Incidental Mutation 'R8227:Gm1968'
ID 637034
Institutional Source Beutler Lab
Gene Symbol Gm1968
Ensembl Gene ENSMUSG00000075286
Gene Name predicted gene 1968
Synonyms
MMRRC Submission 067644-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # R8227 (G1)
Quality Score 105.008
Status Not validated
Chromosome 16
Chromosomal Location 29776745-29797942 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 29777380 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Asparagine at position 93 (K93N)
Ref Sequence ENSEMBL: ENSMUSP00000097593 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100016]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000100016
AA Change: K93N
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.3%
  • 20x: 97.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp7 C A 7: 28,316,073 (GRCm39) S171I probably damaging Het
Arhgap24 A G 5: 103,023,647 (GRCm39) E227G probably benign Het
Atp13a4 A G 16: 29,222,663 (GRCm39) V1087A Het
Csnk1g2 G A 10: 80,474,463 (GRCm39) probably null Het
Dlc1 A G 8: 37,039,825 (GRCm39) L994S probably damaging Het
Dusp13b A G 14: 21,792,869 (GRCm39) S19P probably benign Het
Foxr1 T C 9: 44,347,304 (GRCm39) S78G probably benign Het
Gm4781 G A 10: 100,232,424 (GRCm39) P171S noncoding transcript Het
Gm7276 T A 18: 77,273,158 (GRCm39) Q192L unknown Het
Greb1l T A 18: 10,515,371 (GRCm39) L721H probably damaging Het
Grm3 T C 5: 9,620,242 (GRCm39) D334G possibly damaging Het
Lama3 C T 18: 12,540,608 (GRCm39) A304V probably benign Het
Lamc1 G A 1: 153,099,500 (GRCm39) S1491L probably benign Het
Lepr T C 4: 101,628,559 (GRCm39) S555P probably damaging Het
Mup14 C T 4: 61,258,494 (GRCm39) E97K probably benign Het
Pdss2 A T 10: 43,221,577 (GRCm39) H163L probably damaging Het
Rps16 T A 7: 28,051,926 (GRCm39) D101E probably benign Het
Rpusd4 T C 9: 35,179,831 (GRCm39) V108A probably benign Het
Slc7a14 T C 3: 31,263,361 (GRCm39) K727R probably benign Het
Snx6 A T 12: 54,798,756 (GRCm39) F351I possibly damaging Het
Son CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC 16: 91,453,579 (GRCm39) probably benign Het
Togaram2 T A 17: 72,021,237 (GRCm39) Y675* probably null Het
Other mutations in Gm1968
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01293:Gm1968 APN 16 29,777,632 (GRCm39) exon noncoding transcript
IGL01300:Gm1968 APN 16 29,781,038 (GRCm39) exon noncoding transcript
R1539:Gm1968 UTSW 16 29,777,659 (GRCm39) exon noncoding transcript
R5339:Gm1968 UTSW 16 29,781,077 (GRCm39) exon noncoding transcript
R5359:Gm1968 UTSW 16 29,777,617 (GRCm39) exon noncoding transcript
R5610:Gm1968 UTSW 16 29,777,557 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- CCATGGAGGTCAGAGGCATG -3'
(R):5'- TGCAAGAGTTTGACTTCCATAAG -3'

Sequencing Primer
(F):5'- CATGATGTATGCATGTGTATACCTGC -3'
(R):5'- AACCTTGTCATGGAGCTCAG -3'
Posted On 2020-07-13