89,460,516 (GRCm39) |
I242S |
possibly damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Rabepk |
A |
G |
2: 34,670,752 (GRCm39) |
M228T |
probably damaging |
Het |
Rcn3 |
T |
A |
7: 44,738,092 (GRCm39) |
D92V |
probably damaging |
Het |
Sec1 |
T |
A |
7: 45,328,297 (GRCm39) |
Y250F |
probably damaging |
Het |
Slc39a4 |
T |
C |
15: 76,498,693 (GRCm39) |
T334A |
probably benign |
Het |
Trip11 |
G |
T |
12: 101,803,875 (GRCm39) |
T1669K |
probably damaging |
Het |
Ttbk2 |
A |
G |
2: 120,570,673 (GRCm39) |
L1091P |
probably damaging |
Het |
Vmn1r231 |
A |
G |
17: 21,110,660 (GRCm39) |
V85A |
possibly damaging |
Het |
Zfp280b |
T |
C |
10: 75,874,663 (GRCm39) |
C181R |
probably benign |
Het |
|
Other mutations in Adgrb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01525:Adgrb1
|
APN |
15 |
74,458,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01748:Adgrb1
|
APN |
15 |
74,420,206 (GRCm39) |
splice site |
probably benign |
|
IGL01874:Adgrb1
|
APN |
15 |
74,413,423 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02040:Adgrb1
|
APN |
15 |
74,413,424 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02138:Adgrb1
|
APN |
15 |
74,401,631 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02149:Adgrb1
|
APN |
15 |
74,412,326 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02320:Adgrb1
|
APN |
15 |
74,445,961 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02556:Adgrb1
|
APN |
15 |
74,458,654 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02637:Adgrb1
|
APN |
15 |
74,460,143 (GRCm39) |
splice site |
probably benign |
|
IGL02678:Adgrb1
|
APN |
15 |
74,410,177 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02792:Adgrb1
|
APN |
15 |
74,419,471 (GRCm39) |
missense |
probably damaging |
0.98 |
Bunting
|
UTSW |
15 |
74,415,550 (GRCm39) |
missense |
probably null |
0.94 |
BB005:Adgrb1
|
UTSW |
15 |
74,410,170 (GRCm39) |
missense |
probably damaging |
1.00 |
BB015:Adgrb1
|
UTSW |
15 |
74,410,170 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Adgrb1
|
UTSW |
15 |
74,413,508 (GRCm39) |
missense |
probably damaging |
0.99 |
R0193:Adgrb1
|
UTSW |
15 |
74,444,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Adgrb1
|
UTSW |
15 |
74,458,656 (GRCm39) |
missense |
probably benign |
|
R0267:Adgrb1
|
UTSW |
15 |
74,401,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R0336:Adgrb1
|
UTSW |
15 |
74,458,998 (GRCm39) |
missense |
probably benign |
0.06 |
R0345:Adgrb1
|
UTSW |
15 |
74,415,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R0533:Adgrb1
|
UTSW |
15 |
74,413,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Adgrb1
|
UTSW |
15 |
74,412,741 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0729:Adgrb1
|
UTSW |
15 |
74,420,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Adgrb1
|
UTSW |
15 |
74,452,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R1122:Adgrb1
|
UTSW |
15 |
74,419,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R1295:Adgrb1
|
UTSW |
15 |
74,421,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Adgrb1
|
UTSW |
15 |
74,452,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R1696:Adgrb1
|
UTSW |
15 |
74,459,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R1707:Adgrb1
|
UTSW |
15 |
74,401,192 (GRCm39) |
missense |
probably damaging |
0.99 |
R1750:Adgrb1
|
UTSW |
15 |
74,413,676 (GRCm39) |
missense |
probably benign |
0.23 |
R1804:Adgrb1
|
UTSW |
15 |
74,401,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R1829:Adgrb1
|
UTSW |
15 |
74,452,435 (GRCm39) |
nonsense |
probably null |
|
R1895:Adgrb1
|
UTSW |
15 |
74,412,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Adgrb1
|
UTSW |
15 |
74,411,726 (GRCm39) |
splice site |
probably benign |
|
R2114:Adgrb1
|
UTSW |
15 |
74,412,411 (GRCm39) |
critical splice donor site |
probably null |
|
R2133:Adgrb1
|
UTSW |
15 |
74,401,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R2210:Adgrb1
|
UTSW |
15 |
74,419,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R3701:Adgrb1
|
UTSW |
15 |
74,416,864 (GRCm39) |
missense |
probably damaging |
0.99 |
R3770:Adgrb1
|
UTSW |
15 |
74,460,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R3980:Adgrb1
|
UTSW |
15 |
74,454,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Adgrb1
|
UTSW |
15 |
74,415,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R4412:Adgrb1
|
UTSW |
15 |
74,449,302 (GRCm39) |
unclassified |
probably benign |
|
R4683:Adgrb1
|
UTSW |
15 |
74,459,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4742:Adgrb1
|
UTSW |
15 |
74,401,328 (GRCm39) |
nonsense |
probably null |
|
R4760:Adgrb1
|
UTSW |
15 |
74,443,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R4794:Adgrb1
|
UTSW |
15 |
74,459,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R4880:Adgrb1
|
UTSW |
15 |
74,458,871 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4885:Adgrb1
|
UTSW |
15 |
74,444,011 (GRCm39) |
missense |
probably benign |
0.04 |
R5092:Adgrb1
|
UTSW |
15 |
74,401,664 (GRCm39) |
missense |
probably benign |
0.39 |
R5198:Adgrb1
|
UTSW |
15 |
74,415,550 (GRCm39) |
missense |
probably null |
0.94 |
R5225:Adgrb1
|
UTSW |
15 |
74,449,348 (GRCm39) |
unclassified |
probably benign |
|
R5421:Adgrb1
|
UTSW |
15 |
74,421,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R5764:Adgrb1
|
UTSW |
15 |
74,413,423 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5914:Adgrb1
|
UTSW |
15 |
74,410,219 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6035:Adgrb1
|
UTSW |
15 |
74,412,292 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6035:Adgrb1
|
UTSW |
15 |
74,412,292 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6066:Adgrb1
|
UTSW |
15 |
74,412,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R6423:Adgrb1
|
UTSW |
15 |
74,459,992 (GRCm39) |
critical splice donor site |
probably null |
|
R6811:Adgrb1
|
UTSW |
15 |
74,401,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R6945:Adgrb1
|
UTSW |
15 |
74,421,873 (GRCm39) |
missense |
probably damaging |
0.99 |
R7012:Adgrb1
|
UTSW |
15 |
74,401,750 (GRCm39) |
missense |
probably damaging |
0.97 |
R7015:Adgrb1
|
UTSW |
15 |
74,445,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Adgrb1
|
UTSW |
15 |
74,441,730 (GRCm39) |
missense |
probably benign |
0.00 |
R7209:Adgrb1
|
UTSW |
15 |
74,441,797 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7213:Adgrb1
|
UTSW |
15 |
74,441,733 (GRCm39) |
missense |
probably benign |
|
R7283:Adgrb1
|
UTSW |
15 |
74,452,512 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7329:Adgrb1
|
UTSW |
15 |
74,411,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R7616:Adgrb1
|
UTSW |
15 |
74,420,418 (GRCm39) |
missense |
probably damaging |
0.98 |
R7695:Adgrb1
|
UTSW |
15 |
74,415,487 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7928:Adgrb1
|
UTSW |
15 |
74,410,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R8152:Adgrb1
|
UTSW |
15 |
74,416,849 (GRCm39) |
missense |
probably damaging |
0.98 |
R8152:Adgrb1
|
UTSW |
15 |
74,413,460 (GRCm39) |
missense |
probably benign |
0.00 |
R8198:Adgrb1
|
UTSW |
15 |
74,411,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R8485:Adgrb1
|
UTSW |
15 |
74,420,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R8528:Adgrb1
|
UTSW |
15 |
74,447,700 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8534:Adgrb1
|
UTSW |
15 |
74,415,357 (GRCm39) |
missense |
probably damaging |
0.97 |
R8865:Adgrb1
|
UTSW |
15 |
74,415,507 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9044:Adgrb1
|
UTSW |
15 |
74,441,748 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9098:Adgrb1
|
UTSW |
15 |
74,415,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R9157:Adgrb1
|
UTSW |
15 |
74,411,624 (GRCm39) |
missense |
probably damaging |
0.98 |
R9166:Adgrb1
|
UTSW |
15 |
74,420,475 (GRCm39) |
missense |
probably benign |
0.00 |
R9313:Adgrb1
|
UTSW |
15 |
74,411,624 (GRCm39) |
missense |
probably damaging |
0.98 |
R9445:Adgrb1
|
UTSW |
15 |
74,435,807 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1177:Adgrb1
|
UTSW |
15 |
74,419,532 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Adgrb1
|
UTSW |
15 |
74,413,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|