Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
C |
T |
17: 24,593,274 (GRCm39) |
R224C |
probably damaging |
Het |
Adcy8 |
A |
T |
15: 64,659,207 (GRCm39) |
W528R |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,060,403 (GRCm39) |
R141Q |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,980,595 (GRCm39) |
H626Q |
probably benign |
Het |
Ampd2 |
A |
T |
3: 107,986,549 (GRCm39) |
M245K |
probably damaging |
Het |
Apob |
G |
A |
12: 8,055,219 (GRCm39) |
|
probably null |
Het |
Apool |
C |
T |
X: 111,259,540 (GRCm39) |
Q60* |
probably null |
Het |
Aqp1 |
A |
T |
6: 55,322,520 (GRCm39) |
I172F |
probably damaging |
Het |
Atp7a |
A |
G |
X: 105,153,374 (GRCm39) |
D1092G |
probably benign |
Het |
Bcas3 |
A |
G |
11: 85,261,958 (GRCm39) |
Y110C |
probably damaging |
Het |
Brpf1 |
T |
C |
6: 113,287,215 (GRCm39) |
S148P |
probably damaging |
Het |
Capn3 |
A |
G |
2: 120,322,301 (GRCm39) |
H339R |
probably damaging |
Het |
Ccdc141 |
A |
T |
2: 76,954,722 (GRCm39) |
|
probably null |
Het |
Ccl2 |
A |
G |
11: 81,927,984 (GRCm39) |
|
probably benign |
Het |
Cct8l1 |
G |
A |
5: 25,721,881 (GRCm39) |
V199I |
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,784,742 (GRCm39) |
V7L |
unknown |
Het |
Cit |
T |
A |
5: 116,084,902 (GRCm39) |
M811K |
probably benign |
Het |
Crim1 |
T |
C |
17: 78,588,776 (GRCm39) |
C284R |
possibly damaging |
Het |
Cyp2d10 |
C |
T |
15: 82,287,954 (GRCm39) |
R383H |
probably benign |
Het |
Dbndd2 |
A |
G |
2: 164,332,224 (GRCm39) |
|
probably benign |
Het |
Dnaja3 |
A |
T |
16: 4,514,289 (GRCm39) |
T274S |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,620,480 (GRCm39) |
D514G |
possibly damaging |
Het |
Dysf |
A |
T |
6: 84,114,254 (GRCm39) |
K1226M |
probably damaging |
Het |
Eef1akmt1 |
A |
G |
14: 57,803,464 (GRCm39) |
L30P |
probably damaging |
Het |
Elavl1 |
A |
G |
8: 4,351,741 (GRCm39) |
M125T |
possibly damaging |
Het |
Eml4 |
C |
A |
17: 83,771,006 (GRCm39) |
S723R |
probably damaging |
Het |
Fgf15 |
A |
C |
7: 144,450,576 (GRCm39) |
Y54S |
possibly damaging |
Het |
Fign |
A |
T |
2: 63,810,037 (GRCm39) |
L411* |
probably null |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Fryl |
G |
A |
5: 73,232,110 (GRCm39) |
P1550L |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gprasp2 |
C |
T |
X: 134,743,346 (GRCm39) |
T235I |
possibly damaging |
Het |
H2ab3 |
T |
C |
X: 119,222,543 (GRCm39) |
T84A |
probably damaging |
Het |
Hal |
A |
T |
10: 93,349,904 (GRCm39) |
I555F |
probably damaging |
Het |
Hdac6 |
A |
G |
X: 7,811,036 (GRCm39) |
F104L |
probably damaging |
Het |
Hibadh |
C |
T |
6: 52,597,079 (GRCm39) |
V122M |
possibly damaging |
Het |
Hmga1b |
C |
T |
11: 120,654,012 (GRCm39) |
Q100* |
probably null |
Het |
Hydin |
A |
G |
8: 111,265,105 (GRCm39) |
N2763D |
probably benign |
Het |
Ifi47 |
A |
G |
11: 48,986,361 (GRCm39) |
T43A |
probably benign |
Het |
Ifnlr1 |
A |
G |
4: 135,432,457 (GRCm39) |
T298A |
probably benign |
Het |
Impdh2 |
G |
A |
9: 108,440,535 (GRCm39) |
|
probably null |
Het |
Insr |
A |
G |
8: 3,209,475 (GRCm39) |
F1203L |
probably damaging |
Het |
Kcnq4 |
A |
G |
4: 120,574,714 (GRCm39) |
S117P |
probably damaging |
Het |
Kif19a |
G |
A |
11: 114,658,053 (GRCm39) |
M37I |
probably benign |
Het |
Kif1a |
T |
C |
1: 92,950,227 (GRCm39) |
H1400R |
probably damaging |
Het |
Kiss1r |
C |
A |
10: 79,754,596 (GRCm39) |
S30* |
probably null |
Het |
Krt222 |
T |
A |
11: 99,134,796 (GRCm39) |
|
probably benign |
Het |
Lekr1 |
A |
T |
3: 65,727,215 (GRCm39) |
|
noncoding transcript |
Het |
Ltn1 |
A |
G |
16: 87,224,628 (GRCm39) |
V32A |
probably damaging |
Het |
Marchf1 |
T |
A |
8: 66,839,020 (GRCm39) |
W21R |
probably benign |
Het |
Marchf5 |
A |
G |
19: 37,188,207 (GRCm39) |
N58S |
possibly damaging |
Het |
Mast4 |
G |
A |
13: 102,875,391 (GRCm39) |
Q1158* |
probably null |
Het |
Mib2 |
C |
G |
4: 155,741,233 (GRCm39) |
A535P |
probably damaging |
Het |
Mrtfa |
A |
G |
15: 80,906,627 (GRCm39) |
V91A |
probably damaging |
Het |
Msc |
C |
T |
1: 14,824,537 (GRCm39) |
V178M |
probably benign |
Het |
Muc4 |
C |
A |
16: 32,754,529 (GRCm38) |
H1468N |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,412,999 (GRCm39) |
T1982S |
unknown |
Het |
Mvk |
A |
T |
5: 114,591,013 (GRCm39) |
|
probably benign |
Het |
Myo1a |
T |
C |
10: 127,543,288 (GRCm39) |
|
probably null |
Het |
Myo6 |
T |
G |
9: 80,195,290 (GRCm39) |
S887A |
probably benign |
Het |
Myo7a |
G |
A |
7: 97,722,425 (GRCm39) |
Q1167* |
probably null |
Het |
Ncald |
A |
T |
15: 37,397,478 (GRCm39) |
H67Q |
probably damaging |
Het |
Nmnat1 |
C |
A |
4: 149,553,595 (GRCm39) |
M172I |
probably benign |
Het |
Nudt1 |
G |
T |
5: 140,317,662 (GRCm39) |
|
probably null |
Het |
Nudt5 |
T |
A |
2: 5,869,198 (GRCm39) |
H141Q |
probably benign |
Het |
Or1m1 |
T |
C |
9: 18,666,118 (GRCm39) |
E271G |
possibly damaging |
Het |
Or4e1 |
T |
A |
14: 52,701,032 (GRCm39) |
M118L |
probably damaging |
Het |
Or8h10 |
A |
T |
2: 86,808,666 (GRCm39) |
V158D |
possibly damaging |
Het |
Parp14 |
A |
T |
16: 35,655,077 (GRCm39) |
I1798K |
probably damaging |
Het |
Pcdhga7 |
A |
G |
18: 37,849,025 (GRCm39) |
D344G |
probably damaging |
Het |
Pck1 |
A |
G |
2: 172,998,770 (GRCm39) |
T343A |
probably benign |
Het |
Pik3c2g |
T |
A |
6: 139,665,873 (GRCm39) |
C65S |
probably null |
Het |
Pilra |
A |
G |
5: 137,833,674 (GRCm39) |
F131L |
probably damaging |
Het |
Ppl |
A |
T |
16: 4,906,742 (GRCm39) |
S1184R |
probably benign |
Het |
Prmt2 |
C |
T |
10: 76,058,390 (GRCm39) |
V140I |
probably damaging |
Het |
Prpf38b |
A |
G |
3: 108,818,484 (GRCm39) |
F92S |
probably damaging |
Het |
Psmc3 |
A |
G |
2: 90,884,915 (GRCm39) |
|
probably benign |
Het |
Ptgs1 |
A |
T |
2: 36,141,272 (GRCm39) |
N573I |
probably damaging |
Het |
Rgs9 |
C |
A |
11: 109,118,157 (GRCm39) |
A332S |
probably benign |
Het |
Rptor |
T |
C |
11: 119,787,305 (GRCm39) |
I1290T |
possibly damaging |
Het |
Slc38a7 |
C |
A |
8: 96,568,278 (GRCm39) |
R369L |
probably damaging |
Het |
Slc4a2 |
G |
A |
5: 24,643,760 (GRCm39) |
S855N |
probably benign |
Het |
Slco2a1 |
G |
T |
9: 102,923,925 (GRCm39) |
L46F |
probably damaging |
Het |
Snrpd3 |
G |
T |
10: 75,355,227 (GRCm39) |
C20F |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,699,422 (GRCm39) |
I481N |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,960,176 (GRCm39) |
E143G |
probably damaging |
Het |
Tenm2 |
T |
A |
11: 35,959,208 (GRCm39) |
T1114S |
probably damaging |
Het |
Tg |
A |
C |
15: 66,607,101 (GRCm39) |
M213L |
probably benign |
Het |
Tnc |
A |
G |
4: 63,938,648 (GRCm39) |
C64R |
probably damaging |
Het |
Tpd52l1 |
A |
G |
10: 31,233,916 (GRCm39) |
L79S |
probably damaging |
Het |
Tpp2 |
C |
A |
1: 43,993,896 (GRCm39) |
S260R |
possibly damaging |
Het |
Tppp2 |
G |
A |
14: 52,157,912 (GRCm39) |
R119Q |
probably benign |
Het |
Tshz2 |
A |
T |
2: 169,804,493 (GRCm39) |
|
probably benign |
Het |
Tuba8 |
T |
C |
6: 121,199,862 (GRCm39) |
V182A |
probably damaging |
Het |
Ufl1 |
A |
G |
4: 25,254,780 (GRCm39) |
Y559H |
probably benign |
Het |
Usp53 |
A |
T |
3: 122,727,595 (GRCm39) |
S996T |
probably benign |
Het |
Vcam1 |
A |
G |
3: 115,918,037 (GRCm39) |
V308A |
probably damaging |
Het |
Wdr17 |
T |
A |
8: 55,143,271 (GRCm39) |
|
probably null |
Het |
Wdr6 |
G |
A |
9: 108,451,565 (GRCm39) |
H773Y |
probably damaging |
Het |
Wnk4 |
T |
G |
11: 101,152,014 (GRCm39) |
F173V |
probably damaging |
Het |
Xrcc5 |
T |
C |
1: 72,378,188 (GRCm39) |
Y395H |
probably damaging |
Het |
Zcwpw1 |
T |
A |
5: 137,793,781 (GRCm39) |
M1K |
probably null |
Het |
Zfp263 |
A |
G |
16: 3,564,704 (GRCm39) |
R240G |
possibly damaging |
Het |
Zfp652 |
A |
G |
11: 95,640,890 (GRCm39) |
I272V |
possibly damaging |
Het |
|
Other mutations in Cyp4a29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02687:Cyp4a29
|
APN |
4 |
115,108,397 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03224:Cyp4a29
|
APN |
4 |
115,104,247 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03271:Cyp4a29
|
APN |
4 |
115,111,705 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03387:Cyp4a29
|
APN |
4 |
115,108,368 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0304:Cyp4a29
|
UTSW |
4 |
115,110,129 (GRCm39) |
splice site |
probably benign |
|
R2656:Cyp4a29
|
UTSW |
4 |
115,106,921 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4012:Cyp4a29
|
UTSW |
4 |
115,105,707 (GRCm39) |
missense |
probably benign |
|
R4834:Cyp4a29
|
UTSW |
4 |
115,106,867 (GRCm39) |
missense |
probably benign |
0.00 |
R4856:Cyp4a29
|
UTSW |
4 |
115,110,078 (GRCm39) |
missense |
probably benign |
|
R4886:Cyp4a29
|
UTSW |
4 |
115,110,078 (GRCm39) |
missense |
probably benign |
|
R4939:Cyp4a29
|
UTSW |
4 |
115,104,873 (GRCm39) |
critical splice donor site |
probably null |
|
R4967:Cyp4a29
|
UTSW |
4 |
115,104,196 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Cyp4a29
|
UTSW |
4 |
115,104,860 (GRCm39) |
missense |
probably benign |
0.00 |
R5072:Cyp4a29
|
UTSW |
4 |
115,104,860 (GRCm39) |
missense |
probably benign |
0.00 |
R5620:Cyp4a29
|
UTSW |
4 |
115,108,088 (GRCm39) |
missense |
probably benign |
0.12 |
R5818:Cyp4a29
|
UTSW |
4 |
115,104,229 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6219:Cyp4a29
|
UTSW |
4 |
115,106,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R6318:Cyp4a29
|
UTSW |
4 |
115,107,396 (GRCm39) |
missense |
probably benign |
0.00 |
R6386:Cyp4a29
|
UTSW |
4 |
115,104,272 (GRCm39) |
critical splice donor site |
probably null |
|
R6456:Cyp4a29
|
UTSW |
4 |
115,108,381 (GRCm39) |
missense |
probably benign |
0.30 |
R7393:Cyp4a29
|
UTSW |
4 |
115,099,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R7443:Cyp4a29
|
UTSW |
4 |
115,105,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R7719:Cyp4a29
|
UTSW |
4 |
115,108,137 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7831:Cyp4a29
|
UTSW |
4 |
115,107,367 (GRCm39) |
missense |
probably benign |
0.00 |
R7983:Cyp4a29
|
UTSW |
4 |
115,108,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Cyp4a29
|
UTSW |
4 |
115,111,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R8674:Cyp4a29
|
UTSW |
4 |
115,106,882 (GRCm39) |
missense |
probably benign |
0.08 |
R9109:Cyp4a29
|
UTSW |
4 |
115,108,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R9298:Cyp4a29
|
UTSW |
4 |
115,108,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Cyp4a29
|
UTSW |
4 |
115,106,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Cyp4a29
|
UTSW |
4 |
115,105,772 (GRCm39) |
missense |
probably damaging |
0.98 |
R9667:Cyp4a29
|
UTSW |
4 |
115,111,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R9790:Cyp4a29
|
UTSW |
4 |
115,108,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R9791:Cyp4a29
|
UTSW |
4 |
115,108,380 (GRCm39) |
missense |
probably damaging |
1.00 |
U24488:Cyp4a29
|
UTSW |
4 |
115,108,204 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Cyp4a29
|
UTSW |
4 |
115,105,693 (GRCm39) |
missense |
probably benign |
0.00 |
|