Incidental Mutation 'IGL03156:Gm7276'
ID411266
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7276
Ensembl Gene ENSMUSG00000073532
Gene Namepredicted gene 7276
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.094) question?
Stock #IGL03156
Quality Score
Status
Chromosome18
Chromosomal Location77185006-77186257 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) C to T at 77185603 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000078566 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075290] [ENSMUST00000079618] [ENSMUST00000097520]
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
1700017D01Rik A T 19: 11,105,750 I102K possibly damaging Het
4930430A15Rik T C 2: 111,200,412 D12G possibly damaging Het
Abca16 T C 7: 120,423,851 I70T possibly damaging Het
Acot11 A G 4: 106,754,136 Y365H probably damaging Het
Bdp1 A G 13: 100,061,036 V947A probably benign Het
Ccdc159 G T 9: 21,929,475 V113L probably benign Het
Cep350 T C 1: 155,858,042 D3035G probably damaging Het
Clca1 T A 3: 145,013,911 I433F probably damaging Het
Cntn5 T C 9: 9,673,877 Y740C probably damaging Het
Dennd5a C A 7: 109,919,255 probably benign Het
Des G A 1: 75,362,996 E333K probably damaging Het
Dnah7a T C 1: 53,605,824 R1018G probably damaging Het
Eif2b2 G T 12: 85,219,721 A54S probably damaging Het
Hsbp1l1 A G 18: 80,235,519 probably benign Het
Iars G A 13: 49,703,179 G303S possibly damaging Het
Il18r1 A G 1: 40,498,368 E431G possibly damaging Het
Lrrc14b A G 13: 74,363,904 V19A probably benign Het
Map1lc3a T A 2: 155,277,009 I31N probably damaging Het
Obscn T C 11: 59,054,896 Y4163C probably damaging Het
Olfr478 T A 7: 108,032,351 probably benign Het
Pcsk1 A G 13: 75,131,951 T632A probably benign Het
Ppp1r15a A G 7: 45,525,171 L71P possibly damaging Het
Ptgs2 T G 1: 150,105,477 F504V probably damaging Het
Rimbp2 T G 5: 128,771,757 R908S probably damaging Het
Rnh1 T C 7: 141,163,183 N268S probably damaging Het
Sap30l T C 11: 57,806,168 probably null Het
Scara3 C T 14: 65,931,154 R338H probably damaging Het
Serpina12 T C 12: 104,037,899 Y158C probably damaging Het
Tmem237 A T 1: 59,109,127 D148E probably damaging Het
Trmt13 T C 3: 116,585,802 D232G probably benign Het
Zan T A 5: 137,463,939 T993S unknown Het
Zfp236 G A 18: 82,680,702 L85F probably damaging Het
Zfp352 G A 4: 90,224,087 D155N possibly damaging Het
Zfp867 T C 11: 59,465,008 probably benign Het
Zmiz2 T C 11: 6,399,536 F399L probably damaging Het
Other mutations in Gm7276
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1661:Gm7276 UTSW 18 77185570 unclassified probably benign
R1665:Gm7276 UTSW 18 77185570 unclassified probably benign
R1791:Gm7276 UTSW 18 77185735 unclassified probably benign
R6421:Gm7276 UTSW 18 77185670 unclassified probably benign
R7319:Gm7276 UTSW 18 77185520 missense unknown
R7412:Gm7276 UTSW 18 77185487 missense unknown
R8227:Gm7276 UTSW 18 77185462 missense unknown
Posted On2016-08-02