Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4gnt |
C |
A |
9: 99,502,613 (GRCm39) |
P258T |
probably damaging |
Het |
Adamts1 |
C |
A |
16: 85,593,579 (GRCm39) |
G719* |
probably null |
Het |
Ano5 |
G |
T |
7: 51,194,599 (GRCm39) |
D111Y |
probably damaging |
Het |
Arvcf |
T |
C |
16: 18,221,699 (GRCm39) |
V714A |
possibly damaging |
Het |
AU021092 |
T |
A |
16: 5,038,253 (GRCm39) |
S85C |
probably damaging |
Het |
Capn5 |
T |
C |
7: 97,773,195 (GRCm39) |
D603G |
probably benign |
Het |
Cbr1 |
T |
A |
16: 93,406,692 (GRCm39) |
V136E |
probably damaging |
Het |
Ccr1 |
T |
C |
9: 123,763,765 (GRCm39) |
Y255C |
probably damaging |
Het |
Cdr1 |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
X: 60,228,130 (GRCm39) |
|
probably benign |
Het |
Cep112 |
A |
G |
11: 108,410,722 (GRCm39) |
T553A |
probably benign |
Het |
Chd7 |
C |
T |
4: 8,753,101 (GRCm39) |
L533F |
unknown |
Het |
Cntnap1 |
T |
C |
11: 101,068,131 (GRCm39) |
F48L |
probably benign |
Het |
Cyb5r3 |
T |
C |
15: 83,046,064 (GRCm39) |
D84G |
probably damaging |
Het |
Ddx47 |
T |
C |
6: 134,992,803 (GRCm39) |
I154T |
probably benign |
Het |
Dennd2b |
G |
A |
7: 109,130,337 (GRCm39) |
A888V |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,185,624 (GRCm39) |
L99P |
probably benign |
Het |
Dzank1 |
A |
G |
2: 144,325,293 (GRCm39) |
I558T |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,148,421 (GRCm39) |
D2609G |
possibly damaging |
Het |
Fhl5 |
C |
A |
4: 25,211,194 (GRCm39) |
C166F |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 7,969,206 (GRCm39) |
L1553P |
probably damaging |
Het |
Frem1 |
G |
A |
4: 82,890,374 (GRCm39) |
T1035I |
probably benign |
Het |
Gm3099 |
A |
G |
14: 15,346,517 (GRCm39) |
M128V |
probably benign |
Het |
Gpaa1 |
C |
T |
15: 76,218,940 (GRCm39) |
T594I |
probably benign |
Het |
Hck |
C |
T |
2: 152,966,191 (GRCm39) |
T55M |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,471,123 (GRCm39) |
|
probably null |
Het |
Ica1l |
C |
T |
1: 60,054,995 (GRCm39) |
|
probably null |
Het |
Ilf3 |
T |
C |
9: 21,314,662 (GRCm39) |
Y765H |
unknown |
Het |
Mast4 |
G |
A |
13: 102,941,226 (GRCm39) |
T277M |
probably damaging |
Het |
Mfsd6 |
T |
C |
1: 52,748,056 (GRCm39) |
T270A |
probably benign |
Het |
Mib1 |
G |
A |
18: 10,775,541 (GRCm39) |
D498N |
probably benign |
Het |
Naaladl1 |
A |
T |
19: 6,164,663 (GRCm39) |
T576S |
possibly damaging |
Het |
Ncoa6 |
A |
T |
2: 155,247,577 (GRCm39) |
I1909N |
probably benign |
Het |
Negr1 |
A |
G |
3: 156,565,235 (GRCm39) |
D107G |
probably benign |
Het |
Nlrc4 |
A |
G |
17: 74,734,114 (GRCm39) |
M933T |
probably benign |
Het |
Nmnat3 |
T |
G |
9: 98,292,306 (GRCm39) |
F184V |
probably benign |
Het |
Or4b12 |
A |
T |
2: 90,096,639 (GRCm39) |
V45E |
probably damaging |
Het |
Or5p81 |
T |
C |
7: 108,266,743 (GRCm39) |
V40A |
possibly damaging |
Het |
Or6c76 |
C |
T |
10: 129,612,142 (GRCm39) |
R120C |
probably benign |
Het |
Or7a42 |
C |
A |
10: 78,791,676 (GRCm39) |
F212L |
probably benign |
Het |
Pfkfb4 |
T |
C |
9: 108,828,222 (GRCm39) |
Y86H |
probably benign |
Het |
Pgm5 |
T |
G |
19: 24,801,693 (GRCm39) |
Q178H |
probably damaging |
Het |
Phrf1 |
C |
T |
7: 140,838,725 (GRCm39) |
T640M |
unknown |
Het |
Pramel34 |
A |
C |
5: 93,784,147 (GRCm39) |
L439R |
probably damaging |
Het |
Psg18 |
T |
G |
7: 18,083,241 (GRCm39) |
T305P |
probably benign |
Het |
Skil |
T |
A |
3: 31,152,381 (GRCm39) |
V301D |
probably damaging |
Het |
Slc36a1 |
C |
A |
11: 55,109,895 (GRCm39) |
P68T |
probably damaging |
Het |
Smim6 |
T |
C |
11: 115,804,371 (GRCm39) |
F53L |
probably benign |
Het |
Tpgs2 |
G |
A |
18: 25,301,652 (GRCm39) |
T5M |
possibly damaging |
Het |
Trrap |
T |
A |
5: 144,765,410 (GRCm39) |
V2523D |
probably benign |
Het |
Usp9y |
A |
T |
Y: 1,432,197 (GRCm39) |
D429E |
probably damaging |
Het |
Vmn1r125 |
A |
G |
7: 21,006,818 (GRCm39) |
T239A |
probably benign |
Het |
Vmn1r168 |
T |
C |
7: 23,240,421 (GRCm39) |
F93L |
probably damaging |
Het |
Vmn1r88 |
A |
G |
7: 12,912,403 (GRCm39) |
N253S |
possibly damaging |
Het |
Zfp644 |
C |
T |
5: 106,784,343 (GRCm39) |
A735T |
probably damaging |
Het |
|
Other mutations in Ccdc27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4472001:Ccdc27
|
UTSW |
4 |
154,126,184 (GRCm39) |
missense |
unknown |
|
R0078:Ccdc27
|
UTSW |
4 |
154,120,195 (GRCm39) |
splice site |
probably benign |
|
R0883:Ccdc27
|
UTSW |
4 |
154,120,941 (GRCm39) |
missense |
unknown |
|
R1389:Ccdc27
|
UTSW |
4 |
154,126,226 (GRCm39) |
missense |
unknown |
|
R1773:Ccdc27
|
UTSW |
4 |
154,126,222 (GRCm39) |
missense |
unknown |
|
R1869:Ccdc27
|
UTSW |
4 |
154,111,220 (GRCm39) |
splice site |
probably null |
|
R2020:Ccdc27
|
UTSW |
4 |
154,117,770 (GRCm39) |
missense |
probably null |
0.05 |
R2070:Ccdc27
|
UTSW |
4 |
154,126,270 (GRCm39) |
missense |
unknown |
|
R2131:Ccdc27
|
UTSW |
4 |
154,120,763 (GRCm39) |
small deletion |
probably benign |
|
R3825:Ccdc27
|
UTSW |
4 |
154,120,742 (GRCm39) |
missense |
unknown |
|
R4183:Ccdc27
|
UTSW |
4 |
154,120,763 (GRCm39) |
small deletion |
probably benign |
|
R4254:Ccdc27
|
UTSW |
4 |
154,123,976 (GRCm39) |
missense |
unknown |
|
R5932:Ccdc27
|
UTSW |
4 |
154,111,231 (GRCm39) |
missense |
probably benign |
0.22 |
R6269:Ccdc27
|
UTSW |
4 |
154,122,179 (GRCm39) |
missense |
unknown |
|
R6324:Ccdc27
|
UTSW |
4 |
154,120,648 (GRCm39) |
missense |
probably benign |
0.02 |
R6761:Ccdc27
|
UTSW |
4 |
154,122,155 (GRCm39) |
missense |
unknown |
|
R7090:Ccdc27
|
UTSW |
4 |
154,112,523 (GRCm39) |
missense |
probably benign |
0.03 |
R7163:Ccdc27
|
UTSW |
4 |
154,117,282 (GRCm39) |
missense |
not run |
|
R7488:Ccdc27
|
UTSW |
4 |
154,117,424 (GRCm39) |
missense |
probably benign |
0.22 |
R7555:Ccdc27
|
UTSW |
4 |
154,126,274 (GRCm39) |
missense |
unknown |
|
R7651:Ccdc27
|
UTSW |
4 |
154,112,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7826:Ccdc27
|
UTSW |
4 |
154,123,958 (GRCm39) |
critical splice donor site |
probably null |
|
R8250:Ccdc27
|
UTSW |
4 |
154,126,245 (GRCm39) |
missense |
unknown |
|
R8815:Ccdc27
|
UTSW |
4 |
154,111,205 (GRCm39) |
missense |
probably benign |
0.02 |
R8835:Ccdc27
|
UTSW |
4 |
154,127,023 (GRCm39) |
missense |
unknown |
|
R9019:Ccdc27
|
UTSW |
4 |
154,124,014 (GRCm39) |
missense |
unknown |
|
R9224:Ccdc27
|
UTSW |
4 |
154,122,174 (GRCm39) |
missense |
unknown |
|
R9252:Ccdc27
|
UTSW |
4 |
154,125,507 (GRCm39) |
missense |
unknown |
|
R9267:Ccdc27
|
UTSW |
4 |
154,117,441 (GRCm39) |
missense |
probably damaging |
1.00 |
RF016:Ccdc27
|
UTSW |
4 |
154,120,567 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Ccdc27
|
UTSW |
4 |
154,120,928 (GRCm39) |
missense |
unknown |
|
|