Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam10 |
T |
A |
9: 70,661,516 (GRCm39) |
I363N |
probably damaging |
Het |
Ahcyl2 |
T |
C |
6: 29,890,670 (GRCm39) |
|
probably benign |
Het |
Asap1 |
A |
G |
15: 63,966,213 (GRCm39) |
L941P |
probably damaging |
Het |
Aurka |
G |
A |
2: 172,209,067 (GRCm39) |
R23C |
probably benign |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Casp8ap2 |
T |
A |
4: 32,640,381 (GRCm39) |
H478Q |
probably damaging |
Het |
Clcn4 |
C |
T |
7: 7,293,503 (GRCm39) |
A418T |
possibly damaging |
Het |
Cplx3 |
T |
C |
9: 57,521,384 (GRCm39) |
T193A |
probably benign |
Het |
Cpxm2 |
A |
T |
7: 131,645,772 (GRCm39) |
Y715* |
probably null |
Het |
Csmd1 |
T |
C |
8: 16,235,287 (GRCm39) |
M1179V |
probably benign |
Het |
Ddx21 |
A |
T |
10: 62,423,307 (GRCm39) |
F632I |
probably damaging |
Het |
Dnai1 |
C |
A |
4: 41,625,335 (GRCm39) |
T433K |
possibly damaging |
Het |
Dpyd |
G |
A |
3: 119,225,191 (GRCm39) |
G988D |
probably damaging |
Het |
Dync1i2 |
AAAAGAAGAGGAAAGAAGAGGAAAG |
AAAAGAAGAGGAAAG |
2: 71,044,862 (GRCm39) |
|
probably null |
Het |
Dync1li2 |
A |
T |
8: 105,147,297 (GRCm39) |
S466T |
probably benign |
Het |
Ears2 |
T |
C |
7: 121,647,667 (GRCm39) |
T206A |
probably benign |
Het |
Elmod1 |
A |
T |
9: 53,838,876 (GRCm39) |
|
probably benign |
Het |
Eps8l3 |
C |
A |
3: 107,799,661 (GRCm39) |
D590E |
probably benign |
Het |
Etfdh |
A |
T |
3: 79,513,112 (GRCm39) |
H370Q |
probably benign |
Het |
Fam83g |
C |
A |
11: 61,598,489 (GRCm39) |
A792E |
probably benign |
Het |
Ffar3 |
G |
T |
7: 30,554,962 (GRCm39) |
Y119* |
probably null |
Het |
Fosb |
G |
T |
7: 19,041,138 (GRCm39) |
S118R |
possibly damaging |
Het |
Foxn4 |
G |
A |
5: 114,401,175 (GRCm39) |
L3F |
probably damaging |
Het |
Foxo4 |
A |
G |
X: 100,298,784 (GRCm39) |
K65E |
probably damaging |
Het |
Frem2 |
A |
G |
3: 53,424,281 (GRCm39) |
L3052P |
probably damaging |
Het |
Fubp3 |
G |
A |
2: 31,498,149 (GRCm39) |
R101H |
probably damaging |
Het |
Gba2 |
C |
A |
4: 43,569,927 (GRCm39) |
G429C |
probably damaging |
Het |
Gimap1 |
T |
C |
6: 48,718,363 (GRCm39) |
|
probably benign |
Het |
Gnas |
A |
G |
2: 174,140,304 (GRCm39) |
T158A |
possibly damaging |
Het |
Gpc5 |
T |
C |
14: 115,789,740 (GRCm39) |
V538A |
probably damaging |
Het |
Greb1l |
T |
C |
18: 10,458,781 (GRCm39) |
|
probably benign |
Het |
H2-M10.5 |
G |
A |
17: 37,085,620 (GRCm39) |
G260R |
probably damaging |
Het |
Hbs1l |
A |
C |
10: 21,225,222 (GRCm39) |
Q412H |
probably benign |
Het |
Hecw1 |
G |
T |
13: 14,411,526 (GRCm39) |
T1058N |
probably damaging |
Het |
Heph |
A |
T |
X: 95,601,690 (GRCm39) |
T1027S |
probably damaging |
Het |
Hoga1 |
A |
C |
19: 42,034,514 (GRCm39) |
E53A |
possibly damaging |
Het |
Insrr |
T |
G |
3: 87,721,744 (GRCm39) |
|
probably benign |
Het |
Ipo11 |
A |
T |
13: 107,028,969 (GRCm39) |
V328D |
probably damaging |
Het |
Jakmip1 |
T |
C |
5: 37,276,217 (GRCm39) |
V509A |
probably damaging |
Het |
Jmjd1c |
T |
C |
10: 67,061,568 (GRCm39) |
V1307A |
probably benign |
Het |
Kmt2a |
T |
A |
9: 44,758,868 (GRCm39) |
S1027C |
probably damaging |
Het |
Kprp |
G |
C |
3: 92,731,664 (GRCm39) |
P462R |
unknown |
Het |
Lrit3 |
A |
T |
3: 129,584,945 (GRCm39) |
V271D |
probably damaging |
Het |
Mark4 |
A |
C |
7: 19,182,598 (GRCm39) |
|
probably benign |
Het |
Mfsd14b |
A |
G |
13: 65,226,259 (GRCm39) |
V142A |
probably benign |
Het |
Mis18bp1 |
A |
T |
12: 65,208,227 (GRCm39) |
I162N |
possibly damaging |
Het |
Mrpl43 |
A |
T |
19: 44,994,391 (GRCm39) |
|
probably benign |
Het |
Mrpl47 |
A |
G |
3: 32,790,842 (GRCm39) |
F16S |
probably benign |
Het |
Myh2 |
G |
T |
11: 67,069,793 (GRCm39) |
G380C |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,412,464 (GRCm39) |
Y3284H |
probably damaging |
Het |
Nectin2 |
A |
G |
7: 19,467,148 (GRCm39) |
|
probably benign |
Het |
Neu3 |
A |
G |
7: 99,463,390 (GRCm39) |
V111A |
probably damaging |
Het |
Nol4l |
T |
C |
2: 153,259,604 (GRCm39) |
|
probably null |
Het |
Nphp3 |
C |
A |
9: 103,900,633 (GRCm39) |
H510Q |
probably damaging |
Het |
Nprl3 |
T |
A |
11: 32,183,118 (GRCm39) |
|
probably null |
Het |
Or14c39 |
A |
G |
7: 86,344,516 (GRCm39) |
N284S |
probably damaging |
Het |
Or4c58 |
T |
C |
2: 89,674,787 (GRCm39) |
T177A |
probably benign |
Het |
Or52ab7 |
T |
C |
7: 102,978,170 (GRCm39) |
V159A |
probably benign |
Het |
Or6c2 |
T |
C |
10: 129,362,765 (GRCm39) |
I223T |
possibly damaging |
Het |
Pex1 |
A |
G |
5: 3,656,130 (GRCm39) |
E319G |
possibly damaging |
Het |
Pgap6 |
T |
C |
17: 26,336,088 (GRCm39) |
L130S |
probably benign |
Het |
Phtf1 |
C |
A |
3: 103,911,785 (GRCm39) |
T709K |
probably damaging |
Het |
Plek2 |
A |
T |
12: 78,938,946 (GRCm39) |
L271Q |
probably damaging |
Het |
Plekhg5 |
T |
A |
4: 152,191,926 (GRCm39) |
C421* |
probably null |
Het |
Polk |
A |
C |
13: 96,620,687 (GRCm39) |
C525W |
probably damaging |
Het |
Ppfibp2 |
T |
C |
7: 107,328,381 (GRCm39) |
S471P |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,435,546 (GRCm39) |
F74L |
probably benign |
Het |
Prl7d1 |
A |
T |
13: 27,896,038 (GRCm39) |
V113D |
probably benign |
Het |
Prr14 |
C |
T |
7: 127,071,267 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ret |
A |
G |
6: 118,155,571 (GRCm39) |
V375A |
probably damaging |
Het |
Rora |
T |
C |
9: 69,269,028 (GRCm39) |
F41S |
probably damaging |
Het |
Sall1 |
T |
C |
8: 89,758,386 (GRCm39) |
T573A |
probably benign |
Het |
Shb |
A |
G |
4: 45,458,321 (GRCm39) |
V281A |
possibly damaging |
Het |
Slc25a26 |
A |
T |
6: 94,569,391 (GRCm39) |
|
probably null |
Het |
Sltm |
T |
C |
9: 70,493,363 (GRCm39) |
F769L |
probably damaging |
Het |
Snx9 |
T |
A |
17: 5,968,688 (GRCm39) |
M328K |
probably damaging |
Het |
Stk25 |
G |
T |
1: 93,552,313 (GRCm39) |
Q356K |
probably benign |
Het |
Svep1 |
T |
A |
4: 58,128,858 (GRCm39) |
Y613F |
possibly damaging |
Het |
Syne4 |
G |
A |
7: 30,016,169 (GRCm39) |
A195T |
probably damaging |
Het |
Tmem217b |
A |
T |
17: 29,738,545 (GRCm39) |
F74I |
probably benign |
Het |
Trcg1 |
C |
T |
9: 57,149,616 (GRCm39) |
T396M |
probably damaging |
Het |
Trim30b |
A |
G |
7: 104,006,505 (GRCm39) |
V117A |
possibly damaging |
Het |
Trpc4 |
T |
C |
3: 54,209,511 (GRCm39) |
|
probably benign |
Het |
Ttll4 |
A |
G |
1: 74,727,439 (GRCm39) |
H827R |
probably damaging |
Het |
Tut7 |
A |
G |
13: 59,948,131 (GRCm39) |
V328A |
probably benign |
Het |
Urgcp |
T |
C |
11: 5,667,477 (GRCm39) |
E287G |
probably damaging |
Het |
Usp2 |
G |
T |
9: 44,004,081 (GRCm39) |
L319F |
probably damaging |
Het |
Vmn1r167 |
A |
T |
7: 23,204,512 (GRCm39) |
V168D |
probably damaging |
Het |
Vmn2r100 |
C |
A |
17: 19,742,382 (GRCm39) |
P252Q |
possibly damaging |
Het |
Vmn2r61 |
A |
T |
7: 41,915,442 (GRCm39) |
I130F |
probably benign |
Het |
Vmn2r63 |
A |
T |
7: 42,577,952 (GRCm39) |
Y195* |
probably null |
Het |
Vmn2r81 |
T |
C |
10: 79,129,283 (GRCm39) |
S725P |
probably damaging |
Het |
Wnt10b |
A |
G |
15: 98,670,818 (GRCm39) |
|
probably benign |
Het |
Zfp292 |
T |
C |
4: 34,807,194 (GRCm39) |
E1950G |
probably damaging |
Het |
Zfyve16 |
A |
G |
13: 92,653,028 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Map4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00565:Map4
|
APN |
9 |
109,901,672 (GRCm39) |
splice site |
probably benign |
|
IGL01331:Map4
|
APN |
9 |
109,863,869 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01599:Map4
|
APN |
9 |
109,863,836 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01631:Map4
|
APN |
9 |
109,892,201 (GRCm39) |
unclassified |
probably benign |
|
IGL02208:Map4
|
APN |
9 |
109,807,938 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
IGL02455:Map4
|
APN |
9 |
109,828,901 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02625:Map4
|
APN |
9 |
109,893,485 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Map4
|
UTSW |
9 |
109,901,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Map4
|
UTSW |
9 |
109,896,692 (GRCm39) |
missense |
probably damaging |
0.96 |
R0384:Map4
|
UTSW |
9 |
109,863,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R0392:Map4
|
UTSW |
9 |
109,907,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R0496:Map4
|
UTSW |
9 |
109,868,918 (GRCm39) |
intron |
probably benign |
|
R0526:Map4
|
UTSW |
9 |
109,866,346 (GRCm39) |
splice site |
probably null |
|
R0571:Map4
|
UTSW |
9 |
109,865,834 (GRCm39) |
missense |
probably benign |
0.00 |
R0698:Map4
|
UTSW |
9 |
109,897,856 (GRCm39) |
nonsense |
probably null |
|
R0762:Map4
|
UTSW |
9 |
109,867,546 (GRCm39) |
intron |
probably benign |
|
R0862:Map4
|
UTSW |
9 |
109,808,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:Map4
|
UTSW |
9 |
109,808,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:Map4
|
UTSW |
9 |
109,864,032 (GRCm39) |
missense |
probably benign |
0.00 |
R1238:Map4
|
UTSW |
9 |
109,897,648 (GRCm39) |
missense |
probably benign |
0.00 |
R1735:Map4
|
UTSW |
9 |
109,864,023 (GRCm39) |
missense |
probably benign |
0.00 |
R1869:Map4
|
UTSW |
9 |
109,897,996 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1869:Map4
|
UTSW |
9 |
109,864,032 (GRCm39) |
missense |
probably benign |
0.00 |
R2196:Map4
|
UTSW |
9 |
109,900,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:Map4
|
UTSW |
9 |
109,910,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R2507:Map4
|
UTSW |
9 |
109,866,551 (GRCm39) |
intron |
probably benign |
|
R2512:Map4
|
UTSW |
9 |
109,863,770 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3087:Map4
|
UTSW |
9 |
109,882,257 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3154:Map4
|
UTSW |
9 |
109,828,860 (GRCm39) |
missense |
probably benign |
0.19 |
R3498:Map4
|
UTSW |
9 |
109,864,280 (GRCm39) |
missense |
probably benign |
0.03 |
R3547:Map4
|
UTSW |
9 |
109,881,266 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3751:Map4
|
UTSW |
9 |
109,867,742 (GRCm39) |
intron |
probably benign |
|
R4036:Map4
|
UTSW |
9 |
109,861,283 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4423:Map4
|
UTSW |
9 |
109,896,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R4505:Map4
|
UTSW |
9 |
109,861,253 (GRCm39) |
missense |
probably benign |
0.01 |
R4561:Map4
|
UTSW |
9 |
109,881,439 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4577:Map4
|
UTSW |
9 |
109,910,489 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4601:Map4
|
UTSW |
9 |
109,881,887 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4795:Map4
|
UTSW |
9 |
109,864,331 (GRCm39) |
missense |
probably benign |
0.00 |
R4801:Map4
|
UTSW |
9 |
109,864,325 (GRCm39) |
missense |
probably benign |
0.15 |
R4802:Map4
|
UTSW |
9 |
109,864,325 (GRCm39) |
missense |
probably benign |
0.15 |
R4999:Map4
|
UTSW |
9 |
109,867,445 (GRCm39) |
intron |
probably benign |
|
R5020:Map4
|
UTSW |
9 |
109,897,868 (GRCm39) |
missense |
probably benign |
0.02 |
R5021:Map4
|
UTSW |
9 |
109,867,157 (GRCm39) |
nonsense |
probably null |
|
R5049:Map4
|
UTSW |
9 |
109,908,882 (GRCm39) |
nonsense |
probably null |
|
R5451:Map4
|
UTSW |
9 |
109,866,851 (GRCm39) |
intron |
probably benign |
|
R5452:Map4
|
UTSW |
9 |
109,866,851 (GRCm39) |
intron |
probably benign |
|
R5453:Map4
|
UTSW |
9 |
109,866,851 (GRCm39) |
intron |
probably benign |
|
R5492:Map4
|
UTSW |
9 |
109,881,450 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5532:Map4
|
UTSW |
9 |
109,863,746 (GRCm39) |
missense |
probably benign |
0.24 |
R5602:Map4
|
UTSW |
9 |
109,881,768 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5628:Map4
|
UTSW |
9 |
109,910,915 (GRCm39) |
missense |
probably benign |
0.04 |
R5896:Map4
|
UTSW |
9 |
109,901,702 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6017:Map4
|
UTSW |
9 |
109,863,687 (GRCm39) |
missense |
probably benign |
0.00 |
R6084:Map4
|
UTSW |
9 |
109,893,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R6294:Map4
|
UTSW |
9 |
109,831,814 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6397:Map4
|
UTSW |
9 |
109,856,784 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6773:Map4
|
UTSW |
9 |
109,863,993 (GRCm39) |
missense |
probably benign |
0.00 |
R6997:Map4
|
UTSW |
9 |
109,881,982 (GRCm39) |
missense |
probably benign |
0.35 |
R7141:Map4
|
UTSW |
9 |
109,807,938 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R7187:Map4
|
UTSW |
9 |
109,882,201 (GRCm39) |
missense |
probably benign |
0.03 |
R7320:Map4
|
UTSW |
9 |
109,910,585 (GRCm39) |
missense |
probably benign |
0.24 |
R7469:Map4
|
UTSW |
9 |
109,856,865 (GRCm39) |
splice site |
probably null |
|
R7479:Map4
|
UTSW |
9 |
109,897,892 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7487:Map4
|
UTSW |
9 |
109,856,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7690:Map4
|
UTSW |
9 |
109,828,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R7780:Map4
|
UTSW |
9 |
109,863,720 (GRCm39) |
missense |
probably benign |
0.00 |
R7998:Map4
|
UTSW |
9 |
109,908,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R8028:Map4
|
UTSW |
9 |
109,897,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8557:Map4
|
UTSW |
9 |
109,893,370 (GRCm39) |
splice site |
probably null |
|
R8950:Map4
|
UTSW |
9 |
109,901,702 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8972:Map4
|
UTSW |
9 |
109,864,185 (GRCm39) |
missense |
probably benign |
|
R9145:Map4
|
UTSW |
9 |
109,855,268 (GRCm39) |
missense |
probably damaging |
0.99 |
R9297:Map4
|
UTSW |
9 |
109,882,480 (GRCm39) |
missense |
probably benign |
0.02 |
R9332:Map4
|
UTSW |
9 |
109,864,223 (GRCm39) |
missense |
probably benign |
0.00 |
R9354:Map4
|
UTSW |
9 |
109,897,847 (GRCm39) |
missense |
probably benign |
|
R9419:Map4
|
UTSW |
9 |
109,882,029 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9430:Map4
|
UTSW |
9 |
109,863,760 (GRCm39) |
missense |
probably benign |
0.41 |
R9437:Map4
|
UTSW |
9 |
109,864,155 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9718:Map4
|
UTSW |
9 |
109,901,774 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Map4
|
UTSW |
9 |
109,897,591 (GRCm39) |
critical splice acceptor site |
probably null |
|
|