Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
A |
13: 119,602,659 (GRCm39) |
V7E |
possibly damaging |
Het |
Aars2 |
G |
A |
17: 45,825,535 (GRCm39) |
G333S |
probably damaging |
Het |
Aen |
T |
A |
7: 78,555,592 (GRCm39) |
I85N |
probably damaging |
Het |
Ahnak |
C |
A |
19: 8,985,389 (GRCm39) |
H2224Q |
possibly damaging |
Het |
Aldh18a1 |
C |
T |
19: 40,568,487 (GRCm39) |
R41H |
possibly damaging |
Het |
Bpifb9b |
T |
A |
2: 154,151,284 (GRCm39) |
W2R |
probably damaging |
Het |
Caprin2 |
A |
G |
6: 148,779,390 (GRCm39) |
I139T |
probably benign |
Het |
Cdhr3 |
T |
A |
12: 33,103,474 (GRCm39) |
N381I |
probably damaging |
Het |
Cecr2 |
A |
G |
6: 120,735,011 (GRCm39) |
Y721C |
probably damaging |
Het |
Cfhr4 |
A |
T |
1: 139,680,749 (GRCm39) |
C256* |
probably null |
Het |
Cherp |
G |
T |
8: 73,224,725 (GRCm39) |
A125D |
probably damaging |
Het |
Cped1 |
G |
A |
6: 22,138,714 (GRCm39) |
|
probably null |
Het |
Ctdp1 |
T |
A |
18: 80,502,512 (GRCm39) |
|
probably null |
Het |
Cyp2c55 |
T |
C |
19: 39,007,111 (GRCm39) |
I169T |
probably benign |
Het |
Cyp4a31 |
T |
C |
4: 115,432,117 (GRCm39) |
L418P |
possibly damaging |
Het |
Efcab7 |
T |
C |
4: 99,717,627 (GRCm39) |
|
probably benign |
Het |
Efcab8 |
T |
C |
2: 153,652,188 (GRCm39) |
W466R |
possibly damaging |
Het |
Ehd3 |
C |
A |
17: 74,112,408 (GRCm39) |
N57K |
probably benign |
Het |
Ern2 |
C |
A |
7: 121,772,495 (GRCm39) |
K654N |
probably damaging |
Het |
Fbh1 |
A |
T |
2: 11,753,257 (GRCm39) |
F879L |
probably benign |
Het |
Gde1 |
T |
C |
7: 118,291,004 (GRCm39) |
D92G |
probably null |
Het |
Heatr5b |
A |
G |
17: 79,110,863 (GRCm39) |
V995A |
probably damaging |
Het |
Ifrd2 |
A |
G |
9: 107,469,290 (GRCm39) |
E346G |
probably damaging |
Het |
Ism1 |
AACGGACCCGTTCTTGTGGCTATGCA |
AA |
2: 139,587,962 (GRCm39) |
|
probably benign |
Het |
Itgb4 |
T |
C |
11: 115,888,963 (GRCm39) |
V1102A |
possibly damaging |
Het |
Itgb6 |
A |
T |
2: 60,435,620 (GRCm39) |
I710N |
probably damaging |
Het |
Kif9 |
T |
C |
9: 110,346,902 (GRCm39) |
|
probably null |
Het |
Kitl |
T |
C |
10: 99,925,095 (GRCm39) |
*57Q |
probably null |
Het |
Lrat |
C |
A |
3: 82,810,812 (GRCm39) |
V70F |
probably damaging |
Het |
Lrrc9 |
T |
A |
12: 72,533,797 (GRCm39) |
M1022K |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,566,895 (GRCm39) |
T1875A |
unknown |
Het |
Mup4 |
T |
A |
4: 59,957,890 (GRCm39) |
N171I |
probably damaging |
Het |
Npas4 |
G |
A |
19: 5,036,403 (GRCm39) |
T587I |
probably damaging |
Het |
Oas3 |
A |
G |
5: 120,909,295 (GRCm39) |
V217A |
probably benign |
Het |
Or6c1b |
A |
G |
10: 129,273,557 (GRCm39) |
N292S |
possibly damaging |
Het |
Osbp |
C |
A |
19: 11,955,317 (GRCm39) |
A323D |
possibly damaging |
Het |
Panx2 |
G |
A |
15: 88,951,821 (GRCm39) |
R96H |
probably damaging |
Het |
Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,254,341 (GRCm39) |
R385G |
possibly damaging |
Het |
Pkn2 |
T |
C |
3: 142,517,360 (GRCm39) |
T476A |
probably damaging |
Het |
Plekha4 |
T |
C |
7: 45,203,226 (GRCm39) |
|
probably benign |
Het |
Ppfibp2 |
T |
C |
7: 107,280,969 (GRCm39) |
S94P |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,320,007 (GRCm39) |
I429L |
probably benign |
Het |
Rif1 |
A |
G |
2: 51,975,065 (GRCm39) |
K325E |
probably damaging |
Het |
Ror2 |
T |
C |
13: 53,264,578 (GRCm39) |
Y826C |
probably damaging |
Het |
Rsph10b |
G |
A |
5: 143,896,564 (GRCm39) |
G19R |
probably damaging |
Het |
Slc20a1 |
A |
G |
2: 129,049,924 (GRCm39) |
N361D |
probably damaging |
Het |
Slc26a9 |
A |
G |
1: 131,691,647 (GRCm39) |
D630G |
probably benign |
Het |
Smtnl2 |
G |
A |
11: 72,292,225 (GRCm39) |
A274V |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,181,314 (GRCm39) |
|
probably null |
Het |
Tspan10 |
T |
A |
11: 120,335,368 (GRCm39) |
C159* |
probably null |
Het |
Uba6 |
G |
A |
5: 86,312,624 (GRCm39) |
T23I |
probably benign |
Het |
Vmn2r74 |
T |
C |
7: 85,601,659 (GRCm39) |
T660A |
possibly damaging |
Het |
Vwa5b1 |
T |
C |
4: 138,305,983 (GRCm39) |
N905S |
probably benign |
Het |
Zfp831 |
T |
C |
2: 174,488,214 (GRCm39) |
L963P |
possibly damaging |
Het |
Zfp990 |
T |
A |
4: 145,264,359 (GRCm39) |
N452K |
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 |
R5314:Kif1a
|
UTSW |
1 |
92,946,220 (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 |
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 |
|