Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700016G14Rik |
T |
C |
13: 24,741,506 |
S78P |
probably benign |
Het |
Aars2 |
T |
A |
17: 45,508,961 |
Y221* |
probably null |
Het |
AC166344.1 |
T |
A |
14: 43,300,788 |
F97I |
|
Het |
Ankmy2 |
T |
C |
12: 36,196,312 |
S412P |
probably benign |
Het |
Ap1s3 |
T |
C |
1: 79,609,202 |
T144A |
probably benign |
Het |
Asb3 |
T |
A |
11: 30,998,501 |
L59* |
probably null |
Het |
Asxl3 |
G |
T |
18: 22,517,701 |
G916* |
probably null |
Het |
Asxl3 |
G |
C |
18: 22,517,702 |
G916A |
probably damaging |
Het |
Birc2 |
A |
C |
9: 7,818,761 |
F610V |
probably damaging |
Het |
Camk4 |
G |
A |
18: 33,107,943 |
|
probably null |
Het |
Ccdc162 |
A |
G |
10: 41,673,859 |
S343P |
probably benign |
Het |
Ccnk |
T |
A |
12: 108,186,475 |
L17Q |
probably damaging |
Het |
Cd59b |
G |
A |
2: 104,084,447 |
W63* |
probably null |
Het |
Chrm3 |
C |
T |
13: 9,877,801 |
V400I |
probably benign |
Het |
Crb1 |
C |
A |
1: 139,243,367 |
V762F |
probably damaging |
Het |
Cspp1 |
C |
T |
1: 10,088,936 |
T529I |
possibly damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,448,447 |
I71T |
possibly damaging |
Het |
Cyb561 |
C |
A |
11: 105,935,567 |
G90V |
probably damaging |
Het |
Cyld |
T |
A |
8: 88,744,892 |
D804E |
possibly damaging |
Het |
Dgkg |
T |
C |
16: 22,500,382 |
D643G |
probably damaging |
Het |
Dnah12 |
G |
A |
14: 26,778,912 |
|
probably null |
Het |
Dnah12 |
T |
G |
14: 26,801,413 |
I1953S |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,139,710 |
W848R |
probably damaging |
Het |
Dnah7c |
C |
T |
1: 46,533,208 |
T947M |
probably damaging |
Het |
Dnmt3c |
C |
A |
2: 153,714,952 |
|
probably null |
Het |
Dsp |
A |
T |
13: 38,179,073 |
Y443F |
probably damaging |
Het |
Espl1 |
T |
A |
15: 102,319,524 |
C1603* |
probably null |
Het |
Faiml |
G |
T |
9: 99,234,443 |
R65S |
probably benign |
Het |
Gfpt2 |
T |
C |
11: 49,804,955 |
I4T |
probably damaging |
Het |
Gm10376 |
T |
A |
14: 43,010,493 |
M179L |
probably benign |
Het |
Gm13084 |
A |
T |
4: 143,810,663 |
L366Q |
probably damaging |
Het |
Gm4302 |
T |
A |
10: 100,341,727 |
M291K |
unknown |
Het |
Gm8906 |
C |
T |
5: 11,505,231 |
P83S |
probably damaging |
Het |
Gnb1l |
T |
A |
16: 18,545,168 |
D154E |
probably benign |
Het |
Igkv10-94 |
T |
C |
6: 68,704,743 |
R38G |
possibly damaging |
Het |
Inmt |
A |
T |
6: 55,171,028 |
Y205* |
probably null |
Het |
Krba1 |
A |
G |
6: 48,416,299 |
Q1049R |
probably benign |
Het |
Lpxn |
T |
A |
19: 12,833,319 |
C376S |
probably damaging |
Het |
Lrrc52 |
T |
A |
1: 167,466,450 |
I89F |
probably damaging |
Het |
Map9 |
A |
T |
3: 82,363,458 |
T110S |
probably benign |
Het |
Mccc1 |
T |
C |
3: 35,995,818 |
Y75C |
probably damaging |
Het |
Mff |
T |
A |
1: 82,747,091 |
L203* |
probably null |
Het |
Micall1 |
C |
A |
15: 79,109,424 |
D47E |
unknown |
Het |
Mink1 |
T |
C |
11: 70,603,503 |
F243S |
probably damaging |
Het |
Mlycd |
C |
T |
8: 119,402,477 |
R228W |
probably damaging |
Het |
Msr1 |
A |
T |
8: 39,589,424 |
V370E |
possibly damaging |
Het |
Naip6 |
T |
C |
13: 100,300,419 |
E532G |
probably damaging |
Het |
Nepn |
G |
A |
10: 52,391,719 |
C27Y |
probably damaging |
Het |
Ninl |
T |
C |
2: 150,955,604 |
H592R |
probably benign |
Het |
Nr4a2 |
A |
G |
2: 57,112,249 |
M64T |
possibly damaging |
Het |
Olfr1279 |
T |
A |
2: 111,307,020 |
F272I |
probably benign |
Het |
Olfr484 |
T |
C |
7: 108,124,574 |
K230E |
probably damaging |
Het |
Oprm1 |
A |
T |
10: 6,830,203 |
I171F |
possibly damaging |
Het |
Pcbp1 |
A |
T |
6: 86,525,506 |
M137K |
possibly damaging |
Het |
Pcf11 |
A |
T |
7: 92,657,316 |
S1215T |
probably benign |
Het |
Pdlim5 |
A |
T |
3: 142,311,922 |
|
probably null |
Het |
Pecam1 |
T |
C |
11: 106,689,031 |
I402V |
probably damaging |
Het |
Pex12 |
T |
C |
11: 83,297,642 |
T176A |
probably benign |
Het |
Phf3 |
T |
C |
1: 30,831,109 |
K286R |
possibly damaging |
Het |
Pik3ap1 |
T |
A |
19: 41,332,321 |
D153V |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,584,978 |
|
probably null |
Het |
Plekhn1 |
A |
G |
4: 156,223,335 |
V378A |
probably benign |
Het |
Ptprm |
A |
T |
17: 66,944,288 |
D531E |
possibly damaging |
Het |
Pum2 |
A |
T |
12: 8,728,952 |
Q508L |
possibly damaging |
Het |
Rad54l |
A |
G |
4: 116,105,830 |
S324P |
probably damaging |
Het |
Recql5 |
C |
T |
11: 115,930,672 |
|
probably null |
Het |
Reln |
A |
T |
5: 21,976,596 |
V1763D |
possibly damaging |
Het |
Rp1 |
T |
C |
1: 4,348,168 |
N907S |
possibly damaging |
Het |
Scaf11 |
T |
A |
15: 96,420,328 |
N452Y |
possibly damaging |
Het |
Scgb2b3 |
T |
A |
7: 31,360,214 |
H45L |
possibly damaging |
Het |
Sim1 |
A |
G |
10: 50,895,927 |
T11A |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,616,714 |
M189K |
possibly damaging |
Het |
Slco2b1 |
C |
T |
7: 99,695,063 |
G10S |
probably null |
Het |
Stxbp3 |
A |
G |
3: 108,800,755 |
L410P |
probably damaging |
Het |
Sugct |
T |
C |
13: 17,302,009 |
N297D |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,233,409 |
I4132T |
probably benign |
Het |
Teddm1b |
A |
T |
1: 153,875,166 |
L240F |
probably damaging |
Het |
Tlr5 |
C |
A |
1: 182,975,523 |
D797E |
possibly damaging |
Het |
Tmprss13 |
G |
T |
9: 45,338,345 |
G327C |
probably damaging |
Het |
Tnrc18 |
G |
T |
5: 142,787,817 |
A419D |
|
Het |
Ttc28 |
T |
C |
5: 111,280,007 |
Y1790H |
probably damaging |
Het |
Vmn1r125 |
T |
G |
7: 21,272,402 |
M75R |
probably damaging |
Het |
Vwa3a |
T |
A |
7: 120,773,030 |
D276E |
possibly damaging |
Het |
Wdfy3 |
C |
T |
5: 101,915,437 |
V1322M |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,628,106 |
S872P |
possibly damaging |
Het |
Zc3h13 |
T |
C |
14: 75,321,721 |
S357P |
unknown |
Het |
|