Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
A |
G |
5: 99,382,435 (GRCm39) |
L271P |
probably benign |
Het |
Adamts3 |
A |
C |
5: 89,923,280 (GRCm39) |
D175E |
probably benign |
Het |
Adcy4 |
T |
C |
14: 56,008,929 (GRCm39) |
T833A |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,750,958 (GRCm39) |
I508F |
probably damaging |
Het |
Arhgap9 |
G |
T |
10: 127,163,593 (GRCm39) |
V464L |
probably damaging |
Het |
Atp10a |
T |
A |
7: 58,474,182 (GRCm39) |
D1156E |
probably damaging |
Het |
Atp2a1 |
A |
T |
7: 126,049,314 (GRCm39) |
M576K |
probably benign |
Het |
Atrx |
T |
C |
X: 104,891,235 (GRCm39) |
Q1536R |
probably damaging |
Het |
Ccdc141 |
A |
C |
2: 76,842,015 (GRCm39) |
V1472G |
possibly damaging |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Celsr1 |
G |
T |
15: 85,916,886 (GRCm39) |
N362K |
probably damaging |
Het |
Cep290 |
G |
A |
10: 100,352,058 (GRCm39) |
A755T |
probably benign |
Het |
Cfap70 |
T |
A |
14: 20,445,067 (GRCm39) |
E1071V |
probably damaging |
Het |
Cps1 |
T |
C |
1: 67,248,801 (GRCm39) |
V1176A |
probably damaging |
Het |
Csn1s2a |
G |
A |
5: 87,926,052 (GRCm39) |
V43M |
probably damaging |
Het |
Cyp26b1 |
T |
C |
6: 84,561,254 (GRCm39) |
D136G |
probably benign |
Het |
Cyp7b1 |
A |
G |
3: 18,151,616 (GRCm39) |
L199P |
probably benign |
Het |
Dapk1 |
C |
T |
13: 60,867,468 (GRCm39) |
T225I |
probably damaging |
Het |
Dio2 |
T |
A |
12: 90,696,680 (GRCm39) |
T103S |
probably benign |
Het |
Dipk1a |
C |
A |
5: 108,057,713 (GRCm39) |
V237F |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,304,974 (GRCm39) |
S339T |
probably benign |
Het |
Drc1 |
A |
G |
5: 30,523,841 (GRCm39) |
N737D |
probably damaging |
Het |
Efhc1 |
C |
T |
1: 21,049,762 (GRCm39) |
P541S |
probably benign |
Het |
Elmo2 |
A |
T |
2: 165,134,077 (GRCm39) |
I637N |
probably damaging |
Het |
Eps15 |
T |
A |
4: 109,240,034 (GRCm39) |
D492E |
probably damaging |
Het |
Ermn |
G |
T |
2: 57,938,249 (GRCm39) |
N121K |
probably benign |
Het |
F5 |
A |
G |
1: 164,021,100 (GRCm39) |
T1192A |
possibly damaging |
Het |
Fbxo22 |
T |
C |
9: 55,130,771 (GRCm39) |
F347L |
probably benign |
Het |
Fbxw15 |
G |
A |
9: 109,387,314 (GRCm39) |
S227F |
probably damaging |
Het |
Foxj3 |
A |
G |
4: 119,476,548 (GRCm39) |
N242S |
probably benign |
Het |
Gjb3 |
G |
A |
4: 127,220,224 (GRCm39) |
R103W |
probably damaging |
Het |
Grm4 |
A |
G |
17: 27,691,914 (GRCm39) |
V235A |
probably damaging |
Het |
Gstm4 |
T |
C |
3: 107,950,874 (GRCm39) |
N74S |
probably damaging |
Het |
Gtf3c3 |
A |
G |
1: 54,459,583 (GRCm39) |
V393A |
possibly damaging |
Het |
Hltf |
T |
A |
3: 20,159,855 (GRCm39) |
L702H |
probably damaging |
Het |
Inpp4a |
T |
A |
1: 37,432,059 (GRCm39) |
V153E |
possibly damaging |
Het |
Kmt5c |
T |
C |
7: 4,745,729 (GRCm39) |
|
probably null |
Het |
Kynu |
A |
G |
2: 43,494,169 (GRCm39) |
R201G |
possibly damaging |
Het |
Lrp2 |
T |
A |
2: 69,333,874 (GRCm39) |
T1456S |
probably benign |
Het |
Lrrc40 |
G |
A |
3: 157,742,441 (GRCm39) |
V19I |
probably benign |
Het |
M1ap |
T |
A |
6: 82,982,491 (GRCm39) |
C258* |
probably null |
Het |
Man2a1 |
T |
C |
17: 65,059,452 (GRCm39) |
L1113P |
probably benign |
Het |
Man2a1 |
C |
T |
17: 64,976,492 (GRCm39) |
R427W |
probably damaging |
Het |
Meikin |
C |
A |
11: 54,308,613 (GRCm39) |
Q404K |
probably benign |
Het |
Mfsd4a |
T |
C |
1: 131,981,334 (GRCm39) |
I222V |
possibly damaging |
Het |
N4bp2 |
A |
G |
5: 65,964,168 (GRCm39) |
N739S |
possibly damaging |
Het |
Ncoa2 |
A |
T |
1: 13,232,517 (GRCm39) |
|
probably null |
Het |
Nisch |
G |
T |
14: 30,899,228 (GRCm39) |
|
probably benign |
Het |
Nmur2 |
A |
G |
11: 55,920,447 (GRCm39) |
V266A |
probably damaging |
Het |
Npcd |
G |
A |
15: 79,712,987 (GRCm39) |
R147C |
probably damaging |
Het |
Or4q3 |
T |
A |
14: 50,583,537 (GRCm39) |
M121L |
probably benign |
Het |
Or5ac25 |
T |
A |
16: 59,182,243 (GRCm39) |
I113F |
probably benign |
Het |
Pals2 |
T |
A |
6: 50,173,525 (GRCm39) |
M463K |
probably damaging |
Het |
Parp4 |
A |
T |
14: 56,885,589 (GRCm39) |
H1556L |
unknown |
Het |
Pcdh9 |
G |
T |
14: 94,126,107 (GRCm39) |
A21E |
probably benign |
Het |
Phtf1 |
A |
G |
3: 103,903,958 (GRCm39) |
E436G |
probably benign |
Het |
Piezo2 |
C |
A |
18: 63,165,911 (GRCm39) |
|
probably null |
Het |
Piezo2 |
T |
C |
18: 63,241,158 (GRCm39) |
Y690C |
probably damaging |
Het |
Pla2g4f |
T |
C |
2: 120,141,549 (GRCm39) |
R183G |
possibly damaging |
Het |
Plxnd1 |
T |
C |
6: 115,971,018 (GRCm39) |
D250G |
probably damaging |
Het |
Ppig |
A |
G |
2: 69,579,744 (GRCm39) |
D426G |
unknown |
Het |
Ppp3cb |
T |
C |
14: 20,574,540 (GRCm39) |
E185G |
possibly damaging |
Het |
Qsox1 |
A |
T |
1: 155,670,364 (GRCm39) |
M151K |
probably null |
Het |
Ralgapa2 |
T |
C |
2: 146,184,648 (GRCm39) |
E1453G |
probably benign |
Het |
Rnf167 |
G |
A |
11: 70,540,838 (GRCm39) |
V191I |
probably benign |
Het |
Rp1 |
T |
C |
1: 4,419,055 (GRCm39) |
K686E |
possibly damaging |
Het |
Ryr1 |
T |
G |
7: 28,767,046 (GRCm39) |
Q2979P |
probably damaging |
Het |
Scaf1 |
T |
A |
7: 44,657,443 (GRCm39) |
I479F |
probably damaging |
Het |
Septin8 |
A |
G |
11: 53,425,310 (GRCm39) |
T68A |
probably benign |
Het |
Sh3rf1 |
A |
T |
8: 61,825,661 (GRCm39) |
N552I |
probably damaging |
Het |
Shoc1 |
A |
T |
4: 59,099,383 (GRCm39) |
V103D |
possibly damaging |
Het |
Slc1a3 |
A |
G |
15: 8,717,888 (GRCm39) |
L68P |
probably damaging |
Het |
Slc39a6 |
G |
A |
18: 24,718,524 (GRCm39) |
P511L |
probably benign |
Het |
Slc9c1 |
A |
G |
16: 45,374,652 (GRCm39) |
Y339C |
probably damaging |
Het |
Smarcal1 |
G |
T |
1: 72,625,120 (GRCm39) |
C89F |
probably damaging |
Het |
Smu1 |
A |
T |
4: 40,745,537 (GRCm39) |
M261K |
probably damaging |
Het |
Spag8 |
T |
G |
4: 43,653,087 (GRCm39) |
|
probably benign |
Het |
Spag8 |
T |
C |
4: 43,653,345 (GRCm39) |
|
probably benign |
Het |
Spata31d1a |
T |
C |
13: 59,851,216 (GRCm39) |
D304G |
probably benign |
Het |
Spdl1 |
A |
T |
11: 34,711,856 (GRCm39) |
L298* |
probably null |
Het |
Stac2 |
C |
T |
11: 97,930,444 (GRCm39) |
|
probably null |
Het |
Stag1 |
A |
G |
9: 100,835,515 (GRCm39) |
|
probably null |
Het |
Stpg2 |
C |
T |
3: 139,125,542 (GRCm39) |
P445L |
probably damaging |
Het |
Sult2a8 |
A |
T |
7: 14,157,451 (GRCm39) |
V128E |
probably damaging |
Het |
Synm |
A |
G |
7: 67,385,707 (GRCm39) |
F210L |
probably damaging |
Het |
Tbck |
C |
G |
3: 132,480,263 (GRCm39) |
A714G |
probably benign |
Het |
Tcerg1 |
A |
T |
18: 42,694,012 (GRCm39) |
Y711F |
possibly damaging |
Het |
Tnfrsf25 |
A |
G |
4: 152,201,465 (GRCm39) |
T98A |
probably benign |
Het |
Togaram2 |
T |
C |
17: 71,998,450 (GRCm39) |
S218P |
probably damaging |
Het |
Tpp1 |
A |
T |
7: 105,399,515 (GRCm39) |
D84E |
probably benign |
Het |
Trim30d |
G |
T |
7: 104,132,682 (GRCm39) |
Q202K |
probably damaging |
Het |
Trim37 |
T |
A |
11: 87,068,845 (GRCm39) |
V397E |
probably damaging |
Het |
Triml1 |
A |
T |
8: 43,583,512 (GRCm39) |
I363N |
probably damaging |
Het |
Trpm6 |
T |
A |
19: 18,869,363 (GRCm39) |
|
probably null |
Het |
Tsc2 |
T |
C |
17: 24,823,382 (GRCm39) |
S1055G |
probably benign |
Het |
Ubr5 |
T |
C |
15: 37,989,621 (GRCm39) |
D2065G |
probably damaging |
Het |
Uggt2 |
G |
T |
14: 119,269,688 (GRCm39) |
P948Q |
probably benign |
Het |
Vps13c |
A |
T |
9: 67,851,399 (GRCm39) |
S2345C |
probably damaging |
Het |
Wtap |
G |
T |
17: 13,199,771 (GRCm39) |
R48S |
possibly damaging |
Het |
Zbtb38 |
A |
G |
9: 96,570,934 (GRCm39) |
V50A |
probably damaging |
Het |
Zcchc2 |
T |
A |
1: 105,958,017 (GRCm39) |
S829R |
probably benign |
Het |
Zfp385b |
T |
C |
2: 77,246,316 (GRCm39) |
D237G |
probably benign |
Het |
|
Other mutations in Csf2rb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00585:Csf2rb2
|
APN |
15 |
78,169,047 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00765:Csf2rb2
|
APN |
15 |
78,176,916 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01383:Csf2rb2
|
APN |
15 |
78,181,243 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01975:Csf2rb2
|
APN |
15 |
78,173,086 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02330:Csf2rb2
|
APN |
15 |
78,169,328 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02365:Csf2rb2
|
APN |
15 |
78,171,260 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02756:Csf2rb2
|
APN |
15 |
78,169,049 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0269:Csf2rb2
|
UTSW |
15 |
78,173,065 (GRCm39) |
missense |
probably benign |
0.09 |
R0462:Csf2rb2
|
UTSW |
15 |
78,169,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R0540:Csf2rb2
|
UTSW |
15 |
78,172,108 (GRCm39) |
missense |
probably benign |
0.00 |
R0607:Csf2rb2
|
UTSW |
15 |
78,172,108 (GRCm39) |
missense |
probably benign |
0.00 |
R0636:Csf2rb2
|
UTSW |
15 |
78,176,160 (GRCm39) |
nonsense |
probably null |
|
R0782:Csf2rb2
|
UTSW |
15 |
78,170,951 (GRCm39) |
missense |
probably damaging |
0.98 |
R1387:Csf2rb2
|
UTSW |
15 |
78,182,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R1881:Csf2rb2
|
UTSW |
15 |
78,176,735 (GRCm39) |
splice site |
probably null |
|
R2079:Csf2rb2
|
UTSW |
15 |
78,172,207 (GRCm39) |
missense |
probably benign |
0.13 |
R2108:Csf2rb2
|
UTSW |
15 |
78,176,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R2359:Csf2rb2
|
UTSW |
15 |
78,176,976 (GRCm39) |
missense |
probably benign |
0.39 |
R4614:Csf2rb2
|
UTSW |
15 |
78,175,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Csf2rb2
|
UTSW |
15 |
78,169,490 (GRCm39) |
missense |
probably benign |
0.11 |
R4900:Csf2rb2
|
UTSW |
15 |
78,170,174 (GRCm39) |
splice site |
probably null |
|
R5206:Csf2rb2
|
UTSW |
15 |
78,176,952 (GRCm39) |
missense |
probably benign |
|
R5270:Csf2rb2
|
UTSW |
15 |
78,176,182 (GRCm39) |
splice site |
probably null |
|
R5427:Csf2rb2
|
UTSW |
15 |
78,173,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R6633:Csf2rb2
|
UTSW |
15 |
78,173,152 (GRCm39) |
missense |
probably benign |
0.00 |
R7067:Csf2rb2
|
UTSW |
15 |
78,176,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Csf2rb2
|
UTSW |
15 |
78,181,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Csf2rb2
|
UTSW |
15 |
78,169,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7423:Csf2rb2
|
UTSW |
15 |
78,176,760 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7453:Csf2rb2
|
UTSW |
15 |
78,169,491 (GRCm39) |
missense |
probably benign |
0.14 |
R7705:Csf2rb2
|
UTSW |
15 |
78,168,774 (GRCm39) |
missense |
probably benign |
0.02 |
R7788:Csf2rb2
|
UTSW |
15 |
78,177,041 (GRCm39) |
missense |
probably benign |
0.12 |
R7849:Csf2rb2
|
UTSW |
15 |
78,168,621 (GRCm39) |
missense |
probably benign |
0.09 |
R7851:Csf2rb2
|
UTSW |
15 |
78,173,137 (GRCm39) |
missense |
probably benign |
0.10 |
R8057:Csf2rb2
|
UTSW |
15 |
78,169,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R8405:Csf2rb2
|
UTSW |
15 |
78,172,093 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8406:Csf2rb2
|
UTSW |
15 |
78,171,216 (GRCm39) |
missense |
probably benign |
0.00 |
R8857:Csf2rb2
|
UTSW |
15 |
78,178,613 (GRCm39) |
missense |
probably null |
0.00 |
R8972:Csf2rb2
|
UTSW |
15 |
78,172,115 (GRCm39) |
missense |
probably benign |
|
R9262:Csf2rb2
|
UTSW |
15 |
78,168,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9311:Csf2rb2
|
UTSW |
15 |
78,176,735 (GRCm39) |
splice site |
probably null |
|
R9343:Csf2rb2
|
UTSW |
15 |
78,171,287 (GRCm39) |
intron |
probably benign |
|
R9478:Csf2rb2
|
UTSW |
15 |
78,168,965 (GRCm39) |
missense |
probably benign |
0.00 |
R9713:Csf2rb2
|
UTSW |
15 |
78,176,730 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9789:Csf2rb2
|
UTSW |
15 |
78,169,196 (GRCm39) |
missense |
probably benign |
0.06 |
RF007:Csf2rb2
|
UTSW |
15 |
78,176,126 (GRCm39) |
missense |
probably benign |
0.21 |
RF009:Csf2rb2
|
UTSW |
15 |
78,176,127 (GRCm39) |
missense |
probably benign |
0.02 |
|