Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adra1a |
T |
A |
14: 66,875,273 (GRCm39) |
S83T |
probably damaging |
Het |
Aff1 |
T |
A |
5: 103,994,905 (GRCm39) |
Y1034* |
probably null |
Het |
Ago3 |
A |
T |
4: 126,262,296 (GRCm39) |
M418K |
probably benign |
Het |
Alpk1 |
G |
T |
3: 127,481,241 (GRCm39) |
N175K |
possibly damaging |
Het |
Als2 |
A |
G |
1: 59,254,472 (GRCm39) |
V295A |
probably benign |
Het |
Arhgap32 |
A |
G |
9: 32,040,949 (GRCm39) |
D67G |
probably damaging |
Het |
Arhgap32 |
T |
C |
9: 32,172,076 (GRCm39) |
C1619R |
probably damaging |
Het |
Asns |
T |
G |
6: 7,678,029 (GRCm39) |
K350Q |
probably benign |
Het |
Atp8b5 |
A |
T |
4: 43,356,980 (GRCm39) |
D576V |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,617,590 (GRCm39) |
I122V |
probably damaging |
Het |
Baz1b |
T |
G |
5: 135,246,267 (GRCm39) |
L572R |
possibly damaging |
Het |
C4b |
T |
C |
17: 34,952,380 (GRCm39) |
T1220A |
probably benign |
Het |
Carmil3 |
T |
C |
14: 55,738,778 (GRCm39) |
|
probably null |
Het |
Ccndbp1 |
A |
T |
2: 120,839,003 (GRCm39) |
T5S |
probably benign |
Het |
Chaf1b |
T |
C |
16: 93,681,430 (GRCm39) |
V16A |
probably damaging |
Het |
Chd8 |
C |
A |
14: 52,442,825 (GRCm39) |
C575F |
probably damaging |
Het |
Chrna10 |
G |
A |
7: 101,762,426 (GRCm39) |
P255S |
possibly damaging |
Het |
Clip1 |
T |
C |
5: 123,717,356 (GRCm39) |
D1387G |
probably damaging |
Het |
Col12a1 |
C |
A |
9: 79,585,776 (GRCm39) |
V1228F |
possibly damaging |
Het |
Cxcr5 |
T |
C |
9: 44,424,638 (GRCm39) |
T340A |
probably benign |
Het |
Cyp2e1 |
G |
A |
7: 140,343,821 (GRCm39) |
V20I |
possibly damaging |
Het |
Dchs1 |
A |
G |
7: 105,415,133 (GRCm39) |
Y684H |
probably damaging |
Het |
Dcun1d3 |
T |
C |
7: 119,456,887 (GRCm39) |
E275G |
probably damaging |
Het |
Dgcr8 |
G |
A |
16: 18,076,174 (GRCm39) |
R4* |
probably null |
Het |
Dglucy |
A |
T |
12: 100,804,923 (GRCm39) |
D168V |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 30,985,436 (GRCm39) |
K3818N |
probably damaging |
Het |
Dnajc17 |
T |
C |
2: 119,009,909 (GRCm39) |
D239G |
probably benign |
Het |
Dok2 |
C |
T |
14: 71,015,314 (GRCm39) |
P347L |
probably benign |
Het |
Elavl2 |
T |
C |
4: 91,142,379 (GRCm39) |
R265G |
probably null |
Het |
Elf1 |
T |
A |
14: 79,818,183 (GRCm39) |
N567K |
probably benign |
Het |
Epha8 |
A |
T |
4: 136,660,633 (GRCm39) |
I695N |
probably damaging |
Het |
Fam178b |
C |
A |
1: 36,671,496 (GRCm39) |
|
probably null |
Het |
Fam76a |
A |
T |
4: 132,629,428 (GRCm39) |
|
probably null |
Het |
Fam76a |
A |
G |
4: 132,643,501 (GRCm39) |
Y78H |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,166,839 (GRCm39) |
C2026S |
probably damaging |
Het |
Fbxo4 |
T |
C |
15: 3,998,523 (GRCm39) |
T312A |
probably benign |
Het |
Fscn2 |
T |
C |
11: 120,258,813 (GRCm39) |
F453L |
possibly damaging |
Het |
Gabrb2 |
T |
C |
11: 42,488,469 (GRCm39) |
C312R |
probably damaging |
Het |
Gba2 |
A |
C |
4: 43,568,315 (GRCm39) |
L684R |
probably damaging |
Het |
Golga2 |
T |
A |
2: 32,187,168 (GRCm39) |
N89K |
probably damaging |
Het |
Gpx6 |
C |
T |
13: 21,496,434 (GRCm39) |
Q3* |
probably null |
Het |
Grin1 |
T |
A |
2: 25,182,393 (GRCm39) |
H956L |
possibly damaging |
Het |
H2-Q7 |
T |
G |
17: 35,658,914 (GRCm39) |
C122G |
probably damaging |
Het |
Hcar2 |
C |
G |
5: 124,002,513 (GRCm39) |
G330A |
probably benign |
Het |
Hes3 |
A |
G |
4: 152,372,289 (GRCm39) |
S37P |
probably damaging |
Het |
Hs3st3b1 |
T |
C |
11: 63,780,086 (GRCm39) |
H347R |
probably benign |
Het |
Il1rl1 |
A |
G |
1: 40,489,348 (GRCm39) |
R367G |
probably damaging |
Het |
Kcnc1 |
G |
T |
7: 46,086,711 (GRCm39) |
S570I |
probably benign |
Het |
Kctd3 |
T |
C |
1: 188,706,665 (GRCm39) |
I523M |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Kntc1 |
T |
G |
5: 123,954,825 (GRCm39) |
M2081R |
possibly damaging |
Het |
Krt87 |
A |
G |
15: 101,385,837 (GRCm39) |
S253P |
probably damaging |
Het |
Ktn1 |
T |
A |
14: 47,930,953 (GRCm39) |
|
probably null |
Het |
Lair1 |
T |
A |
7: 4,012,731 (GRCm39) |
M251L |
probably benign |
Het |
Lama3 |
A |
T |
18: 12,582,601 (GRCm39) |
H631L |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,107,486 (GRCm39) |
N1231S |
probably damaging |
Het |
Lin54 |
A |
G |
5: 100,607,597 (GRCm39) |
I250T |
probably damaging |
Het |
Lrit1 |
C |
T |
14: 36,784,193 (GRCm39) |
T507M |
possibly damaging |
Het |
Lrp11 |
A |
G |
10: 7,479,965 (GRCm39) |
H345R |
possibly damaging |
Het |
Lrp6 |
A |
C |
6: 134,456,502 (GRCm39) |
S921A |
probably benign |
Het |
Lrrc27 |
A |
G |
7: 138,822,614 (GRCm39) |
T502A |
probably benign |
Het |
Marf1 |
A |
C |
16: 13,970,321 (GRCm39) |
S133A |
probably benign |
Het |
Mga |
C |
T |
2: 119,733,538 (GRCm39) |
P129S |
probably damaging |
Het |
Mgat4e |
T |
C |
1: 134,469,063 (GRCm39) |
N327S |
probably damaging |
Het |
Mlh1 |
A |
G |
9: 111,068,866 (GRCm39) |
Y499H |
probably benign |
Het |
Mrgpra1 |
A |
G |
7: 46,985,218 (GRCm39) |
S154P |
probably damaging |
Het |
Myo1h |
A |
G |
5: 114,498,660 (GRCm39) |
I919V |
possibly damaging |
Het |
Naalad2 |
T |
C |
9: 18,262,214 (GRCm39) |
R442G |
probably damaging |
Het |
Nat8f4 |
T |
C |
6: 85,878,481 (GRCm39) |
H14R |
probably benign |
Het |
Nav1 |
A |
G |
1: 135,386,477 (GRCm39) |
S1184P |
probably damaging |
Het |
Nckap1 |
T |
A |
2: 80,337,278 (GRCm39) |
N986I |
probably benign |
Het |
Nop9 |
AGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGA |
14: 55,983,859 (GRCm39) |
|
probably benign |
Het |
Nphp4 |
G |
A |
4: 152,639,003 (GRCm39) |
R878K |
probably benign |
Het |
Nutm1 |
G |
A |
2: 112,079,281 (GRCm39) |
A878V |
probably benign |
Het |
Or4f56 |
A |
T |
2: 111,703,395 (GRCm39) |
D268E |
possibly damaging |
Het |
Or52e8b |
A |
C |
7: 104,673,737 (GRCm39) |
I150S |
probably damaging |
Het |
Or5k1b |
G |
T |
16: 58,580,911 (GRCm39) |
F209L |
probably damaging |
Het |
Orc6 |
T |
A |
8: 86,029,579 (GRCm39) |
I41K |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,307,005 (GRCm39) |
T1798A |
probably benign |
Het |
Ppp1r14a |
A |
T |
7: 28,991,486 (GRCm39) |
E98V |
possibly damaging |
Het |
Prpf8 |
T |
A |
11: 75,383,331 (GRCm39) |
D521E |
probably damaging |
Het |
Pudp |
A |
G |
18: 50,701,136 (GRCm39) |
V199A |
probably damaging |
Het |
Rab3c |
T |
C |
13: 110,198,434 (GRCm39) |
E198G |
probably benign |
Het |
Ramac |
T |
A |
7: 81,418,163 (GRCm39) |
W73R |
probably damaging |
Het |
Rbl2 |
A |
G |
8: 91,812,196 (GRCm39) |
Y255C |
probably damaging |
Het |
Rbm12 |
T |
C |
2: 155,938,484 (GRCm39) |
D596G |
possibly damaging |
Het |
Sipa1l3 |
A |
G |
7: 29,077,066 (GRCm39) |
V902A |
probably damaging |
Het |
Slc37a3 |
T |
G |
6: 39,314,157 (GRCm39) |
Q485P |
probably benign |
Het |
Slc44a3 |
T |
C |
3: 121,320,723 (GRCm39) |
T93A |
possibly damaging |
Het |
Slc66a1 |
G |
T |
4: 139,027,312 (GRCm39) |
H343Q |
probably benign |
Het |
Sun3 |
G |
A |
11: 8,988,266 (GRCm39) |
L19F |
probably benign |
Het |
Tas2r125 |
A |
G |
6: 132,886,866 (GRCm39) |
I85V |
probably benign |
Het |
Tenm4 |
A |
C |
7: 96,423,253 (GRCm39) |
K683Q |
probably damaging |
Het |
Tmprss11d |
C |
T |
5: 86,454,140 (GRCm39) |
V222M |
probably damaging |
Het |
Tnip1 |
A |
C |
11: 54,806,365 (GRCm39) |
S570A |
possibly damaging |
Het |
Top1mt |
G |
A |
15: 75,529,552 (GRCm39) |
P554S |
probably damaging |
Het |
Top1mt |
A |
G |
15: 75,547,880 (GRCm39) |
F69L |
possibly damaging |
Het |
Ttc7 |
A |
G |
17: 87,648,325 (GRCm39) |
K508R |
probably benign |
Het |
Ttll4 |
A |
T |
1: 74,718,166 (GRCm39) |
T6S |
possibly damaging |
Het |
Xpo5 |
T |
C |
17: 46,533,643 (GRCm39) |
Y500H |
possibly damaging |
Het |
Xpot |
C |
T |
10: 121,450,968 (GRCm39) |
|
probably null |
Het |
Zbbx |
T |
C |
3: 74,992,348 (GRCm39) |
I268V |
probably benign |
Het |
Zbtb40 |
G |
A |
4: 136,734,408 (GRCm39) |
P360S |
probably damaging |
Het |
Zfp324 |
T |
C |
7: 12,705,233 (GRCm39) |
L474P |
probably damaging |
Het |
Zfp398 |
A |
G |
6: 47,817,186 (GRCm39) |
T9A |
probably benign |
Het |
Zfp692 |
A |
C |
11: 58,200,997 (GRCm39) |
S293R |
probably null |
Het |
|