Incidental Mutation 'IGL02448:Zdhhc25'
ID293600
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zdhhc25
Ensembl Gene ENSMUSG00000054117
Gene Namezinc finger, DHHC domain containing 25
Synonyms1700030J15Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.112) question?
Stock #IGL02448
Quality Score
Status
Chromosome15
Chromosomal Location88600302-88601669 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 88600842 bp
ZygosityHeterozygous
Amino Acid Change Valine to Methionine at position 127 (V127M)
Ref Sequence ENSEMBL: ENSMUSP00000136289 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000066949]
Predicted Effect probably damaging
Transcript: ENSMUST00000066949
AA Change: V127M

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000136289
Gene: ENSMUSG00000054117
AA Change: V127M

DomainStartEndE-ValueType
transmembrane domain 35 55 N/A INTRINSIC
transmembrane domain 65 87 N/A INTRINSIC
Pfam:zf-DHHC 105 235 2.4e-32 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Angptl6 T A 9: 20,875,570 I286F probably damaging Het
Arhgap5 A G 12: 52,562,340 E1366G probably damaging Het
Blzf1 T A 1: 164,295,781 I326F possibly damaging Het
Cc2d2a A C 5: 43,683,205 probably benign Het
Cdc37 T C 9: 21,139,851 E366G possibly damaging Het
Cdh17 T C 4: 11,784,680 S279P probably benign Het
Cdh18 T C 15: 23,173,789 S30P probably benign Het
Cep192 A G 18: 67,869,447 T2238A probably benign Het
Cpped1 C T 16: 11,805,389 E289K probably benign Het
Ctsq A T 13: 61,036,230 Y293N probably damaging Het
Epb41l2 A G 10: 25,493,595 N20S possibly damaging Het
Gcc2 T A 10: 58,292,571 C1304* probably null Het
Hsd3b5 C T 3: 98,622,131 G61E probably damaging Het
Igfals A T 17: 24,880,187 N84I probably damaging Het
Irs2 A T 8: 11,007,862 V190D probably benign Het
Kank1 T A 19: 25,411,375 L804Q probably damaging Het
Kcnj2 G T 11: 111,072,282 V167L probably benign Het
Kif20a T C 18: 34,628,454 V300A possibly damaging Het
Kmt2d T C 15: 98,844,110 probably benign Het
Moxd1 T C 10: 24,282,719 F424L probably damaging Het
Mpeg1 A C 19: 12,462,609 D477A probably benign Het
Mtmr10 A T 7: 64,308,150 Y166F probably damaging Het
Muc5b T G 7: 141,868,489 I4454S possibly damaging Het
Ntng1 G A 3: 109,934,559 probably benign Het
Olfr582 T C 7: 103,042,397 I306T possibly damaging Het
Olfr869 T A 9: 20,137,641 L175* probably null Het
Pex11a A T 7: 79,737,460 probably null Het
Plcg2 A G 8: 117,607,221 D911G probably benign Het
Rc3h2 T C 2: 37,389,805 T471A probably benign Het
Rif1 T A 2: 52,116,696 L2214Q probably damaging Het
Rtel1 T A 2: 181,336,037 S120T probably benign Het
Ryr1 A G 7: 29,105,066 probably benign Het
Sh3yl1 G T 12: 30,939,667 A129S probably damaging Het
Slc25a10 A G 11: 120,497,053 T191A probably benign Het
Slc8b1 T C 5: 120,525,791 S359P probably damaging Het
Srf T C 17: 46,555,423 T136A possibly damaging Het
Stx1a G T 5: 135,023,619 probably benign Het
Taf1d T A 9: 15,310,394 C224* probably null Het
Tnik A G 3: 28,621,077 S700G probably null Het
Ttn T C 2: 76,942,987 H2357R probably benign Het
Ttn T C 2: 76,736,114 E28145G probably damaging Het
Ush1c C A 7: 46,209,137 V576F possibly damaging Het
Xpc T C 6: 91,515,744 E19G probably benign Het
Other mutations in Zdhhc25
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01999:Zdhhc25 APN 15 88601014 missense probably damaging 0.98
IGL02576:Zdhhc25 APN 15 88601269 missense probably benign 0.01
R0001:Zdhhc25 UTSW 15 88600909 missense probably benign 0.00
R0394:Zdhhc25 UTSW 15 88600920 missense probably damaging 0.96
R0622:Zdhhc25 UTSW 15 88601107 missense probably damaging 0.98
R1116:Zdhhc25 UTSW 15 88600620 missense probably benign 0.25
R1132:Zdhhc25 UTSW 15 88600723 missense probably damaging 1.00
R1854:Zdhhc25 UTSW 15 88600486 missense probably benign
R1994:Zdhhc25 UTSW 15 88600824 missense probably benign 0.00
R2102:Zdhhc25 UTSW 15 88600759 missense probably benign 0.10
R3749:Zdhhc25 UTSW 15 88601023 missense probably benign 0.00
R5144:Zdhhc25 UTSW 15 88601056 missense probably damaging 0.98
R5220:Zdhhc25 UTSW 15 88601162 nonsense probably null
Posted On2015-04-16