Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,833,115 (GRCm39) |
Q1195L |
possibly damaging |
Het |
Abcc12 |
A |
G |
8: 87,258,197 (GRCm39) |
I773T |
probably benign |
Het |
Adamtsl1 |
T |
A |
4: 86,260,960 (GRCm39) |
I1057N |
possibly damaging |
Het |
Adgrv1 |
A |
T |
13: 81,651,114 (GRCm39) |
|
probably benign |
Het |
Anxa5 |
G |
A |
3: 36,504,821 (GRCm39) |
A247V |
probably damaging |
Het |
Ascc3 |
T |
G |
10: 50,611,425 (GRCm39) |
W1589G |
probably damaging |
Het |
Atp2b2 |
G |
A |
6: 113,770,743 (GRCm39) |
P389S |
probably damaging |
Het |
Bicd1 |
A |
G |
6: 149,414,445 (GRCm39) |
E386G |
probably damaging |
Het |
Bmal2 |
C |
A |
6: 146,729,601 (GRCm39) |
H471N |
probably benign |
Het |
Bpifa6 |
T |
A |
2: 153,824,851 (GRCm39) |
S9T |
probably benign |
Het |
Cacna1c |
T |
C |
6: 118,602,473 (GRCm39) |
I1428V |
probably damaging |
Het |
Cfhr4 |
T |
A |
1: 139,682,009 (GRCm39) |
T196S |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,442,783 (GRCm39) |
V589A |
probably benign |
Het |
Chrnb2 |
T |
C |
3: 89,671,713 (GRCm39) |
M1V |
probably null |
Het |
Cldnd1 |
T |
C |
16: 58,553,355 (GRCm39) |
L232P |
probably damaging |
Het |
Col16a1 |
T |
A |
4: 129,960,889 (GRCm39) |
V449E |
unknown |
Het |
Col3a1 |
T |
A |
1: 45,368,028 (GRCm39) |
|
probably benign |
Het |
Cttnbp2nl |
T |
G |
3: 104,913,173 (GRCm39) |
K237T |
probably damaging |
Het |
Cyc1 |
G |
A |
15: 76,229,159 (GRCm39) |
V142I |
probably benign |
Het |
Dapk3 |
A |
G |
10: 81,028,141 (GRCm39) |
T265A |
probably benign |
Het |
Ddx21 |
A |
T |
10: 62,420,531 (GRCm39) |
M711K |
possibly damaging |
Het |
Dlg5 |
A |
T |
14: 24,188,717 (GRCm39) |
L1735Q |
probably damaging |
Het |
Dse |
A |
G |
10: 34,029,660 (GRCm39) |
Y341H |
probably damaging |
Het |
Elmod2 |
A |
G |
8: 84,046,133 (GRCm39) |
I148T |
probably damaging |
Het |
Fam187b |
T |
A |
7: 30,688,545 (GRCm39) |
V22E |
probably damaging |
Het |
Faxc |
A |
G |
4: 21,936,659 (GRCm39) |
D98G |
probably damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,837,040 (GRCm39) |
R320G |
probably damaging |
Het |
Fcrl2 |
A |
G |
3: 87,166,266 (GRCm39) |
S170P |
possibly damaging |
Het |
Fsip2 |
G |
A |
2: 82,821,465 (GRCm39) |
D5733N |
probably benign |
Het |
Gbe1 |
T |
C |
16: 70,157,740 (GRCm39) |
|
probably benign |
Het |
Gm6327 |
T |
C |
16: 12,578,909 (GRCm39) |
|
noncoding transcript |
Het |
H2-T24 |
T |
A |
17: 36,325,878 (GRCm39) |
I238F |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,471,087 (GRCm39) |
E2658G |
probably benign |
Het |
Herc1 |
A |
C |
9: 66,388,192 (GRCm39) |
I3826L |
probably benign |
Het |
Hinfp |
A |
G |
9: 44,211,060 (GRCm39) |
C67R |
probably damaging |
Het |
Hp1bp3 |
C |
T |
4: 137,964,520 (GRCm39) |
S348F |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,279,198 (GRCm39) |
Y3094H |
probably damaging |
Het |
Htr1f |
A |
G |
16: 64,747,091 (GRCm39) |
V67A |
probably damaging |
Het |
Idi2l |
T |
A |
13: 8,990,563 (GRCm39) |
|
probably benign |
Het |
Iqcc |
T |
G |
4: 129,510,392 (GRCm39) |
E374D |
probably damaging |
Het |
Kcnj9 |
T |
C |
1: 172,153,765 (GRCm39) |
T120A |
probably damaging |
Het |
Kitl |
C |
T |
10: 99,923,226 (GRCm39) |
P208S |
probably benign |
Het |
Kmt2b |
A |
T |
7: 30,283,346 (GRCm39) |
C296S |
probably damaging |
Het |
Lgals4 |
A |
G |
7: 28,533,657 (GRCm39) |
|
probably null |
Het |
Lpcat4 |
A |
G |
2: 112,077,093 (GRCm39) |
Y479C |
probably damaging |
Het |
Lrrc74b |
T |
C |
16: 17,371,016 (GRCm39) |
N227S |
probably damaging |
Het |
Mdc1 |
T |
A |
17: 36,163,473 (GRCm39) |
V1007D |
probably damaging |
Het |
Mocos |
T |
G |
18: 24,812,819 (GRCm39) |
I571S |
probably benign |
Het |
Myh8 |
A |
G |
11: 67,183,014 (GRCm39) |
N659D |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,695,874 (GRCm39) |
V203A |
probably benign |
Het |
Myom2 |
A |
G |
8: 15,133,329 (GRCm39) |
N407S |
probably damaging |
Het |
Naip2 |
A |
G |
13: 100,320,296 (GRCm39) |
V240A |
probably benign |
Het |
Nap1l1 |
T |
C |
10: 111,321,370 (GRCm39) |
S37P |
probably benign |
Het |
Nin |
T |
G |
12: 70,097,915 (GRCm39) |
K515T |
probably damaging |
Het |
Npl |
T |
A |
1: 153,384,864 (GRCm39) |
K258* |
probably null |
Het |
Ntn4 |
T |
A |
10: 93,480,569 (GRCm39) |
S98T |
possibly damaging |
Het |
Or10x1 |
T |
C |
1: 174,197,152 (GRCm39) |
V223A |
probably damaging |
Het |
Or2t6 |
T |
C |
14: 14,175,620 (GRCm38) |
D154G |
probably benign |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or5k14 |
C |
A |
16: 58,693,269 (GRCm39) |
M81I |
probably benign |
Het |
Or8u10 |
T |
C |
2: 85,915,844 (GRCm39) |
I92M |
probably damaging |
Het |
Pasd1 |
T |
C |
X: 70,983,161 (GRCm39) |
C378R |
possibly damaging |
Het |
Pate3 |
A |
G |
9: 35,557,453 (GRCm39) |
C68R |
probably damaging |
Het |
Pcdh15 |
A |
G |
10: 74,006,440 (GRCm39) |
D106G |
probably null |
Het |
Ppox |
C |
A |
1: 171,106,849 (GRCm39) |
A192S |
possibly damaging |
Het |
Prkdc |
T |
C |
16: 15,531,517 (GRCm39) |
L1380S |
probably benign |
Het |
Proc |
C |
T |
18: 32,268,951 (GRCm39) |
M11I |
probably benign |
Het |
Psd4 |
C |
A |
2: 24,295,363 (GRCm39) |
A839E |
probably damaging |
Het |
Psg21 |
A |
G |
7: 18,388,793 (GRCm39) |
Y100H |
probably benign |
Het |
Pten |
T |
A |
19: 32,753,469 (GRCm39) |
V45E |
probably benign |
Het |
Ptprn2 |
T |
G |
12: 116,685,711 (GRCm39) |
F57V |
probably damaging |
Het |
Ptprt |
C |
T |
2: 162,120,030 (GRCm39) |
V146I |
probably benign |
Het |
R3hdm2 |
T |
A |
10: 127,334,322 (GRCm39) |
M915K |
probably damaging |
Het |
Rab26 |
C |
T |
17: 24,749,759 (GRCm39) |
|
probably null |
Het |
Rab7b |
T |
C |
1: 131,626,293 (GRCm39) |
L107P |
probably damaging |
Het |
Rbm47 |
T |
A |
5: 66,183,872 (GRCm39) |
T244S |
possibly damaging |
Het |
Rhbdf2 |
C |
A |
11: 116,496,170 (GRCm39) |
G122C |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,321,187 (GRCm39) |
E1215G |
probably benign |
Het |
Rprd2 |
T |
C |
3: 95,681,673 (GRCm39) |
K407E |
probably damaging |
Het |
Siah3 |
G |
A |
14: 75,693,574 (GRCm39) |
V27I |
possibly damaging |
Het |
Slc12a3 |
G |
A |
8: 95,067,511 (GRCm39) |
|
probably benign |
Het |
Slc14a2 |
T |
A |
18: 78,235,338 (GRCm39) |
N280Y |
probably damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc25a35 |
A |
G |
11: 68,862,786 (GRCm39) |
Y247C |
probably damaging |
Het |
Slc29a4 |
A |
G |
5: 142,691,285 (GRCm39) |
D55G |
probably benign |
Het |
Slc35d1 |
C |
T |
4: 103,065,378 (GRCm39) |
V189I |
probably benign |
Het |
Spg11 |
T |
C |
2: 121,901,449 (GRCm39) |
E1497G |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,067,884 (GRCm39) |
R322* |
probably null |
Het |
Stac3 |
A |
T |
10: 127,339,519 (GRCm39) |
R138S |
probably damaging |
Het |
Tet3 |
C |
G |
6: 83,345,770 (GRCm39) |
G1556R |
probably damaging |
Het |
Tgfbr3 |
A |
G |
5: 107,280,682 (GRCm39) |
S693P |
probably benign |
Het |
Tmcc2 |
C |
T |
1: 132,308,444 (GRCm39) |
G150D |
probably benign |
Het |
Tmem216 |
T |
C |
19: 10,531,970 (GRCm39) |
Y44C |
probably damaging |
Het |
Tmem260 |
T |
A |
14: 48,720,779 (GRCm39) |
C306* |
probably null |
Het |
Ubr4 |
A |
G |
4: 139,191,362 (GRCm39) |
T4127A |
possibly damaging |
Het |
Ugt2a2 |
T |
A |
5: 87,622,720 (GRCm39) |
K293* |
probably null |
Het |
Vmn2r102 |
A |
C |
17: 19,899,025 (GRCm39) |
T456P |
probably benign |
Het |
Vmn2r90 |
T |
A |
17: 17,932,511 (GRCm39) |
S139R |
probably benign |
Het |
Wrnip1 |
G |
A |
13: 32,990,847 (GRCm39) |
V369I |
probably damaging |
Het |
Zc3h12c |
T |
A |
9: 52,037,923 (GRCm39) |
I305F |
possibly damaging |
Het |
Zmym2 |
A |
G |
14: 57,180,715 (GRCm39) |
N876D |
probably benign |
Het |
|