Incidental Mutation 'IGL01060:Gm12887'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm12887
Ensembl Gene ENSMUSG00000078575
Gene Namepredicted gene 12887
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.084) question?
Stock #IGL01060
Quality Score
Chromosomal Location121614271-121622103 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) C to T at 121616413 bp
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

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