Incidental Mutation 'IGL02701:Zmynd12'
ID 304150
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zmynd12
Ensembl Gene ENSMUSG00000070806
Gene Name zinc finger, MYND domain containing 12
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL02701
Quality Score
Status
Chromosome 4
Chromosomal Location 119279881-119311096 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to T at 119301952 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000092414 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094819]
AlphaFold A2BGJ5
Predicted Effect probably benign
Transcript: ENSMUST00000094819
SMART Domains Protein: ENSMUSP00000092414
Gene: ENSMUSG00000070806

DomainStartEndE-ValueType
Pfam:zf-MYND 17 54 1.2e-10 PFAM
low complexity region 70 87 N/A INTRINSIC
Blast:TPR 88 121 2e-14 BLAST
Pfam:TPR_8 130 157 3.9e-3 PFAM
Pfam:TPR_8 172 196 1.5e-2 PFAM
Blast:TPR 214 247 2e-13 BLAST
low complexity region 305 319 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129150
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134147
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap21 A G 2: 20,896,902 (GRCm39) C125R probably damaging Het
Blmh A G 11: 76,862,736 (GRCm39) D383G probably benign Het
Brca1 T C 11: 101,416,061 (GRCm39) E691G probably damaging Het
Chrm3 G A 13: 9,928,500 (GRCm39) R179* probably null Het
Cnrip1 A G 11: 17,028,415 (GRCm39) T116A probably benign Het
Csmd2 T C 4: 128,389,934 (GRCm39) V2223A probably benign Het
Dalrd3 T A 9: 108,449,483 (GRCm39) V143D possibly damaging Het
Ddx60 A T 8: 62,432,375 (GRCm39) I886L probably damaging Het
Dennd4a T C 9: 64,804,635 (GRCm39) F1325L possibly damaging Het
Dnmt3l A T 10: 77,890,856 (GRCm39) T253S probably benign Het
Fads2b A G 2: 85,314,513 (GRCm39) L480P probably damaging Het
Ftdc1 G A 16: 58,436,170 (GRCm39) S51L probably benign Het
Gde1 T A 7: 118,297,860 (GRCm39) T9S probably damaging Het
Ggcx T A 6: 72,395,455 (GRCm39) probably benign Het
Hspg2 C T 4: 137,284,485 (GRCm39) A3481V probably damaging Het
Igf1r T C 7: 67,850,997 (GRCm39) Y931H possibly damaging Het
Ighv12-3 A C 12: 114,330,421 (GRCm39) S25A probably damaging Het
Itga5 A C 15: 103,256,193 (GRCm39) C920G probably damaging Het
Kmt5b A G 19: 3,846,681 (GRCm39) D118G probably benign Het
Lrp1b T G 2: 41,136,029 (GRCm39) N1647T possibly damaging Het
Lrrc71 T C 3: 87,649,079 (GRCm39) E363G probably benign Het
Mapk1 A G 16: 16,833,770 (GRCm39) Y41C probably benign Het
Mib1 T C 18: 10,747,357 (GRCm39) V178A probably damaging Het
Or13c7d A G 4: 43,770,366 (GRCm39) I215T probably benign Het
Or5m10b A G 2: 85,699,802 (GRCm39) I289V probably benign Het
Or5p52 A T 7: 107,502,649 (GRCm39) T242S probably benign Het
Plb1 T C 5: 32,521,541 (GRCm39) V1464A unknown Het
Plekhg5 T C 4: 152,187,479 (GRCm39) S82P probably damaging Het
Plxna4 T C 6: 32,494,494 (GRCm39) T41A probably benign Het
Ppip5k1 A C 2: 121,147,130 (GRCm39) probably null Het
Pttg1ip2 A G 5: 5,516,623 (GRCm39) probably null Het
Rpl14 T C 9: 120,402,639 (GRCm39) probably benign Het
Slc44a2 T C 9: 21,259,247 (GRCm39) F554L probably benign Het
Slco1b2 T A 6: 141,631,271 (GRCm39) V635E probably benign Het
Sv2a T A 3: 96,094,447 (GRCm39) C261S probably damaging Het
Thbs2 T C 17: 14,903,623 (GRCm39) I353V probably benign Het
Tspan4 G A 7: 141,071,941 (GRCm39) V205M probably damaging Het
Vezf1 A T 11: 87,967,047 (GRCm39) R93* probably null Het
Wwox T A 8: 115,433,108 (GRCm39) V258D probably damaging Het
Other mutations in Zmynd12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01603:Zmynd12 APN 4 119,299,117 (GRCm39) critical splice donor site probably null
IGL02113:Zmynd12 APN 4 119,291,194 (GRCm39) missense probably damaging 1.00
IGL03287:Zmynd12 APN 4 119,310,776 (GRCm39) missense probably damaging 1.00
IGL03138:Zmynd12 UTSW 4 119,280,186 (GRCm39) missense probably damaging 1.00
R4531:Zmynd12 UTSW 4 119,280,194 (GRCm39) critical splice donor site probably null
R5078:Zmynd12 UTSW 4 119,302,047 (GRCm39) missense probably damaging 1.00
R5687:Zmynd12 UTSW 4 119,299,098 (GRCm39) missense probably damaging 0.96
R6995:Zmynd12 UTSW 4 119,310,772 (GRCm39) missense probably benign 0.00
R7707:Zmynd12 UTSW 4 119,302,063 (GRCm39) missense probably damaging 1.00
R8393:Zmynd12 UTSW 4 119,305,352 (GRCm39) missense probably damaging 1.00
R8911:Zmynd12 UTSW 4 119,294,286 (GRCm39) missense probably damaging 1.00
R8952:Zmynd12 UTSW 4 119,302,081 (GRCm39) critical splice donor site probably null
X0019:Zmynd12 UTSW 4 119,307,565 (GRCm39) missense probably benign 0.04
Z1176:Zmynd12 UTSW 4 119,280,074 (GRCm39) unclassified probably benign
Posted On 2015-04-16