Incidental Mutation 'R9258:Cep152'
ID |
701994 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cep152
|
Ensembl Gene |
ENSMUSG00000068394 |
Gene Name |
centrosomal protein 152 |
Synonyms |
|
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R9258 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
125405008-125467033 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
G to A
at 125421356 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Stop codon
at position 1125
(Q1125*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000087208
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000089776]
|
AlphaFold |
A2AUM9 |
Predicted Effect |
probably null
Transcript: ENSMUST00000089776
AA Change: Q1125*
|
SMART Domains |
Protein: ENSMUSP00000087208 Gene: ENSMUSG00000068394 AA Change: Q1125*
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: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
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: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
T |
A |
8: 124,709,347 (GRCm39) |
Q69L |
probably benign |
Het |
Abtb2 |
A |
C |
2: 103,546,410 (GRCm39) |
Q930P |
probably null |
Het |
Adam18 |
G |
A |
8: 25,158,574 (GRCm39) |
T73I |
probably benign |
Het |
Ankrd54 |
A |
T |
15: 78,946,996 (GRCm39) |
M1K |
probably null |
Het |
Anks1 |
T |
C |
17: 28,277,400 (GRCm39) |
V1106A |
probably damaging |
Het |
Aox1 |
A |
T |
1: 58,351,515 (GRCm39) |
I701F |
probably damaging |
Het |
Arfgef3 |
C |
T |
10: 18,465,387 (GRCm39) |
R2152H |
probably damaging |
Het |
Arnt2 |
C |
T |
7: 84,010,798 (GRCm39) |
G37E |
probably damaging |
Het |
Arpp21 |
G |
A |
9: 111,953,956 (GRCm39) |
T581M |
probably benign |
Het |
Arvcf |
A |
G |
16: 18,216,957 (GRCm39) |
N428S |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,098,026 (GRCm39) |
E1471G |
|
Het |
Cadm1 |
A |
G |
9: 47,710,730 (GRCm39) |
K211R |
probably benign |
Het |
Cdh6 |
A |
G |
15: 13,064,462 (GRCm39) |
S143P |
probably damaging |
Het |
Cfap54 |
A |
C |
10: 92,770,960 (GRCm39) |
S2095A |
unknown |
Het |
Col12a1 |
T |
C |
9: 79,613,645 (GRCm39) |
T67A |
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,700,703 (GRCm39) |
N3216S |
unknown |
Het |
Cpeb2 |
T |
A |
5: 43,391,455 (GRCm39) |
L217Q |
|
Het |
Ctbp2 |
A |
T |
7: 132,597,021 (GRCm39) |
N119K |
probably damaging |
Het |
Des |
G |
T |
1: 75,340,289 (GRCm39) |
V399L |
probably benign |
Het |
Dnah2 |
G |
T |
11: 69,368,079 (GRCm39) |
H1753Q |
probably damaging |
Het |
Dnajc6 |
T |
C |
4: 101,475,813 (GRCm39) |
V562A |
probably benign |
Het |
Dusp13b |
T |
C |
14: 21,791,155 (GRCm39) |
D99G |
probably benign |
Het |
Ehd3 |
A |
G |
17: 74,127,561 (GRCm39) |
I165V |
probably benign |
Het |
Eme2 |
C |
T |
17: 25,112,053 (GRCm39) |
V241M |
probably damaging |
Het |
Eml5 |
A |
G |
12: 98,810,376 (GRCm39) |
L860P |
possibly damaging |
Het |
Eogt |
T |
A |
6: 97,089,043 (GRCm39) |
K521M |
possibly damaging |
Het |
Epb41l5 |
T |
C |
1: 119,506,701 (GRCm39) |
T489A |
probably benign |
Het |
Fmo5 |
G |
T |
3: 97,558,802 (GRCm39) |
V421L |
probably benign |
Het |
Gabpa |
C |
T |
16: 84,653,403 (GRCm39) |
P268S |
probably benign |
Het |
Gas2l3 |
G |
T |
10: 89,262,315 (GRCm39) |
H136N |
probably benign |
Het |
Gm5592 |
C |
T |
7: 40,938,407 (GRCm39) |
A563V |
possibly damaging |
Het |
Gpn3 |
A |
T |
5: 122,519,508 (GRCm39) |
D205V |
probably benign |
Het |
H13 |
T |
C |
2: 152,522,999 (GRCm39) |
L104S |
probably damaging |
Het |
H2-Q4 |
T |
A |
17: 35,599,105 (GRCm39) |
V125E |
probably benign |
Het |
Ifih1 |
A |
G |
2: 62,442,242 (GRCm39) |
F374S |
probably damaging |
Het |
Ildr2 |
A |
G |
1: 166,131,158 (GRCm39) |
D338G |
probably damaging |
Het |
Kmt2b |
A |
T |
7: 30,281,893 (GRCm39) |
N1162K |
probably null |
Het |
Lmntd1 |
T |
C |
6: 145,359,256 (GRCm39) |
D298G |
probably damaging |
Het |
Lrrc32 |
T |
A |
7: 98,148,345 (GRCm39) |
V375E |
probably benign |
Het |
Lrrc37a |
A |
C |
11: 103,393,022 (GRCm39) |
I801R |
probably benign |
Het |
Matcap1 |
A |
G |
8: 106,008,775 (GRCm39) |
V414A |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,657,121 (GRCm39) |
E935G |
probably benign |
Het |
Mms22l |
A |
T |
4: 24,588,238 (GRCm39) |
T917S |
probably damaging |
Het |
Myo3a |
A |
T |
2: 22,467,545 (GRCm39) |
E1204D |
possibly damaging |
Het |
Nav3 |
T |
A |
10: 109,550,243 (GRCm39) |
E1829V |
probably damaging |
Het |
Nccrp1 |
C |
T |
7: 28,245,632 (GRCm39) |
G150D |
probably damaging |
Het |
Nlrp4b |
G |
T |
7: 10,444,087 (GRCm39) |
W12L |
probably damaging |
Het |
Nmb |
T |
C |
7: 80,554,001 (GRCm39) |
T71A |
possibly damaging |
Het |
Ogfod2 |
T |
A |
5: 124,250,505 (GRCm39) |
H35Q |
probably benign |
Het |
Ola1 |
A |
T |
2: 72,929,732 (GRCm39) |
S290R |
probably damaging |
Het |
Or1e30 |
T |
G |
11: 73,678,281 (GRCm39) |
N172K |
probably benign |
Het |
Or4k47 |
A |
T |
2: 111,452,329 (GRCm39) |
I30N |
possibly damaging |
Het |
Or51v15-ps1 |
T |
G |
7: 103,278,543 (GRCm39) |
Y208S |
unknown |
Het |
Or52e2 |
C |
A |
7: 102,804,409 (GRCm39) |
E182* |
probably null |
Het |
Or5p68 |
T |
G |
7: 107,945,886 (GRCm39) |
T101P |
probably benign |
Het |
Or9i14 |
A |
T |
19: 13,792,099 (GRCm39) |
L285* |
probably null |
Het |
Pcsk9 |
T |
C |
4: 106,316,047 (GRCm39) |
D132G |
possibly damaging |
Het |
Pkhd1 |
A |
T |
1: 20,444,174 (GRCm39) |
V2296E |
probably damaging |
Het |
Prl2c5 |
A |
T |
13: 13,365,297 (GRCm39) |
I151L |
probably damaging |
Het |
Prl3d3 |
A |
T |
13: 27,344,931 (GRCm39) |
D101V |
possibly damaging |
Het |
Prrt1 |
A |
G |
17: 34,850,120 (GRCm39) |
Y178C |
probably damaging |
Het |
Rasal1 |
A |
T |
5: 120,793,155 (GRCm39) |
I87F |
possibly damaging |
Het |
Rpgrip1l |
A |
T |
8: 91,987,614 (GRCm39) |
Y814* |
probably null |
Het |
Rpl3l |
T |
G |
17: 24,951,447 (GRCm39) |
|
probably null |
Het |
Rrbp1 |
C |
A |
2: 143,853,161 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,483,364 (GRCm39) |
S4158P |
probably damaging |
Het |
Scube2 |
G |
T |
7: 109,398,515 (GRCm39) |
S951Y |
probably damaging |
Het |
Sec14l1 |
T |
C |
11: 117,041,002 (GRCm39) |
V396A |
probably benign |
Het |
Sh3gl1 |
T |
A |
17: 56,325,911 (GRCm39) |
K173* |
probably null |
Het |
Shank3 |
A |
T |
15: 89,388,521 (GRCm39) |
E371V |
probably damaging |
Het |
Slc25a24 |
A |
G |
3: 109,066,751 (GRCm39) |
T302A |
probably damaging |
Het |
Slc25a41 |
A |
T |
17: 57,348,580 (GRCm39) |
H4Q |
probably benign |
Het |
Slc45a1 |
A |
T |
4: 150,723,071 (GRCm39) |
V271D |
possibly damaging |
Het |
Smad6 |
A |
T |
9: 63,927,573 (GRCm39) |
L245Q |
probably damaging |
Het |
Smad7 |
C |
A |
18: 75,527,317 (GRCm39) |
Q388K |
probably damaging |
Het |
Snx29 |
G |
T |
16: 11,532,799 (GRCm39) |
D348Y |
possibly damaging |
Het |
Son |
A |
T |
16: 91,474,570 (GRCm39) |
H2418L |
unknown |
Het |
Sppl3 |
G |
A |
5: 115,233,922 (GRCm39) |
V331M |
probably damaging |
Het |
St13 |
T |
G |
15: 81,272,569 (GRCm39) |
T92P |
probably benign |
Het |
St3gal4 |
A |
G |
9: 34,963,643 (GRCm39) |
W222R |
probably damaging |
Het |
Stk32a |
T |
A |
18: 43,444,999 (GRCm39) |
N264K |
probably benign |
Het |
Stoml3 |
T |
A |
3: 53,405,397 (GRCm39) |
I26N |
possibly damaging |
Het |
Taf7 |
T |
C |
18: 37,776,021 (GRCm39) |
E182G |
probably damaging |
Het |
Tas2r138 |
A |
G |
6: 40,590,129 (GRCm39) |
V39A |
probably damaging |
Het |
Tbc1d12 |
A |
G |
19: 38,889,823 (GRCm39) |
S418G |
possibly damaging |
Het |
Tbr1 |
T |
A |
2: 61,642,723 (GRCm39) |
C663S |
probably benign |
Het |
Tmc5 |
A |
T |
7: 118,222,501 (GRCm39) |
Y67F |
probably benign |
Het |
Tnfsf4 |
A |
C |
1: 161,244,814 (GRCm39) |
I168L |
probably benign |
Het |
Trav5-1 |
T |
G |
14: 52,860,347 (GRCm39) |
S51A |
probably benign |
Het |
Trmt10c |
A |
T |
16: 55,854,646 (GRCm39) |
C330S |
possibly damaging |
Het |
Trpm1 |
T |
C |
7: 63,884,713 (GRCm39) |
M798T |
probably benign |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Unc13d |
CATGCC |
CATGCCTCCGATGCC |
11: 115,959,007 (GRCm39) |
|
probably benign |
Het |
Vmn1r199 |
A |
G |
13: 22,566,822 (GRCm39) |
T39A |
possibly damaging |
Het |
Vmn1r74 |
T |
A |
7: 11,580,999 (GRCm39) |
C100S |
possibly damaging |
Het |
Vmn2r77 |
T |
A |
7: 86,452,302 (GRCm39) |
I494K |
possibly damaging |
Het |
Wdr17 |
G |
A |
8: 55,112,654 (GRCm39) |
Q816* |
probably null |
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 |
|
R0462:Cep152
|
UTSW |
2 |
125,425,854 (GRCm39) |
missense |
possibly damaging |
0.64 |
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 |
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'- CAGTAGACCTGCTGCAATAAAG -3'
(R):5'- TTTGGACCAGAGTCGCAAGG -3'
Sequencing Primer
(F):5'- CCTGCTGCAATAAAGCTTTTAAAATC -3'
(R):5'- GCAGACACAAGTGGAAATCCGTC -3'
|
Posted On |
2022-03-25 |