Incidental Mutation 'R6644:Gm6803'
ID 526031
Institutional Source Beutler Lab
Gene Symbol Gm6803
Ensembl Gene ENSMUSG00000096803
Gene Name predicted gene 6803
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Not available question?
Stock # R6644 (G1)
Quality Score 225.009
Status Not validated
Chromosome 12
Chromosomal Location 88018337-88018771 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 88018690 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 28 (F28L)
Ref Sequence ENSEMBL: ENSMUSP00000137317 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178301]
AlphaFold J3QPI8
Predicted Effect probably benign
Transcript: ENSMUST00000178301
AA Change: F28L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000137317
Gene: ENSMUSG00000096803
AA Change: F28L

DomainStartEndE-ValueType
low complexity region 3 25 N/A INTRINSIC
eIF1a 28 110 7.09e-44 SMART
low complexity region 132 144 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.5%
  • 20x: 92.3%
Validation Efficiency 100% (50/50)
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610037L13Rik T G 4: 107,894,922 I130S probably damaging Het
Abca7 C T 10: 80,008,764 P1461L probably damaging Het
Abhd14a T C 9: 106,444,273 Y10C probably damaging Het
Adcy2 C T 13: 68,668,552 V772M possibly damaging Het
Apob A G 12: 8,009,077 M2487V probably damaging Het
B4galnt1 T C 10: 127,171,793 probably null Het
Cabp7 C T 11: 4,740,396 V76I probably benign Het
Cbr3 A G 16: 93,690,511 Y194C probably damaging Het
Cdk18 G A 1: 132,122,069 Q58* probably null Het
Cryba4 T C 5: 112,246,762 D167G probably damaging Het
Dner T C 1: 84,395,707 N588S probably damaging Het
Dnm1l T C 16: 16,329,873 I343V probably benign Het
Fam168b C A 1: 34,836,741 G21V probably damaging Het
Fam71d T A 12: 78,715,286 D241E probably damaging Het
Fbxw17 G A 13: 50,423,219 R49Q probably damaging Het
Gm10332 T A 14: 54,820,159 F59I probably damaging Het
Gm8765 A G 13: 50,702,035 T570A possibly damaging Het
Gnai3 A G 3: 108,123,536 probably null Het
Helz T A 11: 107,632,261 M75K possibly damaging Het
Hnrnph3 C T 10: 63,018,893 probably benign Het
Ifi211 C T 1: 173,905,552 C181Y probably benign Het
Immp1l A G 2: 105,937,045 K83R probably damaging Het
Itga6 G A 2: 71,841,124 G740R probably damaging Het
Klhl1 T C 14: 96,517,918 T134A probably benign Het
Klhl7 A G 5: 24,149,246 D353G probably damaging Het
Map3k1 A G 13: 111,752,449 S1325P probably benign Het
Map3k4 A G 17: 12,232,410 probably null Het
Meioc G A 11: 102,668,460 probably null Het
Mfap5 T C 6: 122,520,596 F26L probably damaging Het
Myo5a A G 9: 75,146,967 T386A probably damaging Het
Npc1l1 A T 11: 6,214,013 L1266Q probably damaging Het
Npc1l1 G T 11: 6,214,014 L1266M probably damaging Het
Olfr1221 A G 2: 89,111,981 M177T probably benign Het
Olfr612 C A 7: 103,539,058 V59F possibly damaging Het
Pbld1 T A 10: 63,075,063 S233T probably damaging Het
Phf12 A G 11: 78,026,092 *789W probably null Het
Sf3b2 A T 19: 5,279,964 probably null Het
Slc23a3 A G 1: 75,128,547 I459T probably damaging Het
Sptbn2 C G 19: 4,749,012 R2037G probably benign Het
Stard9 A C 2: 120,695,772 M837L probably benign Het
Stx5a A T 19: 8,755,248 probably benign Het
Tmc7 A G 7: 118,538,162 V719A probably benign Het
Trank1 T A 9: 111,364,834 I642K possibly damaging Het
Trim34a T C 7: 104,261,037 Y349H probably damaging Het
Uba7 A G 9: 107,981,472 Y834C possibly damaging Het
Ube2d1 A G 10: 71,256,700 S105P possibly damaging Het
Vps13a A G 19: 16,744,919 V343A possibly damaging Het
Zbtb37 G A 1: 161,032,073 Q221* probably null Het
Zfp119b T C 17: 55,939,148 N346S probably benign Het
Zfp708 G T 13: 67,070,721 T358K possibly damaging Het
Other mutations in Gm6803
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1602:Gm6803 UTSW 12 88018364 missense probably benign 0.00
R1603:Gm6803 UTSW 12 88018364 missense probably benign 0.00
R2157:Gm6803 UTSW 12 88018711 missense unknown
R2508:Gm6803 UTSW 12 88018488 missense probably damaging 1.00
R4092:Gm6803 UTSW 12 88018424 missense possibly damaging 0.50
R4328:Gm6803 UTSW 12 88018515 missense possibly damaging 0.94
R5022:Gm6803 UTSW 12 88018711 missense unknown
R5057:Gm6803 UTSW 12 88018711 missense unknown
R5302:Gm6803 UTSW 12 88018546 missense probably damaging 1.00
R5360:Gm6803 UTSW 12 88018495 missense probably benign 0.03
R5747:Gm6803 UTSW 12 88018596 missense possibly damaging 0.93
R6028:Gm6803 UTSW 12 88018361 missense possibly damaging 0.70
R6275:Gm6803 UTSW 12 88018485 missense probably benign 0.01
R7689:Gm6803 UTSW 12 88018489 missense probably damaging 1.00
R8691:Gm6803 UTSW 12 88018508 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TAGGCCTTCAGACTTCTTGC -3'
(R):5'- AAGCGTATAGTAGCTCTTGGAAC -3'

Sequencing Primer
(F):5'- GGATTGTACTTTAAGATCACATCAGC -3'
(R):5'- CTTGGAACTGATTCAAAGCCACTGTC -3'
Posted On 2018-06-22