Incidental Mutation 'IGL02636:Zfp353-ps'
ID301508
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp353-ps
Ensembl Gene ENSMUSG00000095057
Gene Namezinc finger protein 353, pseudogene
SynonymsZfp353
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.070) question?
Stock #IGL02636
Quality Score
Status
Chromosome8
Chromosomal Location42081460-42083109 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to A at 42082440 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000107130
SMART Domains Protein: ENSMUSP00000102747
Gene: ENSMUSG00000095057

DomainStartEndE-ValueType
ZnF_C2H2 457 481 9.9e-5 SMART
ZnF_C2H2 487 511 2.6e-5 SMART
ZnF_C2H2 517 540 6.1e-4 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alms1 C A 6: 85,628,654 Q1960K probably benign Het
Arhgef40 T A 14: 51,997,408 V1056E probably damaging Het
Cdh26 T A 2: 178,449,962 F105I probably damaging Het
Cep162 A T 9: 87,248,379 D59E possibly damaging Het
Cngb3 A T 4: 19,396,690 T348S probably damaging Het
Eci3 A T 13: 34,946,980 probably null Het
Gapvd1 A G 2: 34,725,404 I409T probably benign Het
Golga2 T C 2: 32,296,723 probably null Het
Hoxd3 G A 2: 74,746,954 A393T probably benign Het
Htr5a T C 5: 27,842,660 F71S probably damaging Het
Hyou1 T C 9: 44,381,410 probably null Het
Igsf6 C A 7: 121,067,280 probably benign Het
Klrb1c C A 6: 128,788,552 C25F probably benign Het
Lrguk C A 6: 34,090,188 T483K probably damaging Het
Lrpprc A T 17: 84,753,104 probably benign Het
Lrrk1 A T 7: 66,308,659 probably null Het
Megf8 G A 7: 25,358,432 G2098D probably damaging Het
Nfkbia T C 12: 55,491,173 Q165R possibly damaging Het
Nipsnap2 A G 5: 129,745,290 probably benign Het
Phykpl C T 11: 51,598,713 T382I probably damaging Het
Prdm10 A G 9: 31,329,681 D206G possibly damaging Het
Rab26 T C 17: 24,533,559 S9G probably benign Het
Sema3e C A 5: 14,225,656 N258K probably benign Het
Slfn10-ps T A 11: 83,030,145 noncoding transcript Het
Tgm5 A T 2: 121,076,796 C149S probably damaging Het
Timp4 C T 6: 115,249,824 probably null Het
Traf7 T C 17: 24,512,990 K251E probably benign Het
Ugcg G T 4: 59,207,763 R34L possibly damaging Het
Unc13d T C 11: 116,073,618 H300R probably damaging Het
Vmn1r20 G T 6: 57,431,761 C24F probably benign Het
Vmn2r13 T C 5: 109,192,017 R31G probably damaging Het
Vsig10l A G 7: 43,463,578 T87A possibly damaging Het
Other mutations in Zfp353-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2040:Zfp353-ps UTSW 8 42082296 exon noncoding transcript
R2111:Zfp353-ps UTSW 8 42082968 exon noncoding transcript
R3922:Zfp353-ps UTSW 8 42083012 exon noncoding transcript
R4679:Zfp353-ps UTSW 8 42082214 exon noncoding transcript
R5270:Zfp353-ps UTSW 8 42081535 exon noncoding transcript
R5524:Zfp353-ps UTSW 8 42082563 exon noncoding transcript
R5772:Zfp353-ps UTSW 8 42082610 exon noncoding transcript
Posted On2015-04-16