Incidental Mutation 'R9653:Ccdc180'
ID |
727168 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ccdc180
|
Ensembl Gene |
ENSMUSG00000035539 |
Gene Name |
coiled-coil domain containing 180 |
Synonyms |
LOC381522, E230008N13Rik |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R9653 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
45890303-45950774 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 45923495 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 1092
(I1092T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000136714
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000178561]
|
AlphaFold |
J3QNE4 |
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000119784 Gene: ENSMUSG00000035539 AA Change: I916T
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 benign
Transcript: ENSMUST00000151024
|
SMART Domains |
Protein: ENSMUSP00000122332 Gene: ENSMUSG00000035539
Domain | Start | End | E-Value | Type |
low complexity region
|
8 |
22 |
N/A |
INTRINSIC |
low complexity region
|
38 |
55 |
N/A |
INTRINSIC |
coiled coil region
|
90 |
160 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000178561
AA Change: I1092T
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000136714 Gene: ENSMUSG00000035539 AA Change: I1092T
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: 99.2%
|
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 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: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
C |
T |
11: 9,243,741 (GRCm39) |
P1868L |
probably benign |
Het |
Abcc1 |
T |
C |
16: 14,214,257 (GRCm39) |
Y191H |
probably damaging |
Het |
Adamtsl5 |
C |
T |
10: 80,180,763 (GRCm39) |
G100R |
probably damaging |
Het |
Adgrg5 |
C |
T |
8: 95,663,864 (GRCm39) |
P235S |
|
Het |
Anks1b |
T |
G |
10: 90,346,524 (GRCm39) |
L608R |
probably damaging |
Het |
Ano10 |
C |
G |
9: 122,080,221 (GRCm39) |
A597P |
possibly damaging |
Het |
Calb2 |
T |
C |
8: 110,881,374 (GRCm39) |
M58V |
probably benign |
Het |
Ces3b |
G |
T |
8: 105,812,257 (GRCm39) |
A169S |
probably damaging |
Het |
Chmp2a |
A |
T |
7: 12,766,456 (GRCm39) |
F129I |
probably damaging |
Het |
Clasp2 |
T |
A |
9: 113,670,993 (GRCm39) |
W365R |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,584,556 (GRCm39) |
K1344R |
probably benign |
Het |
Col3a1 |
A |
G |
1: 45,360,728 (GRCm39) |
I53V |
unknown |
Het |
Coro2b |
T |
C |
9: 62,335,259 (GRCm39) |
Y309C |
probably damaging |
Het |
Cramp1 |
C |
A |
17: 25,201,783 (GRCm39) |
K566N |
probably damaging |
Het |
Crygs |
T |
A |
16: 22,625,304 (GRCm39) |
T46S |
probably benign |
Het |
Ctbp2 |
C |
G |
7: 132,615,933 (GRCm39) |
R334P |
probably damaging |
Het |
Dcstamp |
A |
T |
15: 39,623,792 (GRCm39) |
D469V |
probably benign |
Het |
Dhdh |
T |
C |
7: 45,128,551 (GRCm39) |
D209G |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,252,544 (GRCm39) |
V1742A |
possibly damaging |
Het |
Dnaja2 |
T |
C |
8: 86,265,982 (GRCm39) |
T368A |
probably benign |
Het |
Dscaml1 |
T |
C |
9: 45,643,466 (GRCm39) |
|
probably null |
Het |
Eps8l1 |
A |
T |
7: 4,481,886 (GRCm39) |
K704M |
unknown |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Fgd4 |
T |
A |
16: 16,254,461 (GRCm39) |
H524L |
probably benign |
Het |
Fktn |
T |
A |
4: 53,731,273 (GRCm39) |
F103I |
probably benign |
Het |
Gcc2 |
T |
C |
10: 58,110,822 (GRCm39) |
M1001T |
possibly damaging |
Het |
Gm4847 |
T |
C |
1: 166,467,582 (GRCm39) |
S205G |
possibly damaging |
Het |
Grid2 |
A |
T |
6: 63,907,968 (GRCm39) |
N203Y |
possibly damaging |
Het |
Hif3a |
G |
A |
7: 16,782,641 (GRCm39) |
A308V |
probably damaging |
Het |
Htr5a |
A |
G |
5: 28,047,838 (GRCm39) |
N131S |
possibly damaging |
Het |
Igfn1 |
G |
A |
1: 135,883,323 (GRCm39) |
Q2728* |
probably null |
Het |
Ighv5-16 |
C |
A |
12: 113,802,313 (GRCm39) |
K62N |
possibly damaging |
Het |
Ip6k3 |
A |
T |
17: 27,367,588 (GRCm39) |
Y203N |
possibly damaging |
Het |
Itga2 |
G |
A |
13: 115,020,991 (GRCm39) |
P120L |
probably benign |
Het |
Itpkb |
G |
T |
1: 180,160,056 (GRCm39) |
E61* |
probably null |
Het |
Kcnj3 |
G |
A |
2: 55,484,864 (GRCm39) |
V321M |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,507,819 (GRCm39) |
L3206P |
probably damaging |
Het |
Krtap5-4 |
T |
C |
7: 141,857,908 (GRCm39) |
C193R |
unknown |
Het |
Large1 |
G |
T |
8: 73,564,106 (GRCm39) |
H553Q |
probably benign |
Het |
Lrfn5 |
T |
A |
12: 61,890,418 (GRCm39) |
V569D |
probably damaging |
Het |
Luzp2 |
A |
G |
7: 54,702,580 (GRCm39) |
T48A |
probably damaging |
Het |
Lypd6 |
A |
T |
2: 50,080,758 (GRCm39) |
T149S |
probably benign |
Het |
Map3k1 |
T |
C |
13: 111,890,296 (GRCm39) |
N1301S |
possibly damaging |
Het |
Ndufv2 |
C |
T |
17: 66,396,251 (GRCm39) |
W91* |
probably null |
Het |
Nisch |
A |
T |
14: 30,893,628 (GRCm39) |
V1315E |
probably damaging |
Het |
Npas1 |
T |
C |
7: 16,190,146 (GRCm39) |
I467V |
probably benign |
Het |
Nucb1 |
A |
G |
7: 45,144,202 (GRCm39) |
M337T |
probably benign |
Het |
Oog3 |
T |
G |
4: 143,884,489 (GRCm39) |
R482S |
probably benign |
Het |
Or10d4b |
T |
C |
9: 39,535,154 (GRCm39) |
L243P |
probably damaging |
Het |
Or4f14c |
A |
T |
2: 111,941,261 (GRCm39) |
M112K |
probably damaging |
Het |
Or51ag1 |
C |
T |
7: 103,155,727 (GRCm39) |
R142H |
probably benign |
Het |
Or56a42-ps1 |
A |
T |
7: 104,775,985 (GRCm39) |
N164K |
probably benign |
Het |
Padi2 |
T |
C |
4: 140,662,036 (GRCm39) |
|
probably null |
Het |
Pam |
C |
T |
1: 97,768,469 (GRCm39) |
V660M |
possibly damaging |
Het |
Phc2 |
C |
T |
4: 128,641,012 (GRCm39) |
L700F |
probably damaging |
Het |
Plekha1 |
T |
C |
7: 130,479,494 (GRCm39) |
V4A |
possibly damaging |
Het |
Rai1 |
A |
G |
11: 60,080,142 (GRCm39) |
E1402G |
probably benign |
Het |
Recql5 |
G |
A |
11: 115,788,032 (GRCm39) |
A429V |
probably benign |
Het |
Rere |
A |
G |
4: 150,516,010 (GRCm39) |
N101S |
probably benign |
Het |
Robo1 |
T |
G |
16: 72,821,330 (GRCm39) |
S1357A |
possibly damaging |
Het |
Rsl1 |
T |
A |
13: 67,330,106 (GRCm39) |
Y185N |
probably damaging |
Het |
Rsph3a |
T |
C |
17: 8,165,074 (GRCm39) |
S145P |
possibly damaging |
Het |
Sall1 |
T |
C |
8: 89,757,506 (GRCm39) |
E866G |
probably damaging |
Het |
Sall3 |
A |
T |
18: 81,016,228 (GRCm39) |
S567T |
probably benign |
Het |
Sap30 |
G |
A |
8: 57,938,156 (GRCm39) |
Q154* |
probably null |
Het |
Sbf2 |
T |
C |
7: 110,040,702 (GRCm39) |
Q375R |
possibly damaging |
Het |
Scn8a |
A |
G |
15: 100,937,947 (GRCm39) |
E1772G |
probably damaging |
Het |
Scube3 |
C |
T |
17: 28,375,772 (GRCm39) |
A169V |
probably damaging |
Het |
Sema6c |
T |
C |
3: 95,080,525 (GRCm39) |
S940P |
probably benign |
Het |
Sertad4 |
C |
T |
1: 192,528,836 (GRCm39) |
D327N |
probably damaging |
Het |
Shisal2b |
A |
G |
13: 105,000,296 (GRCm39) |
|
probably benign |
Het |
Skp1 |
A |
G |
11: 52,134,514 (GRCm39) |
T82A |
possibly damaging |
Het |
Slc39a14 |
G |
T |
14: 70,547,248 (GRCm39) |
T366K |
probably damaging |
Het |
Snrnp200 |
G |
T |
2: 127,067,959 (GRCm39) |
V819L |
probably damaging |
Het |
Sntg1 |
T |
A |
1: 8,433,749 (GRCm39) |
T501S |
unknown |
Het |
Srsf12 |
T |
C |
4: 33,231,249 (GRCm39) |
S253P |
possibly damaging |
Het |
Sycp2l |
A |
G |
13: 41,295,381 (GRCm39) |
S315G |
probably benign |
Het |
Tars2 |
T |
C |
3: 95,655,379 (GRCm39) |
Y337C |
probably damaging |
Het |
Thbs4 |
T |
C |
13: 92,898,022 (GRCm39) |
D599G |
probably benign |
Het |
Tmem200c |
A |
G |
17: 69,149,181 (GRCm39) |
H588R |
probably benign |
Het |
Tmem255b |
T |
A |
8: 13,506,005 (GRCm39) |
V204E |
probably damaging |
Het |
Usp24 |
T |
A |
4: 106,204,564 (GRCm39) |
M261K |
probably benign |
Het |
Utrn |
T |
A |
10: 12,497,123 (GRCm39) |
I2429F |
probably benign |
Het |
Utrn |
C |
T |
10: 12,539,189 (GRCm39) |
A1943T |
probably benign |
Het |
Vmn2r85 |
A |
T |
10: 130,261,694 (GRCm39) |
D214E |
probably damaging |
Het |
Wdr81 |
G |
T |
11: 75,340,213 (GRCm39) |
P183T |
|
Het |
Zfp28 |
G |
A |
7: 6,395,623 (GRCm39) |
R134H |
|
Het |
Zfp532 |
T |
A |
18: 65,756,308 (GRCm39) |
D80E |
possibly damaging |
Het |
Zfyve26 |
T |
C |
12: 79,334,418 (GRCm39) |
D200G |
probably benign |
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 |
R7792:Ccdc180
|
UTSW |
4 |
45,890,389 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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'- CCGGATTGAGTTCGTTGAAAG -3'
(R):5'- TCACCCTGTGGACAGTACTG -3'
Sequencing Primer
(F):5'- TGGACCAGGTGGGAGCTC -3'
(R):5'- GGACAGTACTGGTGTGCAG -3'
|
Posted On |
2022-10-06 |