Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Adad1 |
G |
T |
3: 37,139,260 (GRCm39) |
L443F |
probably damaging |
Het |
Amph |
T |
A |
13: 19,268,378 (GRCm39) |
M70K |
probably damaging |
Het |
Ankra2 |
T |
A |
13: 98,409,919 (GRCm39) |
L306H |
probably damaging |
Het |
Arc |
A |
C |
15: 74,543,592 (GRCm39) |
D210E |
probably benign |
Het |
Arhgap10 |
A |
G |
8: 78,159,367 (GRCm39) |
|
probably null |
Het |
Atp8b5 |
T |
A |
4: 43,344,449 (GRCm39) |
N445K |
probably benign |
Het |
C1qc |
G |
T |
4: 136,617,746 (GRCm39) |
Q117K |
probably benign |
Het |
Cadps |
T |
A |
14: 12,822,449 (GRCm38) |
E97V |
unknown |
Het |
Capn13 |
GCA |
G |
17: 73,658,501 (GRCm39) |
|
probably null |
Het |
Cdk13 |
A |
T |
13: 17,895,868 (GRCm39) |
W1014R |
probably damaging |
Het |
Cltb |
C |
T |
13: 54,746,908 (GRCm39) |
E23K |
probably damaging |
Het |
Clvs2 |
A |
T |
10: 33,498,642 (GRCm39) |
I96N |
probably damaging |
Het |
Cwf19l1 |
A |
G |
19: 44,103,006 (GRCm39) |
V403A |
probably damaging |
Het |
Ddr2 |
A |
T |
1: 169,816,066 (GRCm39) |
L547Q |
possibly damaging |
Het |
Fat4 |
A |
G |
3: 38,942,466 (GRCm39) |
Q453R |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gata6 |
A |
G |
18: 11,054,497 (GRCm39) |
E142G |
possibly damaging |
Het |
Gm14221 |
T |
C |
2: 160,416,600 (GRCm39) |
|
noncoding transcript |
Het |
Gm42791 |
C |
A |
5: 148,896,247 (GRCm39) |
|
probably benign |
Het |
Gm6370 |
G |
T |
5: 146,430,621 (GRCm39) |
V269L |
probably benign |
Het |
Gphn |
G |
A |
12: 78,673,984 (GRCm39) |
V526M |
probably damaging |
Het |
Gpt |
A |
T |
15: 76,583,485 (GRCm39) |
E206V |
probably damaging |
Het |
Grm3 |
G |
A |
5: 9,620,047 (GRCm39) |
A399V |
probably damaging |
Het |
Helq |
A |
T |
5: 100,931,025 (GRCm39) |
V575E |
possibly damaging |
Het |
Herc4 |
A |
G |
10: 63,151,437 (GRCm39) |
|
probably null |
Het |
Ifi207 |
A |
T |
1: 173,557,381 (GRCm39) |
N452K |
probably damaging |
Het |
Ikbke |
A |
G |
1: 131,184,848 (GRCm39) |
|
probably null |
Het |
Kbtbd2 |
A |
G |
6: 56,756,687 (GRCm39) |
F350L |
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,519,555 (GRCm39) |
V2185A |
probably benign |
Het |
Lgi2 |
T |
C |
5: 52,695,849 (GRCm39) |
Q362R |
probably damaging |
Het |
Lrit1 |
G |
A |
14: 36,783,773 (GRCm39) |
G367E |
possibly damaging |
Het |
Lrp1 |
G |
A |
10: 127,446,311 (GRCm39) |
H78Y |
probably benign |
Het |
Matk |
A |
G |
10: 81,098,720 (GRCm39) |
|
probably benign |
Het |
Med21 |
G |
A |
6: 146,549,690 (GRCm39) |
G24S |
probably damaging |
Het |
Met |
G |
T |
6: 17,558,796 (GRCm39) |
L1141F |
probably damaging |
Het |
Mroh3 |
A |
T |
1: 136,128,677 (GRCm39) |
|
probably null |
Het |
Mrpl15 |
T |
C |
1: 4,844,683 (GRCm39) |
I203V |
probably benign |
Het |
Naip1 |
T |
C |
13: 100,559,728 (GRCm39) |
|
probably null |
Het |
Ndufa9 |
A |
C |
6: 126,804,505 (GRCm39) |
Y298* |
probably null |
Het |
Neb |
T |
C |
2: 52,188,906 (GRCm39) |
E808G |
probably damaging |
Het |
Nol4l |
C |
T |
2: 153,253,726 (GRCm39) |
G616S |
probably benign |
Het |
Oprm1 |
T |
A |
10: 6,788,468 (GRCm39) |
C408S |
probably benign |
Het |
Or2ag18 |
T |
C |
7: 106,405,463 (GRCm39) |
M69V |
probably benign |
Het |
Or4f14 |
A |
G |
2: 111,742,444 (GRCm39) |
V277A |
probably benign |
Het |
Or4k42 |
T |
G |
2: 111,320,293 (GRCm39) |
D70A |
probably damaging |
Het |
Or52e7 |
T |
A |
7: 104,684,858 (GRCm39) |
I151N |
probably damaging |
Het |
Or5ak20 |
T |
C |
2: 85,183,793 (GRCm39) |
N159S |
possibly damaging |
Het |
Paqr3 |
A |
G |
5: 97,256,053 (GRCm39) |
I107T |
possibly damaging |
Het |
Pex5l |
G |
A |
3: 33,196,989 (GRCm39) |
|
probably benign |
Het |
Phf8-ps |
C |
T |
17: 33,285,713 (GRCm39) |
S363N |
probably benign |
Het |
Pik3ap1 |
T |
C |
19: 41,316,284 (GRCm39) |
D326G |
probably benign |
Het |
Plaa |
G |
T |
4: 94,474,645 (GRCm39) |
D252E |
probably damaging |
Het |
Plxna2 |
G |
A |
1: 194,480,040 (GRCm39) |
V1404I |
probably benign |
Het |
Ppargc1a |
G |
A |
5: 51,631,564 (GRCm39) |
A355V |
possibly damaging |
Het |
Primpol |
A |
G |
8: 47,039,726 (GRCm39) |
S350P |
probably benign |
Het |
Prlr |
T |
C |
15: 10,328,883 (GRCm39) |
S453P |
probably benign |
Het |
Psmd5 |
T |
C |
2: 34,742,564 (GRCm39) |
|
probably benign |
Het |
Robo2 |
A |
T |
16: 73,768,079 (GRCm39) |
V571E |
probably damaging |
Het |
Sbspon |
A |
T |
1: 15,929,264 (GRCm39) |
S176T |
possibly damaging |
Het |
Scyl2 |
G |
A |
10: 89,476,325 (GRCm39) |
|
probably benign |
Het |
Sema3e |
T |
A |
5: 14,280,144 (GRCm39) |
V341E |
probably damaging |
Het |
Serpinb3b |
A |
T |
1: 107,082,270 (GRCm39) |
F331L |
possibly damaging |
Het |
Setd2 |
A |
G |
9: 110,401,022 (GRCm39) |
H1736R |
probably benign |
Het |
Sidt2 |
A |
T |
9: 45,863,327 (GRCm39) |
D180E |
probably benign |
Het |
Skint9 |
A |
T |
4: 112,248,208 (GRCm39) |
Y179N |
probably benign |
Het |
Slc27a5 |
T |
C |
7: 12,722,560 (GRCm39) |
N638S |
probably benign |
Het |
Slc6a4 |
T |
A |
11: 76,904,135 (GRCm39) |
W197R |
probably damaging |
Het |
Spag17 |
A |
T |
3: 99,970,649 (GRCm39) |
M1278L |
probably benign |
Het |
Sptbn1 |
T |
A |
11: 30,092,353 (GRCm39) |
I471F |
probably damaging |
Het |
Tasor2 |
A |
T |
13: 3,616,680 (GRCm39) |
|
probably null |
Het |
Teddm1a |
A |
G |
1: 153,768,382 (GRCm39) |
Q282R |
probably benign |
Het |
Tex35 |
A |
G |
1: 156,927,295 (GRCm39) |
L160P |
probably damaging |
Het |
Tfap2c |
T |
C |
2: 172,393,438 (GRCm39) |
Y118H |
probably damaging |
Het |
Tpp1 |
T |
C |
7: 105,395,930 (GRCm39) |
Q533R |
probably benign |
Het |
Ttc13 |
C |
T |
8: 125,401,174 (GRCm39) |
D730N |
probably damaging |
Het |
Ufc1 |
A |
G |
1: 171,122,375 (GRCm39) |
|
probably benign |
Het |
Vcpip1 |
A |
G |
1: 9,817,589 (GRCm39) |
W265R |
probably damaging |
Het |
Wdr11 |
C |
G |
7: 129,202,158 (GRCm39) |
|
probably null |
Het |
Xirp2 |
A |
G |
2: 67,341,408 (GRCm39) |
I1216M |
possibly damaging |
Het |
Zswim2 |
A |
G |
2: 83,747,187 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ebf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01150:Ebf1
|
APN |
11 |
44,759,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02228:Ebf1
|
APN |
11 |
44,863,739 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02430:Ebf1
|
APN |
11 |
44,815,403 (GRCm39) |
critical splice donor site |
probably null |
|
Befuddled
|
UTSW |
11 |
44,523,602 (GRCm39) |
missense |
probably damaging |
0.98 |
Catastrophic
|
UTSW |
11 |
44,774,712 (GRCm39) |
missense |
probably damaging |
1.00 |
Crabapple
|
UTSW |
11 |
44,774,666 (GRCm39) |
missense |
probably damaging |
1.00 |
Crater_lake
|
UTSW |
11 |
44,863,735 (GRCm39) |
nonsense |
probably null |
|
ebby
|
UTSW |
11 |
44,774,641 (GRCm39) |
missense |
probably damaging |
1.00 |
Oregano
|
UTSW |
11 |
44,759,996 (GRCm39) |
missense |
probably damaging |
1.00 |
Oregano2
|
UTSW |
11 |
44,881,331 (GRCm39) |
splice site |
probably null |
|
Realtor
|
UTSW |
11 |
44,511,374 (GRCm39) |
missense |
probably benign |
0.05 |
Vie
|
UTSW |
11 |
44,863,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Ebf1
|
UTSW |
11 |
44,882,282 (GRCm39) |
missense |
probably benign |
0.02 |
R0102:Ebf1
|
UTSW |
11 |
44,882,282 (GRCm39) |
missense |
probably benign |
0.02 |
R0141:Ebf1
|
UTSW |
11 |
44,798,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0230:Ebf1
|
UTSW |
11 |
44,886,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Ebf1
|
UTSW |
11 |
44,759,915 (GRCm39) |
splice site |
probably benign |
|
R0268:Ebf1
|
UTSW |
11 |
44,534,240 (GRCm39) |
missense |
probably damaging |
0.96 |
R0414:Ebf1
|
UTSW |
11 |
44,815,297 (GRCm39) |
nonsense |
probably null |
|
R0648:Ebf1
|
UTSW |
11 |
44,882,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R0765:Ebf1
|
UTSW |
11 |
44,759,987 (GRCm39) |
missense |
probably damaging |
0.97 |
R1055:Ebf1
|
UTSW |
11 |
44,523,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R1432:Ebf1
|
UTSW |
11 |
44,895,533 (GRCm39) |
splice site |
probably benign |
|
R1713:Ebf1
|
UTSW |
11 |
44,815,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1749:Ebf1
|
UTSW |
11 |
44,798,835 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1989:Ebf1
|
UTSW |
11 |
44,512,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R2405:Ebf1
|
UTSW |
11 |
44,882,349 (GRCm39) |
missense |
probably damaging |
0.98 |
R3110:Ebf1
|
UTSW |
11 |
44,534,225 (GRCm39) |
splice site |
probably benign |
|
R4538:Ebf1
|
UTSW |
11 |
44,798,822 (GRCm39) |
missense |
probably benign |
0.07 |
R4666:Ebf1
|
UTSW |
11 |
44,882,384 (GRCm39) |
missense |
probably damaging |
0.99 |
R4904:Ebf1
|
UTSW |
11 |
44,759,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R5137:Ebf1
|
UTSW |
11 |
44,882,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Ebf1
|
UTSW |
11 |
44,883,228 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5849:Ebf1
|
UTSW |
11 |
44,881,331 (GRCm39) |
splice site |
probably null |
|
R5940:Ebf1
|
UTSW |
11 |
44,512,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R5989:Ebf1
|
UTSW |
11 |
44,886,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Ebf1
|
UTSW |
11 |
44,774,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R6512:Ebf1
|
UTSW |
11 |
44,883,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Ebf1
|
UTSW |
11 |
44,774,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R7031:Ebf1
|
UTSW |
11 |
44,512,795 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7042:Ebf1
|
UTSW |
11 |
44,882,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R8065:Ebf1
|
UTSW |
11 |
44,511,374 (GRCm39) |
missense |
probably benign |
0.05 |
R8067:Ebf1
|
UTSW |
11 |
44,511,374 (GRCm39) |
missense |
probably benign |
0.05 |
R8125:Ebf1
|
UTSW |
11 |
44,863,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R8413:Ebf1
|
UTSW |
11 |
44,534,274 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8863:Ebf1
|
UTSW |
11 |
44,774,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R9178:Ebf1
|
UTSW |
11 |
44,895,548 (GRCm39) |
missense |
probably benign |
0.20 |
R9178:Ebf1
|
UTSW |
11 |
44,883,276 (GRCm39) |
missense |
probably benign |
0.04 |
R9511:Ebf1
|
UTSW |
11 |
44,815,393 (GRCm39) |
missense |
probably benign |
0.03 |
R9603:Ebf1
|
UTSW |
11 |
44,509,006 (GRCm39) |
start codon destroyed |
probably null |
0.07 |
|