Incidental Mutation 'IGL03156:Gm7276'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7276
Ensembl Gene ENSMUSG00000073532
Gene Namepredicted gene 7276
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.094) question?
Stock #IGL03156
Quality Score
Chromosomal Location77185006-77186257 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) C to T at 77185603 bp
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

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

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

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