Incidental Mutation 'R0122:Ciz1'
ID |
21073 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ciz1
|
Ensembl Gene |
ENSMUSG00000039205 |
Gene Name |
CDKN1A interacting zinc finger protein 1 |
Synonyms |
0610038H21Rik, 2900056O04Rik |
MMRRC Submission |
038407-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.136)
|
Stock # |
R0122 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
32252724-32268311 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to G
at 32261431 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000048964]
[ENSMUST00000113331]
[ENSMUST00000113332]
[ENSMUST00000113334]
[ENSMUST00000113338]
[ENSMUST00000132028]
[ENSMUST00000131152]
[ENSMUST00000136079]
[ENSMUST00000125818]
|
AlphaFold |
Q8VEH2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000048964
|
SMART Domains |
Protein: ENSMUSP00000048428 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
low complexity region
|
58 |
80 |
N/A |
INTRINSIC |
low complexity region
|
85 |
99 |
N/A |
INTRINSIC |
low complexity region
|
128 |
140 |
N/A |
INTRINSIC |
low complexity region
|
245 |
256 |
N/A |
INTRINSIC |
low complexity region
|
361 |
390 |
N/A |
INTRINSIC |
ZnF_U1
|
534 |
568 |
1.23e-1 |
SMART |
ZnF_C2H2
|
537 |
561 |
1.99e0 |
SMART |
ZnF_U1
|
626 |
660 |
2.08e-1 |
SMART |
ZnF_C2H2
|
629 |
653 |
3.02e0 |
SMART |
low complexity region
|
689 |
709 |
N/A |
INTRINSIC |
ZnF_U1
|
744 |
779 |
1.43e-4 |
SMART |
ZnF_C2H2
|
747 |
772 |
9.56e1 |
SMART |
low complexity region
|
823 |
845 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113331
|
SMART Domains |
Protein: ENSMUSP00000108957 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
low complexity region
|
58 |
80 |
N/A |
INTRINSIC |
low complexity region
|
85 |
100 |
N/A |
INTRINSIC |
low complexity region
|
104 |
116 |
N/A |
INTRINSIC |
low complexity region
|
221 |
232 |
N/A |
INTRINSIC |
internal_repeat_2
|
252 |
284 |
9.48e-5 |
PROSPERO |
internal_repeat_2
|
301 |
333 |
9.48e-5 |
PROSPERO |
low complexity region
|
337 |
366 |
N/A |
INTRINSIC |
ZnF_U1
|
510 |
544 |
1.23e-1 |
SMART |
ZnF_C2H2
|
513 |
537 |
1.99e0 |
SMART |
ZnF_U1
|
602 |
636 |
2.08e-1 |
SMART |
ZnF_C2H2
|
605 |
629 |
3.02e0 |
SMART |
low complexity region
|
665 |
685 |
N/A |
INTRINSIC |
ZnF_U1
|
720 |
755 |
1.43e-4 |
SMART |
ZnF_C2H2
|
723 |
748 |
9.56e1 |
SMART |
low complexity region
|
799 |
821 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113332
|
SMART Domains |
Protein: ENSMUSP00000108958 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
low complexity region
|
58 |
80 |
N/A |
INTRINSIC |
low complexity region
|
85 |
99 |
N/A |
INTRINSIC |
low complexity region
|
128 |
140 |
N/A |
INTRINSIC |
low complexity region
|
240 |
251 |
N/A |
INTRINSIC |
ZnF_U1
|
480 |
514 |
1.23e-1 |
SMART |
ZnF_C2H2
|
483 |
507 |
1.99e0 |
SMART |
Blast:ZnF_U1
|
543 |
570 |
2e-6 |
BLAST |
ZnF_U1
|
572 |
606 |
2.08e-1 |
SMART |
ZnF_C2H2
|
575 |
599 |
3.02e0 |
SMART |
low complexity region
|
635 |
655 |
N/A |
INTRINSIC |
ZnF_U1
|
690 |
725 |
1.43e-4 |
SMART |
ZnF_C2H2
|
693 |
718 |
9.56e1 |
SMART |
low complexity region
|
769 |
791 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113334
|
SMART Domains |
Protein: ENSMUSP00000108960 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
low complexity region
|
58 |
80 |
N/A |
INTRINSIC |
low complexity region
|
85 |
99 |
N/A |
INTRINSIC |
low complexity region
|
128 |
140 |
N/A |
INTRINSIC |
low complexity region
|
245 |
256 |
N/A |
INTRINSIC |
low complexity region
|
361 |
390 |
N/A |
INTRINSIC |
ZnF_U1
|
534 |
568 |
1.23e-1 |
SMART |
ZnF_C2H2
|
537 |
561 |
1.99e0 |
SMART |
ZnF_U1
|
626 |
660 |
2.08e-1 |
SMART |
ZnF_C2H2
|
629 |
653 |
3.02e0 |
SMART |
low complexity region
|
689 |
709 |
N/A |
INTRINSIC |
ZnF_U1
|
744 |
779 |
1.43e-4 |
SMART |
ZnF_C2H2
|
747 |
772 |
9.56e1 |
SMART |
low complexity region
|
823 |
845 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113338
|
SMART Domains |
Protein: ENSMUSP00000108964 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
low complexity region
|
58 |
80 |
N/A |
INTRINSIC |
low complexity region
|
85 |
99 |
N/A |
INTRINSIC |
low complexity region
|
128 |
140 |
N/A |
INTRINSIC |
low complexity region
|
245 |
256 |
N/A |
INTRINSIC |
low complexity region
|
361 |
390 |
N/A |
INTRINSIC |
ZnF_U1
|
534 |
568 |
1.23e-1 |
SMART |
ZnF_C2H2
|
537 |
561 |
1.99e0 |
SMART |
ZnF_U1
|
626 |
660 |
2.08e-1 |
SMART |
ZnF_C2H2
|
629 |
653 |
3.02e0 |
SMART |
low complexity region
|
689 |
709 |
N/A |
INTRINSIC |
ZnF_U1
|
744 |
779 |
1.43e-4 |
SMART |
ZnF_C2H2
|
747 |
772 |
9.56e1 |
SMART |
low complexity region
|
823 |
845 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000125482
|
SMART Domains |
Protein: ENSMUSP00000120019 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
216 |
240 |
1.99e0 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000151806
|
SMART Domains |
Protein: ENSMUSP00000119429 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
low complexity region
|
70 |
81 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134141
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145957
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125769
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149184
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132290
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000137220
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000132028
|
SMART Domains |
Protein: ENSMUSP00000120295 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
low complexity region
|
58 |
80 |
N/A |
INTRINSIC |
low complexity region
|
85 |
99 |
N/A |
INTRINSIC |
low complexity region
|
128 |
140 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000131152
|
SMART Domains |
Protein: ENSMUSP00000141211 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136079
|
SMART Domains |
Protein: ENSMUSP00000116812 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
coiled coil region
|
5 |
45 |
N/A |
INTRINSIC |
low complexity region
|
58 |
80 |
N/A |
INTRINSIC |
low complexity region
|
85 |
99 |
N/A |
INTRINSIC |
low complexity region
|
128 |
140 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000139637
|
SMART Domains |
Protein: ENSMUSP00000122469 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
low complexity region
|
85 |
96 |
N/A |
INTRINSIC |
low complexity region
|
201 |
230 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000125818
|
SMART Domains |
Protein: ENSMUSP00000117937 Gene: ENSMUSG00000039205
Domain | Start | End | E-Value | Type |
Blast:ZnF_U1
|
4 |
31 |
3e-6 |
BLAST |
ZnF_U1
|
33 |
67 |
2.08e-1 |
SMART |
ZnF_C2H2
|
36 |
60 |
3.02e0 |
SMART |
low complexity region
|
96 |
116 |
N/A |
INTRINSIC |
ZnF_U1
|
151 |
186 |
1.43e-4 |
SMART |
ZnF_C2H2
|
154 |
179 |
9.56e1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192758
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192055
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 95.9%
- 20x: 91.3%
|
Validation Efficiency |
99% (78/79) |
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 zinc finger DNA binding protein that interacts with CIP1, part of a complex with cyclin E. The encoded protein may regulate the cellular localization of CIP1. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012] PHENOTYPE: Mice hoomozygous for a knock-out allele exhibit decreased body size and gender specific effects on motor phenotypes. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,057,789 (GRCm39) |
|
probably benign |
Het |
Adam12 |
T |
A |
7: 133,614,077 (GRCm39) |
I60F |
probably benign |
Het |
Adamts10 |
A |
G |
17: 33,747,454 (GRCm39) |
|
probably benign |
Het |
Adamts12 |
C |
T |
15: 11,215,710 (GRCm39) |
R244C |
probably damaging |
Het |
Adamts7 |
A |
G |
9: 90,061,474 (GRCm39) |
E360G |
probably damaging |
Het |
Atn1 |
A |
T |
6: 124,720,197 (GRCm39) |
|
probably benign |
Het |
Avl9 |
G |
T |
6: 56,713,468 (GRCm39) |
R242L |
probably benign |
Het |
Baz2b |
G |
T |
2: 59,743,963 (GRCm39) |
|
probably null |
Het |
Bloc1s6 |
G |
C |
2: 122,587,963 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
C1qa |
T |
A |
4: 136,625,142 (GRCm39) |
T3S |
probably benign |
Het |
Cacna1e |
A |
T |
1: 154,319,647 (GRCm39) |
F1351Y |
probably damaging |
Het |
Car9 |
C |
T |
4: 43,512,206 (GRCm39) |
A356V |
probably benign |
Het |
Ccdc116 |
T |
A |
16: 16,960,598 (GRCm39) |
D73V |
probably damaging |
Het |
Ces2g |
T |
C |
8: 105,694,932 (GRCm39) |
Y518H |
probably damaging |
Het |
Cmc1 |
A |
T |
9: 117,894,388 (GRCm39) |
C29S |
probably damaging |
Het |
Coil |
T |
A |
11: 88,875,833 (GRCm39) |
|
probably benign |
Het |
Col3a1 |
C |
T |
1: 45,380,057 (GRCm39) |
|
probably benign |
Het |
Cox15 |
A |
G |
19: 43,737,229 (GRCm39) |
I135T |
possibly damaging |
Het |
Cyld |
T |
C |
8: 89,468,920 (GRCm39) |
S564P |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,378,509 (GRCm39) |
N2948K |
probably damaging |
Het |
Dnah7a |
G |
A |
1: 53,436,301 (GRCm39) |
R4014W |
probably damaging |
Het |
Dnmt3b |
T |
C |
2: 153,518,618 (GRCm39) |
Y594H |
probably damaging |
Het |
Dntt |
A |
G |
19: 41,041,477 (GRCm39) |
K387R |
possibly damaging |
Het |
Efcab7 |
G |
A |
4: 99,749,560 (GRCm39) |
|
probably benign |
Het |
Flvcr1 |
G |
T |
1: 190,753,423 (GRCm39) |
P250T |
possibly damaging |
Het |
Gga2 |
C |
A |
7: 121,590,797 (GRCm39) |
V504L |
probably damaging |
Het |
Gm12239 |
T |
A |
11: 55,906,738 (GRCm39) |
|
noncoding transcript |
Het |
Gm6327 |
T |
C |
16: 12,578,890 (GRCm39) |
|
noncoding transcript |
Het |
Krt26 |
G |
T |
11: 99,224,545 (GRCm39) |
Y324* |
probably null |
Het |
Lamb2 |
A |
T |
9: 108,363,713 (GRCm39) |
H939L |
probably benign |
Het |
Lipo3 |
C |
T |
19: 33,600,086 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
G |
A |
9: 7,386,689 (GRCm39) |
T145M |
probably damaging |
Het |
Mrps27 |
G |
T |
13: 99,501,736 (GRCm39) |
V76L |
probably benign |
Het |
Mup6 |
T |
A |
4: 60,003,995 (GRCm39) |
Y29* |
probably null |
Het |
Nlrc3 |
T |
C |
16: 3,776,822 (GRCm39) |
K756E |
probably damaging |
Het |
Nnt |
T |
C |
13: 119,505,133 (GRCm39) |
H527R |
probably damaging |
Het |
Nudt8 |
T |
C |
19: 4,051,306 (GRCm39) |
V59A |
probably benign |
Het |
Ofcc1 |
A |
T |
13: 40,434,032 (GRCm39) |
|
probably null |
Het |
Or10d1 |
A |
T |
9: 39,484,020 (GRCm39) |
D178E |
probably damaging |
Het |
Or2a25 |
T |
C |
6: 42,888,889 (GRCm39) |
V144A |
probably benign |
Het |
Or51q1c |
T |
C |
7: 103,652,565 (GRCm39) |
W28R |
probably damaging |
Het |
Pdgfd |
T |
C |
9: 6,293,851 (GRCm39) |
S142P |
probably damaging |
Het |
Pias4 |
G |
T |
10: 80,992,921 (GRCm39) |
Q22K |
probably damaging |
Het |
Pin1 |
T |
C |
9: 20,573,600 (GRCm39) |
I95T |
probably benign |
Het |
Pramel23 |
A |
T |
4: 143,424,974 (GRCm39) |
D156E |
probably benign |
Het |
Prickle2 |
G |
A |
6: 92,388,326 (GRCm39) |
Q359* |
probably null |
Het |
Qrich2 |
G |
T |
11: 116,337,639 (GRCm39) |
Q1950K |
possibly damaging |
Het |
Rab10 |
C |
A |
12: 3,359,357 (GRCm39) |
G21V |
probably damaging |
Het |
Rbm27 |
T |
A |
18: 42,447,033 (GRCm39) |
|
probably benign |
Het |
Samd4 |
C |
A |
14: 47,254,017 (GRCm39) |
S160R |
probably benign |
Het |
Scube3 |
A |
C |
17: 28,385,502 (GRCm39) |
|
probably benign |
Het |
Serpinf2 |
A |
G |
11: 75,327,372 (GRCm39) |
L185P |
probably damaging |
Het |
Slc16a12 |
A |
G |
19: 34,652,264 (GRCm39) |
I294T |
probably benign |
Het |
Slc45a3 |
T |
A |
1: 131,905,478 (GRCm39) |
M167K |
probably damaging |
Het |
Sspo |
T |
A |
6: 48,450,910 (GRCm39) |
L2673Q |
possibly damaging |
Het |
Supt3 |
A |
G |
17: 45,314,028 (GRCm39) |
D139G |
probably damaging |
Het |
Tas1r3 |
T |
C |
4: 155,945,290 (GRCm39) |
M644V |
probably benign |
Het |
Tgfbi |
A |
G |
13: 56,775,781 (GRCm39) |
T276A |
probably damaging |
Het |
Tmem177 |
T |
C |
1: 119,838,308 (GRCm39) |
I124V |
probably benign |
Het |
Tmprss11f |
G |
T |
5: 86,681,484 (GRCm39) |
|
probably benign |
Het |
Tmprss3 |
G |
A |
17: 31,412,876 (GRCm39) |
|
probably benign |
Het |
Twf1 |
A |
G |
15: 94,484,430 (GRCm39) |
|
probably benign |
Het |
Uba52 |
T |
A |
8: 70,961,951 (GRCm39) |
Q166L |
probably damaging |
Het |
Ubr3 |
G |
T |
2: 69,809,756 (GRCm39) |
G1242V |
probably damaging |
Het |
Unc13d |
C |
T |
11: 115,956,308 (GRCm39) |
S835N |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,680,652 (GRCm39) |
K4877E |
possibly damaging |
Het |
Vmn2r98 |
A |
G |
17: 19,286,662 (GRCm39) |
I387V |
probably benign |
Het |
Vps11 |
A |
T |
9: 44,265,809 (GRCm39) |
I490N |
probably damaging |
Het |
Vstm4 |
T |
A |
14: 32,585,768 (GRCm39) |
|
probably null |
Het |
Zfp110 |
C |
A |
7: 12,582,524 (GRCm39) |
H391N |
possibly damaging |
Het |
Zfp212 |
C |
T |
6: 47,907,957 (GRCm39) |
P312L |
possibly damaging |
Het |
Zfp329 |
A |
T |
7: 12,544,914 (GRCm39) |
H203Q |
probably damaging |
Het |
Zscan12 |
G |
A |
13: 21,553,139 (GRCm39) |
G321E |
probably damaging |
Het |
|
Other mutations in Ciz1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Ciz1
|
APN |
2 |
32,262,400 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Ciz1
|
APN |
2 |
32,268,121 (GRCm39) |
utr 3 prime |
probably benign |
|
R0029:Ciz1
|
UTSW |
2 |
32,261,431 (GRCm39) |
splice site |
probably benign |
|
R0363:Ciz1
|
UTSW |
2 |
32,267,375 (GRCm39) |
critical splice donor site |
probably null |
|
R0373:Ciz1
|
UTSW |
2 |
32,257,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R0653:Ciz1
|
UTSW |
2 |
32,262,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0816:Ciz1
|
UTSW |
2 |
32,266,388 (GRCm39) |
unclassified |
probably benign |
|
R1255:Ciz1
|
UTSW |
2 |
32,255,888 (GRCm39) |
critical splice donor site |
probably null |
|
R2116:Ciz1
|
UTSW |
2 |
32,257,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R3161:Ciz1
|
UTSW |
2 |
32,260,075 (GRCm39) |
missense |
probably benign |
0.11 |
R3732:Ciz1
|
UTSW |
2 |
32,257,495 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4014:Ciz1
|
UTSW |
2 |
32,264,356 (GRCm39) |
missense |
probably damaging |
0.96 |
R4386:Ciz1
|
UTSW |
2 |
32,260,111 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4687:Ciz1
|
UTSW |
2 |
32,257,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R4786:Ciz1
|
UTSW |
2 |
32,267,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Ciz1
|
UTSW |
2 |
32,261,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R4869:Ciz1
|
UTSW |
2 |
32,254,247 (GRCm39) |
missense |
probably damaging |
0.99 |
R4871:Ciz1
|
UTSW |
2 |
32,262,300 (GRCm39) |
splice site |
probably benign |
|
R5270:Ciz1
|
UTSW |
2 |
32,264,511 (GRCm39) |
splice site |
probably null |
|
R5429:Ciz1
|
UTSW |
2 |
32,266,055 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5621:Ciz1
|
UTSW |
2 |
32,261,753 (GRCm39) |
missense |
probably damaging |
0.96 |
R5721:Ciz1
|
UTSW |
2 |
32,266,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R5805:Ciz1
|
UTSW |
2 |
32,257,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R5960:Ciz1
|
UTSW |
2 |
32,261,228 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6187:Ciz1
|
UTSW |
2 |
32,260,063 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6612:Ciz1
|
UTSW |
2 |
32,267,323 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7006:Ciz1
|
UTSW |
2 |
32,261,127 (GRCm39) |
critical splice donor site |
probably null |
|
R7200:Ciz1
|
UTSW |
2 |
32,254,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Ciz1
|
UTSW |
2 |
32,261,761 (GRCm39) |
missense |
probably benign |
|
R7574:Ciz1
|
UTSW |
2 |
32,257,380 (GRCm39) |
missense |
probably benign |
0.16 |
R7910:Ciz1
|
UTSW |
2 |
32,260,139 (GRCm39) |
critical splice donor site |
probably null |
|
R8390:Ciz1
|
UTSW |
2 |
32,257,335 (GRCm39) |
missense |
probably benign |
0.00 |
R8749:Ciz1
|
UTSW |
2 |
32,255,848 (GRCm39) |
missense |
probably benign |
0.03 |
R8765:Ciz1
|
UTSW |
2 |
32,260,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R8784:Ciz1
|
UTSW |
2 |
32,260,262 (GRCm39) |
missense |
probably benign |
0.01 |
R8812:Ciz1
|
UTSW |
2 |
32,254,286 (GRCm39) |
missense |
probably benign |
0.00 |
R8927:Ciz1
|
UTSW |
2 |
32,257,512 (GRCm39) |
nonsense |
probably null |
|
R8928:Ciz1
|
UTSW |
2 |
32,257,512 (GRCm39) |
nonsense |
probably null |
|
R9681:Ciz1
|
UTSW |
2 |
32,260,974 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9744:Ciz1
|
UTSW |
2 |
32,253,859 (GRCm39) |
missense |
unknown |
|
X0018:Ciz1
|
UTSW |
2 |
32,261,264 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGTCCAAATGCTGCCGCGTATC -3'
(R):5'- TGGGCACTTACTGGTTCTGGCAAG -3'
Sequencing Primer
(F):5'- CTCTCCAGAGCACTTAGCG -3'
(R):5'- CCACAGTGTCTACCATTTGGGG -3'
|
Posted On |
2013-04-11 |