Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
G |
A |
12: 55,126,768 (GRCm39) |
T32I |
probably benign |
Het |
4930486L24Rik |
T |
A |
13: 61,000,922 (GRCm39) |
I205L |
probably benign |
Het |
Aatk |
C |
T |
11: 119,901,508 (GRCm39) |
V963M |
probably damaging |
Het |
Adra1b |
C |
A |
11: 43,726,242 (GRCm39) |
R225L |
probably damaging |
Het |
Adrb1 |
T |
C |
19: 56,711,021 (GRCm39) |
V73A |
probably damaging |
Het |
Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
BC035947 |
G |
T |
1: 78,475,527 (GRCm39) |
P335Q |
possibly damaging |
Het |
Capn9 |
A |
G |
8: 125,342,924 (GRCm39) |
I635V |
probably benign |
Het |
Cep55 |
T |
A |
19: 38,046,374 (GRCm39) |
D42E |
probably benign |
Het |
Cftr |
T |
A |
6: 18,274,607 (GRCm39) |
Y878* |
probably null |
Het |
Clpb |
A |
T |
7: 101,312,866 (GRCm39) |
|
probably benign |
Het |
Cpeb3 |
T |
C |
19: 37,022,089 (GRCm39) |
I569V |
possibly damaging |
Het |
Cpne6 |
A |
T |
14: 55,752,701 (GRCm39) |
D297V |
probably damaging |
Het |
Ddhd1 |
T |
C |
14: 45,894,976 (GRCm39) |
T165A |
probably benign |
Het |
Fam98b |
T |
C |
2: 117,093,402 (GRCm39) |
|
probably null |
Het |
Frem2 |
T |
C |
3: 53,561,744 (GRCm39) |
N921S |
probably benign |
Het |
Gbf1 |
T |
A |
19: 46,260,211 (GRCm39) |
V1039E |
probably benign |
Het |
Gmip |
A |
G |
8: 70,266,436 (GRCm39) |
E212G |
probably damaging |
Het |
Gpcpd1 |
C |
T |
2: 132,379,758 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
A |
T |
5: 134,392,766 (GRCm39) |
N796K |
probably damaging |
Het |
Hadhb |
T |
C |
5: 30,360,247 (GRCm39) |
|
probably benign |
Het |
Itga4 |
T |
A |
2: 79,119,609 (GRCm39) |
S472T |
probably damaging |
Het |
Kcna4 |
G |
A |
2: 107,125,670 (GRCm39) |
E135K |
possibly damaging |
Het |
Kmt2c |
G |
T |
5: 25,480,737 (GRCm39) |
|
probably null |
Het |
Lama1 |
T |
C |
17: 68,091,020 (GRCm39) |
I1620T |
unknown |
Het |
Lins1 |
A |
G |
7: 66,363,902 (GRCm39) |
E594G |
probably benign |
Het |
Lrrc38 |
T |
A |
4: 143,096,364 (GRCm39) |
M225K |
probably benign |
Het |
Mphosph9 |
A |
G |
5: 124,399,090 (GRCm39) |
I975T |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 13,095,874 (GRCm39) |
F38S |
probably benign |
Het |
Myo1h |
G |
A |
5: 114,458,714 (GRCm39) |
G150R |
probably damaging |
Het |
Oas2 |
T |
G |
5: 120,876,863 (GRCm39) |
I391L |
possibly damaging |
Het |
Or4a70 |
T |
A |
2: 89,324,378 (GRCm39) |
R93* |
probably null |
Het |
Or5p72 |
T |
C |
7: 108,021,889 (GRCm39) |
I37T |
possibly damaging |
Het |
Or6c3b |
T |
A |
10: 129,527,391 (GRCm39) |
D173V |
possibly damaging |
Het |
Or7e178 |
T |
C |
9: 20,247,221 (GRCm39) |
D14G |
probably benign |
Het |
Pdcd5 |
T |
C |
7: 35,342,063 (GRCm39) |
T182A |
probably damaging |
Het |
Pdlim7 |
T |
C |
13: 55,656,810 (GRCm39) |
D48G |
probably damaging |
Het |
Polr3b |
A |
C |
10: 84,464,489 (GRCm39) |
|
probably null |
Het |
Psmd5 |
C |
T |
2: 34,747,649 (GRCm39) |
|
probably null |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Homo |
Sdhb |
T |
C |
4: 140,703,501 (GRCm39) |
Y208H |
probably damaging |
Het |
Serinc5 |
G |
A |
13: 92,842,740 (GRCm39) |
V397I |
possibly damaging |
Het |
Sik2 |
A |
T |
9: 50,909,834 (GRCm39) |
M73K |
possibly damaging |
Het |
Slc41a1 |
A |
G |
1: 131,770,487 (GRCm39) |
|
probably null |
Het |
Slco1a1 |
T |
C |
6: 141,882,213 (GRCm39) |
I119V |
probably benign |
Het |
Srd5a1 |
T |
C |
13: 69,759,418 (GRCm39) |
|
probably benign |
Het |
Stab2 |
T |
C |
10: 86,754,948 (GRCm39) |
I1111V |
probably benign |
Het |
Stxbp6 |
G |
T |
12: 44,949,779 (GRCm39) |
|
probably null |
Het |
Tbc1d19 |
A |
G |
5: 53,992,591 (GRCm39) |
|
probably null |
Het |
Tnxb |
A |
T |
17: 34,929,710 (GRCm39) |
T2815S |
probably benign |
Het |
Txnip |
T |
A |
3: 96,467,623 (GRCm39) |
I363N |
probably damaging |
Het |
Zfp442 |
A |
T |
2: 150,251,499 (GRCm39) |
N134K |
possibly damaging |
Het |
|
Other mutations in C2cd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00540:C2cd3
|
APN |
7 |
100,040,335 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01420:C2cd3
|
APN |
7 |
100,104,065 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01775:C2cd3
|
APN |
7 |
100,092,638 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01832:C2cd3
|
APN |
7 |
100,076,421 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01883:C2cd3
|
APN |
7 |
100,023,693 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02664:C2cd3
|
APN |
7 |
100,068,922 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02697:C2cd3
|
APN |
7 |
100,076,376 (GRCm39) |
unclassified |
probably benign |
|
IGL02852:C2cd3
|
APN |
7 |
100,079,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03158:C2cd3
|
APN |
7 |
100,023,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:C2cd3
|
UTSW |
7 |
100,067,729 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0012:C2cd3
|
UTSW |
7 |
100,067,729 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0013:C2cd3
|
UTSW |
7 |
100,065,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:C2cd3
|
UTSW |
7 |
100,065,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:C2cd3
|
UTSW |
7 |
100,093,652 (GRCm39) |
unclassified |
probably benign |
|
R0032:C2cd3
|
UTSW |
7 |
100,093,652 (GRCm39) |
unclassified |
probably benign |
|
R0124:C2cd3
|
UTSW |
7 |
100,118,725 (GRCm39) |
missense |
probably benign |
|
R0387:C2cd3
|
UTSW |
7 |
100,071,714 (GRCm39) |
splice site |
probably benign |
|
R0522:C2cd3
|
UTSW |
7 |
100,044,429 (GRCm39) |
missense |
probably benign |
0.14 |
R1124:C2cd3
|
UTSW |
7 |
100,071,888 (GRCm39) |
missense |
probably benign |
0.00 |
R1484:C2cd3
|
UTSW |
7 |
100,089,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:C2cd3
|
UTSW |
7 |
100,055,284 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1631:C2cd3
|
UTSW |
7 |
100,021,704 (GRCm39) |
critical splice donor site |
probably null |
|
R1875:C2cd3
|
UTSW |
7 |
100,056,232 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2059:C2cd3
|
UTSW |
7 |
100,104,700 (GRCm39) |
unclassified |
probably benign |
|
R2060:C2cd3
|
UTSW |
7 |
100,104,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R2348:C2cd3
|
UTSW |
7 |
100,062,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:C2cd3
|
UTSW |
7 |
100,044,459 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3405:C2cd3
|
UTSW |
7 |
100,039,373 (GRCm39) |
missense |
probably benign |
0.01 |
R3687:C2cd3
|
UTSW |
7 |
100,085,040 (GRCm39) |
missense |
probably benign |
0.28 |
R3775:C2cd3
|
UTSW |
7 |
100,081,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R3854:C2cd3
|
UTSW |
7 |
100,103,808 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4359:C2cd3
|
UTSW |
7 |
100,090,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R4403:C2cd3
|
UTSW |
7 |
100,081,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4446:C2cd3
|
UTSW |
7 |
100,023,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:C2cd3
|
UTSW |
7 |
100,021,657 (GRCm39) |
unclassified |
probably benign |
|
R4705:C2cd3
|
UTSW |
7 |
100,044,395 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4770:C2cd3
|
UTSW |
7 |
100,092,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:C2cd3
|
UTSW |
7 |
100,065,539 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4816:C2cd3
|
UTSW |
7 |
100,040,226 (GRCm39) |
missense |
probably benign |
0.01 |
R4842:C2cd3
|
UTSW |
7 |
100,065,397 (GRCm39) |
missense |
probably benign |
0.00 |
R4858:C2cd3
|
UTSW |
7 |
100,104,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:C2cd3
|
UTSW |
7 |
100,062,581 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4898:C2cd3
|
UTSW |
7 |
100,055,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R5026:C2cd3
|
UTSW |
7 |
100,109,049 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5112:C2cd3
|
UTSW |
7 |
100,092,692 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5242:C2cd3
|
UTSW |
7 |
100,039,373 (GRCm39) |
missense |
probably benign |
0.01 |
R5538:C2cd3
|
UTSW |
7 |
100,104,700 (GRCm39) |
critical splice donor site |
probably null |
|
R5861:C2cd3
|
UTSW |
7 |
100,093,682 (GRCm39) |
unclassified |
probably benign |
|
R6110:C2cd3
|
UTSW |
7 |
100,090,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:C2cd3
|
UTSW |
7 |
100,065,635 (GRCm39) |
missense |
probably benign |
0.02 |
R6429:C2cd3
|
UTSW |
7 |
100,081,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:C2cd3
|
UTSW |
7 |
100,104,505 (GRCm39) |
missense |
probably benign |
|
R6613:C2cd3
|
UTSW |
7 |
100,044,448 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6631:C2cd3
|
UTSW |
7 |
100,067,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6837:C2cd3
|
UTSW |
7 |
100,097,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:C2cd3
|
UTSW |
7 |
100,056,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:C2cd3
|
UTSW |
7 |
100,039,448 (GRCm39) |
missense |
probably benign |
0.28 |
R6929:C2cd3
|
UTSW |
7 |
100,100,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:C2cd3
|
UTSW |
7 |
100,081,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:C2cd3
|
UTSW |
7 |
100,065,388 (GRCm39) |
missense |
|
|
R7174:C2cd3
|
UTSW |
7 |
100,081,405 (GRCm39) |
missense |
|
|
R7241:C2cd3
|
UTSW |
7 |
100,056,257 (GRCm39) |
missense |
|
|
R7335:C2cd3
|
UTSW |
7 |
100,071,810 (GRCm39) |
missense |
|
|
R7357:C2cd3
|
UTSW |
7 |
100,079,310 (GRCm39) |
missense |
|
|
R7493:C2cd3
|
UTSW |
7 |
100,076,433 (GRCm39) |
missense |
|
|
R7567:C2cd3
|
UTSW |
7 |
100,080,022 (GRCm39) |
missense |
|
|
R7573:C2cd3
|
UTSW |
7 |
100,068,914 (GRCm39) |
missense |
|
|
R7869:C2cd3
|
UTSW |
7 |
100,118,698 (GRCm39) |
missense |
probably damaging |
0.99 |
R7999:C2cd3
|
UTSW |
7 |
100,109,096 (GRCm39) |
critical splice donor site |
probably null |
|
R8134:C2cd3
|
UTSW |
7 |
100,067,711 (GRCm39) |
missense |
|
|
R8369:C2cd3
|
UTSW |
7 |
100,044,465 (GRCm39) |
missense |
probably benign |
0.03 |
R8372:C2cd3
|
UTSW |
7 |
100,104,487 (GRCm39) |
nonsense |
probably null |
|
R8753:C2cd3
|
UTSW |
7 |
100,049,024 (GRCm39) |
critical splice donor site |
probably null |
|
R8893:C2cd3
|
UTSW |
7 |
100,104,004 (GRCm39) |
missense |
probably benign |
|
R8905:C2cd3
|
UTSW |
7 |
100,074,132 (GRCm39) |
critical splice donor site |
probably null |
|
R8945:C2cd3
|
UTSW |
7 |
100,040,286 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8970:C2cd3
|
UTSW |
7 |
100,068,971 (GRCm39) |
missense |
|
|
R9000:C2cd3
|
UTSW |
7 |
100,065,281 (GRCm39) |
missense |
|
|
R9064:C2cd3
|
UTSW |
7 |
100,059,608 (GRCm39) |
missense |
|
|
R9072:C2cd3
|
UTSW |
7 |
100,040,291 (GRCm39) |
missense |
probably benign |
0.07 |
R9126:C2cd3
|
UTSW |
7 |
100,081,430 (GRCm39) |
missense |
|
|
R9160:C2cd3
|
UTSW |
7 |
100,075,236 (GRCm39) |
missense |
|
|
R9234:C2cd3
|
UTSW |
7 |
100,049,012 (GRCm39) |
missense |
|
|
R9258:C2cd3
|
UTSW |
7 |
100,098,026 (GRCm39) |
missense |
|
|
R9295:C2cd3
|
UTSW |
7 |
100,081,734 (GRCm39) |
missense |
|
|
R9411:C2cd3
|
UTSW |
7 |
100,065,704 (GRCm39) |
missense |
|
|
R9420:C2cd3
|
UTSW |
7 |
100,065,262 (GRCm39) |
missense |
|
|
R9589:C2cd3
|
UTSW |
7 |
100,081,756 (GRCm39) |
missense |
|
|
R9628:C2cd3
|
UTSW |
7 |
100,097,961 (GRCm39) |
missense |
|
|
R9629:C2cd3
|
UTSW |
7 |
100,029,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R9681:C2cd3
|
UTSW |
7 |
100,023,662 (GRCm39) |
missense |
probably benign |
0.32 |
R9775:C2cd3
|
UTSW |
7 |
100,076,458 (GRCm39) |
missense |
|
|
X0002:C2cd3
|
UTSW |
7 |
100,089,442 (GRCm39) |
missense |
possibly damaging |
0.50 |
|