Incidental Mutation 'R9311:Gm5105'
ID 705542
Institutional Source Beutler Lab
Gene Symbol Gm5105
Ensembl Gene ENSMUSG00000049349
Gene Name predicted gene 5105
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.188) question?
Stock # R9311 (G1)
Quality Score 225.009
Status Validated
Chromosome 3
Chromosomal Location 138048761-138067388 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 138049657 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 56 (D56V)
Ref Sequence ENSEMBL: ENSMUSP00000052388 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053318]
AlphaFold Q8C6Y9
Predicted Effect unknown
Transcript: ENSMUST00000053318
AA Change: D56V
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (61/61)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310046K23Rik T G 3: 92,533,090 Q14P unknown Het
5430419D17Rik A T 7: 131,257,761 D1137V unknown Het
A4gnt T C 9: 99,613,763 I84T possibly damaging Het
Adad2 G T 8: 119,615,247 R268L probably damaging Het
Agxt2 A T 15: 10,380,647 N208I probably damaging Het
Brsk1 G T 7: 4,706,723 probably null Het
Cd40 A T 2: 165,070,747 Q235L possibly damaging Het
Cln6 T C 9: 62,850,618 Y220H probably damaging Het
Cngb1 A T 8: 95,284,166 probably null Het
Cpne1 A T 2: 156,077,803 V277E probably damaging Het
Csf2rb2 C T 15: 78,292,535 probably null Het
Cyp4f15 A G 17: 32,686,165 T41A probably benign Het
Dab1 T C 4: 104,512,266 probably null Het
Eif4e1b C A 13: 54,784,519 H56N probably benign Het
Elp3 A T 14: 65,586,339 D78E probably benign Het
Ephx3 C G 17: 32,189,316 D45H probably benign Het
Gabarap T A 11: 69,991,723 V4E probably benign Het
Gosr2 G T 11: 103,683,867 H134Q probably damaging Het
Ifi204 A G 1: 173,761,649 V72A possibly damaging Het
Irx1 A G 13: 71,959,297 V422A probably benign Het
Kcne4 C A 1: 78,818,107 D157E probably benign Het
Kctd13 A G 7: 126,942,173 N195S probably damaging Het
Kirrel A G 3: 87,097,816 V75A probably benign Het
Klkb1 T C 8: 45,269,946 T625A probably benign Het
Lama5 A G 2: 180,196,482 probably null Het
Lifr A G 15: 7,178,937 I599V possibly damaging Het
Lin52 A T 12: 84,529,696 E101V probably damaging Het
Liph C T 16: 21,956,163 R428Q probably damaging Het
Liph T C 16: 21,983,930 I130V probably benign Het
Lrrc4c A C 2: 97,630,735 I569L possibly damaging Het
Mnat1 G A 12: 73,168,142 V78I probably benign Het
Msln C T 17: 25,753,016 D76N probably benign Het
Myh7b A G 2: 155,621,333 H495R probably damaging Het
Ndst4 C T 3: 125,724,736 S354L probably benign Het
Nfu1 T C 6: 87,009,944 V15A probably benign Het
Nphp4 T C 4: 152,524,257 S441P probably damaging Het
Nuak1 T C 10: 84,378,226 probably null Het
Olfr153 A G 2: 87,532,014 probably benign Het
Olfr197 A T 16: 59,185,743 C247S unknown Het
Olfr352 A T 2: 36,870,393 I276F probably damaging Het
Olfr918 A G 9: 38,672,629 S272P probably damaging Het
Palld A G 8: 61,525,155 V1109A unknown Het
Pik3c3 G A 18: 30,312,613 R551H probably benign Het
Plcb1 G A 2: 135,347,465 V838I probably benign Het
Plppr4 G T 3: 117,325,869 T297K probably damaging Het
Ptprd A G 4: 76,133,083 I67T probably benign Het
Rb1cc1 T A 1: 6,240,315 N312K probably damaging Het
Sh3glb1 A C 3: 144,691,898 probably null Het
Siglec1 C T 2: 131,074,093 C1283Y probably damaging Het
Spns1 T C 7: 126,373,823 I204V probably damaging Het
Supt6 T C 11: 78,225,458 Y693C probably damaging Het
Taar9 A G 10: 24,109,254 V94A probably damaging Het
Tchp T C 5: 114,708,816 S55P probably benign Het
Tmem132b A G 5: 125,785,965 H678R possibly damaging Het
Tnr G C 1: 159,850,093 G16A probably benign Het
Top3b T C 16: 16,882,699 probably null Het
Tpmt A G 13: 47,032,416 probably null Het
Treh G A 9: 44,681,358 V87I probably benign Het
Ttc4 T C 4: 106,678,766 D33G probably benign Het
Usp47 A G 7: 112,104,050 D1171G probably benign Het
Vmn2r61 G T 7: 42,300,668 L837F possibly damaging Het
Vmn2r86 T A 10: 130,452,571 N354Y probably damaging Het
Vmn2r88 C G 14: 51,413,046 A72G probably benign Het
Zscan4b C A 7: 10,902,023 V126F probably damaging Het
Other mutations in Gm5105
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3615:Gm5105 UTSW 3 138049688 missense unknown
R3616:Gm5105 UTSW 3 138049688 missense unknown
R7018:Gm5105 UTSW 3 138049558 missense unknown
Predicted Primers PCR Primer
(F):5'- ATCTTTGGGAGCAATAGTTTAGCG -3'
(R):5'- GCTGGGGTTCTTCCAAGAAAG -3'

Sequencing Primer
(F):5'- TGGTGGCCTGTCACTACC -3'
(R):5'- CTGGGGTTCTTCCAAGAAAGACTAC -3'
Posted On 2022-03-25