Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c18 |
T |
C |
13: 4,195,213 (GRCm39) |
T82A |
possibly damaging |
Het |
Alx1 |
A |
G |
10: 102,864,353 (GRCm39) |
S39P |
possibly damaging |
Het |
Atr |
A |
G |
9: 95,802,408 (GRCm39) |
T1767A |
probably benign |
Het |
Brf1 |
A |
T |
12: 112,924,728 (GRCm39) |
|
probably null |
Het |
Cd86 |
A |
G |
16: 36,438,686 (GRCm39) |
|
probably null |
Het |
Cdan1 |
A |
G |
2: 120,549,620 (GRCm39) |
|
probably null |
Het |
Cntln |
A |
G |
4: 84,892,228 (GRCm39) |
D371G |
probably damaging |
Het |
Cypt4 |
A |
G |
9: 24,536,515 (GRCm39) |
T2A |
possibly damaging |
Het |
Dll1 |
G |
T |
17: 15,593,817 (GRCm39) |
Y183* |
probably null |
Het |
Dnmt1 |
G |
T |
9: 20,819,814 (GRCm39) |
P1444Q |
probably damaging |
Het |
Ern2 |
A |
G |
7: 121,776,993 (GRCm39) |
L309P |
probably damaging |
Het |
Fam151a |
A |
G |
4: 106,599,491 (GRCm39) |
K142E |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,156,591 (GRCm39) |
E2378G |
probably damaging |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Kdm5b |
A |
C |
1: 134,558,288 (GRCm39) |
T1432P |
possibly damaging |
Het |
Kif2a |
G |
A |
13: 107,130,423 (GRCm39) |
S15F |
probably damaging |
Het |
Lzic |
A |
G |
4: 149,571,308 (GRCm39) |
E31G |
probably damaging |
Het |
Mmp16 |
A |
G |
4: 18,112,021 (GRCm39) |
M466V |
probably benign |
Het |
Mtm1 |
T |
C |
X: 70,330,837 (GRCm39) |
V203A |
probably benign |
Het |
Muc21 |
T |
A |
17: 35,932,489 (GRCm39) |
|
probably benign |
Het |
Neurl4 |
A |
G |
11: 69,794,702 (GRCm39) |
M249V |
probably benign |
Het |
Or6c76b |
T |
C |
10: 129,692,759 (GRCm39) |
I124T |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,326,794 (GRCm39) |
Y243H |
probably damaging |
Het |
Rbm44 |
A |
G |
1: 91,080,481 (GRCm39) |
N223S |
probably damaging |
Het |
Sel1l3 |
G |
T |
5: 53,357,559 (GRCm39) |
H144Q |
possibly damaging |
Het |
Simc1 |
A |
ANNNNNNNNNNNNNNNNNNNNN |
13: 54,673,060 (GRCm39) |
|
probably benign |
Het |
Snrpb2 |
A |
G |
2: 142,907,086 (GRCm39) |
|
probably benign |
Het |
Spata31d1d |
T |
G |
13: 59,873,838 (GRCm39) |
K1232N |
possibly damaging |
Het |
Spink5 |
A |
T |
18: 44,123,749 (GRCm39) |
E345D |
possibly damaging |
Het |
Sucla2 |
C |
T |
14: 73,798,074 (GRCm39) |
|
probably benign |
Het |
Tarbp1 |
T |
C |
8: 127,175,069 (GRCm39) |
D789G |
probably benign |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tmem232 |
T |
C |
17: 65,757,401 (GRCm39) |
N264S |
possibly damaging |
Het |
Trim43b |
G |
C |
9: 88,967,725 (GRCm39) |
L303V |
possibly damaging |
Het |
Tulp2 |
C |
A |
7: 45,168,145 (GRCm39) |
R298S |
probably benign |
Het |
Usp42 |
A |
G |
5: 143,703,088 (GRCm39) |
V511A |
probably damaging |
Het |
Vav1 |
A |
T |
17: 57,608,214 (GRCm39) |
T321S |
probably benign |
Het |
Vmn1r169 |
A |
C |
7: 23,277,247 (GRCm39) |
H213P |
probably damaging |
Het |
Vmn1r170 |
C |
T |
7: 23,305,787 (GRCm39) |
T63I |
probably benign |
Het |
Vmn2r103 |
T |
G |
17: 20,014,509 (GRCm39) |
W434G |
probably damaging |
Het |
Zfp407 |
C |
T |
18: 84,577,898 (GRCm39) |
A1072T |
probably benign |
Het |
Zfp7 |
T |
C |
15: 76,774,908 (GRCm39) |
S317P |
probably damaging |
Het |
|
Other mutations in 1700001K19Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4304:1700001K19Rik
|
UTSW |
12 |
110,634,884 (GRCm39) |
unclassified |
probably benign |
|
FR4304:1700001K19Rik
|
UTSW |
12 |
110,634,883 (GRCm39) |
unclassified |
probably benign |
|
FR4548:1700001K19Rik
|
UTSW |
12 |
110,634,886 (GRCm39) |
unclassified |
probably benign |
|
FR4548:1700001K19Rik
|
UTSW |
12 |
110,634,883 (GRCm39) |
unclassified |
probably benign |
|
FR4737:1700001K19Rik
|
UTSW |
12 |
110,634,882 (GRCm39) |
unclassified |
probably benign |
|
FR4976:1700001K19Rik
|
UTSW |
12 |
110,634,884 (GRCm39) |
unclassified |
probably benign |
|
FR4976:1700001K19Rik
|
UTSW |
12 |
110,634,881 (GRCm39) |
unclassified |
probably benign |
|
R0266:1700001K19Rik
|
UTSW |
12 |
110,635,188 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1859:1700001K19Rik
|
UTSW |
12 |
110,637,268 (GRCm39) |
start gained |
probably benign |
|
R7020:1700001K19Rik
|
UTSW |
12 |
110,634,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R7225:1700001K19Rik
|
UTSW |
12 |
110,637,299 (GRCm39) |
splice site |
probably benign |
|
R7311:1700001K19Rik
|
UTSW |
12 |
110,635,184 (GRCm39) |
missense |
probably benign |
|
R8410:1700001K19Rik
|
UTSW |
12 |
110,635,145 (GRCm39) |
missense |
probably benign |
0.21 |
R9001:1700001K19Rik
|
UTSW |
12 |
110,637,176 (GRCm39) |
missense |
probably damaging |
1.00 |
RF022:1700001K19Rik
|
UTSW |
12 |
110,634,877 (GRCm39) |
nonsense |
probably null |
|
|