Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aim2 |
A |
G |
1: 173,287,372 (GRCm39) |
D124G |
probably benign |
Het |
Akr1c6 |
T |
C |
13: 4,504,494 (GRCm39) |
M293T |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,709,158 (GRCm39) |
T23A |
probably benign |
Het |
Ankhd1 |
A |
G |
18: 36,722,505 (GRCm39) |
T343A |
probably damaging |
Het |
Ano2 |
T |
C |
6: 125,880,018 (GRCm39) |
|
probably benign |
Het |
Arfgap2 |
G |
A |
2: 91,104,004 (GRCm39) |
G353R |
probably damaging |
Het |
Armc3 |
A |
G |
2: 19,297,791 (GRCm39) |
|
probably null |
Het |
Atp11b |
T |
C |
3: 35,889,528 (GRCm39) |
|
probably null |
Het |
Brd4 |
A |
G |
17: 32,418,214 (GRCm39) |
M13T |
probably benign |
Het |
Btd |
T |
A |
14: 31,384,044 (GRCm39) |
M10K |
possibly damaging |
Het |
C1s2 |
T |
C |
6: 124,602,649 (GRCm39) |
K515E |
probably benign |
Het |
Cars1 |
A |
T |
7: 143,123,587 (GRCm39) |
Y455N |
probably damaging |
Het |
Ccdc110 |
A |
G |
8: 46,396,460 (GRCm39) |
S784G |
probably benign |
Het |
Chic2 |
A |
G |
5: 75,171,872 (GRCm39) |
|
probably benign |
Het |
Chka |
A |
T |
19: 3,942,105 (GRCm39) |
|
probably null |
Het |
Chrne |
A |
G |
11: 70,506,101 (GRCm39) |
I420T |
possibly damaging |
Het |
Clstn1 |
T |
C |
4: 149,729,486 (GRCm39) |
V747A |
probably benign |
Het |
Cobll1 |
A |
G |
2: 64,929,602 (GRCm39) |
S575P |
possibly damaging |
Het |
Col6a6 |
A |
T |
9: 105,666,147 (GRCm39) |
L3Q |
probably damaging |
Het |
Comtd1 |
A |
T |
14: 21,898,813 (GRCm39) |
|
probably benign |
Het |
Cpsf2 |
T |
C |
12: 101,948,243 (GRCm39) |
V13A |
probably benign |
Het |
Creb3l4 |
T |
A |
3: 90,149,521 (GRCm39) |
I115L |
probably benign |
Het |
Cyp2j12 |
C |
T |
4: 95,990,346 (GRCm39) |
A407T |
possibly damaging |
Het |
Ddr2 |
A |
G |
1: 169,825,498 (GRCm39) |
|
probably null |
Het |
Dennd4c |
T |
C |
4: 86,725,775 (GRCm39) |
L743P |
probably damaging |
Het |
Egfl8 |
T |
C |
17: 34,833,171 (GRCm39) |
T192A |
probably benign |
Het |
Elapor1 |
C |
T |
3: 108,379,284 (GRCm39) |
|
probably null |
Het |
Elf3 |
A |
G |
1: 135,184,473 (GRCm39) |
|
probably benign |
Het |
Entrep2 |
A |
G |
7: 64,417,439 (GRCm39) |
S322P |
probably benign |
Het |
Etv3 |
T |
G |
3: 87,443,223 (GRCm39) |
L269R |
possibly damaging |
Het |
Fah |
C |
A |
7: 84,251,260 (GRCm39) |
|
probably benign |
Het |
Fbll1 |
C |
A |
11: 35,688,407 (GRCm39) |
L285F |
probably benign |
Het |
Fcrla |
A |
T |
1: 170,748,682 (GRCm39) |
F154I |
probably damaging |
Het |
Fnip2 |
T |
A |
3: 79,396,701 (GRCm39) |
|
probably null |
Het |
Focad |
T |
C |
4: 88,115,083 (GRCm39) |
|
probably benign |
Het |
Gabrr1 |
T |
A |
4: 33,162,820 (GRCm39) |
I462N |
possibly damaging |
Het |
Gm57859 |
C |
A |
11: 113,579,805 (GRCm39) |
T400K |
probably benign |
Het |
Gnptab |
A |
G |
10: 88,265,485 (GRCm39) |
T366A |
probably benign |
Het |
Hnrnpu |
G |
A |
1: 178,159,017 (GRCm39) |
|
probably benign |
Het |
Il17ra |
T |
A |
6: 120,454,406 (GRCm39) |
V299E |
possibly damaging |
Het |
Impg1 |
G |
A |
9: 80,252,360 (GRCm39) |
Q607* |
probably null |
Het |
Impg1 |
T |
A |
9: 80,252,827 (GRCm39) |
E374V |
probably damaging |
Het |
Itgax |
C |
T |
7: 127,747,700 (GRCm39) |
L1039F |
probably benign |
Het |
Kcnk2 |
A |
T |
1: 189,072,133 (GRCm39) |
V65D |
probably damaging |
Het |
Kif20b |
A |
C |
19: 34,918,611 (GRCm39) |
|
probably null |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lama5 |
T |
G |
2: 179,825,942 (GRCm39) |
I2372L |
probably benign |
Het |
Lilrb4a |
A |
G |
10: 51,368,139 (GRCm39) |
T85A |
possibly damaging |
Het |
Mapk13 |
C |
A |
17: 28,997,197 (GRCm39) |
H330N |
probably benign |
Het |
Mars1 |
C |
A |
10: 127,132,549 (GRCm39) |
|
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,671,608 (GRCm39) |
L476Q |
possibly damaging |
Het |
Mup21 |
T |
C |
4: 62,066,202 (GRCm39) |
E178G |
probably benign |
Het |
Myg1 |
A |
G |
15: 102,240,288 (GRCm39) |
N38S |
probably benign |
Het |
Ncam1 |
A |
T |
9: 49,416,779 (GRCm39) |
D837E |
probably benign |
Het |
Ncam2 |
C |
T |
16: 81,386,679 (GRCm39) |
P686L |
possibly damaging |
Het |
Nck2 |
T |
C |
1: 43,500,231 (GRCm39) |
|
probably benign |
Het |
Nfya |
T |
C |
17: 48,707,563 (GRCm39) |
|
probably benign |
Het |
Npat |
A |
G |
9: 53,482,330 (GRCm39) |
K1346R |
probably damaging |
Het |
Odad2 |
C |
G |
18: 7,181,787 (GRCm39) |
D846H |
probably damaging |
Het |
Or12j3 |
G |
T |
7: 139,952,920 (GRCm39) |
T201K |
probably benign |
Het |
Or4a72 |
T |
C |
2: 89,406,023 (GRCm39) |
T16A |
probably damaging |
Het |
Or6c212 |
A |
G |
10: 129,558,681 (GRCm39) |
V244A |
probably benign |
Het |
Pde7b |
G |
T |
10: 20,288,873 (GRCm39) |
Q325K |
probably damaging |
Het |
Pla2r1 |
A |
T |
2: 60,253,056 (GRCm39) |
M1345K |
probably benign |
Het |
Prkcz |
T |
C |
4: 155,441,946 (GRCm39) |
D62G |
probably damaging |
Het |
Pros1 |
T |
A |
16: 62,723,935 (GRCm39) |
C228S |
possibly damaging |
Het |
Ptprc |
A |
G |
1: 138,006,236 (GRCm39) |
M782T |
possibly damaging |
Het |
Rcn1 |
T |
C |
2: 105,219,518 (GRCm39) |
D225G |
probably benign |
Het |
Recql4 |
G |
A |
15: 76,594,381 (GRCm39) |
R46C |
probably damaging |
Het |
Rnf220 |
C |
T |
4: 117,346,797 (GRCm39) |
R205Q |
possibly damaging |
Het |
Samd13 |
T |
C |
3: 146,368,502 (GRCm39) |
D11G |
probably benign |
Het |
Scp2d1 |
T |
A |
2: 144,666,030 (GRCm39) |
I123K |
probably benign |
Het |
Skap1 |
A |
T |
11: 96,644,870 (GRCm39) |
Y311F |
probably damaging |
Het |
Slc2a10 |
T |
C |
2: 165,356,676 (GRCm39) |
I112T |
possibly damaging |
Het |
Slc34a1 |
G |
A |
13: 24,003,078 (GRCm39) |
V243M |
probably benign |
Het |
Slc39a2 |
G |
A |
14: 52,132,711 (GRCm39) |
G218D |
probably damaging |
Het |
Sos1 |
T |
C |
17: 80,742,381 (GRCm39) |
N382S |
probably benign |
Het |
Spam1 |
C |
T |
6: 24,796,655 (GRCm39) |
T202I |
probably damaging |
Het |
Tas2r138 |
T |
A |
6: 40,589,820 (GRCm39) |
Q142L |
possibly damaging |
Het |
Tec |
T |
A |
5: 72,939,365 (GRCm39) |
R217* |
probably null |
Het |
Tmeff2 |
T |
A |
1: 50,969,804 (GRCm39) |
V90D |
probably benign |
Het |
Tmem119 |
T |
C |
5: 113,933,405 (GRCm39) |
Y132C |
probably damaging |
Het |
Topbp1 |
A |
G |
9: 103,190,035 (GRCm39) |
I204V |
probably benign |
Het |
Trappc14 |
A |
T |
5: 138,260,641 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,601,232 (GRCm39) |
I17001N |
probably damaging |
Het |
Vit |
T |
A |
17: 78,894,270 (GRCm39) |
M224K |
probably benign |
Het |
Vmn1r179 |
T |
G |
7: 23,628,491 (GRCm39) |
H227Q |
possibly damaging |
Het |
Vmn1r84 |
T |
C |
7: 12,095,743 (GRCm39) |
N305D |
probably benign |
Het |
Vmn2r61 |
A |
G |
7: 41,916,520 (GRCm39) |
N378D |
probably damaging |
Het |
Vmn2r87 |
A |
G |
10: 130,314,435 (GRCm39) |
Y384H |
probably damaging |
Het |
Wiz |
C |
T |
17: 32,580,570 (GRCm39) |
A294T |
probably benign |
Het |
Xdh |
C |
A |
17: 74,231,931 (GRCm39) |
V260L |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,343,237 (GRCm39) |
K1826R |
probably benign |
Het |
Zfp445 |
A |
C |
9: 122,681,358 (GRCm39) |
I861R |
probably benign |
Het |
Zfp691 |
T |
C |
4: 119,027,999 (GRCm39) |
T78A |
probably benign |
Het |
|
Other mutations in Mdga1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01576:Mdga1
|
APN |
17 |
30,062,101 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01637:Mdga1
|
APN |
17 |
30,058,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02130:Mdga1
|
APN |
17 |
30,076,643 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02596:Mdga1
|
APN |
17 |
30,051,379 (GRCm39) |
splice site |
probably benign |
|
IGL03258:Mdga1
|
APN |
17 |
30,058,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Mdga1
|
UTSW |
17 |
30,071,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:Mdga1
|
UTSW |
17 |
30,076,682 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1017:Mdga1
|
UTSW |
17 |
30,069,522 (GRCm39) |
missense |
probably damaging |
0.98 |
R1520:Mdga1
|
UTSW |
17 |
30,065,493 (GRCm39) |
missense |
probably benign |
0.12 |
R1545:Mdga1
|
UTSW |
17 |
30,061,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1549:Mdga1
|
UTSW |
17 |
30,056,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1671:Mdga1
|
UTSW |
17 |
30,069,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Mdga1
|
UTSW |
17 |
30,071,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Mdga1
|
UTSW |
17 |
30,068,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Mdga1
|
UTSW |
17 |
30,059,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Mdga1
|
UTSW |
17 |
30,069,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Mdga1
|
UTSW |
17 |
30,068,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2894:Mdga1
|
UTSW |
17 |
30,071,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R2964:Mdga1
|
UTSW |
17 |
30,071,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R3813:Mdga1
|
UTSW |
17 |
30,057,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Mdga1
|
UTSW |
17 |
30,076,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R3982:Mdga1
|
UTSW |
17 |
30,150,238 (GRCm39) |
missense |
unknown |
|
R4063:Mdga1
|
UTSW |
17 |
30,057,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Mdga1
|
UTSW |
17 |
30,052,317 (GRCm39) |
missense |
probably benign |
0.32 |
R4183:Mdga1
|
UTSW |
17 |
30,188,964 (GRCm39) |
missense |
unknown |
|
R4392:Mdga1
|
UTSW |
17 |
30,069,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R4393:Mdga1
|
UTSW |
17 |
30,069,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Mdga1
|
UTSW |
17 |
30,069,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Mdga1
|
UTSW |
17 |
30,061,128 (GRCm39) |
missense |
probably benign |
0.20 |
R4829:Mdga1
|
UTSW |
17 |
30,065,343 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4932:Mdga1
|
UTSW |
17 |
30,076,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Mdga1
|
UTSW |
17 |
30,058,847 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5076:Mdga1
|
UTSW |
17 |
30,069,528 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5141:Mdga1
|
UTSW |
17 |
30,071,467 (GRCm39) |
missense |
probably benign |
0.43 |
R5180:Mdga1
|
UTSW |
17 |
30,076,710 (GRCm39) |
splice site |
probably benign |
|
R5590:Mdga1
|
UTSW |
17 |
30,058,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R5747:Mdga1
|
UTSW |
17 |
30,069,525 (GRCm39) |
missense |
probably benign |
0.11 |
R5748:Mdga1
|
UTSW |
17 |
30,069,525 (GRCm39) |
missense |
probably benign |
0.11 |
R6207:Mdga1
|
UTSW |
17 |
30,057,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R6826:Mdga1
|
UTSW |
17 |
30,189,000 (GRCm39) |
missense |
unknown |
|
R6831:Mdga1
|
UTSW |
17 |
30,106,490 (GRCm39) |
nonsense |
probably null |
|
R7114:Mdga1
|
UTSW |
17 |
30,061,816 (GRCm39) |
splice site |
probably null |
|
R7147:Mdga1
|
UTSW |
17 |
30,065,495 (GRCm39) |
nonsense |
probably null |
|
R7273:Mdga1
|
UTSW |
17 |
30,188,912 (GRCm39) |
missense |
unknown |
|
R7413:Mdga1
|
UTSW |
17 |
30,069,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Mdga1
|
UTSW |
17 |
30,051,353 (GRCm39) |
missense |
probably benign |
0.00 |
R7797:Mdga1
|
UTSW |
17 |
30,061,814 (GRCm39) |
splice site |
probably null |
|
R7812:Mdga1
|
UTSW |
17 |
30,062,115 (GRCm39) |
missense |
probably benign |
0.02 |
R7838:Mdga1
|
UTSW |
17 |
30,058,796 (GRCm39) |
missense |
probably benign |
0.10 |
R8463:Mdga1
|
UTSW |
17 |
30,068,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R8697:Mdga1
|
UTSW |
17 |
30,065,615 (GRCm39) |
missense |
probably damaging |
0.97 |
R8699:Mdga1
|
UTSW |
17 |
30,061,348 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8864:Mdga1
|
UTSW |
17 |
30,150,295 (GRCm39) |
missense |
unknown |
|
R8945:Mdga1
|
UTSW |
17 |
30,058,959 (GRCm39) |
splice site |
probably benign |
|
R9150:Mdga1
|
UTSW |
17 |
30,057,420 (GRCm39) |
missense |
probably damaging |
0.98 |
R9157:Mdga1
|
UTSW |
17 |
30,057,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R9294:Mdga1
|
UTSW |
17 |
30,058,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Mdga1
|
UTSW |
17 |
30,069,512 (GRCm39) |
missense |
probably benign |
0.31 |
R9367:Mdga1
|
UTSW |
17 |
30,051,282 (GRCm39) |
makesense |
probably null |
|
R9567:Mdga1
|
UTSW |
17 |
30,076,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Mdga1
|
UTSW |
17 |
30,051,991 (GRCm39) |
missense |
probably damaging |
0.99 |
|