Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519G04Rik |
T |
G |
5: 115,001,569 (GRCm39) |
M22R |
probably benign |
Het |
Abca8b |
C |
A |
11: 109,841,476 (GRCm39) |
M1039I |
probably benign |
Het |
Actn2 |
A |
T |
13: 12,292,301 (GRCm39) |
I653N |
probably damaging |
Het |
Actr8 |
G |
T |
14: 29,700,513 (GRCm39) |
V31L |
probably benign |
Het |
Adam30 |
T |
C |
3: 98,069,441 (GRCm39) |
C425R |
probably damaging |
Het |
Armc1 |
A |
G |
3: 19,203,659 (GRCm39) |
V89A |
possibly damaging |
Het |
Atr |
T |
C |
9: 95,817,579 (GRCm39) |
M2090T |
probably damaging |
Het |
Braf |
T |
A |
6: 39,641,923 (GRCm39) |
|
probably benign |
Het |
Cant1 |
A |
T |
11: 118,302,091 (GRCm39) |
N75K |
probably benign |
Het |
Chd7 |
C |
T |
4: 8,805,139 (GRCm39) |
|
probably benign |
Het |
Clec16a |
A |
G |
16: 10,432,444 (GRCm39) |
Y488C |
probably damaging |
Het |
Col6a3 |
A |
T |
1: 90,749,520 (GRCm39) |
|
probably benign |
Het |
Col9a2 |
T |
A |
4: 120,911,504 (GRCm39) |
M615K |
probably benign |
Het |
Dedd |
G |
A |
1: 171,168,498 (GRCm39) |
R228H |
probably damaging |
Het |
Dhtkd1 |
C |
T |
2: 5,908,902 (GRCm39) |
D731N |
probably damaging |
Het |
Ercc2 |
A |
G |
7: 19,127,812 (GRCm39) |
T651A |
probably damaging |
Het |
Fam13a |
T |
A |
6: 58,933,684 (GRCm39) |
D302V |
probably damaging |
Het |
Fam193a |
T |
C |
5: 34,583,735 (GRCm39) |
S19P |
probably damaging |
Het |
Fam43a |
T |
C |
16: 30,420,553 (GRCm39) |
V379A |
possibly damaging |
Het |
Fat1 |
C |
A |
8: 45,404,369 (GRCm39) |
Y373* |
probably null |
Het |
Fbxl15 |
A |
C |
19: 46,317,861 (GRCm39) |
D181A |
probably damaging |
Het |
Flt3 |
A |
T |
5: 147,278,080 (GRCm39) |
C831* |
probably null |
Het |
Foxj3 |
T |
A |
4: 119,443,033 (GRCm39) |
|
probably benign |
Het |
Glul |
T |
C |
1: 153,781,132 (GRCm39) |
|
probably benign |
Het |
Gm16380 |
A |
T |
9: 53,791,529 (GRCm39) |
|
noncoding transcript |
Het |
Gm7964 |
A |
T |
7: 83,405,158 (GRCm39) |
|
noncoding transcript |
Het |
Hipk1 |
A |
G |
3: 103,667,890 (GRCm39) |
F559S |
possibly damaging |
Het |
Hnf4g |
A |
T |
3: 3,716,682 (GRCm39) |
I284F |
probably damaging |
Het |
Hoxa13 |
CCG |
CCGCG |
6: 52,237,618 (GRCm39) |
|
probably null |
Het |
Icosl |
A |
G |
10: 77,907,800 (GRCm39) |
N120S |
possibly damaging |
Het |
Ift172 |
A |
G |
5: 31,442,821 (GRCm39) |
V155A |
possibly damaging |
Het |
Kdm4c |
A |
G |
4: 74,252,031 (GRCm39) |
E426G |
probably benign |
Het |
Kif23 |
A |
G |
9: 61,826,257 (GRCm39) |
|
probably benign |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Lama1 |
G |
A |
17: 68,086,129 (GRCm39) |
C1456Y |
possibly damaging |
Het |
Lamc3 |
T |
A |
2: 31,827,980 (GRCm39) |
L1378Q |
probably damaging |
Het |
Larp1b |
T |
A |
3: 40,924,469 (GRCm39) |
L121M |
probably benign |
Het |
Lepr |
T |
A |
4: 101,649,216 (GRCm39) |
D872E |
probably damaging |
Het |
Lepr |
A |
C |
4: 101,671,901 (GRCm39) |
D975A |
possibly damaging |
Het |
Magi1 |
A |
G |
6: 93,671,045 (GRCm39) |
V1068A |
probably damaging |
Het |
Malt1 |
T |
A |
18: 65,591,271 (GRCm39) |
N358K |
probably damaging |
Het |
Mfap4 |
T |
A |
11: 61,378,771 (GRCm39) |
W240R |
probably damaging |
Het |
Mis18a |
A |
G |
16: 90,523,244 (GRCm39) |
V84A |
possibly damaging |
Het |
Mns1 |
A |
G |
9: 72,356,753 (GRCm39) |
E308G |
possibly damaging |
Het |
Mpp2 |
C |
A |
11: 101,953,116 (GRCm39) |
L258F |
possibly damaging |
Het |
Myh2 |
A |
G |
11: 67,079,504 (GRCm39) |
E987G |
probably damaging |
Het |
Myof |
A |
G |
19: 37,942,972 (GRCm39) |
V702A |
possibly damaging |
Het |
Nhs |
C |
A |
X: 160,620,355 (GRCm39) |
R1467I |
probably damaging |
Het |
Nrxn2 |
A |
G |
19: 6,567,228 (GRCm39) |
T1360A |
probably damaging |
Het |
Obox6 |
A |
G |
7: 15,567,874 (GRCm39) |
I191T |
probably benign |
Het |
Pacs2 |
G |
T |
12: 113,014,547 (GRCm39) |
R236L |
probably damaging |
Het |
Pcdhb2 |
T |
G |
18: 37,429,032 (GRCm39) |
V335G |
probably damaging |
Het |
Phyhipl |
T |
C |
10: 70,404,748 (GRCm39) |
I140M |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,380,738 (GRCm39) |
|
probably benign |
Het |
Ppp1r3b |
T |
G |
8: 35,851,571 (GRCm39) |
C137G |
probably damaging |
Het |
Prdm13 |
T |
A |
4: 21,678,490 (GRCm39) |
I667F |
probably damaging |
Het |
Prex2 |
A |
G |
1: 11,270,157 (GRCm39) |
M1281V |
probably benign |
Het |
Rab40b |
A |
G |
11: 121,250,412 (GRCm39) |
F81L |
probably damaging |
Het |
Rb1cc1 |
T |
C |
1: 6,318,767 (GRCm39) |
S729P |
probably damaging |
Het |
Rcl1 |
A |
G |
19: 29,105,497 (GRCm39) |
D228G |
probably damaging |
Het |
Rhbdf1 |
A |
T |
11: 32,160,875 (GRCm39) |
C19* |
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnf150 |
G |
A |
8: 83,590,807 (GRCm39) |
V57M |
probably benign |
Het |
Rp9 |
A |
G |
9: 22,370,015 (GRCm39) |
F51L |
probably benign |
Het |
Sav1 |
A |
T |
12: 70,015,975 (GRCm39) |
Y274* |
probably null |
Het |
Scn4a |
A |
T |
11: 106,236,503 (GRCm39) |
D252E |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,379,724 (GRCm39) |
T187A |
probably damaging |
Het |
Sigirr |
T |
A |
7: 140,672,333 (GRCm39) |
D229V |
probably benign |
Het |
Slc39a13 |
T |
C |
2: 90,896,031 (GRCm39) |
S157G |
possibly damaging |
Het |
Slc6a20a |
A |
G |
9: 123,489,471 (GRCm39) |
S191P |
probably damaging |
Het |
Sorl1 |
C |
A |
9: 41,979,128 (GRCm39) |
A457S |
probably benign |
Het |
Spon1 |
A |
G |
7: 113,436,066 (GRCm39) |
E119G |
possibly damaging |
Het |
Spred2 |
T |
A |
11: 19,958,485 (GRCm39) |
|
probably benign |
Het |
Sprr3 |
T |
G |
3: 92,364,784 (GRCm39) |
Q20P |
possibly damaging |
Het |
Strn3 |
A |
T |
12: 51,673,966 (GRCm39) |
F464L |
possibly damaging |
Het |
Sun1 |
A |
G |
5: 139,220,602 (GRCm39) |
|
probably benign |
Het |
Sypl2 |
A |
G |
3: 108,133,486 (GRCm39) |
W28R |
possibly damaging |
Het |
Syt5 |
A |
T |
7: 4,545,813 (GRCm39) |
V150D |
probably damaging |
Het |
Tasor |
T |
C |
14: 27,168,363 (GRCm39) |
F302L |
probably damaging |
Het |
Thsd7a |
A |
G |
6: 12,379,604 (GRCm39) |
I940T |
possibly damaging |
Het |
Tlcd3b |
C |
T |
7: 126,426,795 (GRCm39) |
R73C |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,785,951 (GRCm39) |
|
probably benign |
Het |
Trp53 |
T |
A |
11: 69,479,509 (GRCm39) |
L203Q |
probably damaging |
Het |
Tubgcp4 |
T |
C |
2: 121,005,900 (GRCm39) |
V96A |
probably benign |
Het |
Usp17la |
A |
G |
7: 104,510,246 (GRCm39) |
T284A |
possibly damaging |
Het |
Usp34 |
T |
C |
11: 23,401,997 (GRCm39) |
M2409T |
probably benign |
Het |
Vmn2r100 |
C |
A |
17: 19,742,382 (GRCm39) |
P252Q |
possibly damaging |
Het |
Vmn2r56 |
A |
G |
7: 12,449,350 (GRCm39) |
I296T |
probably benign |
Het |
Vmn2r67 |
A |
G |
7: 84,799,900 (GRCm39) |
V446A |
probably damaging |
Het |
Zfp217 |
C |
T |
2: 169,957,382 (GRCm39) |
A539T |
probably benign |
Het |
Zfp267 |
T |
C |
3: 36,220,262 (GRCm39) |
C762R |
probably damaging |
Het |
|
Other mutations in Spag5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01380:Spag5
|
APN |
11 |
78,195,443 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01820:Spag5
|
APN |
11 |
78,195,085 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02066:Spag5
|
APN |
11 |
78,195,358 (GRCm39) |
missense |
probably benign |
|
IGL02140:Spag5
|
APN |
11 |
78,206,459 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02251:Spag5
|
APN |
11 |
78,210,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02452:Spag5
|
APN |
11 |
78,195,449 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02658:Spag5
|
APN |
11 |
78,212,157 (GRCm39) |
nonsense |
probably null |
|
boyardee
|
UTSW |
11 |
78,204,017 (GRCm39) |
critical splice donor site |
probably null |
|
Franco
|
UTSW |
11 |
78,205,008 (GRCm39) |
nonsense |
probably null |
|
spaghetto
|
UTSW |
11 |
78,204,205 (GRCm39) |
nonsense |
probably null |
|
IGL02991:Spag5
|
UTSW |
11 |
78,205,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R0477:Spag5
|
UTSW |
11 |
78,205,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R0535:Spag5
|
UTSW |
11 |
78,195,554 (GRCm39) |
missense |
probably benign |
0.00 |
R0557:Spag5
|
UTSW |
11 |
78,205,037 (GRCm39) |
missense |
probably damaging |
0.99 |
R0584:Spag5
|
UTSW |
11 |
78,194,921 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0666:Spag5
|
UTSW |
11 |
78,204,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Spag5
|
UTSW |
11 |
78,210,410 (GRCm39) |
unclassified |
probably benign |
|
R1413:Spag5
|
UTSW |
11 |
78,196,143 (GRCm39) |
nonsense |
probably null |
|
R1680:Spag5
|
UTSW |
11 |
78,211,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R1687:Spag5
|
UTSW |
11 |
78,195,755 (GRCm39) |
missense |
probably benign |
0.32 |
R1696:Spag5
|
UTSW |
11 |
78,212,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1831:Spag5
|
UTSW |
11 |
78,205,082 (GRCm39) |
missense |
probably benign |
0.08 |
R1866:Spag5
|
UTSW |
11 |
78,195,281 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1918:Spag5
|
UTSW |
11 |
78,195,002 (GRCm39) |
missense |
probably benign |
0.01 |
R4004:Spag5
|
UTSW |
11 |
78,212,355 (GRCm39) |
missense |
probably benign |
0.22 |
R4005:Spag5
|
UTSW |
11 |
78,212,355 (GRCm39) |
missense |
probably benign |
0.22 |
R4222:Spag5
|
UTSW |
11 |
78,195,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Spag5
|
UTSW |
11 |
78,210,878 (GRCm39) |
missense |
probably benign |
0.00 |
R4771:Spag5
|
UTSW |
11 |
78,195,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Spag5
|
UTSW |
11 |
78,205,199 (GRCm39) |
missense |
probably damaging |
0.97 |
R5360:Spag5
|
UTSW |
11 |
78,205,588 (GRCm39) |
missense |
probably damaging |
0.99 |
R5366:Spag5
|
UTSW |
11 |
78,211,152 (GRCm39) |
splice site |
probably null |
|
R5618:Spag5
|
UTSW |
11 |
78,194,906 (GRCm39) |
missense |
probably benign |
0.00 |
R5668:Spag5
|
UTSW |
11 |
78,195,542 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5762:Spag5
|
UTSW |
11 |
78,194,972 (GRCm39) |
missense |
probably benign |
0.25 |
R5859:Spag5
|
UTSW |
11 |
78,204,360 (GRCm39) |
missense |
probably benign |
0.38 |
R6564:Spag5
|
UTSW |
11 |
78,206,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R6571:Spag5
|
UTSW |
11 |
78,212,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Spag5
|
UTSW |
11 |
78,205,008 (GRCm39) |
nonsense |
probably null |
|
R7074:Spag5
|
UTSW |
11 |
78,195,868 (GRCm39) |
critical splice donor site |
probably null |
|
R7091:Spag5
|
UTSW |
11 |
78,204,017 (GRCm39) |
critical splice donor site |
probably null |
|
R7332:Spag5
|
UTSW |
11 |
78,204,205 (GRCm39) |
nonsense |
probably null |
|
R8073:Spag5
|
UTSW |
11 |
78,192,803 (GRCm39) |
missense |
probably benign |
0.22 |
R8709:Spag5
|
UTSW |
11 |
78,192,738 (GRCm39) |
missense |
probably benign |
|
R8723:Spag5
|
UTSW |
11 |
78,212,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Spag5
|
UTSW |
11 |
78,195,413 (GRCm39) |
missense |
probably benign |
0.01 |
R9053:Spag5
|
UTSW |
11 |
78,212,575 (GRCm39) |
missense |
probably benign |
0.14 |
R9142:Spag5
|
UTSW |
11 |
78,192,823 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1176:Spag5
|
UTSW |
11 |
78,205,808 (GRCm39) |
missense |
possibly damaging |
0.62 |
|