Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700069L16Rik |
T |
G |
5: 113,861,765 (GRCm39) |
Q35P |
unknown |
Het |
2010109A12Rik |
T |
A |
5: 93,361,305 (GRCm39) |
*120K |
probably null |
Het |
2700049A03Rik |
A |
G |
12: 71,235,448 (GRCm39) |
T1133A |
possibly damaging |
Het |
A830005F24Rik |
G |
A |
13: 48,667,758 (GRCm39) |
R20Q |
unknown |
Het |
Acta2 |
T |
C |
19: 34,223,481 (GRCm39) |
T205A |
probably benign |
Het |
Adcy5 |
A |
G |
16: 35,100,725 (GRCm39) |
D759G |
probably damaging |
Het |
Ankk1 |
T |
A |
9: 49,330,714 (GRCm39) |
M276L |
probably benign |
Het |
Arfgef2 |
G |
A |
2: 166,713,447 (GRCm39) |
E1283K |
probably damaging |
Het |
Arhgef26 |
G |
T |
3: 62,246,803 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
A |
C |
13: 98,133,415 (GRCm39) |
S351A |
probably benign |
Het |
Arih2 |
C |
T |
9: 108,484,504 (GRCm39) |
G436S |
probably damaging |
Het |
Bptf |
T |
C |
11: 106,969,396 (GRCm39) |
T1013A |
probably damaging |
Het |
Camsap1 |
A |
T |
2: 25,828,166 (GRCm39) |
V1186E |
probably benign |
Het |
Capn10 |
G |
T |
1: 92,871,586 (GRCm39) |
A395S |
possibly damaging |
Het |
Ccdc184 |
A |
T |
15: 98,066,737 (GRCm39) |
T181S |
probably damaging |
Het |
Clasp1 |
T |
C |
1: 118,509,108 (GRCm39) |
I1345T |
possibly damaging |
Het |
Cpsf1 |
A |
T |
15: 76,486,779 (GRCm39) |
H252Q |
probably damaging |
Het |
Ctnna2 |
T |
A |
6: 77,582,172 (GRCm39) |
M363L |
probably benign |
Het |
Cyp24a1 |
G |
A |
2: 170,338,625 (GRCm39) |
P24S |
probably benign |
Het |
D130040H23Rik |
A |
G |
8: 69,755,566 (GRCm39) |
H341R |
probably damaging |
Het |
Dclk3 |
A |
G |
9: 111,298,226 (GRCm39) |
E590G |
probably damaging |
Het |
Ear2 |
A |
T |
14: 44,340,729 (GRCm39) |
Y129F |
probably benign |
Het |
Egf |
A |
G |
3: 129,530,514 (GRCm39) |
L216P |
probably damaging |
Het |
Fbxw9 |
T |
A |
8: 85,792,523 (GRCm39) |
H319Q |
probably damaging |
Het |
Gipr |
A |
G |
7: 18,891,487 (GRCm39) |
S397P |
probably damaging |
Het |
Gxylt2 |
G |
T |
6: 100,682,072 (GRCm39) |
E90* |
probably null |
Het |
Hnf1b |
T |
C |
11: 83,784,283 (GRCm39) |
V473A |
probably benign |
Het |
Iffo1 |
G |
A |
6: 125,130,436 (GRCm39) |
E475K |
probably damaging |
Het |
Ifi206 |
T |
A |
1: 173,308,075 (GRCm39) |
R640S |
|
Het |
Ipmk |
A |
G |
10: 71,217,439 (GRCm39) |
S328G |
probably damaging |
Het |
Kcnq1 |
A |
T |
7: 142,737,368 (GRCm39) |
I229F |
probably damaging |
Het |
Klhl36 |
C |
T |
8: 120,601,129 (GRCm39) |
Q383* |
probably null |
Het |
Lrp4 |
G |
T |
2: 91,316,179 (GRCm39) |
V766F |
probably damaging |
Het |
Mettl26 |
T |
A |
17: 26,094,511 (GRCm39) |
M3K |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,570,675 (GRCm39) |
I615F |
unknown |
Het |
Myo7b |
T |
A |
18: 32,133,068 (GRCm39) |
Q427L |
probably benign |
Het |
Naip1 |
A |
G |
13: 100,559,584 (GRCm39) |
M1140T |
probably benign |
Het |
Ncapg |
G |
A |
5: 45,829,834 (GRCm39) |
V179I |
probably damaging |
Het |
Nme4 |
C |
T |
17: 26,314,410 (GRCm39) |
G6E |
possibly damaging |
Het |
Nr1h4 |
T |
C |
10: 89,319,311 (GRCm39) |
Y185C |
probably damaging |
Het |
Nt5c3b |
T |
C |
11: 100,327,012 (GRCm39) |
I95V |
probably benign |
Het |
Ntaq1 |
A |
G |
15: 58,004,913 (GRCm39) |
T9A |
probably benign |
Het |
Or2y3 |
C |
T |
17: 38,393,470 (GRCm39) |
R133H |
probably benign |
Het |
Or5g9 |
A |
T |
2: 85,552,145 (GRCm39) |
Y132F |
probably damaging |
Het |
Or5t16 |
A |
T |
2: 86,819,055 (GRCm39) |
I155N |
probably damaging |
Het |
Pappa2 |
G |
T |
1: 158,611,481 (GRCm39) |
P1494Q |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,457,909 (GRCm39) |
F144S |
probably benign |
Het |
Phactr3 |
A |
G |
2: 177,975,896 (GRCm39) |
H547R |
probably damaging |
Het |
Pik3c2b |
T |
A |
1: 133,018,588 (GRCm39) |
S1012T |
possibly damaging |
Het |
Plppr2 |
G |
A |
9: 21,859,107 (GRCm39) |
G408D |
probably damaging |
Het |
Pom121 |
T |
A |
5: 135,420,554 (GRCm39) |
N289I |
unknown |
Het |
Ppa1 |
T |
A |
10: 61,487,362 (GRCm39) |
S30T |
probably damaging |
Het |
Rgs5 |
A |
T |
1: 169,518,089 (GRCm39) |
K108* |
probably null |
Het |
Rpap1 |
A |
G |
2: 119,607,278 (GRCm39) |
V287A |
probably benign |
Het |
Ryr1 |
A |
G |
7: 28,774,664 (GRCm39) |
Y2326H |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,707,599 (GRCm39) |
S2813P |
probably damaging |
Het |
Sap25 |
T |
C |
5: 137,640,702 (GRCm39) |
|
probably null |
Het |
Senp5 |
T |
C |
16: 31,782,279 (GRCm39) |
Y739C |
probably damaging |
Het |
Slc25a29 |
A |
T |
12: 108,793,017 (GRCm39) |
L187Q |
possibly damaging |
Het |
Slc7a2 |
C |
T |
8: 41,358,641 (GRCm39) |
T328M |
probably damaging |
Het |
Slc7a8 |
T |
C |
14: 55,018,759 (GRCm39) |
N9S |
probably benign |
Het |
Snx18 |
A |
G |
13: 113,754,039 (GRCm39) |
V298A |
probably benign |
Het |
Spo11 |
T |
A |
2: 172,833,904 (GRCm39) |
I342N |
possibly damaging |
Het |
Ssc5d |
A |
G |
7: 4,932,367 (GRCm39) |
K344E |
probably benign |
Het |
Sspo |
A |
T |
6: 48,439,269 (GRCm39) |
D1639V |
probably benign |
Het |
Stk32b |
T |
C |
5: 37,617,001 (GRCm39) |
D285G |
probably benign |
Het |
Sult1b1 |
T |
C |
5: 87,662,815 (GRCm39) |
D295G |
probably benign |
Het |
Syt5 |
A |
G |
7: 4,544,831 (GRCm39) |
L274P |
probably damaging |
Het |
Tas1r2 |
T |
C |
4: 139,396,208 (GRCm39) |
S545P |
possibly damaging |
Het |
Tbc1d17 |
T |
G |
7: 44,490,696 (GRCm39) |
D632A |
probably damaging |
Het |
Tbc1d2 |
A |
G |
4: 46,650,007 (GRCm39) |
S10P |
probably benign |
Het |
Tlk1 |
A |
T |
2: 70,555,908 (GRCm39) |
I417N |
probably damaging |
Het |
Tmem184a |
C |
T |
5: 139,791,984 (GRCm39) |
R348H |
possibly damaging |
Het |
Togaram2 |
T |
A |
17: 72,023,508 (GRCm39) |
V808D |
possibly damaging |
Het |
Tpr |
A |
G |
1: 150,324,939 (GRCm39) |
Q2397R |
probably benign |
Het |
Trav7-4 |
A |
G |
14: 53,698,994 (GRCm39) |
D47G |
possibly damaging |
Het |
Usp17le |
T |
A |
7: 104,419,814 (GRCm39) |
M35L |
probably benign |
Het |
Vegfc |
C |
T |
8: 54,633,829 (GRCm39) |
S262L |
probably benign |
Het |
Vmn2r74 |
T |
A |
7: 85,605,212 (GRCm39) |
I479L |
possibly damaging |
Het |
Vps13a |
A |
T |
19: 16,736,958 (GRCm39) |
F126L |
probably benign |
Het |
Zfp945 |
C |
A |
17: 23,070,582 (GRCm39) |
C460F |
possibly damaging |
Het |
Zmym4 |
G |
T |
4: 126,804,942 (GRCm39) |
S439R |
possibly damaging |
Het |
Zscan4-ps3 |
A |
G |
7: 11,344,093 (GRCm39) |
E17G |
probably damaging |
Het |
|
Other mutations in Kif9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01630:Kif9
|
APN |
9 |
110,314,138 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02273:Kif9
|
APN |
9 |
110,339,538 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02818:Kif9
|
APN |
9 |
110,314,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0034:Kif9
|
UTSW |
9 |
110,348,679 (GRCm39) |
missense |
probably benign |
0.23 |
R0034:Kif9
|
UTSW |
9 |
110,348,679 (GRCm39) |
missense |
probably benign |
0.23 |
R0047:Kif9
|
UTSW |
9 |
110,314,106 (GRCm39) |
missense |
probably benign |
0.05 |
R0047:Kif9
|
UTSW |
9 |
110,314,106 (GRCm39) |
missense |
probably benign |
0.05 |
R0137:Kif9
|
UTSW |
9 |
110,314,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:Kif9
|
UTSW |
9 |
110,340,408 (GRCm39) |
missense |
probably benign |
0.22 |
R1503:Kif9
|
UTSW |
9 |
110,339,506 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1657:Kif9
|
UTSW |
9 |
110,319,034 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1826:Kif9
|
UTSW |
9 |
110,346,701 (GRCm39) |
missense |
probably benign |
0.34 |
R1856:Kif9
|
UTSW |
9 |
110,346,787 (GRCm39) |
missense |
probably null |
1.00 |
R2076:Kif9
|
UTSW |
9 |
110,314,100 (GRCm39) |
splice site |
probably null |
|
R3407:Kif9
|
UTSW |
9 |
110,348,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R4247:Kif9
|
UTSW |
9 |
110,325,027 (GRCm39) |
critical splice donor site |
probably null |
|
R4487:Kif9
|
UTSW |
9 |
110,323,552 (GRCm39) |
missense |
probably null |
1.00 |
R4515:Kif9
|
UTSW |
9 |
110,318,935 (GRCm39) |
missense |
probably benign |
0.38 |
R4880:Kif9
|
UTSW |
9 |
110,330,703 (GRCm39) |
missense |
probably damaging |
0.98 |
R5024:Kif9
|
UTSW |
9 |
110,312,161 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5093:Kif9
|
UTSW |
9 |
110,318,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R5181:Kif9
|
UTSW |
9 |
110,350,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Kif9
|
UTSW |
9 |
110,319,012 (GRCm39) |
missense |
probably damaging |
0.99 |
R5379:Kif9
|
UTSW |
9 |
110,350,371 (GRCm39) |
missense |
probably benign |
0.00 |
R5628:Kif9
|
UTSW |
9 |
110,343,621 (GRCm39) |
nonsense |
probably null |
|
R5653:Kif9
|
UTSW |
9 |
110,353,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Kif9
|
UTSW |
9 |
110,339,532 (GRCm39) |
missense |
probably benign |
|
R5758:Kif9
|
UTSW |
9 |
110,318,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R5986:Kif9
|
UTSW |
9 |
110,319,094 (GRCm39) |
missense |
probably benign |
0.05 |
R6103:Kif9
|
UTSW |
9 |
110,318,917 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6247:Kif9
|
UTSW |
9 |
110,317,612 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6255:Kif9
|
UTSW |
9 |
110,346,902 (GRCm39) |
splice site |
probably null |
|
R6991:Kif9
|
UTSW |
9 |
110,323,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R7113:Kif9
|
UTSW |
9 |
110,335,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R7459:Kif9
|
UTSW |
9 |
110,348,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Kif9
|
UTSW |
9 |
110,350,421 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7892:Kif9
|
UTSW |
9 |
110,343,682 (GRCm39) |
missense |
not run |
|
R8050:Kif9
|
UTSW |
9 |
110,348,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R8370:Kif9
|
UTSW |
9 |
110,317,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R8549:Kif9
|
UTSW |
9 |
110,343,487 (GRCm39) |
splice site |
probably null |
|
R8751:Kif9
|
UTSW |
9 |
110,330,724 (GRCm39) |
missense |
probably benign |
0.03 |
R8830:Kif9
|
UTSW |
9 |
110,353,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R9489:Kif9
|
UTSW |
9 |
110,346,710 (GRCm39) |
missense |
probably benign |
0.01 |
R9519:Kif9
|
UTSW |
9 |
110,350,344 (GRCm39) |
missense |
probably damaging |
0.98 |
R9605:Kif9
|
UTSW |
9 |
110,346,710 (GRCm39) |
missense |
probably benign |
0.01 |
|