Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
C |
T |
4: 53,059,245 (GRCm39) |
|
probably benign |
Het |
Acr |
T |
A |
15: 89,458,535 (GRCm39) |
H405Q |
probably benign |
Het |
Adad1 |
T |
C |
3: 37,137,322 (GRCm39) |
|
probably benign |
Het |
Alox5ap |
T |
C |
5: 149,216,069 (GRCm39) |
|
probably benign |
Het |
Ank2 |
T |
C |
3: 126,730,280 (GRCm39) |
D3568G |
probably damaging |
Het |
Atl3 |
T |
G |
19: 7,506,388 (GRCm39) |
I306S |
probably damaging |
Het |
Atr |
T |
A |
9: 95,809,409 (GRCm39) |
|
probably benign |
Het |
Ccnb2 |
A |
G |
9: 70,326,335 (GRCm39) |
V34A |
probably benign |
Het |
Cdh12 |
A |
C |
15: 21,537,763 (GRCm39) |
|
probably benign |
Het |
Cib1 |
C |
T |
7: 79,880,126 (GRCm39) |
V45M |
probably benign |
Het |
Col6a6 |
T |
C |
9: 105,657,896 (GRCm39) |
E772G |
possibly damaging |
Het |
Dmxl1 |
C |
A |
18: 49,997,102 (GRCm39) |
T466K |
probably benign |
Het |
Dym |
T |
C |
18: 75,258,610 (GRCm39) |
|
probably null |
Het |
Enpp3 |
A |
C |
10: 24,650,722 (GRCm39) |
F805V |
probably damaging |
Het |
Eya1 |
T |
C |
1: 14,254,713 (GRCm39) |
D373G |
probably damaging |
Het |
Gpr179 |
C |
T |
11: 97,225,757 (GRCm39) |
V2133I |
probably benign |
Het |
Grb10 |
G |
T |
11: 11,886,798 (GRCm39) |
H435Q |
probably damaging |
Het |
Gzmm |
T |
C |
10: 79,530,399 (GRCm39) |
I190T |
probably benign |
Het |
Helt |
T |
C |
8: 46,745,433 (GRCm39) |
Y150C |
probably damaging |
Het |
Il17ra |
T |
C |
6: 120,449,086 (GRCm39) |
|
probably benign |
Het |
Inhbc |
A |
G |
10: 127,193,302 (GRCm39) |
I238T |
probably benign |
Het |
Itgb3 |
A |
G |
11: 104,557,966 (GRCm39) |
T787A |
possibly damaging |
Het |
Jakmip2 |
T |
G |
18: 43,685,210 (GRCm39) |
|
probably benign |
Het |
Krt4 |
T |
G |
15: 101,831,187 (GRCm39) |
|
probably benign |
Het |
Lgsn |
C |
T |
1: 31,229,534 (GRCm39) |
T85I |
probably benign |
Het |
Metap1 |
C |
T |
3: 138,177,918 (GRCm39) |
V217I |
probably benign |
Het |
Mib2 |
A |
T |
4: 155,743,897 (GRCm39) |
C48* |
probably null |
Het |
Mroh4 |
T |
A |
15: 74,482,154 (GRCm39) |
I768F |
probably damaging |
Het |
Npas3 |
T |
A |
12: 54,095,624 (GRCm39) |
D361E |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,943,411 (GRCm39) |
L4246P |
probably damaging |
Het |
Or4a78 |
A |
C |
2: 89,497,798 (GRCm39) |
V144G |
probably benign |
Het |
Or7e169 |
A |
G |
9: 19,757,075 (GRCm39) |
M280T |
probably benign |
Het |
Or8h7 |
A |
G |
2: 86,720,835 (GRCm39) |
I228T |
probably damaging |
Het |
P4hb |
G |
A |
11: 120,459,092 (GRCm39) |
R134C |
probably damaging |
Het |
Plcb3 |
T |
C |
19: 6,943,788 (GRCm39) |
D71G |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,150,305 (GRCm39) |
V159E |
probably damaging |
Het |
Prpsap1 |
T |
A |
11: 116,370,482 (GRCm39) |
K158N |
probably benign |
Het |
Prr35 |
C |
A |
17: 26,166,956 (GRCm39) |
E194* |
probably null |
Het |
Ptger1 |
G |
T |
8: 84,394,795 (GRCm39) |
V91L |
probably benign |
Het |
Rdh10 |
T |
C |
1: 16,178,260 (GRCm39) |
|
probably benign |
Het |
Rgs9bp |
C |
A |
7: 35,284,458 (GRCm39) |
R63L |
probably damaging |
Het |
Slc13a5 |
A |
T |
11: 72,149,940 (GRCm39) |
V173E |
probably benign |
Het |
Spata31 |
A |
T |
13: 65,070,377 (GRCm39) |
I842L |
probably benign |
Het |
Stk32b |
A |
C |
5: 37,874,092 (GRCm39) |
D13E |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,123,192 (GRCm39) |
D708G |
possibly damaging |
Het |
Taar6 |
T |
C |
10: 23,861,021 (GRCm39) |
D175G |
probably benign |
Het |
Thbs1 |
A |
C |
2: 117,953,358 (GRCm39) |
D925A |
probably damaging |
Het |
Tnr |
A |
T |
1: 159,714,595 (GRCm39) |
T825S |
probably benign |
Het |
Ttc23l |
A |
C |
15: 10,551,627 (GRCm39) |
L33W |
probably damaging |
Het |
Ttc39d |
T |
C |
17: 80,523,379 (GRCm39) |
Y13H |
probably benign |
Het |
Vmn2r102 |
C |
A |
17: 19,880,851 (GRCm39) |
P64Q |
probably damaging |
Het |
Vps11 |
G |
T |
9: 44,267,588 (GRCm39) |
Y341* |
probably null |
Het |
Vsig8 |
T |
C |
1: 172,387,925 (GRCm39) |
V5A |
possibly damaging |
Het |
Vwce |
C |
T |
19: 10,624,177 (GRCm39) |
A356V |
probably benign |
Het |
|
Other mutations in Hrg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01150:Hrg
|
APN |
16 |
22,777,909 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02795:Hrg
|
APN |
16 |
22,776,303 (GRCm39) |
unclassified |
probably benign |
|
R0184:Hrg
|
UTSW |
16 |
22,772,521 (GRCm39) |
critical splice donor site |
probably null |
|
R1147:Hrg
|
UTSW |
16 |
22,779,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R1147:Hrg
|
UTSW |
16 |
22,779,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R1733:Hrg
|
UTSW |
16 |
22,769,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R1828:Hrg
|
UTSW |
16 |
22,774,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Hrg
|
UTSW |
16 |
22,773,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Hrg
|
UTSW |
16 |
22,774,949 (GRCm39) |
missense |
probably benign |
0.09 |
R2281:Hrg
|
UTSW |
16 |
22,780,059 (GRCm39) |
unclassified |
probably benign |
|
R2447:Hrg
|
UTSW |
16 |
22,779,898 (GRCm39) |
unclassified |
probably benign |
|
R3962:Hrg
|
UTSW |
16 |
22,774,825 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3963:Hrg
|
UTSW |
16 |
22,774,825 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4571:Hrg
|
UTSW |
16 |
22,779,972 (GRCm39) |
unclassified |
probably benign |
|
R4903:Hrg
|
UTSW |
16 |
22,779,901 (GRCm39) |
unclassified |
probably benign |
|
R4904:Hrg
|
UTSW |
16 |
22,770,000 (GRCm39) |
missense |
probably benign |
0.03 |
R5236:Hrg
|
UTSW |
16 |
22,780,263 (GRCm39) |
unclassified |
probably benign |
|
R6020:Hrg
|
UTSW |
16 |
22,773,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R6054:Hrg
|
UTSW |
16 |
22,772,412 (GRCm39) |
missense |
probably benign |
0.05 |
R6207:Hrg
|
UTSW |
16 |
22,773,288 (GRCm39) |
critical splice donor site |
probably null |
|
R6374:Hrg
|
UTSW |
16 |
22,779,742 (GRCm39) |
missense |
probably damaging |
0.98 |
R7516:Hrg
|
UTSW |
16 |
22,780,048 (GRCm39) |
missense |
unknown |
|
R7606:Hrg
|
UTSW |
16 |
22,769,873 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R8190:Hrg
|
UTSW |
16 |
22,779,793 (GRCm39) |
missense |
unknown |
|
R8349:Hrg
|
UTSW |
16 |
22,780,286 (GRCm39) |
missense |
unknown |
|
R8449:Hrg
|
UTSW |
16 |
22,780,286 (GRCm39) |
missense |
unknown |
|
R8973:Hrg
|
UTSW |
16 |
22,777,968 (GRCm39) |
missense |
probably benign |
0.22 |
R8998:Hrg
|
UTSW |
16 |
22,772,455 (GRCm39) |
missense |
probably damaging |
0.99 |
R9334:Hrg
|
UTSW |
16 |
22,780,061 (GRCm39) |
missense |
unknown |
|
Z1177:Hrg
|
UTSW |
16 |
22,772,462 (GRCm39) |
missense |
probably damaging |
1.00 |
|