Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl6 |
G |
T |
11: 54,227,840 (GRCm39) |
|
probably null |
Het |
Anapc5 |
A |
G |
5: 122,957,716 (GRCm39) |
L69P |
possibly damaging |
Het |
Aoc1l3 |
CCTAAATTTCCTATCCCGATCAGCAAGGGTGGCCCTCGAGTGCCCCAGCCCCATGCTAAATTTCC |
CCTAAATTTCC |
6: 48,965,074 (GRCm39) |
|
probably benign |
Het |
Arfgef1 |
A |
T |
1: 10,259,055 (GRCm39) |
S681T |
probably benign |
Het |
Arhgef19 |
A |
G |
4: 140,976,549 (GRCm39) |
D437G |
probably damaging |
Het |
Arhgef25 |
A |
G |
10: 127,019,089 (GRCm39) |
V576A |
probably benign |
Het |
Arl5b |
T |
C |
2: 15,073,012 (GRCm39) |
|
probably null |
Het |
Atg10 |
T |
A |
13: 91,189,071 (GRCm39) |
T80S |
probably benign |
Het |
BC034090 |
A |
G |
1: 155,117,419 (GRCm39) |
V233A |
possibly damaging |
Het |
Bicdl2 |
C |
T |
17: 23,887,158 (GRCm39) |
R482C |
probably damaging |
Het |
Ccdc63 |
G |
A |
5: 122,247,346 (GRCm39) |
P500S |
probably benign |
Het |
Ccn2 |
A |
T |
10: 24,472,647 (GRCm39) |
T186S |
probably benign |
Het |
Ccng1 |
A |
T |
11: 40,643,078 (GRCm39) |
I123K |
possibly damaging |
Het |
Ccp110 |
C |
T |
7: 118,324,680 (GRCm39) |
S734F |
probably damaging |
Het |
Cds2 |
T |
C |
2: 132,139,614 (GRCm39) |
|
probably null |
Het |
Cenpw |
G |
A |
10: 30,074,523 (GRCm39) |
T58I |
probably benign |
Het |
Cfap61 |
T |
A |
2: 145,850,839 (GRCm39) |
L326I |
probably benign |
Het |
Cgn |
T |
A |
3: 94,674,551 (GRCm39) |
Q862L |
possibly damaging |
Het |
Cntrl |
T |
A |
2: 35,016,071 (GRCm39) |
D362E |
probably damaging |
Het |
Col22a1 |
C |
T |
15: 71,762,431 (GRCm39) |
G76E |
probably damaging |
Het |
Cplane1 |
C |
T |
15: 8,252,622 (GRCm39) |
T1948I |
possibly damaging |
Het |
Crip2 |
A |
G |
12: 113,108,030 (GRCm39) |
T140A |
probably benign |
Het |
Csde1 |
T |
C |
3: 102,950,976 (GRCm39) |
V229A |
probably damaging |
Het |
Cyp2d34 |
A |
G |
15: 82,500,523 (GRCm39) |
F439L |
probably damaging |
Het |
Dync1h1 |
A |
G |
12: 110,606,186 (GRCm39) |
T2419A |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,051,495 (GRCm39) |
F3147I |
probably damaging |
Het |
Dynlt1f |
T |
C |
17: 6,916,707 (GRCm39) |
T101A |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,927,601 (GRCm39) |
H4790R |
probably benign |
Het |
Efcab8 |
G |
A |
2: 153,622,888 (GRCm39) |
S19N |
|
Het |
Eno2 |
A |
T |
6: 124,740,091 (GRCm39) |
I315K |
possibly damaging |
Het |
Erich3 |
A |
G |
3: 154,468,886 (GRCm39) |
T1113A |
unknown |
Het |
Fam217a |
A |
T |
13: 35,095,007 (GRCm39) |
Y251N |
possibly damaging |
Het |
Fcrlb |
A |
T |
1: 170,734,938 (GRCm39) |
H396Q |
probably benign |
Het |
Fcsk |
A |
G |
8: 111,614,064 (GRCm39) |
V693A |
probably benign |
Het |
Fgd5 |
A |
T |
6: 92,046,447 (GRCm39) |
K1397* |
probably null |
Het |
Frem1 |
C |
A |
4: 82,831,785 (GRCm39) |
L2010F |
probably benign |
Het |
Fzd8 |
A |
G |
18: 9,214,661 (GRCm39) |
Y581C |
probably damaging |
Het |
Gcnt4 |
G |
A |
13: 97,083,042 (GRCm39) |
V113I |
probably benign |
Het |
Gldn |
A |
G |
9: 54,245,747 (GRCm39) |
I433V |
probably benign |
Het |
Gm3336 |
A |
G |
8: 71,173,069 (GRCm39) |
D27G |
unknown |
Het |
Gm6133 |
T |
A |
18: 78,393,146 (GRCm39) |
Y47N |
probably damaging |
Het |
Gm8257 |
A |
T |
14: 44,893,877 (GRCm39) |
N62K |
probably benign |
Het |
Gpr18 |
T |
G |
14: 122,149,667 (GRCm39) |
R119S |
probably damaging |
Het |
Grm5 |
A |
T |
7: 87,685,397 (GRCm39) |
I505F |
possibly damaging |
Het |
Hdgfl1 |
T |
C |
13: 26,953,428 (GRCm39) |
E215G |
probably benign |
Het |
Heg1 |
T |
A |
16: 33,527,339 (GRCm39) |
C100S |
probably benign |
Het |
Isg20l2 |
T |
C |
3: 87,839,302 (GRCm39) |
V171A |
probably benign |
Het |
Lrrc49 |
A |
T |
9: 60,495,150 (GRCm39) |
C694S |
probably benign |
Het |
Map7d1 |
A |
T |
4: 126,133,911 (GRCm39) |
I217N |
probably damaging |
Het |
Mbnl2 |
A |
T |
14: 120,562,712 (GRCm39) |
Q21L |
probably benign |
Het |
Mfsd10 |
A |
T |
5: 34,792,751 (GRCm39) |
F220Y |
probably benign |
Het |
Mmp1b |
A |
C |
9: 7,387,909 (GRCm39) |
N28K |
probably null |
Het |
Muc16 |
A |
T |
9: 18,555,975 (GRCm39) |
N3439K |
unknown |
Het |
Myef2l |
C |
A |
3: 10,157,341 (GRCm39) |
Q495K |
unknown |
Het |
Myo9a |
A |
T |
9: 59,687,584 (GRCm39) |
K230* |
probably null |
Het |
Mysm1 |
T |
C |
4: 94,835,294 (GRCm39) |
T790A |
probably benign |
Het |
Nell2 |
C |
T |
15: 95,194,117 (GRCm39) |
C532Y |
probably damaging |
Het |
Nmnat1 |
T |
A |
4: 149,553,482 (GRCm39) |
N210I |
probably damaging |
Het |
Or14j7 |
T |
G |
17: 38,235,168 (GRCm39) |
V237G |
probably benign |
Het |
Or2aj6 |
A |
T |
16: 19,443,295 (GRCm39) |
L185* |
probably null |
Het |
Or4k41 |
T |
C |
2: 111,280,343 (GRCm39) |
I286T |
probably damaging |
Het |
Or7g16 |
G |
A |
9: 18,727,569 (GRCm39) |
T7I |
probably damaging |
Het |
Pabpc6 |
T |
C |
17: 9,888,281 (GRCm39) |
D90G |
probably damaging |
Het |
Pacs2 |
A |
T |
12: 113,026,104 (GRCm39) |
I554F |
possibly damaging |
Het |
Padi3 |
C |
A |
4: 140,523,004 (GRCm39) |
V323L |
probably benign |
Het |
Piezo1 |
G |
A |
8: 123,215,090 (GRCm39) |
P1484L |
|
Het |
Pogk |
A |
G |
1: 166,227,254 (GRCm39) |
I299T |
possibly damaging |
Het |
Ptprk |
A |
G |
10: 28,461,928 (GRCm39) |
I1164V |
probably benign |
Het |
Raph1 |
A |
G |
1: 60,542,124 (GRCm39) |
M278T |
unknown |
Het |
Rasa3 |
T |
A |
8: 13,645,851 (GRCm39) |
Q163L |
probably benign |
Het |
Rbm6 |
T |
A |
9: 107,660,911 (GRCm39) |
K884I |
probably damaging |
Het |
Rtl1 |
A |
G |
12: 109,559,691 (GRCm39) |
V716A |
probably benign |
Het |
Sag |
A |
G |
1: 87,749,054 (GRCm39) |
K151R |
probably damaging |
Het |
Scara5 |
G |
A |
14: 66,000,197 (GRCm39) |
V456M |
probably benign |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
Slc4a1 |
A |
T |
11: 102,243,279 (GRCm39) |
V784D |
probably damaging |
Het |
Sstr1 |
T |
C |
12: 58,259,569 (GRCm39) |
I64T |
possibly damaging |
Het |
Steap1 |
A |
G |
5: 5,790,708 (GRCm39) |
I80T |
probably benign |
Het |
Tbc1d24 |
T |
A |
17: 24,427,491 (GRCm39) |
D157V |
probably benign |
Het |
Thsd7a |
T |
C |
6: 12,418,249 (GRCm39) |
E660G |
|
Het |
Trappc3l |
A |
G |
10: 33,932,786 (GRCm39) |
|
probably benign |
Het |
Tsc22d2 |
T |
C |
3: 58,323,497 (GRCm39) |
S130P |
probably benign |
Het |
Tti2 |
T |
A |
8: 31,645,814 (GRCm39) |
I376N |
probably damaging |
Het |
Ttll2 |
C |
A |
17: 7,619,054 (GRCm39) |
W291L |
probably benign |
Het |
Ttll3 |
G |
A |
6: 113,376,657 (GRCm39) |
V345I |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,565,046 (GRCm39) |
Y28394H |
probably damaging |
Het |
Usp45 |
A |
G |
4: 21,832,201 (GRCm39) |
Y684C |
probably damaging |
Het |
Vdr |
A |
G |
15: 97,765,089 (GRCm39) |
S217P |
probably benign |
Het |
Xpot |
A |
G |
10: 121,447,580 (GRCm39) |
L105P |
probably damaging |
Het |
Zan |
A |
G |
5: 137,464,206 (GRCm39) |
I533T |
probably damaging |
Het |
Zbtb8a |
T |
C |
4: 129,248,059 (GRCm39) |
E404G |
probably benign |
Het |
Zfp106 |
T |
A |
2: 120,369,906 (GRCm39) |
I62F |
probably damaging |
Het |
Zfp451 |
A |
T |
1: 33,815,562 (GRCm39) |
F796Y |
probably damaging |
Het |
|
Other mutations in Gcc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Gcc2
|
APN |
10 |
58,128,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00850:Gcc2
|
APN |
10 |
58,094,070 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00935:Gcc2
|
APN |
10 |
58,114,601 (GRCm39) |
splice site |
probably benign |
|
IGL01551:Gcc2
|
APN |
10 |
58,134,691 (GRCm39) |
splice site |
probably benign |
|
IGL01642:Gcc2
|
APN |
10 |
58,116,434 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02041:Gcc2
|
APN |
10 |
58,105,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02215:Gcc2
|
APN |
10 |
58,107,458 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02448:Gcc2
|
APN |
10 |
58,128,393 (GRCm39) |
nonsense |
probably null |
|
IGL02698:Gcc2
|
APN |
10 |
58,107,112 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02888:Gcc2
|
APN |
10 |
58,130,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02936:Gcc2
|
APN |
10 |
58,131,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03223:Gcc2
|
APN |
10 |
58,134,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03249:Gcc2
|
APN |
10 |
58,106,814 (GRCm39) |
nonsense |
probably null |
|
R0179:Gcc2
|
UTSW |
10 |
58,112,472 (GRCm39) |
missense |
probably benign |
0.39 |
R0528:Gcc2
|
UTSW |
10 |
58,134,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1569:Gcc2
|
UTSW |
10 |
58,105,993 (GRCm39) |
missense |
probably benign |
0.00 |
R1606:Gcc2
|
UTSW |
10 |
58,105,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Gcc2
|
UTSW |
10 |
58,139,937 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1916:Gcc2
|
UTSW |
10 |
58,112,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R1956:Gcc2
|
UTSW |
10 |
58,121,965 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2058:Gcc2
|
UTSW |
10 |
58,121,779 (GRCm39) |
missense |
probably benign |
0.10 |
R2114:Gcc2
|
UTSW |
10 |
58,105,362 (GRCm39) |
nonsense |
probably null |
|
R2280:Gcc2
|
UTSW |
10 |
58,105,502 (GRCm39) |
missense |
probably benign |
0.38 |
R2435:Gcc2
|
UTSW |
10 |
58,130,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R2876:Gcc2
|
UTSW |
10 |
58,126,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R4753:Gcc2
|
UTSW |
10 |
58,126,204 (GRCm39) |
missense |
probably benign |
0.20 |
R4827:Gcc2
|
UTSW |
10 |
58,121,953 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4911:Gcc2
|
UTSW |
10 |
58,106,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Gcc2
|
UTSW |
10 |
58,114,628 (GRCm39) |
missense |
probably damaging |
0.98 |
R5224:Gcc2
|
UTSW |
10 |
58,121,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5271:Gcc2
|
UTSW |
10 |
58,105,517 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5398:Gcc2
|
UTSW |
10 |
58,105,329 (GRCm39) |
missense |
probably benign |
0.00 |
R5411:Gcc2
|
UTSW |
10 |
58,106,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R5594:Gcc2
|
UTSW |
10 |
58,123,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R5825:Gcc2
|
UTSW |
10 |
58,130,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R5974:Gcc2
|
UTSW |
10 |
58,094,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R5987:Gcc2
|
UTSW |
10 |
58,091,669 (GRCm39) |
utr 5 prime |
probably benign |
|
R6195:Gcc2
|
UTSW |
10 |
58,106,806 (GRCm39) |
missense |
probably damaging |
0.96 |
R6198:Gcc2
|
UTSW |
10 |
58,128,412 (GRCm39) |
missense |
probably benign |
0.26 |
R6233:Gcc2
|
UTSW |
10 |
58,106,806 (GRCm39) |
missense |
probably damaging |
0.96 |
R6331:Gcc2
|
UTSW |
10 |
58,107,287 (GRCm39) |
missense |
probably benign |
|
R6349:Gcc2
|
UTSW |
10 |
58,105,296 (GRCm39) |
missense |
probably benign |
0.01 |
R6593:Gcc2
|
UTSW |
10 |
58,107,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6632:Gcc2
|
UTSW |
10 |
58,105,871 (GRCm39) |
splice site |
probably null |
|
R6647:Gcc2
|
UTSW |
10 |
58,123,103 (GRCm39) |
critical splice donor site |
probably null |
|
R6774:Gcc2
|
UTSW |
10 |
58,117,261 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6808:Gcc2
|
UTSW |
10 |
58,094,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R7072:Gcc2
|
UTSW |
10 |
58,106,749 (GRCm39) |
missense |
probably benign |
0.02 |
R7220:Gcc2
|
UTSW |
10 |
58,116,416 (GRCm39) |
missense |
probably benign |
0.00 |
R7352:Gcc2
|
UTSW |
10 |
58,116,520 (GRCm39) |
critical splice donor site |
probably null |
|
R7384:Gcc2
|
UTSW |
10 |
58,105,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Gcc2
|
UTSW |
10 |
58,092,723 (GRCm39) |
missense |
probably benign |
0.08 |
R7441:Gcc2
|
UTSW |
10 |
58,092,723 (GRCm39) |
missense |
probably benign |
0.08 |
R7543:Gcc2
|
UTSW |
10 |
58,107,086 (GRCm39) |
missense |
probably benign |
0.02 |
R7843:Gcc2
|
UTSW |
10 |
58,103,843 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7850:Gcc2
|
UTSW |
10 |
58,114,703 (GRCm39) |
missense |
probably damaging |
0.96 |
R7980:Gcc2
|
UTSW |
10 |
58,114,574 (GRCm39) |
splice site |
probably null |
|
R8336:Gcc2
|
UTSW |
10 |
58,108,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R8785:Gcc2
|
UTSW |
10 |
58,107,086 (GRCm39) |
missense |
probably benign |
0.02 |
R8834:Gcc2
|
UTSW |
10 |
58,121,867 (GRCm39) |
critical splice donor site |
probably null |
|
R9006:Gcc2
|
UTSW |
10 |
58,103,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R9240:Gcc2
|
UTSW |
10 |
58,106,398 (GRCm39) |
nonsense |
probably null |
|
R9287:Gcc2
|
UTSW |
10 |
58,105,217 (GRCm39) |
nonsense |
probably null |
|
R9370:Gcc2
|
UTSW |
10 |
58,131,940 (GRCm39) |
missense |
probably benign |
0.00 |
R9433:Gcc2
|
UTSW |
10 |
58,106,592 (GRCm39) |
missense |
probably benign |
0.06 |
R9653:Gcc2
|
UTSW |
10 |
58,110,822 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0018:Gcc2
|
UTSW |
10 |
58,114,636 (GRCm39) |
missense |
probably damaging |
0.98 |
|