Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
G |
T |
7: 29,260,263 (GRCm39) |
|
noncoding transcript |
Het |
Adam21 |
C |
T |
12: 81,606,047 (GRCm39) |
V572I |
probably damaging |
Het |
Arhgap32 |
T |
A |
9: 32,063,315 (GRCm39) |
|
probably null |
Het |
Carmil1 |
A |
T |
13: 24,321,152 (GRCm39) |
I281N |
probably damaging |
Het |
Cdh12 |
T |
A |
15: 21,586,063 (GRCm39) |
|
probably null |
Het |
Cdh20 |
T |
A |
1: 109,976,734 (GRCm39) |
V133E |
probably benign |
Het |
Cntrob |
A |
G |
11: 69,193,708 (GRCm39) |
L814P |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,252,000 (GRCm39) |
N952S |
probably damaging |
Het |
Cspg4 |
A |
G |
9: 56,795,517 (GRCm39) |
Y1084C |
probably damaging |
Het |
Dlg5 |
A |
G |
14: 24,240,378 (GRCm39) |
|
probably benign |
Het |
Glis2 |
T |
C |
16: 4,431,760 (GRCm39) |
|
probably benign |
Het |
Hif3a |
T |
C |
7: 16,788,638 (GRCm39) |
E111G |
probably damaging |
Het |
Kctd4 |
A |
G |
14: 76,200,251 (GRCm39) |
D74G |
probably benign |
Het |
Ktn1 |
G |
A |
14: 47,943,860 (GRCm39) |
|
probably benign |
Het |
Lama2 |
A |
T |
10: 27,335,335 (GRCm39) |
N113K |
probably damaging |
Het |
Ltv1 |
A |
G |
10: 13,054,944 (GRCm39) |
S409P |
probably benign |
Het |
Mgat4c |
A |
G |
10: 102,224,782 (GRCm39) |
E332G |
probably benign |
Het |
Myh6 |
A |
G |
14: 55,201,415 (GRCm39) |
F95L |
probably benign |
Het |
Ndufa4l2 |
A |
G |
10: 127,351,289 (GRCm39) |
I27V |
probably benign |
Het |
Npepl1 |
T |
G |
2: 173,962,447 (GRCm39) |
L371R |
probably damaging |
Het |
Nudt9 |
A |
G |
5: 104,194,972 (GRCm39) |
T23A |
probably benign |
Het |
Ocrl |
G |
A |
X: 47,027,180 (GRCm39) |
V416I |
probably benign |
Het |
Or2g1 |
T |
G |
17: 38,106,895 (GRCm39) |
C187G |
probably damaging |
Het |
Padi2 |
C |
T |
4: 140,645,048 (GRCm39) |
T94I |
probably benign |
Het |
Pcca |
G |
A |
14: 122,922,297 (GRCm39) |
E353K |
probably damaging |
Het |
Pcdhgb2 |
T |
A |
18: 37,824,810 (GRCm39) |
N600K |
probably damaging |
Het |
Pex5l |
A |
G |
3: 33,004,993 (GRCm39) |
L593P |
probably damaging |
Het |
Rbp2 |
G |
A |
9: 98,380,879 (GRCm39) |
D62N |
probably benign |
Het |
Rock1 |
G |
T |
18: 10,067,575 (GRCm39) |
N1319K |
probably benign |
Het |
Ror1 |
A |
C |
4: 100,269,314 (GRCm39) |
D384A |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Sacm1l |
A |
T |
9: 123,381,855 (GRCm39) |
E152D |
probably benign |
Het |
Seh1l |
T |
C |
18: 67,908,087 (GRCm39) |
V3A |
probably benign |
Het |
Serpinb6d |
T |
A |
13: 33,848,097 (GRCm39) |
D20E |
probably benign |
Het |
Serpini1 |
T |
G |
3: 75,521,942 (GRCm39) |
N144K |
probably damaging |
Het |
Slc22a23 |
G |
A |
13: 34,528,323 (GRCm39) |
T153I |
probably benign |
Het |
Slfn8 |
A |
G |
11: 82,908,280 (GRCm39) |
S88P |
probably benign |
Het |
Stpg3 |
T |
A |
2: 25,103,875 (GRCm39) |
M154L |
probably benign |
Het |
Vmn2r115 |
G |
A |
17: 23,564,146 (GRCm39) |
C106Y |
probably damaging |
Het |
Washc3 |
C |
T |
10: 88,055,122 (GRCm39) |
T112M |
probably benign |
Het |
Zfp280d |
C |
T |
9: 72,229,806 (GRCm39) |
T346M |
probably damaging |
Het |
|
Other mutations in Kif21b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Kif21b
|
APN |
1 |
136,080,080 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01020:Kif21b
|
APN |
1 |
136,081,832 (GRCm39) |
splice site |
probably benign |
|
IGL01288:Kif21b
|
APN |
1 |
136,099,922 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02105:Kif21b
|
APN |
1 |
136,099,041 (GRCm39) |
missense |
probably benign |
|
IGL02264:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02308:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02310:Kif21b
|
APN |
1 |
136,087,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02419:Kif21b
|
APN |
1 |
136,079,005 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02553:Kif21b
|
APN |
1 |
136,081,859 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02568:Kif21b
|
APN |
1 |
136,100,605 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02657:Kif21b
|
APN |
1 |
136,099,968 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03068:Kif21b
|
APN |
1 |
136,086,093 (GRCm39) |
unclassified |
probably benign |
|
IGL03230:Kif21b
|
APN |
1 |
136,090,550 (GRCm39) |
missense |
probably benign |
0.03 |
R0629_Kif21b_729
|
UTSW |
1 |
136,099,895 (GRCm39) |
critical splice acceptor site |
probably null |
|
Schiessen
|
UTSW |
1 |
136,075,607 (GRCm39) |
critical splice donor site |
probably null |
|
wolfen
|
UTSW |
1 |
136,072,496 (GRCm39) |
nonsense |
probably null |
|
R0190:Kif21b
|
UTSW |
1 |
136,098,957 (GRCm39) |
missense |
probably benign |
0.32 |
R0349:Kif21b
|
UTSW |
1 |
136,077,049 (GRCm39) |
missense |
probably damaging |
0.97 |
R0501:Kif21b
|
UTSW |
1 |
136,090,837 (GRCm39) |
missense |
probably benign |
0.44 |
R0620:Kif21b
|
UTSW |
1 |
136,087,166 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0629:Kif21b
|
UTSW |
1 |
136,099,895 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0741:Kif21b
|
UTSW |
1 |
136,087,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R1087:Kif21b
|
UTSW |
1 |
136,090,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Kif21b
|
UTSW |
1 |
136,080,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Kif21b
|
UTSW |
1 |
136,083,891 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1464:Kif21b
|
UTSW |
1 |
136,083,891 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1511:Kif21b
|
UTSW |
1 |
136,097,062 (GRCm39) |
critical splice donor site |
probably null |
|
R1512:Kif21b
|
UTSW |
1 |
136,080,543 (GRCm39) |
missense |
probably benign |
0.01 |
R1513:Kif21b
|
UTSW |
1 |
136,083,849 (GRCm39) |
missense |
probably damaging |
0.98 |
R1591:Kif21b
|
UTSW |
1 |
136,077,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Kif21b
|
UTSW |
1 |
136,099,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R1628:Kif21b
|
UTSW |
1 |
136,098,958 (GRCm39) |
missense |
probably benign |
0.01 |
R1658:Kif21b
|
UTSW |
1 |
136,099,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Kif21b
|
UTSW |
1 |
136,087,859 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1741:Kif21b
|
UTSW |
1 |
136,083,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Kif21b
|
UTSW |
1 |
136,087,859 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1807:Kif21b
|
UTSW |
1 |
136,075,531 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1896:Kif21b
|
UTSW |
1 |
136,075,583 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1970:Kif21b
|
UTSW |
1 |
136,098,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R1984:Kif21b
|
UTSW |
1 |
136,075,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1985:Kif21b
|
UTSW |
1 |
136,075,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Kif21b
|
UTSW |
1 |
136,075,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Kif21b
|
UTSW |
1 |
136,080,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R1990:Kif21b
|
UTSW |
1 |
136,089,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Kif21b
|
UTSW |
1 |
136,076,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Kif21b
|
UTSW |
1 |
136,088,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Kif21b
|
UTSW |
1 |
136,080,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R2248:Kif21b
|
UTSW |
1 |
136,100,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R2886:Kif21b
|
UTSW |
1 |
136,075,612 (GRCm39) |
splice site |
probably benign |
|
R2896:Kif21b
|
UTSW |
1 |
136,081,955 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3706:Kif21b
|
UTSW |
1 |
136,087,148 (GRCm39) |
missense |
probably benign |
0.06 |
R3827:Kif21b
|
UTSW |
1 |
136,090,732 (GRCm39) |
critical splice donor site |
probably null |
|
R4227:Kif21b
|
UTSW |
1 |
136,081,831 (GRCm39) |
splice site |
probably null |
|
R4600:Kif21b
|
UTSW |
1 |
136,075,602 (GRCm39) |
missense |
probably benign |
0.39 |
R4608:Kif21b
|
UTSW |
1 |
136,075,924 (GRCm39) |
intron |
probably benign |
|
R4749:Kif21b
|
UTSW |
1 |
136,072,487 (GRCm39) |
nonsense |
probably null |
|
R4841:Kif21b
|
UTSW |
1 |
136,072,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Kif21b
|
UTSW |
1 |
136,072,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Kif21b
|
UTSW |
1 |
136,079,063 (GRCm39) |
splice site |
probably null |
|
R4959:Kif21b
|
UTSW |
1 |
136,076,108 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5018:Kif21b
|
UTSW |
1 |
136,099,972 (GRCm39) |
missense |
probably benign |
0.30 |
R5116:Kif21b
|
UTSW |
1 |
136,080,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R5119:Kif21b
|
UTSW |
1 |
136,090,838 (GRCm39) |
missense |
probably benign |
|
R5197:Kif21b
|
UTSW |
1 |
136,072,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R5230:Kif21b
|
UTSW |
1 |
136,099,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R5249:Kif21b
|
UTSW |
1 |
136,096,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R5337:Kif21b
|
UTSW |
1 |
136,098,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Kif21b
|
UTSW |
1 |
136,100,030 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5466:Kif21b
|
UTSW |
1 |
136,075,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5557:Kif21b
|
UTSW |
1 |
136,097,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R5727:Kif21b
|
UTSW |
1 |
136,097,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Kif21b
|
UTSW |
1 |
136,078,875 (GRCm39) |
nonsense |
probably null |
|
R5929:Kif21b
|
UTSW |
1 |
136,078,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Kif21b
|
UTSW |
1 |
136,077,156 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6349:Kif21b
|
UTSW |
1 |
136,086,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R6648:Kif21b
|
UTSW |
1 |
136,080,135 (GRCm39) |
missense |
probably benign |
0.00 |
R6831:Kif21b
|
UTSW |
1 |
136,072,496 (GRCm39) |
nonsense |
probably null |
|
R7156:Kif21b
|
UTSW |
1 |
136,075,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R7165:Kif21b
|
UTSW |
1 |
136,077,186 (GRCm39) |
missense |
probably damaging |
0.98 |
R7327:Kif21b
|
UTSW |
1 |
136,087,387 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7680:Kif21b
|
UTSW |
1 |
136,075,607 (GRCm39) |
critical splice donor site |
probably null |
|
R7975:Kif21b
|
UTSW |
1 |
136,098,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Kif21b
|
UTSW |
1 |
136,100,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8467:Kif21b
|
UTSW |
1 |
136,100,021 (GRCm39) |
missense |
probably damaging |
0.98 |
R9031:Kif21b
|
UTSW |
1 |
136,073,042 (GRCm39) |
missense |
probably damaging |
0.99 |
R9101:Kif21b
|
UTSW |
1 |
136,078,893 (GRCm39) |
missense |
probably damaging |
0.96 |
R9191:Kif21b
|
UTSW |
1 |
136,100,559 (GRCm39) |
nonsense |
probably null |
|
R9261:Kif21b
|
UTSW |
1 |
136,077,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R9280:Kif21b
|
UTSW |
1 |
136,099,445 (GRCm39) |
critical splice donor site |
probably null |
|
R9307:Kif21b
|
UTSW |
1 |
136,101,800 (GRCm39) |
missense |
probably benign |
|
R9562:Kif21b
|
UTSW |
1 |
136,077,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R9563:Kif21b
|
UTSW |
1 |
136,077,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Kif21b
|
UTSW |
1 |
136,077,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R9758:Kif21b
|
UTSW |
1 |
136,080,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9760:Kif21b
|
UTSW |
1 |
136,076,421 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Kif21b
|
UTSW |
1 |
136,086,079 (GRCm39) |
missense |
probably damaging |
1.00 |
X0053:Kif21b
|
UTSW |
1 |
136,077,054 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Kif21b
|
UTSW |
1 |
136,100,683 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kif21b
|
UTSW |
1 |
136,081,875 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Kif21b
|
UTSW |
1 |
136,076,050 (GRCm39) |
missense |
probably damaging |
1.00 |
|