Incidental Mutation 'R0990:Gm9938'
ID 97678
Institutional Source Beutler Lab
Gene Symbol Gm9938
Ensembl Gene ENSMUSG00000054178
Gene Name predicted gene 9938
Synonyms
MMRRC Submission 039110-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.183) question?
Stock # R0990 (G1)
Quality Score 225
Status Not validated
Chromosome 19
Chromosomal Location 23700643-23702398 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 23701956 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000097156 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067077] [ENSMUST00000099560]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000067077
AA Change: D98G
Predicted Effect probably benign
Transcript: ENSMUST00000099560
SMART Domains Protein: ENSMUSP00000097156
Gene: ENSMUSG00000074925

DomainStartEndE-ValueType
Pfam:PPTA 122 149 3.9e-8 PFAM
Pfam:PPTA 180 207 5e-11 PFAM
Pfam:PPTA 290 315 8e-9 PFAM
Coding Region Coverage
  • 1x: 98.8%
  • 3x: 97.6%
  • 10x: 94.1%
  • 20x: 86.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy7 T C 8: 89,052,080 (GRCm39) V916A possibly damaging Het
Ank2 T C 3: 126,728,315 (GRCm39) I759M possibly damaging Het
Arhgap32 A G 9: 32,166,677 (GRCm39) D438G probably damaging Het
Arhgef12 T C 9: 42,883,677 (GRCm39) Y1285C probably benign Het
Cfap65 A G 1: 74,960,678 (GRCm39) V764A possibly damaging Het
Cog8 T A 8: 107,779,119 (GRCm39) probably null Het
Extl1 TGCGTTGCACCGATACCGGG TG 4: 134,084,988 (GRCm39) probably benign Het
Fam120a G T 13: 49,039,219 (GRCm39) A979E possibly damaging Het
Fbxo24 T C 5: 137,616,701 (GRCm39) N394S probably damaging Het
Iars2 A G 1: 185,050,824 (GRCm39) F422L probably damaging Het
Marchf3 A T 18: 56,940,870 (GRCm39) C87S probably damaging Het
Mettl2 T A 11: 105,028,570 (GRCm39) Y307* probably null Het
Mlh3 T C 12: 85,314,539 (GRCm39) D549G probably benign Het
Muc4 A G 16: 32,752,722 (GRCm38) T867A probably benign Het
Nup210l A T 3: 90,119,232 (GRCm39) T1852S probably benign Het
Or5aq1 T A 2: 86,966,086 (GRCm39) H193L possibly damaging Het
Pdk4 A T 6: 5,485,577 (GRCm39) S371T probably benign Het
Pkm A G 9: 59,585,379 (GRCm39) T454A probably damaging Het
Satb2 G A 1: 56,889,343 (GRCm39) S340F probably damaging Het
Scel G A 14: 103,819,268 (GRCm39) V354I possibly damaging Het
Setdb1 T C 3: 95,247,576 (GRCm39) T440A probably benign Het
Sgk1 T C 10: 21,872,985 (GRCm39) F230S probably damaging Het
Slc22a23 A T 13: 34,379,450 (GRCm39) I439N probably damaging Het
Slc9a5 G A 8: 106,086,078 (GRCm39) R615Q probably damaging Het
Smad1 T A 8: 80,070,417 (GRCm39) I374F probably damaging Het
Tgm4 A G 9: 122,875,576 (GRCm39) E143G probably benign Het
Vmn2r53 A G 7: 12,315,429 (GRCm39) S797P probably benign Het
Other mutations in Gm9938
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0078:Gm9938 UTSW 19 23,701,988 (GRCm39) unclassified probably benign
R0097:Gm9938 UTSW 19 23,701,828 (GRCm39) unclassified probably benign
R0097:Gm9938 UTSW 19 23,701,828 (GRCm39) unclassified probably benign
R1892:Gm9938 UTSW 19 23,701,955 (GRCm39) unclassified probably benign
R7056:Gm9938 UTSW 19 23,701,981 (GRCm39) unclassified probably benign
R8845:Gm9938 UTSW 19 23,701,941 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- ACAAGATGGTGTGTGACATGAGCC -3'
(R):5'- TGTGCCTGCTTCTCTTCAAGCATAG -3'

Sequencing Primer
(F):5'- TGCAACTTGAGAGTAGACCC -3'
(R):5'- GCATAGGCTACACAGCTTTTG -3'
Posted On 2014-01-05