Incidental Mutation 'R5192:Gm9988'
ID 500915
Institutional Source Beutler Lab
Gene Symbol Gm9988
Ensembl Gene ENSMUSG00000055968
Gene Name predicted gene 9988
Synonyms
MMRRC Submission 042768-MU
Accession Numbers
Essential gene? Not available question?
Stock # R5192 (G1)
Quality Score 157
Status Not validated
Chromosome 8
Chromosomal Location 88864707-88865145 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 88865001 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000120121 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034079] [ENSMUST00000095214] [ENSMUST00000121949] [ENSMUST00000127490]
AlphaFold no structure available at present
Predicted Effect silent
Transcript: ENSMUST00000034079
SMART Domains Protein: ENSMUSP00000034079
Gene: ENSMUSG00000031657

DomainStartEndE-ValueType
Pfam:HEAT_EZ 41 106 2.5e-11 PFAM
Blast:ARM 111 171 2e-25 BLAST
Blast:ARM 172 215 1e-15 BLAST
low complexity region 357 366 N/A INTRINSIC
low complexity region 375 393 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000069786
Predicted Effect probably benign
Transcript: ENSMUST00000095214
SMART Domains Protein: ENSMUSP00000092839
Gene: ENSMUSG00000036810

DomainStartEndE-ValueType
Pfam:Tmemb_18A 5 122 1.6e-61 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000121949
SMART Domains Protein: ENSMUSP00000112812
Gene: ENSMUSG00000031657

DomainStartEndE-ValueType
Blast:ARM 1 54 7e-20 BLAST
Blast:ARM 55 98 8e-16 BLAST
low complexity region 240 249 N/A INTRINSIC
low complexity region 258 276 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000127490
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128290
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184847
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef25 A G 10: 127,020,978 (GRCm39) S303P probably damaging Het
Babam1 T C 8: 71,856,897 (GRCm39) V286A probably damaging Het
Becn2 A G 1: 175,748,408 (GRCm39) D158G probably benign Het
Cep192 T C 18: 67,968,075 (GRCm39) I853T probably benign Het
Cfap43 A T 19: 47,814,364 (GRCm39) W157R probably damaging Het
Dnah17 T C 11: 117,925,185 (GRCm39) T3883A possibly damaging Het
Dzip1 C T 14: 119,148,805 (GRCm39) M291I probably damaging Het
Eml2 G A 7: 18,935,088 (GRCm39) V432I probably damaging Het
Fbxw19 T C 9: 109,313,496 (GRCm39) Y234C probably benign Het
Gask1a T G 9: 121,794,727 (GRCm39) S294A probably benign Het
Gstm1 A G 3: 107,922,259 (GRCm39) probably null Het
Hsfy2 T A 1: 56,675,894 (GRCm39) K214N probably benign Het
Kat6a G A 8: 23,401,729 (GRCm39) R366H probably damaging Het
Kctd4 A G 14: 76,200,127 (GRCm39) T33A probably benign Het
Klrh1 T C 6: 129,748,721 (GRCm39) T99A probably benign Het
Marchf10 T C 11: 105,262,752 (GRCm39) H735R possibly damaging Het
Myo1g T C 11: 6,464,816 (GRCm39) D486G probably damaging Het
Or1e16 AGCGGTCGTAGGC AGC 11: 73,286,480 (GRCm39) probably null Het
Or5d46 A G 2: 88,170,092 (GRCm39) Y61C possibly damaging Het
Or8b1 T C 9: 38,400,101 (GRCm39) Y259H possibly damaging Het
Pif1 G T 9: 65,495,374 (GRCm39) A95S probably benign Het
Plppr2 T C 9: 21,852,428 (GRCm39) F104S probably damaging Het
Prep T C 10: 45,029,207 (GRCm39) Y536H probably benign Het
Slc22a30 G A 19: 8,321,757 (GRCm39) Q436* probably null Het
Tmtc2 G A 10: 105,026,038 (GRCm39) P810L probably damaging Het
Tollip C T 7: 141,445,854 (GRCm39) R9H probably damaging Het
Vmn2r57 A T 7: 41,077,363 (GRCm39) S268T probably damaging Het
Vps51 A G 19: 6,120,497 (GRCm39) V472A possibly damaging Het
Zfp608 C A 18: 55,031,569 (GRCm39) K790N probably damaging Het
Zfp661 A G 2: 127,418,982 (GRCm39) V386A possibly damaging Het
Predicted Primers PCR Primer
(F):5'- TCAGTTCTCCCCTATCGAGAG -3'
(R):5'- AACCTGAGCTAACTGGCATG -3'

Sequencing Primer
(F):5'- TCCCCTATCGAGAGCTGTCAG -3'
(R):5'- GGCATGTTATTATTCCCCCAGAAG -3'
Posted On 2017-12-01