Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
A |
G |
2: 19,545,219 (GRCm39) |
I78T |
probably benign |
Het |
4921524J17Rik |
G |
A |
8: 86,159,438 (GRCm39) |
|
probably benign |
Het |
4932438H23Rik |
T |
C |
16: 90,852,744 (GRCm39) |
T131A |
probably benign |
Het |
Acbd6 |
G |
T |
1: 155,463,213 (GRCm39) |
E138* |
probably null |
Het |
Ago3 |
A |
G |
4: 126,239,310 (GRCm39) |
V847A |
probably damaging |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Als2cl |
C |
A |
9: 110,727,174 (GRCm39) |
H913Q |
probably benign |
Het |
Atf6 |
A |
C |
1: 170,643,060 (GRCm39) |
S360R |
possibly damaging |
Het |
Atm |
G |
C |
9: 53,359,425 (GRCm39) |
N2789K |
possibly damaging |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Bpifa6 |
A |
T |
2: 153,831,249 (GRCm39) |
I272F |
possibly damaging |
Het |
Cabin1 |
G |
T |
10: 75,494,481 (GRCm39) |
P1633T |
probably damaging |
Het |
Camsap2 |
A |
G |
1: 136,209,131 (GRCm39) |
V119A |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,153,974 (GRCm39) |
E1082G |
probably benign |
Het |
Cchcr1 |
C |
A |
17: 35,839,248 (GRCm39) |
A479D |
probably damaging |
Het |
Chpt1 |
C |
T |
10: 88,312,230 (GRCm39) |
V349I |
probably benign |
Het |
Cldn13 |
A |
T |
5: 134,943,975 (GRCm39) |
I70K |
probably damaging |
Het |
Col6a6 |
T |
A |
9: 105,659,622 (GRCm39) |
D441V |
probably damaging |
Het |
Cpne5 |
G |
T |
17: 29,423,714 (GRCm39) |
T138K |
probably benign |
Het |
Creb3l3 |
A |
T |
10: 80,925,301 (GRCm39) |
|
probably null |
Het |
Cst5 |
C |
T |
2: 149,247,496 (GRCm39) |
L71F |
probably benign |
Het |
Ctsb |
T |
C |
14: 63,375,550 (GRCm39) |
V172A |
probably benign |
Het |
Cyp19a1 |
A |
G |
9: 54,074,277 (GRCm39) |
Y426H |
possibly damaging |
Het |
Cyth4 |
T |
C |
15: 78,490,094 (GRCm39) |
F72S |
probably damaging |
Het |
D430041D05Rik |
G |
T |
2: 104,240,484 (GRCm39) |
Q9K |
unknown |
Het |
Dnah1 |
T |
A |
14: 30,983,547 (GRCm39) |
I4099F |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 31,022,748 (GRCm39) |
I1130F |
possibly damaging |
Het |
Dnah12 |
A |
G |
14: 26,578,592 (GRCm39) |
K3117R |
probably benign |
Het |
Dpf3 |
A |
T |
12: 83,319,159 (GRCm39) |
S275R |
probably benign |
Het |
Dst |
A |
G |
1: 34,257,578 (GRCm39) |
N2450S |
probably benign |
Het |
Dync1h1 |
C |
T |
12: 110,632,109 (GRCm39) |
R4460W |
probably damaging |
Het |
Ecm1 |
A |
C |
3: 95,642,632 (GRCm39) |
C414G |
possibly damaging |
Het |
Eef2 |
G |
A |
10: 81,015,384 (GRCm39) |
D302N |
probably benign |
Het |
Egf |
T |
C |
3: 129,479,912 (GRCm39) |
D1038G |
possibly damaging |
Het |
Epm2aip1 |
T |
C |
9: 111,101,467 (GRCm39) |
S147P |
probably damaging |
Het |
Esam |
C |
A |
9: 37,448,863 (GRCm39) |
P324T |
possibly damaging |
Het |
Fbxo36 |
A |
G |
1: 84,874,301 (GRCm39) |
D99G |
probably damaging |
Het |
Fhad1 |
G |
A |
4: 141,691,937 (GRCm39) |
R400C |
probably benign |
Het |
Fhip2a |
A |
G |
19: 57,357,017 (GRCm39) |
Y36C |
probably damaging |
Het |
Fndc3b |
T |
C |
3: 27,515,893 (GRCm39) |
T638A |
probably benign |
Het |
Gba2 |
T |
C |
4: 43,568,967 (GRCm39) |
T563A |
probably benign |
Het |
Gm8180 |
T |
A |
14: 44,021,094 (GRCm39) |
N38I |
possibly damaging |
Het |
Hs3st4 |
A |
G |
7: 123,996,249 (GRCm39) |
E305G |
probably damaging |
Het |
Ireb2 |
T |
A |
9: 54,791,338 (GRCm39) |
F191I |
probably benign |
Het |
Irx3 |
T |
G |
8: 92,526,625 (GRCm39) |
T360P |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,380,357 (GRCm39) |
I1375N |
probably benign |
Het |
Klrh1 |
A |
T |
6: 129,752,345 (GRCm39) |
F57I |
probably benign |
Het |
Lama4 |
A |
T |
10: 38,963,369 (GRCm39) |
I1314F |
possibly damaging |
Het |
Lamb2 |
C |
A |
9: 108,363,347 (GRCm39) |
A842D |
probably benign |
Het |
Ldlrap1 |
A |
G |
4: 134,486,307 (GRCm39) |
Y51H |
possibly damaging |
Het |
Leo1 |
A |
G |
9: 75,355,623 (GRCm39) |
D321G |
probably damaging |
Het |
Lrrc14b |
A |
G |
13: 74,511,226 (GRCm39) |
S285P |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,326,860 (GRCm39) |
V4881A |
probably benign |
Het |
Mfsd2b |
A |
T |
12: 4,916,481 (GRCm39) |
F333I |
probably damaging |
Het |
Micall1 |
T |
C |
15: 79,006,760 (GRCm39) |
S196P |
unknown |
Het |
Mrps21 |
T |
C |
3: 95,770,110 (GRCm39) |
N73S |
probably benign |
Het |
Msantd5f5 |
G |
A |
4: 73,542,736 (GRCm39) |
G79S |
probably damaging |
Het |
Msln |
C |
T |
17: 25,969,708 (GRCm39) |
V341M |
possibly damaging |
Het |
Mybpc3 |
A |
T |
2: 90,962,001 (GRCm39) |
M840L |
probably damaging |
Het |
Myo7a |
A |
C |
7: 97,714,000 (GRCm39) |
F1613V |
probably damaging |
Het |
Naprt |
C |
T |
15: 75,763,607 (GRCm39) |
|
probably null |
Het |
Nbr1 |
T |
C |
11: 101,462,765 (GRCm39) |
V572A |
probably damaging |
Het |
Nfkbie |
A |
T |
17: 45,870,233 (GRCm39) |
T193S |
probably damaging |
Het |
Nlrp14 |
T |
G |
7: 106,789,251 (GRCm39) |
N672K |
probably benign |
Het |
Or11l3 |
A |
T |
11: 58,516,260 (GRCm39) |
I204N |
probably damaging |
Het |
Or4b1d |
A |
G |
2: 89,968,668 (GRCm39) |
Y272H |
probably damaging |
Het |
Or52ab2 |
A |
G |
7: 102,969,656 (GRCm39) |
T13A |
|
Het |
Or5b101 |
T |
C |
19: 13,005,439 (GRCm39) |
T85A |
probably benign |
Het |
Or6k14 |
A |
T |
1: 173,927,299 (GRCm39) |
I92F |
probably damaging |
Het |
Or8b49 |
A |
T |
9: 38,506,200 (GRCm39) |
I228L |
probably benign |
Het |
Oscar |
T |
C |
7: 3,614,149 (GRCm39) |
T197A |
possibly damaging |
Het |
P3h3 |
C |
A |
6: 124,827,594 (GRCm39) |
A481S |
possibly damaging |
Het |
Pcdh8 |
T |
C |
14: 80,008,691 (GRCm39) |
|
probably null |
Het |
Pcsk9 |
A |
T |
4: 106,316,094 (GRCm39) |
H116Q |
probably benign |
Het |
Ptcd1 |
A |
G |
5: 145,091,540 (GRCm39) |
F520L |
possibly damaging |
Het |
Rapgef2 |
T |
C |
3: 78,976,580 (GRCm39) |
T1261A |
probably benign |
Het |
Ribc2 |
T |
A |
15: 85,019,446 (GRCm39) |
M76K |
probably benign |
Het |
Sin3b |
A |
G |
8: 73,479,853 (GRCm39) |
E853G |
probably damaging |
Het |
Slit2 |
A |
G |
5: 48,414,180 (GRCm39) |
D940G |
probably damaging |
Het |
Smarcb1 |
T |
A |
10: 75,733,373 (GRCm39) |
N342Y |
probably damaging |
Het |
Smurf2 |
A |
T |
11: 106,726,921 (GRCm39) |
I469N |
probably damaging |
Het |
Spata31h1 |
T |
C |
10: 82,119,421 (GRCm39) |
I4530V |
probably benign |
Het |
Spta1 |
T |
C |
1: 174,074,065 (GRCm39) |
Y2335H |
probably damaging |
Het |
Suz12 |
C |
T |
11: 79,915,801 (GRCm39) |
R425C |
probably benign |
Het |
Synpo |
G |
A |
18: 60,762,895 (GRCm39) |
A4V |
probably benign |
Het |
Tet1 |
A |
C |
10: 62,649,129 (GRCm39) |
S157A |
possibly damaging |
Het |
Themis |
A |
G |
10: 28,637,415 (GRCm39) |
E173G |
possibly damaging |
Het |
Timmdc1 |
A |
T |
16: 38,325,780 (GRCm39) |
L197* |
probably null |
Het |
Tmem63c |
T |
C |
12: 87,115,932 (GRCm39) |
F191S |
possibly damaging |
Het |
Tnn |
G |
A |
1: 159,937,917 (GRCm39) |
T1200I |
probably benign |
Het |
Traf6 |
A |
G |
2: 101,527,537 (GRCm39) |
H429R |
probably benign |
Het |
Trem3 |
T |
C |
17: 48,556,873 (GRCm39) |
S115P |
probably benign |
Het |
Trip11 |
A |
T |
12: 101,851,639 (GRCm39) |
N808K |
probably benign |
Het |
Trub2 |
A |
T |
2: 29,673,385 (GRCm39) |
V106E |
probably damaging |
Het |
Ugcg |
A |
G |
4: 59,217,156 (GRCm39) |
I227V |
probably benign |
Het |
Vat1l |
G |
A |
8: 114,963,539 (GRCm39) |
|
probably null |
Het |
Vmn1r184 |
T |
C |
7: 25,966,824 (GRCm39) |
M190T |
possibly damaging |
Het |
Vmn2r3 |
T |
C |
3: 64,182,953 (GRCm39) |
T249A |
probably benign |
Het |
Zfp729b |
A |
C |
13: 67,742,002 (GRCm39) |
S88A |
probably benign |
Het |
|
Other mutations in Zfp995 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01800:Zfp995
|
APN |
17 |
22,099,972 (GRCm39) |
missense |
possibly damaging |
0.64 |
experienced
|
UTSW |
17 |
22,106,321 (GRCm39) |
start codon destroyed |
probably damaging |
0.98 |
R2906_Zfp995_673
|
UTSW |
17 |
22,099,247 (GRCm39) |
missense |
probably benign |
0.00 |
wise
|
UTSW |
17 |
22,099,493 (GRCm39) |
missense |
probably benign |
0.06 |
R1164:Zfp995
|
UTSW |
17 |
22,098,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1167:Zfp995
|
UTSW |
17 |
22,098,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1592:Zfp995
|
UTSW |
17 |
22,106,321 (GRCm39) |
start codon destroyed |
probably damaging |
0.98 |
R1669:Zfp995
|
UTSW |
17 |
22,098,945 (GRCm39) |
missense |
probably benign |
0.12 |
R1883:Zfp995
|
UTSW |
17 |
22,099,622 (GRCm39) |
missense |
probably benign |
0.00 |
R2044:Zfp995
|
UTSW |
17 |
22,099,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2906:Zfp995
|
UTSW |
17 |
22,099,247 (GRCm39) |
missense |
probably benign |
0.00 |
R4454:Zfp995
|
UTSW |
17 |
22,098,932 (GRCm39) |
missense |
probably benign |
0.17 |
R4670:Zfp995
|
UTSW |
17 |
22,106,320 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R5265:Zfp995
|
UTSW |
17 |
22,099,604 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5393:Zfp995
|
UTSW |
17 |
22,099,473 (GRCm39) |
missense |
probably benign |
0.01 |
R5585:Zfp995
|
UTSW |
17 |
22,106,339 (GRCm39) |
splice site |
probably benign |
|
R5735:Zfp995
|
UTSW |
17 |
22,101,010 (GRCm39) |
missense |
probably benign |
0.05 |
R6243:Zfp995
|
UTSW |
17 |
22,099,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Zfp995
|
UTSW |
17 |
22,099,493 (GRCm39) |
missense |
probably benign |
0.06 |
R7311:Zfp995
|
UTSW |
17 |
22,099,641 (GRCm39) |
missense |
probably benign |
0.01 |
R7529:Zfp995
|
UTSW |
17 |
22,099,333 (GRCm39) |
nonsense |
probably null |
|
R7765:Zfp995
|
UTSW |
17 |
22,100,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8156:Zfp995
|
UTSW |
17 |
22,099,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Zfp995
|
UTSW |
17 |
22,099,172 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Zfp995
|
UTSW |
17 |
22,101,035 (GRCm39) |
missense |
possibly damaging |
0.57 |
|