Incidental Mutation 'R9600:Zeb2'
ID |
723648 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zeb2
|
Ensembl Gene |
ENSMUSG00000026872 |
Gene Name |
zinc finger E-box binding homeobox 2 |
Synonyms |
SIP1, D130016B08Rik, 9130203F04Rik, Zfhx1b, Zfx1b |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R9600 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
44873644-45007407 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 44987180 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Tyrosine
at position 35
(D35Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000135491
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028229]
[ENSMUST00000068415]
[ENSMUST00000076836]
[ENSMUST00000127520]
[ENSMUST00000153561]
[ENSMUST00000176438]
[ENSMUST00000176732]
[ENSMUST00000177302]
[ENSMUST00000200844]
[ENSMUST00000201211]
[ENSMUST00000201490]
[ENSMUST00000201623]
[ENSMUST00000201804]
[ENSMUST00000201969]
[ENSMUST00000202187]
[ENSMUST00000202935]
|
AlphaFold |
Q9R0G7 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000028229
|
SMART Domains |
Protein: ENSMUSP00000028229 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
ZnF_C2H2
|
211 |
234 |
2.09e-3 |
SMART |
ZnF_C2H2
|
241 |
263 |
9.88e-5 |
SMART |
ZnF_C2H2
|
282 |
304 |
4.87e-4 |
SMART |
ZnF_C2H2
|
310 |
330 |
1.86e1 |
SMART |
low complexity region
|
352 |
364 |
N/A |
INTRINSIC |
ZnF_C2H2
|
581 |
601 |
5.54e1 |
SMART |
HOX
|
644 |
706 |
2.05e-3 |
SMART |
low complexity region
|
778 |
808 |
N/A |
INTRINSIC |
low complexity region
|
841 |
856 |
N/A |
INTRINSIC |
low complexity region
|
870 |
881 |
N/A |
INTRINSIC |
ZnF_C2H2
|
999 |
1021 |
4.47e-3 |
SMART |
ZnF_C2H2
|
1027 |
1049 |
2.17e-1 |
SMART |
ZnF_C2H2
|
1055 |
1076 |
1.89e-1 |
SMART |
low complexity region
|
1083 |
1097 |
N/A |
INTRINSIC |
low complexity region
|
1134 |
1150 |
N/A |
INTRINSIC |
low complexity region
|
1158 |
1168 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000068415
|
SMART Domains |
Protein: ENSMUSP00000069685 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
ZnF_C2H2
|
211 |
234 |
2.09e-3 |
SMART |
ZnF_C2H2
|
241 |
263 |
9.88e-5 |
SMART |
ZnF_C2H2
|
282 |
304 |
4.87e-4 |
SMART |
ZnF_C2H2
|
310 |
330 |
1.86e1 |
SMART |
low complexity region
|
352 |
364 |
N/A |
INTRINSIC |
ZnF_C2H2
|
581 |
601 |
5.54e1 |
SMART |
HOX
|
644 |
706 |
2.05e-3 |
SMART |
low complexity region
|
778 |
808 |
N/A |
INTRINSIC |
low complexity region
|
841 |
856 |
N/A |
INTRINSIC |
low complexity region
|
870 |
881 |
N/A |
INTRINSIC |
ZnF_C2H2
|
999 |
1021 |
4.47e-3 |
SMART |
ZnF_C2H2
|
1027 |
1049 |
2.17e-1 |
SMART |
ZnF_C2H2
|
1055 |
1076 |
1.89e-1 |
SMART |
low complexity region
|
1083 |
1097 |
N/A |
INTRINSIC |
low complexity region
|
1134 |
1150 |
N/A |
INTRINSIC |
low complexity region
|
1158 |
1168 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000076836
|
SMART Domains |
Protein: ENSMUSP00000076111 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
ZnF_C2H2
|
210 |
233 |
2.09e-3 |
SMART |
ZnF_C2H2
|
240 |
262 |
9.88e-5 |
SMART |
ZnF_C2H2
|
281 |
303 |
4.87e-4 |
SMART |
ZnF_C2H2
|
309 |
329 |
1.86e1 |
SMART |
low complexity region
|
351 |
363 |
N/A |
INTRINSIC |
ZnF_C2H2
|
580 |
600 |
5.54e1 |
SMART |
HOX
|
643 |
705 |
2.05e-3 |
SMART |
low complexity region
|
777 |
807 |
N/A |
INTRINSIC |
low complexity region
|
840 |
855 |
N/A |
INTRINSIC |
low complexity region
|
869 |
880 |
N/A |
INTRINSIC |
ZnF_C2H2
|
998 |
1020 |
4.47e-3 |
SMART |
ZnF_C2H2
|
1026 |
1048 |
2.17e-1 |
SMART |
ZnF_C2H2
|
1054 |
1075 |
1.89e-1 |
SMART |
low complexity region
|
1082 |
1096 |
N/A |
INTRINSIC |
low complexity region
|
1133 |
1149 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1167 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000127520
|
Predicted Effect |
unknown
Transcript: ENSMUST00000153561
AA Change: D35Y
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176438
|
SMART Domains |
Protein: ENSMUSP00000134849 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
ZnF_C2H2
|
211 |
234 |
2.09e-3 |
SMART |
ZnF_C2H2
|
241 |
263 |
9.88e-5 |
SMART |
ZnF_C2H2
|
282 |
304 |
4.87e-4 |
SMART |
ZnF_C2H2
|
310 |
330 |
1.86e1 |
SMART |
low complexity region
|
352 |
364 |
N/A |
INTRINSIC |
ZnF_C2H2
|
581 |
601 |
5.54e1 |
SMART |
HOX
|
644 |
706 |
2.05e-3 |
SMART |
low complexity region
|
778 |
808 |
N/A |
INTRINSIC |
low complexity region
|
841 |
856 |
N/A |
INTRINSIC |
low complexity region
|
870 |
881 |
N/A |
INTRINSIC |
ZnF_C2H2
|
999 |
1021 |
4.47e-3 |
SMART |
ZnF_C2H2
|
1027 |
1049 |
2.17e-1 |
SMART |
ZnF_C2H2
|
1055 |
1076 |
1.89e-1 |
SMART |
low complexity region
|
1083 |
1097 |
N/A |
INTRINSIC |
low complexity region
|
1134 |
1150 |
N/A |
INTRINSIC |
low complexity region
|
1158 |
1168 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176732
|
SMART Domains |
Protein: ENSMUSP00000135393 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
26 |
N/A |
INTRINSIC |
ZnF_C2H2
|
60 |
83 |
2.09e-3 |
SMART |
ZnF_C2H2
|
90 |
112 |
9.88e-5 |
SMART |
ZnF_C2H2
|
131 |
153 |
4.87e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000177302
|
SMART Domains |
Protein: ENSMUSP00000134747 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
ZnF_C2H2
|
211 |
234 |
2.09e-3 |
SMART |
ZnF_C2H2
|
241 |
263 |
9.88e-5 |
SMART |
ZnF_C2H2
|
282 |
304 |
4.87e-4 |
SMART |
ZnF_C2H2
|
310 |
330 |
1.86e1 |
SMART |
low complexity region
|
352 |
364 |
N/A |
INTRINSIC |
ZnF_C2H2
|
581 |
601 |
5.54e1 |
SMART |
HOX
|
644 |
706 |
2.05e-3 |
SMART |
low complexity region
|
778 |
808 |
N/A |
INTRINSIC |
low complexity region
|
841 |
856 |
N/A |
INTRINSIC |
low complexity region
|
870 |
881 |
N/A |
INTRINSIC |
ZnF_C2H2
|
999 |
1021 |
4.47e-3 |
SMART |
ZnF_C2H2
|
1027 |
1049 |
2.17e-1 |
SMART |
ZnF_C2H2
|
1055 |
1076 |
1.89e-1 |
SMART |
low complexity region
|
1083 |
1097 |
N/A |
INTRINSIC |
low complexity region
|
1134 |
1150 |
N/A |
INTRINSIC |
low complexity region
|
1158 |
1168 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000200844
|
SMART Domains |
Protein: ENSMUSP00000144421 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
ZnF_C2H2
|
187 |
210 |
9.2e-6 |
SMART |
ZnF_C2H2
|
217 |
239 |
4.2e-7 |
SMART |
ZnF_C2H2
|
258 |
280 |
2e-6 |
SMART |
ZnF_C2H2
|
286 |
306 |
8e-2 |
SMART |
low complexity region
|
328 |
340 |
N/A |
INTRINSIC |
ZnF_C2H2
|
557 |
577 |
2.4e-1 |
SMART |
HOX
|
620 |
682 |
1.1e-5 |
SMART |
low complexity region
|
754 |
784 |
N/A |
INTRINSIC |
low complexity region
|
817 |
832 |
N/A |
INTRINSIC |
low complexity region
|
846 |
857 |
N/A |
INTRINSIC |
ZnF_C2H2
|
975 |
997 |
1.9e-5 |
SMART |
ZnF_C2H2
|
1003 |
1025 |
9.6e-4 |
SMART |
ZnF_C2H2
|
1031 |
1052 |
7.9e-4 |
SMART |
low complexity region
|
1059 |
1073 |
N/A |
INTRINSIC |
low complexity region
|
1110 |
1126 |
N/A |
INTRINSIC |
low complexity region
|
1134 |
1144 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201211
|
SMART Domains |
Protein: ENSMUSP00000144406 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201490
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201623
|
SMART Domains |
Protein: ENSMUSP00000144075 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
ZnF_C2H2
|
187 |
210 |
9.2e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201804
|
SMART Domains |
Protein: ENSMUSP00000144637 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
107 |
119 |
N/A |
INTRINSIC |
ZnF_C2H2
|
240 |
263 |
9.2e-6 |
SMART |
ZnF_C2H2
|
270 |
292 |
4.2e-7 |
SMART |
ZnF_C2H2
|
311 |
333 |
2e-6 |
SMART |
ZnF_C2H2
|
339 |
359 |
8e-2 |
SMART |
low complexity region
|
381 |
393 |
N/A |
INTRINSIC |
ZnF_C2H2
|
610 |
630 |
2.4e-1 |
SMART |
HOX
|
673 |
731 |
1.2e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201969
|
SMART Domains |
Protein: ENSMUSP00000144141 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202187
|
SMART Domains |
Protein: ENSMUSP00000144552 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202935
|
SMART Domains |
Protein: ENSMUSP00000143841 Gene: ENSMUSG00000026872
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the Zfh1 family of 2-handed zinc finger/homeodomain proteins. It is located in the nucleus and functions as a DNA-binding transcriptional repressor that interacts with activated SMADs. Mutations in this gene are associated with Hirschsprung disease/Mowat-Wilson syndrome. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jan 2010] PHENOTYPE: Homozygous null mutants exhibit a variety of defects at embryonic day 8.5 and die between embryonic days 9.5 and 10.5. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730455P16Rik |
A |
G |
11: 80,261,197 (GRCm39) |
V210A |
probably damaging |
Het |
Abcc9 |
G |
A |
6: 142,536,102 (GRCm39) |
A1544V |
possibly damaging |
Het |
Akap6 |
A |
G |
12: 52,933,341 (GRCm39) |
T278A |
probably benign |
Het |
Arfgef1 |
T |
A |
1: 10,233,977 (GRCm39) |
I1106F |
probably benign |
Het |
Armc7 |
T |
C |
11: 115,367,038 (GRCm39) |
L61S |
probably damaging |
Het |
Atp1a3 |
G |
A |
7: 24,700,027 (GRCm39) |
T111M |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,095,565 (GRCm39) |
K1103* |
probably null |
Het |
Cacna2d4 |
T |
A |
6: 119,322,023 (GRCm39) |
S962R |
probably benign |
Het |
Camsap2 |
T |
C |
1: 136,204,936 (GRCm39) |
T526A |
|
Het |
Casq2 |
A |
T |
3: 102,052,622 (GRCm39) |
D378V |
unknown |
Het |
Chst8 |
C |
T |
7: 34,374,646 (GRCm39) |
D398N |
possibly damaging |
Het |
Cmya5 |
C |
T |
13: 93,226,604 (GRCm39) |
G2828D |
probably damaging |
Het |
Cntnap2 |
T |
A |
6: 45,969,009 (GRCm39) |
N250K |
probably damaging |
Het |
Cpne5 |
T |
C |
17: 29,380,520 (GRCm39) |
N401D |
probably damaging |
Het |
Cse1l |
A |
G |
2: 166,757,119 (GRCm39) |
N7S |
probably damaging |
Het |
Cyp4f39 |
G |
A |
17: 32,705,920 (GRCm39) |
G337D |
probably damaging |
Het |
Dera |
C |
T |
6: 137,814,135 (GRCm39) |
R308C |
probably benign |
Het |
Drd5 |
T |
A |
5: 38,478,174 (GRCm39) |
I389N |
possibly damaging |
Het |
F830016B08Rik |
A |
G |
18: 60,433,237 (GRCm39) |
T107A |
probably damaging |
Het |
Fbxw22 |
C |
A |
9: 109,212,986 (GRCm39) |
L320F |
probably damaging |
Het |
Fndc3b |
G |
T |
3: 27,552,941 (GRCm39) |
T352K |
probably damaging |
Het |
Gm36864 |
T |
A |
7: 43,886,275 (GRCm39) |
I169K |
unknown |
Het |
Hdac4 |
A |
T |
1: 91,889,277 (GRCm39) |
D749E |
probably damaging |
Het |
Herc1 |
C |
T |
9: 66,304,594 (GRCm39) |
A805V |
possibly damaging |
Het |
Hrh1 |
A |
G |
6: 114,457,453 (GRCm39) |
K245E |
probably benign |
Het |
Khdc1a |
A |
G |
1: 21,421,204 (GRCm39) |
T130A |
probably benign |
Het |
Lrp5 |
C |
G |
19: 3,641,712 (GRCm39) |
A1417P |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,365,002 (GRCm39) |
Q3253R |
possibly damaging |
Het |
Mdn1 |
T |
A |
4: 32,684,723 (GRCm39) |
L811* |
probably null |
Het |
Mettl8 |
T |
C |
2: 70,812,383 (GRCm39) |
D84G |
possibly damaging |
Het |
Miga1 |
T |
G |
3: 151,993,186 (GRCm39) |
T412P |
probably benign |
Het |
Mtor |
G |
T |
4: 148,632,092 (GRCm39) |
R2322L |
possibly damaging |
Het |
Muc16 |
T |
C |
9: 18,567,147 (GRCm39) |
N1791D |
unknown |
Het |
Myo9b |
C |
G |
8: 71,743,075 (GRCm39) |
S45R |
possibly damaging |
Het |
Nup50l |
A |
T |
6: 96,142,156 (GRCm39) |
L296Q |
possibly damaging |
Het |
Olfm4 |
T |
C |
14: 80,243,747 (GRCm39) |
F105S |
probably damaging |
Het |
Or5af2 |
A |
T |
11: 58,708,370 (GRCm39) |
I179F |
possibly damaging |
Het |
Osbpl1a |
T |
C |
18: 13,015,277 (GRCm39) |
I384V |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,030,435 (GRCm39) |
L1131P |
|
Het |
Pex6 |
T |
A |
17: 47,035,322 (GRCm39) |
V827E |
probably damaging |
Het |
Plek |
A |
C |
11: 16,940,119 (GRCm39) |
S197A |
probably benign |
Het |
Pmpca |
T |
C |
2: 26,282,598 (GRCm39) |
Y269H |
probably benign |
Het |
Pop1 |
T |
C |
15: 34,512,881 (GRCm39) |
I493T |
probably benign |
Het |
Rap1gap2 |
T |
C |
11: 74,283,954 (GRCm39) |
N615D |
probably benign |
Het |
Rtp3 |
T |
C |
9: 110,815,198 (GRCm39) |
Y389C |
unknown |
Het |
Rusf1 |
T |
A |
7: 127,875,676 (GRCm39) |
D253V |
possibly damaging |
Het |
Sardh |
T |
C |
2: 27,120,513 (GRCm39) |
Q423R |
probably benign |
Het |
Slc11a1 |
T |
C |
1: 74,422,688 (GRCm39) |
|
probably null |
Het |
Slc5a4b |
T |
C |
10: 75,896,239 (GRCm39) |
D572G |
probably damaging |
Het |
Slco1a8 |
T |
G |
6: 141,949,234 (GRCm39) |
|
probably null |
Het |
Slfn14 |
A |
G |
11: 83,170,048 (GRCm39) |
V532A |
probably benign |
Het |
Spmip10 |
T |
C |
18: 56,725,450 (GRCm39) |
W37R |
probably benign |
Het |
Stxbp1 |
T |
C |
2: 32,701,120 (GRCm39) |
Y264C |
possibly damaging |
Het |
Syce1l |
T |
C |
8: 114,381,750 (GRCm39) |
I230T |
unknown |
Het |
Taf5l |
T |
C |
8: 124,730,173 (GRCm39) |
Y172C |
|
Het |
Trpc4 |
A |
T |
3: 54,102,248 (GRCm39) |
K49* |
probably null |
Het |
Ttc13 |
A |
G |
8: 125,415,284 (GRCm39) |
V285A |
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,204,890 (GRCm39) |
L344Q |
probably damaging |
Het |
Unc79 |
A |
G |
12: 103,135,972 (GRCm39) |
H2469R |
probably benign |
Het |
Xkr7 |
A |
G |
2: 152,896,393 (GRCm39) |
I416V |
probably benign |
Het |
Zfp28 |
A |
G |
7: 6,397,917 (GRCm39) |
H784R |
probably benign |
Het |
Zfp644 |
A |
C |
5: 106,783,909 (GRCm39) |
S848R |
probably benign |
Het |
Zfp809 |
G |
A |
9: 22,150,384 (GRCm39) |
E294K |
possibly damaging |
Het |
Zfp820 |
A |
G |
17: 22,038,861 (GRCm39) |
Y156H |
probably benign |
Het |
|
Other mutations in Zeb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00900:Zeb2
|
APN |
2 |
44,887,287 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01639:Zeb2
|
APN |
2 |
44,887,269 (GRCm39) |
missense |
probably benign |
|
IGL02016:Zeb2
|
APN |
2 |
44,878,886 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02337:Zeb2
|
APN |
2 |
44,887,242 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02745:Zeb2
|
APN |
2 |
44,884,487 (GRCm39) |
unclassified |
probably benign |
|
IGL02893:Zeb2
|
APN |
2 |
44,886,619 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03412:Zeb2
|
APN |
2 |
44,892,720 (GRCm39) |
intron |
probably benign |
|
Blight
|
UTSW |
2 |
45,000,040 (GRCm39) |
missense |
possibly damaging |
0.95 |
Dropped
|
UTSW |
2 |
45,000,053 (GRCm39) |
missense |
possibly damaging |
0.66 |
Okapi
|
UTSW |
2 |
44,887,168 (GRCm39) |
missense |
probably damaging |
1.00 |
sable
|
UTSW |
2 |
44,887,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Zeb2
|
UTSW |
2 |
44,892,659 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0603:Zeb2
|
UTSW |
2 |
44,907,438 (GRCm39) |
missense |
probably benign |
0.45 |
R0608:Zeb2
|
UTSW |
2 |
44,886,138 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1236:Zeb2
|
UTSW |
2 |
44,884,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R1529:Zeb2
|
UTSW |
2 |
44,887,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R1581:Zeb2
|
UTSW |
2 |
44,887,012 (GRCm39) |
missense |
probably damaging |
0.99 |
R1636:Zeb2
|
UTSW |
2 |
44,892,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Zeb2
|
UTSW |
2 |
44,892,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Zeb2
|
UTSW |
2 |
44,887,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R2097:Zeb2
|
UTSW |
2 |
44,887,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Zeb2
|
UTSW |
2 |
44,878,821 (GRCm39) |
missense |
probably benign |
0.20 |
R4385:Zeb2
|
UTSW |
2 |
44,913,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Zeb2
|
UTSW |
2 |
44,913,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Zeb2
|
UTSW |
2 |
44,886,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R4769:Zeb2
|
UTSW |
2 |
44,886,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R4816:Zeb2
|
UTSW |
2 |
44,887,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R4918:Zeb2
|
UTSW |
2 |
44,886,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Zeb2
|
UTSW |
2 |
44,888,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5191:Zeb2
|
UTSW |
2 |
44,892,612 (GRCm39) |
missense |
probably benign |
0.00 |
R5195:Zeb2
|
UTSW |
2 |
44,891,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5322:Zeb2
|
UTSW |
2 |
44,887,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R5699:Zeb2
|
UTSW |
2 |
44,887,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Zeb2
|
UTSW |
2 |
44,887,530 (GRCm39) |
missense |
probably damaging |
0.96 |
R5764:Zeb2
|
UTSW |
2 |
44,886,931 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5914:Zeb2
|
UTSW |
2 |
44,887,064 (GRCm39) |
missense |
probably benign |
0.00 |
R5918:Zeb2
|
UTSW |
2 |
45,001,271 (GRCm39) |
intron |
probably benign |
|
R6037:Zeb2
|
UTSW |
2 |
44,878,652 (GRCm39) |
nonsense |
probably null |
|
R6037:Zeb2
|
UTSW |
2 |
44,878,652 (GRCm39) |
nonsense |
probably null |
|
R6302:Zeb2
|
UTSW |
2 |
44,887,771 (GRCm39) |
missense |
probably benign |
0.18 |
R6372:Zeb2
|
UTSW |
2 |
44,892,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R6402:Zeb2
|
UTSW |
2 |
44,886,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6492:Zeb2
|
UTSW |
2 |
45,000,508 (GRCm39) |
intron |
probably benign |
|
R6554:Zeb2
|
UTSW |
2 |
44,887,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R6675:Zeb2
|
UTSW |
2 |
44,887,457 (GRCm39) |
nonsense |
probably null |
|
R6735:Zeb2
|
UTSW |
2 |
45,000,028 (GRCm39) |
missense |
probably null |
0.99 |
R6870:Zeb2
|
UTSW |
2 |
44,878,922 (GRCm39) |
missense |
probably damaging |
0.98 |
R6925:Zeb2
|
UTSW |
2 |
44,884,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R6963:Zeb2
|
UTSW |
2 |
44,878,811 (GRCm39) |
missense |
probably damaging |
0.97 |
R6972:Zeb2
|
UTSW |
2 |
44,887,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Zeb2
|
UTSW |
2 |
45,000,053 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7178:Zeb2
|
UTSW |
2 |
44,887,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R7379:Zeb2
|
UTSW |
2 |
44,891,829 (GRCm39) |
splice site |
probably null |
|
R7419:Zeb2
|
UTSW |
2 |
44,886,359 (GRCm39) |
missense |
probably benign |
0.20 |
R7580:Zeb2
|
UTSW |
2 |
44,884,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R7599:Zeb2
|
UTSW |
2 |
44,884,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R7625:Zeb2
|
UTSW |
2 |
44,892,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R7917:Zeb2
|
UTSW |
2 |
44,886,421 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8132:Zeb2
|
UTSW |
2 |
44,879,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R8412:Zeb2
|
UTSW |
2 |
44,888,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R8413:Zeb2
|
UTSW |
2 |
44,886,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R8417:Zeb2
|
UTSW |
2 |
44,913,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R8750:Zeb2
|
UTSW |
2 |
44,887,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Zeb2
|
UTSW |
2 |
44,886,139 (GRCm39) |
missense |
probably benign |
0.02 |
R8916:Zeb2
|
UTSW |
2 |
44,886,796 (GRCm39) |
missense |
probably damaging |
0.99 |
R9068:Zeb2
|
UTSW |
2 |
45,000,040 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9094:Zeb2
|
UTSW |
2 |
45,003,136 (GRCm39) |
intron |
probably benign |
|
R9139:Zeb2
|
UTSW |
2 |
44,878,637 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9187:Zeb2
|
UTSW |
2 |
45,000,040 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9309:Zeb2
|
UTSW |
2 |
44,892,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R9310:Zeb2
|
UTSW |
2 |
44,886,988 (GRCm39) |
missense |
probably benign |
0.01 |
R9337:Zeb2
|
UTSW |
2 |
44,912,912 (GRCm39) |
missense |
probably benign |
0.35 |
R9350:Zeb2
|
UTSW |
2 |
44,887,158 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9371:Zeb2
|
UTSW |
2 |
44,888,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9389:Zeb2
|
UTSW |
2 |
44,887,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R9509:Zeb2
|
UTSW |
2 |
44,887,876 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9674:Zeb2
|
UTSW |
2 |
44,891,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R9756:Zeb2
|
UTSW |
2 |
44,887,414 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
Predicted Primers |
PCR Primer
(F):5'- TACTGACATTGGCCCAGGAG -3'
(R):5'- CAGCTTTCGCATCTGCAATTAG -3'
Sequencing Primer
(F):5'- GGTTCCCCAACACTCAAGCTG -3'
(R):5'- CGTGAAAAGCCCTTGTCT -3'
|
Posted On |
2022-09-12 |