Incidental Mutation 'IGL01676:Zfand3'
ID 103628
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: 0.378) question?
Stock # IGL01676
Quality Score
Status
Chromosome 17
Chromosomal Location 30224013-30429797 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 30354337 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Arginine at position 51 (S51R)
Ref Sequence ENSEMBL: ENSMUSP00000154782 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057897] [ENSMUST00000226208]
AlphaFold Q497H0
Predicted Effect possibly damaging
Transcript: ENSMUST00000057897
AA Change: S51R

PolyPhen 2 Score 0.897 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000063158
Gene: ENSMUSG00000044477
AA Change: S51R

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 possibly damaging
Transcript: ENSMUST00000226208
AA Change: S51R

PolyPhen 2 Score 0.897 (Sensitivity: 0.82; Specificity: 0.94)
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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsm4 A T 7: 119,307,866 (GRCm39) R334S probably benign Het
Adamts3 A T 5: 89,825,613 (GRCm39) F1075L probably benign Het
Adamts3 A G 5: 90,029,402 (GRCm39) V30A possibly damaging Het
Bpifb5 A G 2: 154,070,969 (GRCm39) N223D possibly damaging Het
Cacna1e T C 1: 154,274,222 (GRCm39) R2228G probably damaging Het
Cacna1e T C 1: 154,288,196 (GRCm39) E1894G probably damaging Het
Calr4 A G 4: 109,101,447 (GRCm39) K110E probably damaging Het
Catsperz G T 19: 6,902,421 (GRCm39) Y24* probably null Het
Clec9a T G 6: 129,398,118 (GRCm39) S219A probably benign Het
Csrnp3 T A 2: 65,779,336 (GRCm39) I16N probably damaging Het
Ddx19a A G 8: 111,707,621 (GRCm39) probably null Het
Diaph1 G A 18: 37,989,241 (GRCm39) Q905* probably null Het
Dnah10 T C 5: 124,880,392 (GRCm39) M2743T possibly damaging Het
Ears2 A T 7: 121,643,781 (GRCm39) D392E probably benign Het
Fsip1 T C 2: 118,070,865 (GRCm39) probably benign Het
Ighv1-74 T C 12: 115,766,323 (GRCm39) Y98C possibly damaging Het
Igsf10 T C 3: 59,233,432 (GRCm39) K1767R probably benign Het
Igsf10 C T 3: 59,236,756 (GRCm39) A1142T probably benign Het
Lpar6 A G 14: 73,477,010 (GRCm39) N324D probably benign Het
Lrit1 T A 14: 36,779,394 (GRCm39) L109Q probably damaging Het
Nlrp4f A T 13: 65,342,933 (GRCm39) D237E possibly damaging Het
Oas1h G T 5: 121,009,897 (GRCm39) G324V probably damaging Het
Pak1 T G 7: 97,532,738 (GRCm39) D179E probably benign Het
Prop1 T A 11: 50,842,956 (GRCm39) Q77L probably damaging Het
Scn10a A T 9: 119,501,231 (GRCm39) Y184* probably null Het
Sdk1 T C 5: 142,113,591 (GRCm39) F1546S probably damaging Het
Trim67 A T 8: 125,541,899 (GRCm39) I366F possibly damaging Het
Vmn2r94 T G 17: 18,477,272 (GRCm39) M380L probably benign Het
Vmn2r-ps158 A G 7: 42,674,133 (GRCm39) N397S probably damaging Het
Zfp36l3 T C X: 52,777,624 (GRCm39) S197G probably benign Het
Other mutations in Zfand3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01148:Zfand3 APN 17 30,354,374 (GRCm39) missense probably benign 0.01
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 2014-01-21