Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,035,712 (GRCm39) |
|
probably benign |
Het |
Bicdl2 |
G |
A |
17: 23,885,732 (GRCm39) |
|
probably null |
Het |
Cables1 |
A |
G |
18: 12,072,789 (GRCm39) |
D448G |
possibly damaging |
Het |
Casq2 |
A |
T |
3: 102,051,534 (GRCm39) |
N338I |
probably damaging |
Het |
Ccr1l1 |
T |
C |
9: 123,777,553 (GRCm39) |
N298S |
probably damaging |
Het |
Dnajc17 |
A |
G |
2: 119,009,933 (GRCm39) |
V231A |
probably benign |
Het |
Ell2 |
T |
C |
13: 75,911,904 (GRCm39) |
S397P |
probably damaging |
Het |
Gm9966 |
T |
C |
7: 95,607,753 (GRCm39) |
C25R |
unknown |
Het |
H2-DMa |
A |
G |
17: 34,356,121 (GRCm39) |
N41S |
probably damaging |
Het |
Helz2 |
A |
G |
2: 180,882,535 (GRCm39) |
M86T |
probably benign |
Het |
Il17rd |
T |
A |
14: 26,821,510 (GRCm39) |
I268N |
probably damaging |
Het |
Ipcef1 |
C |
T |
10: 6,850,641 (GRCm39) |
V317M |
probably damaging |
Het |
Itgae |
A |
T |
11: 73,031,513 (GRCm39) |
E1076D |
probably benign |
Het |
Kcnq5 |
A |
T |
1: 21,539,771 (GRCm39) |
Y382* |
probably null |
Het |
Lilrb4a |
A |
T |
10: 51,367,709 (GRCm39) |
N84Y |
probably benign |
Het |
Mdga2 |
A |
G |
12: 66,553,044 (GRCm39) |
|
probably benign |
Het |
Naca |
T |
C |
10: 127,877,547 (GRCm39) |
|
probably benign |
Het |
Naif1 |
C |
T |
2: 32,344,887 (GRCm39) |
P197L |
probably benign |
Het |
Nrk |
T |
C |
X: 137,876,197 (GRCm39) |
L466P |
probably damaging |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Pkn1 |
G |
A |
8: 84,407,867 (GRCm39) |
A421V |
probably benign |
Het |
Rusc2 |
A |
G |
4: 43,415,456 (GRCm39) |
Q254R |
probably benign |
Het |
Ryr1 |
G |
T |
7: 28,774,223 (GRCm39) |
R2404S |
probably damaging |
Het |
Selenon |
T |
C |
4: 134,270,380 (GRCm39) |
D324G |
probably null |
Het |
Serpinh1 |
T |
C |
7: 98,998,228 (GRCm39) |
Y134C |
probably damaging |
Het |
Serpini2 |
T |
C |
3: 75,166,921 (GRCm39) |
Y112C |
probably damaging |
Het |
Setx |
T |
G |
2: 29,038,637 (GRCm39) |
C1707W |
probably damaging |
Het |
Sit1 |
C |
T |
4: 43,483,314 (GRCm39) |
R50H |
possibly damaging |
Het |
Slc27a5 |
T |
A |
7: 12,723,487 (GRCm39) |
|
probably benign |
Het |
Slc5a4b |
C |
T |
10: 75,910,907 (GRCm39) |
V310M |
probably damaging |
Het |
Smc6 |
T |
C |
12: 11,326,294 (GRCm39) |
V97A |
probably damaging |
Het |
Ube2frt |
A |
G |
12: 36,140,574 (GRCm39) |
|
probably benign |
Het |
Usp42 |
T |
C |
5: 143,707,384 (GRCm39) |
|
probably benign |
Het |
Utrn |
A |
T |
10: 12,615,105 (GRCm39) |
|
probably null |
Het |
Vmn2r82 |
A |
G |
10: 79,232,082 (GRCm39) |
I694V |
probably benign |
Het |
Vmn2r-ps69 |
T |
C |
7: 84,956,832 (GRCm39) |
|
noncoding transcript |
Het |
Zfpm2 |
A |
G |
15: 40,965,719 (GRCm39) |
T603A |
probably benign |
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 |
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 |
R3780:Kif21b
|
UTSW |
1 |
136,083,964 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|