Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
T |
A |
7: 27,279,871 (GRCm39) |
V278D |
probably damaging |
Het |
Akap12 |
G |
T |
10: 4,307,122 (GRCm39) |
E1311* |
probably null |
Het |
Ankdd1a |
T |
A |
9: 65,415,957 (GRCm39) |
D186V |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,869,090 (GRCm39) |
E346G |
probably damaging |
Het |
Brd10 |
A |
G |
19: 29,696,508 (GRCm39) |
L995S |
possibly damaging |
Het |
Ccr7 |
A |
C |
11: 99,036,130 (GRCm39) |
V264G |
probably damaging |
Het |
Col7a1 |
T |
C |
9: 108,812,987 (GRCm39) |
|
probably null |
Het |
Coq8a |
T |
C |
1: 180,006,633 (GRCm39) |
T132A |
probably benign |
Het |
Cplane1 |
A |
G |
15: 8,281,690 (GRCm39) |
E2843G |
unknown |
Het |
Cyp2b10 |
G |
A |
7: 25,616,780 (GRCm39) |
S407N |
probably benign |
Het |
Ddi2 |
A |
G |
4: 141,412,561 (GRCm39) |
V117A |
probably benign |
Het |
Ddx42 |
G |
A |
11: 106,129,970 (GRCm39) |
V421I |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,601,896 (GRCm39) |
L285* |
probably null |
Het |
Dip2c |
C |
T |
13: 9,684,868 (GRCm39) |
S1232F |
probably damaging |
Het |
Dner |
T |
A |
1: 84,454,123 (GRCm39) |
R402* |
probably null |
Het |
Dpysl3 |
A |
T |
18: 43,486,956 (GRCm39) |
I317N |
probably damaging |
Het |
Dusp23 |
T |
A |
1: 172,459,224 (GRCm39) |
Y146F |
probably benign |
Het |
Eef1a2 |
C |
A |
2: 180,790,421 (GRCm39) |
V412L |
possibly damaging |
Het |
Epha7 |
C |
T |
4: 28,821,489 (GRCm39) |
T218I |
probably damaging |
Het |
Gigyf2 |
T |
A |
1: 87,334,858 (GRCm39) |
C284S |
probably damaging |
Het |
Golm1 |
ACTTCTTCT |
ACTTCT |
13: 59,797,390 (GRCm39) |
|
probably benign |
Het |
Hao2 |
T |
A |
3: 98,784,068 (GRCm39) |
E327V |
probably damaging |
Het |
Hdhd5 |
A |
G |
6: 120,487,130 (GRCm39) |
V409A |
probably damaging |
Het |
Kif9 |
T |
C |
9: 110,323,690 (GRCm39) |
Y236H |
probably damaging |
Het |
Kri1 |
T |
C |
9: 21,199,050 (GRCm39) |
|
probably benign |
Het |
Lig4 |
A |
T |
8: 10,021,098 (GRCm39) |
V894E |
probably damaging |
Het |
Mapk8 |
T |
C |
14: 33,132,841 (GRCm39) |
I32V |
possibly damaging |
Het |
Mast4 |
C |
T |
13: 102,941,155 (GRCm39) |
V301I |
probably damaging |
Het |
Mstn |
T |
C |
1: 53,101,100 (GRCm39) |
I59T |
probably benign |
Het |
Mtrf1l |
T |
C |
10: 5,763,384 (GRCm39) |
E315G |
probably damaging |
Het |
Notch4 |
G |
T |
17: 34,803,774 (GRCm39) |
E1515* |
probably null |
Het |
Npw |
A |
C |
17: 24,877,029 (GRCm39) |
V124G |
probably benign |
Het |
Nxph3 |
A |
G |
11: 95,402,244 (GRCm39) |
S57P |
probably damaging |
Het |
Opn4 |
A |
T |
14: 34,315,864 (GRCm39) |
L390M |
probably benign |
Het |
Or12e10 |
G |
A |
2: 87,640,787 (GRCm39) |
D208N |
possibly damaging |
Het |
Or52e4 |
T |
C |
7: 104,705,771 (GRCm39) |
I106T |
probably damaging |
Het |
Or5b95 |
G |
T |
19: 12,658,112 (GRCm39) |
L213F |
probably benign |
Het |
Or5g23 |
T |
C |
2: 85,438,592 (GRCm39) |
I221V |
possibly damaging |
Het |
Or5p68 |
T |
A |
7: 107,945,295 (GRCm39) |
N298Y |
possibly damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pla2g2e |
G |
A |
4: 138,607,986 (GRCm39) |
C62Y |
probably damaging |
Het |
Plcb4 |
G |
A |
2: 135,752,114 (GRCm39) |
V107M |
probably damaging |
Het |
Pramel33 |
T |
A |
5: 93,632,233 (GRCm39) |
N107I |
probably damaging |
Het |
Prorsd1 |
A |
C |
11: 29,464,486 (GRCm39) |
|
probably benign |
Het |
Prox2 |
A |
G |
12: 85,134,165 (GRCm39) |
L587P |
probably benign |
Het |
Prr22 |
A |
G |
17: 57,078,345 (GRCm39) |
D166G |
possibly damaging |
Het |
Ptprz1 |
G |
A |
6: 23,002,686 (GRCm39) |
R1592Q |
probably benign |
Het |
Rarg |
C |
G |
15: 102,150,350 (GRCm39) |
R74P |
probably damaging |
Het |
Rcan1 |
A |
G |
16: 92,194,251 (GRCm39) |
V54A |
probably benign |
Het |
Rmdn2 |
A |
G |
17: 79,928,739 (GRCm39) |
|
probably benign |
Het |
Sec16a |
G |
A |
2: 26,320,498 (GRCm39) |
R1361C |
probably damaging |
Het |
Serpina1a |
T |
C |
12: 103,820,092 (GRCm39) |
T385A |
probably benign |
Het |
Slc44a3 |
T |
C |
3: 121,325,814 (GRCm39) |
Y12C |
probably benign |
Het |
Smg1 |
C |
A |
7: 117,767,091 (GRCm39) |
|
probably benign |
Het |
Spock3 |
A |
G |
8: 63,808,415 (GRCm39) |
*437W |
probably null |
Het |
Sugct |
T |
A |
13: 17,728,965 (GRCm39) |
Q220H |
probably benign |
Het |
Tesk1 |
A |
G |
4: 43,447,006 (GRCm39) |
T465A |
probably benign |
Het |
Tnks |
C |
A |
8: 35,301,647 (GRCm39) |
R1274I |
probably damaging |
Het |
Trp53bp1 |
C |
T |
2: 121,038,521 (GRCm39) |
R1439H |
probably damaging |
Het |
Vmn1r16 |
G |
T |
6: 57,299,869 (GRCm39) |
S251* |
probably null |
Het |
Vmn2r15 |
T |
A |
5: 109,441,180 (GRCm39) |
Q226L |
probably damaging |
Het |
Vmn2r67 |
T |
G |
7: 84,804,953 (GRCm39) |
Y53S |
possibly damaging |
Het |
Vmn2r99 |
A |
G |
17: 19,598,372 (GRCm39) |
N132S |
probably benign |
Het |
Wdr73 |
T |
G |
7: 80,541,604 (GRCm39) |
T313P |
probably benign |
Het |
Zfp65 |
C |
T |
13: 67,856,640 (GRCm39) |
R213Q |
probably damaging |
Het |
|
Other mutations in Lrriq1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00988:Lrriq1
|
APN |
10 |
102,997,757 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01523:Lrriq1
|
APN |
10 |
103,053,977 (GRCm39) |
nonsense |
probably null |
|
IGL01637:Lrriq1
|
APN |
10 |
103,051,489 (GRCm39) |
missense |
probably benign |
|
IGL02019:Lrriq1
|
APN |
10 |
103,014,661 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02153:Lrriq1
|
APN |
10 |
103,006,340 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02341:Lrriq1
|
APN |
10 |
103,060,802 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02343:Lrriq1
|
APN |
10 |
103,070,024 (GRCm39) |
splice site |
probably benign |
|
IGL02408:Lrriq1
|
APN |
10 |
102,982,142 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02431:Lrriq1
|
APN |
10 |
103,036,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Lrriq1
|
APN |
10 |
103,050,880 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02558:Lrriq1
|
APN |
10 |
102,982,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02613:Lrriq1
|
APN |
10 |
102,980,409 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02642:Lrriq1
|
APN |
10 |
103,057,322 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03027:Lrriq1
|
APN |
10 |
103,063,057 (GRCm39) |
missense |
probably benign |
0.35 |
PIT4362001:Lrriq1
|
UTSW |
10 |
102,907,055 (GRCm39) |
missense |
probably benign |
0.26 |
R0050:Lrriq1
|
UTSW |
10 |
102,904,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R0050:Lrriq1
|
UTSW |
10 |
102,904,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R0068:Lrriq1
|
UTSW |
10 |
102,899,279 (GRCm39) |
missense |
probably benign |
0.02 |
R0068:Lrriq1
|
UTSW |
10 |
102,899,279 (GRCm39) |
missense |
probably benign |
0.02 |
R0124:Lrriq1
|
UTSW |
10 |
103,006,281 (GRCm39) |
critical splice donor site |
probably null |
|
R0244:Lrriq1
|
UTSW |
10 |
103,051,634 (GRCm39) |
missense |
probably damaging |
0.98 |
R0323:Lrriq1
|
UTSW |
10 |
103,057,150 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0515:Lrriq1
|
UTSW |
10 |
102,904,829 (GRCm39) |
splice site |
probably null |
|
R0522:Lrriq1
|
UTSW |
10 |
102,997,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R0701:Lrriq1
|
UTSW |
10 |
103,069,905 (GRCm39) |
missense |
probably benign |
|
R1220:Lrriq1
|
UTSW |
10 |
102,906,990 (GRCm39) |
missense |
probably benign |
0.05 |
R1261:Lrriq1
|
UTSW |
10 |
103,069,998 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1262:Lrriq1
|
UTSW |
10 |
103,069,998 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1451:Lrriq1
|
UTSW |
10 |
103,038,376 (GRCm39) |
splice site |
probably benign |
|
R1642:Lrriq1
|
UTSW |
10 |
103,050,317 (GRCm39) |
missense |
probably benign |
0.13 |
R1643:Lrriq1
|
UTSW |
10 |
103,050,685 (GRCm39) |
missense |
probably benign |
0.00 |
R1647:Lrriq1
|
UTSW |
10 |
103,006,509 (GRCm39) |
nonsense |
probably null |
|
R1830:Lrriq1
|
UTSW |
10 |
102,997,620 (GRCm39) |
missense |
probably benign |
|
R1843:Lrriq1
|
UTSW |
10 |
103,063,034 (GRCm39) |
splice site |
probably null |
|
R2128:Lrriq1
|
UTSW |
10 |
103,050,718 (GRCm39) |
missense |
probably benign |
0.01 |
R2129:Lrriq1
|
UTSW |
10 |
103,050,718 (GRCm39) |
missense |
probably benign |
0.01 |
R2199:Lrriq1
|
UTSW |
10 |
102,904,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2354:Lrriq1
|
UTSW |
10 |
103,025,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R2495:Lrriq1
|
UTSW |
10 |
103,038,242 (GRCm39) |
missense |
probably damaging |
0.97 |
R2897:Lrriq1
|
UTSW |
10 |
103,063,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R2898:Lrriq1
|
UTSW |
10 |
103,063,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R2922:Lrriq1
|
UTSW |
10 |
103,050,536 (GRCm39) |
missense |
probably benign |
0.00 |
R2939:Lrriq1
|
UTSW |
10 |
102,980,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R2965:Lrriq1
|
UTSW |
10 |
103,050,761 (GRCm39) |
missense |
probably benign |
0.07 |
R2966:Lrriq1
|
UTSW |
10 |
103,050,761 (GRCm39) |
missense |
probably benign |
0.07 |
R3081:Lrriq1
|
UTSW |
10 |
102,980,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R3115:Lrriq1
|
UTSW |
10 |
103,006,294 (GRCm39) |
missense |
probably benign |
0.00 |
R3745:Lrriq1
|
UTSW |
10 |
103,006,717 (GRCm39) |
missense |
probably damaging |
0.99 |
R3813:Lrriq1
|
UTSW |
10 |
103,051,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3814:Lrriq1
|
UTSW |
10 |
103,051,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3885:Lrriq1
|
UTSW |
10 |
103,051,967 (GRCm39) |
missense |
probably damaging |
0.96 |
R4378:Lrriq1
|
UTSW |
10 |
103,038,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Lrriq1
|
UTSW |
10 |
103,057,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4633:Lrriq1
|
UTSW |
10 |
103,036,424 (GRCm39) |
nonsense |
probably null |
|
R4663:Lrriq1
|
UTSW |
10 |
102,899,273 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4702:Lrriq1
|
UTSW |
10 |
103,051,610 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4793:Lrriq1
|
UTSW |
10 |
103,006,327 (GRCm39) |
missense |
probably benign |
0.25 |
R4801:Lrriq1
|
UTSW |
10 |
103,057,179 (GRCm39) |
missense |
probably benign |
0.02 |
R4802:Lrriq1
|
UTSW |
10 |
103,057,179 (GRCm39) |
missense |
probably benign |
0.02 |
R4815:Lrriq1
|
UTSW |
10 |
102,980,739 (GRCm39) |
missense |
probably benign |
0.10 |
R4872:Lrriq1
|
UTSW |
10 |
103,014,649 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4877:Lrriq1
|
UTSW |
10 |
103,069,899 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4894:Lrriq1
|
UTSW |
10 |
102,997,613 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4990:Lrriq1
|
UTSW |
10 |
103,036,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R4991:Lrriq1
|
UTSW |
10 |
103,036,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Lrriq1
|
UTSW |
10 |
103,025,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R5013:Lrriq1
|
UTSW |
10 |
103,025,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R5122:Lrriq1
|
UTSW |
10 |
103,023,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R5282:Lrriq1
|
UTSW |
10 |
103,051,206 (GRCm39) |
missense |
probably benign |
0.01 |
R5311:Lrriq1
|
UTSW |
10 |
103,050,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Lrriq1
|
UTSW |
10 |
103,006,457 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5643:Lrriq1
|
UTSW |
10 |
103,051,301 (GRCm39) |
missense |
probably benign |
0.00 |
R5683:Lrriq1
|
UTSW |
10 |
103,009,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Lrriq1
|
UTSW |
10 |
103,057,243 (GRCm39) |
nonsense |
probably null |
|
R6008:Lrriq1
|
UTSW |
10 |
103,006,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R6022:Lrriq1
|
UTSW |
10 |
103,051,395 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6224:Lrriq1
|
UTSW |
10 |
103,051,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Lrriq1
|
UTSW |
10 |
103,051,312 (GRCm39) |
missense |
probably benign |
0.15 |
R6311:Lrriq1
|
UTSW |
10 |
103,009,254 (GRCm39) |
missense |
probably benign |
0.03 |
R6460:Lrriq1
|
UTSW |
10 |
103,036,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R6502:Lrriq1
|
UTSW |
10 |
103,063,045 (GRCm39) |
missense |
probably damaging |
0.99 |
R6637:Lrriq1
|
UTSW |
10 |
103,057,293 (GRCm39) |
missense |
probably benign |
0.06 |
R6719:Lrriq1
|
UTSW |
10 |
102,906,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Lrriq1
|
UTSW |
10 |
103,017,750 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6928:Lrriq1
|
UTSW |
10 |
103,050,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7174:Lrriq1
|
UTSW |
10 |
103,060,826 (GRCm39) |
missense |
probably benign |
|
R7241:Lrriq1
|
UTSW |
10 |
103,051,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Lrriq1
|
UTSW |
10 |
103,059,611 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7287:Lrriq1
|
UTSW |
10 |
103,051,877 (GRCm39) |
missense |
probably benign |
0.00 |
R7402:Lrriq1
|
UTSW |
10 |
103,057,185 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7439:Lrriq1
|
UTSW |
10 |
103,050,380 (GRCm39) |
missense |
probably benign |
0.21 |
R7585:Lrriq1
|
UTSW |
10 |
103,050,807 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7611:Lrriq1
|
UTSW |
10 |
103,036,432 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7634:Lrriq1
|
UTSW |
10 |
103,036,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Lrriq1
|
UTSW |
10 |
103,051,815 (GRCm39) |
missense |
probably damaging |
0.99 |
R7809:Lrriq1
|
UTSW |
10 |
103,051,678 (GRCm39) |
missense |
probably damaging |
0.99 |
R7910:Lrriq1
|
UTSW |
10 |
103,051,055 (GRCm39) |
nonsense |
probably null |
|
R8131:Lrriq1
|
UTSW |
10 |
103,051,572 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8156:Lrriq1
|
UTSW |
10 |
102,992,196 (GRCm39) |
critical splice donor site |
probably null |
|
R8211:Lrriq1
|
UTSW |
10 |
103,006,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Lrriq1
|
UTSW |
10 |
103,069,929 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8487:Lrriq1
|
UTSW |
10 |
103,050,914 (GRCm39) |
missense |
probably damaging |
0.98 |
R8500:Lrriq1
|
UTSW |
10 |
102,882,016 (GRCm39) |
missense |
|
|
R9013:Lrriq1
|
UTSW |
10 |
103,050,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Lrriq1
|
UTSW |
10 |
103,051,864 (GRCm39) |
missense |
probably damaging |
0.98 |
R9155:Lrriq1
|
UTSW |
10 |
103,050,640 (GRCm39) |
missense |
probably benign |
0.03 |
R9320:Lrriq1
|
UTSW |
10 |
103,057,144 (GRCm39) |
missense |
probably benign |
|
R9384:Lrriq1
|
UTSW |
10 |
103,006,458 (GRCm39) |
missense |
probably benign |
0.00 |
R9469:Lrriq1
|
UTSW |
10 |
103,050,761 (GRCm39) |
missense |
probably benign |
0.07 |
R9585:Lrriq1
|
UTSW |
10 |
103,051,250 (GRCm39) |
missense |
probably benign |
|
R9706:Lrriq1
|
UTSW |
10 |
102,881,902 (GRCm39) |
missense |
|
|
R9780:Lrriq1
|
UTSW |
10 |
103,025,824 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Lrriq1
|
UTSW |
10 |
103,051,565 (GRCm39) |
nonsense |
probably null |
|
Z1088:Lrriq1
|
UTSW |
10 |
103,038,307 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lrriq1
|
UTSW |
10 |
103,069,946 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Lrriq1
|
UTSW |
10 |
103,038,221 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lrriq1
|
UTSW |
10 |
103,038,220 (GRCm39) |
missense |
probably damaging |
1.00 |
|