Incidental Mutation 'R5988:Cep295'
ID |
481832 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cep295
|
Ensembl Gene |
ENSMUSG00000046111 |
Gene Name |
centrosomal protein 295 |
Synonyms |
5830418K08Rik, LOC382128 |
MMRRC Submission |
044168-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.952)
|
Stock # |
R5988 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
15228211-15269084 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 15252770 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 353
(F353L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000096578
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098979]
[ENSMUST00000161132]
|
AlphaFold |
no structure available at present |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000059410
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000098979
AA Change: F353L
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000096578 Gene: ENSMUSG00000046111 AA Change: F353L
Domain | Start | End | E-Value | Type |
low complexity region
|
159 |
175 |
N/A |
INTRINSIC |
coiled coil region
|
258 |
288 |
N/A |
INTRINSIC |
coiled coil region
|
536 |
583 |
N/A |
INTRINSIC |
coiled coil region
|
861 |
889 |
N/A |
INTRINSIC |
internal_repeat_1
|
890 |
1104 |
6.8e-5 |
PROSPERO |
internal_repeat_1
|
1277 |
1489 |
6.8e-5 |
PROSPERO |
low complexity region
|
1537 |
1548 |
N/A |
INTRINSIC |
low complexity region
|
1611 |
1625 |
N/A |
INTRINSIC |
coiled coil region
|
1707 |
1736 |
N/A |
INTRINSIC |
low complexity region
|
2003 |
2018 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161132
AA Change: F353L
PolyPhen 2
Score 0.178 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000123788 Gene: ENSMUSG00000046111 AA Change: F353L
Domain | Start | End | E-Value | Type |
low complexity region
|
111 |
127 |
N/A |
INTRINSIC |
coiled coil region
|
210 |
240 |
N/A |
INTRINSIC |
coiled coil region
|
488 |
535 |
N/A |
INTRINSIC |
coiled coil region
|
813 |
841 |
N/A |
INTRINSIC |
coiled coil region
|
1300 |
1327 |
N/A |
INTRINSIC |
low complexity region
|
1489 |
1500 |
N/A |
INTRINSIC |
low complexity region
|
1563 |
1577 |
N/A |
INTRINSIC |
coiled coil region
|
1659 |
1688 |
N/A |
INTRINSIC |
low complexity region
|
2035 |
2050 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000161795
AA Change: F305L
PolyPhen 2
Score 0.904 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000125035 Gene: ENSMUSG00000046111 AA Change: F305L
Domain | Start | End | E-Value | Type |
low complexity region
|
111 |
127 |
N/A |
INTRINSIC |
coiled coil region
|
210 |
240 |
N/A |
INTRINSIC |
coiled coil region
|
488 |
535 |
N/A |
INTRINSIC |
coiled coil region
|
813 |
841 |
N/A |
INTRINSIC |
internal_repeat_1
|
842 |
1056 |
7.14e-5 |
PROSPERO |
internal_repeat_1
|
1229 |
1441 |
7.14e-5 |
PROSPERO |
low complexity region
|
1489 |
1500 |
N/A |
INTRINSIC |
low complexity region
|
1563 |
1577 |
N/A |
INTRINSIC |
coiled coil region
|
1659 |
1688 |
N/A |
INTRINSIC |
low complexity region
|
1955 |
1970 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162689
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000163010
|
Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.1%
- 10x: 95.3%
- 20x: 84.3%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
T |
A |
14: 29,715,030 (GRCm39) |
M615K |
possibly damaging |
Het |
Acvr1c |
A |
T |
2: 58,205,886 (GRCm39) |
C25S |
probably damaging |
Het |
Adk |
A |
T |
14: 21,473,616 (GRCm39) |
E291V |
probably benign |
Het |
Ahnak |
C |
A |
19: 8,986,711 (GRCm39) |
|
probably benign |
Het |
Alg11 |
A |
G |
8: 22,552,044 (GRCm39) |
T63A |
probably benign |
Het |
Alox12 |
A |
T |
11: 70,142,413 (GRCm39) |
S272T |
probably benign |
Het |
Armc10 |
T |
A |
5: 21,865,581 (GRCm39) |
S195T |
probably damaging |
Het |
AW209491 |
C |
T |
13: 14,812,365 (GRCm39) |
A406V |
probably benign |
Het |
Baat |
G |
A |
4: 49,502,871 (GRCm39) |
P84S |
probably damaging |
Het |
BB014433 |
G |
A |
8: 15,091,854 (GRCm39) |
T333I |
probably damaging |
Het |
BC035947 |
G |
A |
1: 78,475,843 (GRCm39) |
R230* |
probably null |
Het |
Bcr |
G |
A |
10: 75,011,167 (GRCm39) |
G26E |
probably benign |
Het |
Ccdc88b |
T |
C |
19: 6,833,348 (GRCm39) |
E233G |
probably damaging |
Het |
Chd8 |
T |
C |
14: 52,455,395 (GRCm39) |
M1031V |
probably damaging |
Het |
Col17a1 |
C |
G |
19: 47,642,659 (GRCm39) |
G885R |
probably damaging |
Het |
Cyp11a1 |
A |
C |
9: 57,928,117 (GRCm39) |
I214L |
probably benign |
Het |
Cyp3a44 |
A |
T |
5: 145,731,728 (GRCm39) |
S139R |
probably damaging |
Het |
Ddhd2 |
G |
A |
8: 26,238,589 (GRCm39) |
R64C |
probably damaging |
Het |
Dll3 |
A |
G |
7: 27,993,537 (GRCm39) |
W561R |
probably damaging |
Het |
Dnajc3 |
T |
C |
14: 119,195,376 (GRCm39) |
V97A |
possibly damaging |
Het |
Drosha |
C |
T |
15: 12,834,582 (GRCm39) |
|
probably benign |
Het |
E2f8 |
T |
C |
7: 48,524,743 (GRCm39) |
D302G |
probably damaging |
Het |
Ecd |
C |
G |
14: 20,374,629 (GRCm39) |
D504H |
probably damaging |
Het |
Eif1ad15 |
T |
A |
12: 88,288,202 (GRCm39) |
N17I |
unknown |
Het |
Eif4g2 |
C |
A |
7: 110,676,437 (GRCm39) |
V331L |
probably benign |
Het |
Fam124a |
T |
C |
14: 62,824,986 (GRCm39) |
I160T |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,482,493 (GRCm39) |
T3051A |
probably benign |
Het |
Gm10271 |
A |
T |
10: 116,808,497 (GRCm39) |
F6L |
probably damaging |
Het |
Gm572 |
A |
G |
4: 148,752,964 (GRCm39) |
E281G |
possibly damaging |
Het |
Gm9944 |
T |
C |
4: 144,179,775 (GRCm39) |
|
probably benign |
Het |
Gstm5 |
A |
C |
3: 107,803,270 (GRCm39) |
M1L |
probably benign |
Het |
Havcr1 |
A |
G |
11: 46,646,964 (GRCm39) |
T133A |
probably damaging |
Het |
Hey1 |
T |
G |
3: 8,731,379 (GRCm39) |
S68R |
probably damaging |
Het |
Hsf2bp |
C |
T |
17: 32,230,149 (GRCm39) |
|
probably null |
Het |
Id2 |
T |
C |
12: 25,145,723 (GRCm39) |
N96S |
probably benign |
Het |
Ifi206 |
A |
C |
1: 173,308,906 (GRCm39) |
S363R |
possibly damaging |
Het |
Il21r |
T |
C |
7: 125,231,460 (GRCm39) |
F296S |
probably damaging |
Het |
Irgm2 |
A |
G |
11: 58,111,013 (GRCm39) |
T247A |
probably benign |
Het |
Irx5 |
T |
A |
8: 93,087,299 (GRCm39) |
Y410* |
probably null |
Het |
Kmt2c |
A |
G |
5: 25,516,118 (GRCm39) |
I2575T |
probably benign |
Het |
Lmbrd2 |
T |
A |
15: 9,182,493 (GRCm39) |
|
probably null |
Het |
Lrig1 |
A |
C |
6: 94,605,023 (GRCm39) |
S191A |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,506,722 (GRCm39) |
|
probably benign |
Het |
Lypd6b |
T |
A |
2: 49,836,178 (GRCm39) |
C120S |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,202,812 (GRCm39) |
|
probably null |
Het |
Myh6 |
G |
T |
14: 55,202,851 (GRCm39) |
R23S |
probably damaging |
Het |
Nat8f6 |
C |
T |
6: 85,786,040 (GRCm39) |
M36I |
probably benign |
Het |
Nol8 |
T |
A |
13: 49,826,090 (GRCm39) |
M970K |
possibly damaging |
Het |
Nrxn2 |
T |
C |
19: 6,542,901 (GRCm39) |
F1042L |
possibly damaging |
Het |
Nup160 |
T |
C |
2: 90,519,553 (GRCm39) |
W277R |
probably damaging |
Het |
Ogfr |
A |
T |
2: 180,236,026 (GRCm39) |
T204S |
probably damaging |
Het |
Or10j5 |
T |
A |
1: 172,784,723 (GRCm39) |
Y120* |
probably null |
Het |
Or1ak2 |
A |
G |
2: 36,827,236 (GRCm39) |
Y35C |
probably damaging |
Het |
Or1p1 |
T |
C |
11: 74,179,679 (GRCm39) |
V69A |
probably benign |
Het |
Or2n1d |
T |
C |
17: 38,646,911 (GRCm39) |
F288L |
probably damaging |
Het |
Or52n2b |
A |
T |
7: 104,566,125 (GRCm39) |
V126E |
probably damaging |
Het |
Or8c20 |
T |
C |
9: 38,261,045 (GRCm39) |
V222A |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,215,189 (GRCm39) |
I648V |
probably benign |
Het |
Pced1b |
T |
A |
15: 97,282,228 (GRCm39) |
V89E |
probably damaging |
Het |
Phax |
G |
T |
18: 56,708,564 (GRCm39) |
A43S |
probably benign |
Het |
Phf20 |
A |
G |
2: 156,149,250 (GRCm39) |
E976G |
probably damaging |
Het |
Plin4 |
T |
C |
17: 56,416,567 (GRCm39) |
T8A |
probably benign |
Het |
Plxna1 |
G |
A |
6: 89,334,522 (GRCm39) |
Q36* |
probably null |
Het |
Pold1 |
T |
C |
7: 44,190,004 (GRCm39) |
Y394C |
probably damaging |
Het |
Ppp1r26 |
T |
A |
2: 28,342,566 (GRCm39) |
V732E |
probably benign |
Het |
Pramel5 |
A |
T |
4: 143,999,716 (GRCm39) |
C124S |
possibly damaging |
Het |
Prorp |
T |
A |
12: 55,424,002 (GRCm39) |
M441K |
probably damaging |
Het |
Prr14l |
C |
A |
5: 32,988,195 (GRCm39) |
L433F |
probably damaging |
Het |
Ptpn14 |
A |
G |
1: 189,582,584 (GRCm39) |
Y477C |
probably damaging |
Het |
Rcl1 |
T |
A |
19: 29,099,167 (GRCm39) |
I154N |
probably damaging |
Het |
Rfpl4 |
T |
C |
7: 5,118,501 (GRCm39) |
Y23C |
probably damaging |
Het |
Rims1 |
T |
C |
1: 22,635,544 (GRCm39) |
K146E |
probably damaging |
Het |
Rims2 |
A |
T |
15: 39,155,577 (GRCm39) |
K126M |
probably damaging |
Het |
Rpusd4 |
T |
A |
9: 35,183,816 (GRCm39) |
|
probably null |
Het |
Scn7a |
C |
T |
2: 66,556,558 (GRCm39) |
W342* |
probably null |
Het |
Sh3pxd2a |
A |
G |
19: 47,353,077 (GRCm39) |
V128A |
probably benign |
Het |
Slc15a5 |
T |
C |
6: 138,020,529 (GRCm39) |
H268R |
probably benign |
Het |
Slc22a3 |
T |
C |
17: 12,652,782 (GRCm39) |
I321V |
possibly damaging |
Het |
Slc7a6os |
A |
G |
8: 106,928,965 (GRCm39) |
S231P |
probably benign |
Het |
Smad5 |
T |
C |
13: 56,883,798 (GRCm39) |
S395P |
probably damaging |
Het |
Sorbs3 |
G |
A |
14: 70,440,752 (GRCm39) |
T20I |
probably benign |
Het |
Spata9 |
A |
G |
13: 76,116,236 (GRCm39) |
I42V |
probably benign |
Het |
Srl |
C |
T |
16: 4,340,892 (GRCm39) |
C9Y |
unknown |
Het |
Sugp2 |
T |
C |
8: 70,695,875 (GRCm39) |
F283L |
probably benign |
Het |
Syne2 |
T |
C |
12: 75,976,191 (GRCm39) |
|
probably null |
Het |
Taar6 |
A |
G |
10: 23,861,154 (GRCm39) |
Y131H |
probably damaging |
Het |
Tango2 |
T |
C |
16: 18,120,554 (GRCm39) |
T137A |
probably damaging |
Het |
Tas2r106 |
T |
A |
6: 131,655,606 (GRCm39) |
I82L |
probably benign |
Het |
Tbc1d32 |
T |
C |
10: 55,964,433 (GRCm39) |
E922G |
probably damaging |
Het |
Tgfb2 |
G |
T |
1: 186,436,778 (GRCm39) |
P65Q |
probably benign |
Het |
Tjp2 |
T |
G |
19: 24,091,464 (GRCm39) |
I566L |
probably benign |
Het |
Tnrc6a |
T |
A |
7: 122,781,603 (GRCm39) |
N1424K |
probably damaging |
Het |
Trim7 |
A |
T |
11: 48,728,513 (GRCm39) |
M54L |
probably benign |
Het |
Trpm1 |
T |
A |
7: 63,876,553 (GRCm39) |
S535R |
probably benign |
Het |
Tsc2 |
T |
A |
17: 24,839,740 (GRCm39) |
N417I |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,800,132 (GRCm39) |
R359G |
probably benign |
Het |
Vim |
A |
G |
2: 13,587,296 (GRCm39) |
T458A |
probably benign |
Het |
Vps11 |
A |
T |
9: 44,265,221 (GRCm39) |
S612R |
probably benign |
Het |
Wdfy3 |
A |
G |
5: 102,032,004 (GRCm39) |
S2273P |
probably benign |
Het |
Wwox |
G |
T |
8: 115,433,081 (GRCm39) |
R249L |
probably benign |
Het |
Zbtb4 |
G |
T |
11: 69,669,790 (GRCm39) |
G838C |
probably damaging |
Het |
Zkscan3 |
A |
T |
13: 21,580,461 (GRCm39) |
C76S |
probably damaging |
Het |
Znrf3 |
C |
T |
11: 5,231,776 (GRCm39) |
C483Y |
probably damaging |
Het |
Zscan2 |
A |
G |
7: 80,525,947 (GRCm39) |
K556R |
possibly damaging |
Het |
|
Other mutations in Cep295 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Cep295
|
APN |
9 |
15,237,368 (GRCm39) |
splice site |
probably null |
|
IGL00769:Cep295
|
APN |
9 |
15,237,440 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00771:Cep295
|
APN |
9 |
15,233,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00850:Cep295
|
APN |
9 |
15,234,148 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01505:Cep295
|
APN |
9 |
15,229,345 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01510:Cep295
|
APN |
9 |
15,265,922 (GRCm39) |
nonsense |
probably null |
|
IGL01759:Cep295
|
APN |
9 |
15,234,855 (GRCm39) |
splice site |
probably null |
|
IGL02415:Cep295
|
APN |
9 |
15,264,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02447:Cep295
|
APN |
9 |
15,243,807 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02502:Cep295
|
APN |
9 |
15,262,209 (GRCm39) |
splice site |
probably benign |
|
IGL02665:Cep295
|
APN |
9 |
15,237,928 (GRCm39) |
splice site |
probably benign |
|
IGL02718:Cep295
|
APN |
9 |
15,237,049 (GRCm39) |
splice site |
probably null |
|
IGL02995:Cep295
|
APN |
9 |
15,244,608 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03024:Cep295
|
APN |
9 |
15,236,868 (GRCm39) |
missense |
probably benign |
|
R0196:Cep295
|
UTSW |
9 |
15,249,509 (GRCm39) |
missense |
probably damaging |
0.96 |
R0398:Cep295
|
UTSW |
9 |
15,266,032 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0595:Cep295
|
UTSW |
9 |
15,243,487 (GRCm39) |
nonsense |
probably null |
|
R0610:Cep295
|
UTSW |
9 |
15,234,050 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0616:Cep295
|
UTSW |
9 |
15,243,618 (GRCm39) |
nonsense |
probably null |
|
R0840:Cep295
|
UTSW |
9 |
15,245,611 (GRCm39) |
missense |
probably benign |
0.02 |
R1215:Cep295
|
UTSW |
9 |
15,239,178 (GRCm39) |
missense |
probably benign |
0.00 |
R1376:Cep295
|
UTSW |
9 |
15,252,164 (GRCm39) |
splice site |
probably benign |
|
R1381:Cep295
|
UTSW |
9 |
15,233,861 (GRCm39) |
missense |
probably benign |
0.02 |
R1484:Cep295
|
UTSW |
9 |
15,246,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R1557:Cep295
|
UTSW |
9 |
15,243,306 (GRCm39) |
nonsense |
probably null |
|
R1655:Cep295
|
UTSW |
9 |
15,252,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1682:Cep295
|
UTSW |
9 |
15,245,217 (GRCm39) |
missense |
probably benign |
0.02 |
R1700:Cep295
|
UTSW |
9 |
15,252,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1734:Cep295
|
UTSW |
9 |
15,252,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1736:Cep295
|
UTSW |
9 |
15,252,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1743:Cep295
|
UTSW |
9 |
15,252,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1765:Cep295
|
UTSW |
9 |
15,239,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R1889:Cep295
|
UTSW |
9 |
15,243,399 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1895:Cep295
|
UTSW |
9 |
15,243,399 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1994:Cep295
|
UTSW |
9 |
15,252,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R1995:Cep295
|
UTSW |
9 |
15,252,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R2071:Cep295
|
UTSW |
9 |
15,252,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R2161:Cep295
|
UTSW |
9 |
15,264,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R2195:Cep295
|
UTSW |
9 |
15,243,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R2354:Cep295
|
UTSW |
9 |
15,246,080 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2427:Cep295
|
UTSW |
9 |
15,245,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R2992:Cep295
|
UTSW |
9 |
15,244,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R3873:Cep295
|
UTSW |
9 |
15,244,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R3981:Cep295
|
UTSW |
9 |
15,228,363 (GRCm39) |
utr 3 prime |
probably benign |
|
R4201:Cep295
|
UTSW |
9 |
15,243,834 (GRCm39) |
missense |
probably benign |
0.19 |
R4297:Cep295
|
UTSW |
9 |
15,233,950 (GRCm39) |
missense |
probably benign |
0.19 |
R4543:Cep295
|
UTSW |
9 |
15,246,549 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4584:Cep295
|
UTSW |
9 |
15,246,095 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4724:Cep295
|
UTSW |
9 |
15,242,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Cep295
|
UTSW |
9 |
15,246,252 (GRCm39) |
missense |
probably benign |
0.11 |
R4884:Cep295
|
UTSW |
9 |
15,263,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Cep295
|
UTSW |
9 |
15,244,456 (GRCm39) |
missense |
probably damaging |
0.97 |
R4990:Cep295
|
UTSW |
9 |
15,243,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Cep295
|
UTSW |
9 |
15,233,979 (GRCm39) |
missense |
probably benign |
0.00 |
R5153:Cep295
|
UTSW |
9 |
15,268,925 (GRCm39) |
missense |
probably benign |
0.32 |
R5180:Cep295
|
UTSW |
9 |
15,243,416 (GRCm39) |
missense |
probably benign |
|
R5285:Cep295
|
UTSW |
9 |
15,233,887 (GRCm39) |
missense |
probably benign |
0.14 |
R5360:Cep295
|
UTSW |
9 |
15,238,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R5419:Cep295
|
UTSW |
9 |
15,235,533 (GRCm39) |
missense |
probably damaging |
0.98 |
R5432:Cep295
|
UTSW |
9 |
15,262,991 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5625:Cep295
|
UTSW |
9 |
15,252,187 (GRCm39) |
missense |
probably damaging |
0.99 |
R5637:Cep295
|
UTSW |
9 |
15,245,108 (GRCm39) |
splice site |
probably null |
|
R5645:Cep295
|
UTSW |
9 |
15,246,404 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5645:Cep295
|
UTSW |
9 |
15,244,090 (GRCm39) |
missense |
probably damaging |
0.98 |
R5678:Cep295
|
UTSW |
9 |
15,234,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R5688:Cep295
|
UTSW |
9 |
15,243,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5807:Cep295
|
UTSW |
9 |
15,243,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R5824:Cep295
|
UTSW |
9 |
15,236,952 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5837:Cep295
|
UTSW |
9 |
15,258,280 (GRCm39) |
missense |
probably damaging |
0.99 |
R5915:Cep295
|
UTSW |
9 |
15,252,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6239:Cep295
|
UTSW |
9 |
15,233,927 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6332:Cep295
|
UTSW |
9 |
15,246,210 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6383:Cep295
|
UTSW |
9 |
15,244,050 (GRCm39) |
missense |
probably damaging |
0.99 |
R6737:Cep295
|
UTSW |
9 |
15,243,647 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6929:Cep295
|
UTSW |
9 |
15,244,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R7428:Cep295
|
UTSW |
9 |
15,244,794 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7697:Cep295
|
UTSW |
9 |
15,266,006 (GRCm39) |
missense |
probably benign |
0.01 |
R7963:Cep295
|
UTSW |
9 |
15,244,737 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8055:Cep295
|
UTSW |
9 |
15,244,905 (GRCm39) |
missense |
probably benign |
0.00 |
R8069:Cep295
|
UTSW |
9 |
15,233,882 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8092:Cep295
|
UTSW |
9 |
15,244,278 (GRCm39) |
missense |
probably benign |
0.17 |
R8117:Cep295
|
UTSW |
9 |
15,245,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R8140:Cep295
|
UTSW |
9 |
15,252,829 (GRCm39) |
missense |
probably benign |
0.00 |
R8178:Cep295
|
UTSW |
9 |
15,244,836 (GRCm39) |
missense |
|
|
R8323:Cep295
|
UTSW |
9 |
15,264,357 (GRCm39) |
missense |
probably damaging |
0.96 |
R8323:Cep295
|
UTSW |
9 |
15,249,529 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8339:Cep295
|
UTSW |
9 |
15,236,846 (GRCm39) |
missense |
|
|
R8351:Cep295
|
UTSW |
9 |
15,234,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R8367:Cep295
|
UTSW |
9 |
15,245,826 (GRCm39) |
missense |
probably benign |
0.09 |
R8725:Cep295
|
UTSW |
9 |
15,243,715 (GRCm39) |
nonsense |
probably null |
|
R8919:Cep295
|
UTSW |
9 |
15,238,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R9015:Cep295
|
UTSW |
9 |
15,244,264 (GRCm39) |
missense |
probably benign |
0.00 |
R9054:Cep295
|
UTSW |
9 |
15,235,551 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9088:Cep295
|
UTSW |
9 |
15,233,815 (GRCm39) |
missense |
probably benign |
0.09 |
R9159:Cep295
|
UTSW |
9 |
15,252,904 (GRCm39) |
missense |
probably benign |
0.05 |
R9243:Cep295
|
UTSW |
9 |
15,243,605 (GRCm39) |
missense |
probably benign |
0.36 |
R9408:Cep295
|
UTSW |
9 |
15,244,619 (GRCm39) |
missense |
probably benign |
0.00 |
R9424:Cep295
|
UTSW |
9 |
15,244,499 (GRCm39) |
missense |
probably damaging |
0.98 |
R9455:Cep295
|
UTSW |
9 |
15,245,046 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9607:Cep295
|
UTSW |
9 |
15,234,009 (GRCm39) |
missense |
probably damaging |
0.98 |
R9648:Cep295
|
UTSW |
9 |
15,234,903 (GRCm39) |
missense |
probably benign |
0.00 |
R9659:Cep295
|
UTSW |
9 |
15,233,846 (GRCm39) |
missense |
probably benign |
0.19 |
R9731:Cep295
|
UTSW |
9 |
15,245,262 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0065:Cep295
|
UTSW |
9 |
15,234,187 (GRCm39) |
missense |
probably benign |
0.36 |
Z1176:Cep295
|
UTSW |
9 |
15,268,993 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cep295
|
UTSW |
9 |
15,242,113 (GRCm39) |
missense |
|
|
|
Predicted Primers |
PCR Primer
(F):5'- GATTGTAGGCAAAGGTTCTGGC -3'
(R):5'- ACTATCTGAAGTTTGACTCTGCAG -3'
Sequencing Primer
(F):5'- AAGATCTGACACCCTCTTCTGGAG -3'
(R):5'- AACCAGGAGCGATTGATG -3'
|
Posted On |
2017-06-26 |