Incidental Mutation 'IGL00272:Gm26870'
ID 88887
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm26870
Ensembl Gene ENSMUSG00000097312
Gene Name predicted gene, 26870
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00272
Quality Score
Status
Chromosome 9
Chromosomal Location (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 3002340 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000136541 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000151376] [ENSMUST00000177722] [ENSMUST00000178077] [ENSMUST00000178348] [ENSMUST00000179881]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000151376
SMART Domains Protein: ENSMUSP00000132394
Gene: ENSMUSG00000091028

DomainStartEndE-ValueType
internal_repeat_2 8 50 1.25e-5 PROSPERO
internal_repeat_1 11 88 6.98e-39 PROSPERO
internal_repeat_2 66 108 1.25e-5 PROSPERO
internal_repeat_1 89 166 6.98e-39 PROSPERO
transmembrane domain 187 209 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000177722
SMART Domains Protein: ENSMUSP00000136598
Gene: ENSMUSG00000096385

DomainStartEndE-ValueType
internal_repeat_1 1 19 1.14e-8 PROSPERO
transmembrane domain 26 48 N/A INTRINSIC
transmembrane domain 68 90 N/A INTRINSIC
internal_repeat_1 118 136 1.14e-8 PROSPERO
transmembrane domain 156 178 N/A INTRINSIC
transmembrane domain 200 222 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000178077
SMART Domains Protein: ENSMUSP00000136761
Gene: ENSMUSG00000096385

DomainStartEndE-ValueType
internal_repeat_1 1 19 4.71e-8 PROSPERO
transmembrane domain 26 48 N/A INTRINSIC
transmembrane domain 68 90 N/A INTRINSIC
internal_repeat_1 118 136 4.71e-8 PROSPERO
transmembrane domain 156 178 N/A INTRINSIC
transmembrane domain 200 222 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000178348
SMART Domains Protein: ENSMUSP00000137273
Gene: ENSMUSG00000096385

DomainStartEndE-ValueType
internal_repeat_1 1 48 1.34e-9 PROSPERO
transmembrane domain 77 99 N/A INTRINSIC
internal_repeat_1 117 165 1.34e-9 PROSPERO
transmembrane domain 196 218 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000179881
SMART Domains Protein: ENSMUSP00000136541
Gene: ENSMUSG00000096385

DomainStartEndE-ValueType
internal_repeat_1 1 46 5.29e-7 PROSPERO
transmembrane domain 53 72 N/A INTRINSIC
transmembrane domain 77 99 N/A INTRINSIC
internal_repeat_1 117 182 5.29e-7 PROSPERO
transmembrane domain 195 217 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181242
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700030J22Rik A G 8: 117,700,279 (GRCm39) V41A probably damaging Het
Ankrd12 C T 17: 66,293,169 (GRCm39) V755I probably benign Het
Arrdc3 T C 13: 81,038,691 (GRCm39) S218P probably damaging Het
Bzw1 T C 1: 58,442,101 (GRCm39) V292A possibly damaging Het
Cers2 T C 3: 95,229,211 (GRCm39) Y228H probably damaging Het
Dnaaf6 A G X: 139,006,711 (GRCm39) I197V probably benign Het
Egf C T 3: 129,505,098 (GRCm39) M625I probably benign Het
Fbxw8 A T 5: 118,206,162 (GRCm39) H595Q probably benign Het
Fshr T A 17: 89,292,699 (GRCm39) I660F probably benign Het
Gapdh C T 6: 125,139,470 (GRCm39) V267M probably damaging Het
Ginm1 T C 10: 7,668,460 (GRCm39) probably benign Het
Gja1 A G 10: 56,264,418 (GRCm39) D259G probably benign Het
Gm21814 T A 6: 149,483,502 (GRCm39) noncoding transcript Het
Habp2 G A 19: 56,306,264 (GRCm39) C482Y probably damaging Het
Knl1 A C 2: 118,894,564 (GRCm39) N79T probably damaging Het
Lama3 G A 18: 12,624,605 (GRCm39) C1450Y probably damaging Het
Lats2 T C 14: 57,929,026 (GRCm39) T950A probably benign Het
Map2k2 T A 10: 80,956,907 (GRCm39) M95K probably damaging Het
Med12l T A 3: 58,949,757 (GRCm39) I160N probably damaging Het
Or9m1b A G 2: 87,836,988 (GRCm39) S45P probably damaging Het
Or9m2 A T 2: 87,820,782 (GRCm39) D109V probably damaging Het
Pes1 T C 11: 3,926,803 (GRCm39) S362P probably damaging Het
Ppp6r2 G T 15: 89,170,016 (GRCm39) A844S probably benign Het
Rnf130 A G 11: 49,984,623 (GRCm39) I308V probably damaging Het
Scn11a T C 9: 119,645,669 (GRCm39) N95S probably damaging Het
Shoc1 A G 4: 59,086,961 (GRCm39) F284L probably benign Het
Skint2 A G 4: 112,481,409 (GRCm39) T91A probably damaging Het
Smg1 A G 7: 117,797,494 (GRCm39) probably benign Het
Snapc1 A G 12: 74,015,148 (GRCm39) probably null Het
Stard10 A T 7: 100,971,173 (GRCm39) Y47F probably damaging Het
Tenm3 C T 8: 48,870,095 (GRCm39) V233I probably damaging Het
Tex14 G A 11: 87,426,469 (GRCm39) S1165N probably damaging Het
Unc5a A G 13: 55,143,633 (GRCm39) I106V probably benign Het
Vps54 T A 11: 21,227,909 (GRCm39) Y275N possibly damaging Het
Wdr87-ps G T 7: 29,237,047 (GRCm39) noncoding transcript Het
Posted On 2013-12-03