Incidental Mutation 'R9623:Zfhx2'
ID |
724995 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfhx2
|
Ensembl Gene |
ENSMUSG00000040721 |
Gene Name |
zinc finger homeobox 2 |
Synonyms |
zfh-5 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.354)
|
Stock # |
R9623 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
55297719-55329781 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 55302191 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Glutamine
at position 1931
(P1931Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000045156
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036328]
|
AlphaFold |
Q2MHN3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000036328
AA Change: P1931Q
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000045156 Gene: ENSMUSG00000040721 AA Change: P1931Q
Domain | Start | End | E-Value | Type |
low complexity region
|
22 |
42 |
N/A |
INTRINSIC |
ZnF_C2H2
|
230 |
252 |
1.43e1 |
SMART |
low complexity region
|
333 |
345 |
N/A |
INTRINSIC |
low complexity region
|
428 |
439 |
N/A |
INTRINSIC |
ZnF_C2H2
|
446 |
469 |
8.94e-3 |
SMART |
ZnF_U1
|
498 |
532 |
6.98e-1 |
SMART |
ZnF_C2H2
|
501 |
525 |
3.21e-4 |
SMART |
ZnF_U1
|
560 |
594 |
1.36e0 |
SMART |
ZnF_C2H2
|
563 |
587 |
3.29e-1 |
SMART |
low complexity region
|
597 |
623 |
N/A |
INTRINSIC |
ZnF_C2H2
|
752 |
776 |
6.4e0 |
SMART |
ZnF_C2H2
|
815 |
839 |
2.02e-1 |
SMART |
ZnF_U1
|
861 |
895 |
1.78e1 |
SMART |
ZnF_C2H2
|
864 |
888 |
5.34e-1 |
SMART |
ZnF_C2H2
|
974 |
997 |
1.51e1 |
SMART |
ZnF_C2H2
|
1003 |
1026 |
1.51e0 |
SMART |
low complexity region
|
1087 |
1103 |
N/A |
INTRINSIC |
low complexity region
|
1106 |
1126 |
N/A |
INTRINSIC |
ZnF_U1
|
1182 |
1216 |
3.42e0 |
SMART |
ZnF_C2H2
|
1185 |
1209 |
8.22e-2 |
SMART |
ZnF_U1
|
1239 |
1273 |
3.73e0 |
SMART |
ZnF_C2H2
|
1242 |
1266 |
6.67e-2 |
SMART |
low complexity region
|
1277 |
1304 |
N/A |
INTRINSIC |
low complexity region
|
1314 |
1326 |
N/A |
INTRINSIC |
low complexity region
|
1332 |
1346 |
N/A |
INTRINSIC |
low complexity region
|
1349 |
1359 |
N/A |
INTRINSIC |
low complexity region
|
1379 |
1400 |
N/A |
INTRINSIC |
low complexity region
|
1457 |
1465 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1474 |
1497 |
5.34e0 |
SMART |
low complexity region
|
1522 |
1531 |
N/A |
INTRINSIC |
low complexity region
|
1542 |
1554 |
N/A |
INTRINSIC |
low complexity region
|
1562 |
1583 |
N/A |
INTRINSIC |
HOX
|
1589 |
1651 |
1.97e-16 |
SMART |
low complexity region
|
1656 |
1665 |
N/A |
INTRINSIC |
coiled coil region
|
1693 |
1723 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1761 |
1783 |
2.53e-2 |
SMART |
low complexity region
|
1837 |
1847 |
N/A |
INTRINSIC |
HOX
|
1851 |
1913 |
2.34e-18 |
SMART |
low complexity region
|
1984 |
1995 |
N/A |
INTRINSIC |
low complexity region
|
2001 |
2051 |
N/A |
INTRINSIC |
HOX
|
2058 |
2120 |
1.52e-17 |
SMART |
ZnF_U1
|
2136 |
2170 |
1.09e1 |
SMART |
ZnF_C2H2
|
2139 |
2163 |
5.4e1 |
SMART |
low complexity region
|
2328 |
2354 |
N/A |
INTRINSIC |
low complexity region
|
2385 |
2426 |
N/A |
INTRINSIC |
ZnF_U1
|
2482 |
2516 |
8.31e-1 |
SMART |
ZnF_C2H2
|
2485 |
2509 |
9.46e0 |
SMART |
low complexity region
|
2523 |
2538 |
N/A |
INTRINSIC |
low complexity region
|
2553 |
2562 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
A |
T |
7: 119,181,975 (GRCm39) |
Y408F |
probably benign |
Het |
Adamts9 |
G |
T |
6: 92,857,661 (GRCm39) |
P876T |
probably benign |
Het |
Afap1l2 |
T |
A |
19: 56,906,462 (GRCm39) |
D479V |
probably damaging |
Het |
Aire |
T |
C |
10: 77,873,809 (GRCm39) |
E300G |
probably damaging |
Het |
Ampd3 |
A |
G |
7: 110,402,307 (GRCm39) |
E428G |
probably damaging |
Het |
Apaf1 |
A |
T |
10: 90,913,463 (GRCm39) |
Y153* |
probably null |
Het |
Arhgap10 |
T |
C |
8: 77,985,786 (GRCm39) |
T694A |
probably benign |
Het |
Arhgef39 |
A |
G |
4: 43,496,819 (GRCm39) |
|
probably null |
Het |
Arhgef5 |
T |
C |
6: 43,251,736 (GRCm39) |
V829A |
possibly damaging |
Het |
Arrdc4 |
A |
G |
7: 68,390,741 (GRCm39) |
M333T |
|
Het |
Boc |
G |
T |
16: 44,322,018 (GRCm39) |
R215S |
|
Het |
Capn2 |
G |
A |
1: 182,344,795 (GRCm39) |
A42V |
probably benign |
Het |
Ccdc136 |
T |
A |
6: 29,405,939 (GRCm39) |
M95K |
probably benign |
Het |
Ccdc183 |
A |
T |
2: 25,499,520 (GRCm39) |
Y438N |
probably benign |
Het |
Ccnf |
C |
A |
17: 24,468,367 (GRCm39) |
R10M |
probably damaging |
Het |
Cd19 |
A |
G |
7: 126,011,284 (GRCm39) |
F300S |
probably damaging |
Het |
Cdkl3 |
G |
T |
11: 51,895,816 (GRCm39) |
C21F |
probably damaging |
Het |
Celf2 |
C |
T |
2: 6,620,522 (GRCm39) |
R183Q |
probably damaging |
Het |
Clca3a1 |
T |
G |
3: 144,719,698 (GRCm39) |
D424A |
probably benign |
Het |
Clec3a |
A |
G |
8: 115,144,887 (GRCm39) |
D21G |
probably benign |
Het |
Clec4e |
T |
C |
6: 123,263,306 (GRCm39) |
N78S |
probably benign |
Het |
Clpb |
A |
T |
7: 101,313,399 (GRCm39) |
S128C |
possibly damaging |
Het |
Cntnap5a |
T |
A |
1: 116,369,985 (GRCm39) |
Y867* |
probably null |
Het |
Dgkg |
G |
C |
16: 22,385,194 (GRCm39) |
N437K |
|
Het |
Dnhd1 |
A |
G |
7: 105,335,773 (GRCm39) |
E1139G |
probably damaging |
Het |
Dnhd1 |
G |
A |
7: 105,344,134 (GRCm39) |
R1826H |
probably damaging |
Het |
Etl4 |
A |
G |
2: 20,811,052 (GRCm39) |
H1413R |
|
Het |
Fibp |
T |
A |
19: 5,513,850 (GRCm39) |
V271D |
possibly damaging |
Het |
Gabra4 |
G |
T |
5: 71,791,023 (GRCm39) |
T273K |
probably damaging |
Het |
Gan |
G |
A |
8: 117,914,219 (GRCm39) |
D206N |
probably damaging |
Het |
Gstz1 |
A |
T |
12: 87,206,923 (GRCm39) |
I106F |
probably damaging |
Het |
Hivep2 |
T |
G |
10: 14,006,546 (GRCm39) |
L1048R |
probably damaging |
Het |
Htr6 |
A |
T |
4: 138,801,750 (GRCm39) |
M108K |
probably damaging |
Het |
Hycc1 |
A |
C |
5: 24,170,255 (GRCm39) |
S365A |
probably benign |
Het |
Itgad |
A |
G |
7: 127,803,723 (GRCm39) |
E1134G |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 41,366,648 (GRCm39) |
G657S |
|
Het |
Lrp2 |
T |
C |
2: 69,307,423 (GRCm39) |
I2879V |
probably benign |
Het |
Lyst |
G |
T |
13: 13,852,587 (GRCm39) |
V2196L |
probably benign |
Het |
Mettl5 |
T |
A |
2: 69,711,717 (GRCm39) |
I50F |
possibly damaging |
Het |
Mmadhc |
A |
G |
2: 50,186,341 (GRCm39) |
|
probably benign |
Het |
Msantd1 |
G |
A |
5: 35,075,076 (GRCm39) |
W46* |
probably null |
Het |
Mto1 |
T |
C |
9: 78,364,712 (GRCm39) |
I317T |
probably damaging |
Het |
Myef2 |
T |
G |
2: 124,957,377 (GRCm39) |
D126A |
probably damaging |
Het |
Net1 |
A |
G |
13: 3,937,569 (GRCm39) |
|
probably null |
Het |
Nnmt |
A |
T |
9: 48,503,660 (GRCm39) |
M122K |
probably benign |
Het |
Nos1 |
A |
G |
5: 118,087,849 (GRCm39) |
K1371E |
probably benign |
Het |
Nrcam |
G |
C |
12: 44,636,931 (GRCm39) |
W1121C |
probably damaging |
Het |
Nt5c2 |
A |
G |
19: 46,877,409 (GRCm39) |
S511P |
|
Het |
Or10w1 |
C |
A |
19: 13,632,414 (GRCm39) |
A207E |
probably damaging |
Het |
Or1j17 |
G |
T |
2: 36,578,778 (GRCm39) |
V255F |
probably benign |
Het |
Or2k2 |
T |
C |
4: 58,785,585 (GRCm39) |
I46V |
possibly damaging |
Het |
Or4a73 |
A |
G |
2: 89,421,261 (GRCm39) |
F66S |
probably benign |
Het |
P2rx7 |
A |
G |
5: 122,790,860 (GRCm39) |
K66E |
probably damaging |
Het |
Paqr4 |
A |
G |
17: 23,956,656 (GRCm39) |
W236R |
probably damaging |
Het |
Parm1 |
A |
G |
5: 91,760,923 (GRCm39) |
Y265C |
probably damaging |
Het |
Pcbp2 |
T |
C |
15: 102,392,628 (GRCm39) |
Y178H |
probably damaging |
Het |
Pidd1 |
G |
A |
7: 141,021,678 (GRCm39) |
P261S |
probably damaging |
Het |
Pik3r6 |
T |
C |
11: 68,442,159 (GRCm39) |
V705A |
possibly damaging |
Het |
Pla2g15 |
G |
T |
8: 106,887,275 (GRCm39) |
V156F |
possibly damaging |
Het |
Prpf6 |
G |
A |
2: 181,289,137 (GRCm39) |
V609M |
possibly damaging |
Het |
Resf1 |
A |
G |
6: 149,226,965 (GRCm39) |
N4D |
possibly damaging |
Het |
Rprd2 |
A |
G |
3: 95,679,505 (GRCm39) |
V491A |
probably benign |
Het |
Rtp3 |
T |
A |
9: 110,818,600 (GRCm39) |
H27L |
probably damaging |
Het |
Sema5b |
G |
A |
16: 35,443,121 (GRCm39) |
R42Q |
possibly damaging |
Het |
Serpina3f |
A |
G |
12: 104,183,743 (GRCm39) |
K202E |
probably damaging |
Het |
Slc25a33 |
T |
G |
4: 149,833,767 (GRCm39) |
M168L |
probably benign |
Het |
Slc7a8 |
A |
G |
14: 54,964,341 (GRCm39) |
C371R |
probably damaging |
Het |
Smyd1 |
T |
C |
6: 71,192,808 (GRCm39) |
N467S |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,107,807 (GRCm39) |
W872R |
probably damaging |
Het |
Syne1 |
A |
T |
10: 5,152,009 (GRCm39) |
I5766N |
probably damaging |
Het |
Syne2 |
A |
G |
12: 75,986,760 (GRCm39) |
S1699G |
probably benign |
Het |
Synpo2 |
T |
C |
3: 122,908,047 (GRCm39) |
D423G |
possibly damaging |
Het |
Tcf19 |
A |
T |
17: 35,825,792 (GRCm39) |
F122I |
probably damaging |
Het |
Tdpoz4 |
A |
T |
3: 93,704,221 (GRCm39) |
T173S |
probably benign |
Het |
Trappc8 |
T |
A |
18: 20,983,975 (GRCm39) |
H681L |
possibly damaging |
Het |
Trim36 |
A |
G |
18: 46,308,623 (GRCm39) |
F413S |
probably benign |
Het |
Tsks |
A |
G |
7: 44,605,931 (GRCm39) |
T466A |
possibly damaging |
Het |
Ubr1 |
T |
C |
2: 120,764,820 (GRCm39) |
I545V |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,159,024 (GRCm39) |
E1170G |
probably benign |
Het |
Usp29 |
A |
G |
7: 6,964,396 (GRCm39) |
R80G |
possibly damaging |
Het |
Utrn |
C |
T |
10: 12,282,225 (GRCm39) |
R3258H |
probably damaging |
Het |
Vmn1r13 |
T |
G |
6: 57,187,549 (GRCm39) |
V236G |
probably benign |
Het |
Vmn1r33 |
T |
A |
6: 66,589,002 (GRCm39) |
D184V |
probably damaging |
Het |
Vmn2r87 |
T |
C |
10: 130,315,794 (GRCm39) |
N91D |
probably damaging |
Het |
Wrn |
A |
G |
8: 33,774,644 (GRCm39) |
|
probably null |
Het |
Zan |
G |
A |
5: 137,461,636 (GRCm39) |
P1181L |
unknown |
Het |
Zbtb47 |
C |
A |
9: 121,591,990 (GRCm39) |
Y103* |
probably null |
Het |
Zfc3h1 |
C |
A |
10: 115,259,362 (GRCm39) |
L1645I |
possibly damaging |
Het |
Zfp352 |
A |
G |
4: 90,113,128 (GRCm39) |
K423E |
probably benign |
Het |
Zfp574 |
T |
A |
7: 24,780,515 (GRCm39) |
H512Q |
|
Het |
Zfp7 |
G |
A |
15: 76,774,531 (GRCm39) |
R191H |
probably benign |
Het |
Zfp771 |
A |
T |
7: 126,844,301 (GRCm39) |
K46* |
probably null |
Het |
Zkscan8 |
T |
C |
13: 21,704,763 (GRCm39) |
E392G |
probably damaging |
Het |
|
Other mutations in Zfhx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Zfhx2
|
APN |
14 |
55,304,022 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00164:Zfhx2
|
APN |
14 |
55,302,483 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00235:Zfhx2
|
APN |
14 |
55,300,714 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00925:Zfhx2
|
APN |
14 |
55,310,518 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01025:Zfhx2
|
APN |
14 |
55,301,717 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01061:Zfhx2
|
APN |
14 |
55,311,339 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01486:Zfhx2
|
APN |
14 |
55,304,547 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01875:Zfhx2
|
APN |
14 |
55,301,372 (GRCm39) |
missense |
unknown |
|
IGL01990:Zfhx2
|
APN |
14 |
55,311,047 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02097:Zfhx2
|
APN |
14 |
55,300,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02269:Zfhx2
|
APN |
14 |
55,309,393 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02488:Zfhx2
|
APN |
14 |
55,302,560 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02624:Zfhx2
|
APN |
14 |
55,304,085 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03087:Zfhx2
|
APN |
14 |
55,310,302 (GRCm39) |
missense |
possibly damaging |
0.85 |
G1patch:Zfhx2
|
UTSW |
14 |
55,301,539 (GRCm39) |
nonsense |
probably null |
|
PIT4403001:Zfhx2
|
UTSW |
14 |
55,312,437 (GRCm39) |
missense |
probably benign |
|
R0148:Zfhx2
|
UTSW |
14 |
55,310,354 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0323:Zfhx2
|
UTSW |
14 |
55,303,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0328:Zfhx2
|
UTSW |
14 |
55,309,445 (GRCm39) |
missense |
probably benign |
|
R0348:Zfhx2
|
UTSW |
14 |
55,300,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R0442:Zfhx2
|
UTSW |
14 |
55,304,357 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0533:Zfhx2
|
UTSW |
14 |
55,301,547 (GRCm39) |
missense |
probably benign |
0.23 |
R0561:Zfhx2
|
UTSW |
14 |
55,303,346 (GRCm39) |
missense |
probably benign |
0.01 |
R0627:Zfhx2
|
UTSW |
14 |
55,302,784 (GRCm39) |
missense |
probably benign |
|
R0659:Zfhx2
|
UTSW |
14 |
55,311,258 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0675:Zfhx2
|
UTSW |
14 |
55,300,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R1301:Zfhx2
|
UTSW |
14 |
55,300,854 (GRCm39) |
missense |
probably benign |
0.32 |
R1563:Zfhx2
|
UTSW |
14 |
55,302,545 (GRCm39) |
missense |
probably benign |
0.33 |
R1607:Zfhx2
|
UTSW |
14 |
55,300,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Zfhx2
|
UTSW |
14 |
55,311,401 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1710:Zfhx2
|
UTSW |
14 |
55,303,455 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1773:Zfhx2
|
UTSW |
14 |
55,310,348 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1879:Zfhx2
|
UTSW |
14 |
55,310,206 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1879:Zfhx2
|
UTSW |
14 |
55,303,074 (GRCm39) |
missense |
probably benign |
0.32 |
R1933:Zfhx2
|
UTSW |
14 |
55,312,695 (GRCm39) |
start gained |
probably benign |
|
R1944:Zfhx2
|
UTSW |
14 |
55,312,189 (GRCm39) |
missense |
probably benign |
0.18 |
R2888:Zfhx2
|
UTSW |
14 |
55,302,260 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2889:Zfhx2
|
UTSW |
14 |
55,302,260 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2915:Zfhx2
|
UTSW |
14 |
55,302,014 (GRCm39) |
missense |
probably damaging |
0.98 |
R3971:Zfhx2
|
UTSW |
14 |
55,311,932 (GRCm39) |
missense |
probably benign |
0.33 |
R4082:Zfhx2
|
UTSW |
14 |
55,302,662 (GRCm39) |
missense |
probably benign |
|
R4134:Zfhx2
|
UTSW |
14 |
55,302,600 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4231:Zfhx2
|
UTSW |
14 |
55,310,991 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4675:Zfhx2
|
UTSW |
14 |
55,304,678 (GRCm39) |
missense |
probably benign |
0.03 |
R4764:Zfhx2
|
UTSW |
14 |
55,304,372 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4866:Zfhx2
|
UTSW |
14 |
55,302,993 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4940:Zfhx2
|
UTSW |
14 |
55,303,891 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5125:Zfhx2
|
UTSW |
14 |
55,312,232 (GRCm39) |
missense |
probably benign |
0.00 |
R5178:Zfhx2
|
UTSW |
14 |
55,312,232 (GRCm39) |
missense |
probably benign |
0.00 |
R5554:Zfhx2
|
UTSW |
14 |
55,301,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R5689:Zfhx2
|
UTSW |
14 |
55,311,360 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5768:Zfhx2
|
UTSW |
14 |
55,311,822 (GRCm39) |
missense |
probably benign |
|
R5792:Zfhx2
|
UTSW |
14 |
55,304,303 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5834:Zfhx2
|
UTSW |
14 |
55,310,787 (GRCm39) |
nonsense |
probably null |
|
R5895:Zfhx2
|
UTSW |
14 |
55,303,348 (GRCm39) |
missense |
probably benign |
|
R5999:Zfhx2
|
UTSW |
14 |
55,311,462 (GRCm39) |
missense |
probably benign |
|
R6025:Zfhx2
|
UTSW |
14 |
55,302,665 (GRCm39) |
missense |
probably benign |
0.00 |
R6106:Zfhx2
|
UTSW |
14 |
55,305,767 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6135:Zfhx2
|
UTSW |
14 |
55,311,653 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6186:Zfhx2
|
UTSW |
14 |
55,300,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R6379:Zfhx2
|
UTSW |
14 |
55,311,795 (GRCm39) |
missense |
probably benign |
|
R6725:Zfhx2
|
UTSW |
14 |
55,301,539 (GRCm39) |
nonsense |
probably null |
|
R7089:Zfhx2
|
UTSW |
14 |
55,303,229 (GRCm39) |
missense |
probably benign |
0.33 |
R7383:Zfhx2
|
UTSW |
14 |
55,305,710 (GRCm39) |
missense |
probably benign |
0.00 |
R7470:Zfhx2
|
UTSW |
14 |
55,304,207 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7606:Zfhx2
|
UTSW |
14 |
55,304,120 (GRCm39) |
missense |
probably benign |
0.12 |
R7607:Zfhx2
|
UTSW |
14 |
55,303,688 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7698:Zfhx2
|
UTSW |
14 |
55,300,306 (GRCm39) |
missense |
probably benign |
0.00 |
R7730:Zfhx2
|
UTSW |
14 |
55,304,357 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8142:Zfhx2
|
UTSW |
14 |
55,310,895 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8188:Zfhx2
|
UTSW |
14 |
55,301,898 (GRCm39) |
missense |
probably benign |
0.18 |
R8212:Zfhx2
|
UTSW |
14 |
55,310,373 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8264:Zfhx2
|
UTSW |
14 |
55,302,969 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8331:Zfhx2
|
UTSW |
14 |
55,309,444 (GRCm39) |
missense |
probably benign |
0.00 |
R8369:Zfhx2
|
UTSW |
14 |
55,304,201 (GRCm39) |
missense |
probably benign |
0.05 |
R8371:Zfhx2
|
UTSW |
14 |
55,301,549 (GRCm39) |
missense |
probably damaging |
0.99 |
R8383:Zfhx2
|
UTSW |
14 |
55,311,528 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8415:Zfhx2
|
UTSW |
14 |
55,308,079 (GRCm39) |
missense |
probably benign |
|
R8441:Zfhx2
|
UTSW |
14 |
55,303,985 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8466:Zfhx2
|
UTSW |
14 |
55,310,353 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8504:Zfhx2
|
UTSW |
14 |
55,303,243 (GRCm39) |
missense |
probably benign |
0.00 |
R8708:Zfhx2
|
UTSW |
14 |
55,312,509 (GRCm39) |
missense |
probably benign |
|
R8804:Zfhx2
|
UTSW |
14 |
55,312,191 (GRCm39) |
missense |
probably benign |
0.18 |
R8913:Zfhx2
|
UTSW |
14 |
55,309,543 (GRCm39) |
missense |
probably benign |
0.02 |
R8952:Zfhx2
|
UTSW |
14 |
55,310,207 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9057:Zfhx2
|
UTSW |
14 |
55,310,027 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9060:Zfhx2
|
UTSW |
14 |
55,311,803 (GRCm39) |
missense |
probably benign |
0.00 |
R9197:Zfhx2
|
UTSW |
14 |
55,312,179 (GRCm39) |
nonsense |
probably null |
|
R9622:Zfhx2
|
UTSW |
14 |
55,303,483 (GRCm39) |
missense |
probably benign |
0.18 |
R9775:Zfhx2
|
UTSW |
14 |
55,304,562 (GRCm39) |
missense |
probably benign |
0.01 |
R9780:Zfhx2
|
UTSW |
14 |
55,312,494 (GRCm39) |
missense |
probably benign |
0.02 |
X0065:Zfhx2
|
UTSW |
14 |
55,304,417 (GRCm39) |
missense |
probably benign |
0.33 |
Z1088:Zfhx2
|
UTSW |
14 |
55,311,637 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Zfhx2
|
UTSW |
14 |
55,304,439 (GRCm39) |
missense |
possibly damaging |
0.70 |
Z1177:Zfhx2
|
UTSW |
14 |
55,303,377 (GRCm39) |
missense |
probably benign |
0.40 |
|
Predicted Primers |
PCR Primer
(F):5'- TAGATGGTTCCTCTGGACCCTC -3'
(R):5'- GGTACATGCAGGACTCCAAC -3'
Sequencing Primer
(F):5'- TCGTCCTCACTGAGTGCTGG -3'
(R):5'- CCCCACACGGAAGATGCTC -3'
|
Posted On |
2022-09-12 |