Incidental Mutation 'IGL01060:Gm12887'
ID50822
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm12887
Ensembl Gene ENSMUSG00000078575
Gene Namepredicted gene 12887
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.084) question?
Stock #IGL01060
Quality Score
Status
Chromosome4
Chromosomal Location121614271-121622103 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) C to T at 121616413 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101872 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106265]
Predicted Effect probably benign
Transcript: ENSMUST00000106265
SMART Domains Protein: ENSMUSP00000101872
Gene: ENSMUSG00000078575

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:Palm_thioest 37 119 2.4e-10 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110038F14Rik G A 15: 76,950,275 V124I probably damaging Het
Anks4b A G 7: 120,173,925 T3A possibly damaging Het
Arhgef26 T A 3: 62,340,121 S209T probably benign Het
Ccdc78 A G 17: 25,788,832 D281G probably damaging Het
Ccnb3 A T X: 6,980,274 N1362K probably benign Het
Dnah2 T C 11: 69,478,092 N1662S possibly damaging Het
Ern2 T A 7: 122,170,092 R904W probably damaging Het
Fam120c C T X: 151,469,587 P1045S probably benign Het
Gpld1 G A 13: 24,982,566 G627S probably damaging Het
Ikbkap C T 4: 56,784,537 probably null Het
Krt77 T A 15: 101,860,880 probably benign Het
Ltf A T 9: 111,022,882 probably null Het
Map3k6 G T 4: 133,247,302 probably null Het
Nsd1 G A 13: 55,263,429 G1431D probably damaging Het
Plekhm2 C T 4: 141,642,645 probably null Het
Popdc2 T A 16: 38,373,965 N249K probably damaging Het
Ppm1h A G 10: 122,907,571 D400G possibly damaging Het
Rps6ka1 A T 4: 133,860,870 S320T probably damaging Het
Rsph6a C T 7: 19,054,868 R42* probably null Het
Sap130 T C 18: 31,715,443 L967P probably damaging Het
Smyd2 T C 1: 189,897,470 E121G possibly damaging Het
Sspo G A 6: 48,449,479 W144* probably null Het
Taar6 A G 10: 23,985,072 V192A probably benign Het
Tbc1d24 A T 17: 24,185,828 V114E probably damaging Het
Trim16 T C 11: 62,820,704 I67T probably benign Het
Ttll7 A G 3: 146,909,582 D267G possibly damaging Het
Ttn T C 2: 76,889,729 probably benign Het
Vmn2r56 T A 7: 12,713,089 I379F probably damaging Het
Zfp14 T C 7: 30,038,085 T492A probably damaging Het
Other mutations in Gm12887
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02113:Gm12887 APN 4 121616495 missense probably benign 0.32
R0055:Gm12887 UTSW 4 121616469 missense probably damaging 0.98
R0055:Gm12887 UTSW 4 121616469 missense probably damaging 0.98
R1673:Gm12887 UTSW 4 121616458 missense probably damaging 0.98
R1784:Gm12887 UTSW 4 121616518 missense probably benign 0.44
R1843:Gm12887 UTSW 4 121622030 missense probably damaging 0.98
R4231:Gm12887 UTSW 4 121622102 start codon destroyed probably null 0.53
R5258:Gm12887 UTSW 4 121615700 missense probably benign
R6528:Gm12887 UTSW 4 121615637 missense probably damaging 1.00
R8037:Gm12887 UTSW 4 121615690 missense probably damaging 1.00
Posted On2013-06-21