Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
G |
A |
9: 55,890,645 (GRCm39) |
Q355* |
probably null |
Het |
Aacs |
A |
T |
5: 125,580,691 (GRCm39) |
N255I |
possibly damaging |
Het |
Abcf2 |
A |
G |
5: 24,779,185 (GRCm39) |
L121P |
probably damaging |
Het |
Amigo1 |
A |
G |
3: 108,095,034 (GRCm39) |
I178V |
probably benign |
Het |
Ankrd13a |
T |
A |
5: 114,933,793 (GRCm39) |
N262K |
probably damaging |
Het |
Apba2 |
A |
G |
7: 64,345,062 (GRCm39) |
E84G |
possibly damaging |
Het |
Arhgap35 |
A |
T |
7: 16,296,914 (GRCm39) |
L717* |
probably null |
Het |
Aspa |
A |
T |
11: 73,199,625 (GRCm39) |
C217* |
probably null |
Het |
Atp5mc3 |
A |
G |
2: 73,739,567 (GRCm39) |
I91T |
probably damaging |
Het |
Birc6 |
T |
C |
17: 75,004,420 (GRCm39) |
M4763T |
possibly damaging |
Het |
Cc2d2b |
A |
G |
19: 40,753,927 (GRCm39) |
Y150C |
unknown |
Het |
Ccdc180 |
C |
T |
4: 45,920,861 (GRCm39) |
Q936* |
probably null |
Het |
Cdc42bpg |
A |
G |
19: 6,370,115 (GRCm39) |
E1103G |
probably benign |
Het |
Cdca2 |
T |
C |
14: 67,915,003 (GRCm39) |
Q752R |
probably benign |
Het |
Ces1b |
A |
T |
8: 93,791,637 (GRCm39) |
S321T |
probably benign |
Het |
Cfap70 |
A |
T |
14: 20,490,690 (GRCm39) |
|
probably null |
Het |
Cpox |
C |
T |
16: 58,490,984 (GRCm39) |
T65I |
possibly damaging |
Het |
Crocc |
C |
T |
4: 140,748,988 (GRCm39) |
E1606K |
probably damaging |
Het |
Cryzl2 |
T |
G |
1: 157,316,038 (GRCm39) |
M337R |
probably benign |
Het |
Cyp4a29 |
C |
A |
4: 115,111,630 (GRCm39) |
A469D |
probably damaging |
Het |
Dpp6 |
T |
A |
5: 27,930,604 (GRCm39) |
I812N |
probably damaging |
Het |
Elovl5 |
A |
G |
9: 77,889,947 (GRCm39) |
T253A |
possibly damaging |
Het |
Fancd2 |
T |
A |
6: 113,530,717 (GRCm39) |
L450* |
probably null |
Het |
Fbxo31 |
C |
T |
8: 122,305,208 (GRCm39) |
R96H |
probably damaging |
Het |
Gls |
A |
T |
1: 52,230,036 (GRCm39) |
|
probably null |
Het |
Gm3045 |
G |
A |
13: 56,577,253 (GRCm39) |
E134K |
possibly damaging |
Het |
Gpr158 |
A |
G |
2: 21,830,054 (GRCm39) |
I700V |
probably damaging |
Het |
H2-Aa |
T |
C |
17: 34,502,295 (GRCm39) |
I209V |
probably benign |
Het |
Ifnar2 |
A |
G |
16: 91,184,984 (GRCm39) |
D125G |
probably benign |
Het |
Igsf8 |
C |
A |
1: 172,145,319 (GRCm39) |
D278E |
possibly damaging |
Het |
Inpp5d |
T |
C |
1: 87,623,128 (GRCm39) |
I407T |
probably damaging |
Het |
Iqcd |
A |
G |
5: 120,744,737 (GRCm39) |
E355G |
probably damaging |
Het |
Klra2 |
T |
A |
6: 131,219,836 (GRCm39) |
D115V |
probably benign |
Het |
Kmt2b |
T |
C |
7: 30,287,784 (GRCm39) |
E120G |
unknown |
Het |
Lhx6 |
A |
G |
2: 35,980,979 (GRCm39) |
I321T |
possibly damaging |
Het |
Lmna |
CAGCACGGTGCGTGAGC |
CAGC |
3: 88,389,857 (GRCm39) |
|
probably null |
Het |
Lztr1 |
T |
C |
16: 17,327,000 (GRCm39) |
Y37H |
probably damaging |
Het |
Malrd1 |
A |
T |
2: 15,570,026 (GRCm39) |
|
probably null |
Het |
Mtmr3 |
C |
T |
11: 4,470,890 (GRCm39) |
V79I |
probably damaging |
Het |
Nbr1 |
A |
G |
11: 101,451,261 (GRCm39) |
I56M |
possibly damaging |
Het |
Ncor2 |
C |
T |
5: 125,125,545 (GRCm39) |
A580T |
unknown |
Het |
Ndst3 |
A |
G |
3: 123,353,866 (GRCm39) |
I601T |
possibly damaging |
Het |
Nectin4 |
C |
A |
1: 171,210,165 (GRCm39) |
P219Q |
probably damaging |
Het |
Nfatc4 |
T |
C |
14: 56,066,964 (GRCm39) |
V501A |
probably benign |
Het |
Nisch |
T |
C |
14: 30,895,646 (GRCm39) |
T1015A |
probably damaging |
Het |
Nr2c1 |
T |
C |
10: 94,017,479 (GRCm39) |
|
probably null |
Het |
Nrg2 |
T |
C |
18: 36,165,430 (GRCm39) |
E394G |
probably benign |
Het |
Oas1e |
A |
G |
5: 120,932,347 (GRCm39) |
F99L |
probably benign |
Het |
Oaz3 |
A |
T |
3: 94,341,835 (GRCm39) |
Y178* |
probably null |
Het |
Or1e35 |
A |
G |
11: 73,798,097 (GRCm39) |
S74P |
possibly damaging |
Het |
Or6c69b |
A |
C |
10: 129,627,022 (GRCm39) |
S145R |
probably damaging |
Het |
Pcdhb20 |
C |
T |
18: 37,637,839 (GRCm39) |
H122Y |
probably benign |
Het |
Pdcd2 |
T |
A |
17: 15,747,535 (GRCm39) |
M1L |
probably damaging |
Het |
Phf11 |
T |
C |
14: 59,482,240 (GRCm39) |
N171S |
probably benign |
Het |
Plcd1 |
C |
A |
9: 118,901,698 (GRCm39) |
G609W |
probably damaging |
Het |
Plscr3 |
T |
C |
11: 69,738,631 (GRCm39) |
F98L |
probably benign |
Het |
Ppp1r8 |
T |
C |
4: 132,570,407 (GRCm39) |
N6S |
probably benign |
Het |
Prpf38b |
G |
A |
3: 108,818,859 (GRCm39) |
|
probably benign |
Het |
Rin2 |
T |
A |
2: 145,702,202 (GRCm39) |
N299K |
possibly damaging |
Het |
Serpina1d |
T |
G |
12: 103,734,299 (GRCm39) |
T2P |
probably benign |
Het |
Slc22a16 |
A |
G |
10: 40,461,125 (GRCm39) |
D330G |
probably benign |
Het |
Slit1 |
G |
A |
19: 41,731,832 (GRCm39) |
Q6* |
probably null |
Het |
Spaca7b |
T |
A |
8: 11,705,681 (GRCm39) |
E142V |
probably benign |
Het |
Spag9 |
T |
C |
11: 93,887,119 (GRCm39) |
V8A |
possibly damaging |
Het |
Spsb3 |
C |
T |
17: 25,105,784 (GRCm39) |
T44I |
unknown |
Het |
Srrt |
T |
C |
5: 137,295,732 (GRCm39) |
Y563C |
probably damaging |
Het |
Syne2 |
A |
G |
12: 75,926,951 (GRCm39) |
D69G |
probably damaging |
Het |
Tcf12 |
A |
G |
9: 71,792,443 (GRCm39) |
V80A |
probably benign |
Het |
Tdpoz3 |
G |
A |
3: 93,733,336 (GRCm39) |
D4N |
possibly damaging |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tmem132d |
G |
A |
5: 128,061,375 (GRCm39) |
T409I |
possibly damaging |
Het |
Tmem245 |
G |
T |
4: 56,947,119 (GRCm39) |
T98K |
probably damaging |
Het |
Tmem70 |
A |
C |
1: 16,735,659 (GRCm39) |
E43A |
probably benign |
Het |
Trim25 |
A |
T |
11: 88,907,188 (GRCm39) |
I516F |
probably damaging |
Het |
Trim3 |
G |
A |
7: 105,267,455 (GRCm39) |
S308L |
possibly damaging |
Het |
Ttll9 |
C |
T |
2: 152,831,989 (GRCm39) |
R189* |
probably null |
Het |
Ttpal |
T |
C |
2: 163,449,596 (GRCm39) |
|
probably null |
Het |
Ubl4b |
A |
T |
3: 107,461,911 (GRCm39) |
H116Q |
probably benign |
Het |
Unc80 |
C |
A |
1: 66,651,287 (GRCm39) |
T1544K |
possibly damaging |
Het |
Usp2 |
T |
C |
9: 44,003,487 (GRCm39) |
|
probably null |
Het |
Usp25 |
T |
C |
16: 76,874,123 (GRCm39) |
|
probably null |
Het |
Vmn1r167 |
C |
T |
7: 23,204,990 (GRCm39) |
V9I |
probably benign |
Het |
Vmn2r87 |
A |
G |
10: 130,314,776 (GRCm39) |
I270T |
probably damaging |
Het |
Vps35l |
G |
A |
7: 118,348,915 (GRCm39) |
|
probably null |
Het |
Wdr24 |
A |
G |
17: 26,046,301 (GRCm39) |
D515G |
possibly damaging |
Het |
Wdr81 |
T |
C |
11: 75,341,650 (GRCm39) |
T87A |
|
Het |
Zcchc14 |
A |
T |
8: 122,331,863 (GRCm39) |
L500Q |
unknown |
Het |
Zzef1 |
A |
G |
11: 72,758,786 (GRCm39) |
T1242A |
probably benign |
Het |
|
Other mutations in Dnaaf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01113:Dnaaf1
|
APN |
8 |
120,309,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Dnaaf1
|
APN |
8 |
120,309,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Dnaaf1
|
APN |
8 |
120,317,410 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03391:Dnaaf1
|
APN |
8 |
120,309,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R7097_Dnaaf1_566
|
UTSW |
8 |
120,323,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0329:Dnaaf1
|
UTSW |
8 |
120,322,756 (GRCm39) |
unclassified |
probably benign |
|
R0467:Dnaaf1
|
UTSW |
8 |
120,317,471 (GRCm39) |
missense |
probably benign |
|
R0483:Dnaaf1
|
UTSW |
8 |
120,317,405 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1464:Dnaaf1
|
UTSW |
8 |
120,306,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R1464:Dnaaf1
|
UTSW |
8 |
120,306,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R1532:Dnaaf1
|
UTSW |
8 |
120,304,162 (GRCm39) |
missense |
probably benign |
|
R1847:Dnaaf1
|
UTSW |
8 |
120,309,616 (GRCm39) |
missense |
probably benign |
0.41 |
R2060:Dnaaf1
|
UTSW |
8 |
120,317,341 (GRCm39) |
missense |
probably benign |
0.27 |
R2108:Dnaaf1
|
UTSW |
8 |
120,309,471 (GRCm39) |
critical splice donor site |
probably null |
|
R2356:Dnaaf1
|
UTSW |
8 |
120,315,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Dnaaf1
|
UTSW |
8 |
120,304,100 (GRCm39) |
missense |
probably benign |
0.10 |
R4802:Dnaaf1
|
UTSW |
8 |
120,304,100 (GRCm39) |
missense |
probably benign |
0.10 |
R5232:Dnaaf1
|
UTSW |
8 |
120,317,329 (GRCm39) |
missense |
probably benign |
0.42 |
R6846:Dnaaf1
|
UTSW |
8 |
120,309,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R7080:Dnaaf1
|
UTSW |
8 |
120,309,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7097:Dnaaf1
|
UTSW |
8 |
120,323,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7360:Dnaaf1
|
UTSW |
8 |
120,304,090 (GRCm39) |
missense |
probably benign |
0.37 |
R7940:Dnaaf1
|
UTSW |
8 |
120,309,454 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8773:Dnaaf1
|
UTSW |
8 |
120,302,194 (GRCm39) |
missense |
probably benign |
|
R9090:Dnaaf1
|
UTSW |
8 |
120,324,392 (GRCm39) |
missense |
probably benign |
0.30 |
R9170:Dnaaf1
|
UTSW |
8 |
120,302,195 (GRCm39) |
missense |
probably benign |
0.00 |
R9271:Dnaaf1
|
UTSW |
8 |
120,324,392 (GRCm39) |
missense |
probably benign |
0.30 |
R9562:Dnaaf1
|
UTSW |
8 |
120,309,392 (GRCm39) |
missense |
probably damaging |
0.99 |
R9607:Dnaaf1
|
UTSW |
8 |
120,309,350 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9622:Dnaaf1
|
UTSW |
8 |
120,315,001 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Dnaaf1
|
UTSW |
8 |
120,302,180 (GRCm39) |
missense |
possibly damaging |
0.52 |
|