Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Accsl |
T |
C |
2: 93,699,498 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
T |
A |
13: 81,530,472 (GRCm39) |
K5867N |
possibly damaging |
Het |
Adh1 |
T |
A |
3: 137,988,571 (GRCm39) |
Y181* |
probably null |
Het |
Agbl2 |
T |
C |
2: 90,631,458 (GRCm39) |
V272A |
possibly damaging |
Het |
Akap13 |
T |
C |
7: 75,354,275 (GRCm39) |
Y80H |
probably benign |
Het |
Amotl1 |
A |
T |
9: 14,526,063 (GRCm39) |
S6T |
probably benign |
Het |
Bicd1 |
T |
A |
6: 149,414,391 (GRCm39) |
V368E |
probably damaging |
Het |
Brinp2 |
G |
A |
1: 158,074,273 (GRCm39) |
T616I |
probably damaging |
Het |
Cacna1e |
T |
A |
1: 154,318,033 (GRCm39) |
I1450F |
probably damaging |
Het |
Camk2a |
A |
G |
18: 61,088,607 (GRCm39) |
|
probably null |
Het |
Ccdc125 |
A |
G |
13: 100,826,875 (GRCm39) |
E244G |
probably benign |
Het |
Cdh23 |
C |
T |
10: 60,166,995 (GRCm39) |
A1884T |
probably damaging |
Het |
Clcn1 |
T |
C |
6: 42,282,462 (GRCm39) |
I510T |
probably damaging |
Het |
Copb1 |
A |
T |
7: 113,831,432 (GRCm39) |
V572D |
probably benign |
Het |
Ctf1 |
AGCAAC |
A |
7: 127,316,180 (GRCm39) |
|
probably null |
Het |
Dnhd1 |
T |
A |
7: 105,354,179 (GRCm39) |
L3053Q |
probably damaging |
Het |
Ephb4 |
T |
A |
5: 137,361,564 (GRCm39) |
H531Q |
possibly damaging |
Het |
Fgl2 |
T |
A |
5: 21,580,790 (GRCm39) |
C377* |
probably null |
Het |
Frmd4a |
T |
C |
2: 4,608,711 (GRCm39) |
F860L |
probably damaging |
Het |
Gbp9 |
T |
C |
5: 105,229,091 (GRCm39) |
N519D |
probably benign |
Het |
Gm1110 |
A |
G |
9: 26,795,083 (GRCm39) |
S468P |
possibly damaging |
Het |
Gm4847 |
A |
T |
1: 166,462,541 (GRCm39) |
D316E |
probably damaging |
Het |
Gnas |
T |
C |
2: 174,185,089 (GRCm39) |
Y916H |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,816,079 (GRCm39) |
D1336G |
possibly damaging |
Het |
Herc2 |
G |
T |
7: 55,762,848 (GRCm39) |
G859V |
probably damaging |
Het |
Hydin |
G |
A |
8: 111,322,114 (GRCm39) |
D4589N |
probably damaging |
Het |
Itfg1 |
A |
T |
8: 86,490,875 (GRCm39) |
N351K |
possibly damaging |
Het |
Kcnd3 |
G |
A |
3: 105,572,863 (GRCm39) |
|
probably null |
Het |
Krt77 |
A |
T |
15: 101,769,779 (GRCm39) |
Y364N |
probably damaging |
Het |
Lcn4 |
C |
T |
2: 26,560,613 (GRCm39) |
|
probably null |
Het |
Lrrn1 |
T |
A |
6: 107,545,505 (GRCm39) |
H434Q |
probably benign |
Het |
Lrrtm2 |
A |
G |
18: 35,346,687 (GRCm39) |
I205T |
probably damaging |
Het |
Mepce |
G |
C |
5: 137,783,759 (GRCm39) |
P189R |
probably damaging |
Het |
Mfap1a |
T |
C |
2: 121,330,084 (GRCm39) |
K221E |
probably benign |
Het |
Myo7a |
A |
G |
7: 97,746,818 (GRCm39) |
|
probably null |
Het |
Ncbp3 |
T |
C |
11: 72,938,727 (GRCm39) |
M1T |
probably null |
Het |
Nck1 |
A |
T |
9: 100,379,369 (GRCm39) |
M294K |
probably benign |
Het |
Nr2f2 |
A |
T |
7: 70,010,056 (GRCm39) |
W8R |
probably damaging |
Het |
Or12e10 |
T |
A |
2: 87,640,187 (GRCm39) |
S8T |
possibly damaging |
Het |
Or1e20-ps1 |
T |
A |
11: 73,324,818 (GRCm39) |
Q78L |
unknown |
Het |
Or4c12b |
A |
T |
2: 89,647,553 (GRCm39) |
R288S |
probably damaging |
Het |
Or6ae1 |
T |
A |
7: 139,742,822 (GRCm39) |
I14F |
possibly damaging |
Het |
Or7e169 |
A |
G |
9: 19,757,816 (GRCm39) |
L33P |
possibly damaging |
Het |
Or8g18 |
T |
C |
9: 39,149,625 (GRCm39) |
T32A |
probably benign |
Het |
Or8j3c |
A |
T |
2: 86,253,707 (GRCm39) |
F104L |
probably damaging |
Het |
Pcdha1 |
A |
G |
18: 37,065,286 (GRCm39) |
K650R |
probably benign |
Het |
Pgm1 |
T |
A |
4: 99,841,242 (GRCm39) |
I532N |
probably damaging |
Het |
Pik3c2a |
T |
A |
7: 115,939,321 (GRCm39) |
K1672N |
probably benign |
Het |
Pou3f1 |
G |
A |
4: 124,552,835 (GRCm39) |
G446S |
probably benign |
Het |
Ppm1j |
T |
C |
3: 104,693,134 (GRCm39) |
I497T |
probably damaging |
Het |
Pprc1 |
C |
T |
19: 46,056,500 (GRCm39) |
Q1202* |
probably null |
Het |
Pramel30 |
T |
A |
4: 144,059,678 (GRCm39) |
I463N |
possibly damaging |
Het |
Prdm15 |
T |
C |
16: 97,607,704 (GRCm39) |
N713S |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,138,142 (GRCm39) |
T62A |
probably benign |
Het |
Rabl2 |
T |
A |
15: 89,474,631 (GRCm39) |
|
probably null |
Het |
Ranbp3l |
A |
T |
15: 9,037,176 (GRCm39) |
R149* |
probably null |
Het |
Resf1 |
T |
A |
6: 149,229,793 (GRCm39) |
Y946* |
probably null |
Het |
Rfx4 |
T |
A |
10: 84,674,050 (GRCm39) |
M1K |
probably null |
Het |
Ripk4 |
G |
T |
16: 97,547,098 (GRCm39) |
S388* |
probably null |
Het |
Rnft1 |
T |
G |
11: 86,377,065 (GRCm39) |
I43R |
possibly damaging |
Het |
Setbp1 |
A |
T |
18: 78,899,781 (GRCm39) |
F1295L |
probably damaging |
Het |
Sez6 |
A |
G |
11: 77,865,409 (GRCm39) |
D682G |
probably damaging |
Het |
Slc1a1 |
T |
C |
19: 28,812,734 (GRCm39) |
|
probably null |
Het |
Slc7a5 |
G |
T |
8: 122,613,616 (GRCm39) |
T312K |
probably benign |
Het |
Slco4c1 |
A |
T |
1: 96,799,643 (GRCm39) |
N64K |
probably benign |
Het |
Spata13 |
C |
T |
14: 60,929,849 (GRCm39) |
T469I |
probably benign |
Het |
Stxbp5 |
T |
A |
10: 9,687,754 (GRCm39) |
N440I |
probably benign |
Het |
Tas2r114 |
T |
A |
6: 131,666,746 (GRCm39) |
Q94L |
probably benign |
Het |
Tasor |
T |
A |
14: 27,186,271 (GRCm39) |
C823* |
probably null |
Het |
Tfr2 |
A |
G |
5: 137,575,769 (GRCm39) |
D295G |
possibly damaging |
Het |
Thap7 |
A |
G |
16: 17,348,152 (GRCm39) |
Y60H |
probably damaging |
Het |
Tjap1 |
G |
T |
17: 46,569,733 (GRCm39) |
P409H |
probably damaging |
Het |
Tmtc4 |
G |
A |
14: 123,209,204 (GRCm39) |
A147V |
probably benign |
Het |
Tpp2 |
T |
A |
1: 44,017,648 (GRCm39) |
S751T |
probably benign |
Het |
Tpra1 |
T |
C |
6: 88,887,221 (GRCm39) |
V193A |
probably benign |
Het |
Trafd1 |
T |
C |
5: 121,516,837 (GRCm39) |
N122S |
possibly damaging |
Het |
Vmn1r151 |
T |
A |
7: 22,199,096 (GRCm39) |
D3V |
probably benign |
Het |
Wdr20rt |
A |
G |
12: 65,272,825 (GRCm39) |
Y96C |
probably damaging |
Het |
Zfp507 |
A |
G |
7: 35,475,573 (GRCm39) |
V880A |
probably benign |
Het |
Zfp598 |
A |
G |
17: 24,896,568 (GRCm39) |
D215G |
probably damaging |
Het |
Zfp7 |
T |
C |
15: 76,775,484 (GRCm39) |
S509P |
probably damaging |
Het |
Zfp738 |
A |
T |
13: 67,817,635 (GRCm39) |
C785* |
probably null |
Het |
Zfp985 |
C |
T |
4: 147,667,999 (GRCm39) |
T289I |
probably damaging |
Het |
Zkscan6 |
T |
A |
11: 65,712,795 (GRCm39) |
Y243N |
probably damaging |
Het |
|
Other mutations in C1rl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02435:C1rl
|
APN |
6 |
124,485,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02549:C1rl
|
APN |
6 |
124,470,796 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02581:C1rl
|
APN |
6 |
124,470,113 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02642:C1rl
|
APN |
6 |
124,470,806 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02950:C1rl
|
APN |
6 |
124,485,820 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02980:C1rl
|
UTSW |
6 |
124,485,487 (GRCm39) |
missense |
probably benign |
0.00 |
R0699:C1rl
|
UTSW |
6 |
124,485,595 (GRCm39) |
missense |
probably benign |
0.14 |
R0848:C1rl
|
UTSW |
6 |
124,485,465 (GRCm39) |
missense |
probably benign |
0.29 |
R1221:C1rl
|
UTSW |
6 |
124,470,940 (GRCm39) |
missense |
probably benign |
0.43 |
R1654:C1rl
|
UTSW |
6 |
124,470,869 (GRCm39) |
missense |
probably damaging |
0.97 |
R1957:C1rl
|
UTSW |
6 |
124,486,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:C1rl
|
UTSW |
6 |
124,470,781 (GRCm39) |
missense |
probably benign |
0.01 |
R2120:C1rl
|
UTSW |
6 |
124,485,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R2262:C1rl
|
UTSW |
6 |
124,483,907 (GRCm39) |
missense |
probably damaging |
0.99 |
R2363:C1rl
|
UTSW |
6 |
124,486,069 (GRCm39) |
missense |
probably benign |
0.13 |
R3933:C1rl
|
UTSW |
6 |
124,485,781 (GRCm39) |
nonsense |
probably null |
|
R4824:C1rl
|
UTSW |
6 |
124,486,040 (GRCm39) |
nonsense |
probably null |
|
R5228:C1rl
|
UTSW |
6 |
124,485,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5414:C1rl
|
UTSW |
6 |
124,485,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:C1rl
|
UTSW |
6 |
124,470,147 (GRCm39) |
missense |
probably benign |
0.00 |
R6467:C1rl
|
UTSW |
6 |
124,485,535 (GRCm39) |
missense |
probably benign |
0.03 |
R6549:C1rl
|
UTSW |
6 |
124,485,487 (GRCm39) |
missense |
probably benign |
0.00 |
R6609:C1rl
|
UTSW |
6 |
124,485,583 (GRCm39) |
missense |
probably benign |
0.44 |
R6998:C1rl
|
UTSW |
6 |
124,485,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:C1rl
|
UTSW |
6 |
124,485,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:C1rl
|
UTSW |
6 |
124,470,844 (GRCm39) |
missense |
probably benign |
0.00 |
R8706:C1rl
|
UTSW |
6 |
124,470,191 (GRCm39) |
critical splice donor site |
probably null |
|
R9274:C1rl
|
UTSW |
6 |
124,485,483 (GRCm39) |
missense |
probably benign |
0.00 |
R9335:C1rl
|
UTSW |
6 |
124,482,341 (GRCm39) |
missense |
probably benign |
0.00 |
R9425:C1rl
|
UTSW |
6 |
124,485,322 (GRCm39) |
missense |
probably benign |
0.02 |
R9516:C1rl
|
UTSW |
6 |
124,485,802 (GRCm39) |
missense |
probably damaging |
0.96 |
R9523:C1rl
|
UTSW |
6 |
124,484,054 (GRCm39) |
missense |
probably benign |
|
Z1088:C1rl
|
UTSW |
6 |
124,485,701 (GRCm39) |
missense |
probably benign |
0.00 |
|