Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432M17Rik |
T |
C |
3: 121,473,172 (GRCm39) |
F109S |
unknown |
Het |
Ankhd1 |
A |
T |
18: 36,694,111 (GRCm39) |
|
probably null |
Het |
Atp8a1 |
C |
T |
5: 67,863,248 (GRCm39) |
|
probably null |
Het |
Ccdc136 |
G |
T |
6: 29,417,497 (GRCm39) |
V707F |
probably benign |
Het |
Ccdc157 |
A |
T |
11: 4,100,078 (GRCm39) |
C91* |
probably null |
Het |
Ceacam3 |
T |
A |
7: 16,892,296 (GRCm39) |
N346K |
possibly damaging |
Het |
Cfap251 |
A |
G |
5: 123,460,626 (GRCm39) |
D1196G |
probably benign |
Het |
Chd4 |
A |
G |
6: 125,077,551 (GRCm39) |
E74G |
probably damaging |
Het |
Cntn1 |
A |
G |
15: 92,192,892 (GRCm39) |
M665V |
probably benign |
Het |
Crtc2 |
C |
T |
3: 90,168,348 (GRCm39) |
Q364* |
probably null |
Het |
Csf1r |
T |
A |
18: 61,262,796 (GRCm39) |
I857N |
probably damaging |
Het |
Dner |
C |
T |
1: 84,558,460 (GRCm39) |
G168D |
probably damaging |
Het |
Edar |
T |
C |
10: 58,443,182 (GRCm39) |
T315A |
probably benign |
Het |
Egflam |
A |
G |
15: 7,333,493 (GRCm39) |
V153A |
probably damaging |
Het |
Enoph1 |
T |
C |
5: 100,211,682 (GRCm39) |
I193T |
possibly damaging |
Het |
Epc1 |
A |
G |
18: 6,462,969 (GRCm39) |
I9T |
probably damaging |
Het |
Fbxw18 |
T |
A |
9: 109,522,246 (GRCm39) |
I208F |
possibly damaging |
Het |
Gm4841 |
A |
G |
18: 60,403,364 (GRCm39) |
V243A |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,869,534 (GRCm39) |
V4297A |
probably damaging |
Het |
Itsn2 |
C |
T |
12: 4,677,960 (GRCm39) |
P106S |
probably benign |
Het |
Kcnu1 |
A |
G |
8: 26,352,486 (GRCm39) |
T218A |
probably damaging |
Het |
Krt14 |
A |
T |
11: 100,095,526 (GRCm39) |
M293K |
probably damaging |
Het |
Meis3 |
T |
A |
7: 15,917,989 (GRCm39) |
V307E |
probably damaging |
Het |
Nadk2 |
A |
C |
15: 9,108,401 (GRCm39) |
I417L |
probably benign |
Het |
Nav2 |
AAGCAGCAGCAGCAGCAGCAGCAGCA |
AAGCAGCAGCAGCAGCAGCAGCA |
7: 49,058,440 (GRCm39) |
|
probably benign |
Het |
Neb |
A |
T |
2: 52,171,515 (GRCm39) |
N1659K |
probably benign |
Het |
Nhsl3 |
T |
C |
4: 129,118,005 (GRCm39) |
T208A |
possibly damaging |
Het |
Or10w1 |
T |
C |
19: 13,632,630 (GRCm39) |
V274A |
probably benign |
Het |
Or8g32 |
T |
C |
9: 39,305,785 (GRCm39) |
S233P |
probably damaging |
Het |
Or8s5 |
G |
A |
15: 98,238,246 (GRCm39) |
A208V |
probably benign |
Het |
Pde3b |
A |
T |
7: 114,093,772 (GRCm39) |
N339Y |
probably damaging |
Het |
Pde8b |
A |
G |
13: 95,223,361 (GRCm39) |
F298L |
possibly damaging |
Het |
Phtf1 |
G |
A |
3: 103,906,603 (GRCm39) |
R606H |
probably damaging |
Het |
Psd4 |
A |
G |
2: 24,290,528 (GRCm39) |
D535G |
possibly damaging |
Het |
Rad51ap1 |
A |
G |
6: 126,905,121 (GRCm39) |
V130A |
probably damaging |
Het |
Rbm11 |
T |
C |
16: 75,393,474 (GRCm39) |
F57L |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,671,401 (GRCm39) |
V1334A |
possibly damaging |
Het |
Satb2 |
T |
C |
1: 56,870,686 (GRCm39) |
E433G |
probably damaging |
Het |
Sema6b |
G |
A |
17: 56,435,413 (GRCm39) |
R277* |
probably null |
Het |
Sepsecs |
A |
T |
5: 52,805,015 (GRCm39) |
S349T |
probably benign |
Het |
Slc35b2 |
T |
C |
17: 45,877,424 (GRCm39) |
Y184H |
probably damaging |
Het |
Slc7a2 |
T |
C |
8: 41,368,067 (GRCm39) |
|
probably null |
Het |
Smc1b |
T |
A |
15: 84,955,066 (GRCm39) |
Y1062F |
probably benign |
Het |
Snrnp70 |
G |
A |
7: 45,026,476 (GRCm39) |
R298* |
probably null |
Het |
Sntb1 |
C |
G |
15: 55,506,191 (GRCm39) |
G461R |
probably damaging |
Het |
Taar8c |
A |
T |
10: 23,977,246 (GRCm39) |
C189S |
probably damaging |
Het |
Tas1r2 |
T |
A |
4: 139,382,672 (GRCm39) |
D103E |
probably damaging |
Het |
Timd2 |
T |
C |
11: 46,568,087 (GRCm39) |
I236V |
probably benign |
Het |
Tmem87a |
A |
G |
2: 120,208,407 (GRCm39) |
V316A |
probably damaging |
Het |
Treml2 |
T |
A |
17: 48,607,601 (GRCm39) |
L16Q |
probably damaging |
Het |
Zcchc14 |
G |
A |
8: 122,335,337 (GRCm39) |
|
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,013,178 (GRCm39) |
Y567H |
probably damaging |
Het |
Zfp551 |
G |
A |
7: 12,150,087 (GRCm39) |
R441* |
probably null |
Het |
Zfp930 |
A |
G |
8: 69,679,373 (GRCm39) |
I59M |
probably benign |
Het |
|
Other mutations in Kif1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Kif1a
|
APN |
1 |
92,982,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01574:Kif1a
|
APN |
1 |
93,010,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01637:Kif1a
|
APN |
1 |
92,967,575 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01895:Kif1a
|
APN |
1 |
92,953,455 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02215:Kif1a
|
APN |
1 |
92,948,271 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02571:Kif1a
|
APN |
1 |
92,948,178 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02734:Kif1a
|
APN |
1 |
92,990,280 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02752:Kif1a
|
APN |
1 |
92,967,569 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02990:Kif1a
|
APN |
1 |
92,966,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03298:Kif1a
|
APN |
1 |
92,993,903 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03309:Kif1a
|
APN |
1 |
92,986,579 (GRCm39) |
nonsense |
probably null |
|
IGL03354:Kif1a
|
APN |
1 |
92,987,957 (GRCm39) |
missense |
probably damaging |
1.00 |
asbestos
|
UTSW |
1 |
92,950,227 (GRCm39) |
missense |
probably damaging |
1.00 |
chrysolite
|
UTSW |
1 |
93,002,670 (GRCm39) |
splice site |
probably benign |
|
osmium
|
UTSW |
1 |
92,986,532 (GRCm39) |
splice site |
probably benign |
|
R4538_Kif1a_397
|
UTSW |
1 |
93,004,769 (GRCm39) |
missense |
probably damaging |
1.00 |
1mM(1):Kif1a
|
UTSW |
1 |
93,004,790 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03046:Kif1a
|
UTSW |
1 |
93,010,128 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4508001:Kif1a
|
UTSW |
1 |
92,974,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Kif1a
|
UTSW |
1 |
92,970,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Kif1a
|
UTSW |
1 |
92,974,500 (GRCm39) |
splice site |
probably benign |
|
R0243:Kif1a
|
UTSW |
1 |
92,969,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Kif1a
|
UTSW |
1 |
92,982,164 (GRCm39) |
splice site |
probably benign |
|
R0335:Kif1a
|
UTSW |
1 |
92,980,288 (GRCm39) |
splice site |
probably benign |
|
R0380:Kif1a
|
UTSW |
1 |
92,983,753 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0472:Kif1a
|
UTSW |
1 |
92,946,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R0501:Kif1a
|
UTSW |
1 |
92,983,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Kif1a
|
UTSW |
1 |
92,971,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R0628:Kif1a
|
UTSW |
1 |
92,947,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R0848:Kif1a
|
UTSW |
1 |
92,947,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Kif1a
|
UTSW |
1 |
92,951,175 (GRCm39) |
splice site |
probably benign |
|
R1132:Kif1a
|
UTSW |
1 |
92,983,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R1387:Kif1a
|
UTSW |
1 |
92,983,672 (GRCm39) |
splice site |
probably benign |
|
R1466:Kif1a
|
UTSW |
1 |
92,982,651 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1466:Kif1a
|
UTSW |
1 |
92,982,651 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1544:Kif1a
|
UTSW |
1 |
93,002,670 (GRCm39) |
splice site |
probably benign |
|
R1569:Kif1a
|
UTSW |
1 |
92,986,532 (GRCm39) |
splice site |
probably benign |
|
R1802:Kif1a
|
UTSW |
1 |
92,993,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Kif1a
|
UTSW |
1 |
92,946,753 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1919:Kif1a
|
UTSW |
1 |
92,946,753 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1999:Kif1a
|
UTSW |
1 |
92,988,517 (GRCm39) |
missense |
probably damaging |
0.98 |
R2000:Kif1a
|
UTSW |
1 |
92,982,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R2276:Kif1a
|
UTSW |
1 |
92,996,199 (GRCm39) |
splice site |
probably benign |
|
R2307:Kif1a
|
UTSW |
1 |
93,006,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Kif1a
|
UTSW |
1 |
92,974,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R3440:Kif1a
|
UTSW |
1 |
92,964,575 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3441:Kif1a
|
UTSW |
1 |
92,964,575 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3618:Kif1a
|
UTSW |
1 |
93,004,765 (GRCm39) |
missense |
probably null |
1.00 |
R3957:Kif1a
|
UTSW |
1 |
92,953,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R4010:Kif1a
|
UTSW |
1 |
92,950,131 (GRCm39) |
missense |
probably benign |
0.42 |
R4013:Kif1a
|
UTSW |
1 |
93,004,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R4017:Kif1a
|
UTSW |
1 |
93,004,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R4115:Kif1a
|
UTSW |
1 |
92,980,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R4386:Kif1a
|
UTSW |
1 |
92,996,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R4538:Kif1a
|
UTSW |
1 |
93,004,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R4608:Kif1a
|
UTSW |
1 |
92,952,368 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4625:Kif1a
|
UTSW |
1 |
92,970,381 (GRCm39) |
missense |
probably benign |
0.00 |
R4701:Kif1a
|
UTSW |
1 |
93,006,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R4794:Kif1a
|
UTSW |
1 |
92,953,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R4830:Kif1a
|
UTSW |
1 |
92,948,931 (GRCm39) |
splice site |
probably null |
|
R4903:Kif1a
|
UTSW |
1 |
92,949,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Kif1a
|
UTSW |
1 |
93,002,700 (GRCm39) |
missense |
probably benign |
0.21 |
R4918:Kif1a
|
UTSW |
1 |
93,002,700 (GRCm39) |
missense |
probably benign |
0.21 |
R4991:Kif1a
|
UTSW |
1 |
93,006,530 (GRCm39) |
missense |
probably benign |
0.00 |
R5028:Kif1a
|
UTSW |
1 |
92,982,049 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5051:Kif1a
|
UTSW |
1 |
93,003,876 (GRCm39) |
splice site |
probably null |
|
R5073:Kif1a
|
UTSW |
1 |
92,950,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5103:Kif1a
|
UTSW |
1 |
92,974,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R5481:Kif1a
|
UTSW |
1 |
92,987,966 (GRCm39) |
missense |
probably benign |
0.01 |
R5510:Kif1a
|
UTSW |
1 |
92,969,414 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5610:Kif1a
|
UTSW |
1 |
92,953,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Kif1a
|
UTSW |
1 |
92,983,489 (GRCm39) |
missense |
probably damaging |
0.98 |
R5808:Kif1a
|
UTSW |
1 |
92,970,420 (GRCm39) |
missense |
probably damaging |
0.99 |
R6027:Kif1a
|
UTSW |
1 |
92,953,365 (GRCm39) |
missense |
probably benign |
0.33 |
R6056:Kif1a
|
UTSW |
1 |
92,952,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R6077:Kif1a
|
UTSW |
1 |
92,982,618 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6120:Kif1a
|
UTSW |
1 |
92,952,296 (GRCm39) |
splice site |
probably null |
|
R6126:Kif1a
|
UTSW |
1 |
92,947,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R6130:Kif1a
|
UTSW |
1 |
92,964,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R6255:Kif1a
|
UTSW |
1 |
92,947,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Kif1a
|
UTSW |
1 |
92,982,663 (GRCm39) |
nonsense |
probably null |
|
R6326:Kif1a
|
UTSW |
1 |
93,004,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R6594:Kif1a
|
UTSW |
1 |
92,949,035 (GRCm39) |
missense |
probably benign |
0.00 |
R6653:Kif1a
|
UTSW |
1 |
93,005,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6791:Kif1a
|
UTSW |
1 |
92,993,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6853:Kif1a
|
UTSW |
1 |
92,967,524 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7022:Kif1a
|
UTSW |
1 |
92,993,820 (GRCm39) |
missense |
probably benign |
0.31 |
R7059:Kif1a
|
UTSW |
1 |
92,974,551 (GRCm39) |
intron |
probably benign |
|
R7103:Kif1a
|
UTSW |
1 |
93,005,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Kif1a
|
UTSW |
1 |
92,969,305 (GRCm39) |
missense |
probably benign |
0.35 |
R7259:Kif1a
|
UTSW |
1 |
93,001,532 (GRCm39) |
nonsense |
probably null |
|
R7424:Kif1a
|
UTSW |
1 |
92,982,039 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7659:Kif1a
|
UTSW |
1 |
92,974,542 (GRCm39) |
intron |
probably benign |
|
R7681:Kif1a
|
UTSW |
1 |
92,982,666 (GRCm39) |
missense |
probably benign |
|
R7976:Kif1a
|
UTSW |
1 |
92,967,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Kif1a
|
UTSW |
1 |
92,982,423 (GRCm39) |
intron |
probably benign |
|
R8420:Kif1a
|
UTSW |
1 |
92,950,141 (GRCm39) |
missense |
probably benign |
|
R8994:Kif1a
|
UTSW |
1 |
92,983,457 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9016:Kif1a
|
UTSW |
1 |
92,953,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R9206:Kif1a
|
UTSW |
1 |
92,979,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R9246:Kif1a
|
UTSW |
1 |
93,005,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R9252:Kif1a
|
UTSW |
1 |
93,002,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Kif1a
|
UTSW |
1 |
93,000,029 (GRCm39) |
critical splice donor site |
probably null |
|
R9413:Kif1a
|
UTSW |
1 |
92,949,019 (GRCm39) |
missense |
probably benign |
0.00 |
R9612:Kif1a
|
UTSW |
1 |
92,953,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R9621:Kif1a
|
UTSW |
1 |
92,983,445 (GRCm39) |
missense |
probably benign |
|
R9625:Kif1a
|
UTSW |
1 |
93,000,766 (GRCm39) |
missense |
probably benign |
0.42 |
R9694:Kif1a
|
UTSW |
1 |
92,950,173 (GRCm39) |
missense |
probably benign |
|
Z1176:Kif1a
|
UTSW |
1 |
92,950,213 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kif1a
|
UTSW |
1 |
92,949,038 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Kif1a
|
UTSW |
1 |
92,983,419 (GRCm39) |
missense |
probably benign |
0.01 |
|