Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,241,058 (GRCm39) |
Y974H |
probably benign |
Het |
Abca2 |
G |
T |
2: 25,324,906 (GRCm39) |
G300V |
probably benign |
Het |
Abi1 |
A |
G |
2: 22,852,516 (GRCm39) |
|
probably benign |
Het |
Actr10 |
T |
A |
12: 71,006,738 (GRCm39) |
Y332N |
probably damaging |
Het |
Adam25 |
G |
T |
8: 41,208,261 (GRCm39) |
C509F |
probably damaging |
Het |
Adck1 |
A |
T |
12: 88,338,461 (GRCm39) |
|
probably benign |
Het |
Adgra3 |
A |
G |
5: 50,166,676 (GRCm39) |
|
probably null |
Het |
Adgrl1 |
G |
T |
8: 84,661,279 (GRCm39) |
|
probably benign |
Het |
Arhgef25 |
T |
C |
10: 127,019,566 (GRCm39) |
I463V |
probably null |
Het |
Atp6v1e2 |
C |
T |
17: 87,252,006 (GRCm39) |
V131M |
probably benign |
Het |
Bdnf |
A |
G |
2: 109,505,688 (GRCm39) |
|
probably null |
Het |
Bltp3b |
T |
C |
10: 89,627,305 (GRCm39) |
S145P |
probably damaging |
Het |
C7 |
A |
T |
15: 5,023,624 (GRCm39) |
|
probably benign |
Het |
Cdc27 |
T |
C |
11: 104,419,114 (GRCm39) |
T273A |
probably benign |
Het |
Cdo1 |
T |
A |
18: 46,848,678 (GRCm39) |
I187F |
probably benign |
Het |
Cep104 |
A |
T |
4: 154,080,761 (GRCm39) |
T742S |
probably benign |
Het |
Ckm |
A |
T |
7: 19,153,377 (GRCm39) |
K223* |
probably null |
Het |
Cmtr1 |
C |
T |
17: 29,895,259 (GRCm39) |
P586L |
probably benign |
Het |
Csmd1 |
C |
T |
8: 16,042,758 (GRCm39) |
R2325Q |
probably damaging |
Het |
Dcpp1 |
A |
T |
17: 24,101,568 (GRCm39) |
I106L |
possibly damaging |
Het |
Diaph3 |
A |
C |
14: 87,328,400 (GRCm39) |
|
probably benign |
Het |
Dnah11 |
A |
G |
12: 118,070,245 (GRCm39) |
V1520A |
probably damaging |
Het |
Dnajc25 |
T |
A |
4: 59,020,438 (GRCm39) |
M168K |
|
Het |
Dpp3 |
T |
C |
19: 4,964,682 (GRCm39) |
N542D |
probably damaging |
Het |
Ebf2 |
A |
T |
14: 67,609,185 (GRCm39) |
K199* |
probably null |
Het |
Eeig2 |
T |
C |
3: 108,887,520 (GRCm39) |
E248G |
probably benign |
Het |
Efcab11 |
T |
A |
12: 99,685,294 (GRCm39) |
Q160L |
probably benign |
Het |
Eif2ak4 |
T |
A |
2: 118,261,517 (GRCm39) |
S686T |
probably benign |
Het |
Epha6 |
C |
T |
16: 60,026,095 (GRCm39) |
S449N |
possibly damaging |
Het |
Ercc4 |
T |
C |
16: 12,944,331 (GRCm39) |
V329A |
probably benign |
Het |
Faf1 |
T |
C |
4: 109,697,600 (GRCm39) |
F309L |
possibly damaging |
Het |
G6pd2 |
C |
A |
5: 61,966,910 (GRCm39) |
D228E |
probably benign |
Het |
Ggt1 |
T |
G |
10: 75,421,791 (GRCm39) |
V546G |
probably damaging |
Het |
Gpatch4 |
G |
T |
3: 87,958,524 (GRCm39) |
V3F |
probably damaging |
Het |
Gprin3 |
A |
G |
6: 59,330,372 (GRCm39) |
L645P |
probably damaging |
Het |
Hyal2 |
A |
G |
9: 107,449,270 (GRCm39) |
Y342C |
probably benign |
Het |
Igf2bp2 |
A |
G |
16: 21,907,849 (GRCm39) |
I16T |
possibly damaging |
Het |
Inca1 |
T |
C |
11: 70,581,025 (GRCm39) |
Y61C |
probably damaging |
Het |
Ipo5 |
T |
C |
14: 121,180,145 (GRCm39) |
W860R |
possibly damaging |
Het |
Kcnj9 |
C |
T |
1: 172,150,591 (GRCm39) |
A341T |
probably benign |
Het |
Kdm5b |
T |
C |
1: 134,530,309 (GRCm39) |
V440A |
probably damaging |
Het |
L3mbtl1 |
C |
T |
2: 162,789,255 (GRCm39) |
|
probably benign |
Het |
Lin54 |
G |
A |
5: 100,600,152 (GRCm39) |
T307I |
probably damaging |
Het |
Lrrc18 |
C |
A |
14: 32,731,096 (GRCm39) |
Q212K |
probably benign |
Het |
Lrrc37a |
A |
G |
11: 103,393,851 (GRCm39) |
S525P |
probably benign |
Het |
Lrrc71 |
T |
A |
3: 87,653,006 (GRCm39) |
S137C |
probably damaging |
Het |
Lrrk1 |
A |
T |
7: 65,940,656 (GRCm39) |
|
probably null |
Het |
Man2b2 |
G |
A |
5: 36,973,542 (GRCm39) |
S58L |
probably benign |
Het |
Masp1 |
T |
A |
16: 23,276,888 (GRCm39) |
H539L |
probably benign |
Het |
Med1 |
G |
A |
11: 98,047,730 (GRCm39) |
P1022L |
probably damaging |
Het |
Meis1 |
T |
A |
11: 18,961,360 (GRCm39) |
H171L |
probably damaging |
Het |
Mier1 |
T |
A |
4: 103,012,820 (GRCm39) |
|
probably benign |
Het |
Mmp13 |
A |
T |
9: 7,272,929 (GRCm39) |
R96S |
probably damaging |
Het |
Mms19 |
G |
A |
19: 41,942,173 (GRCm39) |
T38I |
probably damaging |
Het |
Mrc1 |
G |
A |
2: 14,314,843 (GRCm39) |
C976Y |
probably damaging |
Het |
Mrtfb |
C |
T |
16: 13,230,390 (GRCm39) |
T1025I |
possibly damaging |
Het |
Naalad2 |
A |
G |
9: 18,297,191 (GRCm39) |
Y32H |
probably benign |
Het |
Ndufs1 |
A |
G |
1: 63,183,085 (GRCm39) |
|
probably benign |
Het |
Nefm |
C |
T |
14: 68,361,608 (GRCm39) |
D219N |
probably damaging |
Het |
Nwd1 |
C |
T |
8: 73,388,965 (GRCm39) |
P172L |
probably damaging |
Het |
Nwd2 |
T |
A |
5: 63,962,454 (GRCm39) |
D679E |
probably damaging |
Het |
Ogdh |
T |
A |
11: 6,289,936 (GRCm39) |
|
probably benign |
Het |
Olfm3 |
T |
A |
3: 114,916,330 (GRCm39) |
S421T |
possibly damaging |
Het |
Opn5 |
T |
G |
17: 42,903,844 (GRCm39) |
T164P |
possibly damaging |
Het |
Or4k37 |
A |
T |
2: 111,159,673 (GRCm39) |
N303I |
probably benign |
Het |
Or51a25 |
T |
A |
7: 102,373,236 (GRCm39) |
I154F |
probably damaging |
Het |
Or52a24 |
T |
C |
7: 103,381,583 (GRCm39) |
V150A |
probably benign |
Het |
Or5ak20 |
A |
G |
2: 85,184,093 (GRCm39) |
M59T |
possibly damaging |
Het |
Or5b12b |
T |
C |
19: 12,861,443 (GRCm39) |
L66P |
probably damaging |
Het |
Or5b12b |
A |
G |
19: 12,861,910 (GRCm39) |
T222A |
probably damaging |
Het |
Pde7b |
C |
T |
10: 20,314,492 (GRCm39) |
V166M |
probably damaging |
Het |
Peds1 |
A |
T |
2: 167,486,907 (GRCm39) |
|
probably benign |
Het |
Pik3ap1 |
T |
C |
19: 41,313,003 (GRCm39) |
N370S |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,452,814 (GRCm39) |
D3913V |
probably damaging |
Het |
Pld1 |
A |
G |
3: 28,174,971 (GRCm39) |
I90V |
possibly damaging |
Het |
Plxna2 |
A |
G |
1: 194,326,656 (GRCm39) |
T197A |
possibly damaging |
Het |
Plxna4 |
A |
T |
6: 32,179,054 (GRCm39) |
M987K |
probably benign |
Het |
Pmch |
A |
G |
10: 87,927,221 (GRCm39) |
N75D |
probably benign |
Het |
Prom2 |
T |
A |
2: 127,374,787 (GRCm39) |
Q583L |
possibly damaging |
Het |
Pyroxd1 |
T |
A |
6: 142,299,288 (GRCm39) |
M148K |
possibly damaging |
Het |
R3hdm2 |
C |
T |
10: 127,293,569 (GRCm39) |
L158F |
probably damaging |
Het |
Rapgef6 |
A |
T |
11: 54,516,789 (GRCm39) |
T349S |
probably benign |
Het |
Rfx5 |
C |
T |
3: 94,863,666 (GRCm39) |
T105I |
probably damaging |
Het |
Rif1 |
C |
A |
2: 52,000,749 (GRCm39) |
P1401Q |
probably damaging |
Het |
Robo3 |
G |
A |
9: 37,328,055 (GRCm39) |
|
probably benign |
Het |
Rpn1 |
T |
A |
6: 88,067,224 (GRCm39) |
S195T |
probably benign |
Het |
Rslcan18 |
C |
A |
13: 67,250,183 (GRCm39) |
K17N |
probably benign |
Het |
Rsph3b |
A |
T |
17: 7,209,126 (GRCm39) |
I48N |
probably damaging |
Het |
Sbf2 |
A |
T |
7: 109,998,550 (GRCm39) |
Y628N |
probably damaging |
Het |
Sis |
T |
C |
3: 72,867,629 (GRCm39) |
T139A |
probably benign |
Het |
Slc22a14 |
A |
G |
9: 119,001,100 (GRCm39) |
|
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,364 (GRCm39) |
L781H |
probably damaging |
Het |
Smarcb1 |
T |
C |
10: 75,732,900 (GRCm39) |
T372A |
probably damaging |
Het |
Spidr |
T |
A |
16: 15,855,531 (GRCm39) |
H328L |
probably damaging |
Het |
Sun5 |
T |
A |
2: 153,712,872 (GRCm39) |
D16V |
probably damaging |
Het |
Syde2 |
G |
A |
3: 145,720,135 (GRCm39) |
E1053K |
possibly damaging |
Het |
Syne2 |
T |
C |
12: 76,146,238 (GRCm39) |
S6419P |
probably damaging |
Het |
Tenm3 |
G |
A |
8: 48,794,195 (GRCm39) |
|
probably benign |
Het |
Timm44 |
C |
A |
8: 4,310,532 (GRCm39) |
E407* |
probably null |
Het |
Tnpo2 |
A |
G |
8: 85,773,991 (GRCm39) |
T342A |
probably benign |
Het |
Trio |
A |
G |
15: 27,767,993 (GRCm39) |
C1964R |
probably benign |
Het |
Trip11 |
A |
C |
12: 101,851,931 (GRCm39) |
L711R |
probably damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,100,450 (GRCm39) |
H101Q |
probably damaging |
Het |
Trpm6 |
A |
G |
19: 18,851,266 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,680,335 (GRCm39) |
|
probably benign |
Het |
Ucp1 |
T |
A |
8: 84,021,936 (GRCm39) |
M256K |
possibly damaging |
Het |
Unc5a |
T |
A |
13: 55,152,767 (GRCm39) |
S838T |
probably damaging |
Het |
Uxs1 |
T |
C |
1: 43,804,046 (GRCm39) |
|
probably null |
Het |
Vmn2r108 |
A |
T |
17: 20,683,096 (GRCm39) |
C703S |
possibly damaging |
Het |
Zc3hav1 |
C |
T |
6: 38,309,599 (GRCm39) |
G408R |
probably damaging |
Het |
Zfp1004 |
T |
A |
2: 150,035,000 (GRCm39) |
C471* |
probably null |
Het |
Zfp609 |
G |
A |
9: 65,610,744 (GRCm39) |
L740F |
possibly damaging |
Het |
Zfp69 |
T |
C |
4: 120,788,292 (GRCm39) |
E341G |
probably damaging |
Het |
Zfp707 |
A |
T |
15: 75,847,105 (GRCm39) |
H312L |
probably damaging |
Het |
Zfp773 |
T |
C |
7: 7,136,023 (GRCm39) |
D191G |
probably benign |
Het |
Zgrf1 |
C |
A |
3: 127,366,887 (GRCm39) |
D755E |
probably benign |
Het |
Zscan5b |
T |
A |
7: 6,242,074 (GRCm39) |
I431N |
probably damaging |
Het |
|
Other mutations in Akr1c21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00645:Akr1c21
|
APN |
13 |
4,626,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01093:Akr1c21
|
APN |
13 |
4,631,139 (GRCm39) |
splice site |
probably benign |
|
IGL01408:Akr1c21
|
APN |
13 |
4,627,431 (GRCm39) |
missense |
probably benign |
|
IGL02470:Akr1c21
|
APN |
13 |
4,627,406 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02683:Akr1c21
|
APN |
13 |
4,626,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Akr1c21
|
APN |
13 |
4,630,300 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03126:Akr1c21
|
APN |
13 |
4,627,457 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03365:Akr1c21
|
APN |
13 |
4,633,851 (GRCm39) |
missense |
probably benign |
0.00 |
R0166:Akr1c21
|
UTSW |
13 |
4,631,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0391:Akr1c21
|
UTSW |
13 |
4,631,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R1069:Akr1c21
|
UTSW |
13 |
4,625,333 (GRCm39) |
splice site |
probably benign |
|
R1168:Akr1c21
|
UTSW |
13 |
4,633,836 (GRCm39) |
missense |
probably benign |
0.04 |
R1617:Akr1c21
|
UTSW |
13 |
4,626,351 (GRCm39) |
splice site |
probably null |
|
R1686:Akr1c21
|
UTSW |
13 |
4,627,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Akr1c21
|
UTSW |
13 |
4,625,177 (GRCm39) |
missense |
probably damaging |
0.98 |
R1753:Akr1c21
|
UTSW |
13 |
4,627,134 (GRCm39) |
nonsense |
probably null |
|
R1977:Akr1c21
|
UTSW |
13 |
4,624,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Akr1c21
|
UTSW |
13 |
4,624,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Akr1c21
|
UTSW |
13 |
4,626,305 (GRCm39) |
missense |
probably damaging |
0.98 |
R2198:Akr1c21
|
UTSW |
13 |
4,627,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R2925:Akr1c21
|
UTSW |
13 |
4,626,349 (GRCm39) |
splice site |
probably null |
|
R4965:Akr1c21
|
UTSW |
13 |
4,630,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6245:Akr1c21
|
UTSW |
13 |
4,625,231 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6381:Akr1c21
|
UTSW |
13 |
4,624,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R6711:Akr1c21
|
UTSW |
13 |
4,627,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6843:Akr1c21
|
UTSW |
13 |
4,625,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R6998:Akr1c21
|
UTSW |
13 |
4,633,850 (GRCm39) |
missense |
probably benign |
0.05 |
R7253:Akr1c21
|
UTSW |
13 |
4,627,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Akr1c21
|
UTSW |
13 |
4,626,318 (GRCm39) |
missense |
probably benign |
0.09 |
R8389:Akr1c21
|
UTSW |
13 |
4,626,278 (GRCm39) |
missense |
probably damaging |
0.96 |
R8391:Akr1c21
|
UTSW |
13 |
4,626,278 (GRCm39) |
missense |
probably damaging |
0.96 |
|