Incidental Mutation 'R9622:Zfhx2'
ID |
724897 |
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 # |
R9622 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
55297719-55329781 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 55303483 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 1500
(F1500L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000045156
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036328]
|
AlphaFold |
Q2MHN3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000036328
AA Change: F1500L
PolyPhen 2
Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000045156 Gene: ENSMUSG00000040721 AA Change: F1500L
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: 99.2%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
A |
G |
5: 36,006,889 (GRCm39) |
K435E |
probably damaging |
Het |
Acly |
T |
C |
11: 100,395,785 (GRCm39) |
T412A |
probably damaging |
Het |
Aldh3b2 |
T |
A |
19: 4,029,489 (GRCm39) |
D287E |
probably benign |
Het |
Asphd1 |
G |
A |
7: 126,547,974 (GRCm39) |
P110S |
|
Het |
Atg7 |
T |
C |
6: 114,654,993 (GRCm39) |
L142P |
probably benign |
Het |
Atp13a4 |
T |
C |
16: 29,239,277 (GRCm39) |
I796V |
|
Het |
Bbx |
A |
G |
16: 50,095,022 (GRCm39) |
V98A |
probably damaging |
Het |
Brca2 |
T |
C |
5: 150,480,410 (GRCm39) |
S2727P |
probably damaging |
Het |
Camk1 |
T |
A |
6: 113,318,850 (GRCm39) |
D21V |
possibly damaging |
Het |
Cdc5l |
A |
T |
17: 45,715,709 (GRCm39) |
D634E |
probably benign |
Het |
Cfap418 |
T |
C |
4: 10,893,304 (GRCm39) |
I141T |
possibly damaging |
Het |
Cyfip1 |
A |
T |
7: 55,528,853 (GRCm39) |
D275V |
possibly damaging |
Het |
Cyp4a30b |
A |
G |
4: 115,328,162 (GRCm39) |
E477G |
probably damaging |
Het |
Cyp4f16 |
C |
T |
17: 32,769,246 (GRCm39) |
P379S |
probably damaging |
Het |
Dchs2 |
C |
T |
3: 83,263,766 (GRCm39) |
Q3345* |
probably null |
Het |
Dnaaf1 |
A |
G |
8: 120,315,001 (GRCm39) |
T270A |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,561,356 (GRCm39) |
V334A |
|
Het |
Dnhd1 |
T |
C |
7: 105,353,342 (GRCm39) |
F2832L |
probably benign |
Het |
Dock8 |
A |
G |
19: 25,098,545 (GRCm39) |
N623S |
probably null |
Het |
Eif4enif1 |
T |
C |
11: 3,165,714 (GRCm39) |
I97T |
probably benign |
Het |
Elmo1 |
C |
G |
13: 20,392,310 (GRCm39) |
P29A |
probably benign |
Het |
Erich6 |
G |
C |
3: 58,544,162 (GRCm39) |
P142A |
possibly damaging |
Het |
Fam135b |
T |
C |
15: 71,397,686 (GRCm39) |
R125G |
probably damaging |
Het |
Fcrla |
T |
A |
1: 170,749,808 (GRCm39) |
H83L |
probably damaging |
Het |
Flt3 |
C |
T |
5: 147,303,841 (GRCm39) |
E366K |
possibly damaging |
Het |
Gabbr2 |
C |
T |
4: 46,724,283 (GRCm39) |
|
probably null |
Het |
Gigyf1 |
T |
A |
5: 137,522,926 (GRCm39) |
L809* |
probably null |
Het |
Glg1 |
C |
T |
8: 111,899,133 (GRCm39) |
G711R |
probably damaging |
Het |
Gp1bb |
T |
C |
16: 18,439,527 (GRCm39) |
E189G |
probably benign |
Het |
H2-Q1 |
A |
T |
17: 35,542,532 (GRCm39) |
I326F |
probably benign |
Het |
Hoxb3 |
A |
T |
11: 96,235,420 (GRCm39) |
K116* |
probably null |
Het |
Kcnb1 |
T |
C |
2: 167,030,161 (GRCm39) |
Y128C |
probably damaging |
Het |
Kif5b |
G |
A |
18: 6,225,672 (GRCm39) |
R171C |
probably damaging |
Het |
Lcn4 |
G |
A |
2: 26,561,228 (GRCm39) |
Q18* |
probably null |
Het |
Lrp1b |
G |
A |
2: 40,779,354 (GRCm39) |
Q2677* |
probably null |
Het |
Map4k3 |
T |
A |
17: 80,958,538 (GRCm39) |
T145S |
probably damaging |
Het |
Mas1 |
T |
C |
17: 13,060,898 (GRCm39) |
E175G |
probably benign |
Het |
Metap2 |
T |
C |
10: 93,707,366 (GRCm39) |
T202A |
probably benign |
Het |
Mras |
A |
T |
9: 99,275,054 (GRCm39) |
M131K |
probably benign |
Het |
Mtor |
T |
C |
4: 148,568,169 (GRCm39) |
V1092A |
probably damaging |
Het |
Mug2 |
T |
C |
6: 122,028,751 (GRCm39) |
S582P |
probably benign |
Het |
Myo5b |
A |
G |
18: 74,848,017 (GRCm39) |
N1085S |
probably damaging |
Het |
Nav3 |
T |
C |
10: 109,603,103 (GRCm39) |
T1149A |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,366,373 (GRCm39) |
S1239T |
probably benign |
Het |
Nkpd1 |
C |
A |
7: 19,257,867 (GRCm39) |
R549S |
probably benign |
Het |
Or10a3m |
T |
A |
7: 108,312,677 (GRCm39) |
M39K |
probably benign |
Het |
Or10p1 |
G |
A |
10: 129,444,084 (GRCm39) |
H89Y |
probably benign |
Het |
Or1j1 |
A |
G |
2: 36,702,621 (GRCm39) |
L161P |
probably damaging |
Het |
Or51i2 |
T |
A |
7: 103,689,522 (GRCm39) |
V173D |
probably damaging |
Het |
Pcdh18 |
T |
C |
3: 49,711,229 (GRCm39) |
N29D |
probably benign |
Het |
Pdzrn4 |
T |
C |
15: 92,294,949 (GRCm39) |
W52R |
probably benign |
Het |
Plekhb1 |
T |
C |
7: 100,304,588 (GRCm39) |
K39E |
probably damaging |
Het |
Pramel28 |
A |
G |
4: 143,692,348 (GRCm39) |
S218P |
probably benign |
Het |
Psmb4 |
C |
A |
3: 94,792,285 (GRCm39) |
E212D |
probably benign |
Het |
Rcc1l |
A |
G |
5: 134,205,348 (GRCm39) |
L69P |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,729,952 (GRCm39) |
R1082G |
probably benign |
Het |
Rorb |
T |
C |
19: 18,955,115 (GRCm39) |
Y167C |
probably damaging |
Het |
Sanbr |
T |
A |
11: 23,534,590 (GRCm39) |
K589I |
probably damaging |
Het |
Sbsn |
GGAAATATGGCAGACAAGTTTGGTCAGGGGGCCCACCATGCTTTTGGTCAGGGCAG |
GG |
7: 30,452,067 (GRCm39) |
|
probably benign |
Het |
Scaf8 |
T |
A |
17: 3,248,170 (GRCm39) |
F1164L |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,438,046 (GRCm39) |
M1940K |
probably benign |
Het |
Serpinb2 |
A |
G |
1: 107,452,298 (GRCm39) |
N292S |
probably benign |
Het |
Sparcl1 |
C |
A |
5: 104,234,998 (GRCm39) |
V506L |
possibly damaging |
Het |
Stt3a |
A |
G |
9: 36,661,025 (GRCm39) |
V262A |
possibly damaging |
Het |
Syt17 |
C |
A |
7: 118,036,191 (GRCm39) |
M58I |
probably benign |
Het |
Tas2r134 |
A |
C |
2: 51,518,358 (GRCm39) |
N279T |
possibly damaging |
Het |
Tbc1d2 |
T |
C |
4: 46,609,065 (GRCm39) |
E724G |
probably damaging |
Het |
Teddm1b |
T |
A |
1: 153,750,620 (GRCm39) |
L143Q |
|
Het |
Tlk1 |
T |
A |
2: 70,617,281 (GRCm39) |
R66S |
probably damaging |
Het |
Tmem139 |
A |
T |
6: 42,240,176 (GRCm39) |
|
probably null |
Het |
Tom1l2 |
T |
C |
11: 60,151,942 (GRCm39) |
Y155C |
possibly damaging |
Het |
Trmt1l |
C |
A |
1: 151,304,710 (GRCm39) |
S28* |
probably null |
Het |
Ttf2 |
T |
C |
3: 100,859,918 (GRCm39) |
I679V |
probably benign |
Het |
Unc13b |
T |
G |
4: 43,172,513 (GRCm39) |
F1114V |
|
Het |
Vmn2r25 |
T |
A |
6: 123,816,579 (GRCm39) |
D334V |
probably damaging |
Het |
Vps13c |
T |
G |
9: 67,856,715 (GRCm39) |
Y2581D |
probably damaging |
Het |
Xkr5 |
A |
G |
8: 18,984,247 (GRCm39) |
S432P |
probably benign |
Het |
Zc2hc1b |
G |
A |
10: 13,043,677 (GRCm39) |
P73S |
possibly damaging |
Het |
Zfp3 |
T |
G |
11: 70,662,739 (GRCm39) |
S233A |
possibly damaging |
Het |
Zmat5 |
T |
C |
11: 4,687,453 (GRCm39) |
W169R |
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 |
|
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'- AGCCTTCTTCTTCCTCAGAGGG -3'
(R):5'- AGCAGCCAAAGCCCTTCTAG -3'
Sequencing Primer
(F):5'- GCTCTTCAGAAGTGTGGATCCC -3'
(R):5'- GCCAAAGCCCTTCTAGAAAATTTTGG -3'
|
Posted On |
2022-09-12 |