Incidental Mutation 'IGL02185:Zdhhc14'
ID 283598
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zdhhc14
Ensembl Gene ENSMUSG00000034265
Gene Name zinc finger, DHHC domain containing 14
Synonyms New1cp, B530001K09Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # IGL02185
Quality Score
Status
Chromosome 17
Chromosomal Location 5542832-5804086 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 5803157 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 420 (T420K)
Ref Sequence ENSEMBL: ENSMUSP00000086589 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089185]
AlphaFold Q8BQQ1
Predicted Effect probably benign
Transcript: ENSMUST00000089185
AA Change: T420K

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000086589
Gene: ENSMUSG00000034265
AA Change: T420K

DomainStartEndE-ValueType
transmembrane domain 62 81 N/A INTRINSIC
transmembrane domain 91 110 N/A INTRINSIC
Pfam:zf-DHHC 160 289 1.8e-38 PFAM
low complexity region 351 365 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adh5 A G 3: 138,156,815 (GRCm39) D167G probably benign Het
C9orf72 A T 4: 35,197,046 (GRCm39) W340R probably damaging Het
Cand2 G A 6: 115,766,471 (GRCm39) A359T probably benign Het
Cnnm2 T C 19: 46,751,434 (GRCm39) V408A probably benign Het
Eloa A G 4: 135,740,290 (GRCm39) probably benign Het
Ern2 T C 7: 121,772,598 (GRCm39) probably benign Het
Hs6st3 A G 14: 120,106,296 (GRCm39) probably null Het
Hydin A T 8: 111,233,108 (GRCm39) I1736F possibly damaging Het
Ifrd2 A T 9: 107,468,290 (GRCm39) I253F probably benign Het
Kctd7 G A 5: 130,181,299 (GRCm39) V241I possibly damaging Het
Lcp1 T C 14: 75,466,740 (GRCm39) F616L possibly damaging Het
Lyst C T 13: 13,835,678 (GRCm39) Q1787* probably null Het
Mapkbp1 A T 2: 119,845,144 (GRCm39) T342S possibly damaging Het
Mcph1 A G 8: 18,719,006 (GRCm39) probably benign Het
Mctp2 T C 7: 71,730,571 (GRCm39) H868R probably benign Het
Mefv T C 16: 3,533,714 (GRCm39) T186A probably benign Het
Nol9 T A 4: 152,142,368 (GRCm39) I666N probably damaging Het
Or51t4 T A 7: 102,597,721 (GRCm39) N16K probably damaging Het
Or6c205 G T 10: 129,086,904 (GRCm39) C167F possibly damaging Het
Or8b8 A C 9: 37,809,531 (GRCm39) Y277S probably damaging Het
Pum2 T C 12: 8,798,955 (GRCm39) probably null Het
Rpgrip1 A C 14: 52,349,685 (GRCm39) K24N possibly damaging Het
Ryr3 T A 2: 112,797,548 (GRCm39) T122S probably damaging Het
Sfn A G 4: 133,328,636 (GRCm39) S149P probably benign Het
Slc27a2 T A 2: 126,409,736 (GRCm39) V306D probably damaging Het
Slc35a1 A G 4: 34,675,584 (GRCm39) V81A probably benign Het
Trav21-dv12 A T 14: 54,113,955 (GRCm39) D25V probably benign Het
Ttn T C 2: 76,598,878 (GRCm39) H11018R possibly damaging Het
Txn1 A T 4: 57,950,883 (GRCm39) Y49N probably benign Het
Ulk2 C T 11: 61,672,886 (GRCm39) A903T probably damaging Het
Vmn2r77 G A 7: 86,444,360 (GRCm39) M4I unknown Het
Vmn2r85 G T 10: 130,254,561 (GRCm39) L708I probably benign Het
Vmn2r9 G A 5: 108,991,502 (GRCm39) L620F probably damaging Het
Vrk2 T A 11: 26,485,638 (GRCm39) R117* probably null Het
Xpo6 A T 7: 125,712,980 (GRCm39) probably benign Het
Zfp334 G T 2: 165,228,869 (GRCm39) probably benign Het
Zfp958 T A 8: 4,678,990 (GRCm39) C338* probably null Het
Other mutations in Zdhhc14
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00419:Zdhhc14 APN 17 5,802,959 (GRCm39) splice site probably benign
IGL00909:Zdhhc14 APN 17 5,803,067 (GRCm39) missense probably benign
IGL00964:Zdhhc14 APN 17 5,762,756 (GRCm39) missense probably damaging 1.00
IGL01398:Zdhhc14 APN 17 5,762,738 (GRCm39) missense possibly damaging 0.90
IGL01483:Zdhhc14 APN 17 5,762,733 (GRCm39) missense probably benign 0.01
IGL02801:Zdhhc14 APN 17 5,777,094 (GRCm39) splice site probably null
R0189:Zdhhc14 UTSW 17 5,775,539 (GRCm39) missense possibly damaging 0.90
R0304:Zdhhc14 UTSW 17 5,775,611 (GRCm39) splice site probably benign
R0648:Zdhhc14 UTSW 17 5,543,877 (GRCm39) missense probably benign 0.01
R1017:Zdhhc14 UTSW 17 5,543,924 (GRCm39) missense probably damaging 0.99
R1595:Zdhhc14 UTSW 17 5,543,831 (GRCm39) missense probably benign 0.00
R2416:Zdhhc14 UTSW 17 5,803,283 (GRCm39) missense probably benign
R3420:Zdhhc14 UTSW 17 5,803,366 (GRCm39) makesense probably null
R3421:Zdhhc14 UTSW 17 5,803,366 (GRCm39) makesense probably null
R4063:Zdhhc14 UTSW 17 5,802,983 (GRCm39) missense probably damaging 1.00
R4088:Zdhhc14 UTSW 17 5,777,131 (GRCm39) missense probably benign 0.01
R5359:Zdhhc14 UTSW 17 5,543,821 (GRCm39) missense probably benign
R6236:Zdhhc14 UTSW 17 5,543,918 (GRCm39) missense probably damaging 1.00
R7029:Zdhhc14 UTSW 17 5,698,186 (GRCm39) missense probably damaging 0.97
R7350:Zdhhc14 UTSW 17 5,777,151 (GRCm39) missense probably benign 0.44
R7873:Zdhhc14 UTSW 17 5,762,729 (GRCm39) missense probably benign 0.37
R8247:Zdhhc14 UTSW 17 5,736,031 (GRCm39) missense probably damaging 1.00
R8492:Zdhhc14 UTSW 17 5,762,689 (GRCm39) missense probably damaging 0.98
R8865:Zdhhc14 UTSW 17 5,775,570 (GRCm39) missense possibly damaging 0.58
R8969:Zdhhc14 UTSW 17 5,775,555 (GRCm39) missense probably benign 0.12
R9133:Zdhhc14 UTSW 17 5,803,283 (GRCm39) missense probably benign
R9291:Zdhhc14 UTSW 17 5,698,237 (GRCm39) missense probably benign 0.02
R9433:Zdhhc14 UTSW 17 5,781,779 (GRCm39) missense probably benign 0.03
Posted On 2015-04-16