Incidental Mutation 'R6537:Gm10604'
ID 520458
Institutional Source Beutler Lab
Gene Symbol Gm10604
Ensembl Gene ENSMUSG00000073995
Gene Name predicted gene 10604
Synonyms
MMRRC Submission 044663-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.120) question?
Stock # R6537 (G1)
Quality Score 225.009
Status Validated
Chromosome 4
Chromosomal Location 11979560-11981265 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 11980221 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Alanine at position 28 (S28A)
Ref Sequence ENSEMBL: ENSMUSP00000095860 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098260]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000098260
AA Change: S28A
SMART Domains Protein: ENSMUSP00000095860
Gene: ENSMUSG00000073995
AA Change: S28A

DomainStartEndE-ValueType
SCOP:d1kcma_ 2 72 5e-3 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128443
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146154
Predicted Effect noncoding transcript
Transcript: ENSMUST00000154194
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181295
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
Validation Efficiency 100% (30/30)
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Anapc4 T C 5: 53,000,898 (GRCm39) S224P probably damaging Het
Col6a4 G A 9: 105,945,153 (GRCm39) T987M possibly damaging Het
Cort C T 4: 149,211,081 (GRCm39) G8E probably benign Het
Ctdp1 G T 18: 80,492,766 (GRCm39) D576E probably benign Het
Ctsq A T 13: 61,183,140 (GRCm39) I334N probably damaging Het
Cwc15 A G 9: 14,413,284 (GRCm39) D22G probably damaging Het
Dnmt3l G A 10: 77,887,898 (GRCm39) G136R probably null Het
Fxyd6 A G 9: 45,302,092 (GRCm39) I37V possibly damaging Het
Gm43302 A G 5: 105,438,861 (GRCm39) I9T possibly damaging Het
Hmcn2 T C 2: 31,305,280 (GRCm39) V3151A probably benign Het
Kif1b T C 4: 149,277,053 (GRCm39) M1337V probably benign Het
Kyat3 A G 3: 142,435,573 (GRCm39) T282A probably benign Het
Lrp6 T C 6: 134,457,458 (GRCm39) E782G probably benign Het
Lrrc3b T C 14: 15,357,946 (GRCm38) Y220C probably damaging Het
Macf1 C T 4: 123,386,518 (GRCm39) S1033N probably damaging Het
Mdm1 A G 10: 117,994,481 (GRCm39) T452A probably benign Het
Nrn1l G T 8: 106,621,350 (GRCm39) R99L probably damaging Het
Pappa T A 4: 65,215,519 (GRCm39) I1142N probably damaging Het
Pcsk1 T C 13: 75,280,358 (GRCm39) F728L probably damaging Het
Ptcd3 T C 6: 71,874,094 (GRCm39) probably null Het
Siglecf C T 7: 43,005,423 (GRCm39) T461I probably benign Het
Slc7a8 C T 14: 54,972,576 (GRCm39) A282T probably benign Het
Srcap T C 7: 127,141,392 (GRCm39) V1724A probably damaging Het
Tafa2 T A 10: 123,429,401 (GRCm39) M5K possibly damaging Het
Tek A G 4: 94,725,561 (GRCm39) Q609R probably benign Het
Trim45 C T 3: 100,832,712 (GRCm39) A315V probably benign Het
Ttbk1 C T 17: 46,781,236 (GRCm39) V446M probably damaging Het
Wrap53 T C 11: 69,454,694 (GRCm39) D225G possibly damaging Het
Znhit6 A G 3: 145,300,374 (GRCm39) I193V probably benign Het
Other mutations in Gm10604
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1906:Gm10604 UTSW 4 11,979,989 (GRCm39) missense unknown
R2504:Gm10604 UTSW 4 11,980,083 (GRCm39) missense unknown
R2923:Gm10604 UTSW 4 11,980,122 (GRCm39) missense unknown
R7243:Gm10604 UTSW 4 11,980,113 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TGTGTAGGCCATCACCTTGAAC -3'
(R):5'- ACCTGGTATCCAACTGAAGTC -3'

Sequencing Primer
(F):5'- GTGTAGGCCATCACCTTGAACAAAAC -3'
(R):5'- TGGTATCCAACTGAAGTCACACAAAG -3'
Posted On 2018-06-06