Incidental Mutation 'IGL02475:Zdhhc2'
ID 294910
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zdhhc2
Ensembl Gene ENSMUSG00000039470
Gene Name zinc finger, DHHC domain containing 2
Synonyms
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02475
Quality Score
Status
Chromosome 8
Chromosomal Location 40423815-40510268 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) G to T at 40473025 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glycine to Cysteine at position 354 (G354C)
Ref Sequence ENSEMBL: ENSMUSP00000129996 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049389] [ENSMUST00000128166] [ENSMUST00000167766]
AlphaFold P59267
Predicted Effect probably null
Transcript: ENSMUST00000049389
AA Change: G354C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000041727
Gene: ENSMUSG00000039470
AA Change: G354C

DomainStartEndE-ValueType
transmembrane domain 16 38 N/A INTRINSIC
Pfam:zf-DHHC 66 248 4.1e-43 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000128166
AA Change: G354C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000123070
Gene: ENSMUSG00000039470
AA Change: G354C

DomainStartEndE-ValueType
transmembrane domain 16 38 N/A INTRINSIC
transmembrane domain 48 70 N/A INTRINSIC
Pfam:zf-DHHC 122 248 1.8e-37 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000167766
AA Change: G354C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129996
Gene: ENSMUSG00000039470
AA Change: G354C

DomainStartEndE-ValueType
transmembrane domain 16 38 N/A INTRINSIC
Pfam:zf-DHHC 66 248 4.1e-43 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001J03Rik A T 5: 146,182,533 probably benign Het
5730409E04Rik A G 4: 126,611,949 E90G probably damaging Het
Abhd6 T A 14: 8,039,849 I27N probably damaging Het
Akap6 A T 12: 53,139,494 E1230D probably benign Het
Bcl2l12 A G 7: 44,996,893 V31A possibly damaging Het
Cep350 G A 1: 155,862,595 R2501W probably damaging Het
Cnga3 A G 1: 37,257,991 probably null Het
Crcp T C 5: 130,059,858 probably benign Het
Creb5 G A 6: 53,693,924 S304N probably damaging Het
Csgalnact1 C A 8: 68,401,492 G219V probably damaging Het
Dnah5 A G 15: 28,219,150 D38G probably benign Het
Fam171a1 A G 2: 3,223,490 I293V possibly damaging Het
Fbxw10 T C 11: 62,857,735 V396A possibly damaging Het
Gm10340 G A 14: 3,140,482 probably benign Het
Gm20390 A G 11: 93,955,574 V16A probably damaging Het
Grik3 A G 4: 125,650,517 T344A probably benign Het
Itga7 T C 10: 128,934,089 F34S probably damaging Het
Musk T C 4: 58,353,936 probably benign Het
Neb G T 2: 52,292,819 N1038K probably damaging Het
Nf1 T C 11: 79,535,667 Y1636H probably damaging Het
Ngef G T 1: 87,479,150 T632K possibly damaging Het
Nts A G 10: 102,490,247 probably benign Het
Olfml2b A G 1: 170,682,174 D697G probably damaging Het
Olfr1031 T C 2: 85,992,032 F72L probably benign Het
Olfr1502 T A 19: 13,862,299 C169S probably damaging Het
Olfr205 A T 16: 59,328,725 H261Q probably benign Het
Otof T C 5: 30,376,682 R1428G probably damaging Het
Pgghg T C 7: 140,945,720 S479P Het
Rnaseh2b T A 14: 62,346,615 F37I probably damaging Het
Rtn4 T A 11: 29,733,801 I1031N probably damaging Het
Rxfp2 A G 5: 150,063,686 E344G probably benign Het
Scel A G 14: 103,537,008 R89G possibly damaging Het
Sirt4 T C 5: 115,482,996 E39G probably benign Het
Slc6a12 T A 6: 121,354,375 probably null Het
Snapc3 C A 4: 83,450,096 H277N probably benign Het
Susd2 A G 10: 75,637,499 probably null Het
Tagap1 T C 17: 6,956,427 Q290R probably benign Het
Tenm3 A T 8: 48,279,198 probably benign Het
Tmem54 A T 4: 129,108,280 H40L probably damaging Het
Tnks1bp1 T C 2: 85,059,377 S683P probably damaging Het
Tnpo2 A G 8: 85,050,502 D547G probably benign Het
Tpd52l2 G A 2: 181,499,874 V17M probably benign Het
Trip11 T A 12: 101,895,683 T208S probably benign Het
Ttc17 C A 2: 94,364,376 D551Y probably damaging Het
Ttll12 A T 15: 83,587,101 W222R probably damaging Het
Xkr8 A T 4: 132,728,201 I287N probably damaging Het
Zfp13 C T 17: 23,576,098 A493T probably benign Het
Other mutations in Zdhhc2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01697:Zdhhc2 APN 8 40467419 splice site probably benign
IGL01751:Zdhhc2 APN 8 40473001 missense probably benign
IGL01752:Zdhhc2 APN 8 40473001 missense probably benign
IGL01800:Zdhhc2 APN 8 40464243 missense probably damaging 1.00
IGL02554:Zdhhc2 APN 8 40462114 missense probably damaging 1.00
R0662:Zdhhc2 UTSW 8 40447098 missense probably damaging 1.00
R0720:Zdhhc2 UTSW 8 40472907 splice site probably null
R1511:Zdhhc2 UTSW 8 40467972 missense probably benign 0.00
R4738:Zdhhc2 UTSW 8 40464142 splice site probably null
R5114:Zdhhc2 UTSW 8 40445784 missense probably benign 0.06
R5935:Zdhhc2 UTSW 8 40464236 missense probably damaging 0.96
R6029:Zdhhc2 UTSW 8 40472927 missense probably null
R7210:Zdhhc2 UTSW 8 40467439 missense probably damaging 0.96
R7792:Zdhhc2 UTSW 8 40447141 missense probably benign 0.02
R8756:Zdhhc2 UTSW 8 40467510 missense probably damaging 1.00
R8805:Zdhhc2 UTSW 8 40445805 critical splice donor site probably null
R9142:Zdhhc2 UTSW 8 40467522 missense probably damaging 1.00
Posted On 2015-04-16