Incidental Mutation 'R4732:Zfhx4'
ID |
359041 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfhx4
|
Ensembl Gene |
ENSMUSG00000025255 |
Gene Name |
zinc finger homeodomain 4 |
Synonyms |
Zfh-4, Zfh4, C130041O22Rik |
MMRRC Submission |
042022-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.663)
|
Stock # |
R4732 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
5283586-5480917 bp(+) (GRCm39) |
Type of Mutation |
unclassified |
DNA Base Change (assembly) |
T to C
at 5279867 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000135827
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000026284]
[ENSMUST00000175866]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000026284
|
SMART Domains |
Protein: ENSMUSP00000026284 Gene: ENSMUSG00000025255
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
80 |
99 |
1.78e2 |
SMART |
low complexity region
|
110 |
122 |
N/A |
INTRINSIC |
ZnF_C2H2
|
277 |
300 |
1.55e1 |
SMART |
low complexity region
|
421 |
438 |
N/A |
INTRINSIC |
low complexity region
|
470 |
475 |
N/A |
INTRINSIC |
low complexity region
|
590 |
610 |
N/A |
INTRINSIC |
ZnF_C2H2
|
611 |
634 |
2.45e0 |
SMART |
ZnF_C2H2
|
642 |
665 |
6.78e-3 |
SMART |
ZnF_U1
|
694 |
728 |
1.8e-1 |
SMART |
ZnF_C2H2
|
697 |
721 |
4.87e-4 |
SMART |
low complexity region
|
754 |
763 |
N/A |
INTRINSIC |
ZnF_C2H2
|
765 |
789 |
6.67e-2 |
SMART |
ZnF_C2H2
|
876 |
897 |
2.44e2 |
SMART |
ZnF_U1
|
912 |
946 |
2.88e0 |
SMART |
ZnF_C2H2
|
915 |
939 |
1.23e0 |
SMART |
ZnF_C2H2
|
971 |
993 |
7.05e-1 |
SMART |
ZnF_U1
|
1016 |
1050 |
3.73e0 |
SMART |
ZnF_C2H2
|
1019 |
1043 |
4.98e-1 |
SMART |
ZnF_C2H2
|
1188 |
1211 |
1.1e-2 |
SMART |
ZnF_C2H2
|
1217 |
1240 |
4.94e0 |
SMART |
ZnF_C2H2
|
1368 |
1390 |
7.67e-2 |
SMART |
ZnF_C2H2
|
1396 |
1419 |
1.33e-1 |
SMART |
ZnF_U1
|
1509 |
1543 |
7.4e-1 |
SMART |
ZnF_C2H2
|
1512 |
1536 |
8.22e-2 |
SMART |
ZnF_U1
|
1561 |
1595 |
3.73e0 |
SMART |
ZnF_C2H2
|
1564 |
1588 |
1.16e-1 |
SMART |
low complexity region
|
1664 |
1692 |
N/A |
INTRINSIC |
low complexity region
|
1701 |
1713 |
N/A |
INTRINSIC |
low complexity region
|
1762 |
1808 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1916 |
1939 |
3.07e-1 |
SMART |
low complexity region
|
1964 |
1990 |
N/A |
INTRINSIC |
low complexity region
|
2008 |
2032 |
N/A |
INTRINSIC |
low complexity region
|
2055 |
2072 |
N/A |
INTRINSIC |
HOX
|
2100 |
2162 |
4.23e-16 |
SMART |
HOX
|
2197 |
2259 |
5.62e-21 |
SMART |
ZnF_C2H2
|
2283 |
2303 |
1.13e1 |
SMART |
low complexity region
|
2364 |
2376 |
N/A |
INTRINSIC |
low complexity region
|
2408 |
2425 |
N/A |
INTRINSIC |
low complexity region
|
2449 |
2460 |
N/A |
INTRINSIC |
ZnF_C2H2
|
2461 |
2483 |
2.17e-1 |
SMART |
HOX
|
2573 |
2635 |
3.18e-20 |
SMART |
ZnF_C2H2
|
2643 |
2666 |
6.67e-2 |
SMART |
low complexity region
|
2874 |
2886 |
N/A |
INTRINSIC |
HOX
|
2896 |
2958 |
4.54e-16 |
SMART |
ZnF_U1
|
2971 |
3005 |
6.59e-1 |
SMART |
ZnF_C2H2
|
2974 |
2998 |
1.36e1 |
SMART |
low complexity region
|
3066 |
3078 |
N/A |
INTRINSIC |
low complexity region
|
3106 |
3119 |
N/A |
INTRINSIC |
low complexity region
|
3163 |
3186 |
N/A |
INTRINSIC |
coiled coil region
|
3279 |
3308 |
N/A |
INTRINSIC |
ZnF_C2H2
|
3368 |
3388 |
1.12e2 |
SMART |
ZnF_U1
|
3409 |
3443 |
6.16e-2 |
SMART |
ZnF_C2H2
|
3412 |
3436 |
6.57e0 |
SMART |
low complexity region
|
3461 |
3479 |
N/A |
INTRINSIC |
low complexity region
|
3505 |
3527 |
N/A |
INTRINSIC |
low complexity region
|
3536 |
3547 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128815
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000175641
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000175866
|
SMART Domains |
Protein: ENSMUSP00000135827 Gene: ENSMUSG00000025255
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
80 |
99 |
1.78e2 |
SMART |
low complexity region
|
110 |
122 |
N/A |
INTRINSIC |
ZnF_C2H2
|
277 |
300 |
1.55e1 |
SMART |
low complexity region
|
421 |
438 |
N/A |
INTRINSIC |
low complexity region
|
470 |
475 |
N/A |
INTRINSIC |
low complexity region
|
590 |
610 |
N/A |
INTRINSIC |
ZnF_C2H2
|
611 |
634 |
2.45e0 |
SMART |
ZnF_C2H2
|
642 |
665 |
6.78e-3 |
SMART |
ZnF_U1
|
694 |
728 |
1.8e-1 |
SMART |
ZnF_C2H2
|
697 |
721 |
4.87e-4 |
SMART |
low complexity region
|
754 |
763 |
N/A |
INTRINSIC |
ZnF_C2H2
|
765 |
789 |
6.67e-2 |
SMART |
ZnF_C2H2
|
902 |
923 |
2.44e2 |
SMART |
ZnF_U1
|
938 |
972 |
2.88e0 |
SMART |
ZnF_C2H2
|
941 |
965 |
1.23e0 |
SMART |
ZnF_C2H2
|
997 |
1019 |
7.05e-1 |
SMART |
ZnF_U1
|
1042 |
1076 |
3.73e0 |
SMART |
ZnF_C2H2
|
1045 |
1069 |
4.98e-1 |
SMART |
ZnF_C2H2
|
1213 |
1236 |
1.1e-2 |
SMART |
ZnF_C2H2
|
1242 |
1265 |
4.94e0 |
SMART |
ZnF_C2H2
|
1393 |
1415 |
7.67e-2 |
SMART |
ZnF_C2H2
|
1421 |
1444 |
1.33e-1 |
SMART |
ZnF_U1
|
1534 |
1568 |
7.4e-1 |
SMART |
ZnF_C2H2
|
1537 |
1561 |
8.22e-2 |
SMART |
ZnF_U1
|
1586 |
1620 |
3.73e0 |
SMART |
ZnF_C2H2
|
1589 |
1613 |
1.16e-1 |
SMART |
low complexity region
|
1689 |
1717 |
N/A |
INTRINSIC |
low complexity region
|
1726 |
1738 |
N/A |
INTRINSIC |
low complexity region
|
1787 |
1833 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1941 |
1964 |
3.07e-1 |
SMART |
low complexity region
|
1989 |
2015 |
N/A |
INTRINSIC |
low complexity region
|
2033 |
2057 |
N/A |
INTRINSIC |
low complexity region
|
2080 |
2097 |
N/A |
INTRINSIC |
HOX
|
2125 |
2187 |
4.23e-16 |
SMART |
HOX
|
2222 |
2284 |
5.62e-21 |
SMART |
ZnF_C2H2
|
2308 |
2328 |
1.13e1 |
SMART |
low complexity region
|
2389 |
2401 |
N/A |
INTRINSIC |
low complexity region
|
2433 |
2450 |
N/A |
INTRINSIC |
low complexity region
|
2474 |
2485 |
N/A |
INTRINSIC |
ZnF_C2H2
|
2486 |
2508 |
2.17e-1 |
SMART |
HOX
|
2598 |
2660 |
3.18e-20 |
SMART |
ZnF_C2H2
|
2668 |
2691 |
6.67e-2 |
SMART |
low complexity region
|
2899 |
2911 |
N/A |
INTRINSIC |
HOX
|
2921 |
2983 |
4.54e-16 |
SMART |
ZnF_U1
|
2996 |
3030 |
6.59e-1 |
SMART |
ZnF_C2H2
|
2999 |
3023 |
1.36e1 |
SMART |
low complexity region
|
3091 |
3103 |
N/A |
INTRINSIC |
low complexity region
|
3131 |
3144 |
N/A |
INTRINSIC |
low complexity region
|
3188 |
3211 |
N/A |
INTRINSIC |
coiled coil region
|
3304 |
3333 |
N/A |
INTRINSIC |
ZnF_C2H2
|
3393 |
3413 |
1.12e2 |
SMART |
ZnF_U1
|
3434 |
3468 |
6.16e-2 |
SMART |
ZnF_C2H2
|
3437 |
3461 |
6.57e0 |
SMART |
low complexity region
|
3486 |
3504 |
N/A |
INTRINSIC |
low complexity region
|
3530 |
3552 |
N/A |
INTRINSIC |
low complexity region
|
3561 |
3572 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177440
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000194070
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000194396
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.2%
- 20x: 95.1%
|
Validation Efficiency |
99% (110/111) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 192 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700128F08Rik |
T |
A |
9: 8,222,174 (GRCm39) |
|
noncoding transcript |
Het |
4933409G03Rik |
A |
G |
2: 68,445,065 (GRCm39) |
|
probably benign |
Het |
Acan |
T |
C |
7: 78,748,357 (GRCm39) |
S1043P |
probably damaging |
Het |
Ackr2 |
A |
G |
9: 121,738,249 (GRCm39) |
Y208C |
probably damaging |
Het |
Actg1 |
C |
T |
11: 120,238,305 (GRCm39) |
|
probably benign |
Het |
Actmap |
T |
A |
7: 26,900,468 (GRCm39) |
M149K |
probably damaging |
Het |
Adam1a |
T |
A |
5: 121,657,497 (GRCm39) |
T599S |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,270,748 (GRCm39) |
S668C |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,626,711 (GRCm39) |
V709A |
possibly damaging |
Het |
Adgrf2 |
A |
C |
17: 43,021,645 (GRCm39) |
I393S |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,984,665 (GRCm39) |
G1983V |
probably damaging |
Het |
Aim2 |
T |
A |
1: 173,291,442 (GRCm39) |
D282E |
possibly damaging |
Het |
Ak8 |
A |
G |
2: 28,650,083 (GRCm39) |
Y370C |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,063,901 (GRCm39) |
D1750G |
probably damaging |
Het |
Als2cl |
T |
A |
9: 110,718,204 (GRCm39) |
V315E |
probably damaging |
Het |
Ankrd28 |
A |
C |
14: 31,477,698 (GRCm39) |
C115G |
probably benign |
Het |
Ap3b2 |
C |
T |
7: 81,121,680 (GRCm39) |
A519T |
probably damaging |
Het |
Apool |
C |
T |
X: 111,281,897 (GRCm39) |
T166I |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,539,247 (GRCm39) |
K65* |
probably null |
Het |
Arhgef38 |
G |
T |
3: 132,838,030 (GRCm39) |
Y633* |
probably null |
Het |
Asah2 |
T |
C |
19: 31,972,758 (GRCm39) |
N659S |
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,059,750 (GRCm39) |
D430G |
possibly damaging |
Het |
Atp8a1 |
G |
A |
5: 67,970,463 (GRCm39) |
S92L |
probably benign |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
C130073F10Rik |
C |
A |
4: 101,747,907 (GRCm39) |
S89I |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,334,041 (GRCm39) |
T867A |
probably damaging |
Het |
Ccdc88a |
T |
G |
11: 29,435,906 (GRCm39) |
N1276K |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,361,221 (GRCm39) |
V282E |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,577,530 (GRCm39) |
L92H |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,306,268 (GRCm39) |
D2012V |
probably damaging |
Het |
Cenpt |
A |
G |
8: 106,573,768 (GRCm39) |
V254A |
probably benign |
Het |
Cep104 |
T |
A |
4: 154,072,883 (GRCm39) |
D380E |
probably damaging |
Het |
Cers5 |
C |
T |
15: 99,639,518 (GRCm39) |
R123Q |
probably benign |
Het |
Ces2h |
A |
G |
8: 105,741,236 (GRCm39) |
E76G |
probably damaging |
Het |
Cfap77 |
T |
A |
2: 28,874,400 (GRCm39) |
E143D |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,969,745 (GRCm39) |
R65L |
probably damaging |
Het |
Cldnd2 |
T |
A |
7: 43,091,613 (GRCm39) |
C65S |
possibly damaging |
Het |
Clec2g |
C |
A |
6: 128,958,842 (GRCm39) |
Y142* |
probably null |
Het |
Coch |
A |
T |
12: 51,651,802 (GRCm39) |
E549V |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,563,467 (GRCm39) |
D215G |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,464,779 (GRCm39) |
V348A |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,496,197 (GRCm39) |
H1606R |
probably benign |
Het |
Cpd |
T |
C |
11: 76,702,620 (GRCm39) |
N583D |
probably damaging |
Het |
Cyp2d11 |
T |
A |
15: 82,273,428 (GRCm39) |
Y481F |
probably benign |
Het |
D130043K22Rik |
T |
C |
13: 25,083,648 (GRCm39) |
S1038P |
probably damaging |
Het |
Deptor |
C |
A |
15: 55,044,406 (GRCm39) |
H191N |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,684 (GRCm39) |
I699N |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,503,741 (GRCm39) |
T1653I |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,809,333 (GRCm39) |
N3550K |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,994,035 (GRCm39) |
K3384R |
probably null |
Het |
Dnajc11 |
A |
G |
4: 152,055,424 (GRCm39) |
|
probably benign |
Het |
Dnajc13 |
CT |
C |
9: 104,064,004 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
C |
A |
7: 105,323,056 (GRCm39) |
N521K |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,352,222 (GRCm39) |
|
probably null |
Het |
Dync1h1 |
C |
T |
12: 110,615,941 (GRCm39) |
Q3030* |
probably null |
Het |
Efhb |
G |
A |
17: 53,733,272 (GRCm39) |
T533I |
probably damaging |
Het |
Eif2d |
T |
C |
1: 131,092,464 (GRCm39) |
V374A |
probably damaging |
Het |
Etfb |
T |
C |
7: 43,093,624 (GRCm39) |
V17A |
probably damaging |
Het |
F5 |
C |
T |
1: 164,009,226 (GRCm39) |
T332M |
probably damaging |
Het |
Fcho1 |
T |
C |
8: 72,169,439 (GRCm39) |
T156A |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,641,671 (GRCm39) |
|
probably null |
Het |
Fnip2 |
A |
T |
3: 79,388,959 (GRCm39) |
S561T |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,909,998 (GRCm39) |
T455S |
probably benign |
Het |
Fry |
G |
A |
5: 150,309,472 (GRCm39) |
E639K |
|
Het |
Fto |
T |
A |
8: 92,136,342 (GRCm39) |
D205E |
probably damaging |
Het |
Galnt2l |
A |
G |
8: 122,997,013 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
G |
A |
8: 58,880,847 (GRCm39) |
P147L |
probably damaging |
Het |
Gigyf1 |
T |
A |
5: 137,523,032 (GRCm39) |
D844E |
probably benign |
Het |
Gle1 |
T |
C |
2: 29,830,244 (GRCm39) |
S267P |
probably damaging |
Het |
Glg1 |
G |
A |
8: 111,914,387 (GRCm39) |
R466W |
probably damaging |
Het |
Gm10277 |
T |
C |
11: 77,676,923 (GRCm39) |
|
probably benign |
Het |
Gm6871 |
T |
C |
7: 41,196,173 (GRCm39) |
I39V |
probably benign |
Het |
Gm9970 |
A |
G |
5: 31,398,410 (GRCm39) |
|
probably benign |
Het |
Gpr35 |
T |
G |
1: 92,911,107 (GRCm39) |
I57S |
probably damaging |
Het |
Gprin1 |
C |
T |
13: 54,887,770 (GRCm39) |
G168E |
possibly damaging |
Het |
Gtdc1 |
A |
G |
2: 44,679,067 (GRCm39) |
|
probably benign |
Het |
Gtf3c2 |
G |
T |
5: 31,317,401 (GRCm39) |
P586T |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm39) |
H410L |
probably benign |
Het |
Gucy2c |
A |
G |
6: 136,744,150 (GRCm39) |
S150P |
probably damaging |
Het |
Ifi214 |
T |
C |
1: 173,354,157 (GRCm39) |
Q171R |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,721 (GRCm39) |
I245M |
probably benign |
Het |
Igkv4-50 |
T |
C |
6: 69,677,984 (GRCm39) |
K40R |
probably benign |
Het |
Igkv8-18 |
T |
A |
6: 70,333,280 (GRCm39) |
I74N |
probably damaging |
Het |
Il2ra |
T |
A |
2: 11,681,731 (GRCm39) |
M112K |
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kbtbd7 |
T |
C |
14: 79,666,240 (GRCm39) |
*691Q |
probably null |
Het |
Kcnn2 |
T |
A |
18: 45,693,416 (GRCm39) |
S331T |
possibly damaging |
Het |
Khnyn |
T |
A |
14: 56,123,946 (GRCm39) |
|
probably null |
Het |
Kif26a |
G |
A |
12: 112,142,007 (GRCm39) |
A754T |
probably benign |
Het |
Klra3 |
T |
A |
6: 130,304,095 (GRCm39) |
Y199F |
possibly damaging |
Het |
Lhx2 |
A |
G |
2: 38,250,003 (GRCm39) |
K274R |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,363,899 (GRCm39) |
I313V |
probably benign |
Het |
Lrrfip1 |
A |
T |
1: 91,043,369 (GRCm39) |
E591D |
probably benign |
Het |
Lrrk2 |
A |
C |
15: 91,573,052 (GRCm39) |
E200A |
probably damaging |
Het |
Lrrk2 |
G |
A |
15: 91,649,950 (GRCm39) |
E1696K |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,909,080 (GRCm39) |
M465K |
probably damaging |
Het |
Moxd2 |
T |
G |
6: 40,855,793 (GRCm39) |
I599L |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,048,831 (GRCm39) |
S866P |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,231,772 (GRCm39) |
T79A |
possibly damaging |
Het |
Ncoa6 |
C |
A |
2: 155,263,221 (GRCm39) |
Q404H |
probably damaging |
Het |
Neb |
A |
G |
2: 52,169,091 (GRCm39) |
Y1815H |
probably damaging |
Het |
Nell1 |
A |
G |
7: 50,505,965 (GRCm39) |
D724G |
probably damaging |
Het |
Nkx3-2 |
A |
G |
5: 41,919,487 (GRCm39) |
V167A |
probably benign |
Het |
Nsun3 |
C |
A |
16: 62,555,482 (GRCm39) |
C348F |
possibly damaging |
Het |
Obox6 |
A |
T |
7: 15,568,697 (GRCm39) |
S60T |
possibly damaging |
Het |
Oog2 |
T |
A |
4: 143,920,511 (GRCm39) |
|
probably benign |
Het |
Or10g9b |
A |
T |
9: 39,917,564 (GRCm39) |
I227N |
probably damaging |
Het |
Or11g2 |
T |
A |
14: 50,856,026 (GRCm39) |
C116S |
probably benign |
Het |
Or1ad6 |
G |
A |
11: 50,860,093 (GRCm39) |
V83M |
possibly damaging |
Het |
Or1e16 |
T |
C |
11: 73,286,521 (GRCm39) |
D109G |
probably benign |
Het |
Or2i1 |
T |
C |
17: 37,507,915 (GRCm39) |
T315A |
probably damaging |
Het |
Or2n1e |
T |
A |
17: 38,586,438 (GRCm39) |
Y259N |
probably damaging |
Het |
Or9s18 |
T |
C |
13: 65,300,467 (GRCm39) |
V143A |
possibly damaging |
Het |
Pabpc1 |
A |
T |
15: 36,599,528 (GRCm39) |
V389E |
probably benign |
Het |
Pank4 |
A |
T |
4: 155,055,847 (GRCm39) |
M291L |
probably benign |
Het |
Pcf11 |
T |
C |
7: 92,308,041 (GRCm39) |
D709G |
probably benign |
Het |
Pcgf1 |
T |
A |
6: 83,056,938 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
A |
G |
12: 82,042,525 (GRCm39) |
I2256V |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,035,633 (GRCm39) |
|
probably null |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,163,472 (GRCm39) |
A2149T |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,881,711 (GRCm39) |
E781G |
probably benign |
Het |
Pik3r4 |
G |
A |
9: 105,555,375 (GRCm39) |
V1111I |
possibly damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,722,581 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
T |
A |
10: 3,907,506 (GRCm39) |
S808T |
probably benign |
Het |
Pnkp |
T |
A |
7: 44,509,878 (GRCm39) |
|
probably benign |
Het |
Polr3c |
A |
T |
3: 96,630,977 (GRCm39) |
F148I |
probably damaging |
Het |
Ppard |
A |
T |
17: 28,505,417 (GRCm39) |
T35S |
probably benign |
Het |
Ptov1 |
T |
C |
7: 44,516,533 (GRCm39) |
D134G |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,002,609 (GRCm39) |
S1566R |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,445,504 (GRCm39) |
S158P |
probably benign |
Het |
Qki |
T |
C |
17: 10,435,217 (GRCm39) |
H269R |
probably damaging |
Het |
Qrsl1 |
T |
C |
10: 43,752,659 (GRCm39) |
Y388C |
probably damaging |
Het |
Rapgef1 |
T |
G |
2: 29,579,172 (GRCm39) |
I182S |
probably damaging |
Het |
Ret |
T |
C |
6: 118,140,154 (GRCm39) |
S1013G |
possibly damaging |
Het |
Rimbp3 |
A |
G |
16: 17,028,465 (GRCm39) |
R630G |
possibly damaging |
Het |
Rnmt |
A |
T |
18: 68,451,031 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,592,795 (GRCm39) |
M4653K |
possibly damaging |
Het |
Sacm1l |
G |
A |
9: 123,419,895 (GRCm39) |
V553I |
probably benign |
Het |
Sec31b |
A |
T |
19: 44,521,116 (GRCm39) |
S110T |
probably damaging |
Het |
Serpina3k |
G |
A |
12: 104,307,119 (GRCm39) |
G117D |
probably damaging |
Het |
Sesn2 |
T |
C |
4: 132,221,902 (GRCm39) |
Y410C |
probably damaging |
Het |
Slc24a1 |
G |
A |
9: 64,856,836 (GRCm39) |
R24C |
probably benign |
Het |
Slc35g2 |
A |
C |
9: 100,434,555 (GRCm39) |
V372G |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,646,190 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,152,988 (GRCm39) |
Y135* |
probably null |
Het |
Slco1a7 |
A |
T |
6: 141,668,905 (GRCm39) |
M509K |
probably benign |
Het |
Slco4a1 |
A |
G |
2: 180,115,408 (GRCm39) |
N662D |
probably damaging |
Het |
Slfn4 |
T |
A |
11: 83,080,108 (GRCm39) |
|
probably benign |
Het |
Slmap |
T |
C |
14: 26,189,690 (GRCm39) |
N156S |
probably damaging |
Het |
Smim29 |
A |
G |
17: 27,784,244 (GRCm39) |
|
probably benign |
Het |
Snx18 |
A |
G |
13: 113,754,310 (GRCm39) |
S208P |
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,303,133 (GRCm39) |
R485S |
probably benign |
Het |
Spib |
A |
G |
7: 44,178,309 (GRCm39) |
S154P |
probably damaging |
Het |
Spty2d1 |
T |
C |
7: 46,645,858 (GRCm39) |
D595G |
probably damaging |
Het |
St7 |
T |
A |
6: 17,906,515 (GRCm39) |
|
probably null |
Het |
Susd1 |
T |
C |
4: 59,428,029 (GRCm39) |
T52A |
possibly damaging |
Het |
Svs5 |
T |
A |
2: 164,079,043 (GRCm39) |
D288V |
possibly damaging |
Het |
Syt7 |
T |
A |
19: 10,420,288 (GRCm39) |
I355N |
probably damaging |
Het |
Tarm1 |
G |
A |
7: 3,545,416 (GRCm39) |
Q145* |
probably null |
Het |
Teddm2 |
T |
A |
1: 153,726,487 (GRCm39) |
E76V |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,540,923 (GRCm39) |
S343P |
probably damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,400 (GRCm39) |
H422Q |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,043,256 (GRCm39) |
N538D |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,103,317 (GRCm39) |
|
probably null |
Het |
Tmtc1 |
A |
C |
6: 148,186,478 (GRCm39) |
|
probably null |
Het |
Tns3 |
C |
T |
11: 8,400,986 (GRCm39) |
R1104H |
probably benign |
Het |
Trim6 |
T |
C |
7: 103,881,855 (GRCm39) |
Y369H |
probably damaging |
Het |
Triobp |
G |
A |
15: 78,851,313 (GRCm39) |
R489K |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,814 (GRCm39) |
D732G |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,753,380 (GRCm39) |
V1883I |
probably damaging |
Het |
Tsc2 |
C |
A |
17: 24,822,249 (GRCm39) |
V1141F |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,730,171 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,773,355 (GRCm39) |
M2395K |
unknown |
Het |
Tyrp1 |
A |
T |
4: 80,763,172 (GRCm39) |
D353V |
possibly damaging |
Het |
Ubd |
A |
C |
17: 37,506,593 (GRCm39) |
T160P |
probably benign |
Het |
Ugt2b36 |
G |
T |
5: 87,229,397 (GRCm39) |
Y156* |
probably null |
Het |
Ulk4 |
G |
A |
9: 121,092,704 (GRCm39) |
R178* |
probably null |
Het |
Unc13d |
A |
G |
11: 115,964,408 (GRCm39) |
V312A |
possibly damaging |
Het |
Urb2 |
G |
T |
8: 124,755,636 (GRCm39) |
A448S |
probably damaging |
Het |
Urod |
G |
A |
4: 116,848,870 (GRCm39) |
A92V |
possibly damaging |
Het |
Vmn1r33 |
T |
A |
6: 66,588,803 (GRCm39) |
R250S |
probably benign |
Het |
Vmn1r87 |
A |
T |
7: 12,866,254 (GRCm39) |
M11K |
possibly damaging |
Het |
Vmn2r77 |
C |
T |
7: 86,450,195 (GRCm39) |
T147I |
probably benign |
Het |
Vstm4 |
A |
G |
14: 32,639,859 (GRCm39) |
K96E |
possibly damaging |
Het |
Vxn |
T |
C |
1: 9,677,201 (GRCm39) |
S24P |
probably benign |
Het |
Washc4 |
A |
T |
10: 83,410,343 (GRCm39) |
M644L |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,661,990 (GRCm39) |
D172G |
probably benign |
Het |
Zbtb38 |
A |
T |
9: 96,569,737 (GRCm39) |
V449E |
probably damaging |
Het |
Zfp229 |
C |
T |
17: 21,964,267 (GRCm39) |
H166Y |
possibly damaging |
Het |
Zfp512b |
A |
G |
2: 181,230,532 (GRCm39) |
S453P |
probably benign |
Het |
Zp2 |
C |
A |
7: 119,737,343 (GRCm39) |
V282L |
probably damaging |
Het |
|
Other mutations in Zfhx4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Zfhx4
|
APN |
3 |
5,307,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00915:Zfhx4
|
APN |
3 |
5,310,583 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01145:Zfhx4
|
APN |
3 |
5,310,407 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01302:Zfhx4
|
APN |
3 |
5,308,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01314:Zfhx4
|
APN |
3 |
5,478,154 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01321:Zfhx4
|
APN |
3 |
5,307,388 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01328:Zfhx4
|
APN |
3 |
5,309,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01333:Zfhx4
|
APN |
3 |
5,464,387 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01351:Zfhx4
|
APN |
3 |
5,466,196 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01524:Zfhx4
|
APN |
3 |
5,309,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Zfhx4
|
APN |
3 |
5,464,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01715:Zfhx4
|
APN |
3 |
5,307,105 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01736:Zfhx4
|
APN |
3 |
5,309,152 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01904:Zfhx4
|
APN |
3 |
5,477,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02298:Zfhx4
|
APN |
3 |
5,309,364 (GRCm39) |
splice site |
probably null |
|
IGL02342:Zfhx4
|
APN |
3 |
5,467,434 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02465:Zfhx4
|
APN |
3 |
5,464,663 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02481:Zfhx4
|
APN |
3 |
5,476,903 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02511:Zfhx4
|
APN |
3 |
5,464,243 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02571:Zfhx4
|
APN |
3 |
5,394,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02685:Zfhx4
|
APN |
3 |
5,477,213 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02721:Zfhx4
|
APN |
3 |
5,308,367 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02806:Zfhx4
|
APN |
3 |
5,455,468 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03140:Zfhx4
|
APN |
3 |
5,307,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03185:Zfhx4
|
APN |
3 |
5,468,974 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03209:Zfhx4
|
APN |
3 |
5,466,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03292:Zfhx4
|
APN |
3 |
5,476,840 (GRCm39) |
nonsense |
probably null |
|
IGL03302:Zfhx4
|
APN |
3 |
5,468,773 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03303:Zfhx4
|
APN |
3 |
5,468,410 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03341:Zfhx4
|
APN |
3 |
5,476,910 (GRCm39) |
missense |
probably damaging |
0.98 |
3-1:Zfhx4
|
UTSW |
3 |
5,468,445 (GRCm39) |
missense |
probably benign |
0.14 |
B5639:Zfhx4
|
UTSW |
3 |
5,468,235 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02796:Zfhx4
|
UTSW |
3 |
5,464,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03047:Zfhx4
|
UTSW |
3 |
5,308,793 (GRCm39) |
missense |
probably damaging |
0.99 |
P0025:Zfhx4
|
UTSW |
3 |
5,464,648 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4377001:Zfhx4
|
UTSW |
3 |
5,307,802 (GRCm39) |
missense |
probably damaging |
0.98 |
R0090:Zfhx4
|
UTSW |
3 |
5,308,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Zfhx4
|
UTSW |
3 |
5,464,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Zfhx4
|
UTSW |
3 |
5,466,221 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0465:Zfhx4
|
UTSW |
3 |
5,310,716 (GRCm39) |
splice site |
probably benign |
|
R0506:Zfhx4
|
UTSW |
3 |
5,467,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R0507:Zfhx4
|
UTSW |
3 |
5,466,048 (GRCm39) |
nonsense |
probably null |
|
R0550:Zfhx4
|
UTSW |
3 |
5,465,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R0576:Zfhx4
|
UTSW |
3 |
5,467,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R0590:Zfhx4
|
UTSW |
3 |
5,467,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R0697:Zfhx4
|
UTSW |
3 |
5,466,793 (GRCm39) |
missense |
probably damaging |
0.99 |
R0727:Zfhx4
|
UTSW |
3 |
5,466,133 (GRCm39) |
missense |
probably damaging |
0.98 |
R0762:Zfhx4
|
UTSW |
3 |
5,468,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Zfhx4
|
UTSW |
3 |
5,310,375 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0863:Zfhx4
|
UTSW |
3 |
5,310,375 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0866:Zfhx4
|
UTSW |
3 |
5,477,272 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1109:Zfhx4
|
UTSW |
3 |
5,464,930 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1177:Zfhx4
|
UTSW |
3 |
5,465,891 (GRCm39) |
small deletion |
probably benign |
|
R1338:Zfhx4
|
UTSW |
3 |
5,462,021 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1388:Zfhx4
|
UTSW |
3 |
5,466,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Zfhx4
|
UTSW |
3 |
5,306,919 (GRCm39) |
missense |
probably benign |
0.00 |
R1470:Zfhx4
|
UTSW |
3 |
5,478,206 (GRCm39) |
makesense |
probably null |
|
R1470:Zfhx4
|
UTSW |
3 |
5,478,206 (GRCm39) |
makesense |
probably null |
|
R1552:Zfhx4
|
UTSW |
3 |
5,468,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Zfhx4
|
UTSW |
3 |
5,306,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Zfhx4
|
UTSW |
3 |
5,465,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R1656:Zfhx4
|
UTSW |
3 |
5,478,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R1717:Zfhx4
|
UTSW |
3 |
5,468,164 (GRCm39) |
missense |
probably benign |
0.20 |
R1739:Zfhx4
|
UTSW |
3 |
5,466,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R1760:Zfhx4
|
UTSW |
3 |
5,447,676 (GRCm39) |
missense |
probably benign |
|
R1842:Zfhx4
|
UTSW |
3 |
5,466,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Zfhx4
|
UTSW |
3 |
5,477,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1868:Zfhx4
|
UTSW |
3 |
5,477,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Zfhx4
|
UTSW |
3 |
5,463,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Zfhx4
|
UTSW |
3 |
5,468,223 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2154:Zfhx4
|
UTSW |
3 |
5,466,801 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2165:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R2181:Zfhx4
|
UTSW |
3 |
5,468,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Zfhx4
|
UTSW |
3 |
5,307,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R2209:Zfhx4
|
UTSW |
3 |
5,461,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R2303:Zfhx4
|
UTSW |
3 |
5,462,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R2327:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R2420:Zfhx4
|
UTSW |
3 |
5,455,465 (GRCm39) |
missense |
probably benign |
0.00 |
R2422:Zfhx4
|
UTSW |
3 |
5,455,465 (GRCm39) |
missense |
probably benign |
0.00 |
R2516:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R2518:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R2519:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R2520:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R2566:Zfhx4
|
UTSW |
3 |
5,310,203 (GRCm39) |
missense |
probably damaging |
0.98 |
R2922:Zfhx4
|
UTSW |
3 |
5,468,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R3000:Zfhx4
|
UTSW |
3 |
5,468,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Zfhx4
|
UTSW |
3 |
5,464,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R3409:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R3414:Zfhx4
|
UTSW |
3 |
5,468,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R3746:Zfhx4
|
UTSW |
3 |
5,308,225 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3747:Zfhx4
|
UTSW |
3 |
5,308,225 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3748:Zfhx4
|
UTSW |
3 |
5,308,225 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3749:Zfhx4
|
UTSW |
3 |
5,308,225 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3750:Zfhx4
|
UTSW |
3 |
5,308,225 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3763:Zfhx4
|
UTSW |
3 |
5,468,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Zfhx4
|
UTSW |
3 |
5,466,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R3827:Zfhx4
|
UTSW |
3 |
5,466,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R3830:Zfhx4
|
UTSW |
3 |
5,466,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R3877:Zfhx4
|
UTSW |
3 |
5,465,845 (GRCm39) |
missense |
probably benign |
|
R3919:Zfhx4
|
UTSW |
3 |
5,464,175 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3922:Zfhx4
|
UTSW |
3 |
5,465,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R3927:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R3965:Zfhx4
|
UTSW |
3 |
5,468,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R4004:Zfhx4
|
UTSW |
3 |
5,468,418 (GRCm39) |
missense |
probably benign |
0.32 |
R4049:Zfhx4
|
UTSW |
3 |
5,463,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R4073:Zfhx4
|
UTSW |
3 |
5,464,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R4134:Zfhx4
|
UTSW |
3 |
5,308,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R4401:Zfhx4
|
UTSW |
3 |
5,468,405 (GRCm39) |
nonsense |
probably null |
|
R4439:Zfhx4
|
UTSW |
3 |
5,279,875 (GRCm39) |
unclassified |
probably benign |
|
R4497:Zfhx4
|
UTSW |
3 |
5,464,680 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4518:Zfhx4
|
UTSW |
3 |
5,477,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R4569:Zfhx4
|
UTSW |
3 |
5,466,894 (GRCm39) |
missense |
probably benign |
0.00 |
R4612:Zfhx4
|
UTSW |
3 |
5,462,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R4616:Zfhx4
|
UTSW |
3 |
5,478,127 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4626:Zfhx4
|
UTSW |
3 |
5,467,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R4628:Zfhx4
|
UTSW |
3 |
5,468,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4637:Zfhx4
|
UTSW |
3 |
5,468,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Zfhx4
|
UTSW |
3 |
5,464,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R4708:Zfhx4
|
UTSW |
3 |
5,310,563 (GRCm39) |
splice site |
probably null |
|
R4729:Zfhx4
|
UTSW |
3 |
5,464,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R4757:Zfhx4
|
UTSW |
3 |
5,465,122 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4765:Zfhx4
|
UTSW |
3 |
5,465,212 (GRCm39) |
missense |
probably benign |
|
R4819:Zfhx4
|
UTSW |
3 |
5,468,974 (GRCm39) |
missense |
probably benign |
0.05 |
R4937:Zfhx4
|
UTSW |
3 |
5,307,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R4980:Zfhx4
|
UTSW |
3 |
5,464,039 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5124:Zfhx4
|
UTSW |
3 |
5,307,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Zfhx4
|
UTSW |
3 |
5,468,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Zfhx4
|
UTSW |
3 |
5,464,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R5375:Zfhx4
|
UTSW |
3 |
5,477,485 (GRCm39) |
missense |
probably damaging |
0.99 |
R5485:Zfhx4
|
UTSW |
3 |
5,308,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Zfhx4
|
UTSW |
3 |
5,468,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5609:Zfhx4
|
UTSW |
3 |
5,468,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Zfhx4
|
UTSW |
3 |
5,468,381 (GRCm39) |
missense |
probably benign |
0.02 |
R5758:Zfhx4
|
UTSW |
3 |
5,467,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Zfhx4
|
UTSW |
3 |
5,467,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R5938:Zfhx4
|
UTSW |
3 |
5,467,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R5952:Zfhx4
|
UTSW |
3 |
5,462,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R6043:Zfhx4
|
UTSW |
3 |
5,468,487 (GRCm39) |
missense |
probably benign |
0.00 |
R6045:Zfhx4
|
UTSW |
3 |
5,462,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R6125:Zfhx4
|
UTSW |
3 |
5,463,871 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6354:Zfhx4
|
UTSW |
3 |
5,467,011 (GRCm39) |
missense |
probably benign |
|
R6374:Zfhx4
|
UTSW |
3 |
5,309,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Zfhx4
|
UTSW |
3 |
5,308,410 (GRCm39) |
missense |
probably benign |
0.07 |
R6380:Zfhx4
|
UTSW |
3 |
5,478,170 (GRCm39) |
missense |
probably damaging |
0.99 |
R6413:Zfhx4
|
UTSW |
3 |
5,308,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R6449:Zfhx4
|
UTSW |
3 |
5,307,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R6539:Zfhx4
|
UTSW |
3 |
5,309,168 (GRCm39) |
missense |
probably damaging |
0.99 |
R6714:Zfhx4
|
UTSW |
3 |
5,306,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R6933:Zfhx4
|
UTSW |
3 |
5,478,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R6982:Zfhx4
|
UTSW |
3 |
5,468,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7104:Zfhx4
|
UTSW |
3 |
5,467,549 (GRCm39) |
missense |
probably damaging |
0.97 |
R7127:Zfhx4
|
UTSW |
3 |
5,478,104 (GRCm39) |
missense |
probably damaging |
0.99 |
R7138:Zfhx4
|
UTSW |
3 |
5,477,107 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7161:Zfhx4
|
UTSW |
3 |
5,309,143 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7213:Zfhx4
|
UTSW |
3 |
5,461,704 (GRCm39) |
missense |
probably benign |
|
R7483:Zfhx4
|
UTSW |
3 |
5,477,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R7514:Zfhx4
|
UTSW |
3 |
5,307,267 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7544:Zfhx4
|
UTSW |
3 |
5,477,875 (GRCm39) |
missense |
probably damaging |
0.98 |
R7565:Zfhx4
|
UTSW |
3 |
5,455,426 (GRCm39) |
missense |
probably benign |
0.04 |
R7611:Zfhx4
|
UTSW |
3 |
5,468,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R7640:Zfhx4
|
UTSW |
3 |
5,477,540 (GRCm39) |
missense |
probably benign |
0.19 |
R7649:Zfhx4
|
UTSW |
3 |
5,307,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R7689:Zfhx4
|
UTSW |
3 |
5,476,946 (GRCm39) |
missense |
probably benign |
0.05 |
R7711:Zfhx4
|
UTSW |
3 |
5,462,016 (GRCm39) |
missense |
probably damaging |
0.98 |
R7895:Zfhx4
|
UTSW |
3 |
5,307,259 (GRCm39) |
missense |
probably benign |
0.00 |
R7920:Zfhx4
|
UTSW |
3 |
5,465,515 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7972:Zfhx4
|
UTSW |
3 |
5,477,533 (GRCm39) |
missense |
probably benign |
0.02 |
R7993:Zfhx4
|
UTSW |
3 |
5,478,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R8133:Zfhx4
|
UTSW |
3 |
5,465,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R8158:Zfhx4
|
UTSW |
3 |
5,464,010 (GRCm39) |
nonsense |
probably null |
|
R8272:Zfhx4
|
UTSW |
3 |
5,308,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R8285:Zfhx4
|
UTSW |
3 |
5,466,916 (GRCm39) |
missense |
probably benign |
0.17 |
R8321:Zfhx4
|
UTSW |
3 |
5,466,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8381:Zfhx4
|
UTSW |
3 |
5,447,676 (GRCm39) |
missense |
probably benign |
0.00 |
R8434:Zfhx4
|
UTSW |
3 |
5,463,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R8466:Zfhx4
|
UTSW |
3 |
5,307,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R8515:Zfhx4
|
UTSW |
3 |
5,464,534 (GRCm39) |
missense |
probably benign |
0.00 |
R8525:Zfhx4
|
UTSW |
3 |
5,464,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Zfhx4
|
UTSW |
3 |
5,309,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Zfhx4
|
UTSW |
3 |
5,463,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8839:Zfhx4
|
UTSW |
3 |
5,466,915 (GRCm39) |
missense |
probably benign |
|
R8856:Zfhx4
|
UTSW |
3 |
5,455,484 (GRCm39) |
missense |
probably benign |
0.45 |
R8900:Zfhx4
|
UTSW |
3 |
5,463,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R8917:Zfhx4
|
UTSW |
3 |
5,464,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R9101:Zfhx4
|
UTSW |
3 |
5,477,198 (GRCm39) |
missense |
probably benign |
0.10 |
R9126:Zfhx4
|
UTSW |
3 |
5,394,589 (GRCm39) |
missense |
probably damaging |
0.99 |
R9159:Zfhx4
|
UTSW |
3 |
5,466,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R9159:Zfhx4
|
UTSW |
3 |
5,464,312 (GRCm39) |
missense |
probably damaging |
0.98 |
R9241:Zfhx4
|
UTSW |
3 |
5,308,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Zfhx4
|
UTSW |
3 |
5,394,525 (GRCm39) |
missense |
probably benign |
|
R9376:Zfhx4
|
UTSW |
3 |
5,465,395 (GRCm39) |
missense |
probably benign |
0.04 |
R9376:Zfhx4
|
UTSW |
3 |
5,306,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9550:Zfhx4
|
UTSW |
3 |
5,464,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R9680:Zfhx4
|
UTSW |
3 |
5,465,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R9782:Zfhx4
|
UTSW |
3 |
5,466,514 (GRCm39) |
missense |
probably benign |
0.38 |
R9787:Zfhx4
|
UTSW |
3 |
5,455,506 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9790:Zfhx4
|
UTSW |
3 |
5,464,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R9791:Zfhx4
|
UTSW |
3 |
5,464,922 (GRCm39) |
missense |
probably damaging |
1.00 |
RF019:Zfhx4
|
UTSW |
3 |
5,468,327 (GRCm39) |
missense |
probably benign |
0.08 |
X0025:Zfhx4
|
UTSW |
3 |
5,476,896 (GRCm39) |
missense |
probably damaging |
0.99 |
X0026:Zfhx4
|
UTSW |
3 |
5,477,398 (GRCm39) |
missense |
probably benign |
0.00 |
X0028:Zfhx4
|
UTSW |
3 |
5,468,327 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Zfhx4
|
UTSW |
3 |
5,467,474 (GRCm39) |
missense |
probably benign |
0.13 |
X0054:Zfhx4
|
UTSW |
3 |
5,464,770 (GRCm39) |
nonsense |
probably null |
|
Z1177:Zfhx4
|
UTSW |
3 |
5,307,506 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Zfhx4
|
UTSW |
3 |
5,308,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGTGGATTGGAATGAGCTGC -3'
(R):5'- ATTTCACAAATCCACGCTGAGGAC -3'
Sequencing Primer
(F):5'- TTGGAATGAGCTGCTGAGTTAAAC -3'
(R):5'- GGACACTCTGGGCTTTCCAAAC -3'
|
Posted On |
2015-11-11 |