Incidental Mutation 'R2923:Gm10604'
ID 255610
Institutional Source Beutler Lab
Gene Symbol Gm10604
Ensembl Gene ENSMUSG00000073995
Gene Name predicted gene 10604
Synonyms
MMRRC Submission 040508-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.120) question?
Stock # R2923 (G1)
Quality Score 225
Status Validated
Chromosome 4
Chromosomal Location 11979560-11981265 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 11980122 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Threonine at position 61 (A61T)
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: A61T
SMART Domains Protein: ENSMUSP00000095860
Gene: ENSMUSG00000073995
AA Change: A61T

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: 99.2%
  • 3x: 98.6%
  • 10x: 97.5%
  • 20x: 95.6%
Validation Efficiency 98% (46/47)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam4 A T 12: 81,467,518 (GRCm39) C368S probably damaging Het
Adamts3 T C 5: 90,009,393 (GRCm39) D90G possibly damaging Het
Astn2 T C 4: 65,832,010 (GRCm39) Y500C probably damaging Het
Atp12a A T 14: 56,612,079 (GRCm39) T418S probably benign Het
Atp6v0a2 C T 5: 124,794,981 (GRCm39) T656M possibly damaging Het
Camsap2 G A 1: 136,208,547 (GRCm39) P971S possibly damaging Het
Ccdc116 T C 16: 16,960,307 (GRCm39) H170R probably benign Het
Ccn5 G A 2: 163,674,266 (GRCm39) R222Q probably benign Het
Cemip2 A G 19: 21,795,303 (GRCm39) D732G possibly damaging Het
Clpb A G 7: 101,372,035 (GRCm39) D257G probably benign Het
Cpb2 T C 14: 75,493,473 (GRCm39) probably null Het
D430041D05Rik G A 2: 104,085,660 (GRCm39) T164I possibly damaging Het
Dhx40 T G 11: 86,680,089 (GRCm39) Q416P probably benign Het
Dnah17 A G 11: 117,984,373 (GRCm39) F1636S probably damaging Het
Fhl3 T C 4: 124,599,463 (GRCm39) S13P probably damaging Het
Gapvd1 A T 2: 34,578,875 (GRCm39) I1249N probably damaging Het
Gm20939 T A 17: 95,184,721 (GRCm39) H456Q probably damaging Het
Golga4 T A 9: 118,388,411 (GRCm39) S1844R possibly damaging Het
Grm6 G C 11: 50,755,348 (GRCm39) G827R probably damaging Het
Grm7 T A 6: 111,472,866 (GRCm39) probably null Het
Hdc G A 2: 126,435,910 (GRCm39) P654S probably damaging Het
Hoxb1 T C 11: 96,257,119 (GRCm39) L156P probably benign Het
Ipo9 G T 1: 135,327,867 (GRCm39) Q515K probably benign Het
Kcnk3 T C 5: 30,779,414 (GRCm39) S155P probably damaging Het
Mboat2 T A 12: 25,004,239 (GRCm39) W347R probably damaging Het
Mib1 C T 18: 10,760,831 (GRCm39) Q374* probably null Het
Ncor2 A G 5: 125,132,855 (GRCm39) F44S probably damaging Het
Nipal3 A T 4: 135,204,776 (GRCm39) I125N probably damaging Het
Or4c113 A G 2: 88,884,843 (GRCm39) V309A probably benign Het
Or51a43 A G 7: 103,717,794 (GRCm39) V148A probably benign Het
Ovch2 A G 7: 107,389,596 (GRCm39) L317P possibly damaging Het
Pnpla2 T A 7: 141,035,380 (GRCm39) C61S probably benign Het
Ppp1r16b G T 2: 158,598,877 (GRCm39) L312F probably damaging Het
Rdm1 T A 11: 101,521,716 (GRCm39) L157H possibly damaging Het
Rpl22 C A 4: 152,412,002 (GRCm39) T26N possibly damaging Het
Rptn A G 3: 93,306,015 (GRCm39) Y1116C possibly damaging Het
Serpinb5 G A 1: 106,803,770 (GRCm39) S152N probably benign Het
Setx GTGGCT GT 2: 29,044,073 (GRCm39) 1814 probably null Het
St8sia1 A T 6: 142,774,963 (GRCm39) F205L probably damaging Het
Stab2 A G 10: 86,697,325 (GRCm39) Y1988H probably damaging Het
Susd3 A T 13: 49,401,945 (GRCm39) M1K probably null Het
Syne3 A T 12: 104,934,343 (GRCm39) L55Q probably damaging Het
Tmx1 T A 12: 70,512,895 (GRCm39) C268S probably benign Het
Ttll1 T C 15: 83,376,760 (GRCm39) K321R probably damaging Het
Zdhhc18 G T 4: 133,360,455 (GRCm39) H82Q probably benign Het
Zhx1 T C 15: 57,917,077 (GRCm39) I390V probably damaging 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
R6537:Gm10604 UTSW 4 11,980,221 (GRCm39) missense unknown
R7243:Gm10604 UTSW 4 11,980,113 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TTTAAACACTGGAGGCTGGGG -3'
(R):5'- TTGAAGCCCAGGAACATCAG -3'

Sequencing Primer
(F):5'- CAAGTTCAAGGCCAGTCTGAGTTAC -3'
(R):5'- GGAAAGTAAAGACAGATTTCATCTCC -3'
Posted On 2014-12-29