Other mutations in this stock |
Total: 134 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
T |
G |
8: 87,244,118 (GRCm39) |
K1012Q |
possibly damaging |
Het |
Afmid |
G |
A |
11: 117,718,968 (GRCm39) |
G33R |
probably benign |
Het |
Agbl3 |
G |
T |
6: 34,776,131 (GRCm39) |
W207C |
probably damaging |
Het |
Ajuba |
T |
C |
14: 54,807,855 (GRCm39) |
Y459C |
probably damaging |
Het |
Ak2 |
T |
C |
4: 128,901,965 (GRCm39) |
S213P |
probably benign |
Het |
Alk |
T |
A |
17: 72,182,007 (GRCm39) |
N1339Y |
probably damaging |
Het |
Angpt1 |
T |
C |
15: 42,301,761 (GRCm39) |
S416G |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,775,582 (GRCm39) |
V854M |
probably benign |
Het |
Ankrd61 |
G |
T |
5: 143,828,482 (GRCm39) |
N122K |
possibly damaging |
Het |
Armc9 |
T |
A |
1: 86,126,011 (GRCm39) |
L34Q |
probably null |
Het |
Aspg |
T |
A |
12: 112,089,466 (GRCm39) |
V418E |
probably benign |
Het |
Baz1b |
C |
T |
5: 135,266,913 (GRCm39) |
R1241C |
probably damaging |
Het |
Bclaf1 |
T |
C |
10: 20,201,338 (GRCm39) |
V201A |
possibly damaging |
Het |
C1ql3 |
A |
T |
2: 13,009,169 (GRCm39) |
D225E |
probably damaging |
Het |
Capn9 |
A |
G |
8: 125,332,279 (GRCm39) |
T417A |
possibly damaging |
Het |
Card14 |
C |
T |
11: 119,208,115 (GRCm39) |
R62C |
probably damaging |
Het |
Cc2d2a |
A |
G |
5: 43,887,383 (GRCm39) |
N1271S |
probably benign |
Het |
Ccpg1 |
G |
A |
9: 72,920,326 (GRCm39) |
S647N |
probably benign |
Het |
Cdv3 |
T |
C |
9: 103,232,429 (GRCm39) |
K133R |
possibly damaging |
Het |
Cep128 |
A |
C |
12: 90,966,345 (GRCm39) |
S1087R |
probably benign |
Het |
Cep70 |
T |
A |
9: 99,163,128 (GRCm39) |
L325Q |
probably damaging |
Het |
Chit1 |
T |
G |
1: 134,077,192 (GRCm39) |
F332V |
probably damaging |
Het |
Chodl |
C |
A |
16: 78,743,585 (GRCm39) |
T219K |
probably damaging |
Het |
Cntn4 |
T |
C |
6: 106,158,765 (GRCm39) |
L10P |
possibly damaging |
Het |
Copg1 |
G |
T |
6: 87,867,189 (GRCm39) |
M87I |
possibly damaging |
Het |
Cplane1 |
G |
A |
15: 8,223,897 (GRCm39) |
G887R |
probably damaging |
Het |
Cyp3a59 |
A |
G |
5: 146,022,578 (GRCm39) |
Y28C |
probably benign |
Het |
Dchs1 |
A |
C |
7: 105,407,236 (GRCm39) |
V2119G |
probably damaging |
Het |
Dedd |
T |
C |
1: 171,165,951 (GRCm39) |
L23P |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,286,041 (GRCm39) |
S2715P |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,920,182 (GRCm39) |
N2237S |
probably damaging |
Het |
Drosha |
A |
G |
15: 12,842,207 (GRCm39) |
I337V |
probably benign |
Het |
Duox2 |
A |
G |
2: 122,125,617 (GRCm39) |
V330A |
probably benign |
Het |
Dusp11 |
T |
C |
6: 85,924,587 (GRCm39) |
*322W |
probably null |
Het |
Dusp8 |
T |
A |
7: 141,643,730 (GRCm39) |
Q61L |
possibly damaging |
Het |
Ears2 |
G |
C |
7: 121,643,600 (GRCm39) |
T426S |
probably benign |
Het |
Elmo1 |
T |
C |
13: 20,784,380 (GRCm39) |
Y646H |
probably benign |
Het |
Eps15 |
T |
A |
4: 109,178,422 (GRCm39) |
I220K |
possibly damaging |
Het |
Faap100 |
T |
A |
11: 120,268,458 (GRCm39) |
E105V |
possibly damaging |
Het |
Fam171a2 |
C |
A |
11: 102,328,693 (GRCm39) |
V689L |
possibly damaging |
Het |
Fam91a1 |
G |
A |
15: 58,320,243 (GRCm39) |
S645N |
probably benign |
Het |
Fancg |
G |
A |
4: 43,007,076 (GRCm39) |
Q234* |
probably null |
Het |
Garre1 |
A |
G |
7: 33,941,813 (GRCm39) |
F120L |
probably damaging |
Het |
Gid4 |
T |
A |
11: 60,323,268 (GRCm39) |
|
probably null |
Het |
Gm7361 |
A |
C |
5: 26,463,903 (GRCm39) |
T53P |
probably benign |
Het |
Golgb1 |
T |
A |
16: 36,732,677 (GRCm39) |
C641* |
probably null |
Het |
Gon4l |
T |
A |
3: 88,765,803 (GRCm39) |
M409K |
probably benign |
Het |
Gpatch8 |
A |
T |
11: 102,399,053 (GRCm39) |
|
probably null |
Het |
Gpr156 |
T |
A |
16: 37,768,671 (GRCm39) |
V64E |
possibly damaging |
Het |
Grid2 |
T |
A |
6: 63,908,089 (GRCm39) |
I243K |
probably damaging |
Het |
Gucy2g |
G |
A |
19: 55,203,548 (GRCm39) |
A750V |
probably damaging |
Het |
Hdac5 |
T |
C |
11: 102,092,967 (GRCm39) |
E590G |
possibly damaging |
Het |
Herc3 |
T |
A |
6: 58,851,263 (GRCm39) |
M504K |
probably damaging |
Het |
Hif1a |
A |
G |
12: 73,990,867 (GRCm39) |
E713G |
probably benign |
Het |
Hmx3 |
A |
G |
7: 131,146,033 (GRCm39) |
D247G |
probably damaging |
Het |
Hoxd11 |
G |
T |
2: 74,513,163 (GRCm39) |
E143* |
probably null |
Het |
Ifitm3 |
T |
C |
7: 140,590,554 (GRCm39) |
N2S |
probably benign |
Het |
Il17f |
T |
C |
1: 20,848,181 (GRCm39) |
Q99R |
probably benign |
Het |
Itga6 |
T |
A |
2: 71,671,494 (GRCm39) |
S341R |
probably damaging |
Het |
Itgam |
A |
G |
7: 127,707,152 (GRCm39) |
N661S |
probably benign |
Het |
Jag1 |
A |
T |
2: 136,937,464 (GRCm39) |
H303Q |
possibly damaging |
Het |
Kcnh8 |
T |
A |
17: 53,033,023 (GRCm39) |
N103K |
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,291,636 (GRCm39) |
|
probably benign |
Het |
Keg1 |
A |
C |
19: 12,691,902 (GRCm39) |
N63T |
probably damaging |
Het |
Klf12 |
T |
A |
14: 100,137,595 (GRCm39) |
H317L |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,427,983 (GRCm39) |
V530E |
probably damaging |
Het |
Mrgpra6 |
A |
G |
7: 46,838,629 (GRCm39) |
C190R |
probably damaging |
Het |
Myo1a |
G |
T |
10: 127,541,766 (GRCm39) |
E102* |
probably null |
Het |
Napa |
A |
T |
7: 15,850,397 (GRCm39) |
E265D |
probably benign |
Het |
Ncam1 |
A |
C |
9: 49,476,174 (GRCm39) |
V305G |
probably damaging |
Het |
Nek8 |
T |
C |
11: 78,061,263 (GRCm39) |
|
probably null |
Het |
Or10ag53 |
C |
T |
2: 87,082,827 (GRCm39) |
P182L |
probably benign |
Het |
Or11g24 |
T |
A |
14: 50,662,846 (GRCm39) |
V290E |
possibly damaging |
Het |
Or4a70 |
G |
T |
2: 89,324,481 (GRCm39) |
Y58* |
probably null |
Het |
Or4f52 |
T |
C |
2: 111,061,539 (GRCm39) |
T200A |
probably benign |
Het |
Or52a20 |
T |
C |
7: 103,366,562 (GRCm39) |
F254L |
probably benign |
Het |
Or5ak4 |
T |
C |
2: 85,161,979 (GRCm39) |
T88A |
probably benign |
Het |
Or5h23 |
T |
A |
16: 58,906,253 (GRCm39) |
M198L |
probably benign |
Het |
Or8c11 |
A |
T |
9: 38,289,281 (GRCm39) |
I29F |
probably benign |
Het |
Or8g2b |
A |
G |
9: 39,751,126 (GRCm39) |
Y132C |
possibly damaging |
Het |
Pabpc4 |
A |
G |
4: 123,188,790 (GRCm39) |
Q417R |
probably benign |
Het |
Panx3 |
A |
T |
9: 37,580,320 (GRCm39) |
M11K |
probably damaging |
Het |
Pcbp1 |
C |
T |
6: 86,502,471 (GRCm39) |
E143K |
probably damaging |
Het |
Pdcd7 |
G |
A |
9: 65,265,974 (GRCm39) |
W477* |
probably null |
Het |
Pi4k2a |
G |
A |
19: 42,078,954 (GRCm39) |
S5N |
probably damaging |
Het |
Plag1 |
T |
A |
4: 3,904,075 (GRCm39) |
Q372L |
probably benign |
Het |
Plce1 |
C |
A |
19: 38,748,535 (GRCm39) |
N1755K |
probably damaging |
Het |
Pld4 |
G |
T |
12: 112,730,422 (GRCm39) |
E102* |
probably null |
Het |
Pnlip |
A |
G |
19: 58,668,039 (GRCm39) |
N345S |
probably benign |
Het |
Ppm1e |
A |
T |
11: 87,249,377 (GRCm39) |
L118Q |
possibly damaging |
Het |
Prkra |
T |
G |
2: 76,469,622 (GRCm39) |
T146P |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,386,625 (GRCm39) |
D1038G |
probably damaging |
Het |
Prss51 |
T |
A |
14: 64,334,543 (GRCm39) |
V108E |
probably damaging |
Het |
Prxl2b |
T |
A |
4: 154,983,462 (GRCm39) |
M1L |
probably benign |
Het |
Ptch1 |
A |
G |
13: 63,692,857 (GRCm39) |
Y181H |
probably damaging |
Het |
Reln |
A |
G |
5: 22,244,527 (GRCm39) |
V817A |
probably benign |
Het |
Rictor |
C |
A |
15: 6,818,985 (GRCm39) |
Q1403K |
probably benign |
Het |
Rims1 |
T |
A |
1: 22,482,469 (GRCm39) |
I882F |
probably damaging |
Het |
Rnf19a |
A |
G |
15: 36,242,185 (GRCm39) |
V618A |
probably benign |
Het |
Ryr1 |
A |
T |
7: 28,816,841 (GRCm39) |
I65N |
probably damaging |
Het |
S1pr2 |
T |
C |
9: 20,878,890 (GRCm39) |
T313A |
probably benign |
Het |
Serpine2 |
A |
T |
1: 79,799,004 (GRCm39) |
Y83* |
probably null |
Het |
Sfi1 |
A |
ATCTTCCCAAAGCCAGTGC |
11: 3,103,384 (GRCm39) |
|
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,772,256 (GRCm39) |
V215A |
probably benign |
Het |
Sgsm3 |
T |
C |
15: 80,892,200 (GRCm39) |
V256A |
probably benign |
Het |
Shroom4 |
T |
A |
X: 6,497,523 (GRCm39) |
C894* |
probably null |
Het |
Slc28a2b |
C |
A |
2: 122,353,259 (GRCm39) |
L480I |
probably benign |
Het |
Slc4a10 |
A |
T |
2: 62,120,402 (GRCm39) |
E843V |
probably damaging |
Het |
Smyd4 |
T |
A |
11: 75,280,982 (GRCm39) |
C152S |
probably damaging |
Het |
Snx10 |
T |
C |
6: 51,552,952 (GRCm39) |
Y32H |
probably damaging |
Het |
Sorl1 |
T |
C |
9: 41,968,580 (GRCm39) |
T558A |
possibly damaging |
Het |
Spata31d1b |
G |
A |
13: 59,866,866 (GRCm39) |
C1338Y |
possibly damaging |
Het |
Sppl2c |
T |
A |
11: 104,078,127 (GRCm39) |
I309K |
possibly damaging |
Het |
Stard9 |
A |
G |
2: 120,531,111 (GRCm39) |
E2456G |
probably damaging |
Het |
Stx1b |
A |
T |
7: 127,414,575 (GRCm39) |
D16E |
probably benign |
Het |
Tecpr2 |
T |
C |
12: 110,881,887 (GRCm39) |
V152A |
probably damaging |
Het |
Tedc1 |
T |
C |
12: 113,120,302 (GRCm39) |
V47A |
probably benign |
Het |
Tep1 |
A |
T |
14: 51,105,774 (GRCm39) |
L82Q |
probably damaging |
Het |
Tgm4 |
A |
G |
9: 122,885,559 (GRCm39) |
Y367C |
probably damaging |
Het |
Tle1 |
C |
T |
4: 72,060,081 (GRCm39) |
V258M |
probably damaging |
Het |
Tm9sf1 |
C |
T |
14: 55,880,301 (GRCm39) |
G32D |
possibly damaging |
Het |
Tmco2 |
A |
G |
4: 120,963,181 (GRCm39) |
L106P |
probably damaging |
Het |
Tmem131 |
A |
T |
1: 36,911,639 (GRCm39) |
C103S |
possibly damaging |
Het |
Tmprss7 |
T |
A |
16: 45,489,891 (GRCm39) |
I444F |
possibly damaging |
Het |
Trank1 |
T |
C |
9: 111,191,470 (GRCm39) |
V493A |
probably benign |
Het |
Trim80 |
A |
T |
11: 115,338,843 (GRCm39) |
T558S |
probably benign |
Het |
Trmt6 |
C |
A |
2: 132,650,703 (GRCm39) |
A302S |
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,133,985 (GRCm39) |
W1067R |
probably damaging |
Het |
Tulp4 |
T |
A |
17: 6,286,568 (GRCm39) |
V1532D |
probably damaging |
Het |
Ubqlnl |
T |
G |
7: 103,798,424 (GRCm39) |
I358L |
probably benign |
Het |
Ulk3 |
T |
A |
9: 57,498,023 (GRCm39) |
I108N |
possibly damaging |
Het |
Vps13b |
A |
T |
15: 35,640,674 (GRCm39) |
|
probably null |
Het |
Vwa3a |
A |
G |
7: 120,389,365 (GRCm39) |
K68E |
possibly damaging |
Het |
Zfp746 |
G |
T |
6: 48,041,110 (GRCm39) |
H538N |
possibly damaging |
Het |
|
Other mutations in Slc14a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Slc14a2
|
APN |
18 |
78,193,653 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL00763:Slc14a2
|
APN |
18 |
78,235,453 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01359:Slc14a2
|
APN |
18 |
78,197,323 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01400:Slc14a2
|
APN |
18 |
78,235,428 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01450:Slc14a2
|
APN |
18 |
78,226,745 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01469:Slc14a2
|
APN |
18 |
78,198,781 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02231:Slc14a2
|
APN |
18 |
78,252,236 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02340:Slc14a2
|
APN |
18 |
78,206,341 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02542:Slc14a2
|
APN |
18 |
78,252,302 (GRCm39) |
missense |
probably benign |
|
xi_ning
|
UTSW |
18 |
78,238,962 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02991:Slc14a2
|
UTSW |
18 |
78,249,049 (GRCm39) |
start codon destroyed |
probably null |
0.77 |
R0131:Slc14a2
|
UTSW |
18 |
78,235,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Slc14a2
|
UTSW |
18 |
78,235,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0132:Slc14a2
|
UTSW |
18 |
78,235,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Slc14a2
|
UTSW |
18 |
78,200,394 (GRCm39) |
nonsense |
probably null |
|
R1677:Slc14a2
|
UTSW |
18 |
78,206,419 (GRCm39) |
missense |
probably benign |
|
R1749:Slc14a2
|
UTSW |
18 |
78,190,295 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2014:Slc14a2
|
UTSW |
18 |
78,193,601 (GRCm39) |
splice site |
probably benign |
|
R2034:Slc14a2
|
UTSW |
18 |
78,226,798 (GRCm39) |
missense |
probably damaging |
0.99 |
R2264:Slc14a2
|
UTSW |
18 |
78,206,304 (GRCm39) |
splice site |
probably benign |
|
R2278:Slc14a2
|
UTSW |
18 |
78,203,159 (GRCm39) |
missense |
probably benign |
0.01 |
R2920:Slc14a2
|
UTSW |
18 |
78,201,512 (GRCm39) |
nonsense |
probably null |
|
R3878:Slc14a2
|
UTSW |
18 |
78,202,289 (GRCm39) |
missense |
probably benign |
|
R4086:Slc14a2
|
UTSW |
18 |
78,248,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R4237:Slc14a2
|
UTSW |
18 |
78,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4238:Slc14a2
|
UTSW |
18 |
78,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4239:Slc14a2
|
UTSW |
18 |
78,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:Slc14a2
|
UTSW |
18 |
78,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4373:Slc14a2
|
UTSW |
18 |
78,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4375:Slc14a2
|
UTSW |
18 |
78,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4376:Slc14a2
|
UTSW |
18 |
78,250,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4440:Slc14a2
|
UTSW |
18 |
78,238,962 (GRCm39) |
missense |
probably benign |
0.01 |
R4551:Slc14a2
|
UTSW |
18 |
78,239,068 (GRCm39) |
missense |
probably benign |
0.02 |
R4636:Slc14a2
|
UTSW |
18 |
78,239,007 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4749:Slc14a2
|
UTSW |
18 |
78,198,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Slc14a2
|
UTSW |
18 |
78,235,403 (GRCm39) |
missense |
probably damaging |
0.97 |
R4983:Slc14a2
|
UTSW |
18 |
78,193,616 (GRCm39) |
missense |
probably damaging |
0.98 |
R5114:Slc14a2
|
UTSW |
18 |
78,238,963 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5164:Slc14a2
|
UTSW |
18 |
78,200,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R5433:Slc14a2
|
UTSW |
18 |
78,252,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5558:Slc14a2
|
UTSW |
18 |
78,202,381 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5571:Slc14a2
|
UTSW |
18 |
78,252,282 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5693:Slc14a2
|
UTSW |
18 |
78,190,229 (GRCm39) |
missense |
probably benign |
0.23 |
R5715:Slc14a2
|
UTSW |
18 |
78,201,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Slc14a2
|
UTSW |
18 |
78,252,257 (GRCm39) |
missense |
probably benign |
0.06 |
R6160:Slc14a2
|
UTSW |
18 |
78,202,190 (GRCm39) |
critical splice donor site |
probably null |
|
R6352:Slc14a2
|
UTSW |
18 |
78,252,309 (GRCm39) |
start codon destroyed |
probably null |
|
R6380:Slc14a2
|
UTSW |
18 |
78,190,190 (GRCm39) |
missense |
probably benign |
0.00 |
R6444:Slc14a2
|
UTSW |
18 |
78,197,317 (GRCm39) |
missense |
probably damaging |
0.98 |
R6480:Slc14a2
|
UTSW |
18 |
78,202,297 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6732:Slc14a2
|
UTSW |
18 |
78,235,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R7038:Slc14a2
|
UTSW |
18 |
78,202,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R7553:Slc14a2
|
UTSW |
18 |
78,198,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Slc14a2
|
UTSW |
18 |
78,235,334 (GRCm39) |
missense |
probably benign |
0.07 |
R7617:Slc14a2
|
UTSW |
18 |
78,203,156 (GRCm39) |
missense |
probably benign |
|
R7693:Slc14a2
|
UTSW |
18 |
78,197,218 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7874:Slc14a2
|
UTSW |
18 |
78,203,983 (GRCm39) |
missense |
probably benign |
0.01 |
R8144:Slc14a2
|
UTSW |
18 |
78,227,759 (GRCm39) |
critical splice donor site |
probably null |
|
R9205:Slc14a2
|
UTSW |
18 |
78,238,951 (GRCm39) |
missense |
probably benign |
0.19 |
R9356:Slc14a2
|
UTSW |
18 |
78,227,823 (GRCm39) |
missense |
probably null |
0.02 |
Z1088:Slc14a2
|
UTSW |
18 |
78,238,995 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Slc14a2
|
UTSW |
18 |
78,200,584 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1176:Slc14a2
|
UTSW |
18 |
78,200,583 (GRCm39) |
missense |
probably damaging |
1.00 |
|