Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
CCACGACC |
CCACGACCACGACC |
16: 56,447,952 (GRCm39) |
|
probably benign |
Het |
Acan |
T |
G |
7: 78,742,148 (GRCm39) |
V515G |
possibly damaging |
Het |
Acap3 |
TGG |
TGGACTGCTGCATCCAGG |
4: 155,989,555 (GRCm39) |
|
probably benign |
Het |
AI837181 |
G |
GGCT |
19: 5,475,266 (GRCm39) |
|
probably benign |
Het |
Ankhd1 |
GGCGGC |
GGCGGCAGCGGC |
18: 36,693,977 (GRCm39) |
|
probably benign |
Het |
Anks1b |
G |
A |
10: 89,869,087 (GRCm39) |
G49D |
probably damaging |
Het |
Arid1b |
GCG |
GCGACG |
17: 5,045,869 (GRCm39) |
|
probably benign |
Het |
Arid1b |
CGG |
CGGAGG |
17: 5,045,870 (GRCm39) |
|
probably benign |
Het |
Begain |
G |
GCCGCCC |
12: 108,999,363 (GRCm39) |
|
probably null |
Het |
Cacna1e |
A |
G |
1: 154,317,882 (GRCm39) |
M1500T |
probably damaging |
Het |
Casp16 |
C |
A |
17: 23,774,201 (GRCm39) |
|
probably benign |
Het |
Ccdc174 |
T |
C |
6: 91,876,347 (GRCm39) |
S395P |
possibly damaging |
Het |
Ccdc7a |
T |
G |
8: 129,691,434 (GRCm39) |
Q396H |
probably damaging |
Het |
Ccdc85c |
CC |
CCGGC |
12: 108,240,887 (GRCm39) |
|
probably benign |
Het |
Cemip |
T |
C |
7: 83,610,843 (GRCm39) |
T704A |
probably damaging |
Het |
Cfap68 |
C |
T |
9: 50,677,067 (GRCm39) |
R8H |
probably benign |
Het |
Col7a1 |
C |
T |
9: 108,793,547 (GRCm39) |
P1370S |
unknown |
Het |
Cts8 |
T |
C |
13: 61,397,102 (GRCm39) |
I273V |
probably benign |
Het |
Cyp2c50 |
T |
A |
19: 40,078,268 (GRCm39) |
I42N |
probably damaging |
Het |
Dbt |
T |
G |
3: 116,341,717 (GRCm39) |
Y439* |
probably null |
Het |
Dennd1b |
T |
A |
1: 138,981,135 (GRCm39) |
D116E |
probably damaging |
Het |
Dkk2 |
T |
A |
3: 131,883,863 (GRCm39) |
H254Q |
probably damaging |
Het |
Dpy30 |
C |
A |
17: 74,622,902 (GRCm39) |
V27F |
possibly damaging |
Het |
Efhd2 |
GCCGCC |
GCCGCCCCCGCC |
4: 141,602,069 (GRCm39) |
|
probably benign |
Het |
Eif4g3 |
A |
T |
4: 137,903,235 (GRCm39) |
E1020V |
probably damaging |
Het |
Elmo1 |
T |
A |
13: 20,458,706 (GRCm39) |
S156T |
probably benign |
Het |
Fancd2os |
T |
C |
6: 113,574,881 (GRCm39) |
T42A |
probably damaging |
Het |
Fbrsl1 |
TGTGC |
TGTGCGGGTGTGGGTGC |
5: 110,525,984 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
T |
C |
2: 82,808,184 (GRCm39) |
V1501A |
probably benign |
Het |
Gabrb2 |
A |
G |
11: 42,517,705 (GRCm39) |
Y509C |
probably damaging |
Het |
Gm8369 |
GTGT |
GTGTTTGT |
19: 11,489,118 (GRCm39) |
|
probably null |
Het |
Gpr139 |
T |
C |
7: 118,744,090 (GRCm39) |
D165G |
probably benign |
Het |
Grik2 |
T |
C |
10: 49,120,480 (GRCm39) |
E603G |
probably damaging |
Het |
H13 |
G |
A |
2: 152,511,589 (GRCm39) |
E30K |
probably damaging |
Het |
Ifitm10 |
T |
A |
7: 141,882,330 (GRCm39) |
M147L |
unknown |
Het |
Itpkb |
C |
T |
1: 180,160,887 (GRCm39) |
R338W |
probably damaging |
Het |
Krtap28-10 |
ACCACAGCCACAGCCACCACAGCCACAGCCACCACAGC |
ACCACAGCCACAGCCACCACAGCCACAGCCACCACAGCCACAGCCACCACAGC |
1: 83,019,974 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
AGCCACCACAGC |
AGCCACCACAGCCACCGCCACCACAGC |
1: 83,020,000 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CAGCCA |
CAGCCATAGCCA |
1: 83,019,849 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
AGCCAC |
AGCCACCGCCAC |
1: 83,019,856 (GRCm39) |
|
probably benign |
Het |
Las1l |
AGTGG |
AGTGGTGG |
X: 94,984,422 (GRCm39) |
|
probably benign |
Het |
Mical2 |
T |
C |
7: 111,922,833 (GRCm39) |
Y613H |
probably damaging |
Het |
Mlf2 |
C |
A |
6: 124,911,259 (GRCm39) |
H91Q |
probably benign |
Het |
Nat9 |
A |
T |
11: 115,074,212 (GRCm39) |
I152N |
probably damaging |
Het |
Or10d4c |
T |
C |
9: 39,558,559 (GRCm39) |
M179T |
probably benign |
Het |
Or4a75 |
A |
T |
2: 89,447,711 (GRCm39) |
I275N |
possibly damaging |
Het |
Pdik1l |
CACCAC |
CACCACAACCAC |
4: 134,006,822 (GRCm39) |
|
probably benign |
Het |
Phldb2 |
T |
C |
16: 45,583,337 (GRCm39) |
S1054G |
probably damaging |
Het |
Pkhd1l1 |
TTTT |
TTTTTTTTTTGTTT |
15: 44,421,901 (GRCm39) |
|
probably benign |
Het |
Plcg2 |
T |
A |
8: 118,300,263 (GRCm39) |
|
probably null |
Het |
Polr1has |
CACCACCACCACCACCAC |
CACCACCACCACCACCACCACAACCACCACCACCACCAC |
17: 37,275,946 (GRCm39) |
|
probably benign |
Het |
Prdm16 |
T |
A |
4: 154,426,452 (GRCm39) |
R444S |
probably damaging |
Het |
Rgs6 |
T |
C |
12: 83,110,223 (GRCm39) |
F163L |
probably damaging |
Het |
Rnaseh2a |
A |
T |
8: 85,686,687 (GRCm39) |
L154* |
probably null |
Het |
Rpp38 |
A |
G |
2: 3,330,072 (GRCm39) |
S277P |
unknown |
Het |
Setd1a |
GGTAGTGGT |
GGTAGTGGTTGTAGTGGT |
7: 127,384,486 (GRCm39) |
|
probably benign |
Het |
Shisa6 |
CGACAGCAGCAGAG |
CG |
11: 66,416,749 (GRCm39) |
|
probably benign |
Het |
Slc27a2 |
T |
A |
2: 126,395,175 (GRCm39) |
L34Q |
possibly damaging |
Het |
Slc7a6 |
G |
A |
8: 106,922,030 (GRCm39) |
V386I |
probably benign |
Het |
Spry1 |
C |
T |
3: 37,697,264 (GRCm39) |
T169I |
possibly damaging |
Het |
Sry |
TGCTGCTGCTG |
TGCTGCTGCTGCTG |
Y: 2,662,826 (GRCm39) |
|
probably benign |
Het |
Stk24 |
A |
T |
14: 121,532,172 (GRCm39) |
I275N |
probably benign |
Het |
Strn |
TC |
TCCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCAGGC |
17: 78,984,716 (GRCm39) |
|
probably null |
Het |
Tcp11l2 |
C |
A |
10: 84,449,388 (GRCm39) |
P451Q |
probably damaging |
Het |
Tfeb |
AGC |
AGCTGC |
17: 48,097,027 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
TGCTGCTGCTGCTGCGGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
15: 72,673,138 (GRCm39) |
|
probably benign |
Het |
V1ra8 |
A |
G |
6: 90,180,591 (GRCm39) |
T265A |
probably benign |
Het |
Zfp106 |
CTCCTGGCAGT |
CT |
2: 120,355,026 (GRCm39) |
|
probably benign |
Het |
Zfp612 |
C |
A |
8: 110,816,193 (GRCm39) |
H467N |
probably damaging |
Het |
Zfp777 |
A |
T |
6: 48,018,982 (GRCm39) |
Y317* |
probably null |
Het |
|
Other mutations in Kif1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01311:Kif1b
|
APN |
4 |
149,305,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01943:Kif1b
|
APN |
4 |
149,299,362 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02240:Kif1b
|
APN |
4 |
149,330,871 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02414:Kif1b
|
APN |
4 |
149,283,771 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02490:Kif1b
|
APN |
4 |
149,288,665 (GRCm39) |
missense |
probably benign |
|
IGL02501:Kif1b
|
APN |
4 |
149,299,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02833:Kif1b
|
APN |
4 |
149,330,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02852:Kif1b
|
APN |
4 |
149,375,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02900:Kif1b
|
APN |
4 |
149,265,266 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03287:Kif1b
|
APN |
4 |
149,299,438 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03412:Kif1b
|
APN |
4 |
149,359,396 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4305001:Kif1b
|
UTSW |
4 |
149,305,249 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0005:Kif1b
|
UTSW |
4 |
149,266,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Kif1b
|
UTSW |
4 |
149,348,058 (GRCm39) |
splice site |
probably benign |
|
R0044:Kif1b
|
UTSW |
4 |
149,348,058 (GRCm39) |
splice site |
probably benign |
|
R0129:Kif1b
|
UTSW |
4 |
149,345,658 (GRCm39) |
missense |
probably benign |
|
R0180:Kif1b
|
UTSW |
4 |
149,298,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0288:Kif1b
|
UTSW |
4 |
149,283,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Kif1b
|
UTSW |
4 |
149,347,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Kif1b
|
UTSW |
4 |
149,286,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R0398:Kif1b
|
UTSW |
4 |
149,288,688 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0403:Kif1b
|
UTSW |
4 |
149,266,424 (GRCm39) |
nonsense |
probably null |
|
R0445:Kif1b
|
UTSW |
4 |
149,272,466 (GRCm39) |
missense |
probably benign |
0.01 |
R1466:Kif1b
|
UTSW |
4 |
149,307,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Kif1b
|
UTSW |
4 |
149,307,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R1681:Kif1b
|
UTSW |
4 |
149,279,958 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1728:Kif1b
|
UTSW |
4 |
149,272,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1840:Kif1b
|
UTSW |
4 |
149,272,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Kif1b
|
UTSW |
4 |
149,272,089 (GRCm39) |
missense |
probably benign |
|
R1915:Kif1b
|
UTSW |
4 |
149,351,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Kif1b
|
UTSW |
4 |
149,272,097 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2124:Kif1b
|
UTSW |
4 |
149,306,753 (GRCm39) |
missense |
probably benign |
0.08 |
R2126:Kif1b
|
UTSW |
4 |
149,272,097 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2127:Kif1b
|
UTSW |
4 |
149,272,097 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2128:Kif1b
|
UTSW |
4 |
149,272,097 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2129:Kif1b
|
UTSW |
4 |
149,272,097 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2146:Kif1b
|
UTSW |
4 |
149,268,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R2255:Kif1b
|
UTSW |
4 |
149,359,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R2392:Kif1b
|
UTSW |
4 |
149,305,077 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2883:Kif1b
|
UTSW |
4 |
149,322,105 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2981:Kif1b
|
UTSW |
4 |
149,304,998 (GRCm39) |
critical splice donor site |
probably null |
|
R3038:Kif1b
|
UTSW |
4 |
149,297,790 (GRCm39) |
missense |
probably benign |
0.02 |
R3616:Kif1b
|
UTSW |
4 |
149,346,740 (GRCm39) |
splice site |
probably benign |
|
R3935:Kif1b
|
UTSW |
4 |
149,321,617 (GRCm39) |
missense |
probably benign |
0.00 |
R4347:Kif1b
|
UTSW |
4 |
149,331,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R4423:Kif1b
|
UTSW |
4 |
149,298,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R4637:Kif1b
|
UTSW |
4 |
149,283,768 (GRCm39) |
missense |
probably damaging |
0.97 |
R4745:Kif1b
|
UTSW |
4 |
149,322,339 (GRCm39) |
nonsense |
probably null |
|
R4807:Kif1b
|
UTSW |
4 |
149,332,378 (GRCm39) |
intron |
probably benign |
|
R5618:Kif1b
|
UTSW |
4 |
149,354,346 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5644:Kif1b
|
UTSW |
4 |
149,322,939 (GRCm39) |
missense |
probably damaging |
0.96 |
R5683:Kif1b
|
UTSW |
4 |
149,306,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Kif1b
|
UTSW |
4 |
149,358,306 (GRCm39) |
splice site |
probably null |
|
R6022:Kif1b
|
UTSW |
4 |
149,282,989 (GRCm39) |
missense |
probably benign |
0.01 |
R6048:Kif1b
|
UTSW |
4 |
149,348,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6137:Kif1b
|
UTSW |
4 |
149,322,883 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6139:Kif1b
|
UTSW |
4 |
149,321,989 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6171:Kif1b
|
UTSW |
4 |
149,342,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R6250:Kif1b
|
UTSW |
4 |
149,298,100 (GRCm39) |
missense |
probably benign |
0.00 |
R6423:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6424:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6425:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6443:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6460:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6462:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6463:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6469:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6470:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6471:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6472:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6504:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6536:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6537:Kif1b
|
UTSW |
4 |
149,277,053 (GRCm39) |
missense |
probably benign |
0.16 |
R6668:Kif1b
|
UTSW |
4 |
149,297,864 (GRCm39) |
missense |
probably benign |
0.09 |
R6698:Kif1b
|
UTSW |
4 |
149,359,413 (GRCm39) |
missense |
probably damaging |
0.99 |
R7065:Kif1b
|
UTSW |
4 |
149,286,982 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7222:Kif1b
|
UTSW |
4 |
149,309,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Kif1b
|
UTSW |
4 |
149,298,547 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7720:Kif1b
|
UTSW |
4 |
149,266,812 (GRCm39) |
missense |
probably benign |
0.01 |
R7744:Kif1b
|
UTSW |
4 |
149,321,532 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7797:Kif1b
|
UTSW |
4 |
149,321,844 (GRCm39) |
missense |
probably benign |
|
R7829:Kif1b
|
UTSW |
4 |
149,305,447 (GRCm39) |
splice site |
probably null |
|
R7869:Kif1b
|
UTSW |
4 |
149,268,833 (GRCm39) |
missense |
probably benign |
0.01 |
R7878:Kif1b
|
UTSW |
4 |
149,299,454 (GRCm39) |
missense |
probably damaging |
0.98 |
R7980:Kif1b
|
UTSW |
4 |
149,354,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R8047:Kif1b
|
UTSW |
4 |
149,299,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Kif1b
|
UTSW |
4 |
149,275,642 (GRCm39) |
missense |
probably benign |
0.10 |
R8243:Kif1b
|
UTSW |
4 |
149,288,724 (GRCm39) |
missense |
probably benign |
|
R8252:Kif1b
|
UTSW |
4 |
149,358,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R8342:Kif1b
|
UTSW |
4 |
149,306,805 (GRCm39) |
missense |
probably damaging |
0.96 |
R8460:Kif1b
|
UTSW |
4 |
149,272,077 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8462:Kif1b
|
UTSW |
4 |
149,266,797 (GRCm39) |
missense |
probably benign |
0.05 |
R8496:Kif1b
|
UTSW |
4 |
149,277,068 (GRCm39) |
nonsense |
probably null |
|
R8687:Kif1b
|
UTSW |
4 |
149,345,620 (GRCm39) |
nonsense |
probably null |
|
R8694:Kif1b
|
UTSW |
4 |
149,305,024 (GRCm39) |
missense |
probably damaging |
0.98 |
R8842:Kif1b
|
UTSW |
4 |
149,338,196 (GRCm39) |
missense |
probably damaging |
0.98 |
R8883:Kif1b
|
UTSW |
4 |
149,361,342 (GRCm39) |
missense |
probably benign |
|
R8971:Kif1b
|
UTSW |
4 |
149,332,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R8994:Kif1b
|
UTSW |
4 |
149,279,939 (GRCm39) |
missense |
|
|
R9002:Kif1b
|
UTSW |
4 |
149,275,712 (GRCm39) |
missense |
probably damaging |
0.96 |
R9227:Kif1b
|
UTSW |
4 |
149,322,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Kif1b
|
UTSW |
4 |
149,275,652 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9450:Kif1b
|
UTSW |
4 |
149,322,467 (GRCm39) |
missense |
probably benign |
0.01 |
R9478:Kif1b
|
UTSW |
4 |
149,345,616 (GRCm39) |
critical splice donor site |
probably null |
|
R9571:Kif1b
|
UTSW |
4 |
149,305,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R9644:Kif1b
|
UTSW |
4 |
149,375,836 (GRCm39) |
missense |
probably damaging |
1.00 |
X0009:Kif1b
|
UTSW |
4 |
149,331,721 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Kif1b
|
UTSW |
4 |
149,359,462 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kif1b
|
UTSW |
4 |
149,350,755 (GRCm39) |
missense |
possibly damaging |
0.89 |
|