Incidental Mutation 'IGL03156:Gm7276'
ID 411266
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7276
Ensembl Gene ENSMUSG00000073532
Gene Name predicted gene 7276
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.095) question?
Stock # IGL03156
Quality Score
Status
Chromosome 18
Chromosomal Location 77271965-77274059 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to T at 77273299 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000078566 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075290] [ENSMUST00000079618] [ENSMUST00000097520]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000075290
SMART Domains Protein: ENSMUSP00000074764
Gene: ENSMUSG00000025425

DomainStartEndE-ValueType
transmembrane domain 12 34 N/A INTRINSIC
Pfam:Glyco_transf_29 152 407 6.4e-74 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000079618
SMART Domains Protein: ENSMUSP00000078566
Gene: ENSMUSG00000025425

DomainStartEndE-ValueType
transmembrane domain 12 34 N/A INTRINSIC
Pfam:Glyco_transf_29 112 372 5.4e-79 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000097520
AA Change: R145Q
SMART Domains Protein: ENSMUSP00000095127
Gene: ENSMUSG00000073532
AA Change: R145Q

DomainStartEndE-ValueType
low complexity region 2 21 N/A INTRINSIC
low complexity region 61 82 N/A INTRINSIC
low complexity region 143 157 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T C 7: 120,023,074 (GRCm39) I70T possibly damaging Het
Acot11 A G 4: 106,611,333 (GRCm39) Y365H probably damaging Het
Bdp1 A G 13: 100,197,544 (GRCm39) V947A probably benign Het
Ccdc159 G T 9: 21,840,771 (GRCm39) V113L probably benign Het
Cep350 T C 1: 155,733,788 (GRCm39) D3035G probably damaging Het
Clca3a1 T A 3: 144,719,672 (GRCm39) I433F probably damaging Het
Cntn5 T C 9: 9,673,882 (GRCm39) Y740C probably damaging Het
Dennd5a C A 7: 109,518,462 (GRCm39) probably benign Het
Des G A 1: 75,339,640 (GRCm39) E333K probably damaging Het
Dnah7a T C 1: 53,644,983 (GRCm39) R1018G probably damaging Het
Eif2b2 G T 12: 85,266,495 (GRCm39) A54S probably damaging Het
Hsbp1l1 A G 18: 80,278,734 (GRCm39) probably benign Het
Iars1 G A 13: 49,856,655 (GRCm39) G303S possibly damaging Het
Il18r1 A G 1: 40,537,528 (GRCm39) E431G possibly damaging Het
Lrrc14b A G 13: 74,512,023 (GRCm39) V19A probably benign Het
Map1lc3a T A 2: 155,118,929 (GRCm39) I31N probably damaging Het
Ms4a20 A T 19: 11,083,114 (GRCm39) I102K possibly damaging Het
Obscn T C 11: 58,945,722 (GRCm39) Y4163C probably damaging Het
Or5p6 T A 7: 107,631,558 (GRCm39) probably benign Het
Pcsk1 A G 13: 75,280,070 (GRCm39) T632A probably benign Het
Potefam1 T C 2: 111,030,757 (GRCm39) D12G possibly damaging Het
Ppp1r15a A G 7: 45,174,595 (GRCm39) L71P possibly damaging Het
Ptgs2 T G 1: 149,981,228 (GRCm39) F504V probably damaging Het
Rimbp2 T G 5: 128,848,821 (GRCm39) R908S probably damaging Het
Rnh1 T C 7: 140,743,096 (GRCm39) N268S probably damaging Het
Sap30l T C 11: 57,696,994 (GRCm39) probably null Het
Scara3 C T 14: 66,168,603 (GRCm39) R338H probably damaging Het
Serpina12 T C 12: 104,004,158 (GRCm39) Y158C probably damaging Het
Tmem237 A T 1: 59,148,286 (GRCm39) D148E probably damaging Het
Trmt13 T C 3: 116,379,451 (GRCm39) D232G probably benign Het
Zan T A 5: 137,462,201 (GRCm39) T993S unknown Het
Zfp236 G A 18: 82,698,827 (GRCm39) L85F probably damaging Het
Zfp352 G A 4: 90,112,324 (GRCm39) D155N possibly damaging Het
Zfp867 T C 11: 59,355,834 (GRCm39) probably benign Het
Zmiz2 T C 11: 6,349,536 (GRCm39) F399L probably damaging Het
Other mutations in Gm7276
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1661:Gm7276 UTSW 18 77,273,266 (GRCm39) unclassified probably benign
R1665:Gm7276 UTSW 18 77,273,266 (GRCm39) unclassified probably benign
R1791:Gm7276 UTSW 18 77,273,431 (GRCm39) unclassified probably benign
R6421:Gm7276 UTSW 18 77,273,366 (GRCm39) unclassified probably benign
R7319:Gm7276 UTSW 18 77,273,216 (GRCm39) missense unknown
R7412:Gm7276 UTSW 18 77,273,183 (GRCm39) missense unknown
R8227:Gm7276 UTSW 18 77,273,158 (GRCm39) missense unknown
R9123:Gm7276 UTSW 18 77,273,147 (GRCm39) missense unknown
R9125:Gm7276 UTSW 18 77,273,147 (GRCm39) missense unknown
Posted On 2016-08-02