Incidental Mutation 'R5102:Dnajb5'
ID 392408
Institutional Source Beutler Lab
Gene Symbol Dnajb5
Ensembl Gene ENSMUSG00000036052
Gene Name DnaJ heat shock protein family (Hsp40) member B5
Synonyms Hsp40-3, 1110058L06Rik, Hsc40
MMRRC Submission 042690-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.132) question?
Stock # R5102 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 42949866-42959425 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 42956639 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Asparagine at position 109 (D109N)
Ref Sequence ENSEMBL: ENSMUSP00000103607 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037872] [ENSMUST00000084662] [ENSMUST00000098112] [ENSMUST00000107973]
AlphaFold O89114
Predicted Effect possibly damaging
Transcript: ENSMUST00000037872
AA Change: D143N

PolyPhen 2 Score 0.844 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000040451
Gene: ENSMUSG00000036052
AA Change: D143N

DomainStartEndE-ValueType
DnaJ 37 94 8.21e-33 SMART
low complexity region 109 119 N/A INTRINSIC
low complexity region 159 171 N/A INTRINSIC
Pfam:DnaJ_C 205 364 1.3e-34 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000084662
AA Change: D109N

PolyPhen 2 Score 0.950 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000081712
Gene: ENSMUSG00000036052
AA Change: D109N

DomainStartEndE-ValueType
DnaJ 3 60 8.21e-33 SMART
low complexity region 75 85 N/A INTRINSIC
low complexity region 125 137 N/A INTRINSIC
Pfam:CTDII 260 340 1.5e-24 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000098112
AA Change: D109N

PolyPhen 2 Score 0.950 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000095716
Gene: ENSMUSG00000036052
AA Change: D109N

DomainStartEndE-ValueType
DnaJ 3 60 8.21e-33 SMART
low complexity region 75 85 N/A INTRINSIC
low complexity region 125 137 N/A INTRINSIC
Pfam:CTDII 260 340 1.5e-24 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000107973
AA Change: D109N

PolyPhen 2 Score 0.950 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000103607
Gene: ENSMUSG00000036052
AA Change: D109N

DomainStartEndE-ValueType
DnaJ 3 60 8.21e-33 SMART
low complexity region 75 85 N/A INTRINSIC
low complexity region 125 137 N/A INTRINSIC
Pfam:CTDII 260 340 1.5e-24 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142332
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153807
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 96.0%
  • 20x: 91.3%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] DNAJB5 belongs to the evolutionarily conserved DNAJ/HSP40 protein family. For background information on the DNAJ family, see MIM 608375.[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox4 C T 1: 58,279,937 (GRCm39) R518C probably damaging Het
Apbb2 A T 5: 66,469,592 (GRCm39) probably null Het
Arhgap45 C T 10: 79,857,262 (GRCm39) P254S probably benign Het
Arl4c T C 1: 88,629,322 (GRCm39) D22G probably damaging Het
Asxl1 A G 2: 153,242,875 (GRCm39) T1142A probably benign Het
BC035044 T C 6: 128,861,949 (GRCm39) probably benign Het
Bmp4 T C 14: 46,621,458 (GRCm39) N362S probably damaging Het
Cbll1 G T 12: 31,537,912 (GRCm39) T280N probably damaging Het
Cdh10 A T 15: 18,986,971 (GRCm39) T401S probably benign Het
Cmklr2 A G 1: 63,222,326 (GRCm39) V303A probably damaging Het
Cps1 A T 1: 67,245,952 (GRCm39) M1148L probably benign Het
Crybg1 T C 10: 43,873,832 (GRCm39) D1092G probably damaging Het
Cyth2 A G 7: 45,460,126 (GRCm39) S173P probably damaging Het
D6Ertd527e A T 6: 87,088,793 (GRCm39) I319F unknown Het
Dchs1 A T 7: 105,421,384 (GRCm39) H345Q probably benign Het
Ddx50 A T 10: 62,476,640 (GRCm39) V211E probably damaging Het
Dlx6 AGG AG 6: 6,865,180 (GRCm39) probably null Het
Dner A T 1: 84,383,691 (GRCm39) N564K probably damaging Het
Fam234b T C 6: 135,186,282 (GRCm39) S97P probably benign Het
Fam53b G A 7: 132,317,684 (GRCm39) R60* probably null Het
Fmo3 T G 1: 162,791,546 (GRCm39) K244Q probably benign Het
Golim4 A G 3: 75,810,579 (GRCm39) I192T possibly damaging Het
Gprin1 T C 13: 54,887,576 (GRCm39) M233V probably benign Het
Gtf2f1 A T 17: 57,310,626 (GRCm39) V443D probably damaging Het
Hmgcs2 T C 3: 98,187,786 (GRCm39) probably benign Het
Ide T A 19: 37,292,383 (GRCm39) I271L unknown Het
Kat8 G A 7: 127,523,988 (GRCm39) E343K probably damaging Het
Kif14 A G 1: 136,444,141 (GRCm39) I1378V probably benign Het
Lhx3 TCCTACGGGCCGGCCC TCC 2: 26,091,435 (GRCm39) probably null Het
Lhx6 T C 2: 35,984,222 (GRCm39) probably null Het
Lrp2 C T 2: 69,319,502 (GRCm39) G2007D probably damaging Het
Lrp5 T C 19: 3,709,304 (GRCm39) K142R probably damaging Het
Macroh2a1 C G 13: 56,243,936 (GRCm39) probably null Het
Mrpl2 G A 17: 46,960,964 (GRCm39) R286Q probably benign Het
Mtrfr A G 5: 124,476,954 (GRCm39) N83D probably damaging Het
Nacad T A 11: 6,548,528 (GRCm39) D1402V probably damaging Het
Ndfip2 T C 14: 105,535,539 (GRCm39) I275T possibly damaging Het
Neb A C 2: 52,116,582 (GRCm39) V4131G possibly damaging Het
Nfe2l1 G A 11: 96,712,934 (GRCm39) A83V probably damaging Het
Nos3 A G 5: 24,576,625 (GRCm39) D418G probably damaging Het
Or12e7 A T 2: 87,288,138 (GRCm39) M210L probably benign Het
Or1n1b T A 2: 36,780,056 (GRCm39) K268M possibly damaging Het
Plcd4 A G 1: 74,604,313 (GRCm39) T764A probably damaging Het
Plppr3 G T 10: 79,701,220 (GRCm39) P541T possibly damaging Het
Polr2a A G 11: 69,637,771 (GRCm39) I191T possibly damaging Het
Pramel18 T C 4: 101,766,436 (GRCm39) F40S probably damaging Het
Rab11fip1 T C 8: 27,646,402 (GRCm39) K225E probably damaging Het
Rara A T 11: 98,857,185 (GRCm39) Q64L possibly damaging Het
Rtkn G A 6: 83,126,754 (GRCm39) V305M probably damaging Het
Sh2b1 A C 7: 126,070,408 (GRCm39) F399V probably benign Het
Slc7a4 T C 16: 17,393,482 (GRCm39) T106A probably damaging Het
Srcap G A 7: 127,129,795 (GRCm39) G539D probably damaging Het
Stab1 C T 14: 30,869,974 (GRCm39) probably null Het
Zfp267 G A 3: 36,216,814 (GRCm39) C55Y possibly damaging Het
Other mutations in Dnajb5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01571:Dnajb5 APN 4 42,956,516 (GRCm39) splice site probably benign
FR4737:Dnajb5 UTSW 4 42,957,126 (GRCm39) frame shift probably null
R0522:Dnajb5 UTSW 4 42,957,083 (GRCm39) missense probably damaging 1.00
R0594:Dnajb5 UTSW 4 42,956,577 (GRCm39) missense probably damaging 0.96
R1831:Dnajb5 UTSW 4 42,957,333 (GRCm39) missense probably benign 0.15
R2884:Dnajb5 UTSW 4 42,957,355 (GRCm39) missense probably damaging 1.00
R4594:Dnajb5 UTSW 4 42,950,842 (GRCm39) unclassified probably benign
R4992:Dnajb5 UTSW 4 42,953,386 (GRCm39) critical splice donor site probably null
R6143:Dnajb5 UTSW 4 42,956,990 (GRCm39) missense probably damaging 1.00
R9113:Dnajb5 UTSW 4 42,953,233 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGGAGCCAGCATTTAGTGGC -3'
(R):5'- TAGATCTCCTCCAGGGACAC -3'

Sequencing Primer
(F):5'- CCAGCATTTAGTGGCAGAGG -3'
(R):5'- CAGCTCGTGCACCACAG -3'
Posted On 2016-06-15