Incidental Mutation 'R2843:Jade1'
ID 254369
Institutional Source Beutler Lab
Gene Symbol Jade1
Ensembl Gene ENSMUSG00000025764
Gene Name jade family PHD finger 1
Synonyms Phf17, D530048A03Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R2843 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 41510169-41571299 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 41559280 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Histidine at position 454 (Y454H)
Ref Sequence ENSEMBL: ENSMUSP00000141499 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026865] [ENSMUST00000163764] [ENSMUST00000168086] [ENSMUST00000170711] [ENSMUST00000191952]
AlphaFold Q6ZPI0
Predicted Effect probably damaging
Transcript: ENSMUST00000026865
AA Change: Y454H

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000026865
Gene: ENSMUSG00000025764
AA Change: Y454H

DomainStartEndE-ValueType
Pfam:EPL1 31 182 5.3e-23 PFAM
PHD 206 252 1.91e-10 SMART
PHD 315 370 1.31e-8 SMART
low complexity region 622 634 N/A INTRINSIC
low complexity region 817 831 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000163764
AA Change: Y454H

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000128152
Gene: ENSMUSG00000025764
AA Change: Y454H

DomainStartEndE-ValueType
Pfam:EPL1 31 182 5.3e-23 PFAM
PHD 206 252 1.91e-10 SMART
PHD 315 370 1.31e-8 SMART
low complexity region 622 634 N/A INTRINSIC
low complexity region 817 831 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000168086
AA Change: Y454H

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000131441
Gene: ENSMUSG00000025764
AA Change: Y454H

DomainStartEndE-ValueType
Pfam:EPL1 31 182 5.3e-23 PFAM
PHD 206 252 1.91e-10 SMART
PHD 315 370 1.31e-8 SMART
low complexity region 622 634 N/A INTRINSIC
low complexity region 817 831 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000170711
AA Change: Y454H

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000127113
Gene: ENSMUSG00000025764
AA Change: Y454H

DomainStartEndE-ValueType
Pfam:EPL1 5 182 1.5e-9 PFAM
PHD 206 252 1.91e-10 SMART
PHD 315 370 1.31e-8 SMART
low complexity region 622 634 N/A INTRINSIC
low complexity region 817 831 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000191921
Predicted Effect probably damaging
Transcript: ENSMUST00000191952
AA Change: Y454H

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000141499
Gene: ENSMUSG00000025764
AA Change: Y454H

DomainStartEndE-ValueType
Pfam:EPL1 30 182 2.3e-23 PFAM
PHD 206 252 1.91e-10 SMART
PHD 315 370 1.31e-8 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000192300
Predicted Effect noncoding transcript
Transcript: ENSMUST00000195322
Predicted Effect probably benign
Transcript: ENSMUST00000192451
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency
MGI Phenotype PHENOTYPE: Though mice homozygous for mutations of this locus show no overt phenotype at birth, fewer survive to weaning than expected by Mendelian ratios. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 16 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afm C T 5: 90,674,324 (GRCm39) R279* probably null Het
Arhgef18 A G 8: 3,414,634 (GRCm39) E4G possibly damaging Het
Fbxw7 G A 3: 84,883,527 (GRCm39) R486Q probably damaging Het
Fhad1 G T 4: 141,632,279 (GRCm39) Q1287K probably benign Het
Hmg20b G C 10: 81,182,404 (GRCm39) R209G probably benign Het
Hydin T C 8: 111,245,746 (GRCm39) V2153A probably benign Het
Kcnn3 CGCAGCAGCAGCAGCAGCAGCAG CGCAGCAGCAGCAGCAGCAG 3: 89,427,972 (GRCm39) probably benign Het
Pdlim2 C T 14: 70,403,549 (GRCm39) V288I probably benign Het
Pknox2 T C 9: 36,805,624 (GRCm39) N395S probably benign Het
Ppfia3 C A 7: 45,005,852 (GRCm39) R348L probably damaging Het
Rad51 T C 2: 118,949,114 (GRCm39) V38A probably benign Het
Sla2 G A 2: 156,717,862 (GRCm39) R137C probably damaging Het
Slc15a4 A G 5: 127,681,600 (GRCm39) probably null Het
Vmn2r18 T A 5: 151,485,749 (GRCm39) T582S probably damaging Het
Zbtb8os A T 4: 129,235,309 (GRCm39) E54D probably damaging Het
Zfp84 T G 7: 29,474,758 (GRCm39) probably null Het
Other mutations in Jade1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01482:Jade1 APN 3 41,567,937 (GRCm39) missense probably benign 0.01
IGL01564:Jade1 APN 3 41,551,084 (GRCm39) missense possibly damaging 0.91
IGL02428:Jade1 APN 3 41,568,374 (GRCm39) missense probably benign 0.03
IGL03080:Jade1 APN 3 41,554,510 (GRCm39) nonsense probably null
R0763:Jade1 UTSW 3 41,568,218 (GRCm39) missense possibly damaging 0.93
R1539:Jade1 UTSW 3 41,559,431 (GRCm39) missense probably benign 0.00
R1576:Jade1 UTSW 3 41,546,242 (GRCm39) missense probably damaging 1.00
R1826:Jade1 UTSW 3 41,567,648 (GRCm39) missense probably damaging 1.00
R2143:Jade1 UTSW 3 41,559,143 (GRCm39) missense probably benign
R2255:Jade1 UTSW 3 41,546,185 (GRCm39) missense probably damaging 1.00
R2962:Jade1 UTSW 3 41,567,762 (GRCm39) missense probably benign
R3963:Jade1 UTSW 3 41,555,845 (GRCm39) missense probably damaging 0.98
R4753:Jade1 UTSW 3 41,551,106 (GRCm39) nonsense probably null
R4971:Jade1 UTSW 3 41,555,836 (GRCm39) missense probably damaging 1.00
R5278:Jade1 UTSW 3 41,543,444 (GRCm39) missense possibly damaging 0.84
R5327:Jade1 UTSW 3 41,568,413 (GRCm39) missense possibly damaging 0.60
R5384:Jade1 UTSW 3 41,546,137 (GRCm39) missense probably damaging 1.00
R5385:Jade1 UTSW 3 41,546,137 (GRCm39) missense probably damaging 1.00
R5531:Jade1 UTSW 3 41,567,946 (GRCm39) missense probably benign 0.27
R5566:Jade1 UTSW 3 41,559,338 (GRCm39) missense possibly damaging 0.77
R5776:Jade1 UTSW 3 41,568,227 (GRCm39) missense probably benign 0.27
R6299:Jade1 UTSW 3 41,568,160 (GRCm39) missense probably damaging 1.00
R6520:Jade1 UTSW 3 41,558,917 (GRCm39) missense possibly damaging 0.46
R7481:Jade1 UTSW 3 41,559,125 (GRCm39) missense probably benign
R7951:Jade1 UTSW 3 41,546,190 (GRCm39) missense probably damaging 0.99
R8006:Jade1 UTSW 3 41,568,124 (GRCm39) missense probably benign
R8175:Jade1 UTSW 3 41,567,723 (GRCm39) missense probably benign 0.27
R8382:Jade1 UTSW 3 41,519,369 (GRCm39) splice site probably null
R8493:Jade1 UTSW 3 41,559,113 (GRCm39) missense possibly damaging 0.60
R8985:Jade1 UTSW 3 41,568,148 (GRCm39) missense probably benign 0.05
R9018:Jade1 UTSW 3 41,564,292 (GRCm39) missense probably benign 0.09
R9679:Jade1 UTSW 3 41,567,569 (GRCm39) missense probably damaging 0.98
X0026:Jade1 UTSW 3 41,567,848 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- TCTGGAGCCCTATGGTAGTC -3'
(R):5'- ATGACTGGCTATCATCTCTAGGC -3'

Sequencing Primer
(F):5'- CCTATGGTAGTCTGGAGCCGAATC -3'
(R):5'- ACTGGCTATCATCTCTAGGCAAGTG -3'
Posted On 2014-12-04