Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700088E04Rik |
T |
C |
15: 79,023,453 (GRCm39) |
M51V |
possibly damaging |
Het |
Acad8 |
A |
G |
9: 26,903,563 (GRCm39) |
|
probably benign |
Het |
Atp2a2 |
A |
G |
5: 122,638,855 (GRCm39) |
V53A |
possibly damaging |
Het |
Bicra |
T |
C |
7: 15,722,624 (GRCm39) |
T298A |
probably benign |
Het |
Ccdc185 |
C |
T |
1: 182,576,543 (GRCm39) |
E49K |
possibly damaging |
Het |
Cfhr2 |
A |
G |
1: 139,741,352 (GRCm39) |
S208P |
probably benign |
Het |
Chd1 |
T |
C |
17: 15,990,430 (GRCm39) |
Y1661H |
probably damaging |
Het |
Cntnap5a |
A |
G |
1: 116,085,367 (GRCm39) |
H435R |
probably benign |
Het |
Cog8 |
A |
G |
8: 107,780,697 (GRCm39) |
V187A |
probably benign |
Het |
Col24a1 |
A |
G |
3: 145,244,322 (GRCm39) |
H1532R |
probably benign |
Het |
Dpp6 |
A |
G |
5: 27,836,518 (GRCm39) |
Y336C |
probably damaging |
Het |
Drosha |
T |
A |
15: 12,846,198 (GRCm39) |
Y444* |
probably null |
Het |
Egf |
A |
T |
3: 129,491,371 (GRCm39) |
C374* |
probably null |
Het |
Eif2b3 |
C |
T |
4: 116,916,001 (GRCm39) |
H203Y |
probably damaging |
Het |
Erbb4 |
A |
G |
1: 68,293,722 (GRCm39) |
V723A |
possibly damaging |
Het |
Fbxo21 |
T |
C |
5: 118,126,855 (GRCm39) |
I202T |
probably benign |
Het |
Gbp6 |
T |
C |
5: 105,422,073 (GRCm39) |
M544V |
probably benign |
Het |
Gm10750 |
T |
C |
2: 148,857,964 (GRCm39) |
T96A |
unknown |
Het |
Gm8232 |
A |
T |
14: 44,674,640 (GRCm39) |
|
probably null |
Het |
Gpi-ps |
A |
T |
8: 5,689,896 (GRCm39) |
|
noncoding transcript |
Het |
Gsdma3 |
T |
C |
11: 98,528,782 (GRCm39) |
V412A |
possibly damaging |
Het |
Hs6st1 |
A |
T |
1: 36,108,016 (GRCm39) |
H93L |
probably damaging |
Het |
Hsf2 |
G |
A |
10: 57,372,277 (GRCm39) |
E77K |
probably benign |
Het |
Ing3 |
T |
A |
6: 21,968,879 (GRCm39) |
|
probably benign |
Het |
Ints6 |
T |
C |
14: 62,951,188 (GRCm39) |
I280M |
probably damaging |
Het |
Kazn |
C |
A |
4: 141,886,354 (GRCm39) |
|
probably null |
Het |
Klhl20 |
T |
C |
1: 160,923,157 (GRCm39) |
Y13C |
probably damaging |
Het |
Mga |
T |
A |
2: 119,765,720 (GRCm39) |
I1329K |
probably damaging |
Het |
Mindy4 |
A |
G |
6: 55,200,984 (GRCm39) |
D223G |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,128,001 (GRCm39) |
E124G |
probably damaging |
Het |
Nfat5 |
G |
A |
8: 108,071,611 (GRCm39) |
|
probably null |
Het |
Nkain1 |
A |
G |
4: 130,532,134 (GRCm38) |
F184L |
probably benign |
Het |
Or8k25 |
T |
C |
2: 86,243,677 (GRCm39) |
T240A |
probably damaging |
Het |
Rars1 |
A |
T |
11: 35,719,491 (GRCm39) |
F110L |
probably damaging |
Het |
Rfx6 |
A |
C |
10: 51,599,173 (GRCm39) |
K509N |
probably damaging |
Het |
Serpinb2 |
T |
C |
1: 107,443,333 (GRCm39) |
L44P |
probably damaging |
Het |
Sin3a |
G |
A |
9: 57,002,609 (GRCm39) |
R167Q |
probably damaging |
Het |
Sos2 |
T |
A |
12: 69,650,641 (GRCm39) |
T809S |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,533,811 (GRCm39) |
E3356G |
probably damaging |
Het |
Vmn1r52 |
A |
G |
6: 90,155,905 (GRCm39) |
T70A |
probably benign |
Het |
|
Other mutations in Krtap26-1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00886:Krtap26-1
|
APN |
16 |
88,444,267 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01963:Krtap26-1
|
APN |
16 |
88,444,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02524:Krtap26-1
|
APN |
16 |
88,444,367 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0383:Krtap26-1
|
UTSW |
16 |
88,444,131 (GRCm39) |
nonsense |
probably null |
|
R2367:Krtap26-1
|
UTSW |
16 |
88,444,213 (GRCm39) |
missense |
probably benign |
0.28 |
R4694:Krtap26-1
|
UTSW |
16 |
88,444,108 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6699:Krtap26-1
|
UTSW |
16 |
88,444,603 (GRCm39) |
missense |
unknown |
|
R6884:Krtap26-1
|
UTSW |
16 |
88,444,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Krtap26-1
|
UTSW |
16 |
88,444,132 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7808:Krtap26-1
|
UTSW |
16 |
88,444,198 (GRCm39) |
missense |
not run |
|
R8824:Krtap26-1
|
UTSW |
16 |
88,444,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R8824:Krtap26-1
|
UTSW |
16 |
88,444,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R9034:Krtap26-1
|
UTSW |
16 |
88,444,161 (GRCm39) |
missense |
probably benign |
0.14 |
R9186:Krtap26-1
|
UTSW |
16 |
88,444,609 (GRCm39) |
missense |
unknown |
|
R9279:Krtap26-1
|
UTSW |
16 |
88,444,342 (GRCm39) |
missense |
probably benign |
0.00 |
|