Incidental Mutation 'IGL02400:Gm10720'
ID 291871
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10720
Ensembl Gene ENSMUSG00000074564
Gene Name predicted gene 10720
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02400
Quality Score
Status
Chromosome 9
Chromosomal Location 3015654-3017210 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 3016900 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000136170 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099047] [ENSMUST00000099049] [ENSMUST00000099050] [ENSMUST00000099050] [ENSMUST00000099050] [ENSMUST00000099050] [ENSMUST00000143083] [ENSMUST00000179272]
AlphaFold D3Z1I5
Predicted Effect probably null
Transcript: ENSMUST00000099047
SMART Domains Protein: ENSMUSP00000096646
Gene: ENSMUSG00000095547

DomainStartEndE-ValueType
internal_repeat_1 1 40 1.58e-10 PROSPERO
transmembrane domain 53 72 N/A INTRINSIC
transmembrane domain 77 99 N/A INTRINSIC
internal_repeat_1 117 176 1.58e-10 PROSPERO
transmembrane domain 199 221 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000099049
SMART Domains Protein: ENSMUSP00000096648
Gene: ENSMUSG00000095547

DomainStartEndE-ValueType
internal_repeat_1 1 46 2.19e-9 PROSPERO
transmembrane domain 62 84 N/A INTRINSIC
internal_repeat_1 117 182 2.19e-9 PROSPERO
transmembrane domain 197 219 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000099050
SMART Domains Protein: ENSMUSP00000096649
Gene: ENSMUSG00000074564

DomainStartEndE-ValueType
internal_repeat_1 1 46 7.44e-11 PROSPERO
transmembrane domain 67 89 N/A INTRINSIC
internal_repeat_1 117 182 7.44e-11 PROSPERO
transmembrane domain 192 214 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000099050
SMART Domains Protein: ENSMUSP00000096649
Gene: ENSMUSG00000074564

DomainStartEndE-ValueType
internal_repeat_1 1 46 7.44e-11 PROSPERO
transmembrane domain 67 89 N/A INTRINSIC
internal_repeat_1 117 182 7.44e-11 PROSPERO
transmembrane domain 192 214 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000099050
SMART Domains Protein: ENSMUSP00000096649
Gene: ENSMUSG00000074564

DomainStartEndE-ValueType
internal_repeat_1 1 46 7.44e-11 PROSPERO
transmembrane domain 67 89 N/A INTRINSIC
internal_repeat_1 117 182 7.44e-11 PROSPERO
transmembrane domain 192 214 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000099050
SMART Domains Protein: ENSMUSP00000096649
Gene: ENSMUSG00000074564

DomainStartEndE-ValueType
internal_repeat_1 1 46 7.44e-11 PROSPERO
transmembrane domain 67 89 N/A INTRINSIC
internal_repeat_1 117 182 7.44e-11 PROSPERO
transmembrane domain 192 214 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000143083
SMART Domains Protein: ENSMUSP00000137330
Gene: ENSMUSG00000096519

DomainStartEndE-ValueType
internal_repeat_1 1 19 1.27e-7 PROSPERO
transmembrane domain 20 42 N/A INTRINSIC
transmembrane domain 67 89 N/A INTRINSIC
internal_repeat_1 117 135 1.27e-7 PROSPERO
transmembrane domain 155 177 N/A INTRINSIC
transmembrane domain 192 214 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000179272
SMART Domains Protein: ENSMUSP00000136170
Gene: ENSMUSG00000095547

DomainStartEndE-ValueType
internal_repeat_1 1 49 2.1e-10 PROSPERO
transmembrane domain 74 96 N/A INTRINSIC
internal_repeat_1 118 186 2.1e-10 PROSPERO
transmembrane domain 198 217 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181242
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181572
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610028H24Rik A G 10: 76,290,644 (GRCm39) I128V possibly damaging Het
Arfgef3 G T 10: 18,522,005 (GRCm39) Q674K probably damaging Het
Atp6v0a2 T A 5: 124,798,849 (GRCm39) N851K probably benign Het
Chrna7 A G 7: 62,749,070 (GRCm39) C471R probably damaging Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Egflam T A 15: 7,276,534 (GRCm39) K544M probably benign Het
Erbb3 A C 10: 128,415,393 (GRCm39) N385K probably benign Het
Fancm A G 12: 65,160,589 (GRCm39) R1388G probably damaging Het
Gm20489 A T X: 100,306,944 (GRCm39) N328K possibly damaging Het
Gm5828 G T 1: 16,840,042 (GRCm39) noncoding transcript Het
Gnaq T C 19: 16,293,492 (GRCm39) Y145H probably damaging Het
Itgbl1 A G 14: 124,083,938 (GRCm39) D148G probably damaging Het
Myc T G 15: 61,861,760 (GRCm39) probably benign Het
Or10d5 A G 9: 39,861,635 (GRCm39) V144A probably benign Het
Or5m3b A T 2: 85,872,420 (GRCm39) I254F probably benign Het
Or6c211 A G 10: 129,505,752 (GRCm39) V212A probably damaging Het
Padi3 T G 4: 140,516,179 (GRCm39) K567T probably benign Het
Pi4ka T C 16: 17,111,748 (GRCm39) T1576A probably damaging Het
Pikfyve A G 1: 65,291,728 (GRCm39) R1316G probably damaging Het
Ryr2 A G 13: 11,620,130 (GRCm39) probably benign Het
Sash1 G A 10: 8,609,411 (GRCm39) R713* probably null Het
Tmem214 G A 5: 31,030,090 (GRCm39) A296T probably benign Het
Tnfsf4 T A 1: 161,223,276 (GRCm39) C42S possibly damaging Het
Tpp1 A G 7: 105,396,238 (GRCm39) I487T possibly damaging Het
Trim43a T A 9: 88,464,165 (GRCm39) N25K probably benign Het
Tuft1 T C 3: 94,542,809 (GRCm39) probably benign Het
Usp46 T C 5: 74,197,713 (GRCm39) H26R probably benign Het
Zfp560 A T 9: 20,261,896 (GRCm39) I85N possibly damaging Het
Other mutations in Gm10720
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0153:Gm10720 UTSW 9 3,015,787 (GRCm39) missense probably null
V5622:Gm10720 UTSW 9 3,015,669 (GRCm39) missense probably benign
Posted On 2015-04-16