Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930544D05Rik |
A |
G |
11: 70,506,834 (GRCm39) |
|
probably null |
Het |
Abcb10 |
C |
T |
8: 124,691,757 (GRCm39) |
A403T |
|
Het |
Acan |
C |
T |
7: 78,741,086 (GRCm39) |
P484L |
possibly damaging |
Het |
Amotl2 |
T |
A |
9: 102,597,615 (GRCm39) |
Y125N |
probably damaging |
Het |
Apaf1 |
C |
A |
10: 90,913,420 (GRCm39) |
V168F |
possibly damaging |
Het |
Arhgap32 |
C |
T |
9: 32,158,426 (GRCm39) |
H154Y |
probably damaging |
Het |
B4galnt3 |
A |
G |
6: 120,271,346 (GRCm39) |
|
probably null |
Het |
Bcl11b |
T |
A |
12: 107,931,967 (GRCm39) |
M202L |
probably benign |
Het |
Cdc40 |
C |
A |
10: 40,717,473 (GRCm39) |
R406L |
possibly damaging |
Het |
Cemip |
C |
A |
7: 83,652,616 (GRCm39) |
|
probably benign |
Het |
Col26a1 |
T |
C |
5: 136,775,894 (GRCm39) |
D353G |
probably benign |
Het |
Col6a5 |
T |
A |
9: 105,778,815 (GRCm39) |
Q1682L |
unknown |
Het |
Cul9 |
C |
T |
17: 46,822,168 (GRCm39) |
G1819D |
probably damaging |
Het |
Cyp2b10 |
C |
T |
7: 25,614,242 (GRCm39) |
Q239* |
probably null |
Het |
Dthd1 |
T |
A |
5: 63,000,259 (GRCm39) |
I527N |
probably damaging |
Het |
Dzip3 |
C |
T |
16: 48,754,156 (GRCm39) |
|
probably null |
Het |
Ecm2 |
A |
G |
13: 49,671,940 (GRCm39) |
E147G |
probably benign |
Het |
Ercc6l2 |
C |
T |
13: 63,982,561 (GRCm39) |
T132M |
probably damaging |
Het |
Esf1 |
G |
A |
2: 139,990,751 (GRCm39) |
Q578* |
probably null |
Het |
Gria4 |
C |
T |
9: 4,502,429 (GRCm39) |
R368H |
probably benign |
Het |
Hps5 |
T |
C |
7: 46,421,312 (GRCm39) |
D717G |
probably benign |
Het |
Hrh1 |
A |
T |
6: 114,457,253 (GRCm39) |
D178V |
probably benign |
Het |
Inppl1 |
T |
C |
7: 101,479,268 (GRCm39) |
N537S |
possibly damaging |
Het |
Itih1 |
T |
C |
14: 30,663,521 (GRCm39) |
Y165C |
probably damaging |
Het |
Krt71 |
T |
A |
15: 101,643,141 (GRCm39) |
I456F |
possibly damaging |
Het |
Larp4 |
T |
C |
15: 99,892,570 (GRCm39) |
V255A |
probably damaging |
Het |
Lrriq1 |
T |
G |
10: 103,051,572 (GRCm39) |
R393S |
possibly damaging |
Het |
Mep1a |
T |
A |
17: 43,813,558 (GRCm39) |
I31L |
probably benign |
Het |
Muc5b |
C |
T |
7: 141,396,146 (GRCm39) |
T134I |
unknown |
Het |
Neurl4 |
T |
C |
11: 69,800,067 (GRCm39) |
Y1052H |
probably benign |
Het |
Nlrc5 |
C |
G |
8: 95,208,420 (GRCm39) |
N755K |
probably damaging |
Het |
Nrde2 |
T |
C |
12: 100,108,502 (GRCm39) |
K363R |
probably benign |
Het |
Pcdhb12 |
T |
C |
18: 37,570,335 (GRCm39) |
S494P |
possibly damaging |
Het |
Pcnx1 |
C |
A |
12: 81,965,292 (GRCm39) |
S486R |
possibly damaging |
Het |
Pira13 |
T |
A |
7: 3,825,161 (GRCm39) |
R494* |
probably null |
Het |
Plrg1 |
T |
A |
3: 82,977,081 (GRCm39) |
V374E |
probably damaging |
Het |
Plxnb2 |
A |
G |
15: 89,042,916 (GRCm39) |
I1491T |
probably damaging |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Scn4a |
T |
C |
11: 106,232,367 (GRCm39) |
E490G |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,300,958 (GRCm39) |
V887A |
|
Het |
Serpina3a |
T |
C |
12: 104,082,467 (GRCm39) |
I80T |
probably damaging |
Het |
Setd1b |
A |
T |
5: 123,281,443 (GRCm39) |
I66F |
unknown |
Het |
Slirp |
T |
A |
12: 87,494,428 (GRCm39) |
|
probably null |
Het |
Socs6 |
A |
C |
18: 88,888,169 (GRCm39) |
S249A |
probably benign |
Het |
Thoc2l |
A |
G |
5: 104,669,027 (GRCm39) |
E1183G |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,616,077 (GRCm39) |
I16622N |
probably damaging |
Het |
Uox |
A |
T |
3: 146,331,589 (GRCm39) |
T237S |
probably damaging |
Het |
Vmn2r43 |
T |
A |
7: 8,258,326 (GRCm39) |
I296L |
probably benign |
Het |
Vmn2r74 |
T |
A |
7: 85,601,943 (GRCm39) |
D565V |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,372,255 (GRCm39) |
|
probably null |
Het |
Vps13d |
A |
G |
4: 144,882,707 (GRCm39) |
V962A |
|
Het |
|
Other mutations in Bahcc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Bahcc1
|
APN |
11 |
120,163,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00536:Bahcc1
|
APN |
11 |
120,175,871 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01339:Bahcc1
|
APN |
11 |
120,180,338 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01695:Bahcc1
|
APN |
11 |
120,167,435 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01744:Bahcc1
|
APN |
11 |
120,162,563 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01769:Bahcc1
|
APN |
11 |
120,171,030 (GRCm39) |
splice site |
probably benign |
|
IGL01982:Bahcc1
|
APN |
11 |
120,178,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02341:Bahcc1
|
APN |
11 |
120,163,346 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:Bahcc1
|
APN |
11 |
120,178,362 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02559:Bahcc1
|
APN |
11 |
120,175,998 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02579:Bahcc1
|
APN |
11 |
120,176,175 (GRCm39) |
splice site |
probably benign |
|
IGL02609:Bahcc1
|
APN |
11 |
120,180,224 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02678:Bahcc1
|
APN |
11 |
120,163,697 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02800:Bahcc1
|
APN |
11 |
120,163,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02963:Bahcc1
|
APN |
11 |
120,165,758 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03128:Bahcc1
|
APN |
11 |
120,159,260 (GRCm39) |
splice site |
probably benign |
|
IGL03242:Bahcc1
|
APN |
11 |
120,159,126 (GRCm39) |
splice site |
probably benign |
|
IGL03248:Bahcc1
|
APN |
11 |
120,159,235 (GRCm39) |
missense |
probably damaging |
1.00 |
Dimensionality
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
G1citation:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R0019:Bahcc1
|
UTSW |
11 |
120,180,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Bahcc1
|
UTSW |
11 |
120,159,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Bahcc1
|
UTSW |
11 |
120,175,900 (GRCm39) |
splice site |
probably benign |
|
R0321:Bahcc1
|
UTSW |
11 |
120,164,251 (GRCm39) |
critical splice donor site |
probably null |
|
R0671:Bahcc1
|
UTSW |
11 |
120,178,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R0737:Bahcc1
|
UTSW |
11 |
120,163,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Bahcc1
|
UTSW |
11 |
120,173,065 (GRCm39) |
splice site |
probably benign |
|
R1570:Bahcc1
|
UTSW |
11 |
120,163,009 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1914:Bahcc1
|
UTSW |
11 |
120,176,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Bahcc1
|
UTSW |
11 |
120,163,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Bahcc1
|
UTSW |
11 |
120,162,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Bahcc1
|
UTSW |
11 |
120,178,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R3552:Bahcc1
|
UTSW |
11 |
120,167,598 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3711:Bahcc1
|
UTSW |
11 |
120,165,923 (GRCm39) |
missense |
probably benign |
0.27 |
R3804:Bahcc1
|
UTSW |
11 |
120,174,184 (GRCm39) |
missense |
probably benign |
0.01 |
R4349:Bahcc1
|
UTSW |
11 |
120,150,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Bahcc1
|
UTSW |
11 |
120,165,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
R4908:Bahcc1
|
UTSW |
11 |
120,178,580 (GRCm39) |
missense |
probably benign |
0.36 |
R4941:Bahcc1
|
UTSW |
11 |
120,177,491 (GRCm39) |
missense |
probably benign |
|
R5217:Bahcc1
|
UTSW |
11 |
120,165,285 (GRCm39) |
nonsense |
probably null |
|
R5241:Bahcc1
|
UTSW |
11 |
120,162,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Bahcc1
|
UTSW |
11 |
120,178,814 (GRCm39) |
missense |
probably benign |
0.02 |
R5696:Bahcc1
|
UTSW |
11 |
120,164,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Bahcc1
|
UTSW |
11 |
120,176,192 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5725:Bahcc1
|
UTSW |
11 |
120,165,714 (GRCm39) |
missense |
probably benign |
|
R5788:Bahcc1
|
UTSW |
11 |
120,177,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Bahcc1
|
UTSW |
11 |
120,176,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R5900:Bahcc1
|
UTSW |
11 |
120,175,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Bahcc1
|
UTSW |
11 |
120,180,615 (GRCm39) |
missense |
probably benign |
0.00 |
R6058:Bahcc1
|
UTSW |
11 |
120,178,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6107:Bahcc1
|
UTSW |
11 |
120,163,714 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Bahcc1
|
UTSW |
11 |
120,167,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Bahcc1
|
UTSW |
11 |
120,176,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R6550:Bahcc1
|
UTSW |
11 |
120,167,477 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6822:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R6836:Bahcc1
|
UTSW |
11 |
120,162,583 (GRCm39) |
nonsense |
probably null |
|
R6846:Bahcc1
|
UTSW |
11 |
120,162,422 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6916:Bahcc1
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R6966:Bahcc1
|
UTSW |
11 |
120,173,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R7097:Bahcc1
|
UTSW |
11 |
120,163,472 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7289:Bahcc1
|
UTSW |
11 |
120,171,000 (GRCm39) |
missense |
probably benign |
0.08 |
R7441:Bahcc1
|
UTSW |
11 |
120,177,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R7520:Bahcc1
|
UTSW |
11 |
120,167,031 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7556:Bahcc1
|
UTSW |
11 |
120,178,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R7672:Bahcc1
|
UTSW |
11 |
120,174,172 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7791:Bahcc1
|
UTSW |
11 |
120,159,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Bahcc1
|
UTSW |
11 |
120,163,507 (GRCm39) |
nonsense |
probably null |
|
R7802:Bahcc1
|
UTSW |
11 |
120,165,518 (GRCm39) |
missense |
probably benign |
0.03 |
R7946:Bahcc1
|
UTSW |
11 |
120,163,325 (GRCm39) |
missense |
probably benign |
|
R7985:Bahcc1
|
UTSW |
11 |
120,163,717 (GRCm39) |
missense |
probably damaging |
0.97 |
R8128:Bahcc1
|
UTSW |
11 |
120,163,216 (GRCm39) |
nonsense |
probably null |
|
R8353:Bahcc1
|
UTSW |
11 |
120,165,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Bahcc1
|
UTSW |
11 |
120,165,415 (GRCm39) |
missense |
probably benign |
0.01 |
R8710:Bahcc1
|
UTSW |
11 |
120,174,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8799:Bahcc1
|
UTSW |
11 |
120,177,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Bahcc1
|
UTSW |
11 |
120,164,587 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8920:Bahcc1
|
UTSW |
11 |
120,175,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Bahcc1
|
UTSW |
11 |
120,167,591 (GRCm39) |
missense |
probably benign |
0.09 |
R9014:Bahcc1
|
UTSW |
11 |
120,173,048 (GRCm39) |
missense |
probably benign |
|
R9014:Bahcc1
|
UTSW |
11 |
120,163,715 (GRCm39) |
missense |
probably benign |
0.00 |
R9195:Bahcc1
|
UTSW |
11 |
120,167,337 (GRCm39) |
missense |
probably benign |
|
R9216:Bahcc1
|
UTSW |
11 |
120,177,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Bahcc1
|
UTSW |
11 |
120,165,885 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9392:Bahcc1
|
UTSW |
11 |
120,163,513 (GRCm39) |
nonsense |
probably null |
|
R9562:Bahcc1
|
UTSW |
11 |
120,150,035 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9680:Bahcc1
|
UTSW |
11 |
120,163,286 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9797:Bahcc1
|
UTSW |
11 |
120,159,147 (GRCm39) |
nonsense |
probably null |
|
X0026:Bahcc1
|
UTSW |
11 |
120,162,578 (GRCm39) |
missense |
probably benign |
0.20 |
Z1176:Bahcc1
|
UTSW |
11 |
120,175,220 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Bahcc1
|
UTSW |
11 |
120,167,435 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1177:Bahcc1
|
UTSW |
11 |
120,163,747 (GRCm39) |
missense |
possibly damaging |
0.73 |
|