Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630073D07Rik |
T |
G |
6: 132,603,564 (GRCm39) |
Q64P |
unknown |
Het |
Adgrv1 |
A |
T |
13: 81,668,905 (GRCm39) |
F1830L |
probably benign |
Het |
Anks3 |
C |
T |
16: 4,763,918 (GRCm39) |
|
probably null |
Het |
Aqp12 |
G |
A |
1: 92,934,332 (GRCm39) |
D70N |
probably damaging |
Het |
B4galnt4 |
C |
T |
7: 140,648,061 (GRCm39) |
R526* |
probably null |
Het |
Best2 |
A |
G |
8: 85,737,882 (GRCm39) |
F171S |
probably benign |
Het |
C2cd5 |
A |
T |
6: 142,958,956 (GRCm39) |
V965D |
probably damaging |
Het |
Cd33 |
T |
C |
7: 43,179,303 (GRCm39) |
E282G |
probably benign |
Het |
Cep95 |
C |
T |
11: 106,681,554 (GRCm39) |
|
probably benign |
Het |
Chd6 |
A |
T |
2: 160,809,920 (GRCm39) |
|
probably benign |
Het |
Clec4d |
A |
T |
6: 123,244,120 (GRCm39) |
|
probably null |
Het |
Cntd1 |
C |
T |
11: 101,174,678 (GRCm39) |
S128L |
probably damaging |
Het |
Col19a1 |
T |
C |
1: 24,490,835 (GRCm39) |
|
probably benign |
Het |
Ctrb1 |
C |
A |
8: 112,415,324 (GRCm39) |
V117L |
probably benign |
Het |
Dclk1 |
T |
C |
3: 55,154,942 (GRCm39) |
V124A |
possibly damaging |
Het |
Dcp2 |
T |
C |
18: 44,538,638 (GRCm39) |
|
probably null |
Het |
Dctn1 |
C |
A |
6: 83,176,166 (GRCm39) |
|
probably benign |
Het |
Dennd11 |
A |
G |
6: 40,388,648 (GRCm39) |
F238L |
probably benign |
Het |
Ero1b |
A |
G |
13: 12,616,648 (GRCm39) |
E359G |
probably damaging |
Het |
Exosc8 |
G |
T |
3: 54,636,266 (GRCm39) |
A255E |
probably damaging |
Het |
Fhip1a |
G |
A |
3: 85,595,838 (GRCm39) |
P349L |
probably damaging |
Het |
Fndc3c1 |
C |
T |
X: 105,477,128 (GRCm39) |
A824T |
probably benign |
Het |
Gja10 |
G |
A |
4: 32,601,812 (GRCm39) |
Q191* |
probably null |
Het |
Gm1587 |
C |
T |
14: 78,036,288 (GRCm39) |
R6Q |
unknown |
Het |
Gm3409 |
A |
G |
5: 146,476,418 (GRCm39) |
I190V |
probably benign |
Het |
Gm4952 |
G |
T |
19: 12,600,973 (GRCm39) |
M64I |
probably damaging |
Het |
Gramd1b |
C |
T |
9: 40,217,765 (GRCm39) |
M595I |
possibly damaging |
Het |
Grik1 |
C |
T |
16: 87,848,241 (GRCm39) |
V176M |
probably damaging |
Het |
Grin2b |
A |
G |
6: 136,021,044 (GRCm39) |
C86R |
probably damaging |
Het |
Gtse1 |
C |
T |
15: 85,746,264 (GRCm39) |
|
probably benign |
Het |
Hectd2 |
T |
C |
19: 36,589,719 (GRCm39) |
Y615H |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,229,579 (GRCm39) |
F1552S |
possibly damaging |
Het |
Ifi207 |
A |
G |
1: 173,557,211 (GRCm39) |
V516A |
possibly damaging |
Het |
Igfbp5 |
G |
T |
1: 72,913,184 (GRCm39) |
P39T |
probably damaging |
Het |
Il23r |
T |
A |
6: 67,400,719 (GRCm39) |
D537V |
possibly damaging |
Het |
Invs |
A |
G |
4: 48,390,095 (GRCm39) |
Y251C |
probably damaging |
Het |
Isl1 |
G |
T |
13: 116,444,953 (GRCm39) |
H25Q |
probably damaging |
Het |
Kif13a |
A |
G |
13: 46,966,221 (GRCm39) |
L399P |
probably damaging |
Het |
Klhl1 |
A |
G |
14: 96,584,225 (GRCm39) |
V335A |
probably benign |
Het |
Klhl14 |
C |
A |
18: 21,784,843 (GRCm39) |
A195S |
probably damaging |
Het |
Lepr |
A |
G |
4: 101,639,927 (GRCm39) |
|
probably benign |
Het |
Map1b |
A |
C |
13: 99,567,454 (GRCm39) |
S1756A |
unknown |
Het |
Med23 |
C |
T |
10: 24,785,710 (GRCm39) |
A877V |
probably benign |
Het |
Mfsd4b2 |
T |
C |
10: 39,797,458 (GRCm39) |
Y299C |
probably damaging |
Het |
Mipol1 |
T |
A |
12: 57,379,205 (GRCm39) |
M221K |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,569,350 (GRCm39) |
S137C |
probably damaging |
Het |
Mutyh |
T |
C |
4: 116,673,855 (GRCm39) |
Y189H |
probably damaging |
Het |
Nabp2 |
T |
C |
10: 128,245,182 (GRCm39) |
T21A |
possibly damaging |
Het |
Nalf1 |
T |
C |
8: 9,820,217 (GRCm39) |
T268A |
probably benign |
Het |
Nell1 |
T |
A |
7: 50,350,943 (GRCm39) |
V530E |
possibly damaging |
Het |
Npc1 |
G |
C |
18: 12,346,435 (GRCm39) |
P254A |
possibly damaging |
Het |
Nup153 |
A |
G |
13: 46,854,502 (GRCm39) |
V530A |
probably damaging |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Or10j5 |
T |
C |
1: 172,784,881 (GRCm39) |
V173A |
probably damaging |
Het |
Or11h4b |
A |
G |
14: 50,918,872 (GRCm39) |
V73A |
probably benign |
Het |
Or7e177 |
T |
C |
9: 20,212,354 (GRCm39) |
V287A |
probably benign |
Het |
Pabpc1l |
T |
A |
2: 163,874,174 (GRCm39) |
I193N |
possibly damaging |
Het |
Pabpc4l |
A |
G |
3: 46,401,066 (GRCm39) |
Y193H |
probably damaging |
Het |
Pank1 |
T |
C |
19: 34,856,281 (GRCm39) |
S66G |
probably benign |
Het |
Pcdhb1 |
A |
T |
18: 37,399,233 (GRCm39) |
K395* |
probably null |
Het |
Pcna |
A |
G |
2: 132,093,817 (GRCm39) |
|
probably benign |
Het |
Pgr |
T |
A |
9: 8,903,630 (GRCm39) |
Y550* |
probably null |
Het |
Phf11a |
A |
G |
14: 59,519,316 (GRCm39) |
|
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,151,524 (GRCm39) |
|
probably benign |
Het |
Pofut2 |
T |
A |
10: 77,096,642 (GRCm39) |
Y122* |
probably null |
Het |
Pole |
A |
G |
5: 110,475,644 (GRCm39) |
M1818V |
probably benign |
Het |
Rapgef3 |
A |
G |
15: 97,647,914 (GRCm39) |
L696P |
probably damaging |
Het |
Rasal3 |
T |
C |
17: 32,616,327 (GRCm39) |
D310G |
probably damaging |
Het |
Rhoq |
A |
G |
17: 87,302,486 (GRCm39) |
K141E |
probably benign |
Het |
Rilpl1 |
A |
G |
5: 124,652,813 (GRCm39) |
|
probably benign |
Het |
Rnaseh1 |
T |
C |
12: 28,703,088 (GRCm39) |
S91P |
probably benign |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Saa1 |
C |
A |
7: 46,391,856 (GRCm39) |
G31W |
probably null |
Het |
Saxo5 |
T |
A |
8: 3,536,947 (GRCm39) |
I431K |
possibly damaging |
Het |
Scaf8 |
A |
G |
17: 3,218,352 (GRCm39) |
T241A |
unknown |
Het |
Scarb2 |
C |
T |
5: 92,592,125 (GRCm39) |
A473T |
possibly damaging |
Het |
Scnn1b |
T |
C |
7: 121,509,670 (GRCm39) |
F273S |
probably damaging |
Het |
Sdccag8 |
T |
C |
1: 176,656,536 (GRCm39) |
V136A |
probably damaging |
Het |
Sdr16c6 |
A |
T |
4: 4,069,926 (GRCm39) |
V138E |
probably damaging |
Het |
Sf3a3 |
G |
A |
4: 124,615,886 (GRCm39) |
A180T |
possibly damaging |
Het |
Slc16a5 |
T |
A |
11: 115,360,842 (GRCm39) |
S342T |
probably damaging |
Het |
Slc18a1 |
A |
G |
8: 69,526,464 (GRCm39) |
S75P |
probably benign |
Het |
Slc7a6 |
T |
A |
8: 106,920,120 (GRCm39) |
|
probably benign |
Het |
Smco3 |
G |
A |
6: 136,808,845 (GRCm39) |
Q10* |
probably null |
Het |
Spem2 |
T |
C |
11: 69,708,290 (GRCm39) |
Q225R |
probably benign |
Het |
Ssb |
G |
T |
2: 69,697,901 (GRCm39) |
|
probably null |
Het |
Stx8 |
T |
C |
11: 68,000,106 (GRCm39) |
I182T |
probably damaging |
Het |
Synj2 |
T |
A |
17: 6,040,542 (GRCm39) |
I121N |
probably damaging |
Het |
Tbc1d1 |
T |
C |
5: 64,502,643 (GRCm39) |
Y1055H |
probably damaging |
Het |
Thbs3 |
G |
T |
3: 89,125,067 (GRCm39) |
R52L |
probably damaging |
Het |
Tmem101 |
C |
T |
11: 102,044,222 (GRCm39) |
V222I |
probably benign |
Het |
Tnks2 |
C |
T |
19: 36,823,068 (GRCm39) |
Q112* |
probably null |
Het |
Tnrc6b |
T |
A |
15: 80,764,924 (GRCm39) |
W809R |
probably damaging |
Het |
Trib2 |
T |
A |
12: 15,865,454 (GRCm39) |
R16S |
probably damaging |
Het |
Trim12a |
T |
C |
7: 103,956,331 (GRCm39) |
N70D |
probably damaging |
Het |
Trim55 |
T |
A |
3: 19,716,046 (GRCm39) |
|
probably null |
Het |
Tspyl5 |
T |
A |
15: 33,687,153 (GRCm39) |
D264V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,555,388 (GRCm39) |
V30539A |
probably damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,713,988 (GRCm39) |
F43S |
possibly damaging |
Het |
Tut7 |
A |
G |
13: 59,964,548 (GRCm39) |
L209P |
probably damaging |
Het |
Ube3d |
A |
G |
9: 86,305,056 (GRCm39) |
L262P |
probably damaging |
Het |
Ugt1a7c |
T |
C |
1: 88,023,651 (GRCm39) |
V270A |
probably benign |
Het |
Vav3 |
T |
A |
3: 109,413,738 (GRCm39) |
F225L |
possibly damaging |
Het |
Vmn1r21 |
G |
T |
6: 57,821,077 (GRCm39) |
Y122* |
probably null |
Het |
Vmn1r225 |
C |
A |
17: 20,723,071 (GRCm39) |
Q171K |
probably benign |
Het |
Vmn2r103 |
T |
C |
17: 20,032,029 (GRCm39) |
V601A |
possibly damaging |
Het |
Vmn2r19 |
T |
A |
6: 123,308,589 (GRCm39) |
N555K |
probably damaging |
Het |
Vps33a |
G |
A |
5: 123,696,684 (GRCm39) |
A323V |
probably benign |
Het |
Wdr77 |
C |
T |
3: 105,874,618 (GRCm39) |
P337S |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,929,884 (GRCm39) |
I93N |
probably damaging |
Het |
Zbtb9 |
T |
A |
17: 27,193,612 (GRCm39) |
I339N |
probably damaging |
Het |
Zfp202 |
T |
A |
9: 40,121,083 (GRCm39) |
D241E |
probably damaging |
Het |
Zfp235 |
T |
A |
7: 23,840,563 (GRCm39) |
Y327* |
probably null |
Het |
Zfp820 |
A |
C |
17: 22,038,316 (GRCm39) |
D337E |
probably benign |
Het |
Zfp944 |
T |
C |
17: 22,560,065 (GRCm39) |
T14A |
probably damaging |
Het |
Zfy1 |
A |
G |
Y: 729,733 (GRCm39) |
V303A |
unknown |
Het |
Zfyve26 |
C |
T |
12: 79,286,744 (GRCm39) |
W2281* |
probably null |
Het |
|
Other mutations in Ephb3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Ephb3
|
APN |
16 |
21,039,165 (GRCm39) |
splice site |
probably null |
|
IGL00966:Ephb3
|
APN |
16 |
21,036,044 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02166:Ephb3
|
APN |
16 |
21,039,499 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02245:Ephb3
|
APN |
16 |
21,040,174 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02321:Ephb3
|
APN |
16 |
21,033,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02337:Ephb3
|
APN |
16 |
21,040,253 (GRCm39) |
splice site |
probably null |
|
IGL02507:Ephb3
|
APN |
16 |
21,039,389 (GRCm39) |
splice site |
probably benign |
|
IGL02755:Ephb3
|
APN |
16 |
21,040,448 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02806:Ephb3
|
APN |
16 |
21,041,031 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4362001:Ephb3
|
UTSW |
16 |
21,039,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:Ephb3
|
UTSW |
16 |
21,033,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Ephb3
|
UTSW |
16 |
21,036,859 (GRCm39) |
missense |
probably benign |
0.01 |
R0196:Ephb3
|
UTSW |
16 |
21,036,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R0230:Ephb3
|
UTSW |
16 |
21,039,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0828:Ephb3
|
UTSW |
16 |
21,037,784 (GRCm39) |
unclassified |
probably benign |
|
R1126:Ephb3
|
UTSW |
16 |
21,041,226 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1460:Ephb3
|
UTSW |
16 |
21,037,672 (GRCm39) |
missense |
probably benign |
|
R1592:Ephb3
|
UTSW |
16 |
21,040,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R1632:Ephb3
|
UTSW |
16 |
21,031,687 (GRCm39) |
missense |
probably benign |
0.00 |
R1694:Ephb3
|
UTSW |
16 |
21,040,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1719:Ephb3
|
UTSW |
16 |
21,039,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Ephb3
|
UTSW |
16 |
21,035,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R1956:Ephb3
|
UTSW |
16 |
21,040,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R2378:Ephb3
|
UTSW |
16 |
21,036,993 (GRCm39) |
missense |
probably benign |
|
R3408:Ephb3
|
UTSW |
16 |
21,038,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R4027:Ephb3
|
UTSW |
16 |
21,040,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R4429:Ephb3
|
UTSW |
16 |
21,033,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R4655:Ephb3
|
UTSW |
16 |
21,040,958 (GRCm39) |
missense |
probably damaging |
0.98 |
R4826:Ephb3
|
UTSW |
16 |
21,033,745 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4828:Ephb3
|
UTSW |
16 |
21,033,745 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4960:Ephb3
|
UTSW |
16 |
21,039,245 (GRCm39) |
missense |
probably benign |
0.09 |
R5057:Ephb3
|
UTSW |
16 |
21,039,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5090:Ephb3
|
UTSW |
16 |
21,033,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R5396:Ephb3
|
UTSW |
16 |
21,037,855 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5540:Ephb3
|
UTSW |
16 |
21,039,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R5628:Ephb3
|
UTSW |
16 |
21,036,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Ephb3
|
UTSW |
16 |
21,041,241 (GRCm39) |
missense |
probably benign |
0.08 |
R5838:Ephb3
|
UTSW |
16 |
21,040,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5866:Ephb3
|
UTSW |
16 |
21,030,129 (GRCm39) |
intron |
probably benign |
|
R6017:Ephb3
|
UTSW |
16 |
21,040,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:Ephb3
|
UTSW |
16 |
21,040,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R6510:Ephb3
|
UTSW |
16 |
21,036,861 (GRCm39) |
missense |
probably damaging |
0.98 |
R6539:Ephb3
|
UTSW |
16 |
21,040,218 (GRCm39) |
missense |
probably benign |
|
R6591:Ephb3
|
UTSW |
16 |
21,033,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R6691:Ephb3
|
UTSW |
16 |
21,033,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7101:Ephb3
|
UTSW |
16 |
21,037,268 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7111:Ephb3
|
UTSW |
16 |
21,037,577 (GRCm39) |
nonsense |
probably null |
|
R7236:Ephb3
|
UTSW |
16 |
21,033,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7307:Ephb3
|
UTSW |
16 |
21,040,976 (GRCm39) |
missense |
probably benign |
0.04 |
R7410:Ephb3
|
UTSW |
16 |
21,040,158 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7413:Ephb3
|
UTSW |
16 |
21,033,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Ephb3
|
UTSW |
16 |
21,036,107 (GRCm39) |
splice site |
probably null |
|
R7944:Ephb3
|
UTSW |
16 |
21,040,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R7945:Ephb3
|
UTSW |
16 |
21,040,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9092:Ephb3
|
UTSW |
16 |
21,041,214 (GRCm39) |
missense |
probably benign |
0.01 |
R9504:Ephb3
|
UTSW |
16 |
21,036,830 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9706:Ephb3
|
UTSW |
16 |
21,039,193 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ephb3
|
UTSW |
16 |
21,036,786 (GRCm39) |
missense |
possibly damaging |
0.53 |
|