Incidental Mutation 'IGL01148:Zfand3'
ID 53138
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfand3
Ensembl Gene ENSMUSG00000044477
Gene Name zinc finger, AN1-type domain 3
Synonyms TEG-27, Tex27
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.317) question?
Stock # IGL01148
Quality Score
Status
Chromosome 17
Chromosomal Location 30224013-30429797 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 30354374 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 64 (T64S)
Ref Sequence ENSEMBL: ENSMUSP00000154782 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057897] [ENSMUST00000226208]
AlphaFold Q497H0
Predicted Effect probably benign
Transcript: ENSMUST00000057897
AA Change: T64S

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000063158
Gene: ENSMUSG00000044477
AA Change: T64S

DomainStartEndE-ValueType
Pfam:zf-A20 17 36 8.7e-9 PFAM
low complexity region 43 58 N/A INTRINSIC
low complexity region 61 77 N/A INTRINSIC
Pfam:zf-AN1 135 175 8.6e-11 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000226208
AA Change: T64S

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226308
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226421
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acap1 A T 11: 69,781,729 (GRCm39) C64* probably null Het
Ccng2 G A 5: 93,418,746 (GRCm39) D124N probably damaging Het
Cttnbp2 G A 6: 18,382,817 (GRCm39) P1317L probably damaging Het
Dsg1a T A 18: 20,453,982 (GRCm39) V29E probably damaging Het
Exoc6b T C 6: 84,885,208 (GRCm39) K244E probably benign Het
Fastkd5 A G 2: 130,456,605 (GRCm39) F662L probably benign Het
Fbxl18 T C 5: 142,871,580 (GRCm39) M488V probably damaging Het
Gas2l3 C T 10: 89,249,366 (GRCm39) G584D probably benign Het
Gm28042 T C 2: 119,869,519 (GRCm39) F405L possibly damaging Het
Gtf3c2 T C 5: 31,317,168 (GRCm39) K635E probably damaging Het
H2-Q2 A G 17: 35,561,654 (GRCm39) Y48C probably damaging Het
Hddc2 T C 10: 31,192,330 (GRCm39) I78T probably damaging Het
Hspg2 T A 4: 137,273,969 (GRCm39) M2708K probably benign Het
Ift88 T C 14: 57,677,189 (GRCm39) S119P probably benign Het
Mta2 T C 19: 8,925,668 (GRCm39) C388R probably damaging Het
Mymx G T 17: 45,912,594 (GRCm39) probably benign Het
Naga A G 15: 82,214,861 (GRCm39) Y366H possibly damaging Het
Nlrp9a A G 7: 26,257,006 (GRCm39) E208G probably damaging Het
Nr4a2 C T 2: 57,001,983 (GRCm39) V94M probably benign Het
Or4c124 G T 2: 89,156,368 (GRCm39) T52K probably benign Het
Osbpl8 G T 10: 111,112,424 (GRCm39) probably benign Het
Pitpnb T A 5: 111,486,222 (GRCm39) V42D probably damaging Het
Pitrm1 A G 13: 6,623,141 (GRCm39) R801G probably benign Het
Pthlh G A 6: 147,154,073 (GRCm39) T174M probably benign Het
Sco2 T C 15: 89,255,924 (GRCm39) I243M probably benign Het
Sema5a G A 15: 32,681,641 (GRCm39) V907M probably benign Het
Semp2l1 A G 1: 32,584,735 (GRCm39) S392P possibly damaging Het
Spata31e2 T C 1: 26,724,253 (GRCm39) E309G probably benign Het
Stac2 T A 11: 97,934,387 (GRCm39) K106* probably null Het
Tas2r105 T A 6: 131,663,815 (GRCm39) R204S probably damaging Het
Tgm5 A G 2: 120,877,156 (GRCm39) probably null Het
Trpm1 A G 7: 63,893,312 (GRCm39) I939V probably damaging Het
Ttll11 T A 2: 35,674,205 (GRCm39) N574I probably damaging Het
Zfyve26 G A 12: 79,307,644 (GRCm39) H312Y probably benign Het
Other mutations in Zfand3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01676:Zfand3 APN 17 30,354,337 (GRCm39) missense possibly damaging 0.90
IGL02931:Zfand3 APN 17 30,411,611 (GRCm39) missense probably benign 0.00
IGL03052:Zfand3 UTSW 17 30,279,798 (GRCm39) missense probably benign 0.03
R0083:Zfand3 UTSW 17 30,354,372 (GRCm39) missense probably damaging 1.00
R0108:Zfand3 UTSW 17 30,354,372 (GRCm39) missense probably damaging 1.00
R0661:Zfand3 UTSW 17 30,354,372 (GRCm39) missense probably damaging 1.00
R3732:Zfand3 UTSW 17 30,411,630 (GRCm39) missense probably benign 0.06
R3732:Zfand3 UTSW 17 30,411,630 (GRCm39) missense probably benign 0.06
R3733:Zfand3 UTSW 17 30,411,630 (GRCm39) missense probably benign 0.06
R4694:Zfand3 UTSW 17 30,354,362 (GRCm39) missense possibly damaging 0.66
R8029:Zfand3 UTSW 17 30,354,407 (GRCm39) missense probably benign 0.01
R9383:Zfand3 UTSW 17 30,354,479 (GRCm39) missense probably benign 0.01
R9546:Zfand3 UTSW 17 30,372,302 (GRCm39) missense probably benign 0.00
Posted On 2013-06-21