Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730480H06Rik |
T |
A |
5: 48,536,692 (GRCm39) |
H129Q |
probably damaging |
Het |
Abca14 |
G |
A |
7: 119,807,020 (GRCm39) |
R22Q |
probably damaging |
Het |
Abcg5 |
T |
A |
17: 84,976,503 (GRCm39) |
M445L |
probably benign |
Het |
Abhd3 |
T |
A |
18: 10,645,208 (GRCm39) |
N357I |
possibly damaging |
Het |
Adamts5 |
C |
T |
16: 85,665,580 (GRCm39) |
G574S |
probably damaging |
Het |
Adgrg5 |
T |
A |
8: 95,665,260 (GRCm39) |
N389K |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,329,330 (GRCm39) |
V80A |
probably benign |
Het |
Arhgap20 |
A |
G |
9: 51,761,455 (GRCm39) |
Q1066R |
probably benign |
Het |
Arhgap21 |
T |
A |
2: 20,919,610 (GRCm39) |
K32* |
probably null |
Het |
AW209491 |
T |
C |
13: 14,812,317 (GRCm39) |
F390S |
probably damaging |
Het |
Axl |
A |
T |
7: 25,478,142 (GRCm39) |
|
probably benign |
Het |
Bri3bp |
A |
G |
5: 125,531,603 (GRCm39) |
Y183C |
probably damaging |
Het |
Cad |
T |
C |
5: 31,232,801 (GRCm39) |
|
probably benign |
Het |
Capns2 |
A |
G |
8: 93,628,360 (GRCm39) |
Q83R |
possibly damaging |
Het |
Ccdc180 |
G |
T |
4: 45,922,010 (GRCm39) |
R1028L |
probably damaging |
Het |
Cdh19 |
C |
A |
1: 110,852,892 (GRCm39) |
V348F |
possibly damaging |
Het |
Chrm2 |
T |
C |
6: 36,500,641 (GRCm39) |
V166A |
possibly damaging |
Het |
Clmp |
A |
G |
9: 40,693,782 (GRCm39) |
Y333C |
probably benign |
Het |
Cntn3 |
A |
G |
6: 102,254,178 (GRCm39) |
|
probably null |
Het |
Copz1 |
A |
G |
15: 103,199,792 (GRCm39) |
Y69C |
probably damaging |
Het |
Crybg1 |
T |
C |
10: 43,874,894 (GRCm39) |
D738G |
probably benign |
Het |
Ctnna2 |
T |
A |
6: 76,950,882 (GRCm39) |
I165F |
probably damaging |
Het |
Dcaf7 |
T |
G |
11: 105,942,652 (GRCm39) |
S200A |
probably damaging |
Het |
Deup1 |
T |
A |
9: 15,493,893 (GRCm39) |
R416S |
possibly damaging |
Het |
Dmxl1 |
T |
A |
18: 49,990,497 (GRCm39) |
|
probably benign |
Het |
Dnaaf11 |
A |
T |
15: 66,319,455 (GRCm39) |
V305D |
probably damaging |
Het |
Dnase2b |
A |
T |
3: 146,294,910 (GRCm39) |
|
probably benign |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Eef2 |
C |
CN |
10: 81,014,602 (GRCm39) |
|
probably null |
Het |
Ephb2 |
T |
C |
4: 136,383,287 (GRCm39) |
Y931C |
probably damaging |
Het |
Fam83h |
T |
C |
15: 75,875,076 (GRCm39) |
S754G |
possibly damaging |
Het |
Fibp |
T |
A |
19: 5,513,216 (GRCm39) |
V177D |
probably damaging |
Het |
Gfpt2 |
T |
C |
11: 49,723,725 (GRCm39) |
I571T |
probably damaging |
Het |
Grm7 |
T |
G |
6: 111,336,055 (GRCm39) |
|
probably benign |
Het |
Gsdma3 |
A |
G |
11: 98,526,745 (GRCm39) |
Y335C |
probably damaging |
Het |
H2-T23 |
A |
T |
17: 36,343,033 (GRCm39) |
|
probably benign |
Het |
H4c3 |
A |
G |
13: 23,882,131 (GRCm39) |
F101S |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,249,704 (GRCm39) |
I2216V |
probably benign |
Het |
Ipo8 |
A |
G |
6: 148,719,606 (GRCm39) |
M113T |
probably benign |
Het |
Kdm6a |
A |
G |
X: 18,128,664 (GRCm39) |
E1045G |
probably damaging |
Het |
Kyat1 |
C |
T |
2: 30,078,229 (GRCm39) |
E117K |
probably damaging |
Het |
Lin7b |
A |
G |
7: 45,019,326 (GRCm39) |
|
probably benign |
Het |
Lipn |
G |
A |
19: 34,062,003 (GRCm39) |
|
probably benign |
Het |
Lrfn2 |
C |
A |
17: 49,378,072 (GRCm39) |
N384K |
probably damaging |
Het |
Map1b |
T |
C |
13: 99,570,526 (GRCm39) |
K732E |
unknown |
Het |
Mpl |
A |
G |
4: 118,300,705 (GRCm39) |
M541T |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,631,943 (GRCm39) |
|
probably benign |
Het |
Mrc1 |
T |
C |
2: 14,274,937 (GRCm39) |
|
probably benign |
Het |
Ms4a13 |
T |
C |
19: 11,149,235 (GRCm39) |
|
probably benign |
Het |
Myo18b |
G |
T |
5: 112,871,734 (GRCm39) |
R2116S |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,111,686 (GRCm39) |
T731A |
probably damaging |
Het |
Ncoa6 |
G |
T |
2: 155,257,617 (GRCm39) |
A642D |
probably benign |
Het |
Ndufs7 |
T |
A |
10: 80,090,665 (GRCm39) |
|
probably benign |
Het |
Nfkbiz |
G |
A |
16: 55,638,242 (GRCm39) |
T406M |
probably benign |
Het |
Nr4a1 |
A |
G |
15: 101,168,765 (GRCm39) |
E267G |
probably damaging |
Het |
Nrxn2 |
T |
G |
19: 6,543,434 (GRCm39) |
F1103V |
probably damaging |
Het |
Or10ab4 |
C |
T |
7: 107,655,029 (GRCm39) |
T280I |
probably damaging |
Het |
Or10d3 |
A |
T |
9: 39,461,593 (GRCm39) |
D191E |
probably damaging |
Het |
Or1e22 |
T |
C |
11: 73,376,889 (GRCm39) |
T254A |
probably benign |
Het |
Or5a3 |
C |
T |
19: 12,400,173 (GRCm39) |
L167F |
probably damaging |
Het |
Or5g27 |
T |
A |
2: 85,410,119 (GRCm39) |
C179S |
probably damaging |
Het |
Or5m11 |
G |
T |
2: 85,782,353 (GRCm39) |
M315I |
probably benign |
Het |
Or8u9 |
A |
T |
2: 86,001,387 (GRCm39) |
M258K |
probably damaging |
Het |
Pip |
C |
T |
6: 41,826,819 (GRCm39) |
Q53* |
probably null |
Het |
Ppp2ca |
T |
C |
11: 52,008,989 (GRCm39) |
|
probably null |
Het |
Prl2c5 |
A |
G |
13: 13,363,906 (GRCm39) |
|
probably null |
Het |
Psph |
T |
A |
5: 129,843,641 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
C |
T |
13: 63,691,294 (GRCm39) |
|
probably benign |
Het |
Ptprs |
C |
T |
17: 56,765,255 (GRCm39) |
V10M |
probably damaging |
Het |
Rarg |
T |
C |
15: 102,147,312 (GRCm39) |
R358G |
probably damaging |
Het |
Rbl2 |
T |
C |
8: 91,839,133 (GRCm39) |
|
probably benign |
Het |
Robo2 |
A |
T |
16: 73,782,462 (GRCm39) |
|
probably benign |
Het |
Scin |
A |
T |
12: 40,131,765 (GRCm39) |
D256E |
possibly damaging |
Het |
Scn8a |
T |
C |
15: 100,914,449 (GRCm39) |
Y1152H |
probably damaging |
Het |
Sh2b2 |
T |
G |
5: 136,254,155 (GRCm39) |
|
probably benign |
Het |
Slc13a2 |
G |
A |
11: 78,289,964 (GRCm39) |
P450L |
probably damaging |
Het |
Slc2a12 |
A |
G |
10: 22,568,129 (GRCm39) |
I519V |
probably benign |
Het |
Slc30a9 |
C |
T |
5: 67,491,953 (GRCm39) |
T260M |
probably damaging |
Het |
Slc9a7 |
A |
T |
X: 20,069,001 (GRCm39) |
F184Y |
probably damaging |
Het |
Smc2 |
G |
T |
4: 52,458,558 (GRCm39) |
K466N |
probably benign |
Het |
Snx16 |
T |
C |
3: 10,491,278 (GRCm39) |
E209G |
probably damaging |
Het |
Sp3 |
A |
T |
2: 72,800,876 (GRCm39) |
I423N |
possibly damaging |
Het |
Ssh2 |
G |
T |
11: 77,345,620 (GRCm39) |
V1202F |
probably benign |
Het |
Stam2 |
A |
T |
2: 52,593,268 (GRCm39) |
|
probably benign |
Het |
Stox2 |
T |
C |
8: 47,647,070 (GRCm39) |
Y194C |
probably damaging |
Het |
Sult3a1 |
A |
G |
10: 33,742,519 (GRCm39) |
T49A |
probably damaging |
Het |
Supt3 |
A |
T |
17: 45,314,018 (GRCm39) |
I136F |
possibly damaging |
Het |
Syne2 |
A |
T |
12: 76,070,895 (GRCm39) |
R103S |
possibly damaging |
Het |
Synj2 |
T |
A |
17: 6,047,163 (GRCm39) |
M1K |
probably null |
Het |
Tas2r110 |
T |
C |
6: 132,845,334 (GRCm39) |
S122P |
possibly damaging |
Het |
Tln1 |
A |
G |
4: 43,543,434 (GRCm39) |
|
probably null |
Het |
Tmem117 |
A |
G |
15: 94,612,793 (GRCm39) |
T110A |
possibly damaging |
Het |
Tmem247 |
A |
G |
17: 87,224,906 (GRCm39) |
D5G |
probably benign |
Het |
Tmem39a |
T |
A |
16: 38,411,337 (GRCm39) |
F363I |
probably benign |
Het |
Tmem80 |
G |
A |
7: 140,915,808 (GRCm39) |
A73T |
possibly damaging |
Het |
Trpm4 |
C |
T |
7: 44,954,896 (GRCm39) |
G901S |
probably damaging |
Het |
Upk3bl |
T |
C |
5: 136,092,840 (GRCm39) |
|
probably benign |
Het |
Vmn1r120 |
A |
T |
7: 20,787,397 (GRCm39) |
C105S |
probably damaging |
Het |
Vmn1r69 |
A |
T |
7: 10,314,874 (GRCm39) |
|
probably benign |
Het |
Vmn2r95 |
T |
C |
17: 18,672,362 (GRCm39) |
F700L |
probably damaging |
Het |
Wdr70 |
G |
A |
15: 7,915,118 (GRCm39) |
T550M |
possibly damaging |
Het |
Zbtb22 |
A |
G |
17: 34,137,118 (GRCm39) |
D421G |
possibly damaging |
Het |
Zbtb45 |
G |
A |
7: 12,740,260 (GRCm39) |
R452C |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,527,141 (GRCm39) |
Y1013H |
probably damaging |
Het |
Zfp329 |
C |
T |
7: 12,540,520 (GRCm39) |
|
probably null |
Het |
Zfp532 |
T |
A |
18: 65,756,837 (GRCm39) |
S257T |
probably benign |
Het |
Zfp933 |
G |
A |
4: 147,911,005 (GRCm39) |
T197I |
probably benign |
Het |
Zgrf1 |
T |
A |
3: 127,408,841 (GRCm39) |
N1649K |
probably damaging |
Het |
|
Other mutations in Phf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00905:Phf1
|
APN |
17 |
27,155,568 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01629:Phf1
|
APN |
17 |
27,153,247 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01931:Phf1
|
APN |
17 |
27,154,509 (GRCm39) |
unclassified |
probably benign |
|
IGL02008:Phf1
|
APN |
17 |
27,154,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02048:Phf1
|
APN |
17 |
27,153,515 (GRCm39) |
unclassified |
probably benign |
|
IGL02206:Phf1
|
APN |
17 |
27,155,843 (GRCm39) |
unclassified |
probably benign |
|
IGL02252:Phf1
|
APN |
17 |
27,154,109 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02548:Phf1
|
APN |
17 |
27,154,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03145:Phf1
|
APN |
17 |
27,153,344 (GRCm39) |
critical splice donor site |
probably null |
|
R0815:Phf1
|
UTSW |
17 |
27,156,114 (GRCm39) |
unclassified |
probably benign |
|
R0863:Phf1
|
UTSW |
17 |
27,156,114 (GRCm39) |
unclassified |
probably benign |
|
R1028:Phf1
|
UTSW |
17 |
27,153,307 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1083:Phf1
|
UTSW |
17 |
27,156,244 (GRCm39) |
unclassified |
probably benign |
|
R1537:Phf1
|
UTSW |
17 |
27,154,372 (GRCm39) |
critical splice donor site |
probably null |
|
R1587:Phf1
|
UTSW |
17 |
27,156,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R1656:Phf1
|
UTSW |
17 |
27,156,333 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1956:Phf1
|
UTSW |
17 |
27,154,719 (GRCm39) |
splice site |
probably null |
|
R2566:Phf1
|
UTSW |
17 |
27,156,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R3196:Phf1
|
UTSW |
17 |
27,153,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4223:Phf1
|
UTSW |
17 |
27,156,474 (GRCm39) |
nonsense |
probably null |
|
R4835:Phf1
|
UTSW |
17 |
27,153,652 (GRCm39) |
missense |
probably benign |
|
R6439:Phf1
|
UTSW |
17 |
27,155,586 (GRCm39) |
missense |
probably benign |
|
R7070:Phf1
|
UTSW |
17 |
27,153,307 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7289:Phf1
|
UTSW |
17 |
27,154,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Phf1
|
UTSW |
17 |
27,154,291 (GRCm39) |
nonsense |
probably null |
|
R8165:Phf1
|
UTSW |
17 |
27,156,044 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9645:Phf1
|
UTSW |
17 |
27,154,130 (GRCm39) |
critical splice donor site |
probably null |
|
X0028:Phf1
|
UTSW |
17 |
27,155,162 (GRCm39) |
missense |
possibly damaging |
0.95 |
|