Incidental Mutation 'IGL00720:Zng1'
ID 9422
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zng1
Ensembl Gene ENSMUSG00000024878
Gene Name Zn regulated GTPase metalloprotein activator 1
Synonyms Cbwd1, Zng1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.115) question?
Stock # IGL00720
Quality Score
Status
Chromosome 19
Chromosomal Location 24897280-24938974 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 24898495 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 321 (D321G)
Ref Sequence ENSEMBL: ENSMUSP00000025815 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025815]
AlphaFold Q8VEH6
Predicted Effect probably benign
Transcript: ENSMUST00000025815
AA Change: D321G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000025815
Gene: ENSMUSG00000024878
AA Change: D321G

DomainStartEndE-ValueType
low complexity region 9 16 N/A INTRINSIC
Pfam:cobW 41 229 7.1e-51 PFAM
CobW_C 271 374 5.34e-1 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 11 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cul4a A G 8: 13,177,735 (GRCm39) K292E probably benign Het
Fat2 T C 11: 55,202,070 (GRCm39) T335A probably benign Het
Hrh2 T C 13: 54,368,840 (GRCm39) V272A possibly damaging Het
Jak3 A G 8: 72,136,681 (GRCm39) I663V probably damaging Het
Kifc3 A G 8: 95,864,644 (GRCm39) V22A probably damaging Het
Nat8f1 A G 6: 85,887,957 (GRCm39) M1T probably null Het
Scn7a A T 2: 66,506,388 (GRCm39) S1500R possibly damaging Het
Stambp A T 6: 83,547,419 (GRCm39) S23R probably damaging Het
Tenm3 T C 8: 48,729,456 (GRCm39) N1517D probably damaging Het
Zfp663 A T 2: 165,194,525 (GRCm39) F565I probably damaging Het
Zscan26 C T 13: 21,629,369 (GRCm39) R378H probably benign Het
Other mutations in Zng1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01618:Zng1 APN 19 24,918,140 (GRCm39) missense possibly damaging 0.83
IGL02351:Zng1 APN 19 24,909,026 (GRCm39) critical splice donor site probably null
IGL02358:Zng1 APN 19 24,909,026 (GRCm39) critical splice donor site probably null
IGL02628:Zng1 APN 19 24,935,269 (GRCm39) missense probably damaging 1.00
IGL03001:Zng1 APN 19 24,900,002 (GRCm39) missense probably benign 0.01
IGL03053:Zng1 APN 19 24,932,741 (GRCm39) missense probably damaging 1.00
IGL03409:Zng1 APN 19 24,900,130 (GRCm39) missense probably benign 0.01
R0544:Zng1 UTSW 19 24,926,575 (GRCm39) missense possibly damaging 0.79
R0655:Zng1 UTSW 19 24,930,684 (GRCm39) missense possibly damaging 0.90
R0833:Zng1 UTSW 19 24,918,203 (GRCm39) splice site probably benign
R1296:Zng1 UTSW 19 24,920,039 (GRCm39) splice site probably benign
R1723:Zng1 UTSW 19 24,925,458 (GRCm39) missense possibly damaging 0.89
R1888:Zng1 UTSW 19 24,932,769 (GRCm39) missense probably damaging 1.00
R1888:Zng1 UTSW 19 24,932,769 (GRCm39) missense probably damaging 1.00
R4526:Zng1 UTSW 19 24,935,328 (GRCm39) missense probably benign 0.20
R5092:Zng1 UTSW 19 24,898,383 (GRCm39) critical splice donor site probably null
R5238:Zng1 UTSW 19 24,897,994 (GRCm39) missense probably damaging 0.99
R5852:Zng1 UTSW 19 24,932,769 (GRCm39) missense possibly damaging 0.89
R7248:Zng1 UTSW 19 24,898,505 (GRCm39) missense probably damaging 0.99
R7699:Zng1 UTSW 19 24,920,045 (GRCm39) critical splice donor site probably null
R7700:Zng1 UTSW 19 24,920,045 (GRCm39) critical splice donor site probably null
R7733:Zng1 UTSW 19 24,918,158 (GRCm39) missense probably damaging 1.00
R8363:Zng1 UTSW 19 24,920,091 (GRCm39) missense probably benign 0.01
R8825:Zng1 UTSW 19 24,926,601 (GRCm39) missense probably benign 0.23
R8931:Zng1 UTSW 19 24,932,780 (GRCm39) missense probably damaging 1.00
R9118:Zng1 UTSW 19 24,920,048 (GRCm39) missense probably damaging 1.00
R9467:Zng1 UTSW 19 24,930,684 (GRCm39) missense possibly damaging 0.90
Posted On 2012-12-06