Incidental Mutation 'IGL02304:Cep162'
ID 287531
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cep162
Ensembl Gene ENSMUSG00000056919
Gene Name centrosomal protein 162
Synonyms 4922501C03Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.108) question?
Stock # IGL02304
Quality Score
Status
Chromosome 9
Chromosomal Location 87071630-87137589 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 87109200 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000091319 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093802]
AlphaFold Q6ZQ06
Predicted Effect probably benign
Transcript: ENSMUST00000093802
SMART Domains Protein: ENSMUSP00000091319
Gene: ENSMUSG00000056919

DomainStartEndE-ValueType
low complexity region 198 208 N/A INTRINSIC
low complexity region 528 539 N/A INTRINSIC
coiled coil region 630 674 N/A INTRINSIC
coiled coil region 695 899 N/A INTRINSIC
coiled coil region 953 1124 N/A INTRINSIC
coiled coil region 1235 1386 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144137
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188289
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930546C10Rik G T 18: 69,083,122 (GRCm39) H31N unknown Het
Adamts8 A G 9: 30,867,952 (GRCm39) N592S possibly damaging Het
Atp1a2 C A 1: 172,116,920 (GRCm39) E232D probably benign Het
Cacnb3 A T 15: 98,540,263 (GRCm39) D323V probably damaging Het
Cdh9 A T 15: 16,848,687 (GRCm39) T456S probably benign Het
Clvs2 T C 10: 33,404,443 (GRCm39) M258V probably benign Het
Col6a5 T C 9: 105,805,613 (GRCm39) T1098A unknown Het
Foxs1 T C 2: 152,774,270 (GRCm39) D261G probably benign Het
Gas2l2 T C 11: 83,315,064 (GRCm39) probably benign Het
Gins4 A T 8: 23,722,625 (GRCm39) M98K probably benign Het
Gm9637 A T 14: 19,402,545 (GRCm38) noncoding transcript Het
Herc1 A G 9: 66,383,696 (GRCm39) D3720G probably benign Het
Kcnh5 C T 12: 75,023,471 (GRCm39) M532I probably benign Het
Kcnk18 T C 19: 59,223,295 (GRCm39) Y147H probably damaging Het
Kif21a A T 15: 90,849,738 (GRCm39) F55Y probably damaging Het
Krt15 T A 11: 100,024,503 (GRCm39) I278F possibly damaging Het
L3mbtl4 T A 17: 68,894,180 (GRCm39) Y395* probably null Het
Mcm3ap T A 10: 76,320,572 (GRCm39) N843K possibly damaging Het
Mpdz T C 4: 81,228,394 (GRCm39) K1337E possibly damaging Het
Mpdz G A 4: 81,215,796 (GRCm39) probably benign Het
Ms4a6d T C 19: 11,580,505 (GRCm39) probably benign Het
Myo7a G T 7: 97,726,943 (GRCm39) R922S possibly damaging Het
Nek1 G T 8: 61,465,201 (GRCm39) G97C probably damaging Het
Obscn A G 11: 58,967,448 (GRCm39) Y2963H probably damaging Het
Or4k44 T C 2: 111,367,746 (GRCm39) N296S probably benign Het
Or4k6 T C 14: 50,476,217 (GRCm39) N42D probably damaging Het
Or5w15 C T 2: 87,568,330 (GRCm39) V113M probably benign Het
Prmt3 G A 7: 49,476,485 (GRCm39) V365I probably benign Het
Prrc2c T C 1: 162,511,705 (GRCm39) T958A probably benign Het
Ptprb T C 10: 116,167,164 (GRCm39) Y947H probably damaging Het
Pus10 C T 11: 23,662,275 (GRCm39) S315L probably damaging Het
Rmi1 C A 13: 58,557,290 (GRCm39) S513* probably null Het
Sec14l3 C T 11: 4,024,768 (GRCm39) P239L probably damaging Het
Slc44a3 T C 3: 121,320,723 (GRCm39) T93A possibly damaging Het
Srsf3-ps C T 11: 98,516,364 (GRCm39) R3H probably benign Het
Stat1 G A 1: 52,171,703 (GRCm39) A125T probably benign Het
Tigd2 C T 6: 59,188,683 (GRCm39) Q517* probably null Het
Trav13d-3 C T 14: 53,270,837 (GRCm39) Q100* probably null Het
Trim67 G A 8: 125,552,691 (GRCm39) D598N probably damaging Het
Trio A G 15: 27,735,522 (GRCm39) L2856P probably damaging Het
Other mutations in Cep162
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00422:Cep162 APN 9 87,109,220 (GRCm39) missense probably benign 0.24
IGL00584:Cep162 APN 9 87,103,143 (GRCm39) splice site probably benign
IGL01387:Cep162 APN 9 87,093,864 (GRCm39) missense probably benign 0.08
IGL01862:Cep162 APN 9 87,135,986 (GRCm39) missense possibly damaging 0.90
IGL02558:Cep162 APN 9 87,107,779 (GRCm39) missense probably benign
IGL02558:Cep162 APN 9 87,107,786 (GRCm39) missense probably benign 0.04
IGL02602:Cep162 APN 9 87,128,206 (GRCm39) missense probably benign 0.19
IGL02636:Cep162 APN 9 87,130,432 (GRCm39) missense possibly damaging 0.90
IGL02680:Cep162 APN 9 87,128,797 (GRCm39) missense possibly damaging 0.64
IGL03195:Cep162 APN 9 87,107,839 (GRCm39) missense probably benign 0.00
circus UTSW 9 87,088,915 (GRCm39) missense probably damaging 1.00
moscow UTSW 9 87,075,750 (GRCm39) missense probably damaging 1.00
smiley UTSW 9 87,099,134 (GRCm39) nonsense probably null
PIT4378001:Cep162 UTSW 9 87,099,198 (GRCm39) missense probably benign 0.01
PIT4431001:Cep162 UTSW 9 87,126,398 (GRCm39) missense probably benign 0.00
PIT4434001:Cep162 UTSW 9 87,075,701 (GRCm39) missense probably damaging 1.00
R0060:Cep162 UTSW 9 87,119,878 (GRCm39) splice site probably benign
R0218:Cep162 UTSW 9 87,093,862 (GRCm39) missense possibly damaging 0.73
R0366:Cep162 UTSW 9 87,102,537 (GRCm39) missense probably damaging 0.96
R0468:Cep162 UTSW 9 87,075,750 (GRCm39) missense probably damaging 1.00
R0764:Cep162 UTSW 9 87,083,798 (GRCm39) missense probably damaging 1.00
R1386:Cep162 UTSW 9 87,103,255 (GRCm39) missense probably benign
R1614:Cep162 UTSW 9 87,094,985 (GRCm39) missense probably damaging 1.00
R1633:Cep162 UTSW 9 87,085,736 (GRCm39) missense probably benign 0.23
R1831:Cep162 UTSW 9 87,088,985 (GRCm39) missense probably damaging 1.00
R1847:Cep162 UTSW 9 87,086,133 (GRCm39) missense probably benign 0.06
R1941:Cep162 UTSW 9 87,082,048 (GRCm39) missense probably benign 0.14
R2228:Cep162 UTSW 9 87,126,384 (GRCm39) missense probably benign 0.05
R2256:Cep162 UTSW 9 87,088,967 (GRCm39) missense probably damaging 1.00
R2257:Cep162 UTSW 9 87,088,967 (GRCm39) missense probably damaging 1.00
R2936:Cep162 UTSW 9 87,109,467 (GRCm39) missense probably benign
R3005:Cep162 UTSW 9 87,114,113 (GRCm39) missense probably benign 0.00
R3508:Cep162 UTSW 9 87,114,030 (GRCm39) critical splice donor site probably null
R3689:Cep162 UTSW 9 87,107,747 (GRCm39) nonsense probably null
R3743:Cep162 UTSW 9 87,099,230 (GRCm39) splice site probably benign
R4118:Cep162 UTSW 9 87,086,229 (GRCm39) missense probably benign 0.30
R4380:Cep162 UTSW 9 87,082,056 (GRCm39) missense probably damaging 0.99
R4450:Cep162 UTSW 9 87,107,861 (GRCm39) missense probably damaging 1.00
R4540:Cep162 UTSW 9 87,094,992 (GRCm39) missense probably damaging 1.00
R4598:Cep162 UTSW 9 87,085,848 (GRCm39) missense possibly damaging 0.95
R4700:Cep162 UTSW 9 87,088,915 (GRCm39) missense probably damaging 1.00
R4941:Cep162 UTSW 9 87,108,022 (GRCm39) intron probably benign
R5356:Cep162 UTSW 9 87,088,948 (GRCm39) missense probably damaging 1.00
R5468:Cep162 UTSW 9 87,109,290 (GRCm39) missense probably benign 0.00
R5579:Cep162 UTSW 9 87,085,724 (GRCm39) missense probably benign 0.26
R5859:Cep162 UTSW 9 87,086,145 (GRCm39) missense probably damaging 1.00
R6114:Cep162 UTSW 9 87,085,763 (GRCm39) missense probably benign
R6143:Cep162 UTSW 9 87,094,904 (GRCm39) critical splice donor site probably null
R6422:Cep162 UTSW 9 87,114,069 (GRCm39) missense possibly damaging 0.92
R6517:Cep162 UTSW 9 87,104,227 (GRCm39) missense probably damaging 0.99
R6576:Cep162 UTSW 9 87,099,198 (GRCm39) missense probably benign 0.01
R6782:Cep162 UTSW 9 87,093,737 (GRCm39) missense probably benign 0.07
R6867:Cep162 UTSW 9 87,099,134 (GRCm39) nonsense probably null
R7293:Cep162 UTSW 9 87,085,836 (GRCm39) missense probably benign 0.01
R7355:Cep162 UTSW 9 87,136,008 (GRCm39) nonsense probably null
R7391:Cep162 UTSW 9 87,130,547 (GRCm39) nonsense probably null
R7426:Cep162 UTSW 9 87,074,819 (GRCm39) missense probably damaging 1.00
R7593:Cep162 UTSW 9 87,086,250 (GRCm39) missense probably benign 0.40
R7710:Cep162 UTSW 9 87,114,172 (GRCm39) missense probably damaging 1.00
R7841:Cep162 UTSW 9 87,126,369 (GRCm39) missense probably benign 0.00
R7949:Cep162 UTSW 9 87,088,901 (GRCm39) missense probably benign 0.04
R8351:Cep162 UTSW 9 87,074,903 (GRCm39) nonsense probably null
R8451:Cep162 UTSW 9 87,074,903 (GRCm39) nonsense probably null
R8552:Cep162 UTSW 9 87,126,361 (GRCm39) missense probably benign 0.34
R8755:Cep162 UTSW 9 87,114,064 (GRCm39) missense probably benign 0.02
R8762:Cep162 UTSW 9 87,109,314 (GRCm39) missense probably benign 0.00
R9640:Cep162 UTSW 9 87,126,352 (GRCm39) missense probably benign 0.06
X0063:Cep162 UTSW 9 87,104,095 (GRCm39) critical splice donor site probably null
Z1177:Cep162 UTSW 9 87,082,033 (GRCm39) critical splice donor site probably null
Posted On 2015-04-16