Incidental Mutation 'IGL01463:Fastkd1'
ID 88048
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fastkd1
Ensembl Gene ENSMUSG00000027086
Gene Name FAST kinase domains 1
Synonyms 5330408N05Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # IGL01463
Quality Score
Status
Chromosome 2
Chromosomal Location 69517159-69543860 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 69520405 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000099767 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073152] [ENSMUST00000073152] [ENSMUST00000102706]
AlphaFold Q6DI86
Predicted Effect probably null
Transcript: ENSMUST00000073152
SMART Domains Protein: ENSMUSP00000072896
Gene: ENSMUSG00000027086

DomainStartEndE-ValueType
low complexity region 179 191 N/A INTRINSIC
low complexity region 316 324 N/A INTRINSIC
low complexity region 385 396 N/A INTRINSIC
low complexity region 461 472 N/A INTRINSIC
Pfam:FAST_1 560 628 6.6e-25 PFAM
Pfam:FAST_2 645 730 6.4e-26 PFAM
RAP 763 822 4.38e-25 SMART
Predicted Effect probably null
Transcript: ENSMUST00000073152
SMART Domains Protein: ENSMUSP00000072896
Gene: ENSMUSG00000027086

DomainStartEndE-ValueType
low complexity region 179 191 N/A INTRINSIC
low complexity region 316 324 N/A INTRINSIC
low complexity region 385 396 N/A INTRINSIC
low complexity region 461 472 N/A INTRINSIC
Pfam:FAST_1 560 628 6.6e-25 PFAM
Pfam:FAST_2 645 730 6.4e-26 PFAM
RAP 763 822 4.38e-25 SMART
Predicted Effect probably null
Transcript: ENSMUST00000102706
SMART Domains Protein: ENSMUSP00000099767
Gene: ENSMUSG00000027086

DomainStartEndE-ValueType
low complexity region 179 191 N/A INTRINSIC
low complexity region 316 324 N/A INTRINSIC
low complexity region 385 396 N/A INTRINSIC
low complexity region 461 472 N/A INTRINSIC
Pfam:FAST_1 530 600 2.2e-26 PFAM
Pfam:FAST_2 614 701 4.4e-31 PFAM
RAP 734 793 4.38e-25 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 13 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam22 T C 5: 8,142,790 (GRCm39) D773G probably damaging Het
Clvs1 A G 4: 9,429,818 (GRCm39) T274A probably benign Het
Cyp2c50 G T 19: 40,079,422 (GRCm39) C172F probably damaging Het
Fam83h G T 15: 75,875,637 (GRCm39) R567S possibly damaging Het
Gmds A T 13: 32,418,341 (GRCm39) Y48N probably damaging Het
Mov10 C T 3: 104,707,640 (GRCm39) R578H probably damaging Het
Pcna A T 2: 132,093,349 (GRCm39) Y133N probably damaging Het
Rhag T C 17: 41,139,646 (GRCm39) I126T probably damaging Het
Sdr16c6 C T 4: 4,063,238 (GRCm39) G179D probably damaging Het
Sv2b C T 7: 74,786,203 (GRCm39) G406S probably damaging Het
Tiparp G T 3: 65,460,030 (GRCm39) G442* probably null Het
Vmn2r4 A T 3: 64,313,816 (GRCm39) N388K probably damaging Het
Vmn2r93 T A 17: 18,525,150 (GRCm39) N269K probably damaging Het
Other mutations in Fastkd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00163:Fastkd1 APN 2 69,537,893 (GRCm39) missense probably benign 0.02
IGL00702:Fastkd1 APN 2 69,538,889 (GRCm39) missense probably damaging 0.99
IGL00960:Fastkd1 APN 2 69,524,997 (GRCm39) splice site probably benign
IGL01154:Fastkd1 APN 2 69,520,404 (GRCm39) splice site probably null
IGL01913:Fastkd1 APN 2 69,538,845 (GRCm39) splice site probably benign
IGL01977:Fastkd1 APN 2 69,524,932 (GRCm39) missense possibly damaging 0.64
IGL02408:Fastkd1 APN 2 69,532,945 (GRCm39) missense probably benign
IGL02715:Fastkd1 APN 2 69,542,469 (GRCm39) critical splice donor site probably null
IGL03411:Fastkd1 APN 2 69,537,703 (GRCm39) missense probably damaging 0.99
PIT4519001:Fastkd1 UTSW 2 69,520,501 (GRCm39) missense probably damaging 0.97
R0541:Fastkd1 UTSW 2 69,532,750 (GRCm39) missense probably damaging 1.00
R0612:Fastkd1 UTSW 2 69,542,727 (GRCm39) missense probably benign 0.03
R1170:Fastkd1 UTSW 2 69,538,993 (GRCm39) splice site probably benign
R1499:Fastkd1 UTSW 2 69,538,982 (GRCm39) critical splice acceptor site probably null
R1586:Fastkd1 UTSW 2 69,542,492 (GRCm39) missense probably benign 0.43
R1698:Fastkd1 UTSW 2 69,532,813 (GRCm39) missense probably benign 0.22
R2172:Fastkd1 UTSW 2 69,530,477 (GRCm39) missense probably damaging 1.00
R2240:Fastkd1 UTSW 2 69,527,297 (GRCm39) missense probably benign 0.01
R2327:Fastkd1 UTSW 2 69,535,872 (GRCm39) nonsense probably null
R2897:Fastkd1 UTSW 2 69,532,960 (GRCm39) missense probably damaging 1.00
R4120:Fastkd1 UTSW 2 69,537,654 (GRCm39) missense probably damaging 0.98
R4544:Fastkd1 UTSW 2 69,542,655 (GRCm39) missense probably damaging 1.00
R4546:Fastkd1 UTSW 2 69,542,655 (GRCm39) missense probably damaging 1.00
R4798:Fastkd1 UTSW 2 69,521,651 (GRCm39) missense probably benign 0.38
R4993:Fastkd1 UTSW 2 69,533,084 (GRCm39) missense probably damaging 0.99
R5284:Fastkd1 UTSW 2 69,542,532 (GRCm39) missense probably benign 0.01
R5668:Fastkd1 UTSW 2 69,537,725 (GRCm39) missense possibly damaging 0.92
R6869:Fastkd1 UTSW 2 69,533,104 (GRCm39) missense probably benign 0.02
R6870:Fastkd1 UTSW 2 69,538,958 (GRCm39) missense probably benign 0.05
R7062:Fastkd1 UTSW 2 69,534,666 (GRCm39) missense possibly damaging 0.74
R7576:Fastkd1 UTSW 2 69,524,988 (GRCm39) missense probably damaging 1.00
R7644:Fastkd1 UTSW 2 69,527,184 (GRCm39) splice site probably null
R7971:Fastkd1 UTSW 2 69,537,703 (GRCm39) missense probably benign 0.19
R8336:Fastkd1 UTSW 2 69,542,489 (GRCm39) missense probably damaging 1.00
R8403:Fastkd1 UTSW 2 69,517,425 (GRCm39) nonsense probably null
R8422:Fastkd1 UTSW 2 69,532,778 (GRCm39) missense probably damaging 1.00
R9041:Fastkd1 UTSW 2 69,532,715 (GRCm39) missense probably benign
Posted On 2013-11-18