Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
C |
5: 124,228,176 (GRCm39) |
T22A |
possibly damaging |
Het |
Abi3bp |
A |
G |
16: 56,417,173 (GRCm39) |
D419G |
probably benign |
Het |
Acoxl |
A |
T |
2: 127,696,691 (GRCm39) |
|
probably benign |
Het |
Acvr1 |
T |
C |
2: 58,352,983 (GRCm39) |
T326A |
possibly damaging |
Het |
Adgra2 |
T |
C |
8: 27,610,979 (GRCm39) |
L976P |
probably damaging |
Het |
Adora2b |
A |
G |
11: 62,155,886 (GRCm39) |
|
probably null |
Het |
Ak1 |
A |
T |
2: 32,521,182 (GRCm39) |
Q117L |
probably damaging |
Het |
Akr1c14 |
T |
A |
13: 4,128,029 (GRCm39) |
D143E |
probably damaging |
Het |
Ap4e1 |
A |
T |
2: 126,861,242 (GRCm39) |
H127L |
probably damaging |
Het |
Asxl3 |
T |
A |
18: 22,649,670 (GRCm39) |
I553N |
probably damaging |
Het |
Asxl3 |
T |
A |
18: 22,657,481 (GRCm39) |
N1830K |
possibly damaging |
Het |
Atp11a |
G |
A |
8: 12,863,144 (GRCm39) |
A108T |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,362,437 (GRCm39) |
T582A |
unknown |
Het |
Bbs9 |
T |
C |
9: 22,490,005 (GRCm39) |
S259P |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Bltp3a |
T |
A |
17: 28,104,902 (GRCm39) |
L532* |
probably null |
Het |
Blvrb |
T |
C |
7: 27,165,210 (GRCm39) |
S177P |
probably damaging |
Het |
C1s2 |
T |
A |
6: 124,602,642 (GRCm39) |
D523V |
probably benign |
Het |
Cacna2d1 |
C |
T |
5: 16,558,850 (GRCm39) |
T736I |
probably damaging |
Het |
Card9 |
T |
C |
2: 26,242,397 (GRCm39) |
N513S |
probably benign |
Het |
Casp2 |
A |
G |
6: 42,245,882 (GRCm39) |
T180A |
probably benign |
Het |
Cenpf |
A |
T |
1: 189,404,746 (GRCm39) |
L361Q |
probably damaging |
Het |
Cnbd2 |
T |
C |
2: 156,217,488 (GRCm39) |
I659T |
probably damaging |
Het |
Cped1 |
A |
T |
6: 21,987,012 (GRCm39) |
D68V |
probably damaging |
Het |
Cxcr1 |
T |
C |
1: 74,231,099 (GRCm39) |
I308V |
probably benign |
Het |
Dad1 |
A |
G |
14: 54,491,163 (GRCm39) |
L46P |
probably damaging |
Het |
Defb23 |
G |
A |
2: 152,301,422 (GRCm39) |
A50V |
probably benign |
Het |
Dhx33 |
C |
T |
11: 70,877,992 (GRCm39) |
A684T |
probably damaging |
Het |
Dnai3 |
T |
C |
3: 145,772,589 (GRCm39) |
T486A |
probably benign |
Het |
Epb41l4a |
T |
A |
18: 33,965,729 (GRCm39) |
N366I |
probably benign |
Het |
Erich3 |
A |
G |
3: 154,467,912 (GRCm39) |
E788G |
|
Het |
Fam241b |
T |
C |
10: 61,944,892 (GRCm39) |
N35S |
probably benign |
Het |
Fbxo24 |
T |
A |
5: 137,622,526 (GRCm39) |
Q80L |
probably benign |
Het |
Foxk1 |
T |
G |
5: 142,434,497 (GRCm39) |
F254V |
probably benign |
Het |
Gm10801 |
C |
CGTG |
2: 98,494,152 (GRCm39) |
|
probably null |
Het |
Gm12886 |
T |
C |
4: 121,274,743 (GRCm39) |
I46V |
probably benign |
Het |
Gm20834 |
G |
T |
Y: 10,323,354 (GRCm39) |
H27Q |
probably damaging |
Het |
Gm2888 |
A |
G |
14: 3,032,106 (GRCm38) |
N138S |
probably damaging |
Het |
Gm5773 |
T |
C |
3: 93,681,179 (GRCm39) |
C284R |
possibly damaging |
Het |
Gprin3 |
A |
T |
6: 59,330,273 (GRCm39) |
M678K |
probably benign |
Het |
Grm7 |
T |
C |
6: 111,472,729 (GRCm39) |
V856A |
probably benign |
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Immt |
C |
T |
6: 71,851,403 (GRCm39) |
T588I |
probably damaging |
Het |
Ints1 |
G |
C |
5: 139,737,701 (GRCm39) |
N2145K |
possibly damaging |
Het |
Jade2 |
T |
C |
11: 51,715,951 (GRCm39) |
D418G |
probably benign |
Het |
Kdf1 |
T |
C |
4: 133,256,140 (GRCm39) |
Y286H |
probably damaging |
Het |
Kif18a |
A |
G |
2: 109,171,506 (GRCm39) |
Y861C |
possibly damaging |
Het |
Lama2 |
T |
A |
10: 27,298,515 (GRCm39) |
I194F |
probably damaging |
Het |
Lhx8 |
A |
G |
3: 154,034,063 (GRCm39) |
S33P |
probably benign |
Het |
Lmo7 |
T |
C |
14: 102,118,297 (GRCm39) |
I174T |
probably damaging |
Het |
Lrfn2 |
A |
T |
17: 49,376,976 (GRCm39) |
D19V |
possibly damaging |
Het |
Lrrk1 |
A |
T |
7: 65,928,357 (GRCm39) |
I1257N |
probably damaging |
Het |
Malrd1 |
T |
A |
2: 15,802,516 (GRCm39) |
H1076Q |
unknown |
Het |
Map3k14 |
A |
C |
11: 103,128,364 (GRCm39) |
M419R |
probably damaging |
Het |
Mcm10 |
G |
A |
2: 5,011,372 (GRCm39) |
R200C |
probably benign |
Het |
Mertk |
A |
G |
2: 128,604,035 (GRCm39) |
N390D |
probably benign |
Het |
Mitf |
T |
A |
6: 97,990,680 (GRCm39) |
I361N |
probably damaging |
Het |
Mrgprb1 |
T |
A |
7: 48,097,046 (GRCm39) |
I289F |
possibly damaging |
Het |
Muc5ac |
A |
T |
7: 141,352,218 (GRCm39) |
D659V |
probably damaging |
Het |
Nphp3 |
T |
G |
9: 103,909,214 (GRCm39) |
L808R |
probably damaging |
Het |
Or14c42-ps1 |
G |
A |
7: 86,211,156 (GRCm39) |
C72Y |
unknown |
Het |
Or1e1 |
T |
C |
11: 73,245,316 (GRCm39) |
S246P |
probably damaging |
Het |
Or5an1 |
T |
A |
19: 12,260,808 (GRCm39) |
L132Q |
probably damaging |
Het |
Or5b113 |
T |
A |
19: 13,342,755 (GRCm39) |
S254R |
possibly damaging |
Het |
Pagr1a |
T |
C |
7: 126,615,954 (GRCm39) |
E47G |
probably benign |
Het |
Papss2 |
G |
T |
19: 32,618,764 (GRCm39) |
R274L |
probably damaging |
Het |
Pcdhga10 |
C |
A |
18: 37,880,960 (GRCm39) |
F240L |
probably damaging |
Het |
Pcsk5 |
T |
G |
19: 17,563,472 (GRCm39) |
E555A |
|
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pgrmc2 |
T |
A |
3: 41,023,099 (GRCm39) |
D206V |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,790,976 (GRCm39) |
V1057A |
|
Het |
Plekha5 |
T |
C |
6: 140,480,239 (GRCm39) |
I113T |
probably damaging |
Het |
Prorp |
T |
A |
12: 55,426,189 (GRCm39) |
L513Q |
probably damaging |
Het |
Prss32 |
C |
T |
17: 24,078,199 (GRCm39) |
T295I |
possibly damaging |
Het |
Ptprk |
G |
T |
10: 28,456,413 (GRCm39) |
V1072F |
probably damaging |
Het |
Rasd2 |
T |
A |
8: 75,945,174 (GRCm39) |
M1K |
probably null |
Het |
Rhag |
T |
A |
17: 41,139,302 (GRCm39) |
M79K |
probably damaging |
Het |
Rnf19a |
C |
A |
15: 36,253,310 (GRCm39) |
|
probably null |
Het |
Rnf213 |
G |
T |
11: 119,299,573 (GRCm39) |
G101C |
|
Het |
Sap130 |
T |
A |
18: 31,780,116 (GRCm39) |
D45E |
probably benign |
Het |
Scel |
T |
A |
14: 103,839,626 (GRCm39) |
F510I |
probably benign |
Het |
Sertad2 |
A |
T |
11: 20,598,425 (GRCm39) |
E207V |
probably benign |
Het |
Shoc2 |
T |
A |
19: 53,976,310 (GRCm39) |
S67T |
probably benign |
Het |
Slc22a3 |
T |
C |
17: 12,645,619 (GRCm39) |
I441V |
possibly damaging |
Het |
Slfn5 |
A |
G |
11: 82,851,503 (GRCm39) |
D600G |
probably benign |
Het |
Smim7 |
G |
A |
8: 73,324,757 (GRCm39) |
T10M |
probably damaging |
Het |
Sntb2 |
A |
T |
8: 107,662,831 (GRCm39) |
Q133L |
possibly damaging |
Het |
Steap3 |
A |
C |
1: 120,162,048 (GRCm39) |
M408R |
probably benign |
Het |
Supt4a |
T |
C |
11: 87,633,624 (GRCm39) |
I60T |
probably benign |
Het |
Swt1 |
A |
C |
1: 151,244,239 (GRCm39) |
C899G |
possibly damaging |
Het |
Taok3 |
A |
G |
5: 117,344,744 (GRCm39) |
E157G |
probably damaging |
Het |
Taok3 |
C |
T |
5: 117,379,245 (GRCm39) |
L427F |
possibly damaging |
Het |
Taok3 |
T |
C |
5: 117,379,168 (GRCm39) |
V401A |
probably benign |
Het |
Tcf25 |
A |
G |
8: 124,108,182 (GRCm39) |
E79G |
probably benign |
Het |
Tigit |
G |
A |
16: 43,479,876 (GRCm39) |
L140F |
possibly damaging |
Het |
Tmem143 |
G |
T |
7: 45,546,802 (GRCm39) |
|
probably benign |
Het |
Tmem151b |
C |
T |
17: 45,856,355 (GRCm39) |
V362M |
possibly damaging |
Het |
Tmem230 |
A |
G |
2: 132,085,989 (GRCm39) |
F58L |
probably benign |
Het |
Trim25 |
T |
C |
11: 88,899,988 (GRCm39) |
M245T |
probably benign |
Het |
Trim36 |
A |
C |
18: 46,302,410 (GRCm39) |
V546G |
probably benign |
Het |
Triml1 |
T |
C |
8: 43,583,624 (GRCm39) |
N326D |
probably damaging |
Het |
Trp53bp2 |
T |
C |
1: 182,286,328 (GRCm39) |
V1056A |
probably damaging |
Het |
Trpa1 |
C |
A |
1: 14,952,435 (GRCm39) |
M865I |
probably damaging |
Het |
Ttbk1 |
A |
T |
17: 46,790,132 (GRCm39) |
Y104* |
probably null |
Het |
Tubg1 |
T |
A |
11: 101,014,257 (GRCm39) |
H139Q |
probably damaging |
Het |
Ufsp2 |
A |
G |
8: 46,447,050 (GRCm39) |
|
probably null |
Het |
Usp47 |
A |
T |
7: 111,652,431 (GRCm39) |
N36I |
probably benign |
Het |
Vmn1r32 |
G |
A |
6: 66,530,120 (GRCm39) |
R219* |
probably null |
Het |
Vmn2r59 |
G |
A |
7: 41,693,125 (GRCm39) |
P492S |
probably benign |
Het |
Vmn2r59 |
G |
C |
7: 41,693,127 (GRCm39) |
A491G |
|
Het |
Wdr76 |
T |
C |
2: 121,364,592 (GRCm39) |
Y299H |
probably damaging |
Het |
Wnt5a |
C |
T |
14: 28,240,309 (GRCm39) |
A153V |
probably benign |
Het |
Zfp202 |
T |
C |
9: 40,120,237 (GRCm39) |
V226A |
possibly damaging |
Het |
Zfp219 |
C |
T |
14: 52,244,598 (GRCm39) |
R527H |
probably damaging |
Het |
Zfp408 |
A |
T |
2: 91,475,528 (GRCm39) |
L542H |
probably damaging |
Het |
Zfyve9 |
A |
T |
4: 108,539,386 (GRCm39) |
C271* |
probably null |
Het |
|
Other mutations in Nox4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01455:Nox4
|
APN |
7 |
87,025,424 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02711:Nox4
|
APN |
7 |
87,046,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03234:Nox4
|
APN |
7 |
86,966,521 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03286:Nox4
|
APN |
7 |
87,019,349 (GRCm39) |
splice site |
probably benign |
|
BB001:Nox4
|
UTSW |
7 |
87,023,589 (GRCm39) |
missense |
probably benign |
0.00 |
BB011:Nox4
|
UTSW |
7 |
87,023,589 (GRCm39) |
missense |
probably benign |
0.00 |
LCD18:Nox4
|
UTSW |
7 |
86,892,275 (GRCm39) |
unclassified |
probably benign |
|
PIT4151001:Nox4
|
UTSW |
7 |
86,954,097 (GRCm39) |
missense |
probably benign |
0.02 |
R0717:Nox4
|
UTSW |
7 |
86,954,098 (GRCm39) |
nonsense |
probably null |
|
R1033:Nox4
|
UTSW |
7 |
87,023,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R1135:Nox4
|
UTSW |
7 |
86,972,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R1333:Nox4
|
UTSW |
7 |
86,896,072 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1477:Nox4
|
UTSW |
7 |
86,945,074 (GRCm39) |
missense |
probably benign |
0.16 |
R1489:Nox4
|
UTSW |
7 |
86,954,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R1579:Nox4
|
UTSW |
7 |
87,019,231 (GRCm39) |
missense |
probably damaging |
0.98 |
R1669:Nox4
|
UTSW |
7 |
86,945,097 (GRCm39) |
missense |
probably benign |
0.01 |
R1742:Nox4
|
UTSW |
7 |
86,945,026 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1900:Nox4
|
UTSW |
7 |
87,010,004 (GRCm39) |
nonsense |
probably null |
|
R2112:Nox4
|
UTSW |
7 |
87,021,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R2192:Nox4
|
UTSW |
7 |
87,023,588 (GRCm39) |
missense |
probably benign |
0.02 |
R2496:Nox4
|
UTSW |
7 |
86,955,958 (GRCm39) |
missense |
probably benign |
0.04 |
R2497:Nox4
|
UTSW |
7 |
86,945,084 (GRCm39) |
nonsense |
probably null |
|
R4158:Nox4
|
UTSW |
7 |
87,046,032 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4160:Nox4
|
UTSW |
7 |
87,046,032 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4281:Nox4
|
UTSW |
7 |
86,946,732 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4685:Nox4
|
UTSW |
7 |
86,946,716 (GRCm39) |
missense |
probably benign |
0.36 |
R4791:Nox4
|
UTSW |
7 |
86,954,055 (GRCm39) |
missense |
probably benign |
0.35 |
R5001:Nox4
|
UTSW |
7 |
87,010,011 (GRCm39) |
missense |
probably damaging |
0.96 |
R5091:Nox4
|
UTSW |
7 |
87,025,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Nox4
|
UTSW |
7 |
86,972,974 (GRCm39) |
missense |
probably benign |
0.10 |
R5220:Nox4
|
UTSW |
7 |
87,023,616 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5278:Nox4
|
UTSW |
7 |
87,021,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Nox4
|
UTSW |
7 |
86,954,181 (GRCm39) |
intron |
probably benign |
|
R5840:Nox4
|
UTSW |
7 |
87,010,001 (GRCm39) |
missense |
probably benign |
0.00 |
R5852:Nox4
|
UTSW |
7 |
86,988,172 (GRCm39) |
missense |
probably damaging |
0.98 |
R7516:Nox4
|
UTSW |
7 |
86,970,905 (GRCm39) |
missense |
probably benign |
|
R7529:Nox4
|
UTSW |
7 |
87,044,976 (GRCm39) |
missense |
unknown |
|
R7587:Nox4
|
UTSW |
7 |
86,966,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R7643:Nox4
|
UTSW |
7 |
86,972,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R7660:Nox4
|
UTSW |
7 |
87,019,230 (GRCm39) |
missense |
probably damaging |
0.97 |
R7786:Nox4
|
UTSW |
7 |
86,945,050 (GRCm39) |
missense |
probably damaging |
0.99 |
R7871:Nox4
|
UTSW |
7 |
86,963,335 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7924:Nox4
|
UTSW |
7 |
87,023,589 (GRCm39) |
missense |
probably benign |
0.00 |
R7934:Nox4
|
UTSW |
7 |
86,945,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Nox4
|
UTSW |
7 |
86,954,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R8053:Nox4
|
UTSW |
7 |
87,019,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8269:Nox4
|
UTSW |
7 |
86,955,930 (GRCm39) |
splice site |
probably benign |
|
R8376:Nox4
|
UTSW |
7 |
87,023,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R8461:Nox4
|
UTSW |
7 |
86,966,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R9041:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9100:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9101:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9102:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9109:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9136:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9220:Nox4
|
UTSW |
7 |
86,970,774 (GRCm39) |
missense |
probably benign |
0.01 |
R9252:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9298:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9306:Nox4
|
UTSW |
7 |
86,896,781 (GRCm39) |
missense |
probably benign |
0.01 |
R9338:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9339:Nox4
|
UTSW |
7 |
87,025,448 (GRCm39) |
missense |
probably benign |
0.05 |
R9448:Nox4
|
UTSW |
7 |
87,045,001 (GRCm39) |
missense |
unknown |
|
X0021:Nox4
|
UTSW |
7 |
87,044,886 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nox4
|
UTSW |
7 |
87,044,920 (GRCm39) |
missense |
unknown |
|
|