Incidental Mutation 'R1257:Dnajc9'
ID 262740
Institutional Source Beutler Lab
Gene Symbol Dnajc9
Ensembl Gene ENSMUSG00000021811
Gene Name DnaJ heat shock protein family (Hsp40) member C9
Synonyms 5330419I01Rik
MMRRC Submission 039324-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1257 (G1)
Quality Score 172
Status Not validated
Chromosome 14
Chromosomal Location 20434706-20438978 bp(-) (GRCm39)
Type of Mutation splice site (607 bp from exon)
DNA Base Change (assembly) G to A at 20438765 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000055619 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022345] [ENSMUST00000061444]
AlphaFold Q91WN1
Predicted Effect probably null
Transcript: ENSMUST00000022345
SMART Domains Protein: ENSMUSP00000022345
Gene: ENSMUSG00000021811

DomainStartEndE-ValueType
DnaJ 14 74 2.76e-16 SMART
coiled coil region 176 212 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000061444
SMART Domains Protein: ENSMUSP00000055619
Gene: ENSMUSG00000049960

DomainStartEndE-ValueType
Pfam:Ribosomal_S16 24 84 9.9e-25 PFAM
low complexity region 107 135 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223844
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223889
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223950
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224286
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.2%
  • 10x: 95.9%
  • 20x: 91.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acoxl A T 2: 127,886,286 (GRCm39) T174S probably benign Het
Ank3 C T 10: 69,710,665 (GRCm39) R408* probably null Het
Ceacam15 A G 7: 16,405,949 (GRCm39) S201P possibly damaging Het
Ceacam20 A G 7: 19,708,117 (GRCm39) I241V probably benign Het
Cfap46 A T 7: 139,234,545 (GRCm39) L237* probably null Het
Col4a3 T A 1: 82,694,086 (GRCm39) C133S probably damaging Het
Dnhd1 T A 7: 105,343,360 (GRCm39) V1568D probably damaging Het
Gli3 C T 13: 15,900,581 (GRCm39) Q1323* probably null Het
Grhpr A G 4: 44,989,045 (GRCm39) N287S probably damaging Het
H2bl1 A T 13: 99,121,023 (GRCm39) M1K probably null Het
Hectd4 G A 5: 121,456,687 (GRCm39) W684* probably null Het
Kifc3 A G 8: 95,832,400 (GRCm39) V474A probably damaging Het
Lrrc37 A G 11: 103,425,467 (GRCm39) V1462A unknown Het
Mdn1 A T 4: 32,667,089 (GRCm39) probably null Het
Med7 C G 11: 46,331,460 (GRCm39) I18M probably damaging Het
Nid1 T C 13: 13,658,375 (GRCm39) Y707H probably benign Het
Nol4 A T 18: 22,903,738 (GRCm39) N339K probably damaging Het
Or6c209 A T 10: 129,483,413 (GRCm39) K139* probably null Het
Rbm34 C T 8: 127,697,643 (GRCm39) G23S possibly damaging Het
Rps19bp1 CCTTCTTCTTCTTCTTCTTCTT CCTTCTTCTTCTTCTTCTT 15: 80,145,250 (GRCm39) probably benign Het
Shf G A 2: 122,199,163 (GRCm39) P51S probably damaging Het
Snap25 A T 2: 136,600,268 (GRCm39) E37V probably damaging Het
Taf1a A G 1: 183,179,175 (GRCm39) T118A possibly damaging Het
Tasor2 T C 13: 3,625,049 (GRCm39) T1634A probably benign Het
Thrb T A 14: 18,008,642 (GRCm38) I122K probably damaging Het
Xkr4 T G 1: 3,287,036 (GRCm39) I385L probably benign Het
Zeb1 G T 18: 5,772,699 (GRCm39) R996L possibly damaging Het
Other mutations in Dnajc9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00923:Dnajc9 APN 14 20,435,515 (GRCm39) missense probably benign 0.01
IGL01631:Dnajc9 APN 14 20,438,176 (GRCm39) missense probably benign 0.02
R1258:Dnajc9 UTSW 14 20,438,765 (GRCm39) splice site probably null
R1261:Dnajc9 UTSW 14 20,438,765 (GRCm39) splice site probably null
R1765:Dnajc9 UTSW 14 20,438,158 (GRCm39) missense possibly damaging 0.73
R1835:Dnajc9 UTSW 14 20,438,402 (GRCm39) missense possibly damaging 0.89
R7218:Dnajc9 UTSW 14 20,438,507 (GRCm39) missense probably benign 0.02
R7570:Dnajc9 UTSW 14 20,438,712 (GRCm39) missense probably benign 0.01
R7600:Dnajc9 UTSW 14 20,438,793 (GRCm39) missense probably damaging 1.00
R7960:Dnajc9 UTSW 14 20,438,764 (GRCm39) missense possibly damaging 0.90
R9631:Dnajc9 UTSW 14 20,438,670 (GRCm39) critical splice donor site probably null
R9722:Dnajc9 UTSW 14 20,438,279 (GRCm39) missense probably benign 0.01
Predicted Primers
Posted On 2015-02-04