Incidental Mutation 'IGL03009:Gm7008'
ID 407712
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 # IGL03009
Quality Score
Status
Chromosome 12
Chromosomal Location 40273363-40279182 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 40273546 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 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
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222014
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
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adsl C A 15: 80,836,444 (GRCm39) S67* probably null Het
Arrdc4 A G 7: 68,389,241 (GRCm39) V411A probably damaging Het
Cnnm2 A G 19: 46,865,794 (GRCm39) Y794C probably damaging Het
Flt4 G T 11: 49,517,951 (GRCm39) K330N probably benign Het
Foxs1 T C 2: 152,774,849 (GRCm39) H68R probably damaging Het
Gm21969 C T 4: 139,334,965 (GRCm39) S333L probably damaging Het
Gmppa A G 1: 75,416,014 (GRCm39) Y137C probably damaging Het
Grwd1 A G 7: 45,476,561 (GRCm39) probably benign Het
Kdm5a C T 6: 120,407,047 (GRCm39) R1421W probably damaging Het
Myo5b A G 18: 74,894,039 (GRCm39) T1749A possibly damaging Het
Neb A G 2: 52,069,468 (GRCm39) probably benign Het
Ntng1 T C 3: 109,842,018 (GRCm39) K252E possibly damaging Het
Nup133 A G 8: 124,660,239 (GRCm39) I353T possibly damaging Het
Or51ab3 C A 7: 103,201,734 (GRCm39) C247* probably null Het
Osbpl11 T C 16: 33,062,100 (GRCm39) probably benign Het
Pcsk9 C T 4: 106,311,542 (GRCm39) G230S probably damaging Het
Polr1b A G 2: 128,967,988 (GRCm39) N1127S probably damaging Het
Rasgrf1 A T 9: 89,873,756 (GRCm39) K688N possibly damaging Het
Rhot1 A G 11: 80,111,080 (GRCm39) probably null Het
Rims2 A T 15: 39,430,393 (GRCm39) Q1159L possibly damaging Het
Ros1 T C 10: 52,022,003 (GRCm39) I594V probably benign Het
Slc43a2 G A 11: 75,463,202 (GRCm39) C536Y probably benign Het
Stip1 A T 19: 6,998,489 (GRCm39) V537E probably damaging Het
Stxbp2 A T 8: 3,691,971 (GRCm39) I538F probably benign Het
Vav1 A T 17: 57,603,582 (GRCm39) T94S probably benign Het
Zfr A T 15: 12,162,321 (GRCm39) I824F probably damaging Het
Other mutations in Gm7008
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02150:Gm7008 APN 12 40,273,257 (GRCm39) unclassified probably benign
IGL02311:Gm7008 APN 12 40,273,385 (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 2016-08-02