Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
T |
C |
5: 138,561,271 (GRCm39) |
I130M |
probably damaging |
Het |
4921539E11Rik |
T |
C |
4: 103,092,895 (GRCm39) |
D142G |
probably damaging |
Het |
Abcb10 |
C |
T |
8: 124,691,757 (GRCm39) |
A403T |
|
Het |
Arfgef2 |
T |
A |
2: 166,678,170 (GRCm39) |
S218T |
possibly damaging |
Het |
Armc8 |
C |
T |
9: 99,433,600 (GRCm39) |
V40I |
probably benign |
Het |
Caps2 |
A |
T |
10: 112,018,381 (GRCm39) |
D177V |
probably benign |
Het |
Cdh8 |
A |
T |
8: 99,757,676 (GRCm39) |
F641I |
probably damaging |
Het |
Cemip |
T |
C |
7: 83,596,384 (GRCm39) |
S1127G |
probably benign |
Het |
Cmtm1 |
C |
A |
8: 105,036,088 (GRCm39) |
Q180H |
unknown |
Het |
Col15a1 |
C |
T |
4: 47,312,196 (GRCm39) |
T1337I |
probably damaging |
Het |
Col18a1 |
A |
T |
10: 76,910,284 (GRCm39) |
M555K |
probably benign |
Het |
Ctrb1 |
A |
G |
8: 112,415,823 (GRCm39) |
F89L |
possibly damaging |
Het |
Disp1 |
T |
C |
1: 182,917,199 (GRCm39) |
T76A |
probably benign |
Het |
Dpep1 |
T |
C |
8: 123,926,965 (GRCm39) |
V263A |
probably damaging |
Het |
Dysf |
G |
A |
6: 84,114,358 (GRCm39) |
E1216K |
probably damaging |
Het |
F830016B08Rik |
A |
G |
18: 60,433,052 (GRCm39) |
Y45C |
probably benign |
Het |
Fam186a |
CGG |
CG |
15: 99,841,914 (GRCm39) |
|
probably null |
Het |
Gcm1 |
T |
A |
9: 77,971,816 (GRCm39) |
D252E |
probably benign |
Het |
Gm11559 |
A |
G |
11: 99,755,416 (GRCm39) |
T22A |
unknown |
Het |
Gm4847 |
C |
T |
1: 166,465,917 (GRCm39) |
R224Q |
probably damaging |
Het |
Hypk |
A |
G |
2: 121,286,859 (GRCm39) |
|
probably benign |
Het |
I830077J02Rik |
C |
T |
3: 105,834,233 (GRCm39) |
C64Y |
possibly damaging |
Het |
Igkv4-86 |
T |
C |
6: 68,887,650 (GRCm39) |
I30V |
probably benign |
Het |
Il17ra |
A |
G |
6: 120,455,416 (GRCm39) |
I342V |
probably benign |
Het |
Kcnip3 |
C |
T |
2: 127,352,828 (GRCm39) |
A64T |
possibly damaging |
Het |
Kdm5d |
T |
A |
Y: 940,658 (GRCm39) |
D1056E |
possibly damaging |
Het |
Krtap19-2 |
C |
T |
16: 88,670,903 (GRCm39) |
G81R |
unknown |
Het |
Ldlrad1 |
G |
A |
4: 107,066,688 (GRCm39) |
A8T |
probably benign |
Het |
Lpin1 |
A |
T |
12: 16,629,965 (GRCm39) |
I69N |
|
Het |
Matcap1 |
G |
A |
8: 106,012,145 (GRCm39) |
R101W |
probably benign |
Het |
Mki67 |
C |
T |
7: 135,299,293 (GRCm39) |
D1914N |
probably damaging |
Het |
Mmrn1 |
A |
T |
6: 60,937,707 (GRCm39) |
Q235L |
probably damaging |
Het |
Mndal |
T |
A |
1: 173,699,111 (GRCm39) |
K185* |
probably null |
Het |
Muc6 |
T |
C |
7: 141,233,354 (GRCm39) |
T802A |
probably damaging |
Het |
Necab1 |
A |
T |
4: 15,005,073 (GRCm39) |
F130L |
probably damaging |
Het |
Nemf |
A |
T |
12: 69,402,826 (GRCm39) |
M70K |
possibly damaging |
Het |
Nploc4 |
A |
G |
11: 120,280,240 (GRCm39) |
I436T |
possibly damaging |
Het |
Obscn |
C |
A |
11: 59,015,439 (GRCm39) |
R1011M |
probably damaging |
Het |
Or4k44 |
A |
T |
2: 111,367,825 (GRCm39) |
F270I |
probably damaging |
Het |
Or5aq1b |
T |
C |
2: 86,901,570 (GRCm39) |
K303E |
probably benign |
Het |
Or8k24 |
T |
A |
2: 86,215,911 (GRCm39) |
M284L |
probably benign |
Het |
Ormdl1 |
T |
A |
1: 53,338,139 (GRCm39) |
M1K |
probably null |
Het |
Pramel34 |
A |
T |
5: 93,784,597 (GRCm39) |
L289Q |
probably damaging |
Het |
Psmb3 |
A |
G |
11: 97,594,723 (GRCm39) |
D38G |
probably benign |
Het |
Psme4 |
T |
A |
11: 30,792,026 (GRCm39) |
L1171Q |
probably damaging |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Slc22a18 |
G |
A |
7: 143,052,911 (GRCm39) |
V379I |
probably damaging |
Het |
Speg |
T |
A |
1: 75,392,240 (GRCm39) |
F1632L |
probably damaging |
Het |
Taok1 |
G |
A |
11: 77,470,659 (GRCm39) |
R49C |
possibly damaging |
Het |
Ttll6 |
T |
C |
11: 96,047,425 (GRCm39) |
S675P |
probably benign |
Het |
Usp8 |
A |
T |
2: 126,559,918 (GRCm39) |
|
probably benign |
Het |
Vmn2r81 |
T |
A |
10: 79,110,538 (GRCm39) |
N550K |
possibly damaging |
Het |
Zfp119a |
A |
T |
17: 56,172,971 (GRCm39) |
C291S |
probably damaging |
Het |
Zfp329 |
C |
A |
7: 12,544,313 (GRCm39) |
G404C |
probably damaging |
Het |
Zfp934 |
C |
A |
13: 62,667,985 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Kif19b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6021:Kif19b
|
UTSW |
5 |
140,455,434 (GRCm39) |
missense |
probably damaging |
0.98 |
R6401:Kif19b
|
UTSW |
5 |
140,442,698 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6515:Kif19b
|
UTSW |
5 |
140,480,779 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7126:Kif19b
|
UTSW |
5 |
140,477,073 (GRCm39) |
missense |
probably benign |
0.43 |
R7236:Kif19b
|
UTSW |
5 |
140,457,400 (GRCm39) |
missense |
probably benign |
0.31 |
R7241:Kif19b
|
UTSW |
5 |
140,447,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7273:Kif19b
|
UTSW |
5 |
140,461,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Kif19b
|
UTSW |
5 |
140,457,425 (GRCm39) |
missense |
probably benign |
0.45 |
R7357:Kif19b
|
UTSW |
5 |
140,480,806 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7903:Kif19b
|
UTSW |
5 |
140,461,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Kif19b
|
UTSW |
5 |
140,461,785 (GRCm39) |
missense |
probably damaging |
0.96 |
R8826:Kif19b
|
UTSW |
5 |
140,455,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R8862:Kif19b
|
UTSW |
5 |
140,472,534 (GRCm39) |
missense |
probably damaging |
0.97 |
R9013:Kif19b
|
UTSW |
5 |
140,449,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R9214:Kif19b
|
UTSW |
5 |
140,468,257 (GRCm39) |
missense |
probably benign |
0.01 |
R9605:Kif19b
|
UTSW |
5 |
140,455,461 (GRCm39) |
missense |
probably benign |
0.26 |
R9725:Kif19b
|
UTSW |
5 |
140,460,651 (GRCm39) |
missense |
probably benign |
0.02 |
R9794:Kif19b
|
UTSW |
5 |
140,448,070 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Kif19b
|
UTSW |
5 |
140,464,740 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Kif19b
|
UTSW |
5 |
140,446,615 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Kif19b
|
UTSW |
5 |
140,432,177 (GRCm39) |
missense |
probably damaging |
0.98 |
|