Incidental Mutation 'R4851:Cic'
ID |
373549 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cic
|
Ensembl Gene |
ENSMUSG00000005442 |
Gene Name |
capicua transcriptional repressor |
Synonyms |
1200010B10Rik |
MMRRC Submission |
042463-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.943)
|
Stock # |
R4851 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
24967129-24993584 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 24972327 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Histidine
at position 686
(R686H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000132351
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000169266]
[ENSMUST00000169392]
|
AlphaFold |
Q924A2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000169266
AA Change: R686H
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000132351 Gene: ENSMUSG00000005442 AA Change: R686H
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
23 |
N/A |
INTRINSIC |
low complexity region
|
33 |
73 |
N/A |
INTRINSIC |
low complexity region
|
151 |
165 |
N/A |
INTRINSIC |
Pfam:DUF4819
|
249 |
346 |
1.8e-23 |
PFAM |
low complexity region
|
351 |
367 |
N/A |
INTRINSIC |
low complexity region
|
403 |
427 |
N/A |
INTRINSIC |
low complexity region
|
445 |
457 |
N/A |
INTRINSIC |
low complexity region
|
462 |
475 |
N/A |
INTRINSIC |
low complexity region
|
618 |
633 |
N/A |
INTRINSIC |
low complexity region
|
673 |
685 |
N/A |
INTRINSIC |
low complexity region
|
724 |
734 |
N/A |
INTRINSIC |
low complexity region
|
740 |
751 |
N/A |
INTRINSIC |
low complexity region
|
779 |
786 |
N/A |
INTRINSIC |
low complexity region
|
858 |
883 |
N/A |
INTRINSIC |
low complexity region
|
898 |
911 |
N/A |
INTRINSIC |
PDB:4J2L|D
|
930 |
955 |
5e-10 |
PDB |
low complexity region
|
1013 |
1027 |
N/A |
INTRINSIC |
low complexity region
|
1031 |
1045 |
N/A |
INTRINSIC |
HMG
|
1106 |
1176 |
1.24e-17 |
SMART |
low complexity region
|
1322 |
1338 |
N/A |
INTRINSIC |
low complexity region
|
1380 |
1393 |
N/A |
INTRINSIC |
low complexity region
|
1415 |
1428 |
N/A |
INTRINSIC |
low complexity region
|
1432 |
1462 |
N/A |
INTRINSIC |
low complexity region
|
1474 |
1490 |
N/A |
INTRINSIC |
low complexity region
|
1552 |
1567 |
N/A |
INTRINSIC |
low complexity region
|
1636 |
1647 |
N/A |
INTRINSIC |
low complexity region
|
1689 |
1710 |
N/A |
INTRINSIC |
low complexity region
|
1744 |
1766 |
N/A |
INTRINSIC |
low complexity region
|
1846 |
1858 |
N/A |
INTRINSIC |
low complexity region
|
1971 |
1986 |
N/A |
INTRINSIC |
low complexity region
|
2024 |
2038 |
N/A |
INTRINSIC |
low complexity region
|
2041 |
2061 |
N/A |
INTRINSIC |
low complexity region
|
2129 |
2159 |
N/A |
INTRINSIC |
low complexity region
|
2186 |
2219 |
N/A |
INTRINSIC |
low complexity region
|
2311 |
2324 |
N/A |
INTRINSIC |
low complexity region
|
2389 |
2400 |
N/A |
INTRINSIC |
low complexity region
|
2430 |
2453 |
N/A |
INTRINSIC |
low complexity region
|
2474 |
2509 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000169392
|
SMART Domains |
Protein: ENSMUSP00000131680 Gene: ENSMUSG00000005442
Domain | Start | End | E-Value | Type |
low complexity region
|
9 |
23 |
N/A |
INTRINSIC |
low complexity region
|
33 |
73 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.0%
|
Validation Efficiency |
100% (99/99) |
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 an ortholog of the Drosophila melanogaster capicua gene, and is a member of the high mobility group (HMG)-box superfamily of transcriptional repressors. This protein contains a conserved HMG domain that is involved in DNA binding and nuclear localization, and a conserved C-terminus. Studies suggest that the N-terminal region of this protein interacts with Atxn1 (GeneID:6310), to form a transcription repressor complex, and in vitro studies suggest that polyglutamine-expansion of ATXN1 may alter the repressor activity of this complex. Mutations in this gene have been associated with olidogdendrogliomas (PMID:21817013). In addition, translocation events resulting in gene fusions of this gene with both DUX4 (GeneID:100288687) and FOXO4 (GeneID:4303) have been associated with round cell sarcomas. There are multiple pseudogenes of this gene found on chromosomes 1, 4, 6, 7, 16, 20, and the Y chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2015] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit partial postnatal lethality, decreased body size, and severe lung alveolarization defects. [provided by MGI curators]
|
Allele List at MGI |
All alleles(61) : Targeted, other(4) Gene trapped(57)
|
Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,433,890 (GRCm39) |
R4148S |
probably benign |
Het |
Acoxl |
T |
A |
2: 127,886,311 (GRCm39) |
L182Q |
possibly damaging |
Het |
Aldh7a1 |
T |
C |
18: 56,665,088 (GRCm39) |
T364A |
possibly damaging |
Het |
App |
T |
C |
16: 84,853,322 (GRCm39) |
D252G |
unknown |
Het |
Arid1a |
A |
G |
4: 133,408,672 (GRCm39) |
I1945T |
unknown |
Het |
Arsk |
C |
T |
13: 76,213,398 (GRCm39) |
|
probably null |
Het |
Atad2b |
G |
A |
12: 4,993,251 (GRCm39) |
G257S |
probably benign |
Het |
Best1 |
C |
A |
19: 9,969,062 (GRCm39) |
R218L |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,312,300 (GRCm39) |
|
probably null |
Het |
Cdh13 |
C |
T |
8: 119,484,129 (GRCm39) |
T130I |
possibly damaging |
Het |
Cela2a |
T |
C |
4: 141,552,902 (GRCm39) |
E25G |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,632,314 (GRCm39) |
I346F |
probably damaging |
Het |
Chil6 |
C |
T |
3: 106,297,244 (GRCm39) |
G299D |
possibly damaging |
Het |
Cnpy1 |
T |
C |
5: 28,450,738 (GRCm39) |
I23V |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,707,011 (GRCm39) |
Y2034F |
unknown |
Het |
Coq10b |
T |
C |
1: 55,110,903 (GRCm39) |
Y224H |
probably benign |
Het |
Cryge |
G |
T |
1: 65,090,211 (GRCm39) |
|
probably benign |
Het |
Cyb5rl |
T |
G |
4: 106,941,510 (GRCm39) |
S252A |
probably benign |
Het |
Cyp2ab1 |
T |
A |
16: 20,133,814 (GRCm39) |
R125S |
probably damaging |
Het |
Dclk1 |
G |
A |
3: 55,387,811 (GRCm39) |
G86R |
probably damaging |
Het |
Dmtn |
A |
G |
14: 70,842,254 (GRCm39) |
M382T |
probably damaging |
Het |
Dnaaf8 |
A |
G |
16: 4,794,138 (GRCm39) |
|
noncoding transcript |
Het |
Dnah12 |
T |
A |
14: 26,437,784 (GRCm39) |
L471* |
probably null |
Het |
Dock10 |
A |
T |
1: 80,526,874 (GRCm39) |
S782T |
probably benign |
Het |
Egfem1 |
C |
A |
3: 29,206,032 (GRCm39) |
H90N |
possibly damaging |
Het |
Ephb6 |
T |
A |
6: 41,595,079 (GRCm39) |
W698R |
probably benign |
Het |
Exoc4 |
T |
A |
6: 33,895,343 (GRCm39) |
C787S |
probably damaging |
Het |
Exosc8 |
A |
T |
3: 54,639,523 (GRCm39) |
|
probably benign |
Het |
Galc |
T |
A |
12: 98,193,533 (GRCm39) |
Q352L |
probably benign |
Het |
Galns |
A |
G |
8: 123,327,272 (GRCm39) |
Y167H |
probably damaging |
Het |
Glb1l |
T |
C |
1: 75,185,528 (GRCm39) |
|
probably benign |
Het |
Gm6185 |
A |
T |
1: 161,033,750 (GRCm39) |
|
noncoding transcript |
Het |
Gm7694 |
T |
C |
1: 170,128,794 (GRCm39) |
N245S |
probably benign |
Het |
Gmcl1 |
T |
G |
6: 86,681,538 (GRCm39) |
K385N |
possibly damaging |
Het |
Gramd1c |
A |
T |
16: 43,810,200 (GRCm39) |
W463R |
probably damaging |
Het |
Gtpbp8 |
C |
G |
16: 44,566,433 (GRCm39) |
A90P |
probably benign |
Het |
H2bc11 |
G |
T |
13: 22,227,421 (GRCm39) |
|
probably benign |
Het |
Hcar1 |
T |
C |
5: 124,016,731 (GRCm39) |
E320G |
probably benign |
Het |
Hhatl |
T |
C |
9: 121,618,077 (GRCm39) |
D226G |
probably damaging |
Het |
Hoxc5 |
T |
A |
15: 102,923,801 (GRCm39) |
I199N |
probably damaging |
Het |
Iars2 |
T |
C |
1: 185,059,845 (GRCm39) |
D121G |
probably damaging |
Het |
Il5ra |
T |
A |
6: 106,715,432 (GRCm39) |
H134L |
probably benign |
Het |
Isl2 |
T |
A |
9: 55,452,271 (GRCm39) |
I281N |
possibly damaging |
Het |
Kcnk13 |
T |
C |
12: 99,932,383 (GRCm39) |
F60L |
probably damaging |
Het |
Kdelr3 |
C |
T |
15: 79,409,066 (GRCm39) |
T85M |
possibly damaging |
Het |
Kdf1 |
A |
T |
4: 133,255,676 (GRCm39) |
H131L |
probably damaging |
Het |
Mipol1 |
T |
A |
12: 57,379,087 (GRCm39) |
L182I |
probably damaging |
Het |
Morc1 |
T |
G |
16: 48,381,980 (GRCm39) |
S513R |
probably benign |
Het |
Moxd2 |
A |
T |
6: 40,855,756 (GRCm39) |
L611H |
probably damaging |
Het |
Mpped2 |
T |
C |
2: 106,529,724 (GRCm39) |
|
probably benign |
Het |
Mrpl51 |
T |
C |
6: 125,170,270 (GRCm39) |
V92A |
probably benign |
Het |
Mrps26 |
G |
A |
2: 130,405,681 (GRCm39) |
|
probably benign |
Het |
Mrps5 |
A |
G |
2: 127,432,665 (GRCm39) |
T29A |
probably benign |
Het |
Mustn1 |
A |
G |
14: 30,601,517 (GRCm39) |
|
probably benign |
Het |
Ncor2 |
G |
A |
5: 125,110,431 (GRCm39) |
P858S |
possibly damaging |
Het |
Nfasc |
A |
G |
1: 132,529,759 (GRCm39) |
F807S |
probably damaging |
Het |
Nup50 |
G |
A |
15: 84,823,912 (GRCm39) |
V422I |
probably benign |
Het |
Or10x1 |
T |
A |
1: 174,196,562 (GRCm39) |
F26L |
probably benign |
Het |
Or13a25 |
A |
T |
7: 140,247,226 (GRCm39) |
M2L |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,493,883 (GRCm39) |
H159L |
probably damaging |
Het |
Or2ag13 |
A |
T |
7: 106,473,221 (GRCm39) |
V77D |
probably damaging |
Het |
Or3a1d |
C |
A |
11: 74,237,769 (GRCm39) |
V214L |
probably benign |
Het |
Or4c107 |
A |
G |
2: 88,788,930 (GRCm39) |
N40S |
probably damaging |
Het |
Or8b44 |
T |
A |
9: 38,410,319 (GRCm39) |
M118K |
probably damaging |
Het |
Or8u9 |
T |
A |
2: 86,002,015 (GRCm39) |
I49F |
probably damaging |
Het |
Osbpl8 |
T |
A |
10: 111,040,661 (GRCm39) |
M1K |
probably null |
Het |
Pcdhb22 |
A |
C |
18: 37,652,087 (GRCm39) |
D185A |
possibly damaging |
Het |
Pcdhga8 |
G |
T |
18: 37,949,457 (GRCm39) |
R291L |
probably damaging |
Het |
Saysd1 |
A |
T |
14: 20,127,672 (GRCm39) |
L84Q |
possibly damaging |
Het |
Slc41a1 |
T |
C |
1: 131,758,508 (GRCm39) |
I50T |
probably benign |
Het |
Smg7 |
G |
A |
1: 152,720,020 (GRCm39) |
P834S |
probably benign |
Het |
Speer4a1 |
C |
T |
5: 26,243,210 (GRCm39) |
V92M |
probably damaging |
Het |
Srf |
T |
C |
17: 46,860,400 (GRCm39) |
T461A |
probably benign |
Het |
Ssu72 |
A |
G |
4: 155,800,053 (GRCm39) |
D72G |
possibly damaging |
Het |
Suco |
T |
C |
1: 161,661,761 (GRCm39) |
E890G |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,763,656 (GRCm39) |
|
probably null |
Het |
Tm6sf1 |
A |
G |
7: 81,515,091 (GRCm39) |
E7G |
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,378,616 (GRCm39) |
K240R |
probably benign |
Het |
Tmem52 |
T |
A |
4: 155,554,825 (GRCm39) |
Y149* |
probably null |
Het |
Tpgs2 |
A |
T |
18: 25,284,305 (GRCm39) |
Y68N |
possibly damaging |
Het |
Vmn1r205 |
T |
A |
13: 22,777,074 (GRCm39) |
E9D |
probably benign |
Het |
Vmn2r32 |
A |
G |
7: 7,482,953 (GRCm39) |
V7A |
possibly damaging |
Het |
Vmn2r80 |
T |
C |
10: 79,030,156 (GRCm39) |
Y661H |
possibly damaging |
Het |
Vps39 |
G |
A |
2: 120,152,312 (GRCm39) |
|
probably benign |
Het |
Vwde |
A |
T |
6: 13,196,047 (GRCm39) |
V326D |
possibly damaging |
Het |
Zfp641 |
T |
A |
15: 98,186,598 (GRCm39) |
S342C |
probably damaging |
Het |
Zfp961 |
T |
C |
8: 72,722,847 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cic |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Cic
|
APN |
7 |
24,991,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01668:Cic
|
APN |
7 |
24,990,629 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02229:Cic
|
APN |
7 |
24,990,375 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02506:Cic
|
APN |
7 |
24,990,282 (GRCm39) |
missense |
probably benign |
|
IGL02794:Cic
|
APN |
7 |
24,985,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03065:Cic
|
APN |
7 |
24,985,246 (GRCm39) |
splice site |
probably benign |
|
IGL03304:Cic
|
APN |
7 |
24,984,274 (GRCm39) |
missense |
probably damaging |
1.00 |
Capuccino
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
Cassock
|
UTSW |
7 |
24,988,338 (GRCm39) |
nonsense |
probably null |
|
Monkey
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850_Cic_466
|
UTSW |
7 |
24,972,327 (GRCm39) |
missense |
probably damaging |
0.98 |
1mM(1):Cic
|
UTSW |
7 |
24,990,214 (GRCm39) |
splice site |
probably benign |
|
IGL03046:Cic
|
UTSW |
7 |
24,990,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0027:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0038:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0063:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0064:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0118:Cic
|
UTSW |
7 |
24,985,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0241:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0377:Cic
|
UTSW |
7 |
24,985,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R0462:Cic
|
UTSW |
7 |
24,986,565 (GRCm39) |
missense |
probably damaging |
0.98 |
R0462:Cic
|
UTSW |
7 |
24,986,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Cic
|
UTSW |
7 |
24,984,662 (GRCm39) |
missense |
probably benign |
|
R1253:Cic
|
UTSW |
7 |
24,990,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Cic
|
UTSW |
7 |
24,979,162 (GRCm39) |
intron |
probably benign |
|
R1462:Cic
|
UTSW |
7 |
24,971,032 (GRCm39) |
missense |
probably damaging |
0.98 |
R1462:Cic
|
UTSW |
7 |
24,971,032 (GRCm39) |
missense |
probably damaging |
0.98 |
R1519:Cic
|
UTSW |
7 |
24,993,235 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1586:Cic
|
UTSW |
7 |
24,985,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Cic
|
UTSW |
7 |
24,987,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Cic
|
UTSW |
7 |
24,986,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Cic
|
UTSW |
7 |
24,970,961 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2063:Cic
|
UTSW |
7 |
24,972,876 (GRCm39) |
missense |
probably damaging |
0.98 |
R2161:Cic
|
UTSW |
7 |
24,987,559 (GRCm39) |
splice site |
probably null |
|
R2495:Cic
|
UTSW |
7 |
24,991,201 (GRCm39) |
splice site |
probably benign |
|
R2865:Cic
|
UTSW |
7 |
24,972,646 (GRCm39) |
missense |
probably damaging |
0.96 |
R3692:Cic
|
UTSW |
7 |
24,988,338 (GRCm39) |
nonsense |
probably null |
|
R3709:Cic
|
UTSW |
7 |
24,986,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R3710:Cic
|
UTSW |
7 |
24,986,406 (GRCm39) |
missense |
probably damaging |
0.99 |
R3872:Cic
|
UTSW |
7 |
24,971,124 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3946:Cic
|
UTSW |
7 |
24,971,771 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4199:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
frame shift |
probably null |
|
R4426:Cic
|
UTSW |
7 |
24,993,433 (GRCm39) |
utr 3 prime |
probably benign |
|
R4502:Cic
|
UTSW |
7 |
24,987,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Cic
|
UTSW |
7 |
24,972,203 (GRCm39) |
missense |
probably benign |
0.33 |
R4586:Cic
|
UTSW |
7 |
24,972,203 (GRCm39) |
missense |
probably benign |
0.33 |
R4614:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
frame shift |
probably null |
|
R4664:Cic
|
UTSW |
7 |
24,990,099 (GRCm39) |
small deletion |
probably benign |
|
R4688:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
frame shift |
probably null |
|
R4695:Cic
|
UTSW |
7 |
24,973,013 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4696:Cic
|
UTSW |
7 |
24,987,908 (GRCm39) |
missense |
probably benign |
|
R4746:Cic
|
UTSW |
7 |
24,987,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Cic
|
UTSW |
7 |
24,991,636 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4767:Cic
|
UTSW |
7 |
24,971,025 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4776:Cic
|
UTSW |
7 |
24,982,308 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4820:Cic
|
UTSW |
7 |
24,971,157 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4850:Cic
|
UTSW |
7 |
24,972,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R4922:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
small insertion |
probably benign |
|
R4989:Cic
|
UTSW |
7 |
24,986,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5131:Cic
|
UTSW |
7 |
24,991,095 (GRCm39) |
small insertion |
probably benign |
|
R5718:Cic
|
UTSW |
7 |
24,972,203 (GRCm39) |
missense |
probably benign |
0.33 |
R5801:Cic
|
UTSW |
7 |
24,970,863 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5949:Cic
|
UTSW |
7 |
24,971,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Cic
|
UTSW |
7 |
24,971,423 (GRCm39) |
missense |
probably benign |
0.33 |
R6246:Cic
|
UTSW |
7 |
24,971,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R6283:Cic
|
UTSW |
7 |
24,985,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Cic
|
UTSW |
7 |
24,972,248 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6481:Cic
|
UTSW |
7 |
24,987,706 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6919:Cic
|
UTSW |
7 |
24,971,202 (GRCm39) |
missense |
probably benign |
0.04 |
R6920:Cic
|
UTSW |
7 |
24,990,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Cic
|
UTSW |
7 |
24,970,736 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7002:Cic
|
UTSW |
7 |
24,971,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R7113:Cic
|
UTSW |
7 |
24,972,869 (GRCm39) |
missense |
probably benign |
0.08 |
R7560:Cic
|
UTSW |
7 |
24,972,278 (GRCm39) |
missense |
probably damaging |
0.98 |
R7680:Cic
|
UTSW |
7 |
24,991,856 (GRCm39) |
missense |
probably damaging |
0.96 |
R7698:Cic
|
UTSW |
7 |
24,972,597 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7746:Cic
|
UTSW |
7 |
24,988,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7841:Cic
|
UTSW |
7 |
24,985,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Cic
|
UTSW |
7 |
24,984,551 (GRCm39) |
missense |
probably benign |
0.10 |
R7916:Cic
|
UTSW |
7 |
24,987,715 (GRCm39) |
missense |
probably damaging |
0.99 |
R7920:Cic
|
UTSW |
7 |
24,971,384 (GRCm39) |
missense |
probably benign |
|
R8056:Cic
|
UTSW |
7 |
24,990,366 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8226:Cic
|
UTSW |
7 |
24,987,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8281:Cic
|
UTSW |
7 |
24,971,249 (GRCm39) |
missense |
probably benign |
|
R8847:Cic
|
UTSW |
7 |
24,970,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R8991:Cic
|
UTSW |
7 |
24,988,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Cic
|
UTSW |
7 |
24,985,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R9140:Cic
|
UTSW |
7 |
24,985,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R9200:Cic
|
UTSW |
7 |
24,971,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R9208:Cic
|
UTSW |
7 |
24,987,502 (GRCm39) |
missense |
probably benign |
0.07 |
R9301:Cic
|
UTSW |
7 |
24,991,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Cic
|
UTSW |
7 |
24,971,414 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9569:Cic
|
UTSW |
7 |
24,972,120 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9752:Cic
|
UTSW |
7 |
24,971,403 (GRCm39) |
missense |
probably damaging |
0.96 |
V7732:Cic
|
UTSW |
7 |
24,991,670 (GRCm39) |
missense |
probably benign |
|
Z1176:Cic
|
UTSW |
7 |
24,970,444 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
Predicted Primers |
PCR Primer
(F):5'- CACGCTTCGAGTTTGATGAGTG -3'
(R):5'- AGCTGTCACTCTTGGGGAAG -3'
Sequencing Primer
(F):5'- GTGTCACTTGGCAGCTCC -3'
(R):5'- CACTCTTGGGGAAGTCTGG -3'
|
Posted On |
2016-03-01 |