Incidental Mutation 'R0462:Cep152'
| ID |
41346 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cep152
|
| Ensembl Gene |
ENSMUSG00000068394 |
| Gene Name |
centrosomal protein 152 |
| Synonyms |
|
| MMRRC Submission |
038662-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R0462 (G1)
|
| Quality Score |
188 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
125405008-125467033 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 125425854 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glutamic Acid
at position 837
(V837E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000087208
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000089776]
|
| AlphaFold |
A2AUM9 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000089776
AA Change: V837E
PolyPhen 2
Score 0.645 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000087208
Gene: ENSMUSG00000068394
AA Change: V837E
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
29 |
N/A |
INTRINSIC |
|
low complexity region
|
106 |
124 |
N/A |
INTRINSIC |
|
coiled coil region
|
228 |
481 |
N/A |
INTRINSIC |
|
low complexity region
|
582 |
593 |
N/A |
INTRINSIC |
|
coiled coil region
|
602 |
651 |
N/A |
INTRINSIC |
|
coiled coil region
|
692 |
770 |
N/A |
INTRINSIC |
|
low complexity region
|
780 |
793 |
N/A |
INTRINSIC |
|
coiled coil region
|
835 |
868 |
N/A |
INTRINSIC |
|
coiled coil region
|
954 |
1038 |
N/A |
INTRINSIC |
|
coiled coil region
|
1205 |
1277 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.2%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
PHENOTYPE: Embryos homozygous for a null allele exhibit reduced numbers of centrosomes and cilia, increased apoptosis, and midgestation lethality. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aarsd1 |
A |
T |
11: 101,304,917 (GRCm39) |
D190E |
probably damaging |
Het |
| Acnat2 |
A |
G |
4: 49,383,084 (GRCm39) |
|
probably null |
Het |
| Acot10 |
T |
G |
15: 20,666,712 (GRCm39) |
T10P |
possibly damaging |
Het |
| Aldh7a1 |
T |
C |
18: 56,667,286 (GRCm39) |
|
probably null |
Het |
| Alkbh7 |
G |
A |
17: 57,305,443 (GRCm39) |
V87I |
probably benign |
Het |
| Ano2 |
A |
T |
6: 125,689,238 (GRCm39) |
H121L |
probably benign |
Het |
| Apob |
A |
T |
12: 8,050,896 (GRCm39) |
Y1040F |
probably damaging |
Het |
| Arhgap25 |
A |
T |
6: 87,436,942 (GRCm39) |
V636E |
possibly damaging |
Het |
| Atad2b |
A |
T |
12: 4,991,973 (GRCm39) |
T191S |
possibly damaging |
Het |
| Atpsckmt |
T |
C |
15: 31,617,018 (GRCm39) |
M161T |
probably damaging |
Het |
| Btbd9 |
A |
T |
17: 30,749,191 (GRCm39) |
V41D |
possibly damaging |
Het |
| Bzw2 |
G |
A |
12: 36,174,023 (GRCm39) |
R25C |
probably damaging |
Het |
| Carmil1 |
T |
C |
13: 24,206,494 (GRCm39) |
S1326G |
probably benign |
Het |
| Cdh18 |
A |
G |
15: 23,366,971 (GRCm39) |
R226G |
probably damaging |
Het |
| Cdh3 |
A |
G |
8: 107,282,012 (GRCm39) |
N800S |
possibly damaging |
Het |
| Cep85 |
G |
A |
4: 133,858,732 (GRCm39) |
T713M |
possibly damaging |
Het |
| Chd7 |
T |
C |
4: 8,850,821 (GRCm39) |
Y1736H |
probably damaging |
Het |
| Chst3 |
T |
C |
10: 60,022,535 (GRCm39) |
E104G |
probably benign |
Het |
| Cic |
T |
A |
7: 24,986,565 (GRCm39) |
S1299T |
probably damaging |
Het |
| Cic |
C |
A |
7: 24,986,566 (GRCm39) |
S1299Y |
probably damaging |
Het |
| Cmah |
T |
A |
13: 24,620,724 (GRCm39) |
S319R |
possibly damaging |
Het |
| Cnbd1 |
A |
G |
4: 18,895,044 (GRCm39) |
F233L |
probably benign |
Het |
| Cpne5 |
T |
C |
17: 29,395,163 (GRCm39) |
E251G |
probably benign |
Het |
| Csf2rb2 |
G |
A |
15: 78,169,373 (GRCm39) |
P485L |
probably damaging |
Het |
| Dimt1 |
T |
C |
13: 107,085,264 (GRCm39) |
M70T |
possibly damaging |
Het |
| Dlk2 |
A |
G |
17: 46,614,024 (GRCm39) |
*383W |
probably null |
Het |
| Dnah2 |
G |
A |
11: 69,350,027 (GRCm39) |
R2369C |
probably damaging |
Het |
| Dock2 |
A |
G |
11: 34,218,052 (GRCm39) |
F1173L |
possibly damaging |
Het |
| Dok7 |
A |
G |
5: 35,223,806 (GRCm39) |
H115R |
possibly damaging |
Het |
| Dpy19l1 |
A |
G |
9: 24,325,645 (GRCm39) |
I720T |
probably benign |
Het |
| Eps8 |
A |
T |
6: 137,491,309 (GRCm39) |
D356E |
probably benign |
Het |
| Exoc1 |
A |
G |
5: 76,691,464 (GRCm39) |
N263D |
probably benign |
Het |
| Fbxl3 |
T |
C |
14: 103,320,322 (GRCm39) |
D375G |
probably damaging |
Het |
| Fcgbpl1 |
A |
T |
7: 27,836,765 (GRCm39) |
D228V |
probably damaging |
Het |
| Flg2 |
A |
T |
3: 93,108,744 (GRCm39) |
E257D |
probably benign |
Het |
| Fstl4 |
A |
G |
11: 53,077,229 (GRCm39) |
D662G |
probably benign |
Het |
| Gbp10 |
G |
T |
5: 105,366,390 (GRCm39) |
Q505K |
possibly damaging |
Het |
| Gemin2 |
C |
T |
12: 59,060,305 (GRCm39) |
P15S |
probably damaging |
Het |
| Grhl2 |
A |
G |
15: 37,344,919 (GRCm39) |
M514V |
probably benign |
Het |
| Hgs |
A |
G |
11: 120,369,970 (GRCm39) |
N413D |
possibly damaging |
Het |
| Il12rb2 |
T |
C |
6: 67,280,594 (GRCm39) |
S538G |
possibly damaging |
Het |
| Kdm5a |
A |
G |
6: 120,379,561 (GRCm39) |
D623G |
probably damaging |
Het |
| Kifbp |
A |
T |
10: 62,395,235 (GRCm39) |
I469N |
probably damaging |
Het |
| Matk |
G |
T |
10: 81,095,527 (GRCm39) |
V116F |
probably damaging |
Het |
| Mcm3 |
T |
C |
1: 20,875,556 (GRCm39) |
T694A |
probably benign |
Het |
| Mctp1 |
C |
A |
13: 76,949,520 (GRCm39) |
H260Q |
probably damaging |
Het |
| Mios |
T |
A |
6: 8,215,743 (GRCm39) |
I313K |
probably benign |
Het |
| Muc4 |
T |
A |
16: 32,582,910 (GRCm39) |
Y2562N |
possibly damaging |
Het |
| Naip5 |
T |
A |
13: 100,358,240 (GRCm39) |
I999F |
probably damaging |
Het |
| Or11h4 |
T |
A |
14: 50,974,554 (GRCm39) |
I22L |
probably benign |
Het |
| Or14j7 |
A |
T |
17: 38,234,667 (GRCm39) |
D70V |
probably damaging |
Het |
| Or1x6 |
A |
G |
11: 50,939,336 (GRCm39) |
Y134C |
probably damaging |
Het |
| Or52a5 |
A |
T |
7: 103,426,770 (GRCm39) |
S261T |
probably benign |
Het |
| Or7g12 |
A |
T |
9: 18,900,198 (GRCm39) |
I305F |
probably benign |
Het |
| Or8g52 |
T |
A |
9: 39,630,706 (GRCm39) |
F61Y |
probably benign |
Het |
| Pafah1b1 |
A |
G |
11: 74,568,541 (GRCm39) |
V396A |
probably benign |
Het |
| Pard6b |
T |
A |
2: 167,929,467 (GRCm39) |
I91N |
possibly damaging |
Het |
| Pdzd2 |
T |
C |
15: 12,592,246 (GRCm39) |
S133G |
probably damaging |
Het |
| Plcg2 |
T |
G |
8: 118,312,044 (GRCm39) |
S445R |
probably benign |
Het |
| Plekhd1 |
G |
T |
12: 80,768,352 (GRCm39) |
V396L |
probably damaging |
Het |
| Ppp4r2 |
A |
G |
6: 100,843,518 (GRCm39) |
D294G |
possibly damaging |
Het |
| Ppwd1 |
T |
C |
13: 104,359,468 (GRCm39) |
|
probably null |
Het |
| Prr22 |
A |
G |
17: 57,077,551 (GRCm39) |
|
probably benign |
Het |
| Psme4 |
A |
G |
11: 30,798,117 (GRCm39) |
D1370G |
probably damaging |
Het |
| Rac3 |
T |
A |
11: 120,613,684 (GRCm39) |
V86D |
probably damaging |
Het |
| Rnf207 |
T |
C |
4: 152,397,829 (GRCm39) |
S335G |
possibly damaging |
Het |
| Rxfp3 |
A |
G |
15: 11,037,063 (GRCm39) |
L103P |
probably damaging |
Het |
| Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
| Smpdl3a |
G |
T |
10: 57,670,827 (GRCm39) |
C17F |
probably benign |
Het |
| Spaca7b |
T |
A |
8: 11,711,749 (GRCm39) |
|
probably benign |
Het |
| Spata31g1 |
T |
A |
4: 42,973,429 (GRCm39) |
F921I |
probably benign |
Het |
| Spen |
A |
T |
4: 141,200,962 (GRCm39) |
I2555N |
probably damaging |
Het |
| Srpk2 |
G |
T |
5: 23,723,424 (GRCm39) |
T564K |
probably damaging |
Het |
| Stard4 |
C |
T |
18: 33,338,202 (GRCm39) |
R116H |
probably damaging |
Het |
| Supt7l |
A |
T |
5: 31,677,640 (GRCm39) |
S175R |
probably damaging |
Het |
| Sycp1 |
A |
T |
3: 102,726,422 (GRCm39) |
Y932N |
possibly damaging |
Het |
| Tas2r122 |
T |
C |
6: 132,688,141 (GRCm39) |
M251V |
probably benign |
Het |
| Tbx15 |
A |
T |
3: 99,223,634 (GRCm39) |
E274V |
probably damaging |
Het |
| Tex52 |
A |
G |
6: 128,361,917 (GRCm39) |
E298G |
probably benign |
Het |
| Tmem101 |
T |
C |
11: 102,046,693 (GRCm39) |
M59V |
probably benign |
Het |
| Tmem132b |
T |
C |
5: 125,862,990 (GRCm39) |
V665A |
probably damaging |
Het |
| Trim23 |
T |
C |
13: 104,334,541 (GRCm39) |
V347A |
probably damaging |
Het |
| Ush2a |
A |
G |
1: 188,643,136 (GRCm39) |
H4166R |
probably benign |
Het |
| Vmn2r101 |
G |
T |
17: 19,810,431 (GRCm39) |
V406L |
probably benign |
Het |
| Vrk3 |
A |
G |
7: 44,413,624 (GRCm39) |
D166G |
possibly damaging |
Het |
| Washc4 |
T |
A |
10: 83,392,777 (GRCm39) |
M259K |
probably benign |
Het |
| Wdr70 |
T |
C |
15: 8,108,645 (GRCm39) |
D167G |
probably benign |
Het |
| Zfp1005 |
A |
G |
2: 150,111,122 (GRCm39) |
E604G |
possibly damaging |
Het |
| Zfp28 |
A |
T |
7: 6,395,239 (GRCm39) |
Q248L |
possibly damaging |
Het |
| Zfp39 |
A |
G |
11: 58,781,232 (GRCm39) |
I510T |
probably benign |
Het |
| Zfp710 |
T |
A |
7: 79,740,089 (GRCm39) |
*646R |
probably null |
Het |
| Zfp90 |
C |
T |
8: 107,151,892 (GRCm39) |
S535L |
possibly damaging |
Het |
| Zfp949 |
C |
T |
9: 88,450,787 (GRCm39) |
T119I |
possibly damaging |
Het |
|
| Other mutations in Cep152 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00155:Cep152
|
APN |
2 |
125,405,808 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL00561:Cep152
|
APN |
2 |
125,405,643 (GRCm39) |
nonsense |
probably null |
|
|
IGL01082:Cep152
|
APN |
2 |
125,411,465 (GRCm39) |
splice site |
probably benign |
|
|
IGL01420:Cep152
|
APN |
2 |
125,405,572 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
IGL01832:Cep152
|
APN |
2 |
125,460,414 (GRCm39) |
nonsense |
probably null |
|
|
IGL02106:Cep152
|
APN |
2 |
125,444,856 (GRCm39) |
splice site |
probably null |
|
|
IGL02124:Cep152
|
APN |
2 |
125,405,381 (GRCm39) |
missense |
probably benign |
0.23 |
|
IGL02349:Cep152
|
APN |
2 |
125,436,876 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02541:Cep152
|
APN |
2 |
125,447,274 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02659:Cep152
|
APN |
2 |
125,421,469 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02711:Cep152
|
APN |
2 |
125,405,862 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02737:Cep152
|
APN |
2 |
125,428,394 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
IGL03060:Cep152
|
APN |
2 |
125,461,907 (GRCm39) |
splice site |
probably benign |
|
|
IGL03095:Cep152
|
APN |
2 |
125,460,371 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03186:Cep152
|
APN |
2 |
125,405,895 (GRCm39) |
missense |
probably benign |
|
|
IGL03306:Cep152
|
APN |
2 |
125,447,328 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0034:Cep152
|
UTSW |
2 |
125,425,813 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0034:Cep152
|
UTSW |
2 |
125,425,813 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0079:Cep152
|
UTSW |
2 |
125,460,373 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0244:Cep152
|
UTSW |
2 |
125,406,134 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0390:Cep152
|
UTSW |
2 |
125,418,789 (GRCm39) |
splice site |
probably benign |
|
|
R0480:Cep152
|
UTSW |
2 |
125,423,639 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0595:Cep152
|
UTSW |
2 |
125,436,983 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0973:Cep152
|
UTSW |
2 |
125,436,819 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0973:Cep152
|
UTSW |
2 |
125,436,819 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1634:Cep152
|
UTSW |
2 |
125,425,809 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1664:Cep152
|
UTSW |
2 |
125,408,174 (GRCm39) |
missense |
probably benign |
0.38 |
|
R1693:Cep152
|
UTSW |
2 |
125,408,174 (GRCm39) |
missense |
probably benign |
0.38 |
|
R1887:Cep152
|
UTSW |
2 |
125,462,225 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1930:Cep152
|
UTSW |
2 |
125,460,291 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2178:Cep152
|
UTSW |
2 |
125,421,954 (GRCm39) |
splice site |
probably null |
|
|
R2225:Cep152
|
UTSW |
2 |
125,423,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2324:Cep152
|
UTSW |
2 |
125,405,382 (GRCm39) |
missense |
probably benign |
0.38 |
|
R2416:Cep152
|
UTSW |
2 |
125,406,092 (GRCm39) |
nonsense |
probably null |
|
|
R2845:Cep152
|
UTSW |
2 |
125,429,894 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3753:Cep152
|
UTSW |
2 |
125,466,972 (GRCm39) |
unclassified |
probably benign |
|
|
R4212:Cep152
|
UTSW |
2 |
125,461,921 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4304:Cep152
|
UTSW |
2 |
125,405,643 (GRCm39) |
nonsense |
probably null |
|
|
R4371:Cep152
|
UTSW |
2 |
125,454,967 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4399:Cep152
|
UTSW |
2 |
125,429,900 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R4536:Cep152
|
UTSW |
2 |
125,444,867 (GRCm39) |
splice site |
probably null |
|
|
R4713:Cep152
|
UTSW |
2 |
125,429,868 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R4777:Cep152
|
UTSW |
2 |
125,406,015 (GRCm39) |
missense |
probably benign |
0.29 |
|
R4779:Cep152
|
UTSW |
2 |
125,410,812 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R4785:Cep152
|
UTSW |
2 |
125,428,249 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4816:Cep152
|
UTSW |
2 |
125,405,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4847:Cep152
|
UTSW |
2 |
125,460,394 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4898:Cep152
|
UTSW |
2 |
125,428,301 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4934:Cep152
|
UTSW |
2 |
125,453,016 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R4997:Cep152
|
UTSW |
2 |
125,428,271 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5068:Cep152
|
UTSW |
2 |
125,413,736 (GRCm39) |
missense |
probably benign |
0.25 |
|
R5183:Cep152
|
UTSW |
2 |
125,408,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5198:Cep152
|
UTSW |
2 |
125,429,544 (GRCm39) |
missense |
probably benign |
|
|
R5261:Cep152
|
UTSW |
2 |
125,406,125 (GRCm39) |
missense |
probably benign |
0.06 |
|
R5272:Cep152
|
UTSW |
2 |
125,452,950 (GRCm39) |
missense |
probably benign |
0.27 |
|
R5284:Cep152
|
UTSW |
2 |
125,421,941 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6029:Cep152
|
UTSW |
2 |
125,405,552 (GRCm39) |
missense |
probably benign |
0.44 |
|
R6155:Cep152
|
UTSW |
2 |
125,423,620 (GRCm39) |
missense |
probably benign |
|
|
R6239:Cep152
|
UTSW |
2 |
125,421,332 (GRCm39) |
missense |
probably benign |
0.40 |
|
R6590:Cep152
|
UTSW |
2 |
125,406,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6690:Cep152
|
UTSW |
2 |
125,406,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6754:Cep152
|
UTSW |
2 |
125,429,588 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6798:Cep152
|
UTSW |
2 |
125,408,447 (GRCm39) |
splice site |
probably null |
|
|
R6816:Cep152
|
UTSW |
2 |
125,436,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6977:Cep152
|
UTSW |
2 |
125,410,742 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7125:Cep152
|
UTSW |
2 |
125,408,593 (GRCm39) |
nonsense |
probably null |
|
|
R7146:Cep152
|
UTSW |
2 |
125,456,325 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7588:Cep152
|
UTSW |
2 |
125,411,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7852:Cep152
|
UTSW |
2 |
125,432,033 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R7883:Cep152
|
UTSW |
2 |
125,454,978 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8047:Cep152
|
UTSW |
2 |
125,406,247 (GRCm39) |
missense |
probably benign |
0.10 |
|
R8082:Cep152
|
UTSW |
2 |
125,428,313 (GRCm39) |
missense |
probably benign |
|
|
R8680:Cep152
|
UTSW |
2 |
125,406,131 (GRCm39) |
nonsense |
probably null |
|
|
R8739:Cep152
|
UTSW |
2 |
125,461,975 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8744:Cep152
|
UTSW |
2 |
125,436,791 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8896:Cep152
|
UTSW |
2 |
125,408,155 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R8924:Cep152
|
UTSW |
2 |
125,444,778 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8971:Cep152
|
UTSW |
2 |
125,421,770 (GRCm39) |
nonsense |
probably null |
|
|
R9004:Cep152
|
UTSW |
2 |
125,453,020 (GRCm39) |
missense |
probably benign |
0.29 |
|
R9149:Cep152
|
UTSW |
2 |
125,463,127 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9149:Cep152
|
UTSW |
2 |
125,461,803 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9161:Cep152
|
UTSW |
2 |
125,408,574 (GRCm39) |
nonsense |
probably null |
|
|
R9239:Cep152
|
UTSW |
2 |
125,425,830 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9249:Cep152
|
UTSW |
2 |
125,405,904 (GRCm39) |
missense |
probably benign |
0.38 |
|
R9258:Cep152
|
UTSW |
2 |
125,421,356 (GRCm39) |
nonsense |
probably null |
|
|
R9619:Cep152
|
UTSW |
2 |
125,436,827 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9643:Cep152
|
UTSW |
2 |
125,406,150 (GRCm39) |
nonsense |
probably null |
|
|
R9775:Cep152
|
UTSW |
2 |
125,423,660 (GRCm39) |
nonsense |
probably null |
|
|
X0009:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0010:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0011:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0014:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0017:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0021:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0022:Cep152
|
UTSW |
2 |
125,461,983 (GRCm39) |
missense |
probably benign |
0.07 |
|
X0023:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0028:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0033:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0064:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0067:Cep152
|
UTSW |
2 |
125,456,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Cep152
|
UTSW |
2 |
125,425,891 (GRCm39) |
missense |
probably benign |
0.23 |
|
Z1177:Cep152
|
UTSW |
2 |
125,461,624 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Cep152
|
UTSW |
2 |
125,456,244 (GRCm39) |
missense |
probably benign |
0.33 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCAGTTCAAAGGCAGTGTTTCCCAG -3'
(R):5'- GCCCAGTGTGCAAAGCTCTAAACTC -3'
Sequencing Primer
(F):5'- AAGGCAGTGTTTCCCAGATTTTC -3'
(R):5'- CAGTGACAACTTTTGTACCACAGTG -3'
|
| Posted On |
2013-05-23 |
Incidental Mutation