Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
A |
T |
1: 11,633,211 (GRCm39) |
D168V |
probably damaging |
Het |
Abcb4 |
A |
T |
5: 9,008,441 (GRCm39) |
D1203V |
probably damaging |
Het |
Acat2 |
G |
A |
17: 13,178,979 (GRCm39) |
|
probably benign |
Het |
Adam3 |
C |
T |
8: 25,179,484 (GRCm39) |
C611Y |
probably damaging |
Het |
Adgrb1 |
A |
G |
15: 74,415,189 (GRCm39) |
D638G |
probably damaging |
Het |
Adra1b |
T |
C |
11: 43,667,218 (GRCm39) |
N340D |
probably damaging |
Het |
Ankrd31 |
A |
G |
13: 96,916,879 (GRCm39) |
H131R |
probably damaging |
Het |
Aoc2 |
T |
C |
11: 101,217,164 (GRCm39) |
S416P |
possibly damaging |
Het |
Armc8 |
G |
A |
9: 99,387,362 (GRCm39) |
R419* |
probably null |
Het |
Atp6v1h |
T |
G |
1: 5,163,638 (GRCm39) |
V90G |
probably damaging |
Het |
Avl9 |
T |
C |
6: 56,707,628 (GRCm39) |
V191A |
probably benign |
Het |
Bsn |
G |
A |
9: 107,990,173 (GRCm39) |
P1860S |
possibly damaging |
Het |
Btd |
A |
G |
14: 31,384,233 (GRCm39) |
K73R |
probably benign |
Het |
Cd22 |
T |
C |
7: 30,567,391 (GRCm39) |
K731R |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,956,911 (GRCm39) |
L332F |
probably damaging |
Het |
Cirop |
T |
G |
14: 54,932,686 (GRCm39) |
S393R |
probably damaging |
Het |
Cldn11 |
A |
G |
3: 31,217,276 (GRCm39) |
E148G |
probably damaging |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 105,036,334 (GRCm39) |
|
probably null |
Het |
Cnbd1 |
A |
T |
4: 18,886,061 (GRCm39) |
Y319* |
probably null |
Het |
Cnnm4 |
A |
G |
1: 36,511,170 (GRCm39) |
T133A |
probably benign |
Het |
Cpeb4 |
A |
T |
11: 31,822,679 (GRCm39) |
E131V |
probably benign |
Het |
Ctns |
A |
G |
11: 73,078,561 (GRCm39) |
|
probably null |
Het |
Dhx36 |
C |
A |
3: 62,414,142 (GRCm39) |
Q73H |
probably benign |
Het |
Dhx36 |
C |
A |
3: 62,414,141 (GRCm39) |
E74* |
probably null |
Het |
Dnah5 |
A |
G |
15: 28,420,107 (GRCm39) |
T3802A |
|
Het |
Fbxo31 |
G |
A |
8: 122,281,136 (GRCm39) |
R337C |
probably damaging |
Het |
Flnc |
C |
T |
6: 29,455,518 (GRCm39) |
Q2056* |
probably null |
Het |
Fmo9 |
T |
C |
1: 166,492,199 (GRCm39) |
D408G |
possibly damaging |
Het |
Gipr |
C |
T |
7: 18,897,495 (GRCm39) |
S117N |
unknown |
Het |
Gm14412 |
T |
A |
2: 177,006,356 (GRCm39) |
H513L |
probably damaging |
Het |
Gm21663 |
G |
C |
5: 26,147,167 (GRCm39) |
C46W |
probably benign |
Het |
Gucy1a2 |
A |
T |
9: 3,634,489 (GRCm39) |
I178L |
probably benign |
Het |
Htr1b |
A |
T |
9: 81,514,481 (GRCm39) |
L42Q |
|
Het |
Htr2b |
T |
C |
1: 86,027,481 (GRCm39) |
T342A |
probably damaging |
Het |
Jkampl |
T |
C |
6: 73,446,517 (GRCm39) |
T11A |
probably benign |
Het |
Jph2 |
C |
T |
2: 163,181,473 (GRCm39) |
V564M |
probably damaging |
Het |
Kcnmb1 |
A |
G |
11: 33,914,806 (GRCm39) |
T36A |
probably damaging |
Het |
Krit1 |
A |
C |
5: 3,863,135 (GRCm39) |
K310N |
probably benign |
Het |
Lama1 |
C |
T |
17: 68,111,508 (GRCm39) |
T2253M |
|
Het |
Megf6 |
G |
A |
4: 154,354,160 (GRCm39) |
G1355R |
probably damaging |
Het |
Mmp3 |
T |
A |
9: 7,446,936 (GRCm39) |
Y39N |
probably damaging |
Het |
Mrtfb |
A |
G |
16: 13,221,053 (GRCm39) |
H743R |
probably benign |
Het |
Ms4a18 |
C |
A |
19: 10,990,741 (GRCm39) |
V118F |
|
Het |
Mthfr |
G |
A |
4: 148,126,082 (GRCm39) |
S51N |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,554,975 (GRCm39) |
T3773S |
unknown |
Het |
Mus81 |
T |
A |
19: 5,534,032 (GRCm39) |
K400* |
probably null |
Het |
Naaladl2 |
A |
T |
3: 24,487,344 (GRCm39) |
D192E |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,366,127 (GRCm39) |
D329G |
possibly damaging |
Het |
Nek11 |
T |
A |
9: 105,170,856 (GRCm39) |
H393L |
probably benign |
Het |
Nmt2 |
T |
A |
2: 3,306,315 (GRCm39) |
|
probably benign |
Het |
Nmur2 |
T |
C |
11: 55,920,408 (GRCm39) |
D279G |
possibly damaging |
Het |
Nol4l |
C |
A |
2: 153,312,630 (GRCm39) |
R226L |
probably damaging |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or10d4c |
A |
G |
9: 39,558,379 (GRCm39) |
D119G |
probably damaging |
Het |
Or1o2 |
T |
C |
17: 37,542,961 (GRCm39) |
Y100C |
probably benign |
Het |
Or5ak22 |
T |
C |
2: 85,229,995 (GRCm39) |
N294S |
probably damaging |
Het |
Palm |
A |
G |
10: 79,654,988 (GRCm39) |
T249A |
probably benign |
Het |
Pramel22 |
A |
T |
4: 143,381,097 (GRCm39) |
Y309N |
probably benign |
Het |
Rhobtb3 |
A |
G |
13: 76,087,702 (GRCm39) |
I95T |
probably damaging |
Het |
Rnpep |
A |
T |
1: 135,206,559 (GRCm39) |
F178L |
possibly damaging |
Het |
Rsl1d1 |
A |
G |
16: 11,019,227 (GRCm39) |
S105P |
probably damaging |
Het |
Rxra |
C |
T |
2: 27,638,756 (GRCm39) |
T253I |
possibly damaging |
Het |
Schip1 |
A |
G |
3: 67,972,318 (GRCm39) |
D15G |
|
Het |
Sis |
T |
A |
3: 72,844,578 (GRCm39) |
I719F |
possibly damaging |
Het |
Snx18 |
A |
G |
13: 113,754,310 (GRCm39) |
S208P |
probably benign |
Het |
Srcap |
T |
C |
7: 127,151,816 (GRCm39) |
V2125A |
probably damaging |
Het |
Stx7 |
C |
T |
10: 24,058,724 (GRCm39) |
Q199* |
probably null |
Het |
Syt6 |
T |
C |
3: 103,492,895 (GRCm39) |
I134T |
probably damaging |
Het |
Tlr12 |
A |
G |
4: 128,510,870 (GRCm39) |
M460T |
probably benign |
Het |
Tnni3k |
T |
C |
3: 154,647,314 (GRCm39) |
T398A |
possibly damaging |
Het |
Tspan4 |
T |
C |
7: 141,071,816 (GRCm39) |
S188P |
probably benign |
Het |
Ubap2l |
A |
G |
3: 89,909,756 (GRCm39) |
S1025P |
unknown |
Het |
Ubl7 |
A |
G |
9: 57,829,035 (GRCm39) |
D219G |
probably benign |
Het |
Vmn2r115 |
C |
A |
17: 23,564,803 (GRCm39) |
T230K |
probably benign |
Het |
Vmn2r95 |
T |
A |
17: 18,660,167 (GRCm39) |
M193K |
possibly damaging |
Het |
Zfp639 |
A |
G |
3: 32,573,885 (GRCm39) |
E170G |
probably damaging |
Het |
Zfy1 |
A |
G |
Y: 725,987 (GRCm39) |
S593P |
possibly damaging |
Het |
Zscan4-ps1 |
T |
A |
7: 10,799,495 (GRCm39) |
T465S |
probably damaging |
Het |
|
Other mutations in Lpar6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01143:Lpar6
|
APN |
14 |
73,476,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01611:Lpar6
|
APN |
14 |
73,476,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01618:Lpar6
|
APN |
14 |
73,476,506 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01676:Lpar6
|
APN |
14 |
73,477,010 (GRCm39) |
missense |
probably benign |
0.24 |
IGL03031:Lpar6
|
APN |
14 |
73,476,882 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03061:Lpar6
|
APN |
14 |
73,476,510 (GRCm39) |
missense |
probably benign |
0.03 |
R1900:Lpar6
|
UTSW |
14 |
73,476,579 (GRCm39) |
missense |
probably benign |
0.01 |
R2895:Lpar6
|
UTSW |
14 |
73,476,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R2896:Lpar6
|
UTSW |
14 |
73,476,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R3972:Lpar6
|
UTSW |
14 |
73,476,513 (GRCm39) |
missense |
probably benign |
0.01 |
R4305:Lpar6
|
UTSW |
14 |
73,476,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Lpar6
|
UTSW |
14 |
73,476,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Lpar6
|
UTSW |
14 |
73,476,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5024:Lpar6
|
UTSW |
14 |
73,476,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R5133:Lpar6
|
UTSW |
14 |
73,476,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5173:Lpar6
|
UTSW |
14 |
73,476,537 (GRCm39) |
missense |
probably benign |
0.01 |
R5931:Lpar6
|
UTSW |
14 |
73,476,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R6283:Lpar6
|
UTSW |
14 |
73,476,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6316:Lpar6
|
UTSW |
14 |
73,476,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7414:Lpar6
|
UTSW |
14 |
73,476,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R7868:Lpar6
|
UTSW |
14 |
73,476,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R8749:Lpar6
|
UTSW |
14 |
73,476,950 (GRCm39) |
missense |
probably benign |
|
|