Incidental Mutation 'IGL01622:Cdk17'
ID 278653
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cdk17
Ensembl Gene ENSMUSG00000020015
Gene Name cyclin dependent kinase 17
Synonyms Pctk2, 6430598J10Rik
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.295) question?
Stock # IGL01622
Quality Score
Status
Chromosome 10
Chromosomal Location 92996492-93086956 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 93074824 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000069965] [ENSMUST00000215286]
AlphaFold Q8K0D0
Predicted Effect probably benign
Transcript: ENSMUST00000069965
SMART Domains Protein: ENSMUSP00000070355
Gene: ENSMUSG00000020015

DomainStartEndE-ValueType
S_TKc 192 473 4.67e-97 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000215286
Predicted Effect probably benign
Transcript: ENSMUST00000216729
Coding Region Coverage
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 belongs to the cdc2/cdkx subfamily of the ser/thr family of protein kinases. It has similarity to a rat protein that is thought to play a role in terminally differentiated neurons. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, Jul 2010]
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930596D02Rik G A 14: 35,532,024 (GRCm39) Q184* probably null Het
A1bg A C 15: 60,789,742 (GRCm39) I502S possibly damaging Het
Actl11 T C 9: 107,805,775 (GRCm39) S33P probably benign Het
Aftph G T 11: 20,659,632 (GRCm39) D730E probably damaging Het
Arhgap29 A G 3: 121,767,773 (GRCm39) probably benign Het
Brf1 T G 12: 112,924,795 (GRCm39) E643A probably benign Het
Caskin1 G T 17: 24,722,914 (GRCm39) probably null Het
Ccnjl T C 11: 43,476,154 (GRCm39) V259A probably benign Het
Ccser2 G T 14: 36,662,920 (GRCm39) T88K probably benign Het
Clec16a G A 16: 10,395,774 (GRCm39) S309N possibly damaging Het
Cpxm1 C A 2: 130,233,191 (GRCm39) A633S probably benign Het
Ctnnbl1 A T 2: 157,661,468 (GRCm39) N326I probably damaging Het
Cyp46a1 T C 12: 108,318,234 (GRCm39) V215A possibly damaging Het
Daxx A G 17: 34,132,454 (GRCm39) D528G probably benign Het
Dnah6 T C 6: 73,121,701 (GRCm39) Y1427C probably damaging Het
Dpy19l3 G A 7: 35,422,169 (GRCm39) T228I probably damaging Het
Fam131c C T 4: 141,109,761 (GRCm39) A131V possibly damaging Het
Fat1 A G 8: 45,482,592 (GRCm39) T3061A possibly damaging Het
Fgl2 T A 5: 21,578,175 (GRCm39) L154H possibly damaging Het
Fhod3 T A 18: 25,155,924 (GRCm39) I514K probably benign Het
Ficd G A 5: 113,876,622 (GRCm39) G266S probably damaging Het
Frem3 A G 8: 81,340,544 (GRCm39) T946A probably benign Het
Gan T A 8: 117,913,917 (GRCm39) V105D probably damaging Het
Garin5b A G 7: 4,761,722 (GRCm39) V330A probably benign Het
Gramd1c A G 16: 43,811,061 (GRCm39) V221A probably damaging Het
Hacd1 A G 2: 14,040,667 (GRCm39) V196A probably benign Het
Kcna6 C A 6: 126,715,576 (GRCm39) V438L probably damaging Het
Kif14 T C 1: 136,425,094 (GRCm39) probably benign Het
Klhl41 T C 2: 69,508,582 (GRCm39) V512A probably benign Het
Lrfn1 A G 7: 28,166,111 (GRCm39) T502A probably damaging Het
Notch3 A T 17: 32,377,844 (GRCm39) F105I possibly damaging Het
Or4b13 T G 2: 90,082,953 (GRCm39) K126N probably damaging Het
Or5m10 A T 2: 85,717,306 (GRCm39) H54L probably benign Het
P3h1 C T 4: 119,092,480 (GRCm39) T171I probably damaging Het
Pcdhb1 A G 18: 37,399,366 (GRCm39) E439G possibly damaging Het
Pik3c3 A T 18: 30,423,578 (GRCm39) K225* probably null Het
Pik3c3 A G 18: 30,426,102 (GRCm39) probably benign Het
Pik3r5 T A 11: 68,377,452 (GRCm39) probably null Het
Pnpt1 A C 11: 29,098,272 (GRCm39) probably benign Het
Ppp2r1b T A 9: 50,789,422 (GRCm39) V495D probably damaging Het
Rbfox3 C A 11: 118,396,440 (GRCm39) probably benign Het
Sec14l2 G A 11: 4,053,966 (GRCm39) P234S possibly damaging Het
Sec16a A C 2: 26,328,915 (GRCm39) D1033E probably benign Het
Septin14 A G 5: 129,763,019 (GRCm39) V357A probably damaging Het
Sf3a3 C T 4: 124,612,136 (GRCm39) T131I possibly damaging Het
Snrpa A T 7: 26,892,395 (GRCm39) M55K probably benign Het
Swt1 G T 1: 151,286,760 (GRCm39) T244N probably benign Het
Tbl1xr1 A G 3: 22,246,238 (GRCm39) T253A probably benign Het
Tst G T 15: 78,283,964 (GRCm39) R288S probably benign Het
Vmn2r60 A G 7: 41,785,910 (GRCm39) I238V probably benign Het
Zbtb14 A G 17: 69,695,184 (GRCm39) K294R probably benign Het
Zfp710 T A 7: 79,730,871 (GRCm39) V16E probably damaging Het
Zfpm2 A G 15: 40,965,320 (GRCm39) T602A probably benign Het
Zfr2 G A 10: 81,087,193 (GRCm39) M850I probably benign Het
Other mutations in Cdk17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:Cdk17 APN 10 93,062,633 (GRCm39) missense probably damaging 1.00
IGL00781:Cdk17 APN 10 93,068,278 (GRCm39) missense probably damaging 1.00
IGL01623:Cdk17 APN 10 93,074,824 (GRCm39) unclassified probably benign
IGL01732:Cdk17 APN 10 93,053,907 (GRCm39) missense probably benign 0.01
IGL01768:Cdk17 APN 10 93,044,123 (GRCm39) missense probably damaging 0.99
IGL02942:Cdk17 APN 10 93,074,830 (GRCm39) missense probably benign
IGL03308:Cdk17 APN 10 93,057,506 (GRCm39) critical splice donor site probably null
delude UTSW 10 93,053,823 (GRCm39) splice site probably null
Imagine UTSW 10 93,068,277 (GRCm39) missense probably damaging 1.00
Magician UTSW 10 93,064,565 (GRCm39) missense probably damaging 1.00
prestidigitator UTSW 10 93,061,979 (GRCm39) missense probably damaging 1.00
R4436_Cdk17_536 UTSW 10 93,047,758 (GRCm39) splice site probably null
R0039:Cdk17 UTSW 10 93,062,640 (GRCm39) splice site probably benign
R0398:Cdk17 UTSW 10 93,073,702 (GRCm39) missense probably benign 0.01
R0432:Cdk17 UTSW 10 93,073,652 (GRCm39) unclassified probably benign
R0609:Cdk17 UTSW 10 93,052,334 (GRCm39) missense probably benign
R0781:Cdk17 UTSW 10 93,074,895 (GRCm39) nonsense probably null
R1110:Cdk17 UTSW 10 93,074,895 (GRCm39) nonsense probably null
R1604:Cdk17 UTSW 10 93,068,360 (GRCm39) missense probably damaging 1.00
R1674:Cdk17 UTSW 10 93,057,492 (GRCm39) missense probably benign 0.21
R1758:Cdk17 UTSW 10 93,044,112 (GRCm39) missense probably damaging 1.00
R1797:Cdk17 UTSW 10 93,044,114 (GRCm39) missense possibly damaging 0.76
R1864:Cdk17 UTSW 10 93,061,967 (GRCm39) missense probably damaging 1.00
R1924:Cdk17 UTSW 10 93,061,979 (GRCm39) missense probably damaging 1.00
R1929:Cdk17 UTSW 10 93,064,540 (GRCm39) missense probably damaging 1.00
R2143:Cdk17 UTSW 10 93,053,881 (GRCm39) missense probably damaging 1.00
R2207:Cdk17 UTSW 10 93,064,624 (GRCm39) missense probably damaging 1.00
R2261:Cdk17 UTSW 10 93,047,820 (GRCm39) missense possibly damaging 0.90
R2262:Cdk17 UTSW 10 93,047,820 (GRCm39) missense possibly damaging 0.90
R3737:Cdk17 UTSW 10 93,057,506 (GRCm39) critical splice donor site probably null
R3883:Cdk17 UTSW 10 93,047,939 (GRCm39) critical splice donor site probably null
R4436:Cdk17 UTSW 10 93,047,758 (GRCm39) splice site probably null
R5372:Cdk17 UTSW 10 93,061,901 (GRCm39) missense probably benign 0.03
R5444:Cdk17 UTSW 10 93,053,823 (GRCm39) splice site probably null
R5488:Cdk17 UTSW 10 93,068,274 (GRCm39) missense probably damaging 1.00
R5489:Cdk17 UTSW 10 93,068,274 (GRCm39) missense probably damaging 1.00
R5815:Cdk17 UTSW 10 93,064,559 (GRCm39) missense probably damaging 1.00
R6164:Cdk17 UTSW 10 93,071,331 (GRCm39) missense probably benign 0.26
R6209:Cdk17 UTSW 10 93,044,093 (GRCm39) missense probably benign 0.05
R6384:Cdk17 UTSW 10 93,047,827 (GRCm39) missense probably damaging 0.99
R6627:Cdk17 UTSW 10 93,068,274 (GRCm39) missense probably damaging 1.00
R6698:Cdk17 UTSW 10 93,064,540 (GRCm39) missense probably damaging 1.00
R7164:Cdk17 UTSW 10 93,068,343 (GRCm39) missense probably benign 0.07
R8096:Cdk17 UTSW 10 93,052,229 (GRCm39) missense probably damaging 0.98
R8118:Cdk17 UTSW 10 93,052,252 (GRCm39) missense possibly damaging 0.46
R8459:Cdk17 UTSW 10 93,068,289 (GRCm39) missense probably damaging 0.99
R8670:Cdk17 UTSW 10 93,061,958 (GRCm39) nonsense probably null
R8722:Cdk17 UTSW 10 93,064,565 (GRCm39) missense probably damaging 1.00
R8829:Cdk17 UTSW 10 93,042,920 (GRCm39) unclassified probably benign
R9077:Cdk17 UTSW 10 93,068,277 (GRCm39) missense probably damaging 1.00
R9488:Cdk17 UTSW 10 93,044,066 (GRCm39) missense probably damaging 0.98
R9789:Cdk17 UTSW 10 93,060,891 (GRCm39) missense probably damaging 0.98
Posted On 2015-04-16