Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
A |
T |
8: 111,769,338 (GRCm39) |
D287V |
probably damaging |
Het |
Abca12 |
A |
G |
1: 71,334,188 (GRCm39) |
C1105R |
probably benign |
Het |
Abca8b |
T |
A |
11: 109,833,167 (GRCm39) |
N1178Y |
probably damaging |
Het |
Abhd12 |
A |
G |
2: 150,685,318 (GRCm39) |
L189P |
probably damaging |
Het |
Acap2 |
G |
T |
16: 30,929,752 (GRCm39) |
N435K |
probably damaging |
Het |
Adam6b |
G |
T |
12: 113,453,545 (GRCm39) |
G121C |
probably damaging |
Het |
Adgrb1 |
C |
A |
15: 74,452,435 (GRCm39) |
C200* |
probably null |
Het |
Agbl5 |
T |
C |
5: 31,060,408 (GRCm39) |
S730P |
possibly damaging |
Het |
Ahsg |
G |
A |
16: 22,711,078 (GRCm39) |
|
probably benign |
Het |
Alpk2 |
T |
A |
18: 65,427,165 (GRCm39) |
H1857L |
possibly damaging |
Het |
Apip |
T |
A |
2: 102,919,007 (GRCm39) |
N102K |
probably benign |
Het |
Asxl2 |
T |
C |
12: 3,507,125 (GRCm39) |
S106P |
probably damaging |
Het |
Atp2b2 |
G |
T |
6: 113,750,329 (GRCm39) |
R677S |
probably damaging |
Het |
Barhl1 |
A |
C |
2: 28,799,857 (GRCm39) |
M256R |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,990,775 (GRCm39) |
Q619L |
possibly damaging |
Het |
Ccdc137 |
C |
T |
11: 120,349,038 (GRCm39) |
P23L |
probably benign |
Het |
Cdh11 |
A |
T |
8: 103,361,273 (GRCm39) |
N688K |
possibly damaging |
Het |
Cdh18 |
C |
T |
15: 23,173,938 (GRCm39) |
P51S |
probably damaging |
Het |
Cdin1 |
G |
T |
2: 115,473,173 (GRCm39) |
R101L |
possibly damaging |
Het |
Cfhr1 |
A |
T |
1: 139,481,338 (GRCm39) |
Y181N |
probably damaging |
Het |
Chmp3 |
A |
G |
6: 71,537,923 (GRCm39) |
D50G |
probably benign |
Het |
Crem |
T |
C |
18: 3,295,037 (GRCm39) |
|
probably null |
Het |
Cyb561a3 |
G |
A |
19: 10,559,757 (GRCm39) |
W27* |
probably null |
Het |
Cyp2d12 |
C |
A |
15: 82,442,257 (GRCm39) |
N297K |
possibly damaging |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dnah12 |
T |
A |
14: 26,522,032 (GRCm39) |
N1948K |
probably damaging |
Het |
Dnah12 |
T |
C |
14: 26,494,980 (GRCm39) |
L1346P |
probably damaging |
Het |
Dsp |
T |
G |
13: 38,377,171 (GRCm39) |
L1652R |
probably damaging |
Het |
Dstyk |
G |
A |
1: 132,377,333 (GRCm39) |
S66N |
probably benign |
Het |
Ehhadh |
T |
C |
16: 21,580,928 (GRCm39) |
E688G |
probably damaging |
Het |
Emsy |
G |
T |
7: 98,251,937 (GRCm39) |
H688N |
possibly damaging |
Het |
Emsy |
T |
A |
7: 98,251,936 (GRCm39) |
H688L |
possibly damaging |
Het |
Endod1 |
A |
G |
9: 14,268,222 (GRCm39) |
L421P |
probably damaging |
Het |
Fam222b |
C |
T |
11: 78,045,861 (GRCm39) |
P346L |
probably damaging |
Het |
Fam3c |
G |
A |
6: 22,309,436 (GRCm39) |
R182W |
probably damaging |
Het |
Gck |
T |
C |
11: 5,860,984 (GRCm39) |
D29G |
probably damaging |
Het |
Gm10320 |
C |
A |
13: 98,626,207 (GRCm39) |
R59L |
probably damaging |
Het |
Gm21798 |
C |
T |
15: 64,689,675 (GRCm39) |
|
probably benign |
Het |
Gm9376 |
A |
G |
14: 118,504,957 (GRCm39) |
T130A |
possibly damaging |
Het |
Gpr153 |
T |
A |
4: 152,366,849 (GRCm39) |
I334N |
possibly damaging |
Het |
Greb1l |
T |
C |
18: 10,509,314 (GRCm39) |
L542P |
probably damaging |
Het |
H2-T15 |
G |
T |
17: 36,368,896 (GRCm39) |
F61L |
probably damaging |
Het |
Hacl1 |
T |
C |
14: 31,362,491 (GRCm39) |
E52G |
probably benign |
Het |
Ice2 |
A |
G |
9: 69,314,635 (GRCm39) |
Y128C |
probably damaging |
Het |
Ikzf2 |
T |
A |
1: 69,581,446 (GRCm39) |
I121L |
probably benign |
Het |
Ipcef1 |
C |
T |
10: 6,869,900 (GRCm39) |
A167T |
probably benign |
Het |
Jakmip2 |
T |
A |
18: 43,715,145 (GRCm39) |
D127V |
possibly damaging |
Het |
Jph4 |
T |
C |
14: 55,352,368 (GRCm39) |
T122A |
probably damaging |
Het |
Kcns2 |
A |
G |
15: 34,838,949 (GRCm39) |
E104G |
probably damaging |
Het |
Lars2 |
A |
C |
9: 123,260,982 (GRCm39) |
R384S |
probably benign |
Het |
Lsmem1 |
T |
A |
12: 40,235,407 (GRCm39) |
H3L |
possibly damaging |
Het |
Lsmem1 |
G |
T |
12: 40,235,408 (GRCm39) |
H3N |
possibly damaging |
Het |
Ly6g2 |
T |
G |
15: 75,088,605 (GRCm39) |
|
probably null |
Het |
Mfhas1 |
A |
C |
8: 36,057,222 (GRCm39) |
S566R |
probably benign |
Het |
Mfhas1 |
C |
G |
8: 36,057,402 (GRCm39) |
R626G |
probably benign |
Het |
Mgam |
A |
G |
6: 40,643,826 (GRCm39) |
T585A |
probably damaging |
Het |
Mmp25 |
T |
C |
17: 23,858,997 (GRCm39) |
K185E |
probably benign |
Het |
Mtch1 |
T |
C |
17: 29,557,750 (GRCm39) |
I243V |
probably damaging |
Het |
Mtcp1 |
A |
T |
X: 74,455,271 (GRCm39) |
Y25* |
probably null |
Het |
Mybl2 |
A |
G |
2: 162,901,503 (GRCm39) |
T35A |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,041,744 (GRCm39) |
E736G |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,067,385 (GRCm39) |
I224T |
probably damaging |
Het |
Mymx |
T |
C |
17: 45,912,759 (GRCm39) |
|
probably benign |
Het |
Nek10 |
A |
G |
14: 14,863,454 (GRCm38) |
|
probably null |
Het |
Nsd1 |
A |
T |
13: 55,394,182 (GRCm39) |
K697N |
probably damaging |
Het |
Nynrin |
A |
G |
14: 56,110,404 (GRCm39) |
D1837G |
possibly damaging |
Het |
Or14j4 |
G |
A |
17: 37,921,168 (GRCm39) |
T158I |
probably benign |
Het |
Or2ag2b |
A |
G |
7: 106,418,214 (GRCm39) |
H308R |
probably benign |
Het |
Or52s1 |
A |
T |
7: 102,861,093 (GRCm39) |
T9S |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,266,851 (GRCm39) |
I76N |
probably benign |
Het |
Or6k4 |
T |
A |
1: 173,964,760 (GRCm39) |
I150N |
probably benign |
Het |
Pgap6 |
T |
C |
17: 26,341,194 (GRCm39) |
Y766H |
probably damaging |
Het |
Phf19 |
T |
C |
2: 34,801,781 (GRCm39) |
T10A |
probably benign |
Het |
Pkd1 |
A |
T |
17: 24,784,558 (GRCm39) |
H368L |
probably benign |
Het |
Plscr2 |
A |
G |
9: 92,172,808 (GRCm39) |
R156G |
probably damaging |
Het |
Ppp1r42 |
G |
A |
1: 10,070,311 (GRCm39) |
R61C |
probably benign |
Het |
Pptc7 |
T |
G |
5: 122,451,679 (GRCm39) |
V45G |
probably damaging |
Het |
Prlhr |
G |
A |
19: 60,455,867 (GRCm39) |
T233I |
probably damaging |
Het |
Prr23a4 |
T |
A |
9: 98,785,446 (GRCm39) |
I37N |
possibly damaging |
Het |
Reps1 |
C |
T |
10: 17,983,462 (GRCm39) |
T435I |
probably damaging |
Het |
Ret |
T |
A |
6: 118,130,912 (GRCm39) |
T1084S |
probably damaging |
Het |
Rgl2 |
T |
A |
17: 34,152,595 (GRCm39) |
M402K |
probably benign |
Het |
Rp2 |
A |
G |
X: 20,243,154 (GRCm39) |
K43R |
probably benign |
Het |
Rundc3b |
A |
T |
5: 8,629,117 (GRCm39) |
W95R |
probably damaging |
Het |
Samd9l |
T |
C |
6: 3,375,107 (GRCm39) |
D718G |
possibly damaging |
Het |
Scnn1b |
G |
A |
7: 121,502,068 (GRCm39) |
R242H |
probably benign |
Het |
Smad4 |
G |
T |
18: 73,774,965 (GRCm39) |
Q445K |
probably benign |
Het |
Smchd1 |
G |
T |
17: 71,677,332 (GRCm39) |
P1486T |
probably damaging |
Het |
Snx25 |
G |
T |
8: 46,488,669 (GRCm39) |
N895K |
possibly damaging |
Het |
Sox2 |
A |
G |
3: 34,704,890 (GRCm39) |
D109G |
probably damaging |
Het |
Stfa2 |
A |
T |
16: 36,225,564 (GRCm39) |
N38K |
probably damaging |
Het |
Stfa2 |
C |
A |
16: 36,225,573 (GRCm39) |
E35D |
possibly damaging |
Het |
Stfa3 |
A |
G |
16: 36,271,023 (GRCm39) |
L87P |
probably damaging |
Het |
Strbp |
T |
C |
2: 37,530,921 (GRCm39) |
D111G |
possibly damaging |
Het |
Supt20 |
C |
A |
3: 54,635,079 (GRCm39) |
|
probably benign |
Het |
Svep1 |
A |
G |
4: 58,096,310 (GRCm39) |
Y1437H |
possibly damaging |
Het |
Tbx4 |
T |
A |
11: 85,802,746 (GRCm39) |
|
probably null |
Het |
Tmem117 |
A |
T |
15: 94,992,432 (GRCm39) |
N364I |
probably damaging |
Het |
Trat1 |
T |
C |
16: 48,581,742 (GRCm39) |
E45G |
probably damaging |
Het |
Trpc2 |
G |
A |
7: 101,733,326 (GRCm39) |
D92N |
probably damaging |
Het |
Trpm1 |
G |
A |
7: 63,876,530 (GRCm39) |
D528N |
probably damaging |
Het |
Ttll9 |
A |
G |
2: 152,842,156 (GRCm39) |
S337G |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,351,018 (GRCm39) |
I355N |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,070,782 (GRCm39) |
S385P |
probably benign |
Het |
Vmn1r209 |
A |
G |
13: 22,990,409 (GRCm39) |
S94P |
possibly damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,496,810 (GRCm39) |
Q14L |
probably benign |
Het |
Vps45 |
A |
G |
3: 95,954,557 (GRCm39) |
|
probably null |
Het |
Wdr48 |
T |
C |
9: 119,733,396 (GRCm39) |
V81A |
probably benign |
Het |
Xpnpep2 |
A |
G |
X: 47,214,230 (GRCm39) |
N476S |
probably benign |
Het |
Zbtb41 |
A |
T |
1: 139,374,660 (GRCm39) |
K707* |
probably null |
Het |
Zfp442 |
A |
C |
2: 150,250,983 (GRCm39) |
C306W |
probably damaging |
Het |
Zfp811 |
T |
C |
17: 33,017,116 (GRCm39) |
N307S |
possibly damaging |
Het |
Zfp976 |
A |
G |
7: 42,265,735 (GRCm39) |
W17R |
probably damaging |
Het |
Zyg11b |
T |
C |
4: 108,123,290 (GRCm39) |
T226A |
possibly damaging |
Het |
|
Other mutations in Aldh9a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01126:Aldh9a1
|
APN |
1 |
167,192,143 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01432:Aldh9a1
|
APN |
1 |
167,183,354 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02370:Aldh9a1
|
APN |
1 |
167,184,101 (GRCm39) |
missense |
probably damaging |
1.00 |
Yummy
|
UTSW |
1 |
167,180,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Aldh9a1
|
UTSW |
1 |
167,184,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R0197:Aldh9a1
|
UTSW |
1 |
167,189,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R0520:Aldh9a1
|
UTSW |
1 |
167,188,960 (GRCm39) |
splice site |
probably benign |
|
R0836:Aldh9a1
|
UTSW |
1 |
167,177,824 (GRCm39) |
missense |
probably benign |
0.03 |
R1224:Aldh9a1
|
UTSW |
1 |
167,180,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R1340:Aldh9a1
|
UTSW |
1 |
167,184,913 (GRCm39) |
missense |
probably benign |
0.00 |
R2849:Aldh9a1
|
UTSW |
1 |
167,180,197 (GRCm39) |
missense |
probably damaging |
0.98 |
R4937:Aldh9a1
|
UTSW |
1 |
167,189,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R4965:Aldh9a1
|
UTSW |
1 |
167,193,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R5065:Aldh9a1
|
UTSW |
1 |
167,180,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Aldh9a1
|
UTSW |
1 |
167,183,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Aldh9a1
|
UTSW |
1 |
167,182,021 (GRCm39) |
missense |
probably benign |
0.31 |
R7184:Aldh9a1
|
UTSW |
1 |
167,184,965 (GRCm39) |
missense |
probably benign |
0.05 |
R7531:Aldh9a1
|
UTSW |
1 |
167,177,895 (GRCm39) |
missense |
probably benign |
|
R7673:Aldh9a1
|
UTSW |
1 |
167,189,119 (GRCm39) |
missense |
probably benign |
0.35 |
R8026:Aldh9a1
|
UTSW |
1 |
167,180,236 (GRCm39) |
critical splice donor site |
probably null |
|
R8147:Aldh9a1
|
UTSW |
1 |
167,184,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8826:Aldh9a1
|
UTSW |
1 |
167,184,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R9441:Aldh9a1
|
UTSW |
1 |
167,177,919 (GRCm39) |
missense |
probably benign |
0.34 |
R9643:Aldh9a1
|
UTSW |
1 |
167,184,904 (GRCm39) |
missense |
possibly damaging |
0.85 |
|