Incidental Mutation 'R6056:Zfp292'
| ID |
484371 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp292
|
| Ensembl Gene |
ENSMUSG00000039967 |
| Gene Name |
zinc finger protein 292 |
| Synonyms |
Zfp-15, 9430062L07Rik, Zn-16, Zfp15, Zn-15, 5730450D02Rik, Krox-10 |
| MMRRC Submission |
044223-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.843)
|
| Stock # |
R6056 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
34803113-34882960 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 34809784 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Serine
at position 1087
(C1087S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000095766
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047950]
[ENSMUST00000098163]
|
| AlphaFold |
Q9Z2U2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000047950
AA Change: C1092S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000037233
Gene: ENSMUSG00000039967
AA Change: C1092S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
101 |
120 |
N/A |
INTRINSIC |
|
low complexity region
|
512 |
523 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
540 |
561 |
5.12e1 |
SMART |
|
ZnF_C2H2
|
567 |
589 |
4.72e-2 |
SMART |
|
low complexity region
|
649 |
664 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
681 |
705 |
3.52e-1 |
SMART |
|
ZnF_C2H2
|
722 |
744 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
750 |
774 |
1.62e0 |
SMART |
|
ZnF_C2H2
|
779 |
803 |
1.08e1 |
SMART |
|
ZnF_C2H2
|
807 |
831 |
1.95e-3 |
SMART |
|
low complexity region
|
1062 |
1078 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1085 |
1110 |
7.67e-2 |
SMART |
|
ZnF_C2H2
|
1361 |
1381 |
1.93e2 |
SMART |
|
low complexity region
|
1606 |
1618 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1879 |
1904 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
1924 |
1949 |
5.42e-2 |
SMART |
|
low complexity region
|
2004 |
2014 |
N/A |
INTRINSIC |
|
low complexity region
|
2024 |
2037 |
N/A |
INTRINSIC |
|
coiled coil region
|
2050 |
2072 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2091 |
2116 |
4.45e0 |
SMART |
|
low complexity region
|
2121 |
2143 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2149 |
2174 |
1.64e-1 |
SMART |
|
ZnF_C2H2
|
2193 |
2218 |
3.24e0 |
SMART |
|
ZnF_C2H2
|
2233 |
2258 |
1.18e-2 |
SMART |
|
low complexity region
|
2301 |
2314 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2362 |
2386 |
2.86e-1 |
SMART |
|
low complexity region
|
2589 |
2605 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000098163
AA Change: C1087S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000095766
Gene: ENSMUSG00000039967
AA Change: C1087S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
39 |
N/A |
INTRINSIC |
|
low complexity region
|
101 |
120 |
N/A |
INTRINSIC |
|
low complexity region
|
507 |
518 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
535 |
556 |
5.12e1 |
SMART |
|
ZnF_C2H2
|
562 |
584 |
4.72e-2 |
SMART |
|
low complexity region
|
644 |
659 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
676 |
700 |
3.52e-1 |
SMART |
|
ZnF_C2H2
|
717 |
739 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
745 |
769 |
1.62e0 |
SMART |
|
ZnF_C2H2
|
774 |
798 |
1.08e1 |
SMART |
|
ZnF_C2H2
|
802 |
826 |
1.95e-3 |
SMART |
|
low complexity region
|
1057 |
1073 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1080 |
1105 |
7.67e-2 |
SMART |
|
ZnF_C2H2
|
1356 |
1376 |
1.93e2 |
SMART |
|
low complexity region
|
1601 |
1613 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1874 |
1899 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
1919 |
1944 |
5.42e-2 |
SMART |
|
low complexity region
|
1999 |
2009 |
N/A |
INTRINSIC |
|
low complexity region
|
2019 |
2032 |
N/A |
INTRINSIC |
|
coiled coil region
|
2045 |
2067 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2086 |
2111 |
4.45e0 |
SMART |
|
low complexity region
|
2116 |
2138 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2144 |
2169 |
1.64e-1 |
SMART |
|
ZnF_C2H2
|
2188 |
2213 |
3.24e0 |
SMART |
|
ZnF_C2H2
|
2228 |
2253 |
1.18e-2 |
SMART |
|
low complexity region
|
2296 |
2309 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
2357 |
2381 |
2.86e-1 |
SMART |
|
low complexity region
|
2584 |
2600 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.8933 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.4%
- 20x: 95.4%
|
| Validation Efficiency |
96% (99/103) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 101 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310002L09Rik |
A |
T |
4: 73,861,115 (GRCm39) |
W162R |
probably benign |
Het |
| 4930438A08Rik |
C |
A |
11: 58,184,464 (GRCm39) |
P394H |
probably damaging |
Het |
| Aggf1 |
C |
T |
13: 95,508,123 (GRCm39) |
C81Y |
probably benign |
Het |
| Agxt2 |
A |
T |
15: 10,378,963 (GRCm39) |
D188V |
probably damaging |
Het |
| Angpt2 |
T |
C |
8: 18,748,132 (GRCm39) |
K376R |
probably benign |
Het |
| Anxa5 |
A |
G |
3: 36,504,840 (GRCm39) |
S241P |
probably damaging |
Het |
| Aox3 |
A |
T |
1: 58,209,018 (GRCm39) |
K850N |
probably damaging |
Het |
| Arid5a |
T |
C |
1: 36,358,473 (GRCm39) |
M415T |
probably benign |
Het |
| Aspa |
T |
A |
11: 73,199,578 (GRCm39) |
N233I |
probably damaging |
Het |
| Atp4b |
C |
T |
8: 13,438,782 (GRCm39) |
R198Q |
probably damaging |
Het |
| Atp8b2 |
A |
T |
3: 89,853,528 (GRCm39) |
V719E |
possibly damaging |
Het |
| Bltp2 |
C |
A |
11: 78,162,210 (GRCm39) |
L691I |
possibly damaging |
Het |
| Cacna1s |
T |
G |
1: 136,033,574 (GRCm39) |
V1017G |
probably damaging |
Het |
| Chrna4 |
G |
T |
2: 180,671,235 (GRCm39) |
Q174K |
probably damaging |
Het |
| Chrnb1 |
A |
T |
11: 69,677,765 (GRCm39) |
V329D |
probably damaging |
Het |
| Chst14 |
T |
C |
2: 118,758,214 (GRCm39) |
L336P |
probably damaging |
Het |
| Clec2e |
T |
C |
6: 129,077,772 (GRCm39) |
D22G |
probably benign |
Het |
| Csrnp2 |
A |
C |
15: 100,380,263 (GRCm39) |
S343A |
probably benign |
Het |
| Dapl1 |
C |
A |
2: 59,315,057 (GRCm39) |
A2E |
probably damaging |
Het |
| Dlec1 |
G |
T |
9: 118,950,991 (GRCm39) |
R519L |
probably damaging |
Het |
| Dmgdh |
T |
A |
13: 93,845,251 (GRCm39) |
F415I |
possibly damaging |
Het |
| Dmgdh |
T |
C |
13: 93,888,834 (GRCm39) |
V824A |
probably damaging |
Het |
| Dnah11 |
T |
G |
12: 117,892,191 (GRCm39) |
T3661P |
probably benign |
Het |
| Dnah3 |
A |
G |
7: 119,629,254 (GRCm39) |
F1434L |
probably damaging |
Het |
| Dnajc11 |
C |
A |
4: 152,062,583 (GRCm39) |
|
probably benign |
Het |
| Dot1l |
A |
G |
10: 80,621,929 (GRCm39) |
E527G |
probably damaging |
Het |
| Drc7 |
T |
C |
8: 95,801,679 (GRCm39) |
L680P |
probably damaging |
Het |
| Dysf |
T |
C |
6: 84,083,844 (GRCm39) |
Y742H |
probably benign |
Het |
| Ece1 |
A |
G |
4: 137,688,958 (GRCm39) |
Y665C |
probably damaging |
Het |
| Emc1 |
A |
G |
4: 139,081,533 (GRCm39) |
K54E |
possibly damaging |
Het |
| Enoph1 |
C |
T |
5: 100,215,760 (GRCm39) |
T247M |
probably damaging |
Het |
| Exoc2 |
T |
C |
13: 31,084,812 (GRCm39) |
K383R |
probably benign |
Het |
| Fam227b |
A |
T |
2: 125,962,972 (GRCm39) |
H181Q |
probably damaging |
Het |
| Fsip2 |
A |
T |
2: 82,816,017 (GRCm39) |
M3917L |
probably benign |
Het |
| Gtf3a |
T |
A |
5: 146,892,338 (GRCm39) |
|
probably benign |
Het |
| Hgfac |
T |
A |
5: 35,198,973 (GRCm39) |
C11* |
probably null |
Het |
| Hmcn1 |
C |
A |
1: 150,539,660 (GRCm39) |
A2944S |
probably damaging |
Het |
| Hps5 |
T |
A |
7: 46,416,521 (GRCm39) |
Y947F |
probably benign |
Het |
| Ighv2-5 |
A |
T |
12: 113,649,120 (GRCm39) |
I111K |
probably benign |
Het |
| Inpp5e |
A |
T |
2: 26,297,860 (GRCm39) |
L247* |
probably null |
Het |
| Kbtbd11 |
T |
C |
8: 15,077,577 (GRCm39) |
S59P |
probably benign |
Het |
| Kctd19 |
G |
A |
8: 106,123,082 (GRCm39) |
H111Y |
probably damaging |
Het |
| Kif1a |
T |
C |
1: 92,952,370 (GRCm39) |
D1303G |
probably damaging |
Het |
| Kif7 |
A |
G |
7: 79,363,842 (GRCm39) |
V22A |
possibly damaging |
Het |
| Lrit3 |
A |
T |
3: 129,583,004 (GRCm39) |
C328S |
probably damaging |
Het |
| Lrrc37a |
G |
T |
11: 103,388,484 (GRCm39) |
Q2314K |
unknown |
Het |
| LTO1 |
G |
T |
7: 144,469,023 (GRCm39) |
V17L |
possibly damaging |
Het |
| Lurap1 |
G |
T |
4: 115,994,599 (GRCm39) |
P211T |
possibly damaging |
Het |
| Mbd2 |
T |
A |
18: 70,713,874 (GRCm39) |
N5K |
possibly damaging |
Het |
| Mbtps1 |
A |
C |
8: 120,242,341 (GRCm39) |
L894V |
probably benign |
Het |
| Mefv |
G |
A |
16: 3,525,906 (GRCm39) |
S787F |
possibly damaging |
Het |
| Miip |
T |
A |
4: 147,946,792 (GRCm39) |
I289F |
probably damaging |
Het |
| Mogat2 |
T |
A |
7: 98,872,720 (GRCm39) |
I155F |
possibly damaging |
Het |
| Mpp3 |
C |
A |
11: 101,902,515 (GRCm39) |
|
probably null |
Het |
| Mrrf |
A |
G |
2: 36,067,233 (GRCm39) |
K220E |
probably damaging |
Het |
| Mtmr6 |
C |
T |
14: 60,535,619 (GRCm39) |
P485L |
probably damaging |
Het |
| Mtor |
G |
A |
4: 148,621,892 (GRCm39) |
R1896K |
probably benign |
Het |
| Myh3 |
C |
T |
11: 66,978,371 (GRCm39) |
P453S |
probably benign |
Het |
| Nebl |
A |
G |
2: 17,455,045 (GRCm39) |
V112A |
probably benign |
Het |
| Nmnat2 |
G |
A |
1: 152,950,480 (GRCm39) |
W55* |
probably null |
Het |
| Nprl3 |
A |
G |
11: 32,217,432 (GRCm39) |
S37P |
probably damaging |
Het |
| Or4a73 |
T |
C |
2: 89,421,445 (GRCm39) |
N5D |
possibly damaging |
Het |
| Pcdhga4 |
T |
G |
18: 37,819,383 (GRCm39) |
S311A |
probably benign |
Het |
| Pcdhgb6 |
T |
C |
18: 37,876,165 (GRCm39) |
V291A |
probably benign |
Het |
| Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
| Peg3 |
T |
C |
7: 6,712,570 (GRCm39) |
E884G |
probably damaging |
Het |
| Pgpep1 |
G |
A |
8: 71,105,101 (GRCm39) |
T53M |
probably damaging |
Het |
| Phf12 |
A |
G |
11: 77,900,341 (GRCm39) |
T146A |
probably benign |
Het |
| Polr3k |
C |
G |
2: 181,506,281 (GRCm39) |
N10K |
probably damaging |
Het |
| Prickle4 |
C |
A |
17: 48,001,135 (GRCm39) |
G144C |
probably damaging |
Het |
| Ptpn6 |
T |
C |
6: 124,709,398 (GRCm39) |
Y25C |
probably damaging |
Het |
| Rad1 |
A |
G |
15: 10,488,160 (GRCm39) |
I95V |
probably damaging |
Het |
| Rad23b |
A |
G |
4: 55,382,540 (GRCm39) |
T248A |
probably benign |
Het |
| Rapgef3 |
T |
C |
15: 97,656,742 (GRCm39) |
D299G |
probably damaging |
Het |
| Rcc2 |
T |
G |
4: 140,444,335 (GRCm39) |
V342G |
possibly damaging |
Het |
| Rgs3 |
G |
T |
4: 62,544,143 (GRCm39) |
R136L |
probably damaging |
Het |
| Scube2 |
A |
T |
7: 109,432,220 (GRCm39) |
C399* |
probably null |
Het |
| Serpinb3d |
T |
C |
1: 107,007,452 (GRCm39) |
Y178C |
probably damaging |
Het |
| Slc1a7 |
A |
G |
4: 107,869,458 (GRCm39) |
T508A |
probably benign |
Het |
| Slc29a4 |
C |
T |
5: 142,705,832 (GRCm39) |
R439C |
probably damaging |
Het |
| Sntg2 |
A |
G |
12: 30,362,560 (GRCm39) |
I62T |
probably benign |
Het |
| Sowaha |
G |
A |
11: 53,369,914 (GRCm39) |
P274L |
probably damaging |
Het |
| Sptan1 |
A |
G |
2: 29,886,794 (GRCm39) |
N869S |
probably benign |
Het |
| Stx18 |
C |
A |
5: 38,263,908 (GRCm39) |
A64D |
probably damaging |
Het |
| Stxbp5 |
A |
G |
10: 9,646,430 (GRCm39) |
V94A |
probably benign |
Het |
| Sult1a1 |
T |
A |
7: 126,275,624 (GRCm39) |
|
probably null |
Het |
| Susd1 |
G |
T |
4: 59,379,687 (GRCm39) |
H313Q |
possibly damaging |
Het |
| Tdrd9 |
A |
T |
12: 111,951,475 (GRCm39) |
K88N |
probably damaging |
Het |
| Tlr5 |
A |
C |
1: 182,801,603 (GRCm39) |
R302S |
possibly damaging |
Het |
| Tnr |
C |
T |
1: 159,714,479 (GRCm39) |
T786I |
probably damaging |
Het |
| Tprg1l |
A |
G |
4: 154,244,552 (GRCm39) |
S148P |
probably damaging |
Het |
| Trpc4ap |
T |
A |
2: 155,512,994 (GRCm39) |
N127I |
probably damaging |
Het |
| Tulp2 |
T |
A |
7: 45,139,797 (GRCm39) |
|
probably null |
Het |
| Uggt2 |
C |
T |
14: 119,273,381 (GRCm39) |
|
probably null |
Het |
| Ulk4 |
T |
A |
9: 121,102,021 (GRCm39) |
Y19F |
probably damaging |
Het |
| Upf1 |
T |
C |
8: 70,785,687 (GRCm39) |
Y1053C |
probably damaging |
Het |
| Vars2 |
A |
T |
17: 35,976,680 (GRCm39) |
H223Q |
probably benign |
Het |
| Vmn2r106 |
T |
A |
17: 20,487,806 (GRCm39) |
|
probably null |
Het |
| Ythdc2 |
T |
A |
18: 44,973,277 (GRCm39) |
F305I |
probably damaging |
Het |
| Zfp281 |
T |
C |
1: 136,553,178 (GRCm39) |
F52S |
possibly damaging |
Het |
| Zfp335 |
A |
T |
2: 164,737,018 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Zfp292 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00401:Zfp292
|
APN |
4 |
34,808,683 (GRCm39) |
missense |
probably benign |
0.15 |
|
IGL00502:Zfp292
|
APN |
4 |
34,809,775 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
IGL00539:Zfp292
|
APN |
4 |
34,808,790 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL00676:Zfp292
|
APN |
4 |
34,807,827 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01068:Zfp292
|
APN |
4 |
34,806,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01311:Zfp292
|
APN |
4 |
34,807,961 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01639:Zfp292
|
APN |
4 |
34,809,048 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL01688:Zfp292
|
APN |
4 |
34,807,855 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02345:Zfp292
|
APN |
4 |
34,809,244 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL02444:Zfp292
|
APN |
4 |
34,808,810 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL02548:Zfp292
|
APN |
4 |
34,805,416 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02551:Zfp292
|
APN |
4 |
34,806,462 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02702:Zfp292
|
APN |
4 |
34,809,415 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL02715:Zfp292
|
APN |
4 |
34,819,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03273:Zfp292
|
APN |
4 |
34,806,163 (GRCm39) |
missense |
probably benign |
0.00 |
|
F5770:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
PIT4362001:Zfp292
|
UTSW |
4 |
34,807,524 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0153:Zfp292
|
UTSW |
4 |
34,811,185 (GRCm39) |
missense |
probably benign |
0.26 |
|
R0184:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0295:Zfp292
|
UTSW |
4 |
34,806,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0367:Zfp292
|
UTSW |
4 |
34,808,227 (GRCm39) |
missense |
probably benign |
0.25 |
|
R0433:Zfp292
|
UTSW |
4 |
34,839,959 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0481:Zfp292
|
UTSW |
4 |
34,810,059 (GRCm39) |
missense |
probably benign |
0.28 |
|
R0555:Zfp292
|
UTSW |
4 |
34,807,194 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0597:Zfp292
|
UTSW |
4 |
34,807,399 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0748:Zfp292
|
UTSW |
4 |
34,816,424 (GRCm39) |
splice site |
probably benign |
|
|
R0782:Zfp292
|
UTSW |
4 |
34,839,382 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0834:Zfp292
|
UTSW |
4 |
34,809,114 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0879:Zfp292
|
UTSW |
4 |
34,811,218 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1083:Zfp292
|
UTSW |
4 |
34,807,569 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1343:Zfp292
|
UTSW |
4 |
34,805,238 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1498:Zfp292
|
UTSW |
4 |
34,805,397 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1714:Zfp292
|
UTSW |
4 |
34,808,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1724:Zfp292
|
UTSW |
4 |
34,811,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1755:Zfp292
|
UTSW |
4 |
34,811,043 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1837:Zfp292
|
UTSW |
4 |
34,810,264 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1914:Zfp292
|
UTSW |
4 |
34,805,100 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1915:Zfp292
|
UTSW |
4 |
34,805,100 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1936:Zfp292
|
UTSW |
4 |
34,807,452 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2107:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2108:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2136:Zfp292
|
UTSW |
4 |
34,810,266 (GRCm39) |
missense |
probably benign |
0.13 |
|
R2182:Zfp292
|
UTSW |
4 |
34,807,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2186:Zfp292
|
UTSW |
4 |
34,807,962 (GRCm39) |
missense |
probably benign |
0.07 |
|
R2306:Zfp292
|
UTSW |
4 |
34,809,468 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2350:Zfp292
|
UTSW |
4 |
34,811,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2382:Zfp292
|
UTSW |
4 |
34,806,426 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2872:Zfp292
|
UTSW |
4 |
34,808,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2872:Zfp292
|
UTSW |
4 |
34,808,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3018:Zfp292
|
UTSW |
4 |
34,808,814 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3812:Zfp292
|
UTSW |
4 |
34,810,326 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4006:Zfp292
|
UTSW |
4 |
34,807,744 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4006:Zfp292
|
UTSW |
4 |
34,809,611 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4060:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4062:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4063:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4064:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4207:Zfp292
|
UTSW |
4 |
34,806,079 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4641:Zfp292
|
UTSW |
4 |
34,807,828 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4684:Zfp292
|
UTSW |
4 |
34,807,078 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4718:Zfp292
|
UTSW |
4 |
34,819,521 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4865:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4870:Zfp292
|
UTSW |
4 |
34,808,917 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5097:Zfp292
|
UTSW |
4 |
34,839,878 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5233:Zfp292
|
UTSW |
4 |
34,809,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5246:Zfp292
|
UTSW |
4 |
34,805,842 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R5369:Zfp292
|
UTSW |
4 |
34,807,491 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5527:Zfp292
|
UTSW |
4 |
34,806,261 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5621:Zfp292
|
UTSW |
4 |
34,811,703 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5770:Zfp292
|
UTSW |
4 |
34,806,747 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5900:Zfp292
|
UTSW |
4 |
34,805,125 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5905:Zfp292
|
UTSW |
4 |
34,819,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5994:Zfp292
|
UTSW |
4 |
34,805,464 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6028:Zfp292
|
UTSW |
4 |
34,819,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6093:Zfp292
|
UTSW |
4 |
34,811,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6126:Zfp292
|
UTSW |
4 |
34,808,497 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6209:Zfp292
|
UTSW |
4 |
34,809,442 (GRCm39) |
missense |
probably benign |
0.14 |
|
R6275:Zfp292
|
UTSW |
4 |
34,808,883 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6523:Zfp292
|
UTSW |
4 |
34,816,301 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6747:Zfp292
|
UTSW |
4 |
34,806,894 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6752:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6967:Zfp292
|
UTSW |
4 |
34,807,812 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7038:Zfp292
|
UTSW |
4 |
34,816,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7056:Zfp292
|
UTSW |
4 |
34,809,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7088:Zfp292
|
UTSW |
4 |
34,806,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7158:Zfp292
|
UTSW |
4 |
34,808,679 (GRCm39) |
missense |
probably benign |
|
|
R7254:Zfp292
|
UTSW |
4 |
34,819,476 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7350:Zfp292
|
UTSW |
4 |
34,806,839 (GRCm39) |
missense |
probably benign |
|
|
R7378:Zfp292
|
UTSW |
4 |
34,808,384 (GRCm39) |
missense |
probably benign |
0.26 |
|
R7535:Zfp292
|
UTSW |
4 |
34,811,487 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7589:Zfp292
|
UTSW |
4 |
34,806,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7816:Zfp292
|
UTSW |
4 |
34,809,865 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7979:Zfp292
|
UTSW |
4 |
34,809,198 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7997:Zfp292
|
UTSW |
4 |
34,808,688 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8129:Zfp292
|
UTSW |
4 |
34,807,386 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8211:Zfp292
|
UTSW |
4 |
34,806,163 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8302:Zfp292
|
UTSW |
4 |
34,810,893 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R8500:Zfp292
|
UTSW |
4 |
34,826,691 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8709:Zfp292
|
UTSW |
4 |
34,805,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8947:Zfp292
|
UTSW |
4 |
34,811,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9099:Zfp292
|
UTSW |
4 |
34,809,228 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R9190:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9256:Zfp292
|
UTSW |
4 |
34,839,899 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9371:Zfp292
|
UTSW |
4 |
34,810,800 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9492:Zfp292
|
UTSW |
4 |
34,810,794 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9574:Zfp292
|
UTSW |
4 |
34,839,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|
V7580:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
V7581:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
V7582:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
V7583:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
Z1177:Zfp292
|
UTSW |
4 |
34,811,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGCTGCTCACTTGTGATGGC -3'
(R):5'- TTTTCTGTACAAAATGAGGCAGGAC -3'
|
| Posted On |
2017-07-14 |
Incidental Mutation