Incidental Mutation 'IGL01160:Dnajc5g'
ID 53559
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dnajc5g
Ensembl Gene ENSMUSG00000053856
Gene Name DnaJ heat shock protein family (Hsp40) member C5 gamma
Synonyms 4922503E23Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01160
Quality Score
Status
Chromosome 5
Chromosomal Location 31265637-31269870 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 31267529 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 112 (V112A)
Ref Sequence ENSEMBL: ENSMUSP00000064587 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000066544] [ENSMUST00000201396] [ENSMUST00000201740] [ENSMUST00000202433] [ENSMUST00000202740] [ENSMUST00000202760]
AlphaFold Q8C632
Predicted Effect probably benign
Transcript: ENSMUST00000066544
AA Change: V112A

PolyPhen 2 Score 0.370 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000064587
Gene: ENSMUSG00000053856
AA Change: V112A

DomainStartEndE-ValueType
DnaJ 16 74 4.3e-27 SMART
low complexity region 114 132 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000201396
SMART Domains Protein: ENSMUSP00000144295
Gene: ENSMUSG00000029151

DomainStartEndE-ValueType
Pfam:Cation_efflux 27 124 1.1e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000201740
SMART Domains Protein: ENSMUSP00000144137
Gene: ENSMUSG00000053856

DomainStartEndE-ValueType
DnaJ 16 74 2.8e-29 SMART
Predicted Effect silent
Transcript: ENSMUST00000202433
SMART Domains Protein: ENSMUSP00000143997
Gene: ENSMUSG00000053856

DomainStartEndE-ValueType
SCOP:d1gh6a_ 10 41 1e-5 SMART
Blast:DnaJ 17 48 4e-8 BLAST
low complexity region 49 61 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000202740
SMART Domains Protein: ENSMUSP00000144566
Gene: ENSMUSG00000029151

DomainStartEndE-ValueType
Pfam:Cation_efflux 27 244 3e-46 PFAM
Predicted Effect silent
Transcript: ENSMUST00000202760
SMART Domains Protein: ENSMUSP00000144548
Gene: ENSMUSG00000053856

DomainStartEndE-ValueType
SCOP:d1gh6a_ 10 41 1e-5 SMART
Blast:DnaJ 17 48 4e-8 BLAST
low complexity region 49 61 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp11a A G 8: 12,894,609 (GRCm39) T188A probably damaging Het
Bfsp2 A G 9: 103,357,367 (GRCm39) V20A probably benign Het
Btn1a1 G A 13: 23,645,907 (GRCm39) T154M possibly damaging Het
Ccdc117 T C 11: 5,481,532 (GRCm39) S200G probably benign Het
Col24a1 G A 3: 145,213,468 (GRCm39) G1358S probably damaging Het
Crlf2 T C 5: 109,705,436 (GRCm39) T40A possibly damaging Het
Cstf2 T A X: 132,961,478 (GRCm39) probably benign Het
Dcdc2a A G 13: 25,303,312 (GRCm39) D281G probably benign Het
Dmd T C X: 82,968,567 (GRCm39) L1855P probably damaging Het
Dnmt1 G A 9: 20,828,615 (GRCm39) P828S possibly damaging Het
Dock3 A T 9: 106,783,887 (GRCm39) S268R probably damaging Het
Dpep2 C T 8: 106,713,076 (GRCm39) V440M possibly damaging Het
F8 A T X: 74,331,667 (GRCm39) M741K probably damaging Het
Fermt3 C T 19: 6,980,626 (GRCm39) probably null Het
Fosb A G 7: 19,041,039 (GRCm39) probably null Het
Gm3238 C A 10: 77,606,717 (GRCm39) probably benign Het
Hyal5 T A 6: 24,876,480 (GRCm39) S118T possibly damaging Het
Igf2r T C 17: 12,923,662 (GRCm39) D1140G possibly damaging Het
Ighmbp2 G T 19: 3,326,750 (GRCm39) probably benign Het
Irf3 C A 7: 44,648,220 (GRCm39) D28E possibly damaging Het
Ly6i A T 15: 74,851,881 (GRCm39) I96N possibly damaging Het
Macrod2 T C 2: 140,666,962 (GRCm39) probably benign Het
Or2b4 A G 17: 38,116,941 (GRCm39) R302G probably benign Het
Or4c117 A T 2: 88,956,072 (GRCm39) M1K probably null Het
Or4f15 A G 2: 111,814,278 (GRCm39) L47P probably damaging Het
Or52z1 C T 7: 103,436,843 (GRCm39) G214R probably damaging Het
Otof A T 5: 30,538,879 (GRCm39) M1128K probably benign Het
Parp9 A T 16: 35,768,368 (GRCm39) I183F probably damaging Het
Pbsn T C X: 76,886,177 (GRCm39) N147S probably benign Het
Pcf11 A G 7: 92,310,894 (GRCm39) S365P possibly damaging Het
Pcnx4 T G 12: 72,626,151 (GRCm39) V1119G probably damaging Het
Qng1 A G 13: 58,529,790 (GRCm39) V274A probably damaging Het
Rsf1 C T 7: 97,334,791 (GRCm39) T1308M probably damaging Het
Sidt2 A G 9: 45,854,024 (GRCm39) L647P probably damaging Het
Slc28a2b A C 2: 122,355,277 (GRCm39) probably null Het
Slc7a8 A G 14: 54,972,581 (GRCm39) V280A probably benign Het
Spart T A 3: 55,029,177 (GRCm39) F323I probably damaging Het
Supt16 A T 14: 52,420,589 (GRCm39) D70E probably benign Het
Tmc4 T C 7: 3,678,517 (GRCm39) Y38C possibly damaging Het
Tmco5b G T 2: 113,118,143 (GRCm39) probably benign Het
Trav10 G A 14: 53,743,239 (GRCm39) probably benign Het
Vmn2r28 A T 7: 5,489,477 (GRCm39) M454K probably damaging Het
Vmn2r85 T C 10: 130,254,690 (GRCm39) T665A probably benign Het
Yipf7 T C 5: 69,676,660 (GRCm39) I160V probably benign Het
Zc3h18 T C 8: 123,134,989 (GRCm39) probably benign Het
Zfp429 G A 13: 67,539,132 (GRCm39) S91L probably damaging Het
Other mutations in Dnajc5g
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5046:Dnajc5g UTSW 5 31,267,036 (GRCm39) missense probably benign 0.22
R7395:Dnajc5g UTSW 5 31,269,009 (GRCm39) missense possibly damaging 0.61
R8073:Dnajc5g UTSW 5 31,269,029 (GRCm39) missense probably benign 0.00
Posted On 2013-06-28