Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
G |
A |
19: 8,994,098 (GRCm39) |
M5127I |
probably benign |
Het |
Akr1c13 |
T |
C |
13: 4,244,111 (GRCm39) |
Y55H |
probably damaging |
Het |
Armh3 |
A |
T |
19: 45,922,307 (GRCm39) |
|
probably null |
Het |
Atp2b2 |
C |
T |
6: 113,750,349 (GRCm39) |
R625H |
probably damaging |
Het |
Bpifb2 |
T |
C |
2: 153,720,439 (GRCm39) |
V66A |
probably benign |
Het |
Ccdc33 |
T |
C |
9: 57,936,046 (GRCm39) |
T950A |
possibly damaging |
Het |
Ceacam19 |
A |
T |
7: 19,616,557 (GRCm39) |
|
probably null |
Het |
Ces1f |
A |
T |
8: 93,998,517 (GRCm39) |
Y160N |
possibly damaging |
Het |
Clca3a1 |
A |
C |
3: 144,710,615 (GRCm39) |
S863A |
probably benign |
Het |
Cntrl |
T |
A |
2: 35,045,291 (GRCm39) |
I781K |
possibly damaging |
Het |
Dock4 |
C |
T |
12: 40,754,480 (GRCm39) |
R490W |
probably damaging |
Het |
Evpl |
T |
A |
11: 116,118,549 (GRCm39) |
Q686L |
probably damaging |
Het |
Fbxw10 |
A |
G |
11: 62,738,282 (GRCm39) |
S59G |
probably benign |
Het |
Glb1l2 |
A |
G |
9: 26,681,047 (GRCm39) |
V218A |
possibly damaging |
Het |
Gpatch1 |
A |
T |
7: 34,980,801 (GRCm39) |
|
probably benign |
Het |
Grin2c |
G |
A |
11: 115,141,472 (GRCm39) |
P882L |
probably damaging |
Het |
H2-Ob |
C |
A |
17: 34,461,588 (GRCm39) |
T109N |
probably damaging |
Het |
Ipo8 |
A |
G |
6: 148,723,225 (GRCm39) |
V64A |
possibly damaging |
Het |
Jpt2 |
C |
A |
17: 25,167,647 (GRCm39) |
A101S |
probably benign |
Het |
Lamc1 |
C |
A |
1: 153,110,326 (GRCm39) |
Q1116H |
possibly damaging |
Het |
Lamc1 |
T |
C |
1: 153,110,358 (GRCm39) |
S1106G |
probably benign |
Het |
Lamc1 |
T |
G |
1: 153,110,341 (GRCm39) |
Q1111H |
probably damaging |
Het |
Large1 |
A |
G |
8: 73,775,107 (GRCm39) |
|
probably benign |
Het |
Lig4 |
A |
T |
8: 10,023,012 (GRCm39) |
V256E |
possibly damaging |
Het |
Mpz |
C |
A |
1: 170,986,343 (GRCm39) |
Q86K |
possibly damaging |
Het |
Mrps24 |
A |
G |
11: 5,654,684 (GRCm39) |
V90A |
possibly damaging |
Het |
Mtdh |
A |
G |
15: 34,116,528 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
C |
4: 148,547,367 (GRCm39) |
V450A |
probably benign |
Het |
Mycbpap |
A |
G |
11: 94,402,449 (GRCm39) |
|
probably null |
Het |
Myo6 |
T |
A |
9: 80,169,656 (GRCm39) |
|
probably benign |
Het |
Myom1 |
A |
T |
17: 71,428,131 (GRCm39) |
I1450F |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,532,634 (GRCm39) |
S1781T |
probably benign |
Het |
Nedd1 |
T |
C |
10: 92,555,476 (GRCm39) |
E3G |
probably damaging |
Het |
Nt5c3 |
T |
C |
6: 56,863,734 (GRCm39) |
T149A |
probably benign |
Het |
Or5p56 |
A |
G |
7: 107,589,740 (GRCm39) |
H56R |
probably benign |
Het |
Osbp2 |
G |
A |
11: 3,661,882 (GRCm39) |
|
probably benign |
Het |
Paip1 |
T |
C |
13: 119,566,854 (GRCm39) |
S54P |
possibly damaging |
Het |
Pole2 |
G |
A |
12: 69,254,703 (GRCm39) |
L381F |
probably benign |
Het |
Prdm14 |
G |
T |
1: 13,195,968 (GRCm39) |
A31E |
probably benign |
Het |
Ptpn14 |
C |
T |
1: 189,568,637 (GRCm39) |
|
probably benign |
Het |
Rims2 |
A |
G |
15: 39,543,021 (GRCm39) |
|
probably benign |
Het |
Rnf20 |
A |
G |
4: 49,638,197 (GRCm39) |
N103S |
possibly damaging |
Het |
Sema3g |
T |
A |
14: 30,942,861 (GRCm39) |
|
probably benign |
Het |
Slc30a6 |
T |
C |
17: 74,722,640 (GRCm39) |
S236P |
possibly damaging |
Het |
Slc5a1 |
T |
C |
5: 33,315,421 (GRCm39) |
|
probably benign |
Het |
Snx25 |
A |
T |
8: 46,577,119 (GRCm39) |
M1K |
probably null |
Het |
Synpo2 |
A |
G |
3: 122,906,835 (GRCm39) |
V827A |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trak2 |
A |
T |
1: 58,942,820 (GRCm39) |
M862K |
probably benign |
Het |
Trim42 |
A |
T |
9: 97,247,732 (GRCm39) |
H321Q |
probably damaging |
Het |
Twnk |
T |
C |
19: 44,998,693 (GRCm39) |
|
probably benign |
Het |
Tymp |
T |
C |
15: 89,259,021 (GRCm39) |
K221R |
probably damaging |
Het |
Uaca |
C |
A |
9: 60,779,341 (GRCm39) |
Q1243K |
possibly damaging |
Het |
Vwa8 |
T |
C |
14: 79,232,016 (GRCm39) |
|
probably benign |
Het |
Wnt4 |
C |
T |
4: 137,016,594 (GRCm39) |
R83W |
probably damaging |
Het |
Zfp820 |
T |
C |
17: 22,038,509 (GRCm39) |
D273G |
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,609,510 (GRCm39) |
Y738* |
probably null |
Het |
Zkscan4 |
A |
C |
13: 21,668,081 (GRCm39) |
E177D |
probably benign |
Het |
|
Other mutations in Cenpn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Cenpn
|
APN |
8 |
117,655,326 (GRCm39) |
splice site |
probably null |
|
IGL02084:Cenpn
|
APN |
8 |
117,667,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R0843:Cenpn
|
UTSW |
8 |
117,660,045 (GRCm39) |
missense |
probably benign |
0.09 |
R1166:Cenpn
|
UTSW |
8 |
117,652,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Cenpn
|
UTSW |
8 |
117,661,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Cenpn
|
UTSW |
8 |
117,661,536 (GRCm39) |
critical splice donor site |
probably null |
|
R4512:Cenpn
|
UTSW |
8 |
117,660,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R4513:Cenpn
|
UTSW |
8 |
117,660,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Cenpn
|
UTSW |
8 |
117,660,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R4865:Cenpn
|
UTSW |
8 |
117,661,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5969:Cenpn
|
UTSW |
8 |
117,667,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R6518:Cenpn
|
UTSW |
8 |
117,663,904 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6795:Cenpn
|
UTSW |
8 |
117,652,887 (GRCm39) |
missense |
probably benign |
0.02 |
R7143:Cenpn
|
UTSW |
8 |
117,663,966 (GRCm39) |
missense |
probably benign |
0.00 |
R7556:Cenpn
|
UTSW |
8 |
117,664,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R7961:Cenpn
|
UTSW |
8 |
117,663,976 (GRCm39) |
missense |
probably benign |
0.00 |
R8009:Cenpn
|
UTSW |
8 |
117,663,976 (GRCm39) |
missense |
probably benign |
0.00 |
R8172:Cenpn
|
UTSW |
8 |
117,658,333 (GRCm39) |
missense |
probably benign |
0.05 |
R9034:Cenpn
|
UTSW |
8 |
117,661,478 (GRCm39) |
missense |
probably benign |
0.22 |
R9196:Cenpn
|
UTSW |
8 |
117,658,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R9199:Cenpn
|
UTSW |
8 |
117,664,014 (GRCm39) |
critical splice donor site |
probably null |
|
R9534:Cenpn
|
UTSW |
8 |
117,661,474 (GRCm39) |
nonsense |
probably null |
|
R9574:Cenpn
|
UTSW |
8 |
117,660,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|