Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A030005L19Rik |
GCTGTG |
GCTGTGCCTCCTGTG |
1: 82,891,299 (GRCm39) |
|
probably benign |
Het |
A030005L19Rik |
TGTGGCTGC |
TGTGGCTGCCGTGGCTGC |
1: 82,891,301 (GRCm39) |
|
probably benign |
Het |
Acap3 |
TGCATCCTGGGCTGC |
TGCATCCTGGGCTGCAGCATCCTGGGCTGC |
4: 155,989,548 (GRCm39) |
|
probably benign |
Het |
Arid1b |
C |
CGGG |
17: 5,045,873 (GRCm39) |
|
probably benign |
Het |
Blm |
CCTCCTCCTCCTCCTCCTCCTCCT |
CCTCCTCCTCCTACTCCTCCTCCTCCTCCTCCTCCT |
7: 80,162,653 (GRCm39) |
|
probably null |
Het |
Boc |
GAC |
G |
16: 44,316,796 (GRCm39) |
|
probably null |
Het |
Cacna1f |
GAG |
GAGAAG |
X: 7,486,299 (GRCm39) |
|
probably benign |
Het |
Cacna1f |
GAG |
GAGAAG |
X: 7,486,302 (GRCm39) |
|
probably benign |
Het |
Catsper2 |
ATCGCTTTCCTCGTTTTCG |
ATCG |
2: 121,228,207 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
GAGGAG |
GAGGAGTAGGAG |
9: 99,465,750 (GRCm39) |
|
probably null |
Het |
E4f1 |
CGC |
CGCGGC |
17: 24,674,164 (GRCm39) |
|
probably benign |
Het |
Eps8 |
TCGCTC |
TCGCTCGCTC |
6: 137,494,061 (GRCm39) |
|
probably benign |
Het |
Ermn |
AACT |
AACTACT |
2: 57,938,078 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
TAGATGTGAAACCCTTAGAGGTAAGATGTGAAACTCTTAGAGGTAAGA |
TAGATGTGAAACTCTTAGAGGTAAGA |
2: 82,824,352 (GRCm39) |
|
probably null |
Het |
Gab3 |
CTTCTT |
CTTATTCTT |
X: 74,043,606 (GRCm39) |
|
probably null |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,623 (GRCm39) |
|
probably benign |
Het |
Gabre |
CTC |
CTCTGGGTC |
X: 71,314,369 (GRCm39) |
|
probably benign |
Het |
Gm7579 |
GGCTGTGGCTCCTGTGGGGGCTGCAAGGGAAGCTGTGGCTCCTGTGGGGGCTGCAAGGGAAGCTGTGGCTCCTGTGGGGGATGCAAGGGAGGCTGTGGCTCCTGTGGGGG |
GGCTGTGGCTCCTGTGGGGGCTGCAAGGGAAGCTGTGGCTCCTGTGGGGGATGCAAGGGAGGCTGTGGCTCCTGTGGGGG |
7: 141,765,782 (GRCm39) |
|
probably benign |
Het |
Gm8369 |
TG |
TGGGTGAG |
19: 11,489,137 (GRCm39) |
|
probably null |
Het |
Hsdl2 |
CAGCTGCAG |
CAGCTGCAGCAGCAGCCATAGCTGCAG |
4: 59,610,650 (GRCm39) |
|
probably null |
Het |
Iqcf4 |
TTTTCCTTTT |
TTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCGTTTCCTTTT |
9: 106,447,813 (GRCm39) |
|
probably benign |
Het |
Kmt2e |
TTT |
TTTTATT |
5: 23,683,507 (GRCm39) |
|
probably benign |
Het |
Kri1 |
CTCCTCCT |
C |
9: 21,192,367 (GRCm39) |
|
probably null |
Het |
Krtap28-10 |
AGCCACAGCCACCACAGCCACAGCCACCAC |
AGCCACAGCCACCACCGCCACAGCCACCACAGCCACAGCCACCAC |
1: 83,019,979 (GRCm39) |
|
probably benign |
Het |
Lce1m |
GTTGCTGCCACTG |
GTTGCTGCCACTGTTGCTGCCACTG |
3: 92,925,438 (GRCm39) |
|
probably benign |
Het |
Loricrin |
CGCCGCCT |
C |
3: 91,989,206 (GRCm39) |
|
probably null |
Het |
Luzp1 |
A |
AGGTGGCCTCTTCAGG |
4: 136,270,507 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
CCAACA |
CCAACAGGTCCCTCGCCTCTGTTACCCCACAAATAAACAACA |
11: 58,281,065 (GRCm39) |
|
probably benign |
Het |
Mn1 |
CAG |
CAGGAG |
5: 111,567,577 (GRCm39) |
|
probably benign |
Het |
Nefh |
GGGACTTGGCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
GGGACTTGGCCTCACCTGTGGACTTGGCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,012 (GRCm39) |
|
probably benign |
Het |
Nefh |
GGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
GGGGACTTGGCCTCACCTTGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,029 (GRCm39) |
|
probably benign |
Het |
Nf2 |
AAAAG |
A |
11: 4,779,936 (GRCm39) |
|
probably null |
Het |
Nusap1 |
AGAT |
AGATCCACGTTAGCAGTGAGGAGCAAGCTGCGAT |
2: 119,458,059 (GRCm39) |
|
probably benign |
Het |
Nusap1 |
CAGTGAGGAGCAAGCTGAGA |
CAGTGAGGAGCAAGCTGAGATACACGTTAGTAGTGAGGAGCAAGCTGAGA |
2: 119,458,072 (GRCm39) |
|
probably benign |
Het |
Phf20 |
CCCCCC |
CCCCCCGCCCCC |
2: 156,146,543 (GRCm39) |
|
probably benign |
Het |
Ppp1r8 |
TCTCTCTCAC |
TC |
4: 132,557,926 (GRCm39) |
|
probably benign |
Het |
Prr5l |
GCCTC |
G |
2: 101,627,918 (GRCm39) |
|
probably null |
Het |
Rbm12 |
CGGGACCGGGCATTGCGGGACCGGGCATTGCGGG |
CGG |
2: 155,938,050 (GRCm39) |
|
probably null |
Het |
Rpgrip1 |
GA |
GAGTA |
14: 52,386,855 (GRCm39) |
|
probably null |
Het |
Spmap2l |
AGCGATCCTCCCCAGTCCCGCAAGGCC |
AGCGATCCTCCCCAGTCCCGCAAGGCCCGCGATCCTCCCCAGTCCCGCAAGGCC |
5: 77,164,248 (GRCm39) |
|
probably benign |
Het |
Tanc1 |
GTGAGCAGAAACCAGCATTTAGAGGGAACCGGTCCCTTCACTGCAGGAA |
G |
2: 59,673,613 (GRCm39) |
|
probably benign |
Het |
Tfeb |
GCA |
GCATCA |
17: 48,097,022 (GRCm39) |
|
probably benign |
Het |
Tgoln1 |
T |
TTGTCTTGTCAGAATCACCTCCTGG |
6: 72,593,019 (GRCm39) |
|
probably benign |
Het |
Tob1 |
CACA |
CACAACA |
11: 94,105,277 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
GCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
15: 72,673,139 (GRCm39) |
|
probably benign |
Het |
Triobp |
CAGGACT |
CAGGACTGCCTGTGCCCAACGGAACAACCCAAGGACT |
15: 78,851,239 (GRCm39) |
|
probably benign |
Het |
Zfhx3 |
AACAGCAGC |
AACAGCAGCTACAGCAGC |
8: 109,682,728 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp933 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00576:Zfp933
|
APN |
4 |
147,910,778 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03377:Zfp933
|
APN |
4 |
147,913,168 (GRCm39) |
missense |
possibly damaging |
0.65 |
F5770:Zfp933
|
UTSW |
4 |
147,910,927 (GRCm39) |
missense |
probably damaging |
0.98 |
FR4340:Zfp933
|
UTSW |
4 |
147,910,186 (GRCm39) |
frame shift |
probably null |
|
FR4548:Zfp933
|
UTSW |
4 |
147,910,188 (GRCm39) |
frame shift |
probably null |
|
R0388:Zfp933
|
UTSW |
4 |
147,910,899 (GRCm39) |
missense |
probably benign |
0.35 |
R0523:Zfp933
|
UTSW |
4 |
147,910,919 (GRCm39) |
nonsense |
probably null |
|
R0539:Zfp933
|
UTSW |
4 |
147,911,005 (GRCm39) |
missense |
probably benign |
0.08 |
R1672:Zfp933
|
UTSW |
4 |
147,910,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R4049:Zfp933
|
UTSW |
4 |
147,910,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4895:Zfp933
|
UTSW |
4 |
147,910,892 (GRCm39) |
nonsense |
probably null |
|
R5133:Zfp933
|
UTSW |
4 |
147,911,321 (GRCm39) |
missense |
probably benign |
|
R5786:Zfp933
|
UTSW |
4 |
147,912,864 (GRCm39) |
splice site |
probably null |
|
R5891:Zfp933
|
UTSW |
4 |
147,911,231 (GRCm39) |
missense |
probably benign |
0.03 |
R6111:Zfp933
|
UTSW |
4 |
147,913,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R6382:Zfp933
|
UTSW |
4 |
147,910,325 (GRCm39) |
missense |
probably benign |
0.07 |
R6968:Zfp933
|
UTSW |
4 |
147,910,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Zfp933
|
UTSW |
4 |
147,910,636 (GRCm39) |
missense |
probably benign |
0.16 |
R7555:Zfp933
|
UTSW |
4 |
147,910,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R7902:Zfp933
|
UTSW |
4 |
147,911,058 (GRCm39) |
missense |
probably damaging |
0.96 |
R8319:Zfp933
|
UTSW |
4 |
147,912,910 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8688:Zfp933
|
UTSW |
4 |
147,911,249 (GRCm39) |
missense |
probably benign |
0.14 |
R9019:Zfp933
|
UTSW |
4 |
147,911,021 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Zfp933
|
UTSW |
4 |
147,910,898 (GRCm39) |
missense |
probably damaging |
1.00 |
RF035:Zfp933
|
UTSW |
4 |
147,910,188 (GRCm39) |
makesense |
probably null |
|
RF043:Zfp933
|
UTSW |
4 |
147,910,188 (GRCm39) |
frame shift |
probably null |
|
V7581:Zfp933
|
UTSW |
4 |
147,910,927 (GRCm39) |
missense |
probably damaging |
0.98 |
V7582:Zfp933
|
UTSW |
4 |
147,910,927 (GRCm39) |
missense |
probably damaging |
0.98 |
V7583:Zfp933
|
UTSW |
4 |
147,910,927 (GRCm39) |
missense |
probably damaging |
0.98 |
|