Incidental Mutation 'IGL00419:Zdhhc14'
ID 3931
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 # IGL00419
Quality Score
Status
Chromosome 17
Chromosomal Location 5542832-5804086 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 5802959 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000086589 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089185]
AlphaFold Q8BQQ1
Predicted Effect probably benign
Transcript: ENSMUST00000089185
SMART Domains Protein: ENSMUSP00000086589
Gene: ENSMUSG00000034265

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: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp1a4 A C 1: 172,067,373 (GRCm39) N586K probably damaging Het
AU040320 T C 4: 126,686,027 (GRCm39) M201T probably benign Het
Bcap29 A T 12: 31,680,871 (GRCm39) F38L probably benign Het
Bdkrb2 A G 12: 105,554,562 (GRCm39) probably benign Het
Ceacam5 G T 7: 17,493,481 (GRCm39) E835* probably null Het
Cenpp T C 13: 49,801,132 (GRCm39) probably null Het
Clca3a2 A G 3: 144,804,574 (GRCm39) V51A probably damaging Het
Dmxl2 T C 9: 54,313,951 (GRCm39) N1660D probably damaging Het
Exosc9 T C 3: 36,607,288 (GRCm39) probably benign Het
Ezh1 T C 11: 101,085,332 (GRCm39) probably null Het
Fbxo24 G A 5: 137,622,563 (GRCm39) R68C probably damaging Het
Gbp9 T C 5: 105,241,943 (GRCm39) I205V probably benign Het
Gpc5 A G 14: 115,607,436 (GRCm39) Y346C probably damaging Het
Hectd1 A G 12: 51,810,818 (GRCm39) Y1706H probably damaging Het
Igsf9b A G 9: 27,230,951 (GRCm39) Y318C probably damaging Het
Map1a A T 2: 121,129,508 (GRCm39) Q182L probably damaging Het
Rab11fip3 A T 17: 26,210,783 (GRCm39) probably benign Het
Rbm20 G A 19: 53,831,695 (GRCm39) R643Q probably damaging Het
Ros1 A T 10: 51,967,150 (GRCm39) C1707S probably damaging Het
Rpgrip1l G T 8: 91,990,202 (GRCm39) R747S possibly damaging Het
Rsph10b T C 5: 143,873,905 (GRCm39) *166R probably null Het
Sft2d1 G A 17: 8,539,437 (GRCm39) C80Y possibly damaging Het
Zfp300 T A X: 20,948,531 (GRCm39) Y411F probably damaging Het
Zfp92 T C X: 72,463,764 (GRCm39) probably benign Het
Zhx1 A G 15: 57,916,711 (GRCm39) F512L probably damaging Het
Other mutations in Zdhhc14
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
IGL02185:Zdhhc14 APN 17 5,803,157 (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 2012-04-20