Incidental Mutation 'IGL01813:Gm11627'
ID 154330
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11627
Ensembl Gene ENSMUSG00000078640
Gene Name predicted gene 11627
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.122) question?
Stock # IGL01813
Quality Score
Status
Chromosome 11
Chromosomal Location 102467225-102469945 bp(-) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) T to C at 102469634 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000102696 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000107080] [ENSMUST00000107081]
AlphaFold A6PWP4
Predicted Effect probably benign
Transcript: ENSMUST00000107080
Predicted Effect probably benign
Transcript: ENSMUST00000107081
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139829
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 T A 2: 69,117,936 (GRCm39) probably benign Het
Adgrb2 T C 4: 129,906,359 (GRCm39) V929A probably benign Het
Aldh2 T C 5: 121,710,136 (GRCm39) I400V probably benign Het
Atxn2l T C 7: 126,099,425 (GRCm39) D84G probably damaging Het
Avpr1a T A 10: 122,284,916 (GRCm39) N69K probably damaging Het
BC034090 G A 1: 155,102,085 (GRCm39) Q60* probably null Het
Bltp1 G A 3: 36,982,669 (GRCm39) S778N possibly damaging Het
Bub3 T C 7: 131,170,362 (GRCm39) S295P probably benign Het
Cacna1b T C 2: 24,499,902 (GRCm39) S161G probably damaging Het
Clba1 C T 12: 112,779,179 (GRCm39) T272M probably damaging Het
Col6a4 T A 9: 105,954,452 (GRCm39) S296C probably damaging Het
Cyp4f15 G A 17: 32,905,131 (GRCm39) R38H probably benign Het
Dync2h1 T C 9: 7,122,799 (GRCm39) I2052M probably damaging Het
Jmjd8 A T 17: 26,048,212 (GRCm39) probably null Het
Kmt2c A G 5: 25,495,802 (GRCm39) V629A possibly damaging Het
Kremen1 T C 11: 5,149,667 (GRCm39) T335A probably benign Het
Oosp2 T C 19: 11,628,847 (GRCm39) T85A probably benign Het
Or12d17 A G 17: 37,777,649 (GRCm39) E184G probably damaging Het
Or8s10 A G 15: 98,335,530 (GRCm39) Y60C possibly damaging Het
Pex5l T C 3: 33,136,204 (GRCm39) E5G probably benign Het
Pigk A T 3: 152,448,156 (GRCm39) Q173L probably damaging Het
Pik3c2g T A 6: 139,599,407 (GRCm39) N174K possibly damaging Het
Plb1 C T 5: 32,486,429 (GRCm39) H893Y probably damaging Het
Pus7 T C 5: 23,965,302 (GRCm39) probably benign Het
R3hdm1 G A 1: 128,102,970 (GRCm39) probably null Het
Samd7 C T 3: 30,808,435 (GRCm39) P83S probably benign Het
Supt5 T A 7: 28,023,400 (GRCm39) Y293F probably damaging Het
Tbc1d30 T C 10: 121,102,956 (GRCm39) D692G probably benign Het
Tmpo G A 10: 90,999,104 (GRCm39) R228C probably benign Het
Tnn A T 1: 159,916,008 (GRCm39) H1236Q probably damaging Het
Ubr3 T C 2: 69,781,914 (GRCm39) I667T probably benign Het
Vmn1r183 T A 7: 23,754,985 (GRCm39) F263I probably benign Het
Other mutations in Gm11627
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2036:Gm11627 UTSW 11 102,467,580 (GRCm39) missense unknown
R4630:Gm11627 UTSW 11 102,469,657 (GRCm39) start gained probably benign
Posted On 2014-02-04