Incidental Mutation 'IGL01300:Gm1968'
ID 75223
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm1968
Ensembl Gene ENSMUSG00000075286
Gene Name predicted gene 1968
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # IGL01300
Quality Score
Status
Chromosome 16
Chromosomal Location 29776745-29797942 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 29781038 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000100016]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000100016
Predicted Effect noncoding transcript
Transcript: ENSMUST00000231469
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Anxa8 A G 14: 33,821,700 (GRCm39) D300G probably benign Het
Cacna1g T C 11: 94,324,738 (GRCm39) H1161R probably benign Het
Col14a1 G A 15: 55,331,372 (GRCm39) R1471Q unknown Het
Gm14496 A T 2: 181,642,753 (GRCm39) E808V probably damaging Het
Gzmb G A 14: 56,497,653 (GRCm39) R196C probably benign Het
Hkdc1 A G 10: 62,231,040 (GRCm39) probably benign Het
Itgal T A 7: 126,913,290 (GRCm39) V629E probably damaging Het
Jak2 T A 19: 29,287,083 (GRCm39) Y1050N probably damaging Het
Lrrc69 C T 4: 14,773,663 (GRCm39) probably benign Het
Mmd T C 11: 90,140,537 (GRCm39) M1T probably null Het
Myh6 A G 14: 55,200,548 (GRCm39) V191A possibly damaging Het
Mynn A G 3: 30,667,755 (GRCm39) N485S probably damaging Het
Naa30 C T 14: 49,410,714 (GRCm39) T214M probably damaging Het
Ncoa3 A T 2: 165,910,381 (GRCm39) T1265S probably benign Het
Or10al2 C A 17: 37,983,778 (GRCm39) T288K probably damaging Het
Or1j10 T C 2: 36,267,054 (GRCm39) S89P probably benign Het
Prex1 A G 2: 166,480,327 (GRCm39) C138R possibly damaging Het
Prom2 A T 2: 127,377,009 (GRCm39) L535H probably benign Het
Pros1 T C 16: 62,734,174 (GRCm39) F327L possibly damaging Het
Ros1 A G 10: 51,977,809 (GRCm39) M1479T probably benign Het
Scn9a G A 2: 66,318,397 (GRCm39) Q1465* probably null Het
Serpinb3b A G 1: 107,083,573 (GRCm39) probably benign Het
Sipa1l3 G A 7: 29,099,253 (GRCm39) Q339* probably null Het
Slc34a2 A C 5: 53,225,469 (GRCm39) probably null Het
Smc3 T A 19: 53,630,283 (GRCm39) probably benign Het
Tmem30a A G 9: 79,682,382 (GRCm39) probably null Het
Trappc11 A T 8: 47,954,903 (GRCm39) D878E probably benign Het
Trrap C T 5: 144,741,628 (GRCm39) T1325M probably damaging Het
Ttc12 A T 9: 49,359,222 (GRCm39) probably benign Het
Vmn1r237 T A 17: 21,534,337 (GRCm39) I20N probably damaging Het
Vmn2r115 T A 17: 23,578,755 (GRCm39) S743T probably damaging Het
Vmn2r74 A G 7: 85,606,414 (GRCm39) Y311H probably benign Het
Vnn3 T A 10: 23,740,263 (GRCm39) F189I possibly damaging Het
Other mutations in Gm1968
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01293:Gm1968 APN 16 29,777,632 (GRCm39) exon noncoding transcript
R1539:Gm1968 UTSW 16 29,777,659 (GRCm39) exon noncoding transcript
R5339:Gm1968 UTSW 16 29,781,077 (GRCm39) exon noncoding transcript
R5359:Gm1968 UTSW 16 29,777,617 (GRCm39) exon noncoding transcript
R5610:Gm1968 UTSW 16 29,777,557 (GRCm39) exon noncoding transcript
R8227:Gm1968 UTSW 16 29,777,380 (GRCm39) missense noncoding transcript
Posted On 2013-10-07