Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
T |
11: 109,980,810 (GRCm39) |
|
probably null |
Het |
AI987944 |
T |
C |
7: 41,023,815 (GRCm39) |
Y391C |
probably benign |
Het |
Ankfn1 |
A |
T |
11: 89,346,946 (GRCm39) |
S296T |
probably benign |
Het |
Apob |
A |
G |
12: 8,057,488 (GRCm39) |
D1957G |
probably benign |
Het |
Baz1a |
G |
T |
12: 54,976,431 (GRCm39) |
P415Q |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,464,134 (GRCm39) |
H1299Q |
probably benign |
Het |
C7 |
G |
T |
15: 5,063,720 (GRCm39) |
S227* |
probably null |
Het |
Catsperb |
A |
T |
12: 101,474,221 (GRCm39) |
R306S |
probably damaging |
Het |
Cbx3 |
T |
A |
6: 51,448,793 (GRCm39) |
|
probably null |
Het |
Ccnt2 |
A |
G |
1: 127,731,136 (GRCm39) |
Y671C |
probably damaging |
Het |
Crocc |
A |
G |
4: 140,774,253 (GRCm39) |
|
probably null |
Het |
Ctr9 |
G |
A |
7: 110,646,014 (GRCm39) |
V669I |
probably benign |
Het |
Dck |
T |
G |
5: 88,920,576 (GRCm39) |
Y99D |
probably damaging |
Het |
Ddx52 |
T |
A |
11: 83,835,432 (GRCm39) |
D119E |
probably benign |
Het |
Dnah10 |
A |
T |
5: 124,823,768 (GRCm39) |
K596N |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,621,741 (GRCm39) |
V1128E |
probably benign |
Het |
Dph1 |
A |
T |
11: 75,076,679 (GRCm39) |
|
probably null |
Het |
Enah |
G |
A |
1: 181,749,537 (GRCm39) |
P415L |
probably damaging |
Het |
Erc1 |
A |
C |
6: 119,699,216 (GRCm39) |
V802G |
possibly damaging |
Het |
F8 |
ATCTCTCTC |
ATCTCTC |
X: 74,366,604 (GRCm39) |
|
probably null |
Het |
Fam169a |
C |
A |
13: 97,243,600 (GRCm39) |
A210E |
probably benign |
Het |
Fcmr |
A |
G |
1: 130,806,070 (GRCm39) |
D342G |
possibly damaging |
Het |
Fgfr4 |
T |
G |
13: 55,315,702 (GRCm39) |
V743G |
possibly damaging |
Het |
Fsip2 |
A |
G |
2: 82,808,856 (GRCm39) |
D1725G |
probably damaging |
Het |
Heatr5b |
A |
T |
17: 79,136,934 (GRCm39) |
C195* |
probably null |
Het |
Herc2 |
G |
A |
7: 55,855,709 (GRCm39) |
A3882T |
probably damaging |
Het |
Il20 |
T |
A |
1: 130,836,115 (GRCm39) |
N143Y |
probably damaging |
Het |
Inpp5b |
A |
G |
4: 124,692,092 (GRCm39) |
S892G |
probably damaging |
Het |
Ipo13 |
A |
T |
4: 117,761,858 (GRCm39) |
Y447* |
probably null |
Het |
Itprid1 |
A |
G |
6: 55,874,860 (GRCm39) |
N270S |
probably benign |
Het |
Kbtbd12 |
A |
T |
6: 88,594,779 (GRCm39) |
N350K |
probably benign |
Het |
Kiz |
T |
C |
2: 146,811,880 (GRCm39) |
F663S |
probably damaging |
Het |
Matn2 |
A |
G |
15: 34,433,263 (GRCm39) |
D870G |
probably benign |
Het |
Methig1 |
C |
T |
15: 100,251,467 (GRCm39) |
A126V |
probably benign |
Het |
Mme |
A |
G |
3: 63,235,681 (GRCm39) |
D209G |
probably null |
Het |
Mroh4 |
A |
G |
15: 74,481,610 (GRCm39) |
F811L |
possibly damaging |
Het |
Myo9b |
G |
T |
8: 71,743,510 (GRCm39) |
K190N |
probably damaging |
Het |
Ncf1 |
T |
C |
5: 134,258,406 (GRCm39) |
I6V |
probably damaging |
Het |
Nmt2 |
T |
C |
2: 3,310,618 (GRCm39) |
F121L |
probably damaging |
Het |
Nol10 |
A |
G |
12: 17,411,152 (GRCm39) |
D183G |
probably benign |
Het |
Nsun7 |
T |
C |
5: 66,418,429 (GRCm39) |
V53A |
probably benign |
Het |
Or10u4 |
T |
C |
10: 129,802,009 (GRCm39) |
I187V |
probably benign |
Het |
Or8j3 |
T |
C |
2: 86,028,176 (GRCm39) |
S307G |
probably benign |
Het |
Or8k22 |
T |
C |
2: 86,162,774 (GRCm39) |
N309D |
probably benign |
Het |
Pappa2 |
A |
T |
1: 158,784,214 (GRCm39) |
Y265* |
probably null |
Het |
Pigg |
G |
A |
5: 108,486,518 (GRCm39) |
A724T |
probably damaging |
Het |
Pik3r4 |
C |
T |
9: 105,527,534 (GRCm39) |
R296C |
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,431,617 (GRCm39) |
|
probably null |
Het |
Pld4 |
A |
G |
12: 112,734,992 (GRCm39) |
D483G |
probably damaging |
Het |
Ppip5k1 |
C |
T |
2: 121,173,674 (GRCm39) |
R399H |
probably damaging |
Het |
Qrfpr |
A |
T |
3: 36,236,806 (GRCm39) |
H198Q |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,050,748 (GRCm39) |
D883E |
probably damaging |
Het |
Retnlg |
T |
C |
16: 48,694,615 (GRCm39) |
C88R |
probably damaging |
Het |
Sin3a |
C |
T |
9: 57,004,109 (GRCm39) |
T287I |
probably benign |
Het |
Slc44a1 |
GCC |
GCCCCC |
4: 53,563,243 (GRCm39) |
|
probably benign |
Het |
Sppl2c |
G |
C |
11: 104,077,307 (GRCm39) |
V36L |
probably benign |
Het |
Srp72 |
T |
A |
5: 77,124,338 (GRCm39) |
I68N |
probably damaging |
Het |
Srrm3 |
T |
A |
5: 135,883,231 (GRCm39) |
S195R |
probably damaging |
Het |
Srrm4 |
T |
A |
5: 116,605,887 (GRCm39) |
|
probably benign |
Het |
Ssb |
A |
G |
2: 69,699,163 (GRCm39) |
S199G |
probably benign |
Het |
Sult2a6 |
T |
A |
7: 13,988,634 (GRCm39) |
Y42F |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,072,343 (GRCm39) |
T120A |
probably benign |
Het |
Tas1r1 |
A |
G |
4: 152,112,627 (GRCm39) |
F809L |
probably damaging |
Het |
Tead3 |
A |
G |
17: 28,555,544 (GRCm39) |
S117P |
probably damaging |
Het |
Tefm |
C |
T |
11: 80,031,056 (GRCm39) |
R60H |
probably damaging |
Het |
Tmem104 |
G |
A |
11: 115,092,221 (GRCm39) |
R110H |
possibly damaging |
Het |
Tnxb |
G |
A |
17: 34,918,179 (GRCm39) |
G2364D |
probably damaging |
Het |
Vmn1r211 |
T |
A |
13: 23,036,134 (GRCm39) |
I178F |
probably damaging |
Het |
Vmn1r6 |
A |
T |
6: 56,980,109 (GRCm39) |
Y235F |
probably damaging |
Het |
Xrcc5 |
C |
A |
1: 72,385,529 (GRCm39) |
T540K |
probably benign |
Het |
|
Other mutations in Enthd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01726:Enthd1
|
APN |
15 |
80,336,652 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02127:Enthd1
|
APN |
15 |
80,336,943 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4151001:Enthd1
|
UTSW |
15 |
80,336,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R0190:Enthd1
|
UTSW |
15 |
80,418,695 (GRCm39) |
splice site |
probably null |
|
R1237:Enthd1
|
UTSW |
15 |
80,418,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Enthd1
|
UTSW |
15 |
80,336,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R1697:Enthd1
|
UTSW |
15 |
80,337,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Enthd1
|
UTSW |
15 |
80,358,482 (GRCm39) |
missense |
probably damaging |
0.99 |
R3420:Enthd1
|
UTSW |
15 |
80,444,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R3814:Enthd1
|
UTSW |
15 |
80,336,883 (GRCm39) |
missense |
probably benign |
0.11 |
R4049:Enthd1
|
UTSW |
15 |
80,444,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R4403:Enthd1
|
UTSW |
15 |
80,337,025 (GRCm39) |
missense |
probably benign |
0.00 |
R4720:Enthd1
|
UTSW |
15 |
80,444,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Enthd1
|
UTSW |
15 |
80,336,916 (GRCm39) |
missense |
probably damaging |
0.96 |
R6143:Enthd1
|
UTSW |
15 |
80,393,487 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6984:Enthd1
|
UTSW |
15 |
80,444,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R7062:Enthd1
|
UTSW |
15 |
80,336,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7105:Enthd1
|
UTSW |
15 |
80,393,410 (GRCm39) |
missense |
probably benign |
0.17 |
R7177:Enthd1
|
UTSW |
15 |
80,358,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Enthd1
|
UTSW |
15 |
80,444,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R8359:Enthd1
|
UTSW |
15 |
80,358,356 (GRCm39) |
missense |
probably benign |
0.01 |
R8511:Enthd1
|
UTSW |
15 |
80,358,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Enthd1
|
UTSW |
15 |
80,444,235 (GRCm39) |
missense |
probably damaging |
0.99 |
R9620:Enthd1
|
UTSW |
15 |
80,336,901 (GRCm39) |
missense |
probably benign |
0.04 |
|