Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A3galt2 |
A |
T |
4: 128,655,934 (GRCm39) |
T101S |
probably damaging |
Het |
Abraxas2 |
C |
T |
7: 132,484,875 (GRCm39) |
A306V |
probably benign |
Het |
Acvr1c |
T |
A |
2: 58,173,518 (GRCm39) |
N248I |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,587,560 (GRCm39) |
R4537Q |
probably damaging |
Het |
Adrb3 |
A |
C |
8: 27,717,798 (GRCm39) |
M217R |
probably damaging |
Het |
Afg3l1 |
T |
C |
8: 124,216,532 (GRCm39) |
V257A |
probably benign |
Het |
Agbl1 |
C |
A |
7: 76,071,904 (GRCm39) |
Q334K |
probably benign |
Het |
Aox4 |
A |
T |
1: 58,275,835 (GRCm39) |
D389V |
probably benign |
Het |
Apob |
A |
T |
12: 8,058,898 (GRCm39) |
Q2427L |
probably damaging |
Het |
Asxl3 |
T |
C |
18: 22,649,765 (GRCm39) |
C585R |
probably damaging |
Het |
Baz2a |
G |
A |
10: 127,951,995 (GRCm39) |
G571D |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,792,368 (GRCm39) |
S587T |
probably benign |
Het |
Bicdl2 |
T |
C |
17: 23,880,795 (GRCm39) |
L14P |
unknown |
Het |
Cachd1 |
G |
A |
4: 100,851,935 (GRCm39) |
S1177N |
probably damaging |
Het |
Cacna2d3 |
A |
G |
14: 29,015,135 (GRCm39) |
F86L |
possibly damaging |
Het |
Ccdc192 |
C |
T |
18: 57,697,041 (GRCm39) |
T65I |
possibly damaging |
Het |
Cd3d |
A |
T |
9: 44,896,296 (GRCm39) |
E28D |
probably damaging |
Het |
Cmya5 |
T |
C |
13: 93,229,880 (GRCm39) |
K1736R |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,512,456 (GRCm39) |
V2913A |
probably damaging |
Het |
Cops8 |
A |
G |
1: 90,538,724 (GRCm39) |
D51G |
probably damaging |
Het |
Csgalnact1 |
T |
C |
8: 68,913,623 (GRCm39) |
E194G |
probably benign |
Het |
Csn1s1 |
A |
G |
5: 87,828,737 (GRCm39) |
D267G |
possibly damaging |
Het |
Cyp2c40 |
T |
C |
19: 39,795,663 (GRCm39) |
N172S |
probably benign |
Het |
Dhtkd1 |
T |
A |
2: 5,908,813 (GRCm39) |
K760N |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 118,007,939 (GRCm39) |
K691E |
probably benign |
Het |
Dppa4 |
G |
A |
16: 48,113,334 (GRCm39) |
R189Q |
probably benign |
Het |
Dsp |
G |
A |
13: 38,381,678 (GRCm39) |
D2808N |
possibly damaging |
Het |
Egr2 |
A |
G |
10: 67,375,605 (GRCm39) |
E17G |
probably damaging |
Het |
Ehmt1 |
G |
T |
2: 24,767,509 (GRCm39) |
P135T |
probably damaging |
Het |
Epas1 |
A |
G |
17: 87,116,882 (GRCm39) |
N184S |
probably damaging |
Het |
Ezh2 |
C |
T |
6: 47,517,684 (GRCm39) |
C584Y |
probably damaging |
Het |
F10 |
T |
C |
8: 13,105,698 (GRCm39) |
V421A |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam186a |
T |
G |
15: 99,853,374 (GRCm39) |
D122A |
unknown |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fam234b |
T |
C |
6: 135,186,193 (GRCm39) |
V67A |
probably benign |
Het |
Fbn2 |
T |
C |
18: 58,172,412 (GRCm39) |
D2131G |
probably damaging |
Het |
Fgfr4 |
T |
C |
13: 55,307,828 (GRCm39) |
Y271H |
probably damaging |
Het |
Gnmt |
A |
T |
17: 47,036,860 (GRCm39) |
S250T |
probably benign |
Het |
Golgb1 |
C |
A |
16: 36,711,819 (GRCm39) |
Q208K |
possibly damaging |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
Grwd1 |
T |
C |
7: 45,475,298 (GRCm39) |
T415A |
probably benign |
Het |
Gsk3b |
G |
A |
16: 38,060,882 (GRCm39) |
R418H |
probably damaging |
Het |
Hap1 |
T |
G |
11: 100,242,357 (GRCm39) |
M382L |
probably benign |
Het |
Hspa12b |
A |
G |
2: 130,981,428 (GRCm39) |
E221G |
possibly damaging |
Het |
Hspa4l |
T |
A |
3: 40,741,179 (GRCm39) |
D709E |
possibly damaging |
Het |
Il17ra |
A |
G |
6: 120,458,514 (GRCm39) |
E555G |
possibly damaging |
Het |
Il27ra |
T |
C |
8: 84,760,688 (GRCm39) |
T426A |
possibly damaging |
Het |
Jup |
T |
C |
11: 100,273,941 (GRCm39) |
D200G |
probably benign |
Het |
Kcnq1 |
T |
C |
7: 142,748,083 (GRCm39) |
|
probably null |
Het |
Kctd9 |
C |
T |
14: 67,966,805 (GRCm39) |
T106I |
probably damaging |
Het |
Kmt5b |
T |
A |
19: 3,852,240 (GRCm39) |
H159Q |
probably damaging |
Het |
Kprp |
C |
T |
3: 92,731,829 (GRCm39) |
R407Q |
unknown |
Het |
Kras |
T |
C |
6: 145,177,879 (GRCm39) |
Q131R |
probably benign |
Het |
Krt16 |
T |
A |
11: 100,138,457 (GRCm39) |
R230S |
probably damaging |
Het |
Lpar6 |
G |
A |
14: 73,476,147 (GRCm39) |
C36Y |
probably damaging |
Het |
Lrp10 |
T |
C |
14: 54,707,067 (GRCm39) |
S635P |
probably benign |
Het |
Mapre2 |
C |
A |
18: 23,991,190 (GRCm39) |
H153N |
possibly damaging |
Het |
Mark3 |
C |
A |
12: 111,621,762 (GRCm39) |
R703S |
probably damaging |
Het |
Mboat2 |
A |
G |
12: 25,009,065 (GRCm39) |
D457G |
probably benign |
Het |
Med13 |
T |
C |
11: 86,210,675 (GRCm39) |
D489G |
probably benign |
Het |
Msh2 |
C |
A |
17: 88,030,841 (GRCm39) |
A906E |
probably benign |
Het |
Mtus1 |
T |
C |
8: 41,536,229 (GRCm39) |
T496A |
probably benign |
Het |
Nckap5 |
T |
C |
1: 125,961,697 (GRCm39) |
H204R |
probably benign |
Het |
Nlrc4 |
G |
T |
17: 74,753,712 (GRCm39) |
P224T |
possibly damaging |
Het |
Oprl1 |
T |
A |
2: 181,360,403 (GRCm39) |
I153N |
probably damaging |
Het |
Or13a27 |
A |
T |
7: 139,925,236 (GRCm39) |
I222N |
probably damaging |
Het |
Or4c116 |
A |
T |
2: 88,942,140 (GRCm39) |
|
probably null |
Het |
Or5an1 |
T |
C |
19: 12,260,670 (GRCm39) |
L86P |
possibly damaging |
Het |
Or5b121 |
T |
A |
19: 13,507,442 (GRCm39) |
M135K |
probably damaging |
Het |
Otud4 |
G |
A |
8: 80,382,318 (GRCm39) |
V176I |
probably damaging |
Het |
Pcdhb5 |
T |
C |
18: 37,453,943 (GRCm39) |
F108L |
probably benign |
Het |
Pde8b |
T |
C |
13: 95,223,250 (GRCm39) |
I335V |
probably benign |
Het |
Pdzd7 |
T |
A |
19: 45,016,868 (GRCm39) |
I886L |
possibly damaging |
Het |
Prune2 |
C |
T |
19: 16,980,995 (GRCm39) |
P51S |
probably damaging |
Het |
Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
Pwwp3a |
T |
C |
10: 80,068,702 (GRCm39) |
L282P |
probably benign |
Het |
Rab27b |
T |
C |
18: 70,122,659 (GRCm39) |
D100G |
probably damaging |
Het |
Rpf1 |
A |
G |
3: 146,212,293 (GRCm39) |
L349S |
probably damaging |
Het |
Samd14 |
T |
C |
11: 94,912,409 (GRCm39) |
S233P |
probably damaging |
Het |
Sema6a |
C |
A |
18: 47,433,195 (GRCm39) |
V79F |
probably damaging |
Het |
Setbp1 |
A |
G |
18: 78,900,697 (GRCm39) |
I990T |
probably damaging |
Het |
Setx |
A |
G |
2: 29,070,093 (GRCm39) |
R2633G |
probably benign |
Het |
Siae |
T |
G |
9: 37,557,816 (GRCm39) |
I541S |
possibly damaging |
Het |
Smarcc2 |
T |
C |
10: 128,297,342 (GRCm39) |
|
probably null |
Het |
Snrpf |
T |
C |
10: 93,423,985 (GRCm39) |
S2G |
probably benign |
Het |
Speer2 |
C |
A |
16: 69,655,708 (GRCm39) |
K39N |
probably null |
Het |
Spink5 |
T |
G |
18: 44,119,490 (GRCm39) |
F267C |
probably damaging |
Het |
Tgfbrap1 |
G |
T |
1: 43,114,666 (GRCm39) |
R145S |
probably damaging |
Het |
Tmem161b |
C |
A |
13: 84,442,887 (GRCm39) |
T269K |
possibly damaging |
Het |
Tmem64 |
T |
C |
4: 15,281,119 (GRCm39) |
I304T |
probably damaging |
Het |
Tomm7 |
A |
G |
5: 24,049,004 (GRCm39) |
I23T |
probably benign |
Het |
Top6bl |
T |
A |
19: 4,708,449 (GRCm39) |
S194C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ttr |
C |
T |
18: 20,803,167 (GRCm39) |
A111V |
possibly damaging |
Het |
Usp47 |
T |
A |
7: 111,683,089 (GRCm39) |
Y561N |
probably damaging |
Het |
Vmn1r17 |
A |
G |
6: 57,337,828 (GRCm39) |
V130A |
probably benign |
Het |
Wdr45b |
A |
G |
11: 121,219,621 (GRCm39) |
I309T |
probably benign |
Het |
Wnt6 |
T |
C |
1: 74,823,755 (GRCm39) |
L364P |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,573,449 (GRCm39) |
L1530P |
probably damaging |
Het |
Zfp933 |
A |
G |
4: 147,911,321 (GRCm39) |
W60R |
probably benign |
Het |
|
Other mutations in Slc13a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00773:Slc13a1
|
APN |
6 |
24,118,016 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01096:Slc13a1
|
APN |
6 |
24,104,076 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01788:Slc13a1
|
APN |
6 |
24,134,371 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02028:Slc13a1
|
APN |
6 |
24,118,030 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02238:Slc13a1
|
APN |
6 |
24,103,482 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02525:Slc13a1
|
APN |
6 |
24,137,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02741:Slc13a1
|
APN |
6 |
24,150,707 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02894:Slc13a1
|
APN |
6 |
24,137,041 (GRCm39) |
splice site |
probably benign |
|
IGL03086:Slc13a1
|
APN |
6 |
24,118,002 (GRCm39) |
missense |
probably damaging |
1.00 |
Liliput
|
UTSW |
6 |
24,108,194 (GRCm39) |
missense |
probably damaging |
0.97 |
munchkin
|
UTSW |
6 |
24,090,795 (GRCm39) |
nonsense |
probably null |
|
R0294:Slc13a1
|
UTSW |
6 |
24,090,779 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0419:Slc13a1
|
UTSW |
6 |
24,100,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R1249:Slc13a1
|
UTSW |
6 |
24,133,649 (GRCm39) |
missense |
probably benign |
0.01 |
R1401:Slc13a1
|
UTSW |
6 |
24,118,082 (GRCm39) |
splice site |
probably null |
|
R1868:Slc13a1
|
UTSW |
6 |
24,117,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Slc13a1
|
UTSW |
6 |
24,134,396 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2940:Slc13a1
|
UTSW |
6 |
24,090,779 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3740:Slc13a1
|
UTSW |
6 |
24,134,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R4326:Slc13a1
|
UTSW |
6 |
24,103,478 (GRCm39) |
missense |
probably benign |
0.00 |
R4327:Slc13a1
|
UTSW |
6 |
24,103,478 (GRCm39) |
missense |
probably benign |
0.00 |
R4389:Slc13a1
|
UTSW |
6 |
24,092,397 (GRCm39) |
splice site |
probably null |
|
R4520:Slc13a1
|
UTSW |
6 |
24,134,512 (GRCm39) |
missense |
probably benign |
0.18 |
R4771:Slc13a1
|
UTSW |
6 |
24,100,339 (GRCm39) |
nonsense |
probably null |
|
R4883:Slc13a1
|
UTSW |
6 |
24,134,356 (GRCm39) |
missense |
probably benign |
0.01 |
R5213:Slc13a1
|
UTSW |
6 |
24,108,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Slc13a1
|
UTSW |
6 |
24,134,373 (GRCm39) |
missense |
probably benign |
0.02 |
R5504:Slc13a1
|
UTSW |
6 |
24,150,743 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5971:Slc13a1
|
UTSW |
6 |
24,133,656 (GRCm39) |
missense |
probably benign |
0.00 |
R6214:Slc13a1
|
UTSW |
6 |
24,090,795 (GRCm39) |
nonsense |
probably null |
|
R6215:Slc13a1
|
UTSW |
6 |
24,090,795 (GRCm39) |
nonsense |
probably null |
|
R6526:Slc13a1
|
UTSW |
6 |
24,097,611 (GRCm39) |
missense |
probably damaging |
0.97 |
R6562:Slc13a1
|
UTSW |
6 |
24,150,792 (GRCm39) |
missense |
probably benign |
0.35 |
R6573:Slc13a1
|
UTSW |
6 |
24,137,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R6902:Slc13a1
|
UTSW |
6 |
24,097,665 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7184:Slc13a1
|
UTSW |
6 |
24,092,311 (GRCm39) |
missense |
probably damaging |
0.99 |
R7536:Slc13a1
|
UTSW |
6 |
24,100,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R7918:Slc13a1
|
UTSW |
6 |
24,118,065 (GRCm39) |
missense |
probably benign |
0.35 |
R8919:Slc13a1
|
UTSW |
6 |
24,108,194 (GRCm39) |
missense |
probably damaging |
0.97 |
R8971:Slc13a1
|
UTSW |
6 |
24,090,785 (GRCm39) |
missense |
probably benign |
0.30 |
R9151:Slc13a1
|
UTSW |
6 |
24,097,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R9163:Slc13a1
|
UTSW |
6 |
24,097,578 (GRCm39) |
critical splice donor site |
probably null |
|
R9313:Slc13a1
|
UTSW |
6 |
24,108,203 (GRCm39) |
missense |
probably benign |
0.00 |
R9594:Slc13a1
|
UTSW |
6 |
24,089,100 (GRCm39) |
missense |
probably damaging |
0.98 |
R9755:Slc13a1
|
UTSW |
6 |
24,134,407 (GRCm39) |
missense |
probably benign |
0.01 |
U15987:Slc13a1
|
UTSW |
6 |
24,133,656 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Slc13a1
|
UTSW |
6 |
24,133,694 (GRCm39) |
missense |
probably benign |
0.00 |
|