Incidental Mutation 'IGL02382:Gm14406'
ID 291430
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm14406
Ensembl Gene ENSMUSG00000078865
Gene Name predicted gene 14406
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02382
Quality Score
Status
Chromosome 2
Chromosomal Location 177260997-177270003 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to A at 177260988 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104573 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108943] [ENSMUST00000108945]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000108943
SMART Domains Protein: ENSMUSP00000104571
Gene: ENSMUSG00000078865

DomainStartEndE-ValueType
KRAB 4 64 1.1e-11 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000108945
SMART Domains Protein: ENSMUSP00000104573
Gene: ENSMUSG00000078865

DomainStartEndE-ValueType
KRAB 4 66 1.47e-12 SMART
ZnF_C2H2 78 97 2.2e2 SMART
ZnF_C2H2 103 125 7.78e-3 SMART
ZnF_C2H2 131 153 2.12e-4 SMART
ZnF_C2H2 159 181 2.43e-4 SMART
ZnF_C2H2 187 209 2.53e-2 SMART
ZnF_C2H2 215 237 4.87e-4 SMART
ZnF_C2H2 243 265 1.12e-3 SMART
ZnF_C2H2 271 293 4.54e-4 SMART
ZnF_C2H2 299 321 3.04e-5 SMART
ZnF_C2H2 327 349 4.87e-4 SMART
ZnF_C2H2 355 377 1.03e-2 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aim2 A G 1: 173,287,315 (GRCm39) probably null Het
Aoc2 T C 11: 101,217,498 (GRCm39) L527P probably damaging Het
Arhgef15 C A 11: 68,844,856 (GRCm39) R247L probably damaging Het
Armcx2 T C X: 133,706,416 (GRCm39) T406A probably benign Het
Armcx5 T C X: 134,647,577 (GRCm39) F551S probably damaging Het
Ccrl2 T C 9: 110,884,947 (GRCm39) K184E probably benign Het
Cenpe A G 3: 134,953,147 (GRCm39) I1534V probably benign Het
Cflar T A 1: 58,791,840 (GRCm39) I381K probably benign Het
Crb1 T A 1: 139,165,352 (GRCm39) N924I probably damaging Het
Crebbp A G 16: 3,925,934 (GRCm39) V729A probably damaging Het
Dab2 T A 15: 6,466,468 (GRCm39) V615D possibly damaging Het
Edrf1 T C 7: 133,252,344 (GRCm39) probably benign Het
Ep400 G A 5: 110,849,594 (GRCm39) T1409I unknown Het
Kptn T A 7: 15,857,945 (GRCm39) S258T probably benign Het
Mbnl1 G T 3: 60,532,563 (GRCm39) E291* probably null Het
Mcm4 A T 16: 15,442,602 (GRCm39) L843Q probably damaging Het
Mgrn1 A G 16: 4,740,482 (GRCm39) N274D probably damaging Het
Or13a21 T A 7: 139,999,516 (GRCm39) T57S possibly damaging Het
Or8d1 G A 9: 38,766,364 (GRCm39) G2D probably benign Het
Phactr4 A T 4: 132,098,152 (GRCm39) V335E probably damaging Het
Ptgr2 T C 12: 84,360,722 (GRCm39) S331P probably damaging Het
Ranbp9 T C 13: 43,589,622 (GRCm39) probably null Het
Setd5 A G 6: 113,120,601 (GRCm39) T937A probably benign Het
Slc27a4 C T 2: 29,699,855 (GRCm39) R265C probably damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Tenm3 A G 8: 48,688,511 (GRCm39) Y2359H probably damaging Het
Tnip3 T C 6: 65,591,779 (GRCm39) probably null Het
Zfc3h1 C T 10: 115,252,781 (GRCm39) Q1365* probably null Het
Other mutations in Gm14406
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01023:Gm14406 APN 2 177,261,032 (GRCm39) missense probably damaging 1.00
R9602:Gm14406 UTSW 2 177,261,028 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16