Incidental Mutation 'R1914:Zfp292'
| ID |
214662 |
| 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 |
039932-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.843)
|
| Stock # |
R1914 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
34803113-34882960 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 34805100 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Phenylalanine
at position 2648
(S2648F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000095766
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047950]
[ENSMUST00000098163]
|
| AlphaFold |
Q9Z2U2 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000047950
AA Change: S2653F
PolyPhen 2
Score 0.868 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000037233
Gene: ENSMUSG00000039967
AA Change: S2653F
| 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 |
possibly damaging
Transcript: ENSMUST00000098163
AA Change: S2648F
PolyPhen 2
Score 0.919 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000095766
Gene: ENSMUSG00000039967
AA Change: S2648F
| 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 |
0.1795 |
| Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.1%
- 20x: 91.6%
|
| Validation Efficiency |
99% (90/91) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4833420G17Rik |
T |
A |
13: 119,622,386 (GRCm39) |
V618E |
possibly damaging |
Het |
| Abca6 |
T |
C |
11: 110,103,036 (GRCm39) |
R852G |
probably benign |
Het |
| Akap12 |
G |
A |
10: 4,306,685 (GRCm39) |
R1165H |
probably benign |
Het |
| Asxl1 |
T |
C |
2: 153,243,826 (GRCm39) |
S1459P |
probably damaging |
Het |
| Bahcc1 |
C |
T |
11: 120,176,225 (GRCm39) |
R1957C |
probably damaging |
Het |
| Bcar1 |
A |
G |
8: 112,442,030 (GRCm39) |
V270A |
probably damaging |
Het |
| Camsap3 |
C |
T |
8: 3,654,708 (GRCm39) |
R782C |
probably damaging |
Het |
| Capn15 |
C |
A |
17: 26,183,837 (GRCm39) |
A215S |
probably benign |
Het |
| Casz1 |
T |
C |
4: 149,017,415 (GRCm39) |
F235L |
probably damaging |
Het |
| Ccdc57 |
A |
T |
11: 120,794,134 (GRCm39) |
|
probably benign |
Het |
| Cdh23 |
A |
G |
10: 60,159,349 (GRCm39) |
V2142A |
probably damaging |
Het |
| Cdx1 |
A |
G |
18: 61,152,970 (GRCm39) |
V212A |
probably benign |
Het |
| Cep104 |
T |
C |
4: 154,074,296 (GRCm39) |
L516P |
possibly damaging |
Het |
| Cep95 |
C |
T |
11: 106,705,464 (GRCm39) |
T483I |
probably damaging |
Het |
| Cfap100 |
T |
C |
6: 90,389,329 (GRCm39) |
|
probably benign |
Het |
| Chia1 |
T |
A |
3: 106,035,875 (GRCm39) |
N238K |
probably benign |
Het |
| Cntrl |
T |
C |
2: 35,052,873 (GRCm39) |
M1126T |
probably benign |
Het |
| Col28a1 |
A |
G |
6: 8,176,333 (GRCm39) |
F8S |
probably benign |
Het |
| Cpeb3 |
C |
T |
19: 37,031,665 (GRCm39) |
R579Q |
probably damaging |
Het |
| Dbh |
A |
G |
2: 27,058,234 (GRCm39) |
D134G |
probably damaging |
Het |
| Diaph3 |
A |
C |
14: 86,893,921 (GRCm39) |
N29K |
probably damaging |
Het |
| Dnajc2 |
A |
G |
5: 21,986,317 (GRCm39) |
|
probably null |
Het |
| Ephb1 |
C |
T |
9: 101,806,577 (GRCm39) |
C819Y |
probably damaging |
Het |
| Eps8l2 |
G |
A |
7: 140,941,765 (GRCm39) |
V650M |
probably damaging |
Het |
| Erlin1 |
T |
C |
19: 44,047,504 (GRCm39) |
Y139C |
probably damaging |
Het |
| Fezf2 |
A |
T |
14: 12,343,988 (GRCm38) |
V301E |
probably damaging |
Het |
| Fnbp4 |
T |
C |
2: 90,609,537 (GRCm39) |
|
probably benign |
Het |
| Gal3st4 |
T |
A |
5: 138,263,672 (GRCm39) |
K442N |
probably benign |
Het |
| Gas6 |
T |
C |
8: 13,527,152 (GRCm39) |
T199A |
probably benign |
Het |
| Gm10644 |
G |
A |
8: 84,660,479 (GRCm39) |
|
probably benign |
Het |
| Gpr88 |
G |
T |
3: 116,046,073 (GRCm39) |
S79R |
possibly damaging |
Het |
| Grm4 |
A |
T |
17: 27,653,686 (GRCm39) |
C755S |
probably damaging |
Het |
| Hdgfl2 |
A |
G |
17: 56,403,978 (GRCm39) |
D278G |
probably damaging |
Het |
| Heatr5a |
G |
T |
12: 51,952,250 (GRCm39) |
A1130E |
probably damaging |
Het |
| Heatr9 |
T |
G |
11: 83,409,035 (GRCm39) |
I171L |
possibly damaging |
Het |
| Hectd4 |
A |
G |
5: 121,460,357 (GRCm39) |
T2209A |
probably benign |
Het |
| Hsh2d |
A |
G |
8: 72,947,365 (GRCm39) |
T21A |
probably damaging |
Het |
| Ing1 |
T |
A |
8: 11,611,577 (GRCm39) |
V63E |
probably damaging |
Het |
| Irf4 |
A |
T |
13: 30,945,445 (GRCm39) |
Q397L |
probably benign |
Het |
| Itgae |
T |
A |
11: 73,009,469 (GRCm39) |
|
probably benign |
Het |
| Jrkl |
A |
T |
9: 13,245,609 (GRCm39) |
D17E |
possibly damaging |
Het |
| Kcnh6 |
T |
A |
11: 105,908,270 (GRCm39) |
Y295* |
probably null |
Het |
| Klf5 |
T |
C |
14: 99,539,357 (GRCm39) |
S177P |
probably benign |
Het |
| Lats1 |
T |
A |
10: 7,586,221 (GRCm39) |
|
probably benign |
Het |
| Lilrb4a |
A |
G |
10: 51,368,045 (GRCm39) |
I53M |
probably benign |
Het |
| Lrrc2 |
T |
A |
9: 110,810,007 (GRCm39) |
Y348N |
probably damaging |
Het |
| Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
| Med25 |
A |
G |
7: 44,534,046 (GRCm39) |
S245P |
probably benign |
Het |
| Mlh3 |
T |
C |
12: 85,308,442 (GRCm39) |
Y1115C |
probably benign |
Het |
| Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
| Myh10 |
T |
C |
11: 68,681,034 (GRCm39) |
L1025P |
probably damaging |
Het |
| Myof |
T |
A |
19: 37,966,141 (GRCm39) |
N393I |
probably damaging |
Het |
| Naip6 |
T |
A |
13: 100,435,936 (GRCm39) |
E862D |
probably benign |
Het |
| Ncald |
C |
T |
15: 37,397,324 (GRCm39) |
A119T |
probably benign |
Het |
| Nipbl |
T |
C |
15: 8,373,114 (GRCm39) |
E1044G |
possibly damaging |
Het |
| Nyap2 |
T |
C |
1: 81,169,602 (GRCm39) |
S120P |
probably damaging |
Het |
| Oas1a |
A |
T |
5: 121,043,876 (GRCm39) |
N85K |
possibly damaging |
Het |
| Or8b12i |
T |
C |
9: 20,082,324 (GRCm39) |
Y181C |
probably benign |
Het |
| Pappa2 |
A |
T |
1: 158,578,133 (GRCm39) |
D1721E |
probably damaging |
Het |
| Pcid2 |
A |
T |
8: 13,144,141 (GRCm39) |
|
probably null |
Het |
| Pou2f2 |
C |
T |
7: 24,799,581 (GRCm39) |
A92T |
possibly damaging |
Het |
| Ppp1r16a |
T |
C |
15: 76,577,268 (GRCm39) |
L212P |
probably damaging |
Het |
| Ptbp3 |
A |
T |
4: 59,517,635 (GRCm39) |
L84Q |
probably damaging |
Het |
| Ptgr2 |
A |
T |
12: 84,349,096 (GRCm39) |
Q145L |
probably benign |
Het |
| Pudp |
T |
C |
18: 50,701,278 (GRCm39) |
N152D |
probably benign |
Het |
| Rabggta |
A |
T |
14: 55,958,646 (GRCm39) |
F62L |
possibly damaging |
Het |
| Rasal3 |
G |
A |
17: 32,615,324 (GRCm39) |
Q505* |
probably null |
Het |
| Rbm20 |
T |
A |
19: 53,852,518 (GRCm39) |
L1166Q |
probably damaging |
Het |
| Rictor |
T |
G |
15: 6,789,053 (GRCm39) |
I223R |
probably damaging |
Het |
| Ripor1 |
A |
T |
8: 106,343,518 (GRCm39) |
E270D |
probably damaging |
Het |
| Rorc |
T |
C |
3: 94,298,480 (GRCm39) |
C322R |
probably damaging |
Het |
| Rpgrip1l |
T |
C |
8: 91,959,552 (GRCm39) |
D1116G |
probably benign |
Het |
| Rsph4a |
A |
T |
10: 33,789,068 (GRCm39) |
N638Y |
probably damaging |
Het |
| Scn9a |
A |
G |
2: 66,396,594 (GRCm39) |
F100L |
probably damaging |
Het |
| Siglece |
A |
G |
7: 43,307,219 (GRCm39) |
V256A |
probably benign |
Het |
| Slc23a2 |
A |
T |
2: 131,898,686 (GRCm39) |
L617Q |
probably damaging |
Het |
| Snx9 |
T |
C |
17: 5,978,531 (GRCm39) |
I567T |
possibly damaging |
Het |
| Sptan1 |
C |
G |
2: 29,901,048 (GRCm39) |
Q1425E |
probably benign |
Het |
| Srd5a3 |
G |
A |
5: 76,295,552 (GRCm39) |
V81I |
probably benign |
Het |
| Sugp2 |
T |
A |
8: 70,706,310 (GRCm39) |
I790K |
probably damaging |
Het |
| Syde2 |
T |
G |
3: 145,720,071 (GRCm39) |
Y764* |
probably null |
Het |
| Tbl1xr1 |
T |
C |
3: 22,245,074 (GRCm39) |
|
probably benign |
Het |
| Tmem130 |
A |
G |
5: 144,674,666 (GRCm39) |
F353S |
probably damaging |
Het |
| Tmem131 |
T |
A |
1: 36,835,347 (GRCm39) |
K1591N |
probably damaging |
Het |
| Trim43c |
T |
A |
9: 88,722,670 (GRCm39) |
D105E |
probably benign |
Het |
| Urb2 |
C |
A |
8: 124,756,537 (GRCm39) |
T748K |
possibly damaging |
Het |
| Vmn2r18 |
T |
C |
5: 151,499,286 (GRCm39) |
N393D |
probably benign |
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 |
|
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 |
|
R6056:Zfp292
|
UTSW |
4 |
34,809,784 (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'- AGCTCACAACAGCATGCTTG -3'
(R):5'- GTGGAAGTAAAAGAGGATCCCATTCC -3'
Sequencing Primer
(F):5'- CAACAGCATGCTTGATGGC -3'
(R):5'- TTCCAGCTCCAGAAGACATGTTG -3'
|
| Posted On |
2014-07-14 |
Incidental Mutation