Incidental Mutation 'IGL02155:Dnajc22'
ID 282185
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dnajc22
Ensembl Gene ENSMUSG00000038009
Gene Name DnaJ heat shock protein family (Hsp40) member C22
Synonyms 2810451A06Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # IGL02155
Quality Score
Status
Chromosome 15
Chromosomal Location 98991102-99002618 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 98998886 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 24 (Y24H)
Ref Sequence ENSEMBL: ENSMUSP00000055482 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061295]
AlphaFold Q8CHS2
Predicted Effect probably damaging
Transcript: ENSMUST00000061295
AA Change: Y24H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000055482
Gene: ENSMUSG00000038009
AA Change: Y24H

DomainStartEndE-ValueType
Pfam:TM2 1 50 1e-10 PFAM
transmembrane domain 76 98 N/A INTRINSIC
transmembrane domain 105 124 N/A INTRINSIC
transmembrane domain 139 161 N/A INTRINSIC
transmembrane domain 206 228 N/A INTRINSIC
DnaJ 276 335 1.09e-19 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146173
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aacs A G 5: 125,583,350 (GRCm39) H302R probably null Het
Abi3bp A T 16: 56,408,327 (GRCm39) H254L probably damaging Het
Adcy3 G A 12: 4,262,142 (GRCm39) W1064* probably null Het
Arvcf C T 16: 18,222,650 (GRCm39) P70S probably damaging Het
Ceacam3 A G 7: 16,896,906 (GRCm39) D624G possibly damaging Het
Cntrl T A 2: 35,050,250 (GRCm39) probably benign Het
Cyp2a5 T A 7: 26,542,471 (GRCm39) F491Y probably benign Het
Disp2 C T 2: 118,622,285 (GRCm39) R1006C probably damaging Het
Fat2 A G 11: 55,153,245 (GRCm39) F3656L probably benign Het
Fbxo31 A G 8: 122,285,814 (GRCm39) F212S probably damaging Het
Fsip2 T C 2: 82,828,696 (GRCm39) M6831T probably benign Het
Gpi1 G T 7: 33,929,614 (GRCm39) Q9K possibly damaging Het
Hmcn1 T A 1: 150,439,349 (GRCm39) S5495C probably damaging Het
Ift74 A G 4: 94,567,488 (GRCm39) I394V probably benign Het
Kcnh5 G A 12: 75,223,312 (GRCm39) probably benign Het
Lars2 A G 9: 123,284,047 (GRCm39) D745G probably damaging Het
Mitd1 T A 1: 37,924,356 (GRCm39) I65F probably benign Het
Mlxip T C 5: 123,591,455 (GRCm39) M878T probably benign Het
Mrgpra4 T C 7: 47,631,292 (GRCm39) Y103C probably damaging Het
Notch2 T C 3: 98,045,806 (GRCm39) I1657T probably damaging Het
Or5m11 T A 2: 85,782,352 (GRCm39) M315K probably benign Het
Orc1 T A 4: 108,447,874 (GRCm39) D40E probably benign Het
Rnf40 T C 7: 127,189,888 (GRCm39) probably benign Het
Ro60 C T 1: 143,637,007 (GRCm39) probably null Het
Sema4d A G 13: 51,857,303 (GRCm39) V643A probably benign Het
Taf7 A T 18: 37,776,564 (GRCm39) M1K probably null Het
Tnfsf10 A T 3: 27,389,380 (GRCm39) D147V possibly damaging Het
Usp45 T A 4: 21,798,743 (GRCm39) probably null Het
Wdr62 T C 7: 29,962,068 (GRCm39) D2G probably damaging Het
Zp2 T A 7: 119,743,340 (GRCm39) I50F probably benign Het
Other mutations in Dnajc22
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00091:Dnajc22 APN 15 98,999,059 (GRCm39) missense possibly damaging 0.73
IGL00922:Dnajc22 APN 15 98,999,460 (GRCm39) missense possibly damaging 0.89
IGL02726:Dnajc22 APN 15 98,998,881 (GRCm39) missense probably damaging 1.00
IGL03074:Dnajc22 APN 15 98,999,403 (GRCm39) missense probably damaging 1.00
F5770:Dnajc22 UTSW 15 98,999,363 (GRCm39) missense probably damaging 0.99
R1138:Dnajc22 UTSW 15 99,002,308 (GRCm39) small deletion probably benign
R1628:Dnajc22 UTSW 15 98,998,817 (GRCm39) start codon destroyed probably null 1.00
R2018:Dnajc22 UTSW 15 98,999,114 (GRCm39) missense probably benign 0.06
R2146:Dnajc22 UTSW 15 99,002,264 (GRCm39) missense probably benign 0.04
R4342:Dnajc22 UTSW 15 99,002,345 (GRCm39) nonsense probably null
R4950:Dnajc22 UTSW 15 98,999,615 (GRCm39) missense probably benign 0.29
R7123:Dnajc22 UTSW 15 98,999,085 (GRCm39) missense possibly damaging 0.89
R7173:Dnajc22 UTSW 15 98,999,187 (GRCm39) missense probably benign 0.06
R7640:Dnajc22 UTSW 15 98,998,995 (GRCm39) missense probably damaging 1.00
R7997:Dnajc22 UTSW 15 98,999,514 (GRCm39) missense probably damaging 1.00
R8338:Dnajc22 UTSW 15 98,999,022 (GRCm39) missense probably benign 0.00
R8745:Dnajc22 UTSW 15 98,999,345 (GRCm39) missense probably benign 0.01
V7580:Dnajc22 UTSW 15 98,999,363 (GRCm39) missense probably damaging 0.99
V7581:Dnajc22 UTSW 15 98,999,363 (GRCm39) missense probably damaging 0.99
V7582:Dnajc22 UTSW 15 98,999,363 (GRCm39) missense probably damaging 0.99
V7583:Dnajc22 UTSW 15 98,999,363 (GRCm39) missense probably damaging 0.99
Posted On 2015-04-16