Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox4 |
C |
T |
1: 58,279,937 (GRCm39) |
R518C |
probably damaging |
Het |
Apbb2 |
A |
T |
5: 66,469,592 (GRCm39) |
|
probably null |
Het |
Arhgap45 |
C |
T |
10: 79,857,262 (GRCm39) |
P254S |
probably benign |
Het |
Arl4c |
T |
C |
1: 88,629,322 (GRCm39) |
D22G |
probably damaging |
Het |
Asxl1 |
A |
G |
2: 153,242,875 (GRCm39) |
T1142A |
probably benign |
Het |
BC035044 |
T |
C |
6: 128,861,949 (GRCm39) |
|
probably benign |
Het |
Bmp4 |
T |
C |
14: 46,621,458 (GRCm39) |
N362S |
probably damaging |
Het |
Cbll1 |
G |
T |
12: 31,537,912 (GRCm39) |
T280N |
probably damaging |
Het |
Cdh10 |
A |
T |
15: 18,986,971 (GRCm39) |
T401S |
probably benign |
Het |
Cmklr2 |
A |
G |
1: 63,222,326 (GRCm39) |
V303A |
probably damaging |
Het |
Cps1 |
A |
T |
1: 67,245,952 (GRCm39) |
M1148L |
probably benign |
Het |
Crybg1 |
T |
C |
10: 43,873,832 (GRCm39) |
D1092G |
probably damaging |
Het |
Cyth2 |
A |
G |
7: 45,460,126 (GRCm39) |
S173P |
probably damaging |
Het |
D6Ertd527e |
A |
T |
6: 87,088,793 (GRCm39) |
I319F |
unknown |
Het |
Dchs1 |
A |
T |
7: 105,421,384 (GRCm39) |
H345Q |
probably benign |
Het |
Ddx50 |
A |
T |
10: 62,476,640 (GRCm39) |
V211E |
probably damaging |
Het |
Dlx6 |
AGG |
AG |
6: 6,865,180 (GRCm39) |
|
probably null |
Het |
Dnajb5 |
G |
A |
4: 42,956,639 (GRCm39) |
D109N |
possibly damaging |
Het |
Dner |
A |
T |
1: 84,383,691 (GRCm39) |
N564K |
probably damaging |
Het |
Fam234b |
T |
C |
6: 135,186,282 (GRCm39) |
S97P |
probably benign |
Het |
Fam53b |
G |
A |
7: 132,317,684 (GRCm39) |
R60* |
probably null |
Het |
Fmo3 |
T |
G |
1: 162,791,546 (GRCm39) |
K244Q |
probably benign |
Het |
Golim4 |
A |
G |
3: 75,810,579 (GRCm39) |
I192T |
possibly damaging |
Het |
Gprin1 |
T |
C |
13: 54,887,576 (GRCm39) |
M233V |
probably benign |
Het |
Gtf2f1 |
A |
T |
17: 57,310,626 (GRCm39) |
V443D |
probably damaging |
Het |
Hmgcs2 |
T |
C |
3: 98,187,786 (GRCm39) |
|
probably benign |
Het |
Ide |
T |
A |
19: 37,292,383 (GRCm39) |
I271L |
unknown |
Het |
Kat8 |
G |
A |
7: 127,523,988 (GRCm39) |
E343K |
probably damaging |
Het |
Kif14 |
A |
G |
1: 136,444,141 (GRCm39) |
I1378V |
probably benign |
Het |
Lhx3 |
TCCTACGGGCCGGCCC |
TCC |
2: 26,091,435 (GRCm39) |
|
probably null |
Het |
Lhx6 |
T |
C |
2: 35,984,222 (GRCm39) |
|
probably null |
Het |
Lrp2 |
C |
T |
2: 69,319,502 (GRCm39) |
G2007D |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,709,304 (GRCm39) |
K142R |
probably damaging |
Het |
Macroh2a1 |
C |
G |
13: 56,243,936 (GRCm39) |
|
probably null |
Het |
Mrpl2 |
G |
A |
17: 46,960,964 (GRCm39) |
R286Q |
probably benign |
Het |
Mtrfr |
A |
G |
5: 124,476,954 (GRCm39) |
N83D |
probably damaging |
Het |
Nacad |
T |
A |
11: 6,548,528 (GRCm39) |
D1402V |
probably damaging |
Het |
Ndfip2 |
T |
C |
14: 105,535,539 (GRCm39) |
I275T |
possibly damaging |
Het |
Neb |
A |
C |
2: 52,116,582 (GRCm39) |
V4131G |
possibly damaging |
Het |
Nfe2l1 |
G |
A |
11: 96,712,934 (GRCm39) |
A83V |
probably damaging |
Het |
Nos3 |
A |
G |
5: 24,576,625 (GRCm39) |
D418G |
probably damaging |
Het |
Or12e7 |
A |
T |
2: 87,288,138 (GRCm39) |
M210L |
probably benign |
Het |
Or1n1b |
T |
A |
2: 36,780,056 (GRCm39) |
K268M |
possibly damaging |
Het |
Plcd4 |
A |
G |
1: 74,604,313 (GRCm39) |
T764A |
probably damaging |
Het |
Plppr3 |
G |
T |
10: 79,701,220 (GRCm39) |
P541T |
possibly damaging |
Het |
Polr2a |
A |
G |
11: 69,637,771 (GRCm39) |
I191T |
possibly damaging |
Het |
Rab11fip1 |
T |
C |
8: 27,646,402 (GRCm39) |
K225E |
probably damaging |
Het |
Rara |
A |
T |
11: 98,857,185 (GRCm39) |
Q64L |
possibly damaging |
Het |
Rtkn |
G |
A |
6: 83,126,754 (GRCm39) |
V305M |
probably damaging |
Het |
Sh2b1 |
A |
C |
7: 126,070,408 (GRCm39) |
F399V |
probably benign |
Het |
Slc7a4 |
T |
C |
16: 17,393,482 (GRCm39) |
T106A |
probably damaging |
Het |
Srcap |
G |
A |
7: 127,129,795 (GRCm39) |
G539D |
probably damaging |
Het |
Stab1 |
C |
T |
14: 30,869,974 (GRCm39) |
|
probably null |
Het |
Zfp267 |
G |
A |
3: 36,216,814 (GRCm39) |
C55Y |
possibly damaging |
Het |
|
Other mutations in Pramel18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02430:Pramel18
|
APN |
4 |
101,767,477 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02683:Pramel18
|
APN |
4 |
101,767,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03403:Pramel18
|
APN |
4 |
101,767,125 (GRCm39) |
missense |
probably benign |
0.40 |
R0833:Pramel18
|
UTSW |
4 |
101,767,294 (GRCm39) |
missense |
probably damaging |
0.97 |
R1054:Pramel18
|
UTSW |
4 |
101,766,361 (GRCm39) |
missense |
probably benign |
0.00 |
R1953:Pramel18
|
UTSW |
4 |
101,767,312 (GRCm39) |
missense |
probably benign |
|
R2216:Pramel18
|
UTSW |
4 |
101,767,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3747:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3750:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4931:Pramel18
|
UTSW |
4 |
101,766,367 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5586:Pramel18
|
UTSW |
4 |
101,767,317 (GRCm39) |
missense |
probably benign |
0.00 |
R5822:Pramel18
|
UTSW |
4 |
101,767,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Pramel18
|
UTSW |
4 |
101,767,189 (GRCm39) |
missense |
probably benign |
|
R6904:Pramel18
|
UTSW |
4 |
101,767,291 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7544:Pramel18
|
UTSW |
4 |
101,768,599 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7768:Pramel18
|
UTSW |
4 |
101,769,010 (GRCm39) |
missense |
probably benign |
|
R8342:Pramel18
|
UTSW |
4 |
101,767,581 (GRCm39) |
missense |
probably benign |
0.01 |
R8917:Pramel18
|
UTSW |
4 |
101,768,935 (GRCm39) |
missense |
probably benign |
0.09 |
Z1088:Pramel18
|
UTSW |
4 |
101,766,315 (GRCm39) |
splice site |
probably null |
|
Z1088:Pramel18
|
UTSW |
4 |
101,767,383 (GRCm39) |
missense |
probably benign |
0.00 |
|