Incidental Mutation 'R2217:Gm10608'
ID 241218
Institutional Source Beutler Lab
Gene Symbol Gm10608
Ensembl Gene ENSMUSG00000074029
Gene Name predicted gene 10608
Synonyms EG546165
MMRRC Submission 040219-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # R2217 (G1)
Quality Score 163
Status Not validated
Chromosome 9
Chromosomal Location 118991798-118992473 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA to CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA at 118989784 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000091246 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000010795] [ENSMUST00000093527]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000010795
SMART Domains Protein: ENSMUSP00000010795
Gene: ENSMUSG00000010651

DomainStartEndE-ValueType
Pfam:Thiolase_N 38 291 6.7e-90 PFAM
Pfam:Thiolase_C 298 421 3e-53 PFAM
Pfam:ACP_syn_III_C 329 420 1.8e-7 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000093527
SMART Domains Protein: ENSMUSP00000091246
Gene: ENSMUSG00000074029

DomainStartEndE-ValueType
Pfam:DUF3915 11 80 3.1e-10 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213924
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adat1 T C 8: 112,709,128 (GRCm39) K232E probably benign Het
Apba1 T C 19: 23,871,326 (GRCm39) M386T probably damaging Het
Appl2 G T 10: 83,444,601 (GRCm39) F472L possibly damaging Het
Atxn2 T C 5: 121,941,140 (GRCm39) Y56H probably damaging Het
Cacna1c T C 6: 118,647,368 (GRCm39) Y809C probably damaging Het
Canx C T 11: 50,201,694 (GRCm39) V59I probably benign Het
Catsperb T C 12: 101,560,478 (GRCm39) L823P probably damaging Het
Crb3 T C 17: 57,372,090 (GRCm39) S46P probably benign Het
Daam1 G A 12: 72,036,601 (GRCm39) R1058H probably damaging Het
Ehd1 T A 19: 6,348,502 (GRCm39) D493E probably damaging Het
Eml6 T A 11: 29,768,907 (GRCm39) Q746L probably damaging Het
Epg5 T A 18: 77,992,287 (GRCm39) M328K probably benign Het
Flt4 T A 11: 49,515,555 (GRCm39) S48T probably benign Het
Gm7535 A G 17: 18,131,936 (GRCm39) probably benign Het
Gpat4 G A 8: 23,670,171 (GRCm39) P286L probably damaging Het
Hmcn2 A T 2: 31,240,586 (GRCm39) T494S probably benign Het
Hydin G A 8: 111,145,138 (GRCm39) V830I probably benign Het
Map3k6 T A 4: 132,973,983 (GRCm39) H487Q possibly damaging Het
Myh14 G A 7: 44,283,800 (GRCm39) P735S probably damaging Het
Nfkb2 T C 19: 46,296,163 (GRCm39) probably null Het
Nlrp4c T C 7: 6,076,113 (GRCm39) V671A probably benign Het
Nsrp1 A T 11: 76,936,587 (GRCm39) Y536* probably null Het
Or4c112 G T 2: 88,853,770 (GRCm39) H192Q probably benign Het
Pak5 A G 2: 135,958,123 (GRCm39) S322P probably damaging Het
Pank2 A G 2: 131,124,601 (GRCm39) probably null Het
Phf6 A T X: 52,031,525 (GRCm39) I272F probably damaging Het
Plxna2 T C 1: 194,480,056 (GRCm39) L1409P probably damaging Het
Polr2a A G 11: 69,633,511 (GRCm39) probably null Het
Pp2d1 C A 17: 53,822,482 (GRCm39) V195L probably benign Het
Psma1 C T 7: 113,864,173 (GRCm39) E227K unknown Het
Ptger1 C T 8: 84,395,357 (GRCm39) T278I probably benign Het
Slc20a2 C A 8: 23,050,532 (GRCm39) S250R probably benign Het
Slc27a2 A G 2: 126,409,672 (GRCm39) T285A probably damaging Het
Slc47a2 T C 11: 61,204,497 (GRCm39) T285A probably benign Het
Slf1 T A 13: 77,194,825 (GRCm39) probably null Het
Tiam2 A G 17: 3,465,389 (GRCm39) T373A probably benign Het
Timd2 T A 11: 46,577,844 (GRCm39) I96L probably damaging Het
Tmem59l A G 8: 70,939,951 (GRCm39) L6S unknown Het
Tmem64 T C 4: 15,266,658 (GRCm39) I236T possibly damaging Het
Trpm2 T A 10: 77,777,016 (GRCm39) D427V probably damaging Het
Vax2 A T 6: 83,714,871 (GRCm39) Y262F probably damaging Het
Virma T C 4: 11,544,924 (GRCm39) S1628P probably damaging Het
Zan C A 5: 137,408,568 (GRCm39) probably benign Het
Zbtb22 T G 17: 34,136,939 (GRCm39) D361E probably damaging Het
Zfp27 A G 7: 29,595,536 (GRCm39) L143P possibly damaging Het
Other mutations in Gm10608
AlleleSourceChrCoordTypePredicted EffectPPH Score
3-1:Gm10608 UTSW 9 118,990,156 (GRCm39) unclassified probably benign
R1023:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R1053:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R1148:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R1148:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R1167:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R1172:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R1211:Gm10608 UTSW 9 118,989,780 (GRCm39) frame shift probably null
R1601:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R1743:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R1766:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R1939:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R2016:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R2127:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R2270:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R2372:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R2844:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R2959:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R2968:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R3084:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R3607:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R3702:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R3779:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R3839:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R3900:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R3947:Gm10608 UTSW 9 118,989,730 (GRCm39) small deletion probably benign
R4015:Gm10608 UTSW 9 118,989,784 (GRCm39) frame shift probably null
R4024:Gm10608 UTSW 9 118,989,784 (GRCm39) small deletion probably benign
R5346:Gm10608 UTSW 9 118,989,792 (GRCm39) frame shift probably null
R8225:Gm10608 UTSW 9 118,989,776 (GRCm39) frame shift probably null
X0065:Gm10608 UTSW 9 118,989,931 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- TGTGACAGGTGCCACAACAG -3'
(R):5'- GCCTCTTCATAGGTCACATGCC -3'

Sequencing Primer
(F):5'- GTGCCACAACAGGGCAG -3'
(R):5'- TCAGATGGCAAAGCTTCCTG -3'
Posted On 2014-10-15