Incidental Mutation 'IGL03367:Gm11149'
ID 420156
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11149
Ensembl Gene ENSMUSG00000079564
Gene Name predicted gene 11149
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL03367
Quality Score
Status
Chromosome 9
Chromosomal Location 49429588-49479325 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to A at 49457646 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000114476] [ENSMUST00000166811] [ENSMUST00000192584] [ENSMUST00000193547]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000068730
Predicted Effect probably benign
Transcript: ENSMUST00000114476
SMART Domains Protein: ENSMUSP00000110120
Gene: ENSMUSG00000039542

DomainStartEndE-ValueType
IGc2 32 103 2.88e-4 SMART
IGc2 130 196 6.35e-6 SMART
IGc2 226 295 6.38e-20 SMART
IGc2 321 393 4.12e-14 SMART
IGc2 418 487 9.7e-11 SMART
FN3 501 586 4.77e-8 SMART
FN3 602 683 6.97e-1 SMART
low complexity region 711 725 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000166811
SMART Domains Protein: ENSMUSP00000130668
Gene: ENSMUSG00000039542

DomainStartEndE-ValueType
IGc2 32 103 2.88e-4 SMART
IGc2 130 196 6.35e-6 SMART
IGc2 226 295 6.38e-20 SMART
IGc2 321 393 4.12e-14 SMART
IGc2 418 487 9.7e-11 SMART
FN3 501 586 4.77e-8 SMART
FN3 602 683 6.97e-1 SMART
transmembrane domain 706 728 N/A INTRINSIC
low complexity region 797 809 N/A INTRINSIC
low complexity region 814 830 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000192584
SMART Domains Protein: ENSMUSP00000141700
Gene: ENSMUSG00000039542

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGc2 32 103 1.2e-6 SMART
IGc2 130 196 2.6e-8 SMART
IGc2 226 295 2.6e-22 SMART
IGc2 321 393 1.6e-16 SMART
IGc2 418 487 4e-13 SMART
FN3 501 586 2.4e-10 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000193547
SMART Domains Protein: ENSMUSP00000142275
Gene: ENSMUSG00000039542

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
IGc2 32 103 2.88e-4 SMART
IGc2 130 196 6.35e-6 SMART
IGc2 226 295 6.38e-20 SMART
IGc2 321 393 4.12e-14 SMART
IGc2 418 487 9.7e-11 SMART
FN3 501 586 4.77e-8 SMART
FN3 602 683 6.97e-1 SMART
transmembrane domain 706 728 N/A INTRINSIC
low complexity region 797 809 N/A INTRINSIC
low complexity region 814 830 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000194252
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215070
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215465
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216483
Predicted Effect probably benign
Transcript: ENSMUST00000194844
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc5 A T 16: 20,211,561 (GRCm39) probably benign Het
Adra1a G A 14: 66,875,438 (GRCm39) V138I possibly damaging Het
Alpk3 A G 7: 80,744,738 (GRCm39) I1278V probably benign Het
Asb6 A T 2: 30,714,691 (GRCm39) I185N possibly damaging Het
Atg9a A G 1: 75,164,601 (GRCm39) V121A probably benign Het
Cdc42bpb A G 12: 111,302,593 (GRCm39) Y155H probably damaging Het
Ceacam15 A C 7: 16,409,512 (GRCm39) S8A possibly damaging Het
Cep170b T A 12: 112,703,672 (GRCm39) D615E probably benign Het
Cntn6 G T 6: 104,781,299 (GRCm39) G462C probably damaging Het
Col8a2 A G 4: 126,205,991 (GRCm39) D667G probably damaging Het
Cyp2c29 A G 19: 39,317,659 (GRCm39) K382E probably damaging Het
Dgkd T C 1: 87,868,030 (GRCm39) probably null Het
Dkk2 C T 3: 131,883,838 (GRCm39) T246I probably damaging Het
Dnah5 T C 15: 28,234,473 (GRCm39) L294P possibly damaging Het
Erbb2 G T 11: 98,313,701 (GRCm39) probably null Het
Fn1 A G 1: 71,636,712 (GRCm39) F2147L probably benign Het
Gnrhr C T 5: 86,330,190 (GRCm39) V277I probably benign Het
H2-T10 T A 17: 36,431,285 (GRCm39) E129V possibly damaging Het
Hmgcr T C 13: 96,802,361 (GRCm39) T108A probably damaging Het
Hnrnph3 A T 10: 62,853,008 (GRCm39) I196N probably damaging Het
Insyn1 A G 9: 58,406,381 (GRCm39) H97R probably damaging Het
Kcnq5 T C 1: 21,473,289 (GRCm39) K653E probably damaging Het
Lgi2 C A 5: 52,719,502 (GRCm39) D100Y probably damaging Het
Mettl15 T A 2: 108,961,916 (GRCm39) H231L probably benign Het
Mthfd1l A G 10: 4,056,536 (GRCm39) probably benign Het
Pik3cg A G 12: 32,242,120 (GRCm39) S997P probably benign Het
Pla2g1b T C 5: 115,610,173 (GRCm39) C105R probably damaging Het
Ppil1 A T 17: 29,471,218 (GRCm39) probably benign Het
Pramel22 C T 4: 143,382,193 (GRCm39) V168I possibly damaging Het
Rbbp8 A G 18: 11,854,776 (GRCm39) T334A probably benign Het
Slc15a4 T C 5: 127,679,005 (GRCm39) Y445C probably damaging Het
Sox14 A C 9: 99,757,715 (GRCm39) I8S probably damaging Het
Spice1 A G 16: 44,176,541 (GRCm39) T44A probably damaging Het
Sult3a1 G T 10: 33,753,342 (GRCm39) V213L probably benign Het
Vkorc1l1 C A 5: 130,011,148 (GRCm39) Y111* probably null Het
Wdr47 G T 3: 108,537,089 (GRCm39) probably benign Het
Wdr90 A G 17: 26,066,765 (GRCm39) probably benign Het
Other mutations in Gm11149
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03194:Gm11149 APN 9 49,457,646 (GRCm39) unclassified probably benign
R2233:Gm11149 UTSW 9 49,473,446 (GRCm39) intron probably benign
R5746:Gm11149 UTSW 9 49,457,494 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02