Incidental Mutation 'IGL03009:Gm7008'
ID407712
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7008
Ensembl Gene ENSMUSG00000035983
Gene Namepredicted gene 7008
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL03009
Quality Score
Status
Chromosome12
Chromosomal Location40222758-40229184 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to A at 40223547 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000128635 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000001672] [ENSMUST00000164354] [ENSMUST00000169319] [ENSMUST00000169926] [ENSMUST00000171530]
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 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: 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
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adsl C A 15: 80,952,243 S67* probably null Het
Arrdc4 A G 7: 68,739,493 V411A probably damaging Het
Cnnm2 A G 19: 46,877,355 Y794C probably damaging Het
Flt4 G T 11: 49,627,124 K330N probably benign Het
Foxs1 T C 2: 152,932,929 H68R probably damaging Het
Gm21969 C T 4: 139,607,654 S333L probably damaging Het
Gmppa A G 1: 75,439,370 Y137C probably damaging Het
Grwd1 A G 7: 45,827,137 probably benign Het
Kdm5a C T 6: 120,430,086 R1421W probably damaging Het
Myo5b A G 18: 74,760,968 T1749A possibly damaging Het
Neb A G 2: 52,179,456 probably benign Het
Ntng1 T C 3: 109,934,702 K252E possibly damaging Het
Nup133 A G 8: 123,933,500 I353T possibly damaging Het
Olfr613 C A 7: 103,552,527 C247* probably null Het
Osbpl11 T C 16: 33,241,730 probably benign Het
Pcsk9 C T 4: 106,454,345 G230S probably damaging Het
Polr1b A G 2: 129,126,068 N1127S probably damaging Het
Rasgrf1 A T 9: 89,991,703 K688N possibly damaging Het
Rhot1 A G 11: 80,220,254 probably null Het
Rims2 A T 15: 39,566,997 Q1159L possibly damaging Het
Ros1 T C 10: 52,145,907 I594V probably benign Het
Slc43a2 G A 11: 75,572,376 C536Y probably benign Het
Stip1 A T 19: 7,021,121 V537E probably damaging Het
Stxbp2 A T 8: 3,641,971 I538F probably benign Het
Vav1 A T 17: 57,296,582 T94S probably benign Het
Zfr A T 15: 12,162,235 I824F probably damaging Het
Other mutations in Gm7008
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02150:Gm7008 APN 12 40223258 unclassified probably benign
IGL02311:Gm7008 APN 12 40223386 unclassified probably benign
R0271:Gm7008 UTSW 12 40223560 unclassified probably benign
R5224:Gm7008 UTSW 12 40223343 unclassified probably benign
Posted On2016-08-02