Incidental Mutation 'R2365:Gm826'
ID 246283
Institutional Source Beutler Lab
Gene Symbol Gm826
Ensembl Gene ENSMUSG00000074623
Gene Name predicted gene 826
Synonyms Gm46773, LOC329554
MMRRC Submission 040346-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # R2365 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 160153313-160176082 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 160169130 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 60 (S60P)
Ref Sequence ENSEMBL: ENSMUSP00000096729 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099127]
AlphaFold Q3UQ74
Predicted Effect unknown
Transcript: ENSMUST00000099127
AA Change: S60P
SMART Domains Protein: ENSMUSP00000096729
Gene: ENSMUSG00000074623
AA Change: S60P

DomainStartEndE-ValueType
low complexity region 72 89 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138905
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 94.9%
Validation Efficiency 94% (34/36)
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp13a5 T A 16: 29,070,008 (GRCm39) K959N probably benign Het
C4b G A 17: 34,955,032 (GRCm39) probably benign Het
Cdhr2 T G 13: 54,865,901 (GRCm39) S268R probably benign Het
Erc1 A G 6: 119,552,656 (GRCm39) L1094P probably damaging Het
Fat3 G A 9: 15,909,567 (GRCm39) S2145F probably damaging Het
Fat4 A G 3: 39,034,568 (GRCm39) H2740R probably benign Het
Galnt13 A G 2: 54,744,709 (GRCm39) Y136C possibly damaging Het
Gipc2 A G 3: 151,833,831 (GRCm39) I150T possibly damaging Het
Gkn3 C T 6: 87,360,507 (GRCm39) A163T probably damaging Het
Gm21957 T C 7: 124,818,629 (GRCm39) noncoding transcript Het
Gm5591 T A 7: 38,218,825 (GRCm39) R683W probably damaging Het
Hsd17b7 T C 1: 169,792,009 (GRCm39) D133G probably damaging Het
Kera A G 10: 97,444,805 (GRCm39) T55A probably benign Het
Mff T C 1: 82,713,192 (GRCm39) V129A possibly damaging Het
Myo7b A G 18: 32,147,384 (GRCm39) L53P probably damaging Het
Neo1 A G 9: 58,863,286 (GRCm39) V427A probably benign Het
Or10ak7 C T 4: 118,791,230 (GRCm39) E272K probably benign Het
Or52e19 A T 7: 102,959,380 (GRCm39) I151L probably benign Het
Pfkfb3 C T 2: 11,498,713 (GRCm39) probably null Het
Pom121l2 A G 13: 22,167,954 (GRCm39) T742A probably benign Het
Pon1 A G 6: 5,171,746 (GRCm39) S302P probably damaging Het
Rhox3f G T X: 36,763,672 (GRCm39) E140* probably null Het
Sall3 G C 18: 81,015,007 (GRCm39) P974A probably benign Het
Slc1a2 T A 2: 102,578,798 (GRCm39) probably null Het
Slc22a6 A G 19: 8,596,761 (GRCm39) T180A probably benign Het
Slc40a1 T C 1: 45,963,873 (GRCm39) probably null Het
Slc6a5 T C 7: 49,596,284 (GRCm39) S585P possibly damaging Het
Tbpl1 A G 10: 22,581,785 (GRCm39) V164A possibly damaging Het
Tmem98 A T 11: 80,706,511 (GRCm39) I95F probably damaging Het
Ush2a C A 1: 188,111,188 (GRCm39) P571T possibly damaging Het
Vars1 A G 17: 35,234,428 (GRCm39) N1125D probably benign Het
Vps13d T C 4: 144,813,894 (GRCm39) probably benign Het
Zbtb18 A T 1: 177,275,723 (GRCm39) E361V probably benign Het
Zc3hav1 A G 6: 38,317,168 (GRCm39) F144S probably damaging Het
Other mutations in Gm826
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03182:Gm826 APN 2 160,169,035 (GRCm39) missense unknown
R3762:Gm826 UTSW 2 160,155,423 (GRCm39) intron probably benign
R3769:Gm826 UTSW 2 160,169,165 (GRCm39) missense unknown
R4564:Gm826 UTSW 2 160,153,913 (GRCm39) utr 3 prime probably benign
R6125:Gm826 UTSW 2 160,169,034 (GRCm39) missense unknown
R6442:Gm826 UTSW 2 160,169,328 (GRCm39) start gained probably benign
R7048:Gm826 UTSW 2 160,169,026 (GRCm39) nonsense probably null
R7074:Gm826 UTSW 2 160,153,810 (GRCm39) missense unknown
R7491:Gm826 UTSW 2 160,153,942 (GRCm39) missense unknown
R7883:Gm826 UTSW 2 160,169,213 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CTTTTCACACTGAACATAGTCACAC -3'
(R):5'- TGGAAGTCTCTTTGCCTTCAGC -3'

Sequencing Primer
(F):5'- TGAACATAGTCACACAAACATGTCTG -3'
(R):5'- TTCAGCAGCCCCGCTCAG -3'
Posted On 2014-10-30