Incidental Mutation 'R3025:Gm10842'
ID 265803
Institutional Source Beutler Lab
Gene Symbol Gm10842
Ensembl Gene ENSMUSG00000075485
Gene Name predicted gene 10842
Synonyms
MMRRC Submission 040541-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.147) question?
Stock # R3025 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 105037719-105039610 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 105037902 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 62 (S62P)
Ref Sequence ENSEMBL: ENSMUSP00000097911 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100338]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000100338
AA Change: S62P
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ace T A 11: 105,864,919 (GRCm39) probably null Het
Akap6 A G 12: 53,186,926 (GRCm39) T1447A probably benign Het
Atp13a2 C T 4: 140,721,659 (GRCm39) R250C probably damaging Het
Cacna1a T A 8: 85,306,854 (GRCm39) probably null Het
Chd6 GATCAT GAT 2: 160,808,472 (GRCm39) probably benign Het
Cptp T C 4: 155,951,678 (GRCm39) E5G possibly damaging Het
Dnajc16 C A 4: 141,501,922 (GRCm39) V303F probably benign Het
Gm17509 T C 13: 117,357,112 (GRCm39) probably benign Het
Homer1 C T 13: 93,538,582 (GRCm39) Q142* probably null Het
Kcnb2 C A 1: 15,781,059 (GRCm39) Q644K possibly damaging Het
Map3k19 T C 1: 127,766,290 (GRCm39) probably null Het
Msh4 T A 3: 153,569,128 (GRCm39) H621L probably damaging Het
Ogfod1 A T 8: 94,789,680 (GRCm39) E460D probably damaging Het
Or6c65 T A 10: 129,603,542 (GRCm39) F59Y probably damaging Het
Or8k41 A T 2: 86,314,083 (GRCm39) M1K probably null Het
Rp1 G A 1: 4,422,898 (GRCm39) R61W probably damaging Het
Scaf4 A T 16: 90,048,826 (GRCm39) H329Q unknown Het
Sec61a1 A T 6: 88,489,202 (GRCm39) D166E probably damaging Het
Tars2 C T 3: 95,654,952 (GRCm39) R63H possibly damaging Het
Vmn1r57 A T 7: 5,223,714 (GRCm39) K80* probably null Het
Vmn2r106 A G 17: 20,499,147 (GRCm39) W255R probably benign Het
Wdr49 C G 3: 75,240,663 (GRCm39) C402S possibly damaging Het
Other mutations in Gm10842
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0544:Gm10842 UTSW 11 105,037,880 (GRCm39) missense unknown
R1803:Gm10842 UTSW 11 105,037,867 (GRCm39) missense unknown
R2082:Gm10842 UTSW 11 105,037,909 (GRCm39) missense unknown
R9393:Gm10842 UTSW 11 105,037,885 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGACACTTGGGAAATGTTGCTC -3'
(R):5'- ACACTGTGACTCTGGGTGAC -3'

Sequencing Primer
(F):5'- ACTTGGGAAATGTTGCTCAGATTTTC -3'
(R):5'- AGGGGCTTCTCCATTTGTTAACAAC -3'
Posted On 2015-02-05