Incidental Mutation 'R7792:Ccdc180'
ID |
599926 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ccdc180
|
Ensembl Gene |
ENSMUSG00000035539 |
Gene Name |
coiled-coil domain containing 180 |
Synonyms |
LOC381522, E230008N13Rik |
MMRRC Submission |
045848-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7792 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
45890303-45950774 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 45890389 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000136714
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030011]
[ENSMUST00000107782]
[ENSMUST00000107783]
[ENSMUST00000178561]
|
AlphaFold |
J3QNE4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000030011
|
SMART Domains |
Protein: ENSMUSP00000030011 Gene: ENSMUSG00000028327
Domain | Start | End | E-Value | Type |
Pfam:RBP_receptor
|
13 |
602 |
8.7e-228 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000107782
|
SMART Domains |
Protein: ENSMUSP00000103411 Gene: ENSMUSG00000028327
Domain | Start | End | E-Value | Type |
Pfam:RBP_receptor
|
1 |
512 |
2.8e-221 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000107783
|
SMART Domains |
Protein: ENSMUSP00000103412 Gene: ENSMUSG00000028327
Domain | Start | End | E-Value | Type |
Pfam:RBP_receptor
|
12 |
603 |
1e-254 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000149903
|
SMART Domains |
Protein: ENSMUSP00000119784 Gene: ENSMUSG00000035539
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
42 |
N/A |
INTRINSIC |
coiled coil region
|
90 |
117 |
N/A |
INTRINSIC |
Pfam:DUF4455
|
141 |
609 |
2e-189 |
PFAM |
low complexity region
|
628 |
642 |
N/A |
INTRINSIC |
low complexity region
|
658 |
675 |
N/A |
INTRINSIC |
coiled coil region
|
710 |
780 |
N/A |
INTRINSIC |
coiled coil region
|
945 |
979 |
N/A |
INTRINSIC |
low complexity region
|
1100 |
1123 |
N/A |
INTRINSIC |
Pfam:DUF4456
|
1169 |
1372 |
9.5e-77 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000178561
|
SMART Domains |
Protein: ENSMUSP00000136714 Gene: ENSMUSG00000035539
Domain | Start | End | E-Value | Type |
low complexity region
|
32 |
49 |
N/A |
INTRINSIC |
coiled coil region
|
98 |
125 |
N/A |
INTRINSIC |
Pfam:DUF4455
|
148 |
616 |
7.3e-189 |
PFAM |
low complexity region
|
635 |
649 |
N/A |
INTRINSIC |
low complexity region
|
665 |
682 |
N/A |
INTRINSIC |
coiled coil region
|
718 |
788 |
N/A |
INTRINSIC |
coiled coil region
|
1121 |
1155 |
N/A |
INTRINSIC |
low complexity region
|
1275 |
1298 |
N/A |
INTRINSIC |
Pfam:DUF4456
|
1344 |
1547 |
2.2e-76 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
100% (97/97) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a coiled-coil domain. Alternative splicing results in multiple transcript variants encoding different isoforms. A single nucleotide polymorphism (SNP) in this gene has been associated with increased susceptibility to Behcet's Disease (PMID: 19442274). [provided by RefSeq, Dec 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
G |
T |
8: 111,769,896 (GRCm39) |
V332F |
possibly damaging |
Het |
Abhd15 |
T |
A |
11: 77,409,560 (GRCm39) |
S425T |
probably benign |
Het |
Acads |
A |
T |
5: 115,250,840 (GRCm39) |
F152L |
probably damaging |
Het |
Acp3 |
T |
A |
9: 104,204,165 (GRCm39) |
H43L |
probably damaging |
Het |
Adora2a |
A |
G |
10: 75,169,480 (GRCm39) |
S315G |
probably benign |
Het |
Agxt2 |
A |
T |
15: 10,381,472 (GRCm39) |
D242V |
probably damaging |
Het |
Alx4 |
A |
G |
2: 93,473,056 (GRCm39) |
D18G |
probably damaging |
Het |
Ankrd11 |
A |
G |
8: 123,610,970 (GRCm39) |
S2639P |
probably damaging |
Het |
Arhgap35 |
A |
T |
7: 16,295,453 (GRCm39) |
V1204D |
possibly damaging |
Het |
Arid2 |
A |
G |
15: 96,267,256 (GRCm39) |
T579A |
probably benign |
Het |
B4galt1 |
C |
T |
4: 40,809,373 (GRCm39) |
G332S |
probably benign |
Het |
B4galt4 |
C |
A |
16: 38,578,172 (GRCm39) |
Y206* |
probably null |
Het |
Bcl2l14 |
A |
T |
6: 134,409,277 (GRCm39) |
T284S |
possibly damaging |
Het |
Bop1 |
C |
T |
15: 76,338,548 (GRCm39) |
V465M |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,567,977 (GRCm39) |
L1037H |
probably damaging |
Het |
Cadm2 |
G |
A |
16: 66,568,523 (GRCm39) |
T254M |
probably benign |
Het |
Ccdc7a |
A |
T |
8: 129,618,918 (GRCm39) |
D875E |
possibly damaging |
Het |
Cenpu |
A |
G |
8: 47,015,502 (GRCm39) |
D139G |
possibly damaging |
Het |
Cep57l1 |
A |
T |
10: 41,598,936 (GRCm39) |
C292* |
probably null |
Het |
Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
Chst14 |
A |
G |
2: 118,758,256 (GRCm39) |
H350R |
probably benign |
Het |
Clca3a1 |
T |
A |
3: 144,455,492 (GRCm39) |
I434F |
possibly damaging |
Het |
Crispld2 |
A |
G |
8: 120,757,809 (GRCm39) |
T385A |
probably benign |
Het |
Crmp1 |
A |
C |
5: 37,441,439 (GRCm39) |
N507T |
probably damaging |
Het |
Cyp4f40 |
T |
A |
17: 32,890,143 (GRCm39) |
I271N |
probably damaging |
Het |
D630003M21Rik |
G |
T |
2: 158,052,082 (GRCm39) |
Q670K |
possibly damaging |
Het |
Ddx42 |
T |
C |
11: 106,127,822 (GRCm39) |
I342T |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 65,740,839 (GRCm39) |
I4116F |
probably damaging |
Het |
Ehd2 |
T |
C |
7: 15,684,683 (GRCm39) |
H372R |
probably benign |
Het |
Gja8 |
C |
A |
3: 96,827,092 (GRCm39) |
C190F |
probably damaging |
Het |
Gm8297 |
A |
T |
14: 16,165,939 (GRCm39) |
D72V |
possibly damaging |
Het |
Golgb1 |
A |
G |
16: 36,739,092 (GRCm39) |
D2518G |
probably benign |
Het |
Hsd17b12 |
C |
A |
2: 93,863,986 (GRCm39) |
M285I |
probably benign |
Het |
Hus1 |
T |
C |
11: 8,950,133 (GRCm39) |
E196G |
probably damaging |
Het |
Ift70a2 |
T |
C |
2: 75,807,273 (GRCm39) |
N413S |
probably benign |
Het |
Irf2 |
G |
A |
8: 47,260,314 (GRCm39) |
R82Q |
probably damaging |
Het |
Irx2 |
A |
G |
13: 72,779,493 (GRCm39) |
D259G |
possibly damaging |
Het |
Jph1 |
T |
A |
1: 17,074,602 (GRCm39) |
Q472L |
probably benign |
Het |
Kif2a |
T |
C |
13: 107,124,490 (GRCm39) |
Q142R |
probably benign |
Het |
Lonp1 |
T |
C |
17: 56,929,515 (GRCm39) |
Y174C |
probably damaging |
Het |
Mapk14 |
T |
C |
17: 28,965,271 (GRCm39) |
F348L |
probably damaging |
Het |
Marchf10 |
G |
T |
11: 105,281,054 (GRCm39) |
D410E |
probably benign |
Het |
Mff |
A |
T |
1: 82,724,802 (GRCm39) |
|
probably null |
Het |
Mtrex |
A |
T |
13: 113,009,443 (GRCm39) |
D985E |
probably benign |
Het |
Necab3 |
G |
A |
2: 154,388,200 (GRCm39) |
R271C |
probably damaging |
Het |
Nlrp4e |
T |
A |
7: 23,021,182 (GRCm39) |
F556L |
possibly damaging |
Het |
Nt5c2 |
T |
C |
19: 46,878,385 (GRCm39) |
K425E |
probably benign |
Het |
Ofcc1 |
A |
T |
13: 40,296,302 (GRCm39) |
W511R |
probably damaging |
Het |
Or1j18 |
A |
C |
2: 36,624,342 (GRCm39) |
E3A |
probably benign |
Het |
Or2v1 |
T |
A |
11: 49,025,496 (GRCm39) |
I159N |
possibly damaging |
Het |
Or4k77 |
T |
C |
2: 111,199,748 (GRCm39) |
I257T |
probably benign |
Het |
Or52p2 |
T |
A |
7: 102,238,090 (GRCm39) |
|
probably benign |
Het |
P2rx2 |
G |
C |
5: 110,488,210 (GRCm39) |
A448G |
possibly damaging |
Het |
Pcnx2 |
A |
T |
8: 126,618,757 (GRCm39) |
N56K |
possibly damaging |
Het |
Pdzd7 |
A |
C |
19: 45,028,657 (GRCm39) |
M162R |
possibly damaging |
Het |
Phyhd1 |
A |
G |
2: 30,156,782 (GRCm39) |
M1V |
probably null |
Het |
Plaat3 |
T |
C |
19: 7,556,660 (GRCm39) |
C154R |
probably benign |
Het |
Plekha5 |
A |
G |
6: 140,534,950 (GRCm39) |
E1126G |
possibly damaging |
Het |
Plekhm1 |
A |
T |
11: 103,287,886 (GRCm39) |
V87D |
probably damaging |
Het |
Pole |
G |
A |
5: 110,445,332 (GRCm39) |
|
probably null |
Het |
Pramel22 |
A |
G |
4: 143,381,123 (GRCm39) |
L300P |
probably benign |
Het |
R3hcc1 |
T |
C |
14: 69,942,957 (GRCm39) |
M207V |
probably benign |
Het |
R3hcc1l |
T |
A |
19: 42,552,403 (GRCm39) |
S467T |
probably damaging |
Het |
Rasgrp4 |
G |
T |
7: 28,842,527 (GRCm39) |
R267L |
probably damaging |
Het |
Rbm20 |
T |
C |
19: 53,838,567 (GRCm39) |
I848T |
probably benign |
Het |
Rims2 |
T |
C |
15: 39,061,923 (GRCm39) |
S56P |
possibly damaging |
Het |
Rmc1 |
G |
A |
18: 12,314,656 (GRCm39) |
D289N |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,447,222 (GRCm39) |
D3089E |
probably benign |
Het |
Sall2 |
C |
T |
14: 52,553,521 (GRCm39) |
G16R |
probably damaging |
Het |
Scgb1b19 |
G |
A |
7: 32,987,912 (GRCm39) |
C93Y |
probably damaging |
Het |
Scn3a |
T |
A |
2: 65,297,334 (GRCm39) |
K1442* |
probably null |
Het |
Sepsecs |
A |
G |
5: 52,801,391 (GRCm39) |
S424P |
probably damaging |
Het |
Set |
G |
T |
2: 29,960,323 (GRCm39) |
V219F |
probably benign |
Het |
Sh3tc1 |
A |
T |
5: 35,868,295 (GRCm39) |
F390I |
probably damaging |
Het |
Simc1 |
G |
A |
13: 54,695,143 (GRCm39) |
V1269M |
probably damaging |
Het |
Ska3 |
T |
G |
14: 58,047,512 (GRCm39) |
D341A |
probably damaging |
Het |
Slc16a10 |
A |
T |
10: 39,913,411 (GRCm39) |
|
probably null |
Het |
Srgap1 |
T |
A |
10: 121,761,872 (GRCm39) |
N92I |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,431,624 (GRCm39) |
V639A |
probably damaging |
Het |
Stk11 |
A |
T |
10: 79,961,271 (GRCm39) |
|
probably benign |
Het |
Sult5a1 |
G |
A |
8: 123,872,180 (GRCm39) |
H221Y |
probably benign |
Het |
Sytl3 |
T |
A |
17: 7,003,977 (GRCm39) |
M559K |
probably benign |
Het |
Tab2 |
A |
C |
10: 7,794,897 (GRCm39) |
D528E |
possibly damaging |
Het |
Tbc1d15 |
A |
G |
10: 115,057,492 (GRCm39) |
I218T |
possibly damaging |
Het |
Tenm4 |
T |
A |
7: 96,423,221 (GRCm39) |
M672K |
possibly damaging |
Het |
Tent4b |
A |
T |
8: 88,979,182 (GRCm39) |
Q561L |
probably benign |
Het |
Tfrc |
A |
G |
16: 32,437,985 (GRCm39) |
K346R |
probably benign |
Het |
Thsd1 |
G |
T |
8: 22,733,114 (GRCm39) |
G54W |
probably damaging |
Het |
Tmprss15 |
A |
T |
16: 78,800,275 (GRCm39) |
L618I |
probably damaging |
Het |
Top3a |
T |
C |
11: 60,633,790 (GRCm39) |
S769G |
probably benign |
Het |
Trp63 |
C |
A |
16: 25,686,974 (GRCm39) |
P396Q |
possibly damaging |
Het |
Uggt1 |
T |
C |
1: 36,247,065 (GRCm39) |
S311G |
probably damaging |
Het |
Usp10 |
G |
A |
8: 120,678,740 (GRCm39) |
E574K |
possibly damaging |
Het |
Wfdc6b |
T |
A |
2: 164,459,822 (GRCm39) |
I148K |
probably damaging |
Het |
Zcchc2 |
T |
G |
1: 105,945,982 (GRCm39) |
I474R |
probably damaging |
Het |
Zdhhc2 |
A |
G |
8: 40,900,182 (GRCm39) |
K82R |
probably benign |
Het |
Zfp273 |
A |
G |
13: 67,974,135 (GRCm39) |
D421G |
possibly damaging |
Het |
Zfp280d |
T |
C |
9: 72,238,601 (GRCm39) |
I639T |
probably damaging |
Het |
Zfp429 |
A |
T |
13: 67,538,558 (GRCm39) |
C295* |
probably null |
Het |
|
Other mutations in Ccdc180 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01369:Ccdc180
|
APN |
4 |
45,900,256 (GRCm39) |
missense |
probably benign |
|
IGL01713:Ccdc180
|
APN |
4 |
45,921,025 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01915:Ccdc180
|
APN |
4 |
45,904,544 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01935:Ccdc180
|
APN |
4 |
45,906,889 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02539:Ccdc180
|
APN |
4 |
45,921,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Ccdc180
|
APN |
4 |
45,903,840 (GRCm39) |
splice site |
probably benign |
|
IGL03071:Ccdc180
|
APN |
4 |
45,903,840 (GRCm39) |
splice site |
probably benign |
|
IGL03146:Ccdc180
|
APN |
4 |
45,903,840 (GRCm39) |
splice site |
probably benign |
|
PIT4687001:Ccdc180
|
UTSW |
4 |
45,949,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Ccdc180
|
UTSW |
4 |
45,930,119 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0049:Ccdc180
|
UTSW |
4 |
45,930,119 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0054:Ccdc180
|
UTSW |
4 |
45,890,900 (GRCm39) |
missense |
probably benign |
0.01 |
R0054:Ccdc180
|
UTSW |
4 |
45,890,900 (GRCm39) |
missense |
probably benign |
0.01 |
R0080:Ccdc180
|
UTSW |
4 |
45,896,205 (GRCm39) |
missense |
probably null |
0.00 |
R0082:Ccdc180
|
UTSW |
4 |
45,896,205 (GRCm39) |
missense |
probably null |
0.00 |
R0126:Ccdc180
|
UTSW |
4 |
45,912,866 (GRCm39) |
critical splice donor site |
probably null |
|
R0193:Ccdc180
|
UTSW |
4 |
45,914,803 (GRCm39) |
missense |
probably benign |
0.01 |
R0276:Ccdc180
|
UTSW |
4 |
45,923,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R0362:Ccdc180
|
UTSW |
4 |
45,923,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Ccdc180
|
UTSW |
4 |
45,930,197 (GRCm39) |
critical splice donor site |
probably null |
|
R0468:Ccdc180
|
UTSW |
4 |
45,923,271 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0539:Ccdc180
|
UTSW |
4 |
45,922,010 (GRCm39) |
missense |
probably damaging |
0.97 |
R0543:Ccdc180
|
UTSW |
4 |
45,900,041 (GRCm39) |
nonsense |
probably null |
|
R0546:Ccdc180
|
UTSW |
4 |
45,904,597 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0612:Ccdc180
|
UTSW |
4 |
45,927,969 (GRCm39) |
missense |
probably damaging |
0.98 |
R0792:Ccdc180
|
UTSW |
4 |
45,927,975 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1056:Ccdc180
|
UTSW |
4 |
45,916,375 (GRCm39) |
missense |
probably benign |
0.01 |
R1099:Ccdc180
|
UTSW |
4 |
45,914,225 (GRCm39) |
missense |
probably benign |
0.03 |
R1136:Ccdc180
|
UTSW |
4 |
45,914,589 (GRCm39) |
missense |
probably benign |
0.00 |
R1263:Ccdc180
|
UTSW |
4 |
45,903,887 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1331:Ccdc180
|
UTSW |
4 |
45,909,359 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1522:Ccdc180
|
UTSW |
4 |
45,927,975 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1819:Ccdc180
|
UTSW |
4 |
45,926,195 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2022:Ccdc180
|
UTSW |
4 |
45,944,418 (GRCm39) |
missense |
probably benign |
0.18 |
R2056:Ccdc180
|
UTSW |
4 |
45,932,477 (GRCm39) |
missense |
probably benign |
0.03 |
R2219:Ccdc180
|
UTSW |
4 |
45,944,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Ccdc180
|
UTSW |
4 |
45,948,856 (GRCm39) |
critical splice donor site |
probably null |
|
R2229:Ccdc180
|
UTSW |
4 |
45,948,856 (GRCm39) |
critical splice donor site |
probably null |
|
R2255:Ccdc180
|
UTSW |
4 |
45,921,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R2427:Ccdc180
|
UTSW |
4 |
45,929,545 (GRCm39) |
missense |
probably benign |
0.03 |
R3001:Ccdc180
|
UTSW |
4 |
45,899,988 (GRCm39) |
missense |
probably benign |
|
R3002:Ccdc180
|
UTSW |
4 |
45,899,988 (GRCm39) |
missense |
probably benign |
|
R3003:Ccdc180
|
UTSW |
4 |
45,899,988 (GRCm39) |
missense |
probably benign |
|
R3110:Ccdc180
|
UTSW |
4 |
45,900,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3111:Ccdc180
|
UTSW |
4 |
45,900,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3112:Ccdc180
|
UTSW |
4 |
45,900,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3898:Ccdc180
|
UTSW |
4 |
45,912,799 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4022:Ccdc180
|
UTSW |
4 |
45,904,560 (GRCm39) |
nonsense |
probably null |
|
R4084:Ccdc180
|
UTSW |
4 |
45,950,632 (GRCm39) |
missense |
probably benign |
0.19 |
R4377:Ccdc180
|
UTSW |
4 |
45,941,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R4595:Ccdc180
|
UTSW |
4 |
45,945,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R4637:Ccdc180
|
UTSW |
4 |
45,914,443 (GRCm39) |
missense |
probably benign |
|
R4811:Ccdc180
|
UTSW |
4 |
45,928,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Ccdc180
|
UTSW |
4 |
45,912,794 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4858:Ccdc180
|
UTSW |
4 |
45,923,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Ccdc180
|
UTSW |
4 |
45,909,308 (GRCm39) |
missense |
probably damaging |
0.98 |
R4940:Ccdc180
|
UTSW |
4 |
45,917,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R4940:Ccdc180
|
UTSW |
4 |
45,917,453 (GRCm39) |
missense |
probably damaging |
0.96 |
R5042:Ccdc180
|
UTSW |
4 |
45,916,255 (GRCm39) |
missense |
probably damaging |
0.98 |
R5119:Ccdc180
|
UTSW |
4 |
45,914,603 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5177:Ccdc180
|
UTSW |
4 |
45,917,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Ccdc180
|
UTSW |
4 |
45,917,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R5333:Ccdc180
|
UTSW |
4 |
45,890,935 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5448:Ccdc180
|
UTSW |
4 |
45,920,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R5510:Ccdc180
|
UTSW |
4 |
45,928,046 (GRCm39) |
missense |
probably damaging |
0.96 |
R6018:Ccdc180
|
UTSW |
4 |
45,926,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R6108:Ccdc180
|
UTSW |
4 |
45,911,389 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6283:Ccdc180
|
UTSW |
4 |
45,902,486 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6483:Ccdc180
|
UTSW |
4 |
45,921,950 (GRCm39) |
missense |
probably benign |
0.32 |
R6618:Ccdc180
|
UTSW |
4 |
45,950,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R7017:Ccdc180
|
UTSW |
4 |
45,940,934 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7205:Ccdc180
|
UTSW |
4 |
45,914,588 (GRCm39) |
missense |
probably benign |
|
R7341:Ccdc180
|
UTSW |
4 |
45,898,644 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7351:Ccdc180
|
UTSW |
4 |
45,903,887 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7418:Ccdc180
|
UTSW |
4 |
45,904,616 (GRCm39) |
missense |
probably damaging |
0.98 |
R7492:Ccdc180
|
UTSW |
4 |
45,930,009 (GRCm39) |
splice site |
probably null |
|
R7573:Ccdc180
|
UTSW |
4 |
45,922,015 (GRCm39) |
missense |
probably benign |
0.33 |
R7639:Ccdc180
|
UTSW |
4 |
45,928,043 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7806:Ccdc180
|
UTSW |
4 |
45,912,801 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7812:Ccdc180
|
UTSW |
4 |
45,906,952 (GRCm39) |
critical splice donor site |
probably null |
|
R7840:Ccdc180
|
UTSW |
4 |
45,900,461 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7842:Ccdc180
|
UTSW |
4 |
45,909,428 (GRCm39) |
missense |
probably benign |
0.00 |
R8712:Ccdc180
|
UTSW |
4 |
45,920,842 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8818:Ccdc180
|
UTSW |
4 |
45,900,484 (GRCm39) |
missense |
probably benign |
0.02 |
R8961:Ccdc180
|
UTSW |
4 |
45,929,573 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8983:Ccdc180
|
UTSW |
4 |
45,909,359 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9035:Ccdc180
|
UTSW |
4 |
45,906,922 (GRCm39) |
nonsense |
probably null |
|
R9095:Ccdc180
|
UTSW |
4 |
45,949,466 (GRCm39) |
nonsense |
probably null |
|
R9240:Ccdc180
|
UTSW |
4 |
45,917,566 (GRCm39) |
critical splice donor site |
probably null |
|
R9293:Ccdc180
|
UTSW |
4 |
45,944,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Ccdc180
|
UTSW |
4 |
45,902,447 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9346:Ccdc180
|
UTSW |
4 |
45,927,953 (GRCm39) |
missense |
probably benign |
0.09 |
R9521:Ccdc180
|
UTSW |
4 |
45,916,283 (GRCm39) |
missense |
probably null |
0.50 |
R9653:Ccdc180
|
UTSW |
4 |
45,923,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R9667:Ccdc180
|
UTSW |
4 |
45,920,861 (GRCm39) |
nonsense |
probably null |
|
X0017:Ccdc180
|
UTSW |
4 |
45,909,350 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Ccdc180
|
UTSW |
4 |
45,920,910 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ccdc180
|
UTSW |
4 |
45,916,406 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CTTTTAAAGGGCGCTCCAAG -3'
(R):5'- TGTCAGATGGGACTGGAACC -3'
Sequencing Primer
(F):5'- GAGTTTCACTACTCCACGTGGG -3'
(R):5'- TCAGATGGGACTGGAACCCTAGTC -3'
|
Posted On |
2019-11-26 |