Incidental Mutation 'IGL01614:Gm7808'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7808
Ensembl Gene ENSMUSG00000091460
Gene Namepredicted pseudogene 7808
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01614
Quality Score
Chromosomal Location19927896-19928282 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) G to A at 19928146 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149055 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057596] [ENSMUST00000217347]
Predicted Effect probably benign
Transcript: ENSMUST00000057596
SMART Domains Protein: ENSMUSP00000058810
Gene: ENSMUSG00000051118

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

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: 43,424,471 S143T possibly damaging Het
Arhgap32 G T 9: 32,260,505 S1527I probably damaging Het
Atp8a2 A G 14: 60,044,988 V128A probably damaging Het
Bpi T C 2: 158,271,946 F255L probably damaging Het
Clptm1 A T 7: 19,637,700 D269E probably benign Het
E2f7 T C 10: 110,759,978 V63A probably damaging Het
Eif4e1b T A 13: 54,786,916 I184N probably damaging Het
Fam49a T C 12: 12,361,573 probably null Het
Gal3st1 T A 11: 3,998,996 L401Q probably damaging Het
Hdac5 G A 11: 102,200,028 T741I probably benign Het
Ipo5 A G 14: 120,935,095 T522A probably benign Het
Lama5 A C 2: 180,180,864 F2832V probably damaging Het
Ltk A C 2: 119,753,487 L230R probably damaging Het
Mettl14 A T 3: 123,373,960 probably benign Het
Myom1 T C 17: 71,126,178 F1507L possibly damaging Het
Nsd3 T A 8: 25,666,079 I554K possibly damaging Het
Olfr1044 A T 2: 86,171,397 I140N possibly damaging Het
Olfr107 G A 17: 37,405,638 C30Y probably benign Het
Olfr340 T G 2: 36,452,624 I13S probably benign Het
Olfr644 C T 7: 104,068,369 V221I probably benign Het
Prr14 T A 7: 127,475,133 L279H probably damaging Het
Rbm25 G T 12: 83,659,567 D229Y probably damaging Het
Sdk2 T C 11: 113,793,858 K1926E probably damaging Het
Slc25a23 C T 17: 57,045,579 R435Q probably null Het
Srebf2 A G 15: 82,178,853 N457S probably benign Het
Stac2 T C 11: 98,052,948 D12G probably benign Het
Tal1 A C 4: 115,063,128 probably null Het
Usp25 G A 16: 77,077,117 R527Q probably damaging Het
Other mutations in Gm7808
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01878:Gm7808 APN 9 19928246 unclassified probably benign
IGL02120:Gm7808 APN 9 19928017 unclassified probably benign
IGL02285:Gm7808 APN 9 19928051 unclassified probably benign
R1718:Gm7808 UTSW 9 19928003 unclassified probably benign
R1900:Gm7808 UTSW 9 19928114 unclassified probably benign
Posted On2013-12-09