Incidental Mutation 'R4940:Zfhx2'
ID |
383037 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfhx2
|
Ensembl Gene |
ENSMUSG00000040721 |
Gene Name |
zinc finger homeobox 2 |
Synonyms |
zfh-5 |
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.354)
|
Stock # |
R4940 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
55297719-55329781 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 55303891 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Glutamine
at position 1364
(H1364Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000045156
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036328]
[ENSMUST00000183822]
[ENSMUST00000185121]
|
AlphaFold |
Q2MHN3 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000036328
AA Change: H1364Q
PolyPhen 2
Score 0.533 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000045156 Gene: ENSMUSG00000040721 AA Change: H1364Q
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 |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000176665
|
SMART Domains |
Protein: ENSMUSP00000134955 Gene: ENSMUSG00000040721
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
13 |
37 |
5.34e-1 |
SMART |
ZnF_C2H2
|
133 |
156 |
1.51e1 |
SMART |
ZnF_C2H2
|
162 |
185 |
1.51e0 |
SMART |
low complexity region
|
246 |
262 |
N/A |
INTRINSIC |
low complexity region
|
265 |
285 |
N/A |
INTRINSIC |
ZnF_C2H2
|
344 |
368 |
8.22e-2 |
SMART |
ZnF_C2H2
|
401 |
425 |
6.67e-2 |
SMART |
low complexity region
|
436 |
463 |
N/A |
INTRINSIC |
low complexity region
|
473 |
485 |
N/A |
INTRINSIC |
low complexity region
|
491 |
505 |
N/A |
INTRINSIC |
low complexity region
|
508 |
518 |
N/A |
INTRINSIC |
low complexity region
|
538 |
559 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000176872
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183750
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183822
|
SMART Domains |
Protein: ENSMUSP00000140371 Gene: ENSMUSG00000045691
Domain | Start | End | E-Value | Type |
PDB:2JMU|A
|
5 |
64 |
3e-23 |
PDB |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183993
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000185121
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.5%
- 20x: 93.3%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931414P19Rik |
T |
C |
14: 54,828,782 (GRCm39) |
T240A |
probably benign |
Het |
Abca15 |
T |
C |
7: 119,931,917 (GRCm39) |
Y57H |
probably benign |
Het |
Adgrf4 |
A |
G |
17: 42,977,420 (GRCm39) |
I641T |
possibly damaging |
Het |
Ankrd11 |
A |
G |
8: 123,616,560 (GRCm39) |
Y2410H |
probably damaging |
Het |
Apbb2 |
C |
A |
5: 66,609,604 (GRCm39) |
L14F |
probably null |
Het |
Arhgdia |
T |
C |
11: 120,470,061 (GRCm39) |
D204G |
probably damaging |
Het |
Armh4 |
A |
T |
14: 50,010,939 (GRCm39) |
M256K |
probably benign |
Het |
Catsperd |
A |
T |
17: 56,969,736 (GRCm39) |
Y610F |
possibly damaging |
Het |
Cblb |
T |
A |
16: 51,853,466 (GRCm39) |
D27E |
probably damaging |
Het |
Ccdc180 |
A |
T |
4: 45,917,453 (GRCm39) |
I893F |
probably damaging |
Het |
Ccdc180 |
A |
G |
4: 45,917,508 (GRCm39) |
H911R |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,143,714 (GRCm39) |
I2966F |
probably damaging |
Het |
Cfap299 |
A |
G |
5: 98,885,495 (GRCm39) |
H134R |
possibly damaging |
Het |
Chat |
G |
A |
14: 32,141,062 (GRCm39) |
P445L |
probably damaging |
Het |
Chdh |
G |
T |
14: 29,754,809 (GRCm39) |
R273L |
possibly damaging |
Het |
Clic3 |
T |
C |
2: 25,347,929 (GRCm39) |
V72A |
probably benign |
Het |
Cyp2d12 |
T |
A |
15: 82,442,251 (GRCm39) |
D244E |
probably benign |
Het |
Ddr1 |
T |
A |
17: 36,001,022 (GRCm39) |
D241V |
probably damaging |
Het |
Dock7 |
T |
A |
4: 98,908,314 (GRCm39) |
K605N |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,712,487 (GRCm39) |
F164I |
probably damaging |
Het |
Dstyk |
T |
A |
1: 132,380,844 (GRCm39) |
N446K |
probably damaging |
Het |
Epb42 |
A |
T |
2: 120,864,932 (GRCm39) |
L53Q |
probably damaging |
Het |
Extl2 |
G |
C |
3: 115,820,841 (GRCm39) |
K229N |
probably benign |
Het |
Frmd4b |
T |
A |
6: 97,275,051 (GRCm39) |
S617C |
probably damaging |
Het |
Fscb |
C |
T |
12: 64,520,588 (GRCm39) |
V293I |
probably benign |
Het |
Glp2r |
G |
T |
11: 67,648,419 (GRCm39) |
Y94* |
probably null |
Het |
Gm4978 |
A |
C |
9: 69,358,154 (GRCm39) |
|
probably benign |
Het |
Gm6729 |
A |
G |
10: 86,376,252 (GRCm39) |
|
noncoding transcript |
Het |
Gnat2 |
A |
C |
3: 108,007,932 (GRCm39) |
N293T |
probably benign |
Het |
Herpud1 |
T |
C |
8: 95,117,470 (GRCm39) |
I142T |
probably benign |
Het |
Irak2 |
G |
A |
6: 113,670,691 (GRCm39) |
V536I |
probably benign |
Het |
Kcnu1 |
A |
T |
8: 26,387,890 (GRCm39) |
|
probably null |
Het |
Kdm4a |
A |
G |
4: 118,018,951 (GRCm39) |
S422P |
probably benign |
Het |
Lair1 |
T |
A |
7: 4,031,948 (GRCm39) |
D53V |
probably benign |
Het |
Lhx1 |
G |
T |
11: 84,410,735 (GRCm39) |
Y196* |
probably null |
Het |
Lrrc37a |
G |
A |
11: 103,388,438 (GRCm39) |
T2329I |
unknown |
Het |
Mag |
T |
C |
7: 30,608,625 (GRCm39) |
D163G |
probably damaging |
Het |
Magi3 |
A |
G |
3: 103,958,708 (GRCm39) |
V459A |
probably damaging |
Het |
Med13 |
A |
G |
11: 86,178,944 (GRCm39) |
Y1451H |
probably damaging |
Het |
Megf8 |
T |
A |
7: 25,060,131 (GRCm39) |
C2341S |
probably damaging |
Het |
Mppe1 |
A |
G |
18: 67,361,095 (GRCm39) |
C221R |
probably damaging |
Het |
Mtus1 |
T |
A |
8: 41,494,515 (GRCm39) |
H39L |
possibly damaging |
Het |
Nkpd1 |
C |
T |
7: 19,257,498 (GRCm39) |
Q276* |
probably null |
Het |
Nkx3-1 |
G |
A |
14: 69,428,367 (GRCm39) |
G72S |
probably benign |
Het |
Nutm2 |
T |
C |
13: 50,628,909 (GRCm39) |
C658R |
possibly damaging |
Het |
Olfm1 |
T |
C |
2: 28,112,602 (GRCm39) |
V239A |
possibly damaging |
Het |
Pcnx1 |
C |
T |
12: 81,964,567 (GRCm39) |
H245Y |
possibly damaging |
Het |
Pgm3 |
A |
G |
9: 86,441,529 (GRCm39) |
L356S |
probably damaging |
Het |
Pik3r4 |
C |
G |
9: 105,546,193 (GRCm39) |
H207D |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,794,585 (GRCm39) |
T1859A |
probably benign |
Het |
Pon3 |
A |
T |
6: 5,221,625 (GRCm39) |
V335E |
possibly damaging |
Het |
Ppp4r3b |
A |
G |
11: 29,161,740 (GRCm39) |
T705A |
probably benign |
Het |
Prmt7 |
T |
C |
8: 106,963,910 (GRCm39) |
V268A |
probably benign |
Het |
Psd |
C |
T |
19: 46,310,856 (GRCm39) |
G398R |
probably damaging |
Het |
Pygl |
A |
G |
12: 70,253,155 (GRCm39) |
V188A |
probably damaging |
Het |
Rnf13 |
T |
A |
3: 57,703,627 (GRCm39) |
N110K |
probably damaging |
Het |
Rnf170 |
C |
T |
8: 26,615,939 (GRCm39) |
Q77* |
probably null |
Het |
Rrp8 |
A |
T |
7: 105,383,284 (GRCm39) |
Y327* |
probably null |
Het |
Ruvbl2 |
T |
C |
7: 45,074,150 (GRCm39) |
D228G |
probably damaging |
Het |
Scgn |
T |
A |
13: 24,173,807 (GRCm39) |
T35S |
probably benign |
Het |
Scyl3 |
C |
T |
1: 163,762,316 (GRCm39) |
P74S |
probably damaging |
Het |
Sec61b |
T |
G |
4: 47,483,074 (GRCm39) |
S123A |
probably benign |
Het |
Sertad2 |
T |
C |
11: 20,597,899 (GRCm39) |
S32P |
possibly damaging |
Het |
Slc23a3 |
T |
C |
1: 75,110,447 (GRCm39) |
|
probably null |
Het |
Sult2a2 |
T |
G |
7: 13,472,223 (GRCm39) |
V140G |
probably benign |
Het |
Tbc1d4 |
A |
T |
14: 101,744,667 (GRCm39) |
S320T |
probably benign |
Het |
Trabd2b |
T |
C |
4: 114,266,141 (GRCm39) |
Y52H |
probably damaging |
Het |
Traf2 |
T |
C |
2: 25,420,300 (GRCm39) |
E183G |
probably null |
Het |
Trip10 |
G |
T |
17: 57,570,017 (GRCm39) |
V561F |
possibly damaging |
Het |
Ttc7 |
G |
T |
17: 87,614,386 (GRCm39) |
V184F |
probably benign |
Het |
Ubc |
A |
G |
5: 125,463,293 (GRCm39) |
V678A |
probably benign |
Het |
Unk |
A |
G |
11: 115,944,491 (GRCm39) |
E414G |
possibly damaging |
Het |
Usp42 |
T |
C |
5: 143,705,517 (GRCm39) |
N365D |
probably damaging |
Het |
Zbtb26 |
A |
T |
2: 37,326,781 (GRCm39) |
I85K |
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 |
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 |
R9623:Zfhx2
|
UTSW |
14 |
55,302,191 (GRCm39) |
missense |
probably damaging |
0.98 |
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'- CAAAATTTTCTAGAAGGGCTTTGGC -3'
(R):5'- TGGCTTCATGTCTGGACTGC -3'
Sequencing Primer
(F):5'- GCGGGCAGCTTCATTGG -3'
(R):5'- ATGTCTGGACTGCCTTTCTTG -3'
|
Posted On |
2016-04-27 |