Incidental Mutation 'IGL01614:Gm7808'
ID 92315
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7808
Ensembl Gene ENSMUSG00000091460
Gene Name predicted pseudogene 7808
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01614
Quality Score
Status
Chromosome 9
Chromosomal Location 19839192-19839578 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to A at 19839442 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149055 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057596] [ENSMUST00000217347]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000057596
SMART Domains Protein: ENSMUSP00000058810
Gene: ENSMUSG00000051118

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 3e-53 PFAM
Pfam:7tm_1 41 290 1.2e-24 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000082002
SMART Domains Protein: ENSMUSP00000136791
Gene: ENSMUSG00000091460

DomainStartEndE-ValueType
UBQ 1 72 3.73e-36 SMART
Ribosomal_L40e 77 128 1.02e-31 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000217347
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrf5 T A 17: 43,735,362 (GRCm39) S143T possibly damaging Het
Arhgap32 G T 9: 32,171,801 (GRCm39) S1527I probably damaging Het
Atp8a2 A G 14: 60,282,437 (GRCm39) V128A probably damaging Het
Bpi T C 2: 158,113,866 (GRCm39) F255L probably damaging Het
Clptm1 A T 7: 19,371,625 (GRCm39) D269E probably benign Het
Cyria T C 12: 12,411,574 (GRCm39) probably null Het
E2f7 T C 10: 110,595,839 (GRCm39) V63A probably damaging Het
Eif4e1b T A 13: 54,934,729 (GRCm39) I184N probably damaging Het
Gal3st1 T A 11: 3,948,996 (GRCm39) L401Q probably damaging Het
Hdac5 G A 11: 102,090,854 (GRCm39) T741I probably benign Het
Ipo5 A G 14: 121,172,507 (GRCm39) T522A probably benign Het
Lama5 A C 2: 179,822,657 (GRCm39) F2832V probably damaging Het
Ltk A C 2: 119,583,968 (GRCm39) L230R probably damaging Het
Mettl14 A T 3: 123,167,609 (GRCm39) probably benign Het
Myom1 T C 17: 71,433,173 (GRCm39) F1507L possibly damaging Het
Nsd3 T A 8: 26,156,095 (GRCm39) I554K possibly damaging Het
Or1j12 T G 2: 36,342,636 (GRCm39) I13S probably benign Het
Or1o1 G A 17: 37,716,529 (GRCm39) C30Y probably benign Het
Or51a43 C T 7: 103,717,576 (GRCm39) V221I probably benign Het
Or8u9 A T 2: 86,001,741 (GRCm39) I140N possibly damaging Het
Prr14 T A 7: 127,074,305 (GRCm39) L279H probably damaging Het
Rbm25 G T 12: 83,706,341 (GRCm39) D229Y probably damaging Het
Sdk2 T C 11: 113,684,684 (GRCm39) K1926E probably damaging Het
Slc25a23 C T 17: 57,352,579 (GRCm39) R435Q probably null Het
Srebf2 A G 15: 82,063,054 (GRCm39) N457S probably benign Het
Stac2 T C 11: 97,943,774 (GRCm39) D12G probably benign Het
Tal1 A C 4: 114,920,325 (GRCm39) probably null Het
Usp25 G A 16: 76,874,005 (GRCm39) R527Q probably damaging Het
Other mutations in Gm7808
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01878:Gm7808 APN 9 19,839,542 (GRCm39) unclassified probably benign
IGL02120:Gm7808 APN 9 19,839,313 (GRCm39) unclassified probably benign
IGL02285:Gm7808 APN 9 19,839,347 (GRCm39) unclassified probably benign
R1718:Gm7808 UTSW 9 19,839,299 (GRCm39) unclassified probably benign
R1900:Gm7808 UTSW 9 19,839,410 (GRCm39) unclassified probably benign
Posted On 2013-12-09