Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl3 |
T |
A |
7: 81,986,415 (GRCm39) |
I9K |
probably benign |
Het |
Arhgap31 |
T |
C |
16: 38,457,362 (GRCm39) |
E82G |
probably damaging |
Het |
Asap2 |
T |
A |
12: 21,317,767 (GRCm39) |
S993T |
probably damaging |
Het |
Bmpr1a |
A |
T |
14: 34,156,624 (GRCm39) |
L134* |
probably null |
Het |
Cacna1e |
A |
G |
1: 154,509,442 (GRCm39) |
V271A |
probably damaging |
Het |
Cacna2d4 |
A |
G |
6: 119,218,124 (GRCm39) |
E153G |
probably damaging |
Het |
Cage1 |
A |
C |
13: 38,209,705 (GRCm39) |
F91V |
possibly damaging |
Het |
Cdh24 |
T |
C |
14: 54,869,637 (GRCm39) |
D760G |
possibly damaging |
Het |
Col9a1 |
T |
C |
1: 24,271,312 (GRCm39) |
|
probably null |
Het |
Cts6 |
A |
T |
13: 61,349,972 (GRCm39) |
Y36* |
probably null |
Het |
Dennd3 |
C |
G |
15: 73,394,083 (GRCm39) |
A36G |
probably benign |
Het |
Dmxl1 |
G |
A |
18: 50,068,384 (GRCm39) |
G2719D |
probably damaging |
Het |
Dnajc28 |
G |
A |
16: 91,413,755 (GRCm39) |
T187M |
probably damaging |
Het |
Ep300 |
T |
A |
15: 81,532,790 (GRCm39) |
V1676E |
unknown |
Het |
Ercc4 |
C |
T |
16: 12,962,360 (GRCm39) |
T668M |
probably benign |
Het |
G530012D18Rik |
CAGAGAGA |
CAGAGAGAGA |
1: 85,504,945 (GRCm39) |
|
probably null |
Het |
Gm10985 |
GCTCTCTCTCTCTCTCTCTCTCTCTCTCT |
GCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT |
3: 53,752,645 (GRCm39) |
|
probably null |
Het |
H1f4 |
T |
A |
13: 23,806,240 (GRCm39) |
K81* |
probably null |
Het |
Havcr1 |
G |
T |
11: 46,643,407 (GRCm39) |
R109L |
probably damaging |
Het |
Layn |
T |
C |
9: 50,970,856 (GRCm39) |
E229G |
probably benign |
Het |
Lpcat3 |
T |
A |
6: 124,676,955 (GRCm39) |
|
probably null |
Het |
Lrrn1 |
T |
A |
6: 107,546,169 (GRCm39) |
F656I |
possibly damaging |
Het |
Lypd1 |
A |
G |
1: 125,838,121 (GRCm39) |
|
probably benign |
Het |
Or4k41 |
T |
A |
2: 111,279,602 (GRCm39) |
V39E |
possibly damaging |
Het |
Or5v1b |
T |
A |
17: 37,841,246 (GRCm39) |
I126N |
probably damaging |
Het |
Or6c207 |
T |
C |
10: 129,104,934 (GRCm39) |
D86G |
probably damaging |
Het |
Ptprt |
A |
T |
2: 161,653,950 (GRCm39) |
L560Q |
probably damaging |
Het |
Rbm11 |
T |
C |
16: 75,393,469 (GRCm39) |
V55A |
probably damaging |
Het |
Scn11a |
C |
T |
9: 119,632,569 (GRCm39) |
V434I |
probably benign |
Het |
Serpinc1 |
A |
G |
1: 160,829,935 (GRCm39) |
T434A |
probably benign |
Het |
Setd2 |
T |
C |
9: 110,402,753 (GRCm39) |
I1798T |
probably damaging |
Het |
Sfswap |
A |
G |
5: 129,590,298 (GRCm39) |
Y265C |
probably damaging |
Het |
Slc9a8 |
C |
A |
2: 167,266,050 (GRCm39) |
T9K |
probably benign |
Het |
Synpo |
T |
C |
18: 60,736,062 (GRCm39) |
D389G |
probably damaging |
Het |
Vmn1r181 |
C |
T |
7: 23,683,909 (GRCm39) |
L125F |
possibly damaging |
Het |
Wdfy4 |
A |
C |
14: 32,745,331 (GRCm39) |
H2296Q |
probably benign |
Het |
|
Other mutations in Krtap4-9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01949:Krtap4-9
|
APN |
11 |
99,676,391 (GRCm39) |
unclassified |
probably benign |
|
IGL02697:Krtap4-9
|
APN |
11 |
99,676,574 (GRCm39) |
missense |
unknown |
|
IGL03176:Krtap4-9
|
APN |
11 |
99,676,106 (GRCm39) |
unclassified |
probably benign |
|
R0988:Krtap4-9
|
UTSW |
11 |
99,676,362 (GRCm39) |
nonsense |
probably null |
|
R1773:Krtap4-9
|
UTSW |
11 |
99,676,396 (GRCm39) |
unclassified |
probably benign |
|
R1838:Krtap4-9
|
UTSW |
11 |
99,676,222 (GRCm39) |
unclassified |
probably benign |
|
R2566:Krtap4-9
|
UTSW |
11 |
99,676,492 (GRCm39) |
unclassified |
probably benign |
|
R2888:Krtap4-9
|
UTSW |
11 |
99,676,245 (GRCm39) |
nonsense |
probably null |
|
R4633:Krtap4-9
|
UTSW |
11 |
99,676,380 (GRCm39) |
unclassified |
probably benign |
|
R5930:Krtap4-9
|
UTSW |
11 |
99,676,462 (GRCm39) |
unclassified |
probably benign |
|
R6092:Krtap4-9
|
UTSW |
11 |
99,676,481 (GRCm39) |
unclassified |
probably benign |
|
R6501:Krtap4-9
|
UTSW |
11 |
99,676,255 (GRCm39) |
unclassified |
probably benign |
|
R6934:Krtap4-9
|
UTSW |
11 |
99,676,708 (GRCm39) |
nonsense |
probably null |
|
R7131:Krtap4-9
|
UTSW |
11 |
99,676,283 (GRCm39) |
missense |
unknown |
|
R8809:Krtap4-9
|
UTSW |
11 |
99,676,454 (GRCm39) |
missense |
unknown |
|
RF017:Krtap4-9
|
UTSW |
11 |
99,676,225 (GRCm39) |
unclassified |
probably benign |
|
RF023:Krtap4-9
|
UTSW |
11 |
99,676,217 (GRCm39) |
unclassified |
probably benign |
|
|