Incidental Mutation 'IGL00927:Zscan30'
ID29414
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zscan30
Ensembl Gene ENSMUSG00000024274
Gene Namezinc finger and SCAN domain containing 30
SynonymsC230097I24Rik, Zfp397os
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.094) question?
Stock #IGL00927
Quality Score
Status
Chromosome18
Chromosomal Location23970975-23981555 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to C at 23971777 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000115829
SMART Domains Protein: ENSMUSP00000111495
Gene: ENSMUSG00000024274

DomainStartEndE-ValueType
SCAN 44 149 7.42e-54 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224144
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310033P09Rik A G 11: 59,208,848 T92A probably damaging Het
Ankhd1 A G 18: 36,632,072 S1007G probably benign Het
Cabp4 A T 19: 4,139,407 S50R possibly damaging Het
Camp A T 9: 109,849,268 L56Q probably damaging Het
Cblb A G 16: 52,166,098 N568S probably benign Het
Ccr6 C A 17: 8,255,993 T10K probably benign Het
Chit1 T C 1: 134,145,254 F106S probably damaging Het
Cyb561d1 A G 3: 108,199,627 L34P probably damaging Het
Dcun1d1 A T 3: 35,920,965 probably benign Het
Deup1 A G 9: 15,610,671 probably benign Het
Erich1 A G 8: 14,033,518 F184S probably damaging Het
Fmnl3 A G 15: 99,337,628 probably null Het
Grk2 T C 19: 4,287,954 N508S probably benign Het
Herc4 A G 10: 63,273,537 I184V probably benign Het
Hnrnpm C A 17: 33,649,902 R517L probably damaging Het
Kif3b G A 2: 153,316,461 A61T possibly damaging Het
Kmt2d G A 15: 98,845,009 probably benign Het
Lrrc7 C A 3: 158,161,090 V1005L possibly damaging Het
Lrrtm1 A T 6: 77,244,063 M168L probably benign Het
Ndc1 C T 4: 107,384,780 probably benign Het
Nphs1 A G 7: 30,460,739 probably benign Het
Olfr692 A T 7: 105,369,247 Y298F probably damaging Het
Pbld2 T C 10: 63,071,955 V200A probably benign Het
Pcdhb21 A G 18: 37,514,553 Y245C probably damaging Het
Pcm1 A G 8: 41,287,881 T1055A probably damaging Het
Plcl2 C T 17: 50,606,920 S319L probably benign Het
Plekha8 C A 6: 54,629,837 Y372* probably null Het
Ralb T A 1: 119,471,776 N184I probably benign Het
Robo3 C T 9: 37,427,754 probably null Het
Slc41a1 T A 1: 131,839,176 L144H probably damaging Het
Smg1 C T 7: 118,140,632 G3364D probably damaging Het
Theg A G 10: 79,576,599 S329P probably damaging Het
Ttc26 T C 6: 38,382,220 probably benign Het
Vmn1r123 T A 7: 21,162,291 V36D possibly damaging Het
Zbtb7c T C 18: 76,145,850 S460P possibly damaging Het
Other mutations in Zscan30
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02427:Zscan30 APN 18 23971476 exon noncoding transcript
R0349:Zscan30 UTSW 18 23971398 exon noncoding transcript
R1857:Zscan30 UTSW 18 23971467 exon noncoding transcript
R1858:Zscan30 UTSW 18 23971467 exon noncoding transcript
R1859:Zscan30 UTSW 18 23971467 exon noncoding transcript
R2114:Zscan30 UTSW 18 23971116 exon noncoding transcript
R5423:Zscan30 UTSW 18 23971716 exon noncoding transcript
Posted On2013-04-17