Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
A |
10: 79,844,821 (GRCm39) |
N1514K |
probably damaging |
Het |
Abcb4 |
G |
T |
5: 8,984,219 (GRCm39) |
G650* |
probably null |
Het |
Acsbg1 |
T |
A |
9: 54,535,751 (GRCm39) |
|
probably null |
Het |
Alms1 |
A |
T |
6: 85,605,717 (GRCm39) |
K2456* |
probably null |
Het |
Alppl2 |
A |
T |
1: 87,016,184 (GRCm39) |
M225K |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,737,206 (GRCm39) |
V2806I |
probably benign |
Het |
Atxn10 |
A |
T |
15: 85,346,612 (GRCm39) |
I457F |
probably benign |
Het |
Cad |
G |
T |
5: 31,224,144 (GRCm39) |
M800I |
probably null |
Het |
Carmil3 |
T |
A |
14: 55,737,889 (GRCm39) |
L815Q |
probably damaging |
Het |
Ccz1 |
A |
G |
5: 143,940,859 (GRCm39) |
|
probably null |
Het |
Cdc73 |
G |
A |
1: 143,567,211 (GRCm39) |
T104I |
probably benign |
Het |
Cfap52 |
A |
T |
11: 67,829,780 (GRCm39) |
C330S |
possibly damaging |
Het |
Clec16a |
C |
T |
16: 10,512,712 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
A |
G |
6: 102,254,178 (GRCm39) |
|
probably null |
Het |
Crocc2 |
A |
G |
1: 93,141,360 (GRCm39) |
K1171R |
possibly damaging |
Het |
Ctsa |
T |
C |
2: 164,676,281 (GRCm39) |
V86A |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Ddhd2 |
A |
G |
8: 26,242,144 (GRCm39) |
F244L |
probably benign |
Het |
Ddn |
A |
G |
15: 98,703,735 (GRCm39) |
V519A |
possibly damaging |
Het |
Dip2b |
G |
T |
15: 100,060,583 (GRCm39) |
V253L |
probably benign |
Het |
Dnah17 |
C |
A |
11: 118,017,148 (GRCm39) |
W197C |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 118,017,150 (GRCm39) |
W197R |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 118,017,149 (GRCm39) |
W197* |
probably null |
Het |
Ercc6 |
T |
A |
14: 32,279,813 (GRCm39) |
D609E |
probably benign |
Het |
Erg |
C |
A |
16: 95,181,100 (GRCm39) |
R147L |
probably damaging |
Het |
Fbxo41 |
A |
T |
6: 85,455,537 (GRCm39) |
L549H |
probably damaging |
Het |
Foxd4 |
A |
G |
19: 24,876,968 (GRCm39) |
S411P |
probably benign |
Het |
Gaa |
C |
A |
11: 119,171,997 (GRCm39) |
A700D |
probably benign |
Het |
Galntl6 |
T |
A |
8: 58,337,515 (GRCm39) |
D135V |
probably damaging |
Het |
Gm1043 |
G |
C |
5: 37,331,816 (GRCm39) |
G832A |
probably benign |
Het |
Gm21103 |
C |
T |
14: 17,484,841 (GRCm39) |
E68K |
probably damaging |
Het |
Gpam |
A |
G |
19: 55,071,838 (GRCm39) |
V301A |
probably benign |
Het |
H2-M10.1 |
T |
A |
17: 36,634,994 (GRCm39) |
I304F |
unknown |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Jak3 |
C |
A |
8: 72,131,954 (GRCm39) |
Q177K |
probably benign |
Het |
Kcnu1 |
G |
A |
8: 26,341,919 (GRCm39) |
R88H |
probably damaging |
Het |
Kng1 |
A |
T |
16: 22,877,371 (GRCm39) |
I60F |
possibly damaging |
Het |
Krt77 |
A |
T |
15: 101,772,807 (GRCm39) |
Y257* |
probably null |
Het |
Lcor |
A |
T |
19: 41,570,809 (GRCm39) |
S1C |
probably null |
Het |
Lcor |
G |
T |
19: 41,570,810 (GRCm39) |
S1I |
possibly damaging |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Map4k5 |
C |
A |
12: 69,878,336 (GRCm39) |
R355L |
probably benign |
Het |
Mefv |
C |
T |
16: 3,530,898 (GRCm39) |
R498H |
probably benign |
Het |
Mical3 |
A |
T |
6: 120,985,991 (GRCm39) |
L150Q |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,650,536 (GRCm39) |
Q1340L |
probably damaging |
Het |
Nfic |
A |
T |
10: 81,256,351 (GRCm39) |
C126* |
probably null |
Het |
Nisch |
T |
A |
14: 30,899,085 (GRCm39) |
|
probably benign |
Het |
Nt5dc3 |
A |
G |
10: 86,647,395 (GRCm39) |
Y130C |
probably damaging |
Het |
Or2ag1b |
A |
T |
7: 106,288,079 (GRCm39) |
N286K |
probably damaging |
Het |
Or4f15 |
C |
T |
2: 111,814,396 (GRCm39) |
V8I |
probably benign |
Het |
Or6c65 |
C |
A |
10: 129,603,389 (GRCm39) |
T8K |
probably benign |
Het |
Pcdhb12 |
T |
C |
18: 37,569,892 (GRCm39) |
V346A |
probably benign |
Het |
Pla2g4a |
A |
G |
1: 149,733,238 (GRCm39) |
S504P |
probably benign |
Het |
Plin2 |
G |
T |
4: 86,575,526 (GRCm39) |
A341D |
probably damaging |
Het |
Plxnb2 |
A |
T |
15: 89,049,494 (GRCm39) |
I575N |
probably benign |
Het |
Pnma8b |
T |
G |
7: 16,680,158 (GRCm39) |
W381G |
probably benign |
Het |
Psma8 |
A |
G |
18: 14,854,324 (GRCm39) |
D68G |
probably damaging |
Het |
Rcor3 |
G |
A |
1: 191,808,559 (GRCm39) |
H207Y |
probably benign |
Het |
Rwdd2b |
C |
A |
16: 87,231,356 (GRCm39) |
G266V |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,490,449 (GRCm39) |
F3795S |
probably damaging |
Het |
Sord |
T |
A |
2: 122,089,613 (GRCm39) |
|
probably null |
Het |
Spdl1 |
T |
A |
11: 34,710,713 (GRCm39) |
N345I |
probably damaging |
Het |
St8sia2 |
T |
A |
7: 73,626,441 (GRCm39) |
R42S |
possibly damaging |
Het |
Syt9 |
G |
T |
7: 107,035,717 (GRCm39) |
V245F |
possibly damaging |
Het |
Tbpl2 |
T |
A |
2: 23,984,898 (GRCm39) |
N82I |
possibly damaging |
Het |
Tcerg1 |
T |
A |
18: 42,686,530 (GRCm39) |
Y696N |
probably damaging |
Het |
Thsd7b |
A |
G |
1: 129,595,655 (GRCm39) |
T492A |
probably benign |
Het |
Timm13 |
A |
C |
10: 80,736,135 (GRCm39) |
|
probably benign |
Het |
Trdmt1 |
T |
A |
2: 13,524,870 (GRCm39) |
Q195L |
probably benign |
Het |
Ttc27 |
T |
A |
17: 75,165,086 (GRCm39) |
V764D |
probably damaging |
Het |
Ttc39d |
C |
A |
17: 80,524,076 (GRCm39) |
S245* |
probably null |
Het |
Ttc41 |
A |
G |
10: 86,567,023 (GRCm39) |
E563G |
probably benign |
Het |
Ttc41 |
A |
T |
10: 86,569,571 (GRCm39) |
T650S |
probably benign |
Het |
U2surp |
A |
C |
9: 95,358,210 (GRCm39) |
L723R |
probably damaging |
Het |
Ubqln3 |
G |
A |
7: 103,791,524 (GRCm39) |
Q189* |
probably null |
Het |
Vezf1 |
A |
G |
11: 87,972,326 (GRCm39) |
N229S |
probably damaging |
Het |
Vmn2r79 |
T |
A |
7: 86,686,365 (GRCm39) |
M582K |
probably benign |
Het |
Zfp518a |
A |
G |
19: 40,902,567 (GRCm39) |
D832G |
probably benign |
Het |
Zfyve28 |
T |
C |
5: 34,356,216 (GRCm39) |
N762D |
probably damaging |
Het |
|
Other mutations in Slc28a2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00964:Slc28a2b
|
APN |
2 |
122,347,527 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01160:Slc28a2b
|
APN |
2 |
122,355,277 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01838:Slc28a2b
|
APN |
2 |
122,348,464 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01895:Slc28a2b
|
APN |
2 |
122,355,572 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02999:Slc28a2b
|
APN |
2 |
122,344,995 (GRCm39) |
splice site |
probably benign |
|
Wilted
|
UTSW |
2 |
122,353,963 (GRCm39) |
missense |
probably damaging |
1.00 |
K2124:Slc28a2b
|
UTSW |
2 |
122,355,634 (GRCm39) |
missense |
probably benign |
0.00 |
R0084:Slc28a2b
|
UTSW |
2 |
122,353,314 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0092:Slc28a2b
|
UTSW |
2 |
122,348,078 (GRCm39) |
splice site |
probably benign |
|
R0127:Slc28a2b
|
UTSW |
2 |
122,347,550 (GRCm39) |
critical splice donor site |
probably null |
|
R0200:Slc28a2b
|
UTSW |
2 |
122,357,928 (GRCm39) |
makesense |
probably null |
|
R0276:Slc28a2b
|
UTSW |
2 |
122,352,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Slc28a2b
|
UTSW |
2 |
122,348,034 (GRCm39) |
missense |
probably benign |
0.04 |
R0403:Slc28a2b
|
UTSW |
2 |
122,352,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R0600:Slc28a2b
|
UTSW |
2 |
122,344,879 (GRCm39) |
missense |
probably damaging |
0.97 |
R0612:Slc28a2b
|
UTSW |
2 |
122,352,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R1676:Slc28a2b
|
UTSW |
2 |
122,352,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R1801:Slc28a2b
|
UTSW |
2 |
122,352,133 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1986:Slc28a2b
|
UTSW |
2 |
122,357,910 (GRCm39) |
missense |
probably benign |
0.00 |
R2050:Slc28a2b
|
UTSW |
2 |
122,353,349 (GRCm39) |
missense |
probably benign |
0.21 |
R3078:Slc28a2b
|
UTSW |
2 |
122,344,895 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4075:Slc28a2b
|
UTSW |
2 |
122,344,892 (GRCm39) |
missense |
probably benign |
0.00 |
R4096:Slc28a2b
|
UTSW |
2 |
122,353,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R4744:Slc28a2b
|
UTSW |
2 |
122,353,286 (GRCm39) |
nonsense |
probably null |
|
R4796:Slc28a2b
|
UTSW |
2 |
122,344,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R5033:Slc28a2b
|
UTSW |
2 |
122,353,395 (GRCm39) |
critical splice donor site |
probably null |
|
R5069:Slc28a2b
|
UTSW |
2 |
122,324,854 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5288:Slc28a2b
|
UTSW |
2 |
122,353,259 (GRCm39) |
missense |
probably benign |
0.01 |
R5385:Slc28a2b
|
UTSW |
2 |
122,353,259 (GRCm39) |
missense |
probably benign |
0.01 |
R5386:Slc28a2b
|
UTSW |
2 |
122,353,259 (GRCm39) |
missense |
probably benign |
0.01 |
R5442:Slc28a2b
|
UTSW |
2 |
122,317,350 (GRCm39) |
missense |
probably benign |
|
R5795:Slc28a2b
|
UTSW |
2 |
122,348,475 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6258:Slc28a2b
|
UTSW |
2 |
122,353,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Slc28a2b
|
UTSW |
2 |
122,355,288 (GRCm39) |
missense |
probably benign |
0.00 |
R7226:Slc28a2b
|
UTSW |
2 |
122,353,013 (GRCm39) |
missense |
probably benign |
0.00 |
R7574:Slc28a2b
|
UTSW |
2 |
122,353,325 (GRCm39) |
missense |
not run |
|
R7633:Slc28a2b
|
UTSW |
2 |
122,317,161 (GRCm39) |
missense |
probably null |
0.05 |
R7705:Slc28a2b
|
UTSW |
2 |
122,352,110 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7726:Slc28a2b
|
UTSW |
2 |
122,317,214 (GRCm39) |
missense |
probably damaging |
0.99 |
R7998:Slc28a2b
|
UTSW |
2 |
122,324,839 (GRCm39) |
missense |
probably damaging |
0.97 |
R8269:Slc28a2b
|
UTSW |
2 |
122,352,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8337:Slc28a2b
|
UTSW |
2 |
122,355,617 (GRCm39) |
missense |
probably benign |
0.06 |
R8546:Slc28a2b
|
UTSW |
2 |
122,353,235 (GRCm39) |
missense |
probably benign |
0.14 |
R8817:Slc28a2b
|
UTSW |
2 |
122,348,988 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8931:Slc28a2b
|
UTSW |
2 |
122,348,983 (GRCm39) |
missense |
|
|
R9070:Slc28a2b
|
UTSW |
2 |
122,352,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R9542:Slc28a2b
|
UTSW |
2 |
122,324,822 (GRCm39) |
missense |
probably benign |
0.26 |
R9702:Slc28a2b
|
UTSW |
2 |
122,354,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R9782:Slc28a2b
|
UTSW |
2 |
122,352,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|