Incidental Mutation 'R5648:Gm9847'
ID 441283
Institutional Source Beutler Lab
Gene Symbol Gm9847
Ensembl Gene ENSMUSG00000050974
Gene Name predicted pseudogene 9847
Synonyms
MMRRC Submission 043169-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.545) question?
Stock # R5648 (G1)
Quality Score 220
Status Not validated
Chromosome 12
Chromosomal Location 14544562-14545160 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 14545130 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000052528
SMART Domains Protein: ENSMUSP00000052625
Gene: ENSMUSG00000050974

DomainStartEndE-ValueType
low complexity region 32 43 N/A INTRINSIC
SH2 46 135 1.27e-20 SMART
SOCS 154 195 3.15e-16 SMART
SOCS_box 160 194 1.06e-9 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000220577
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca2 T C 2: 25,326,510 (GRCm39) probably null Het
Alpk2 A G 18: 65,482,988 (GRCm39) V340A probably damaging Het
Cald1 G T 6: 34,739,267 (GRCm39) probably null Het
Col24a1 C T 3: 145,064,321 (GRCm39) T702I probably benign Het
Ddx50 T C 10: 62,452,049 (GRCm39) R725G unknown Het
Dnah9 A T 11: 65,818,581 (GRCm39) F68L probably benign Het
Dnmt3b G A 2: 153,519,118 (GRCm39) V651M probably damaging Het
Dock1 G A 7: 134,348,683 (GRCm39) C299Y probably damaging Het
Epha4 T C 1: 77,375,162 (GRCm39) I562V probably benign Het
Esco2 A T 14: 66,068,641 (GRCm39) V223D probably damaging Het
Ggt6 T C 11: 72,326,542 (GRCm39) I33T possibly damaging Het
Gm10392 A T 11: 77,408,306 (GRCm39) D104E probably benign Het
Gnao1 A T 8: 94,676,070 (GRCm39) Y116F probably damaging Het
Gvin1 A T 7: 105,762,606 (GRCm39) I621K possibly damaging Het
Hyal6 T C 6: 24,734,235 (GRCm39) M56T possibly damaging Het
Hyou1 T A 9: 44,296,546 (GRCm39) D490E probably damaging Het
Igsf10 G C 3: 59,235,574 (GRCm39) Q1536E probably benign Het
Klk1b8 T C 7: 43,448,068 (GRCm39) S31P possibly damaging Het
Map3k6 A C 4: 132,970,646 (GRCm39) I178L probably benign Het
Mycbp2 T A 14: 103,528,778 (GRCm39) N427Y probably damaging Het
Ncr1 T A 7: 4,347,519 (GRCm39) I228N probably damaging Het
Nefh A T 11: 4,895,233 (GRCm39) Y319N probably damaging Het
Or4a80 A C 2: 89,582,417 (GRCm39) C252G probably damaging Het
Pakap T C 4: 57,854,848 (GRCm39) V120A probably damaging Het
Pcdhb18 G A 18: 37,623,537 (GRCm39) R289Q probably benign Het
Pkhd1 T A 1: 20,628,850 (GRCm39) Y699F probably benign Het
Plekhd1 T C 12: 80,767,362 (GRCm39) L250P probably damaging Het
Reln A G 5: 22,203,570 (GRCm39) V1228A probably benign Het
Rhobtb2 G T 14: 70,034,593 (GRCm39) R211S probably damaging Het
Rps6kb1 T C 11: 86,403,697 (GRCm39) I305V possibly damaging Het
Slc12a2 G A 18: 58,029,382 (GRCm39) G256E possibly damaging Het
Slc4a1ap A G 5: 31,708,129 (GRCm39) probably null Het
Thoc1 A G 18: 9,962,390 (GRCm39) T92A possibly damaging Het
Ticam1 TCACACA TCACA 17: 56,577,629 (GRCm39) probably null Het
Tmem117 T G 15: 94,992,653 (GRCm39) S438A possibly damaging Het
Ttll7 A G 3: 146,667,465 (GRCm39) N777S probably damaging Het
Ubd T A 17: 37,506,345 (GRCm39) V77E probably damaging Het
Ubqln3 A G 7: 103,790,117 (GRCm39) S658P probably damaging Het
Vmn1r78 G A 7: 11,886,693 (GRCm39) M101I possibly damaging Het
Wdr93 T C 7: 79,426,974 (GRCm39) C638R probably benign Het
Zfp983 T A 17: 21,877,947 (GRCm39) V50D probably damaging Het
Zhx3 A T 2: 160,623,881 (GRCm39) H95Q probably damaging Het
Other mutations in Gm9847
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0178:Gm9847 UTSW 12 14,544,649 (GRCm39) unclassified noncoding transcript
R1276:Gm9847 UTSW 12 14,544,932 (GRCm39) unclassified noncoding transcript
R2137:Gm9847 UTSW 12 14,545,082 (GRCm39) unclassified noncoding transcript
R3810:Gm9847 UTSW 12 14,545,148 (GRCm39) unclassified noncoding transcript
R5196:Gm9847 UTSW 12 14,545,016 (GRCm39) unclassified noncoding transcript
R5566:Gm9847 UTSW 12 14,545,000 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- TGTCCAGATGTGCAAGGATAAACG -3'
(R):5'- GACTGGACCAGAAAAGAAATTCCTC -3'

Sequencing Primer
(F):5'- CAAGGATAAACGGACAGGCCC -3'
(R):5'- TTCCTCCCGACACATAATAATCAG -3'
Posted On 2016-11-08