Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy10 |
A |
G |
1: 165,342,875 (GRCm39) |
N247S |
probably benign |
Het |
Ago3 |
T |
C |
4: 126,248,862 (GRCm39) |
|
probably null |
Het |
Aldh16a1 |
A |
G |
7: 44,797,223 (GRCm39) |
V168A |
probably damaging |
Het |
Aqp7 |
G |
A |
4: 41,035,510 (GRCm39) |
T115I |
probably benign |
Het |
Arhgap26 |
T |
A |
18: 39,254,945 (GRCm39) |
V274E |
probably damaging |
Het |
Clec4d |
T |
C |
6: 123,245,104 (GRCm39) |
|
probably null |
Het |
Dennd4b |
T |
C |
3: 90,185,090 (GRCm39) |
Y1166H |
probably damaging |
Het |
Egln3 |
T |
C |
12: 54,227,447 (GRCm39) |
|
probably null |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Fhad1 |
T |
A |
4: 141,690,768 (GRCm39) |
M434L |
probably benign |
Het |
Gfm1 |
T |
G |
3: 67,342,955 (GRCm39) |
M163R |
probably damaging |
Het |
Isg15 |
A |
T |
4: 156,284,279 (GRCm39) |
L83Q |
probably damaging |
Het |
Ly9 |
GCCTTTGGGGGACAATTCC |
GCC |
1: 171,432,755 (GRCm39) |
|
probably null |
Het |
Med1 |
G |
T |
11: 98,047,206 (GRCm39) |
|
probably benign |
Het |
Mrc2 |
T |
A |
11: 105,227,468 (GRCm39) |
V567D |
probably damaging |
Het |
Nnmt |
G |
T |
9: 48,514,780 (GRCm39) |
T79K |
probably benign |
Het |
Opn1sw |
G |
A |
6: 29,379,840 (GRCm39) |
|
probably benign |
Het |
Optc |
G |
T |
1: 133,828,714 (GRCm39) |
|
probably benign |
Het |
Pcdh17 |
C |
T |
14: 84,685,980 (GRCm39) |
P816S |
probably benign |
Het |
Pcdhb15 |
T |
C |
18: 37,607,502 (GRCm39) |
S245P |
probably benign |
Het |
Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
Sacs |
T |
C |
14: 61,445,288 (GRCm39) |
F2445L |
probably benign |
Het |
Sel1l |
T |
C |
12: 91,778,652 (GRCm39) |
N721S |
probably benign |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Slc7a11 |
C |
G |
3: 50,326,780 (GRCm39) |
V494L |
probably benign |
Het |
Sulf2 |
C |
A |
2: 165,923,426 (GRCm39) |
A598S |
probably benign |
Het |
Tph2 |
A |
T |
10: 115,020,732 (GRCm39) |
D21E |
probably damaging |
Het |
Trf |
T |
C |
9: 103,103,324 (GRCm39) |
Y110C |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,628,202 (GRCm39) |
E14653K |
possibly damaging |
Het |
Vmn2r18 |
A |
G |
5: 151,485,724 (GRCm39) |
I590T |
possibly damaging |
Het |
Zfp607b |
G |
T |
7: 27,402,889 (GRCm39) |
K448N |
probably benign |
Het |
Zfp689 |
T |
C |
7: 127,048,071 (GRCm39) |
|
probably benign |
Het |
Zfp709 |
C |
T |
8: 72,643,999 (GRCm39) |
P476L |
probably damaging |
Het |
|
Other mutations in 1700128F08Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0472:1700128F08Rik
|
UTSW |
9 |
8,222,123 (GRCm39) |
exon |
noncoding transcript |
|
R1114:1700128F08Rik
|
UTSW |
9 |
8,222,179 (GRCm39) |
exon |
noncoding transcript |
|
R4732:1700128F08Rik
|
UTSW |
9 |
8,222,174 (GRCm39) |
exon |
noncoding transcript |
|
R4733:1700128F08Rik
|
UTSW |
9 |
8,222,174 (GRCm39) |
exon |
noncoding transcript |
|
R4970:1700128F08Rik
|
UTSW |
9 |
8,222,066 (GRCm39) |
exon |
noncoding transcript |
|
R5699:1700128F08Rik
|
UTSW |
9 |
8,225,320 (GRCm39) |
unclassified |
noncoding transcript |
|
|