Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
G |
5: 109,884,098 (GRCm39) |
C587R |
probably damaging |
Het |
Abca16 |
T |
A |
7: 120,133,986 (GRCm39) |
S1320T |
probably benign |
Het |
Abra |
C |
A |
15: 41,732,430 (GRCm39) |
R212L |
probably damaging |
Het |
Acadsb |
T |
A |
7: 131,045,958 (GRCm39) |
|
probably null |
Het |
Adam26a |
A |
G |
8: 44,022,578 (GRCm39) |
V304A |
possibly damaging |
Het |
Adgre1 |
T |
C |
17: 57,748,363 (GRCm39) |
V521A |
probably benign |
Het |
Adh5 |
G |
A |
3: 138,159,539 (GRCm39) |
V288I |
probably benign |
Het |
Astn1 |
A |
C |
1: 158,429,515 (GRCm39) |
N753T |
probably damaging |
Het |
Best3 |
A |
G |
10: 116,829,178 (GRCm39) |
T153A |
probably damaging |
Het |
Ccdc122 |
G |
A |
14: 77,348,847 (GRCm39) |
V226I |
probably damaging |
Het |
Ccdc175 |
T |
C |
12: 72,152,700 (GRCm39) |
Q735R |
probably benign |
Het |
Cd19 |
T |
A |
7: 126,008,813 (GRCm39) |
I499F |
probably damaging |
Het |
Cftr |
T |
A |
6: 18,268,288 (GRCm39) |
L749H |
probably benign |
Het |
Clec2h |
G |
T |
6: 128,652,790 (GRCm39) |
G186W |
probably damaging |
Het |
Cpsf3 |
T |
A |
12: 21,346,733 (GRCm39) |
I202N |
probably damaging |
Het |
Crebbp |
G |
T |
16: 3,905,600 (GRCm39) |
T1669N |
possibly damaging |
Het |
Csmd3 |
A |
T |
15: 47,522,588 (GRCm39) |
C2694S |
probably damaging |
Het |
Cul4a |
G |
A |
8: 13,173,565 (GRCm39) |
R204Q |
probably damaging |
Het |
Derl2 |
A |
G |
11: 70,909,169 (GRCm39) |
F43S |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,591,525 (GRCm39) |
N3348K |
probably damaging |
Het |
Dnhd1 |
T |
C |
7: 105,353,412 (GRCm39) |
V2855A |
probably benign |
Het |
Dpysl4 |
G |
T |
7: 138,670,215 (GRCm39) |
C27F |
probably benign |
Het |
Fam228b |
G |
A |
12: 4,798,314 (GRCm39) |
A163V |
probably damaging |
Het |
Fscn1 |
T |
C |
5: 142,955,818 (GRCm39) |
|
probably null |
Het |
Fzd5 |
C |
A |
1: 64,774,153 (GRCm39) |
R536L |
probably damaging |
Het |
Gm8180 |
T |
A |
14: 44,021,196 (GRCm39) |
H4L |
probably benign |
Het |
Gpr176 |
T |
A |
2: 118,203,659 (GRCm39) |
N4Y |
probably damaging |
Het |
Grin3a |
T |
C |
4: 49,665,309 (GRCm39) |
I1109V |
possibly damaging |
Het |
Hcar1 |
T |
A |
5: 124,017,092 (GRCm39) |
I200F |
probably damaging |
Het |
Heatr4 |
G |
A |
12: 84,026,502 (GRCm39) |
Q252* |
probably null |
Het |
Hps1 |
G |
A |
19: 42,750,888 (GRCm39) |
H371Y |
probably damaging |
Het |
Ikzf2 |
T |
C |
1: 69,609,661 (GRCm39) |
T195A |
probably damaging |
Het |
Kdm1b |
G |
A |
13: 47,202,666 (GRCm39) |
A34T |
probably benign |
Het |
Lef1 |
A |
G |
3: 130,905,290 (GRCm39) |
N57S |
probably damaging |
Het |
Ltn1 |
A |
T |
16: 87,213,231 (GRCm39) |
D443E |
probably benign |
Het |
Macroh2a1 |
A |
G |
13: 56,231,017 (GRCm39) |
L287P |
probably damaging |
Het |
Mamdc2 |
T |
C |
19: 23,336,517 (GRCm39) |
T331A |
probably damaging |
Het |
Marchf10 |
A |
T |
11: 105,287,904 (GRCm39) |
S133T |
probably damaging |
Het |
Mb |
A |
G |
15: 76,901,784 (GRCm39) |
Y104H |
probably damaging |
Het |
Mrc1 |
C |
A |
2: 14,333,390 (GRCm39) |
P1357Q |
probably benign |
Het |
Nfib |
C |
T |
4: 82,241,917 (GRCm39) |
V425M |
probably damaging |
Het |
Or12j2 |
G |
A |
7: 139,916,132 (GRCm39) |
R119H |
possibly damaging |
Het |
Or4a27 |
T |
G |
2: 88,559,674 (GRCm39) |
I90L |
probably damaging |
Het |
Or4b1b |
C |
A |
2: 90,112,502 (GRCm39) |
C139F |
probably damaging |
Het |
Or4c127 |
G |
A |
2: 89,833,490 (GRCm39) |
V247I |
probably benign |
Het |
Or4n4 |
A |
T |
14: 50,518,848 (GRCm39) |
Y287* |
probably null |
Het |
Or52u1 |
T |
C |
7: 104,237,112 (GRCm39) |
S34P |
probably damaging |
Het |
Or5b113 |
T |
A |
19: 13,342,705 (GRCm39) |
S238T |
possibly damaging |
Het |
Or5p53 |
A |
G |
7: 107,533,597 (GRCm39) |
Y290C |
probably damaging |
Het |
Or6c208 |
T |
C |
10: 129,223,955 (GRCm39) |
F151S |
probably damaging |
Het |
Or8b51 |
A |
T |
9: 38,569,661 (GRCm39) |
V9E |
probably damaging |
Het |
Phaf1 |
A |
G |
8: 105,966,703 (GRCm39) |
E150G |
probably null |
Het |
Piezo1 |
T |
C |
8: 123,222,489 (GRCm39) |
N919S |
possibly damaging |
Het |
Prkaca |
T |
C |
8: 84,707,852 (GRCm39) |
S46P |
probably benign |
Het |
Prkcb |
T |
G |
7: 122,167,424 (GRCm39) |
V378G |
probably damaging |
Het |
Ptprf |
A |
T |
4: 118,081,129 (GRCm39) |
L576Q |
probably damaging |
Het |
Rapgef4 |
T |
C |
2: 72,065,064 (GRCm39) |
V687A |
probably benign |
Het |
Rsad2 |
C |
T |
12: 26,500,616 (GRCm39) |
V224I |
probably damaging |
Het |
Ryr1 |
A |
T |
7: 28,708,977 (GRCm39) |
D4796E |
unknown |
Het |
Scn1a |
C |
T |
2: 66,148,326 (GRCm39) |
S1073N |
probably damaging |
Het |
Slc26a3 |
A |
G |
12: 31,515,845 (GRCm39) |
M582V |
probably benign |
Het |
Tbc1d32 |
A |
T |
10: 55,999,633 (GRCm39) |
Y846* |
probably null |
Het |
Tbk1 |
A |
T |
10: 121,383,076 (GRCm39) |
M719K |
probably benign |
Het |
Timeless |
A |
G |
10: 128,081,983 (GRCm39) |
K536R |
probably benign |
Het |
Tle6 |
G |
T |
10: 81,430,163 (GRCm39) |
Q330K |
probably damaging |
Het |
Tmem208 |
A |
G |
8: 106,061,438 (GRCm39) |
K155E |
possibly damaging |
Het |
Toe1 |
T |
C |
4: 116,662,426 (GRCm39) |
Y273C |
probably damaging |
Het |
Tppp2 |
A |
C |
14: 52,158,062 (GRCm39) |
N169T |
probably benign |
Het |
Ttll6 |
T |
A |
11: 96,029,700 (GRCm39) |
Y204* |
probably null |
Het |
Ubxn11 |
G |
A |
4: 133,852,149 (GRCm39) |
S32N |
probably damaging |
Het |
Usp8 |
G |
A |
2: 126,597,960 (GRCm39) |
C961Y |
probably damaging |
Het |
Vdac3 |
A |
T |
8: 23,070,515 (GRCm39) |
I132K |
possibly damaging |
Het |
Vmn2r124 |
G |
T |
17: 18,269,759 (GRCm39) |
W5L |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,264,782 (GRCm39) |
D38V |
probably damaging |
Het |
Vmn2r87 |
C |
T |
10: 130,315,755 (GRCm39) |
V104I |
probably benign |
Het |
Vmn2r97 |
C |
T |
17: 19,167,648 (GRCm39) |
T634I |
probably benign |
Het |
Vps50 |
T |
C |
6: 3,520,279 (GRCm39) |
|
probably null |
Het |
Wwc2 |
T |
C |
8: 48,443,137 (GRCm39) |
N32S |
possibly damaging |
Het |
Ythdc2 |
T |
A |
18: 45,006,023 (GRCm39) |
I1172K |
possibly damaging |
Het |
Zfp14 |
C |
T |
7: 29,738,116 (GRCm39) |
V290M |
probably damaging |
Het |
Zfp317 |
G |
A |
9: 19,553,280 (GRCm39) |
A18T |
possibly damaging |
Het |
Zfp354b |
A |
T |
11: 50,814,369 (GRCm39) |
N185K |
probably benign |
Het |
Zscan21 |
T |
A |
5: 138,124,892 (GRCm39) |
D269E |
probably benign |
Het |
|
Other mutations in Atad2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00498:Atad2
|
APN |
15 |
57,980,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00556:Atad2
|
APN |
15 |
57,963,476 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00674:Atad2
|
APN |
15 |
57,971,782 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01407:Atad2
|
APN |
15 |
57,967,921 (GRCm39) |
missense |
probably benign |
|
IGL02557:Atad2
|
APN |
15 |
57,985,993 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03060:Atad2
|
APN |
15 |
57,985,842 (GRCm39) |
unclassified |
probably benign |
|
IGL03308:Atad2
|
APN |
15 |
57,965,919 (GRCm39) |
missense |
probably benign |
0.00 |
R0113:Atad2
|
UTSW |
15 |
57,984,330 (GRCm39) |
unclassified |
probably benign |
|
R0195:Atad2
|
UTSW |
15 |
57,963,350 (GRCm39) |
splice site |
probably benign |
|
R0310:Atad2
|
UTSW |
15 |
57,977,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R0499:Atad2
|
UTSW |
15 |
57,984,345 (GRCm39) |
missense |
probably benign |
|
R0499:Atad2
|
UTSW |
15 |
57,966,636 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0564:Atad2
|
UTSW |
15 |
57,989,229 (GRCm39) |
splice site |
probably benign |
|
R0578:Atad2
|
UTSW |
15 |
57,968,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Atad2
|
UTSW |
15 |
57,990,060 (GRCm39) |
missense |
probably benign |
|
R0667:Atad2
|
UTSW |
15 |
57,962,115 (GRCm39) |
missense |
probably benign |
0.01 |
R0697:Atad2
|
UTSW |
15 |
57,968,939 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1219:Atad2
|
UTSW |
15 |
57,998,307 (GRCm39) |
missense |
probably benign |
0.00 |
R1271:Atad2
|
UTSW |
15 |
57,989,985 (GRCm39) |
missense |
probably benign |
0.00 |
R1544:Atad2
|
UTSW |
15 |
57,966,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Atad2
|
UTSW |
15 |
57,963,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Atad2
|
UTSW |
15 |
57,960,685 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1854:Atad2
|
UTSW |
15 |
57,960,685 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1855:Atad2
|
UTSW |
15 |
57,960,685 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1861:Atad2
|
UTSW |
15 |
57,960,114 (GRCm39) |
splice site |
probably null |
|
R1876:Atad2
|
UTSW |
15 |
57,970,264 (GRCm39) |
missense |
probably benign |
0.00 |
R1938:Atad2
|
UTSW |
15 |
57,960,101 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2158:Atad2
|
UTSW |
15 |
57,961,962 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3756:Atad2
|
UTSW |
15 |
57,963,119 (GRCm39) |
missense |
probably benign |
0.01 |
R4256:Atad2
|
UTSW |
15 |
57,980,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R4762:Atad2
|
UTSW |
15 |
57,971,758 (GRCm39) |
missense |
probably benign |
|
R4827:Atad2
|
UTSW |
15 |
57,971,744 (GRCm39) |
missense |
probably benign |
0.07 |
R4838:Atad2
|
UTSW |
15 |
57,966,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5238:Atad2
|
UTSW |
15 |
57,971,733 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5247:Atad2
|
UTSW |
15 |
57,967,874 (GRCm39) |
nonsense |
probably null |
|
R5685:Atad2
|
UTSW |
15 |
57,980,194 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5790:Atad2
|
UTSW |
15 |
57,989,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Atad2
|
UTSW |
15 |
57,963,250 (GRCm39) |
missense |
probably benign |
0.42 |
R5886:Atad2
|
UTSW |
15 |
57,961,910 (GRCm39) |
nonsense |
probably null |
|
R5955:Atad2
|
UTSW |
15 |
57,969,055 (GRCm39) |
missense |
probably benign |
0.06 |
R6034:Atad2
|
UTSW |
15 |
57,971,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Atad2
|
UTSW |
15 |
57,971,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6111:Atad2
|
UTSW |
15 |
57,971,487 (GRCm39) |
missense |
probably benign |
0.07 |
R6209:Atad2
|
UTSW |
15 |
57,981,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6587:Atad2
|
UTSW |
15 |
57,984,444 (GRCm39) |
missense |
probably benign |
0.03 |
R6856:Atad2
|
UTSW |
15 |
57,970,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R7106:Atad2
|
UTSW |
15 |
57,980,162 (GRCm39) |
critical splice donor site |
probably null |
|
R7178:Atad2
|
UTSW |
15 |
57,980,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R7290:Atad2
|
UTSW |
15 |
57,962,047 (GRCm39) |
missense |
probably benign |
0.00 |
R7421:Atad2
|
UTSW |
15 |
57,998,322 (GRCm39) |
missense |
probably benign |
0.40 |
R7583:Atad2
|
UTSW |
15 |
57,990,060 (GRCm39) |
missense |
probably benign |
|
R7861:Atad2
|
UTSW |
15 |
57,989,176 (GRCm39) |
missense |
probably benign |
0.10 |
R7886:Atad2
|
UTSW |
15 |
57,989,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R8072:Atad2
|
UTSW |
15 |
57,963,374 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8126:Atad2
|
UTSW |
15 |
57,968,987 (GRCm39) |
missense |
probably benign |
0.02 |
R8845:Atad2
|
UTSW |
15 |
57,989,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R9027:Atad2
|
UTSW |
15 |
57,995,628 (GRCm39) |
missense |
probably benign |
0.04 |
R9079:Atad2
|
UTSW |
15 |
57,989,223 (GRCm39) |
missense |
probably benign |
0.35 |
R9161:Atad2
|
UTSW |
15 |
57,989,185 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9209:Atad2
|
UTSW |
15 |
57,980,194 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9266:Atad2
|
UTSW |
15 |
57,985,967 (GRCm39) |
missense |
probably benign |
0.00 |
R9306:Atad2
|
UTSW |
15 |
57,959,994 (GRCm39) |
nonsense |
probably null |
|
R9546:Atad2
|
UTSW |
15 |
57,989,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R9547:Atad2
|
UTSW |
15 |
57,989,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R9614:Atad2
|
UTSW |
15 |
57,970,119 (GRCm39) |
critical splice donor site |
probably null |
|
R9655:Atad2
|
UTSW |
15 |
57,998,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Atad2
|
UTSW |
15 |
57,971,540 (GRCm39) |
missense |
probably benign |
0.06 |
|