Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
C |
T |
8: 120,872,132 (GRCm39) |
T20I |
probably benign |
Het |
Adamts2 |
C |
T |
11: 50,679,516 (GRCm39) |
T832I |
possibly damaging |
Het |
Agbl1 |
G |
A |
7: 76,239,298 (GRCm39) |
|
probably null |
Het |
Ankrd61 |
T |
C |
5: 143,833,894 (GRCm39) |
|
probably benign |
Het |
Anpep |
T |
G |
7: 79,488,039 (GRCm39) |
Y506S |
possibly damaging |
Het |
Aox1 |
T |
A |
1: 58,382,832 (GRCm39) |
H1037Q |
probably benign |
Het |
Auh |
G |
A |
13: 53,052,755 (GRCm39) |
R47* |
probably null |
Het |
B4galt5 |
T |
A |
2: 167,148,558 (GRCm39) |
M187L |
probably benign |
Het |
Bub1 |
A |
T |
2: 127,643,343 (GRCm39) |
D1000E |
probably benign |
Het |
Cacna1f |
T |
G |
X: 7,492,687 (GRCm39) |
|
probably null |
Het |
Cdh3 |
T |
C |
8: 107,279,039 (GRCm39) |
L667P |
probably damaging |
Het |
Cenpe |
A |
T |
3: 134,946,834 (GRCm39) |
R1116S |
possibly damaging |
Het |
Ces1b |
T |
A |
8: 93,799,969 (GRCm39) |
M136L |
possibly damaging |
Het |
Cfap54 |
T |
C |
10: 92,833,236 (GRCm39) |
E1130G |
possibly damaging |
Het |
Chd9 |
C |
T |
8: 91,760,615 (GRCm39) |
P2120L |
probably benign |
Het |
Clu |
T |
C |
14: 66,212,452 (GRCm39) |
V135A |
probably damaging |
Het |
Cmip |
T |
A |
8: 118,163,432 (GRCm39) |
S388T |
probably benign |
Het |
Cnga1 |
C |
T |
5: 72,776,404 (GRCm39) |
V20I |
possibly damaging |
Het |
Cox4i1 |
T |
A |
8: 121,400,029 (GRCm39) |
V51E |
possibly damaging |
Het |
Crym |
T |
C |
7: 119,801,050 (GRCm39) |
N33S |
probably benign |
Het |
Ctcf |
T |
A |
8: 106,398,016 (GRCm39) |
V434E |
probably damaging |
Het |
Daam1 |
G |
A |
12: 72,021,997 (GRCm39) |
D732N |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,262,485 (GRCm39) |
T957A |
probably benign |
Het |
Duox1 |
A |
G |
2: 122,163,619 (GRCm39) |
D817G |
probably benign |
Het |
Eif1ad16 |
T |
C |
12: 87,985,258 (GRCm39) |
Y95C |
probably damaging |
Het |
Fads3 |
A |
G |
19: 10,033,818 (GRCm39) |
Y401C |
probably damaging |
Het |
Fam72a |
T |
C |
1: 131,456,592 (GRCm39) |
|
probably null |
Het |
Fbxw21 |
C |
A |
9: 108,974,553 (GRCm39) |
K322N |
probably benign |
Het |
Fdxr |
G |
A |
11: 115,162,806 (GRCm39) |
T100I |
probably damaging |
Het |
Galnt11 |
C |
G |
5: 25,452,610 (GRCm39) |
P41A |
probably damaging |
Het |
Glb1l |
T |
C |
1: 75,178,473 (GRCm39) |
T322A |
probably damaging |
Het |
Gm6871 |
T |
A |
7: 41,197,414 (GRCm39) |
T149S |
probably benign |
Het |
Gpr26 |
C |
T |
7: 131,568,823 (GRCm39) |
T56I |
probably damaging |
Het |
Grik4 |
C |
A |
9: 42,533,438 (GRCm39) |
G361C |
probably damaging |
Het |
Gsr |
T |
G |
8: 34,170,316 (GRCm39) |
D200E |
probably benign |
Het |
Igsf5 |
T |
A |
16: 96,165,247 (GRCm39) |
D7E |
probably benign |
Het |
Inpp5e |
T |
A |
2: 26,289,355 (GRCm39) |
I522F |
probably damaging |
Het |
Insm2 |
C |
A |
12: 55,647,096 (GRCm39) |
T280K |
probably benign |
Het |
Itih4 |
T |
C |
14: 30,617,435 (GRCm39) |
V585A |
probably damaging |
Het |
Katnip |
T |
A |
7: 125,394,515 (GRCm39) |
V197D |
probably benign |
Het |
Knl1 |
A |
T |
2: 118,888,849 (GRCm39) |
R17* |
probably null |
Het |
Lag3 |
G |
T |
6: 124,888,272 (GRCm39) |
L15I |
possibly damaging |
Het |
Lepr |
T |
A |
4: 101,648,093 (GRCm39) |
S861T |
probably damaging |
Het |
Mcur1 |
A |
T |
13: 43,697,941 (GRCm39) |
Y320N |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,736,717 (GRCm39) |
D872V |
probably damaging |
Het |
Mlycd |
T |
C |
8: 120,134,446 (GRCm39) |
|
probably null |
Het |
Mpl |
C |
A |
4: 118,312,954 (GRCm39) |
C193F |
probably damaging |
Het |
Mycbp2 |
C |
A |
14: 103,368,681 (GRCm39) |
A4142S |
probably damaging |
Het |
Myh1 |
T |
A |
11: 67,104,424 (GRCm39) |
D993E |
possibly damaging |
Het |
N4bp2 |
T |
A |
5: 65,947,404 (GRCm39) |
D11E |
probably benign |
Het |
Neb |
T |
C |
2: 52,085,533 (GRCm39) |
I1521V |
probably benign |
Het |
Notch1 |
A |
G |
2: 26,355,485 (GRCm39) |
V1744A |
possibly damaging |
Het |
Numa1 |
T |
C |
7: 101,644,731 (GRCm39) |
S236P |
possibly damaging |
Het |
Or4p20 |
T |
C |
2: 88,253,800 (GRCm39) |
T190A |
possibly damaging |
Het |
Or6c66 |
T |
A |
10: 129,461,784 (GRCm39) |
I49L |
probably benign |
Het |
Or8k23 |
A |
G |
2: 86,186,708 (GRCm39) |
L6P |
possibly damaging |
Het |
Otogl |
A |
G |
10: 107,710,361 (GRCm39) |
L576P |
probably damaging |
Het |
P2ry1 |
C |
T |
3: 60,910,900 (GRCm39) |
T13M |
probably damaging |
Het |
Pak6 |
A |
T |
2: 118,525,050 (GRCm39) |
R559* |
probably null |
Het |
Parvb |
A |
T |
15: 84,182,171 (GRCm39) |
M234L |
probably benign |
Het |
Pcdha11 |
T |
C |
18: 37,145,907 (GRCm39) |
V666A |
possibly damaging |
Het |
Pde3b |
T |
A |
7: 114,126,092 (GRCm39) |
Y775* |
probably null |
Het |
Pgam5 |
A |
G |
5: 110,413,869 (GRCm39) |
L98P |
probably damaging |
Het |
Phip |
T |
C |
9: 82,797,392 (GRCm39) |
H537R |
possibly damaging |
Het |
Pkib |
T |
G |
10: 57,604,205 (GRCm39) |
D4E |
probably damaging |
Het |
Plcb1 |
A |
T |
2: 135,102,428 (GRCm39) |
I202F |
probably benign |
Het |
Pold3 |
A |
G |
7: 99,770,590 (GRCm39) |
V14A |
probably damaging |
Het |
Prdm1 |
T |
A |
10: 44,322,803 (GRCm39) |
T249S |
probably benign |
Het |
Prpf39 |
T |
A |
12: 65,104,589 (GRCm39) |
F551L |
probably benign |
Het |
Prune2 |
A |
G |
19: 17,099,986 (GRCm39) |
E1830G |
probably benign |
Het |
Ralgapa1 |
G |
A |
12: 55,764,986 (GRCm39) |
P889S |
probably damaging |
Het |
Rassf2 |
A |
T |
2: 131,840,163 (GRCm39) |
|
probably null |
Het |
Rnf185 |
A |
G |
11: 3,368,067 (GRCm39) |
Y204H |
probably benign |
Het |
Rpap1 |
A |
G |
2: 119,610,535 (GRCm39) |
|
probably null |
Het |
Rufy3 |
T |
C |
5: 88,797,757 (GRCm39) |
S645P |
probably damaging |
Het |
Scn11a |
T |
A |
9: 119,594,595 (GRCm39) |
Y1266F |
probably damaging |
Het |
Senp7 |
T |
A |
16: 55,971,725 (GRCm39) |
H287Q |
probably benign |
Het |
Sgsm3 |
T |
C |
15: 80,888,073 (GRCm39) |
|
probably null |
Het |
Slc25a11 |
A |
T |
11: 70,536,658 (GRCm39) |
V104E |
possibly damaging |
Het |
Slc25a13 |
G |
A |
6: 6,117,190 (GRCm39) |
T175I |
probably benign |
Het |
Slc26a3 |
T |
A |
12: 31,520,902 (GRCm39) |
F702Y |
probably damaging |
Het |
Smco2 |
T |
A |
6: 146,761,465 (GRCm39) |
L184H |
probably damaging |
Het |
Ssc4d |
A |
T |
5: 135,994,461 (GRCm39) |
C90S |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,441,298 (GRCm39) |
S1835P |
probably damaging |
Het |
Stk35 |
A |
G |
2: 129,643,435 (GRCm39) |
T140A |
probably damaging |
Het |
Syngr1 |
C |
T |
15: 79,995,941 (GRCm39) |
T160M |
probably damaging |
Het |
Tent2 |
A |
G |
13: 93,320,726 (GRCm39) |
L109S |
probably damaging |
Het |
Tgfb1i1 |
A |
G |
7: 127,848,085 (GRCm39) |
|
probably null |
Het |
Thoc1 |
T |
A |
18: 9,977,947 (GRCm39) |
V296E |
probably damaging |
Het |
Timp2 |
C |
T |
11: 118,201,412 (GRCm39) |
C75Y |
probably damaging |
Het |
Tlr1 |
T |
C |
5: 65,082,639 (GRCm39) |
Y646C |
probably damaging |
Het |
Tprn |
G |
A |
2: 25,158,940 (GRCm39) |
E655K |
possibly damaging |
Het |
Trbv14 |
A |
C |
6: 41,112,424 (GRCm39) |
I74L |
probably benign |
Het |
Trbv5 |
T |
A |
6: 41,039,555 (GRCm39) |
Y53* |
probably null |
Het |
Trpm5 |
T |
C |
7: 142,642,656 (GRCm39) |
Q97R |
possibly damaging |
Het |
Tut1 |
A |
G |
19: 8,932,931 (GRCm39) |
D88G |
probably damaging |
Het |
Ucp2 |
A |
T |
7: 100,147,620 (GRCm39) |
I200F |
probably benign |
Het |
Unc45a |
G |
A |
7: 79,988,623 (GRCm39) |
S131L |
probably benign |
Het |
Uty |
A |
T |
Y: 1,158,182 (GRCm39) |
H573Q |
probably damaging |
Het |
Vmn1r17 |
T |
A |
6: 57,337,855 (GRCm39) |
Y121F |
possibly damaging |
Het |
Vmn1r53 |
T |
C |
6: 90,200,554 (GRCm39) |
I257V |
probably benign |
Het |
Vmn2r90 |
C |
T |
17: 17,954,229 (GRCm39) |
L798F |
probably damaging |
Het |
Vmn2r94 |
A |
T |
17: 18,477,736 (GRCm39) |
M225K |
probably benign |
Het |
Wdr24 |
A |
T |
17: 26,043,273 (GRCm39) |
I32F |
possibly damaging |
Het |
Zc3h11a |
T |
A |
1: 133,552,521 (GRCm39) |
T529S |
probably benign |
Het |
Zc3h4 |
A |
G |
7: 16,168,264 (GRCm39) |
H791R |
unknown |
Het |
Zfp24 |
A |
G |
18: 24,150,927 (GRCm39) |
L73P |
probably damaging |
Het |
Zfp616 |
T |
C |
11: 73,974,121 (GRCm39) |
I130T |
probably benign |
Het |
Zim1 |
ACAGCAG |
ACAGCAGCAG |
7: 6,680,429 (GRCm39) |
|
probably benign |
Het |
Zim1 |
CAG |
CAGAAG |
7: 6,680,430 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Dcaf13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00787:Dcaf13
|
APN |
15 |
39,007,027 (GRCm39) |
nonsense |
probably null |
|
IGL01081:Dcaf13
|
APN |
15 |
38,982,201 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01766:Dcaf13
|
APN |
15 |
38,982,145 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02174:Dcaf13
|
APN |
15 |
39,001,544 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02262:Dcaf13
|
APN |
15 |
38,982,102 (GRCm39) |
splice site |
probably benign |
|
IGL02740:Dcaf13
|
APN |
15 |
39,008,495 (GRCm39) |
nonsense |
probably null |
|
IGL03092:Dcaf13
|
APN |
15 |
38,991,371 (GRCm39) |
splice site |
probably benign |
|
IGL03374:Dcaf13
|
APN |
15 |
39,008,543 (GRCm39) |
nonsense |
probably null |
|
R0590:Dcaf13
|
UTSW |
15 |
39,008,480 (GRCm39) |
splice site |
probably benign |
|
R0594:Dcaf13
|
UTSW |
15 |
38,986,663 (GRCm39) |
missense |
probably benign |
0.00 |
R0711:Dcaf13
|
UTSW |
15 |
39,001,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R1036:Dcaf13
|
UTSW |
15 |
39,007,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R1770:Dcaf13
|
UTSW |
15 |
38,993,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Dcaf13
|
UTSW |
15 |
38,982,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R1933:Dcaf13
|
UTSW |
15 |
39,001,483 (GRCm39) |
missense |
probably damaging |
0.99 |
R4113:Dcaf13
|
UTSW |
15 |
38,993,615 (GRCm39) |
missense |
probably damaging |
0.98 |
R4595:Dcaf13
|
UTSW |
15 |
38,982,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Dcaf13
|
UTSW |
15 |
39,001,637 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5431:Dcaf13
|
UTSW |
15 |
38,986,619 (GRCm39) |
missense |
probably benign |
0.16 |
R5454:Dcaf13
|
UTSW |
15 |
38,987,759 (GRCm39) |
missense |
probably benign |
|
R5834:Dcaf13
|
UTSW |
15 |
39,007,037 (GRCm39) |
nonsense |
probably null |
|
R5929:Dcaf13
|
UTSW |
15 |
39,007,048 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5944:Dcaf13
|
UTSW |
15 |
39,010,072 (GRCm39) |
missense |
probably benign |
|
R6319:Dcaf13
|
UTSW |
15 |
39,007,067 (GRCm39) |
missense |
probably benign |
0.00 |
R6394:Dcaf13
|
UTSW |
15 |
39,007,132 (GRCm39) |
missense |
probably benign |
0.04 |
R6664:Dcaf13
|
UTSW |
15 |
38,982,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6884:Dcaf13
|
UTSW |
15 |
38,986,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R7419:Dcaf13
|
UTSW |
15 |
38,993,615 (GRCm39) |
missense |
probably damaging |
0.98 |
R8750:Dcaf13
|
UTSW |
15 |
38,982,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R8944:Dcaf13
|
UTSW |
15 |
39,001,612 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9294:Dcaf13
|
UTSW |
15 |
38,993,687 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9300:Dcaf13
|
UTSW |
15 |
39,010,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Dcaf13
|
UTSW |
15 |
38,982,178 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9696:Dcaf13
|
UTSW |
15 |
39,001,496 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9778:Dcaf13
|
UTSW |
15 |
39,008,586 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Dcaf13
|
UTSW |
15 |
39,008,642 (GRCm39) |
missense |
probably damaging |
1.00 |
|