Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
A |
G |
11: 94,242,750 (GRCm39) |
S1326P |
probably damaging |
Het |
Alpk1 |
A |
T |
3: 127,466,970 (GRCm39) |
L1103Q |
probably damaging |
Het |
Arhgap11a |
A |
C |
2: 113,667,906 (GRCm39) |
|
probably benign |
Het |
Arl6ip6 |
A |
G |
2: 53,082,226 (GRCm39) |
Y31C |
possibly damaging |
Het |
Arpin |
G |
T |
7: 79,577,395 (GRCm39) |
D217E |
possibly damaging |
Het |
Atp13a4 |
C |
T |
16: 29,241,521 (GRCm39) |
V735I |
probably benign |
Het |
Ccdc146 |
A |
T |
5: 21,502,631 (GRCm39) |
F753L |
probably benign |
Het |
Cdh3 |
T |
A |
8: 107,270,880 (GRCm39) |
L511* |
probably null |
Het |
Chrna1 |
A |
T |
2: 73,397,206 (GRCm39) |
I361N |
possibly damaging |
Het |
Clk2 |
G |
A |
3: 89,083,020 (GRCm39) |
R432H |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,261,018 (GRCm39) |
|
probably benign |
Het |
Cstf1 |
G |
T |
2: 172,219,774 (GRCm39) |
R295L |
probably benign |
Het |
Dsg2 |
A |
G |
18: 20,725,467 (GRCm39) |
D526G |
probably damaging |
Het |
Dsg4 |
T |
A |
18: 20,595,577 (GRCm39) |
H593Q |
probably benign |
Het |
Dysf |
T |
C |
6: 84,107,109 (GRCm39) |
Y1171H |
possibly damaging |
Het |
Erbb4 |
A |
G |
1: 68,345,023 (GRCm39) |
L566P |
probably benign |
Het |
Fam185a |
T |
A |
5: 21,660,829 (GRCm39) |
D281E |
probably damaging |
Het |
Fam185a |
T |
A |
5: 21,634,839 (GRCm39) |
|
probably benign |
Het |
Fam91a1 |
T |
A |
15: 58,304,831 (GRCm39) |
|
probably null |
Het |
Fat2 |
A |
G |
11: 55,202,109 (GRCm39) |
W322R |
probably damaging |
Het |
Fbxw8 |
T |
A |
5: 118,204,125 (GRCm39) |
|
probably benign |
Het |
Ganc |
A |
G |
2: 120,288,615 (GRCm39) |
T874A |
probably benign |
Het |
Gm3543 |
T |
C |
14: 41,802,048 (GRCm39) |
I145M |
probably benign |
Het |
Gtf2i |
G |
A |
5: 134,274,015 (GRCm39) |
T712I |
probably damaging |
Het |
Hk1 |
A |
G |
10: 62,131,552 (GRCm39) |
S268P |
possibly damaging |
Het |
Hmcn1 |
A |
G |
1: 150,868,774 (GRCm39) |
V10A |
probably benign |
Het |
Hsd17b4 |
C |
T |
18: 50,295,164 (GRCm39) |
|
probably benign |
Het |
Ighv1-75 |
A |
T |
12: 115,797,725 (GRCm39) |
W66R |
probably damaging |
Het |
Kif5b |
A |
T |
18: 6,220,914 (GRCm39) |
I398N |
probably benign |
Het |
Metap2 |
T |
C |
10: 93,701,311 (GRCm39) |
M165V |
probably damaging |
Het |
Mterf2 |
A |
C |
10: 84,956,331 (GRCm39) |
L98V |
probably damaging |
Het |
Muc16 |
A |
G |
9: 18,409,849 (GRCm39) |
|
probably null |
Het |
Myo3b |
A |
G |
2: 69,925,568 (GRCm39) |
M12V |
probably benign |
Het |
Nat10 |
C |
A |
2: 103,583,013 (GRCm39) |
R136I |
probably damaging |
Het |
Nsd2 |
T |
G |
5: 34,003,542 (GRCm39) |
S231A |
probably damaging |
Het |
Or4a71 |
T |
C |
2: 89,358,275 (GRCm39) |
T160A |
probably benign |
Het |
Or4k37 |
A |
T |
2: 111,159,333 (GRCm39) |
M190L |
probably benign |
Het |
Pcdhb14 |
T |
A |
18: 37,581,071 (GRCm39) |
L59* |
probably null |
Het |
Pias4 |
A |
G |
10: 80,999,621 (GRCm39) |
L144P |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,433,746 (GRCm39) |
N598K |
probably benign |
Het |
Polq |
A |
G |
16: 36,862,130 (GRCm39) |
Y550C |
probably damaging |
Het |
Pot1b |
T |
A |
17: 56,002,024 (GRCm39) |
|
probably benign |
Het |
Proz |
T |
C |
8: 13,115,260 (GRCm39) |
V92A |
probably benign |
Het |
Rab4a |
T |
C |
8: 124,550,561 (GRCm39) |
F14L |
probably benign |
Het |
Riok3 |
T |
A |
18: 12,276,073 (GRCm39) |
C256* |
probably null |
Het |
Slc6a1 |
T |
A |
6: 114,279,451 (GRCm39) |
|
probably benign |
Het |
Socs5 |
C |
T |
17: 87,442,419 (GRCm39) |
T453M |
probably damaging |
Het |
Spata3 |
T |
C |
1: 85,952,211 (GRCm39) |
L135P |
probably damaging |
Het |
Spata46 |
A |
G |
1: 170,139,534 (GRCm39) |
K178E |
probably damaging |
Het |
Spr |
T |
C |
6: 85,114,430 (GRCm39) |
N100D |
probably damaging |
Het |
Srrm4 |
C |
T |
5: 116,582,624 (GRCm39) |
|
probably benign |
Het |
Stard3 |
T |
C |
11: 98,267,389 (GRCm39) |
F169S |
possibly damaging |
Het |
Tbx1 |
T |
A |
16: 18,402,847 (GRCm39) |
D222V |
probably damaging |
Het |
Trbv23 |
C |
T |
6: 41,193,279 (GRCm39) |
Q56* |
probably null |
Het |
Tsc22d1 |
A |
G |
14: 76,654,838 (GRCm39) |
N357S |
possibly damaging |
Het |
Ugt1a6a |
C |
T |
1: 88,066,811 (GRCm39) |
P206S |
probably benign |
Het |
Utp20 |
A |
G |
10: 88,600,657 (GRCm39) |
V19A |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,646,447 (GRCm39) |
N1517S |
probably benign |
Het |
Washc2 |
T |
C |
6: 116,218,571 (GRCm39) |
I672T |
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 |
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 |
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 |
|