Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
G |
T |
4: 144,396,760 (GRCm39) |
S324* |
probably null |
Het |
Actl11 |
T |
G |
9: 107,806,772 (GRCm39) |
V365G |
probably benign |
Het |
Adgrg6 |
T |
A |
10: 14,317,227 (GRCm39) |
D531V |
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,616,728 (GRCm39) |
S2354P |
probably benign |
Het |
Ano9 |
A |
T |
7: 140,684,221 (GRCm39) |
W514R |
probably damaging |
Het |
Arfgef3 |
A |
T |
10: 18,528,589 (GRCm39) |
V266E |
probably damaging |
Het |
Bpifb4 |
G |
A |
2: 153,801,587 (GRCm39) |
M355I |
probably benign |
Het |
Catsperb |
T |
C |
12: 101,554,402 (GRCm39) |
S699P |
possibly damaging |
Het |
Cdh23 |
T |
G |
10: 60,140,872 (GRCm39) |
I3161L |
possibly damaging |
Het |
Chd3 |
T |
C |
11: 69,244,604 (GRCm39) |
T1257A |
probably damaging |
Het |
Cnnm4 |
C |
T |
1: 36,539,036 (GRCm39) |
T638I |
probably benign |
Het |
Cspg4b |
A |
G |
13: 113,504,646 (GRCm39) |
D1925G |
probably damaging |
Het |
Cyp26c1 |
A |
G |
19: 37,674,936 (GRCm39) |
T86A |
probably damaging |
Het |
Cyp3a63-ps |
A |
G |
5: 145,564,847 (GRCm39) |
|
noncoding transcript |
Het |
Dnah14 |
T |
A |
1: 181,428,771 (GRCm39) |
I259N |
possibly damaging |
Het |
Dnah17 |
T |
C |
11: 118,019,981 (GRCm39) |
D22G |
probably benign |
Het |
Epn2 |
T |
G |
11: 61,437,312 (GRCm39) |
T87P |
probably damaging |
Het |
Fbxl18 |
A |
G |
5: 142,874,578 (GRCm39) |
L81P |
probably damaging |
Het |
Gas1 |
A |
T |
13: 60,323,970 (GRCm39) |
D221E |
probably damaging |
Het |
Gm8356 |
T |
C |
14: 17,691,275 (GRCm39) |
Y130C |
probably damaging |
Het |
Gpr151 |
T |
G |
18: 42,712,459 (GRCm39) |
K73T |
probably damaging |
Het |
Helq |
A |
C |
5: 100,946,305 (GRCm39) |
V12G |
probably damaging |
Het |
Inpp4b |
A |
G |
8: 82,494,806 (GRCm39) |
T74A |
probably benign |
Het |
Kirrel3 |
G |
A |
9: 34,919,045 (GRCm39) |
V234I |
probably damaging |
Het |
Kxd1 |
T |
A |
8: 70,972,713 (GRCm39) |
|
probably null |
Het |
Lif |
T |
C |
11: 4,218,924 (GRCm39) |
Y68H |
probably damaging |
Het |
Map6 |
A |
G |
7: 98,985,314 (GRCm39) |
Q406R |
probably damaging |
Het |
Mcoln3 |
A |
T |
3: 145,830,527 (GRCm39) |
M86L |
probably benign |
Het |
Mei1 |
T |
A |
15: 81,987,439 (GRCm39) |
Y834* |
probably null |
Het |
Mroh1 |
T |
C |
15: 76,320,319 (GRCm39) |
|
probably null |
Het |
Myo15b |
T |
C |
11: 115,777,065 (GRCm39) |
I2319T |
possibly damaging |
Het |
Myo7b |
T |
G |
18: 32,127,439 (GRCm39) |
D621A |
probably damaging |
Het |
Naip5 |
C |
T |
13: 100,359,674 (GRCm39) |
A521T |
possibly damaging |
Het |
Nek7 |
T |
C |
1: 138,426,351 (GRCm39) |
D254G |
probably damaging |
Het |
Nsd2 |
A |
G |
5: 34,024,921 (GRCm39) |
R560G |
possibly damaging |
Het |
Or2t46 |
T |
C |
11: 58,472,464 (GRCm39) |
F265L |
probably benign |
Het |
Or52x1 |
A |
T |
7: 104,852,926 (GRCm39) |
L208H |
probably damaging |
Het |
Pbx1 |
T |
A |
1: 168,018,910 (GRCm39) |
T312S |
probably benign |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
A |
G |
13: 6,610,097 (GRCm39) |
S390G |
probably damaging |
Het |
Plcxd3 |
C |
T |
15: 4,546,239 (GRCm39) |
T81M |
probably damaging |
Het |
Pmf1 |
C |
T |
3: 88,307,017 (GRCm39) |
|
probably null |
Het |
Rabep1 |
T |
C |
11: 70,825,947 (GRCm39) |
V739A |
probably damaging |
Het |
Rex2 |
A |
G |
4: 147,142,451 (GRCm39) |
D313G |
possibly damaging |
Het |
Rpia |
C |
T |
6: 70,750,485 (GRCm39) |
V216I |
probably damaging |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Sec13 |
T |
A |
6: 113,712,167 (GRCm39) |
H56L |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,315,817 (GRCm39) |
V1733D |
probably damaging |
Het |
Sim2 |
G |
A |
16: 93,898,089 (GRCm39) |
A108T |
probably damaging |
Het |
Slc27a5 |
T |
C |
7: 12,722,479 (GRCm39) |
D665G |
probably damaging |
Het |
Slc38a6 |
T |
A |
12: 73,383,849 (GRCm39) |
V180E |
probably damaging |
Het |
Smarcad1 |
T |
G |
6: 65,052,122 (GRCm39) |
N38K |
possibly damaging |
Het |
Spem2 |
T |
C |
11: 69,709,091 (GRCm39) |
T45A |
possibly damaging |
Het |
Svil |
T |
C |
18: 5,057,432 (GRCm39) |
S714P |
probably benign |
Het |
Taar7b |
T |
A |
10: 23,876,158 (GRCm39) |
S108T |
possibly damaging |
Het |
Tbl3 |
T |
C |
17: 24,923,645 (GRCm39) |
K256E |
probably benign |
Het |
Tcam1 |
T |
G |
11: 106,177,276 (GRCm39) |
C423G |
probably damaging |
Het |
Trpm4 |
A |
T |
7: 44,977,143 (GRCm39) |
|
probably null |
Het |
Ttyh2 |
T |
C |
11: 114,592,662 (GRCm39) |
C231R |
probably damaging |
Het |
Ugt3a1 |
C |
T |
15: 9,365,397 (GRCm39) |
P337S |
probably damaging |
Het |
Vmn2r83 |
A |
C |
10: 79,304,837 (GRCm39) |
T16P |
possibly damaging |
Het |
Vps52 |
T |
C |
17: 34,182,189 (GRCm39) |
F589S |
probably damaging |
Het |
Xkr4 |
T |
C |
1: 3,286,961 (GRCm39) |
T410A |
probably damaging |
Het |
Xkr9 |
A |
G |
1: 13,742,726 (GRCm39) |
T4A |
probably damaging |
Het |
Yars2 |
T |
C |
16: 16,122,438 (GRCm39) |
L268P |
probably damaging |
Het |
Zbtb41 |
C |
A |
1: 139,357,027 (GRCm39) |
N427K |
possibly damaging |
Het |
Zeb2 |
T |
C |
2: 44,887,771 (GRCm39) |
T414A |
probably benign |
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 |
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 |
|
R8131:Bahcc1
|
UTSW |
11 |
120,163,664 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|