Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
G |
2: 69,158,355 (GRCm39) |
|
probably benign |
Het |
Adh1 |
C |
T |
3: 137,986,193 (GRCm39) |
T60I |
probably benign |
Het |
Agtpbp1 |
T |
A |
13: 59,661,966 (GRCm39) |
I282F |
probably damaging |
Het |
Arih2 |
G |
T |
9: 108,493,916 (GRCm39) |
Q166K |
probably damaging |
Het |
Cacna1s |
A |
G |
1: 136,025,947 (GRCm39) |
T1031A |
probably benign |
Het |
Ccdc102a |
C |
A |
8: 95,629,914 (GRCm39) |
E542D |
probably benign |
Het |
Cdk1 |
T |
C |
10: 69,180,929 (GRCm39) |
I94V |
probably benign |
Het |
Cep290 |
C |
T |
10: 100,359,176 (GRCm39) |
Q969* |
probably null |
Het |
Cilp2 |
A |
G |
8: 70,335,643 (GRCm39) |
S452P |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,606,642 (GRCm39) |
T594A |
probably damaging |
Het |
Cpox |
A |
G |
16: 58,491,232 (GRCm39) |
T148A |
possibly damaging |
Het |
Csf3r |
A |
G |
4: 125,933,460 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,760,530 (GRCm39) |
C202S |
probably damaging |
Het |
Dlgap4 |
T |
C |
2: 156,604,746 (GRCm39) |
S261P |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 65,998,961 (GRCm39) |
Y1029F |
probably damaging |
Het |
Dok5 |
T |
C |
2: 170,671,880 (GRCm39) |
|
probably benign |
Het |
Dusp11 |
A |
T |
6: 85,929,352 (GRCm39) |
|
probably benign |
Het |
Edar |
T |
C |
10: 58,465,262 (GRCm39) |
N34D |
probably benign |
Het |
Efcab7 |
C |
T |
4: 99,766,943 (GRCm39) |
T56I |
probably damaging |
Het |
Entpd1 |
G |
A |
19: 40,699,729 (GRCm39) |
V47I |
probably benign |
Het |
Ephx4 |
A |
G |
5: 107,551,601 (GRCm39) |
N62S |
probably benign |
Het |
Etaa1 |
A |
T |
11: 17,896,350 (GRCm39) |
L589* |
probably null |
Het |
Fam135b |
T |
A |
15: 71,335,670 (GRCm39) |
N508I |
probably benign |
Het |
Fam193a |
T |
C |
5: 34,623,552 (GRCm39) |
V27A |
possibly damaging |
Het |
Fmnl1 |
A |
G |
11: 103,084,889 (GRCm39) |
|
probably benign |
Het |
Fstl1 |
A |
C |
16: 37,641,516 (GRCm39) |
|
probably null |
Het |
Gbp4 |
G |
A |
5: 105,268,972 (GRCm39) |
R394C |
possibly damaging |
Het |
Gemin4 |
T |
C |
11: 76,102,148 (GRCm39) |
Y871C |
probably benign |
Het |
Get1 |
T |
G |
16: 95,954,217 (GRCm39) |
S105R |
probably benign |
Het |
Gm7247 |
T |
C |
14: 51,760,929 (GRCm39) |
V166A |
probably benign |
Het |
Gpcpd1 |
A |
T |
2: 132,406,543 (GRCm39) |
|
probably benign |
Het |
Gpnmb |
A |
G |
6: 49,019,737 (GRCm39) |
D36G |
probably benign |
Het |
Ido2 |
C |
T |
8: 25,048,159 (GRCm39) |
|
probably null |
Het |
Igfn1 |
G |
A |
1: 135,895,334 (GRCm39) |
T1744I |
probably benign |
Het |
Itga10 |
T |
A |
3: 96,556,375 (GRCm39) |
I170N |
probably damaging |
Het |
Lrp6 |
A |
T |
6: 134,484,587 (GRCm39) |
D345E |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,366,062 (GRCm39) |
S2900T |
probably benign |
Het |
Med13 |
C |
A |
11: 86,190,033 (GRCm39) |
|
probably benign |
Het |
Morc3 |
T |
C |
16: 93,667,362 (GRCm39) |
V507A |
probably damaging |
Het |
Myadm |
AC |
ACC |
7: 3,345,276 (GRCm39) |
|
probably null |
Het |
Myl6 |
C |
T |
10: 128,328,091 (GRCm39) |
|
probably benign |
Het |
Mylk |
T |
C |
16: 34,742,314 (GRCm39) |
V942A |
probably benign |
Het |
Myorg |
G |
T |
4: 41,498,585 (GRCm39) |
H348Q |
probably benign |
Het |
Ncdn |
G |
T |
4: 126,644,327 (GRCm39) |
T165K |
possibly damaging |
Het |
Ncf1 |
T |
C |
5: 134,251,656 (GRCm39) |
|
probably benign |
Het |
Neb |
T |
C |
2: 52,180,751 (GRCm39) |
|
probably benign |
Het |
Nid1 |
T |
A |
13: 13,656,681 (GRCm39) |
I604N |
probably benign |
Het |
Nsrp1 |
T |
C |
11: 76,936,997 (GRCm39) |
R400G |
probably benign |
Het |
Nup43 |
T |
G |
10: 7,546,791 (GRCm39) |
I137S |
probably benign |
Het |
Nynrin |
A |
G |
14: 56,109,648 (GRCm39) |
N1585S |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,893,823 (GRCm39) |
Y6748F |
probably benign |
Het |
Omg |
A |
G |
11: 79,393,661 (GRCm39) |
S66P |
possibly damaging |
Het |
Or13a27 |
A |
T |
7: 139,925,108 (GRCm39) |
S265T |
possibly damaging |
Het |
Or2y1d |
T |
C |
11: 49,322,212 (GRCm39) |
V303A |
possibly damaging |
Het |
Or4c15 |
A |
G |
2: 88,759,906 (GRCm39) |
V251A |
probably benign |
Het |
Or51b6b |
A |
T |
7: 103,309,957 (GRCm39) |
F167I |
possibly damaging |
Het |
Or52z1 |
A |
G |
7: 103,437,362 (GRCm39) |
Y41H |
probably damaging |
Het |
Or5ak22 |
T |
C |
2: 85,230,019 (GRCm39) |
N286S |
probably damaging |
Het |
Or8g27 |
A |
G |
9: 39,129,566 (GRCm39) |
I304M |
probably benign |
Het |
Or8k24 |
G |
A |
2: 86,216,058 (GRCm39) |
R235C |
probably benign |
Het |
Ormdl1 |
C |
T |
1: 53,347,978 (GRCm39) |
|
probably benign |
Het |
Ovch2 |
T |
A |
7: 107,381,243 (GRCm39) |
I552L |
probably benign |
Het |
Pcare |
T |
G |
17: 72,059,212 (GRCm39) |
D155A |
probably benign |
Het |
Pcsk9 |
G |
T |
4: 106,311,538 (GRCm39) |
T231N |
probably damaging |
Het |
Pgpep1 |
T |
C |
8: 71,110,100 (GRCm39) |
N22S |
probably damaging |
Het |
Plb1 |
T |
C |
5: 32,512,706 (GRCm39) |
F1355L |
probably damaging |
Het |
Plcg1 |
G |
T |
2: 160,603,349 (GRCm39) |
L1173F |
probably damaging |
Het |
Plch2 |
A |
T |
4: 155,091,373 (GRCm39) |
|
probably null |
Het |
Ppp1r3g |
T |
A |
13: 36,153,331 (GRCm39) |
F250L |
probably damaging |
Het |
Prkcg |
A |
G |
7: 3,368,095 (GRCm39) |
I381V |
probably benign |
Het |
Pum2 |
C |
T |
12: 8,763,464 (GRCm39) |
A207V |
probably benign |
Het |
Rabac1 |
T |
C |
7: 24,669,607 (GRCm39) |
E166G |
probably damaging |
Het |
Rad21l |
G |
A |
2: 151,493,851 (GRCm39) |
S450L |
probably benign |
Het |
Rangap1 |
ACACTCA |
ACA |
15: 81,600,876 (GRCm39) |
|
probably null |
Het |
Reg3b |
G |
T |
6: 78,348,824 (GRCm39) |
C40F |
probably damaging |
Het |
Rfx2 |
A |
G |
17: 57,091,418 (GRCm39) |
|
probably benign |
Het |
Rrp15 |
G |
A |
1: 186,481,346 (GRCm39) |
|
probably benign |
Het |
Schip1 |
G |
T |
3: 68,401,946 (GRCm39) |
G36C |
probably damaging |
Het |
Sec61a2 |
A |
T |
2: 5,881,165 (GRCm39) |
|
probably benign |
Het |
Sema5a |
A |
G |
15: 32,669,590 (GRCm39) |
K705E |
probably damaging |
Het |
Setx |
A |
G |
2: 29,029,290 (GRCm39) |
Y186C |
probably damaging |
Het |
Slc22a23 |
T |
C |
13: 34,367,115 (GRCm39) |
E631G |
probably damaging |
Het |
Slc5a5 |
T |
C |
8: 71,344,319 (GRCm39) |
T134A |
possibly damaging |
Het |
Stx7 |
T |
C |
10: 24,057,492 (GRCm39) |
S173P |
probably damaging |
Het |
Sybu |
T |
C |
15: 44,536,668 (GRCm39) |
T353A |
probably damaging |
Het |
Syde2 |
T |
A |
3: 145,712,887 (GRCm39) |
N1008K |
probably damaging |
Het |
Tiam1 |
T |
C |
16: 89,606,253 (GRCm39) |
|
probably benign |
Het |
Timm10b |
G |
A |
7: 105,327,537 (GRCm39) |
E61K |
probably benign |
Het |
Tm2d1 |
A |
G |
4: 98,253,810 (GRCm39) |
I121T |
probably damaging |
Het |
Trim75 |
T |
C |
8: 65,435,892 (GRCm39) |
E186G |
probably benign |
Het |
Tti1 |
T |
C |
2: 157,837,396 (GRCm39) |
K895E |
probably benign |
Het |
Vmn1r43 |
A |
G |
6: 89,846,830 (GRCm39) |
S219P |
probably damaging |
Het |
Vmn2r73 |
A |
T |
7: 85,521,087 (GRCm39) |
S294T |
possibly damaging |
Het |
Vmn2r94 |
A |
T |
17: 18,464,080 (GRCm39) |
F737I |
probably damaging |
Het |
Vsx2 |
A |
T |
12: 84,616,777 (GRCm39) |
T21S |
probably benign |
Het |
Zfp462 |
G |
T |
4: 55,010,534 (GRCm39) |
R833S |
probably damaging |
Het |
Zfpl1 |
G |
A |
19: 6,132,482 (GRCm39) |
P143L |
probably damaging |
Het |
|
Other mutations in Inf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Inf2
|
APN |
12 |
112,578,290 (GRCm39) |
nonsense |
probably null |
|
IGL01582:Inf2
|
APN |
12 |
112,576,993 (GRCm39) |
missense |
unknown |
|
IGL02078:Inf2
|
APN |
12 |
112,568,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02534:Inf2
|
APN |
12 |
112,576,930 (GRCm39) |
missense |
unknown |
|
IGL03122:Inf2
|
APN |
12 |
112,570,663 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03296:Inf2
|
APN |
12 |
112,570,642 (GRCm39) |
nonsense |
probably null |
|
Talon
|
UTSW |
12 |
112,576,721 (GRCm39) |
splice site |
probably benign |
|
R0552:Inf2
|
UTSW |
12 |
112,579,008 (GRCm39) |
intron |
probably benign |
|
R0920:Inf2
|
UTSW |
12 |
112,576,721 (GRCm39) |
splice site |
probably benign |
|
R1240:Inf2
|
UTSW |
12 |
112,577,210 (GRCm39) |
missense |
unknown |
|
R1452:Inf2
|
UTSW |
12 |
112,567,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R1974:Inf2
|
UTSW |
12 |
112,574,771 (GRCm39) |
missense |
unknown |
|
R2422:Inf2
|
UTSW |
12 |
112,577,258 (GRCm39) |
missense |
unknown |
|
R3877:Inf2
|
UTSW |
12 |
112,577,264 (GRCm39) |
missense |
unknown |
|
R4108:Inf2
|
UTSW |
12 |
112,574,015 (GRCm39) |
missense |
unknown |
|
R4490:Inf2
|
UTSW |
12 |
112,566,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5071:Inf2
|
UTSW |
12 |
112,578,473 (GRCm39) |
splice site |
probably null |
|
R5074:Inf2
|
UTSW |
12 |
112,578,473 (GRCm39) |
splice site |
probably null |
|
R5306:Inf2
|
UTSW |
12 |
112,567,987 (GRCm39) |
missense |
probably benign |
0.26 |
R5383:Inf2
|
UTSW |
12 |
112,566,579 (GRCm39) |
missense |
probably damaging |
0.99 |
R5569:Inf2
|
UTSW |
12 |
112,568,113 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5664:Inf2
|
UTSW |
12 |
112,578,162 (GRCm39) |
missense |
unknown |
|
R6157:Inf2
|
UTSW |
12 |
112,571,222 (GRCm39) |
unclassified |
probably benign |
|
R6221:Inf2
|
UTSW |
12 |
112,570,179 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6429:Inf2
|
UTSW |
12 |
112,570,690 (GRCm39) |
missense |
probably benign |
0.01 |
R6955:Inf2
|
UTSW |
12 |
112,577,165 (GRCm39) |
missense |
unknown |
|
R7423:Inf2
|
UTSW |
12 |
112,576,172 (GRCm39) |
missense |
unknown |
|
R7444:Inf2
|
UTSW |
12 |
112,571,821 (GRCm39) |
missense |
unknown |
|
R7496:Inf2
|
UTSW |
12 |
112,566,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R7605:Inf2
|
UTSW |
12 |
112,567,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Inf2
|
UTSW |
12 |
112,573,428 (GRCm39) |
missense |
unknown |
|
R7708:Inf2
|
UTSW |
12 |
112,573,991 (GRCm39) |
missense |
unknown |
|
R7752:Inf2
|
UTSW |
12 |
112,576,118 (GRCm39) |
missense |
unknown |
|
R7903:Inf2
|
UTSW |
12 |
112,578,988 (GRCm39) |
missense |
unknown |
|
R8024:Inf2
|
UTSW |
12 |
112,575,336 (GRCm39) |
missense |
unknown |
|
R8118:Inf2
|
UTSW |
12 |
112,567,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R8139:Inf2
|
UTSW |
12 |
112,568,074 (GRCm39) |
nonsense |
probably null |
|
R8229:Inf2
|
UTSW |
12 |
112,578,030 (GRCm39) |
missense |
unknown |
|
R8299:Inf2
|
UTSW |
12 |
112,570,546 (GRCm39) |
missense |
probably benign |
0.00 |
R8918:Inf2
|
UTSW |
12 |
112,572,703 (GRCm39) |
missense |
unknown |
|
R8955:Inf2
|
UTSW |
12 |
112,576,998 (GRCm39) |
missense |
unknown |
|
R8973:Inf2
|
UTSW |
12 |
112,573,949 (GRCm39) |
missense |
unknown |
|
R9171:Inf2
|
UTSW |
12 |
112,567,965 (GRCm39) |
nonsense |
probably null |
|
R9218:Inf2
|
UTSW |
12 |
112,567,858 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9779:Inf2
|
UTSW |
12 |
112,574,786 (GRCm39) |
missense |
unknown |
|
|