Incidental Mutation 'IGL02311:Gm7008'
ID 287795
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7008
Ensembl Gene ENSMUSG00000035983
Gene Name predicted gene 7008
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02311
Quality Score
Status
Chromosome 12
Chromosomal Location 40273363-40279182 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to A at 40273385 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000128635 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000001672] [ENSMUST00000164354] [ENSMUST00000169319] [ENSMUST00000169926] [ENSMUST00000171530]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000001672
SMART Domains Protein: ENSMUSP00000001672
Gene: ENSMUSG00000001627

DomainStartEndE-ValueType
low complexity region 13 31 N/A INTRINSIC
Pfam:IFRD 40 345 1.1e-115 PFAM
Pfam:IFRD_C 390 443 6.7e-28 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000038121
Predicted Effect noncoding transcript
Transcript: ENSMUST00000158746
Predicted Effect probably benign
Transcript: ENSMUST00000164354
SMART Domains Protein: ENSMUSP00000130846
Gene: ENSMUSG00000001627

DomainStartEndE-ValueType
Pfam:IFRD 1 87 1.1e-29 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000169319
SMART Domains Protein: ENSMUSP00000130824
Gene: ENSMUSG00000001627

DomainStartEndE-ValueType
Pfam:IFRD 1 100 8.9e-35 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000169926
SMART Domains Protein: ENSMUSP00000127673
Gene: ENSMUSG00000001627

DomainStartEndE-ValueType
Pfam:IFRD 1 138 5.6e-50 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170019
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170752
Predicted Effect probably benign
Transcript: ENSMUST00000171530
SMART Domains Protein: ENSMUSP00000128635
Gene: ENSMUSG00000001627

DomainStartEndE-ValueType
low complexity region 13 31 N/A INTRINSIC
Pfam:IFRD 40 137 1.8e-33 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222014
Predicted Effect noncoding transcript
Transcript: ENSMUST00000171356
Predicted Effect noncoding transcript
Transcript: ENSMUST00000171553
SMART Domains Protein: ENSMUSP00000127954
Gene: ENSMUSG00000001627

DomainStartEndE-ValueType
low complexity region 13 31 N/A INTRINSIC
transmembrane domain 84 106 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1500035N22Rik C A 5: 25,202,705 (GRCm39) probably benign Het
Adam21 T G 12: 81,607,666 (GRCm39) D32A probably benign Het
Asns A G 6: 7,676,233 (GRCm39) probably null Het
Bin3 A T 14: 70,361,666 (GRCm39) M45L probably benign Het
Cfap44 A T 16: 44,225,134 (GRCm39) probably benign Het
Cmya5 T C 13: 93,227,163 (GRCm39) T2642A probably benign Het
Dbndd2 T C 2: 164,330,622 (GRCm39) S92P possibly damaging Het
Dclre1b A C 3: 103,715,409 (GRCm39) F30V probably damaging Het
Dock6 T C 9: 21,755,624 (GRCm39) D200G probably damaging Het
Epb41l4b C A 4: 57,076,456 (GRCm39) R335L probably damaging Het
Fscn1 T C 5: 142,957,765 (GRCm39) V304A probably benign Het
Gm8237 A G 14: 5,864,425 (GRCm38) probably null Het
Ifih1 T C 2: 62,440,847 (GRCm39) T440A probably damaging Het
Mepe C T 5: 104,485,571 (GRCm39) S237F probably damaging Het
Nr4a2 T C 2: 57,001,743 (GRCm39) I174V probably benign Het
Or2ag2 A G 7: 106,485,101 (GRCm39) Y308H probably benign Het
Or8c11 C T 9: 38,289,194 (GRCm39) Q6* probably null Het
Orc1 G T 4: 108,457,171 (GRCm39) V404L probably benign Het
Pcsk5 G T 19: 17,410,784 (GRCm39) Y1869* probably null Het
Phf21b A G 15: 84,678,095 (GRCm39) probably null Het
Pigg A G 5: 108,484,246 (GRCm39) T631A probably benign Het
Plxnb1 A G 9: 108,930,190 (GRCm39) N349D probably benign Het
Scaf11 T C 15: 96,316,637 (GRCm39) S976G probably benign Het
Scn8a G T 15: 100,911,164 (GRCm39) M861I probably damaging Het
Stau1 T C 2: 166,792,239 (GRCm39) N433S probably damaging Het
Synrg A G 11: 83,910,630 (GRCm39) K854R probably benign Het
Tbata T A 10: 61,015,234 (GRCm39) C150* probably null Het
Tcn2 G A 11: 3,867,692 (GRCm39) P417S probably damaging Het
Tlr1 A T 5: 65,083,290 (GRCm39) L429* probably null Het
Tpr G T 1: 150,274,404 (GRCm39) D104Y probably damaging Het
Ubash3b T C 9: 40,958,333 (GRCm39) T16A probably benign Het
Uso1 T A 5: 92,335,635 (GRCm39) S548T probably benign Het
Vps13b T A 15: 35,709,660 (GRCm39) V1869E probably benign Het
Vps18 T C 2: 119,120,732 (GRCm39) C64R probably benign Het
Zic2 C A 14: 122,713,606 (GRCm39) N173K probably damaging Het
Other mutations in Gm7008
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02150:Gm7008 APN 12 40,273,257 (GRCm39) unclassified probably benign
IGL03009:Gm7008 APN 12 40,273,546 (GRCm39) unclassified probably benign
R0271:Gm7008 UTSW 12 40,273,559 (GRCm39) unclassified probably benign
R5224:Gm7008 UTSW 12 40,273,342 (GRCm39) unclassified probably benign
Posted On 2015-04-16