Incidental Mutation 'IGL01093:Zscan4c'
ID 51508
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zscan4c
Ensembl Gene ENSMUSG00000054272
Gene Name zinc finger and SCAN domain containing 4C
Synonyms LOC245109
Accession Numbers
Essential gene? Possibly essential (E-score: 0.525) question?
Stock # IGL01093
Quality Score
Status
Chromosome 7
Chromosomal Location 10739672-10744474 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 10743544 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Tyrosine at position 381 (C381Y)
Ref Sequence ENSEMBL: ENSMUSP00000118506 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000131379]
AlphaFold Q80VJ6
Predicted Effect probably benign
Transcript: ENSMUST00000131379
AA Change: C381Y

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000118506
Gene: ENSMUSG00000054272
AA Change: C381Y

DomainStartEndE-ValueType
Pfam:SCAN 43 122 3.7e-17 PFAM
low complexity region 181 197 N/A INTRINSIC
ZnF_C2H2 395 417 2.75e-3 SMART
ZnF_C2H2 424 446 7.68e0 SMART
ZnF_C2H2 452 474 4.17e-3 SMART
ZnF_C2H2 480 503 3.83e-2 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Compound heterozygous knock-out mice display no phenotype. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c21 C T 13: 4,631,139 (GRCm39) probably benign Het
Alpk2 A G 18: 65,482,400 (GRCm39) L69P probably damaging Het
C3 G T 17: 57,530,949 (GRCm39) P384Q probably damaging Het
Cobll1 T C 2: 64,928,581 (GRCm39) E953G probably damaging Het
Dnaaf9 T C 2: 130,619,156 (GRCm39) T281A probably benign Het
Dnmt1 C T 9: 20,821,081 (GRCm39) E1269K possibly damaging Het
Dync2h1 T C 9: 7,145,611 (GRCm39) R1012G probably benign Het
Fbxw24 T A 9: 109,434,041 (GRCm39) Q423L probably benign Het
Flg2 T C 3: 93,109,678 (GRCm39) S569P unknown Het
Ier5 A G 1: 154,975,139 (GRCm39) I13T probably damaging Het
Kat6a A G 8: 23,429,337 (GRCm39) D1564G possibly damaging Het
Lcn5 T C 2: 25,550,729 (GRCm39) V139A probably benign Het
Naca A G 10: 127,883,982 (GRCm39) S2138G probably damaging Het
Or1j15 T G 2: 36,458,838 (GRCm39) V76G probably damaging Het
Or5p59 T A 7: 107,702,851 (GRCm39) S112T probably benign Het
Or5w14 T G 2: 87,541,477 (GRCm39) M258L possibly damaging Het
Or6c66 A C 10: 129,461,432 (GRCm39) F166C probably damaging Het
Or6c74 A G 10: 129,869,761 (GRCm39) T89A probably benign Het
Pcdhgb8 A G 18: 37,958,089 (GRCm39) T813A probably damaging Het
Pkd1l1 T C 11: 8,851,345 (GRCm39) T696A probably benign Het
Rif1 T G 2: 51,985,960 (GRCm39) H648Q probably damaging Het
Secisbp2l C A 2: 125,582,245 (GRCm39) K1070N probably benign Het
Spock3 G A 8: 63,801,993 (GRCm39) R327Q probably benign Het
Trpm2 A G 10: 77,768,114 (GRCm39) I795T probably benign Het
Ube4b T C 4: 149,414,726 (GRCm39) I1128V probably benign Het
Vmn1r225 A T 17: 20,723,081 (GRCm39) D174V probably damaging Het
Xpnpep3 T A 15: 81,320,969 (GRCm39) Y283N possibly damaging Het
Zfp9 C T 6: 118,442,800 (GRCm39) A99T probably benign Het
Zfp944 A G 17: 22,562,615 (GRCm39) probably benign Het
Other mutations in Zscan4c
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5305:Zscan4c UTSW 7 10,743,462 (GRCm39) missense probably benign 0.00
R5771:Zscan4c UTSW 7 10,743,574 (GRCm39) missense probably benign 0.00
R6182:Zscan4c UTSW 7 10,740,709 (GRCm39) missense probably benign 0.05
R6431:Zscan4c UTSW 7 10,740,856 (GRCm39) missense probably benign 0.02
R7638:Zscan4c UTSW 7 10,743,658 (GRCm39) missense possibly damaging 0.96
R7920:Zscan4c UTSW 7 10,743,699 (GRCm39) missense possibly damaging 0.53
R9172:Zscan4c UTSW 7 10,743,819 (GRCm39) missense possibly damaging 0.71
R9181:Zscan4c UTSW 7 10,743,741 (GRCm39) missense probably benign 0.00
R9265:Zscan4c UTSW 7 10,740,824 (GRCm39) missense probably benign 0.09
R9499:Zscan4c UTSW 7 10,740,853 (GRCm39) missense probably benign
Posted On 2013-06-21