Incidental Mutation 'R7797:Jade2'
ID 600299
Institutional Source Beutler Lab
Gene Symbol Jade2
Ensembl Gene ENSMUSG00000020387
Gene Name jade family PHD finger 2
Synonyms 1200017K05Rik, Phf15
MMRRC Submission 045853-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7797 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 51704282-51748480 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 51708126 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 696 (S696P)
Ref Sequence ENSEMBL: ENSMUSP00000020655 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020655] [ENSMUST00000109090] [ENSMUST00000109091]
AlphaFold Q6ZQF7
Predicted Effect probably benign
Transcript: ENSMUST00000020655
AA Change: S696P

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000020655
Gene: ENSMUSG00000020387
AA Change: S696P

DomainStartEndE-ValueType
Pfam:EPL1 39 177 3.4e-17 PFAM
PHD 201 247 1.35e-10 SMART
PHD 310 365 1.74e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000109090
SMART Domains Protein: ENSMUSP00000104718
Gene: ENSMUSG00000020387

DomainStartEndE-ValueType
Pfam:EPL1 39 177 2e-17 PFAM
PHD 201 247 1.35e-10 SMART
PHD 310 365 1.74e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000109091
AA Change: S696P

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000104719
Gene: ENSMUSG00000020387
AA Change: S696P

DomainStartEndE-ValueType
Pfam:EPL1 2 176 9.6e-9 PFAM
PHD 201 247 1.35e-10 SMART
PHD 310 365 1.74e-4 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
Validation Efficiency 100% (68/68)
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b A G 11: 109,862,509 (GRCm39) probably null Het
Adam3 T G 8: 25,184,660 (GRCm39) N535T probably damaging Het
Adam34l T A 8: 44,079,411 (GRCm39) E271V probably benign Het
Adamts4 A G 1: 171,085,387 (GRCm39) K679E probably damaging Het
Arnt G A 3: 95,387,572 (GRCm39) probably null Het
Asah2 A G 19: 31,999,761 (GRCm39) F321L probably damaging Het
Asb15 T C 6: 24,562,505 (GRCm39) S156P probably damaging Het
Baiap2l1 A C 5: 144,255,760 (GRCm39) S65A probably damaging Het
Bend7 T G 2: 4,754,455 (GRCm39) M186R probably damaging Het
Blnk T C 19: 40,948,232 (GRCm39) K146E possibly damaging Het
Cd19 A G 7: 126,012,680 (GRCm39) W238R probably damaging Het
Cd44 T A 2: 102,679,079 (GRCm39) N241I probably benign Het
Cdh23 T C 10: 60,220,973 (GRCm39) E1257G probably benign Het
Cfap300 G T 9: 8,027,130 (GRCm39) P136Q possibly damaging Het
Cntnap5c T C 17: 58,666,270 (GRCm39) V1100A probably benign Het
Cul7 T C 17: 46,969,568 (GRCm39) V945A possibly damaging Het
Dock2 C T 11: 34,232,652 (GRCm39) C1116Y probably damaging Het
Ehbp1 T C 11: 22,046,109 (GRCm39) M547V possibly damaging Het
Fam50b G A 13: 34,931,084 (GRCm39) E187K possibly damaging Het
Grhl3 C G 4: 135,286,416 (GRCm39) K88N possibly damaging Het
Hbb-y T A 7: 103,501,088 (GRCm39) Y146F probably damaging Het
Hivep2 T C 10: 14,005,847 (GRCm39) V815A probably benign Het
Hoxa7 T A 6: 52,192,870 (GRCm39) I173F probably damaging Het
Igkv1-110 T G 6: 68,247,977 (GRCm39) S29A probably benign Het
Kif1b T A 4: 149,321,844 (GRCm39) Q1025L probably benign Het
Kif2c A T 4: 117,028,940 (GRCm39) C241S probably benign Het
Kmt2d G T 15: 98,762,287 (GRCm39) H400N probably benign Het
Krt35 T A 11: 99,985,713 (GRCm39) N174Y probably damaging Het
Ldlrad1 G A 4: 107,066,688 (GRCm39) A8T probably benign Het
Magi3 A G 3: 103,958,618 (GRCm39) V489A probably damaging Het
Mapk7 T C 11: 61,380,241 (GRCm39) E739G possibly damaging Het
Mcidas G A 13: 113,135,521 (GRCm39) G315S probably damaging Het
Mdga1 C T 17: 30,061,814 (GRCm39) probably null Het
Megf8 G A 7: 25,034,022 (GRCm39) R607H probably damaging Het
Met T A 6: 17,533,952 (GRCm39) N634K probably damaging Het
Miip C T 4: 147,947,375 (GRCm39) G236S probably benign Het
Mmp11 G T 10: 75,759,314 (GRCm39) T107K Het
Mroh2b A C 15: 4,978,587 (GRCm39) N1378H probably benign Het
Naa15 G A 3: 51,356,031 (GRCm39) C322Y probably damaging Het
Naip1 T A 13: 100,580,986 (GRCm39) Y87F probably damaging Het
Ngrn A G 7: 79,914,185 (GRCm39) D112G probably benign Het
Osbpl1a C A 18: 13,015,321 (GRCm39) C369F probably damaging Het
Pcnx2 G C 8: 126,512,087 (GRCm39) D1406E possibly damaging Het
Phf8-ps T C 17: 33,286,664 (GRCm39) D46G probably damaging Het
Pold1 G A 7: 44,191,213 (GRCm39) P206L probably benign Het
Psen1 A G 12: 83,746,396 (GRCm39) S20G probably benign Het
Ptpn23 C T 9: 110,222,875 (GRCm39) D61N possibly damaging Het
Rbfox3 A T 11: 118,387,310 (GRCm39) L268Q possibly damaging Het
Rbm22 A G 18: 60,694,344 (GRCm39) T26A probably damaging Het
Rpgrip1 G A 14: 52,371,277 (GRCm39) R332Q possibly damaging Het
Rrm2b A T 15: 37,927,505 (GRCm39) L347* probably null Het
Rsf1 A T 7: 97,310,692 (GRCm39) D474V Het
Ryr2 C T 13: 11,816,066 (GRCm39) R640Q probably damaging Het
Sec16b A G 1: 157,389,245 (GRCm39) E691G unknown Het
Septin1 A T 7: 126,813,937 (GRCm39) V365E unknown Het
Tlk2 A G 11: 105,101,444 (GRCm39) H114R probably benign Het
Tmem200a A G 10: 25,869,864 (GRCm39) I135T possibly damaging Het
Tpst2 T A 5: 112,455,782 (GRCm39) V107E probably damaging Het
Trim30a A T 7: 104,060,407 (GRCm39) D456E possibly damaging Het
Ttll3 T C 6: 113,371,738 (GRCm39) V45A possibly damaging Het
Ulk2 A G 11: 61,672,928 (GRCm39) Y889H probably benign Het
Umodl1 A G 17: 31,178,125 (GRCm39) S34G probably benign Het
Vmn1r67 A G 7: 10,180,903 (GRCm39) I56V probably benign Het
Vmn2r120 C T 17: 57,815,874 (GRCm39) G827E probably damaging Het
Zc3h6 T C 2: 128,857,555 (GRCm39) probably null Het
Other mutations in Jade2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01323:Jade2 APN 11 51,716,165 (GRCm39) missense possibly damaging 0.95
IGL01935:Jade2 APN 11 51,719,211 (GRCm39) missense possibly damaging 0.95
IGL02885:Jade2 APN 11 51,722,123 (GRCm39) missense probably damaging 1.00
IGL02987:Jade2 APN 11 51,721,308 (GRCm39) missense probably damaging 1.00
IGL02990:Jade2 APN 11 51,722,074 (GRCm39) splice site probably benign
IGL03172:Jade2 APN 11 51,716,198 (GRCm39) missense probably damaging 1.00
R0116:Jade2 UTSW 11 51,722,136 (GRCm39) missense probably damaging 1.00
R1917:Jade2 UTSW 11 51,709,365 (GRCm39) missense possibly damaging 0.95
R3410:Jade2 UTSW 11 51,708,050 (GRCm39) missense probably benign
R3886:Jade2 UTSW 11 51,721,326 (GRCm39) missense possibly damaging 0.79
R4846:Jade2 UTSW 11 51,711,975 (GRCm39) missense probably benign
R4916:Jade2 UTSW 11 51,707,909 (GRCm39) missense probably benign 0.01
R5420:Jade2 UTSW 11 51,709,434 (GRCm39) missense probably benign 0.21
R5446:Jade2 UTSW 11 51,707,786 (GRCm39) missense probably benign
R5657:Jade2 UTSW 11 51,707,814 (GRCm39) missense probably damaging 1.00
R6031:Jade2 UTSW 11 51,717,413 (GRCm39) nonsense probably null
R6031:Jade2 UTSW 11 51,717,413 (GRCm39) nonsense probably null
R6116:Jade2 UTSW 11 51,726,460 (GRCm39) missense probably damaging 0.99
R7039:Jade2 UTSW 11 51,719,186 (GRCm39) missense probably damaging 0.97
R7270:Jade2 UTSW 11 51,708,011 (GRCm39) missense possibly damaging 0.89
R7702:Jade2 UTSW 11 51,707,744 (GRCm39) missense probably damaging 1.00
R8054:Jade2 UTSW 11 51,709,441 (GRCm39) missense probably benign 0.00
R8243:Jade2 UTSW 11 51,708,045 (GRCm39) missense probably benign
R8371:Jade2 UTSW 11 51,715,959 (GRCm39) missense probably benign 0.04
R8984:Jade2 UTSW 11 51,715,906 (GRCm39) missense probably damaging 1.00
R9020:Jade2 UTSW 11 51,708,454 (GRCm39) missense probably benign 0.00
R9135:Jade2 UTSW 11 51,715,951 (GRCm39) missense probably benign
R9143:Jade2 UTSW 11 51,715,930 (GRCm39) missense probably benign 0.00
Z1177:Jade2 UTSW 11 51,739,821 (GRCm39) missense probably null 0.20
Z1177:Jade2 UTSW 11 51,707,817 (GRCm39) missense probably damaging 0.96
Predicted Primers PCR Primer
(F):5'- GACTGACCTTCATCTCTCGG -3'
(R):5'- TGCTCAGCTTCATGAGGGAC -3'

Sequencing Primer
(F):5'- ACCTTCATCTCTCGGGGTGG -3'
(R):5'- TGGTGACCCTGCCAGAAAG -3'
Posted On 2019-11-26