Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,058,078 (GRCm39) |
T14A |
|
Het |
2610008E11Rik |
T |
C |
10: 78,930,289 (GRCm39) |
N42D |
probably benign |
Het |
Ajm1 |
A |
G |
2: 25,469,246 (GRCm39) |
F222L |
probably benign |
Het |
Ankrd54 |
T |
A |
15: 78,939,641 (GRCm39) |
M183L |
|
Het |
Apob |
G |
A |
12: 8,056,435 (GRCm39) |
G1639D |
probably damaging |
Het |
B3gat2 |
A |
G |
1: 23,884,061 (GRCm39) |
T283A |
probably benign |
Het |
Bmpr2 |
T |
G |
1: 59,886,252 (GRCm39) |
S296R |
probably damaging |
Het |
Cand1 |
G |
A |
10: 119,042,721 (GRCm39) |
T1123I |
probably damaging |
Het |
Cc2d2a |
T |
C |
5: 43,869,781 (GRCm39) |
F943S |
probably damaging |
Het |
Ccdc40 |
T |
C |
11: 119,144,211 (GRCm39) |
I912T |
probably benign |
Het |
Cdkn2d |
G |
A |
9: 21,200,447 (GRCm39) |
S108L |
probably benign |
Het |
Cep295 |
G |
A |
9: 15,245,660 (GRCm39) |
T932I |
probably damaging |
Het |
Cntn5 |
A |
G |
9: 9,673,955 (GRCm39) |
S716P |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,895,808 (GRCm39) |
E903G |
probably benign |
Het |
Ctrc |
T |
A |
4: 141,565,972 (GRCm39) |
I229F |
probably damaging |
Het |
Cyb561d2 |
C |
T |
9: 107,418,771 (GRCm39) |
A18T |
probably benign |
Het |
Dnajb4 |
T |
A |
3: 151,899,089 (GRCm39) |
K46* |
probably null |
Het |
Dsc2 |
C |
T |
18: 20,165,331 (GRCm39) |
G881R |
possibly damaging |
Het |
Dsg1c |
C |
T |
18: 20,410,016 (GRCm39) |
H495Y |
probably benign |
Het |
Eif2b3 |
A |
G |
4: 116,879,414 (GRCm39) |
D18G |
probably damaging |
Het |
Enam |
A |
T |
5: 88,651,385 (GRCm39) |
I965L |
probably benign |
Het |
Fhod3 |
T |
A |
18: 25,248,910 (GRCm39) |
I1363K |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,855,245 (GRCm39) |
Y1918C |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,823,296 (GRCm39) |
I6343N |
possibly damaging |
Het |
Gpr45 |
G |
C |
1: 43,072,475 (GRCm39) |
V373L |
probably damaging |
Het |
Hdac2 |
G |
T |
10: 36,873,966 (GRCm39) |
Q365H |
probably damaging |
Het |
Hspa12b |
A |
G |
2: 130,980,389 (GRCm39) |
T103A |
possibly damaging |
Het |
Ifrd1 |
A |
T |
12: 40,262,350 (GRCm39) |
S287T |
probably benign |
Het |
Igkv6-15 |
G |
A |
6: 70,383,622 (GRCm39) |
P60S |
possibly damaging |
Het |
Ippk |
C |
T |
13: 49,599,818 (GRCm39) |
P226S |
|
Het |
Kctd19 |
T |
A |
8: 106,122,069 (GRCm39) |
D109V |
unknown |
Het |
Matn4 |
G |
A |
2: 164,234,851 (GRCm39) |
S540L |
probably damaging |
Het |
Matn4 |
T |
C |
2: 164,241,682 (GRCm39) |
K248E |
probably benign |
Het |
Muc16 |
G |
A |
9: 18,420,206 (GRCm39) |
Q97* |
probably null |
Het |
Mup18 |
A |
G |
4: 61,592,238 (GRCm39) |
C9R |
unknown |
Het |
Myh1 |
A |
G |
11: 67,113,031 (GRCm39) |
K1845R |
probably damaging |
Het |
Mysm1 |
G |
A |
4: 94,848,627 (GRCm39) |
R469* |
probably null |
Het |
Naip1 |
T |
C |
13: 100,563,509 (GRCm39) |
D552G |
possibly damaging |
Het |
Nrcam |
A |
G |
12: 44,618,371 (GRCm39) |
D787G |
probably benign |
Het |
Nrcam |
G |
A |
12: 44,645,365 (GRCm39) |
V1256I |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,932,980 (GRCm39) |
H4799N |
possibly damaging |
Het |
Or1f12 |
T |
C |
13: 21,722,122 (GRCm39) |
K3E |
probably benign |
Het |
Or4p4 |
A |
G |
2: 88,482,729 (GRCm39) |
K78E |
probably damaging |
Het |
Or52e18 |
T |
C |
7: 104,609,356 (GRCm39) |
I194M |
probably damaging |
Het |
Or7g22 |
A |
G |
9: 19,048,353 (GRCm39) |
I21M |
probably benign |
Het |
Pcdhgb5 |
T |
C |
18: 37,866,302 (GRCm39) |
F699S |
probably damaging |
Het |
Pira1 |
G |
A |
7: 3,740,075 (GRCm39) |
T340I |
probably damaging |
Het |
Ppp2r5c |
A |
G |
12: 110,517,519 (GRCm39) |
H218R |
possibly damaging |
Het |
Ptgs2 |
A |
G |
1: 149,979,785 (GRCm39) |
R297G |
probably damaging |
Het |
Rapgef3 |
A |
T |
15: 97,648,747 (GRCm39) |
D619E |
probably benign |
Het |
Ric1 |
G |
A |
19: 29,552,191 (GRCm39) |
V321I |
probably benign |
Het |
Ripor1 |
T |
C |
8: 106,344,105 (GRCm39) |
V413A |
probably damaging |
Het |
Rsf1 |
G |
T |
7: 97,288,464 (GRCm39) |
|
probably null |
Het |
Sccpdh |
A |
G |
1: 179,504,017 (GRCm39) |
D122G |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,331,441 (GRCm39) |
H191Q |
probably benign |
Het |
Slco1a5 |
G |
T |
6: 142,208,418 (GRCm39) |
N124K |
probably damaging |
Het |
Snrnp200 |
A |
G |
2: 127,071,051 (GRCm39) |
T1111A |
probably benign |
Het |
Stard9 |
G |
A |
2: 120,534,911 (GRCm39) |
G3723S |
probably benign |
Het |
Tanc2 |
T |
A |
11: 105,725,988 (GRCm39) |
V384E |
probably damaging |
Het |
Tbrg1 |
A |
G |
9: 37,568,296 (GRCm39) |
F49L |
possibly damaging |
Het |
Tecta |
A |
G |
9: 42,288,927 (GRCm39) |
F546S |
probably damaging |
Het |
Tmem132c |
A |
G |
5: 127,437,176 (GRCm39) |
R222G |
probably benign |
Het |
Trub2 |
C |
T |
2: 29,668,739 (GRCm39) |
|
probably null |
Het |
Tti1 |
G |
T |
2: 157,849,418 (GRCm39) |
P607Q |
probably damaging |
Het |
Vmn1r62 |
T |
A |
7: 5,678,726 (GRCm39) |
F136I |
possibly damaging |
Het |
Vmn2r111 |
T |
A |
17: 22,790,469 (GRCm39) |
H179L |
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,699,063 (GRCm39) |
C2703* |
probably null |
Het |
Wdfy4 |
G |
A |
14: 32,826,072 (GRCm39) |
P1193L |
|
Het |
Wipf3 |
A |
G |
6: 54,460,816 (GRCm39) |
K88R |
probably benign |
Het |
Zfp641 |
C |
T |
15: 98,186,856 (GRCm39) |
G256R |
probably damaging |
Het |
Zfp993 |
T |
A |
4: 146,741,972 (GRCm39) |
C99S |
probably benign |
Het |
|
Other mutations in Phtf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01443:Phtf2
|
APN |
5 |
20,987,265 (GRCm39) |
unclassified |
probably benign |
|
IGL01789:Phtf2
|
APN |
5 |
20,999,372 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01816:Phtf2
|
APN |
5 |
21,008,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02266:Phtf2
|
APN |
5 |
21,010,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02295:Phtf2
|
APN |
5 |
21,012,428 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03086:Phtf2
|
APN |
5 |
20,969,273 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03179:Phtf2
|
APN |
5 |
20,987,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03192:Phtf2
|
APN |
5 |
20,966,717 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03256:Phtf2
|
APN |
5 |
21,008,250 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4480001:Phtf2
|
UTSW |
5 |
21,018,242 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4802001:Phtf2
|
UTSW |
5 |
21,006,904 (GRCm39) |
missense |
probably damaging |
0.96 |
R0589:Phtf2
|
UTSW |
5 |
21,018,249 (GRCm39) |
nonsense |
probably null |
|
R1732:Phtf2
|
UTSW |
5 |
20,994,625 (GRCm39) |
critical splice donor site |
probably null |
|
R3151:Phtf2
|
UTSW |
5 |
20,970,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R3791:Phtf2
|
UTSW |
5 |
20,987,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R3843:Phtf2
|
UTSW |
5 |
20,979,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R4080:Phtf2
|
UTSW |
5 |
21,018,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R4569:Phtf2
|
UTSW |
5 |
20,994,593 (GRCm39) |
intron |
probably benign |
|
R4627:Phtf2
|
UTSW |
5 |
20,978,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Phtf2
|
UTSW |
5 |
21,010,722 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5131:Phtf2
|
UTSW |
5 |
20,979,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R5276:Phtf2
|
UTSW |
5 |
20,977,195 (GRCm39) |
missense |
probably benign |
0.19 |
R5871:Phtf2
|
UTSW |
5 |
20,999,399 (GRCm39) |
missense |
probably benign |
0.16 |
R5941:Phtf2
|
UTSW |
5 |
20,979,071 (GRCm39) |
missense |
probably damaging |
0.98 |
R5964:Phtf2
|
UTSW |
5 |
20,980,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R6318:Phtf2
|
UTSW |
5 |
21,006,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R6621:Phtf2
|
UTSW |
5 |
21,017,954 (GRCm39) |
intron |
probably benign |
|
R6684:Phtf2
|
UTSW |
5 |
21,017,937 (GRCm39) |
critical splice donor site |
probably benign |
|
R7003:Phtf2
|
UTSW |
5 |
20,999,399 (GRCm39) |
missense |
probably benign |
0.16 |
R7253:Phtf2
|
UTSW |
5 |
20,970,856 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7566:Phtf2
|
UTSW |
5 |
20,970,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7654:Phtf2
|
UTSW |
5 |
20,987,459 (GRCm39) |
missense |
probably damaging |
0.99 |
R8514:Phtf2
|
UTSW |
5 |
21,007,030 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8921:Phtf2
|
UTSW |
5 |
21,008,275 (GRCm39) |
missense |
probably benign |
0.00 |
R8975:Phtf2
|
UTSW |
5 |
20,969,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R9028:Phtf2
|
UTSW |
5 |
20,999,373 (GRCm39) |
missense |
probably benign |
|
R9164:Phtf2
|
UTSW |
5 |
21,008,190 (GRCm39) |
nonsense |
probably null |
|
|