Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
G |
A |
17: 9,220,665 (GRCm39) |
C388Y |
probably damaging |
Het |
4930522L14Rik |
G |
A |
5: 109,884,230 (GRCm39) |
H543Y |
probably damaging |
Het |
Abca1 |
A |
T |
4: 53,046,135 (GRCm39) |
V1711E |
possibly damaging |
Het |
Abca3 |
A |
T |
17: 24,602,997 (GRCm39) |
K531* |
probably null |
Het |
Adgrf5 |
A |
T |
17: 43,752,729 (GRCm39) |
D557V |
possibly damaging |
Het |
Adgrl3 |
A |
G |
5: 81,842,467 (GRCm39) |
E865G |
probably benign |
Het |
Adprhl1 |
T |
A |
8: 13,275,316 (GRCm39) |
R481* |
probably null |
Het |
Afap1l1 |
T |
A |
18: 61,879,853 (GRCm39) |
D339V |
probably damaging |
Het |
Atp9b |
T |
A |
18: 80,890,412 (GRCm39) |
H309L |
|
Het |
Baiap3 |
A |
G |
17: 25,470,112 (GRCm39) |
V122A |
probably damaging |
Het |
Btg4 |
T |
C |
9: 51,029,240 (GRCm39) |
S142P |
probably benign |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cdca2 |
T |
A |
14: 67,914,665 (GRCm39) |
T865S |
probably benign |
Het |
Cdk12 |
A |
G |
11: 98,131,661 (GRCm39) |
Y964C |
unknown |
Het |
Cenpo |
A |
T |
12: 4,264,573 (GRCm39) |
F273Y |
probably damaging |
Het |
Cfap96 |
T |
A |
8: 46,423,436 (GRCm39) |
K92M |
probably damaging |
Het |
Chac1 |
T |
A |
2: 119,183,987 (GRCm39) |
D196E |
probably damaging |
Het |
Clec4n |
T |
C |
6: 123,209,063 (GRCm39) |
F43L |
probably benign |
Het |
Colgalt1 |
T |
A |
8: 72,074,508 (GRCm39) |
C407S |
probably damaging |
Het |
Csnk1g1 |
T |
A |
9: 65,906,830 (GRCm39) |
|
probably null |
Het |
Cyp2b23 |
T |
A |
7: 26,385,851 (GRCm39) |
E2V |
probably damaging |
Het |
Cyp51 |
T |
A |
5: 4,152,929 (GRCm39) |
K91M |
probably damaging |
Het |
Cyria |
A |
C |
12: 12,414,798 (GRCm39) |
Y263S |
probably benign |
Het |
Dnah8 |
G |
T |
17: 30,882,348 (GRCm39) |
G640V |
probably benign |
Het |
Dnajc2 |
G |
T |
5: 21,965,637 (GRCm39) |
S505R |
possibly damaging |
Het |
Fam124b |
A |
T |
1: 80,191,053 (GRCm39) |
L110H |
probably damaging |
Het |
Fem1b |
T |
A |
9: 62,703,844 (GRCm39) |
Y472F |
probably benign |
Het |
Frem1 |
A |
G |
4: 82,932,049 (GRCm39) |
|
probably null |
Het |
Gabrg1 |
A |
T |
5: 70,973,415 (GRCm39) |
D46E |
probably damaging |
Het |
Gbp4 |
T |
C |
5: 105,266,161 (GRCm39) |
K627E |
probably benign |
Het |
Glis1 |
A |
G |
4: 107,491,900 (GRCm39) |
D776G |
probably damaging |
Het |
Gm4847 |
A |
G |
1: 166,467,575 (GRCm39) |
V207A |
possibly damaging |
Het |
Gm7298 |
T |
A |
6: 121,759,741 (GRCm39) |
Y1213* |
probably null |
Het |
Gm8229 |
T |
A |
14: 44,604,033 (GRCm39) |
L74* |
probably null |
Het |
Hc |
A |
T |
2: 34,887,411 (GRCm39) |
Y1364* |
probably null |
Het |
Hnrnpa2b1 |
A |
T |
6: 51,443,302 (GRCm39) |
S186R |
unknown |
Het |
Hrh4 |
A |
G |
18: 13,155,582 (GRCm39) |
I374V |
possibly damaging |
Het |
Ighmbp2 |
A |
G |
19: 3,311,490 (GRCm39) |
L975P |
probably damaging |
Het |
Intu |
G |
A |
3: 40,654,222 (GRCm39) |
V905I |
probably benign |
Het |
Large1 |
T |
A |
8: 73,843,071 (GRCm39) |
R151W |
probably damaging |
Het |
Limd2 |
G |
A |
11: 106,050,004 (GRCm39) |
T24M |
probably benign |
Het |
Med16 |
A |
T |
10: 79,734,206 (GRCm39) |
C569* |
probably null |
Het |
Mettl1 |
T |
G |
10: 126,880,390 (GRCm39) |
V104G |
possibly damaging |
Het |
Mgat4c |
A |
G |
10: 102,220,900 (GRCm39) |
T61A |
probably benign |
Het |
Mrps31 |
T |
A |
8: 22,914,367 (GRCm39) |
Y238N |
probably benign |
Het |
Mrs2 |
T |
C |
13: 25,181,113 (GRCm39) |
E236G |
probably damaging |
Het |
Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
Noxred1 |
G |
A |
12: 87,271,761 (GRCm39) |
A136V |
probably benign |
Het |
Obscn |
T |
A |
11: 59,024,588 (GRCm39) |
D484V |
probably damaging |
Het |
Picalm |
C |
A |
7: 89,779,876 (GRCm39) |
H32Q |
probably benign |
Het |
Pik3r5 |
G |
A |
11: 68,381,431 (GRCm39) |
G206R |
probably damaging |
Het |
Plekhh2 |
G |
A |
17: 84,882,434 (GRCm39) |
C680Y |
probably benign |
Het |
Plxna1 |
A |
G |
6: 89,300,241 (GRCm39) |
F1614S |
probably damaging |
Het |
Ppip5k1 |
T |
C |
2: 121,147,235 (GRCm39) |
M1129V |
probably benign |
Het |
Prp2 |
C |
T |
6: 132,572,928 (GRCm39) |
T7I |
unknown |
Het |
Rrbp1 |
A |
T |
2: 143,789,815 (GRCm39) |
|
probably benign |
Het |
Sdhaf3 |
C |
T |
6: 7,038,855 (GRCm39) |
T59M |
probably benign |
Het |
Slc17a6 |
T |
A |
7: 51,275,253 (GRCm39) |
I104N |
probably benign |
Het |
Slc35c1 |
A |
T |
2: 92,289,402 (GRCm39) |
W48R |
probably damaging |
Het |
Smim13 |
G |
T |
13: 41,403,650 (GRCm39) |
|
probably benign |
Het |
Snrpg |
T |
C |
6: 86,355,761 (GRCm39) |
V76A |
probably benign |
Het |
Sntb2 |
C |
T |
8: 107,738,164 (GRCm39) |
T509I |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,079,601 (GRCm39) |
D1276G |
possibly damaging |
Het |
Sptbn2 |
A |
G |
19: 4,794,290 (GRCm39) |
E1498G |
possibly damaging |
Het |
Stau1 |
T |
A |
2: 166,792,787 (GRCm39) |
N393Y |
possibly damaging |
Het |
Tars2 |
A |
T |
3: 95,653,401 (GRCm39) |
S500T |
probably damaging |
Het |
Tbc1d23 |
A |
T |
16: 56,993,488 (GRCm39) |
D559E |
probably benign |
Het |
Trav14-2 |
T |
C |
14: 53,878,508 (GRCm39) |
Y64H |
possibly damaging |
Het |
Trpm3 |
A |
C |
19: 22,882,148 (GRCm39) |
E838D |
probably benign |
Het |
Vmn1r23 |
G |
A |
6: 57,903,541 (GRCm39) |
A79V |
probably benign |
Het |
Vmn1r48 |
G |
T |
6: 90,013,431 (GRCm39) |
N131K |
probably benign |
Het |
Vmn2r18 |
A |
T |
5: 151,508,437 (GRCm39) |
M229K |
probably damaging |
Het |
Zbtb4 |
G |
A |
11: 69,666,863 (GRCm39) |
R56K |
probably benign |
Het |
Zfp616 |
G |
T |
11: 73,975,188 (GRCm39) |
G486W |
probably damaging |
Het |
Zkscan8 |
A |
T |
13: 21,704,580 (GRCm39) |
F453Y |
possibly damaging |
Het |
|
Other mutations in Slc5a4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01348:Slc5a4b
|
APN |
10 |
75,906,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01433:Slc5a4b
|
APN |
10 |
75,906,329 (GRCm39) |
splice site |
probably benign |
|
IGL01754:Slc5a4b
|
APN |
10 |
75,906,449 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01904:Slc5a4b
|
APN |
10 |
75,896,260 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01990:Slc5a4b
|
APN |
10 |
75,896,188 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02211:Slc5a4b
|
APN |
10 |
75,896,297 (GRCm39) |
splice site |
probably benign |
|
IGL02254:Slc5a4b
|
APN |
10 |
75,896,264 (GRCm39) |
missense |
probably benign |
|
IGL02389:Slc5a4b
|
APN |
10 |
75,908,299 (GRCm39) |
nonsense |
probably null |
|
IGL02427:Slc5a4b
|
APN |
10 |
75,894,713 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02493:Slc5a4b
|
APN |
10 |
75,910,849 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02554:Slc5a4b
|
APN |
10 |
75,946,685 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02670:Slc5a4b
|
APN |
10 |
75,910,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Slc5a4b
|
UTSW |
10 |
75,906,462 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0285:Slc5a4b
|
UTSW |
10 |
75,898,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R0294:Slc5a4b
|
UTSW |
10 |
75,917,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R0522:Slc5a4b
|
UTSW |
10 |
75,926,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R0601:Slc5a4b
|
UTSW |
10 |
75,899,870 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0714:Slc5a4b
|
UTSW |
10 |
75,917,341 (GRCm39) |
missense |
probably benign |
0.09 |
R0975:Slc5a4b
|
UTSW |
10 |
75,917,241 (GRCm39) |
missense |
probably benign |
0.09 |
R1934:Slc5a4b
|
UTSW |
10 |
75,917,307 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2339:Slc5a4b
|
UTSW |
10 |
75,944,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R2886:Slc5a4b
|
UTSW |
10 |
75,910,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R3552:Slc5a4b
|
UTSW |
10 |
75,917,358 (GRCm39) |
missense |
probably damaging |
0.99 |
R3890:Slc5a4b
|
UTSW |
10 |
75,898,094 (GRCm39) |
missense |
probably benign |
0.01 |
R4012:Slc5a4b
|
UTSW |
10 |
75,910,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R4259:Slc5a4b
|
UTSW |
10 |
75,939,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R4260:Slc5a4b
|
UTSW |
10 |
75,939,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Slc5a4b
|
UTSW |
10 |
75,894,725 (GRCm39) |
nonsense |
probably null |
|
R4667:Slc5a4b
|
UTSW |
10 |
75,910,879 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4846:Slc5a4b
|
UTSW |
10 |
75,898,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R4939:Slc5a4b
|
UTSW |
10 |
75,917,301 (GRCm39) |
missense |
probably benign |
0.44 |
R5181:Slc5a4b
|
UTSW |
10 |
75,896,221 (GRCm39) |
nonsense |
probably null |
|
R5319:Slc5a4b
|
UTSW |
10 |
75,898,233 (GRCm39) |
missense |
probably benign |
0.08 |
R6306:Slc5a4b
|
UTSW |
10 |
75,917,185 (GRCm39) |
missense |
probably benign |
0.01 |
R6422:Slc5a4b
|
UTSW |
10 |
75,939,696 (GRCm39) |
missense |
probably damaging |
0.97 |
R6837:Slc5a4b
|
UTSW |
10 |
75,898,220 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6997:Slc5a4b
|
UTSW |
10 |
75,925,812 (GRCm39) |
missense |
probably damaging |
0.97 |
R7140:Slc5a4b
|
UTSW |
10 |
75,910,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Slc5a4b
|
UTSW |
10 |
75,946,742 (GRCm39) |
missense |
probably benign |
0.01 |
R7683:Slc5a4b
|
UTSW |
10 |
75,899,906 (GRCm39) |
missense |
probably damaging |
0.96 |
R7718:Slc5a4b
|
UTSW |
10 |
75,906,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Slc5a4b
|
UTSW |
10 |
75,898,133 (GRCm39) |
missense |
probably benign |
0.19 |
R8150:Slc5a4b
|
UTSW |
10 |
75,939,680 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8843:Slc5a4b
|
UTSW |
10 |
75,910,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R9111:Slc5a4b
|
UTSW |
10 |
75,925,827 (GRCm39) |
splice site |
probably benign |
|
R9163:Slc5a4b
|
UTSW |
10 |
75,917,165 (GRCm39) |
nonsense |
probably null |
|
R9195:Slc5a4b
|
UTSW |
10 |
75,898,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Slc5a4b
|
UTSW |
10 |
75,896,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9643:Slc5a4b
|
UTSW |
10 |
75,945,896 (GRCm39) |
missense |
probably benign |
0.01 |
R9656:Slc5a4b
|
UTSW |
10 |
75,944,391 (GRCm39) |
missense |
probably damaging |
0.98 |
R9699:Slc5a4b
|
UTSW |
10 |
75,946,674 (GRCm39) |
missense |
probably damaging |
0.99 |
X0019:Slc5a4b
|
UTSW |
10 |
75,946,685 (GRCm39) |
missense |
possibly damaging |
0.75 |
|