Incidental Mutation 'R4382:Gm6811'
ID 325394
Institutional Source Beutler Lab
Gene Symbol Gm6811
Ensembl Gene ENSMUSG00000091550
Gene Name predicted gene 6811
Synonyms
MMRRC Submission 041679-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.094) question?
Stock # R4382 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 21313434-21314966 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 21314865 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000169389]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000169389
SMART Domains Protein: ENSMUSP00000127210
Gene: ENSMUSG00000091550

DomainStartEndE-ValueType
low complexity region 4 16 N/A INTRINSIC
S_TKc 28 276 2.2e-84 SMART
low complexity region 290 301 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188185
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.0%
  • 20x: 94.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm2 T A 4: 144,281,596 (GRCm39) T399S possibly damaging Het
Acp2 T C 2: 91,038,454 (GRCm39) S309P possibly damaging Het
Adam23 T C 1: 63,605,787 (GRCm39) Y624H probably damaging Het
B4galnt4 T C 7: 140,650,449 (GRCm39) V772A probably damaging Het
Boc A T 16: 44,311,545 (GRCm39) L726H probably damaging Het
Calr3 T A 8: 73,182,008 (GRCm39) D120V probably damaging Het
Ccdc92b G A 11: 74,520,842 (GRCm39) S48N probably damaging Het
Ceacam12 C T 7: 17,799,959 (GRCm39) probably benign Het
Clca3a1 T A 3: 144,466,483 (GRCm39) M1L probably benign Het
Cnot1 T C 8: 96,496,407 (GRCm39) T300A probably damaging Het
Col12a1 A T 9: 79,538,023 (GRCm39) Y2514* probably null Het
Col6a6 G A 9: 105,660,889 (GRCm39) R407W probably damaging Het
Csnk1g1 T C 9: 65,927,190 (GRCm39) V119A probably damaging Het
Cspg4b T C 13: 113,459,288 (GRCm39) I1273T probably benign Het
Ddx60 G A 8: 62,402,012 (GRCm39) probably null Het
Dnajb12 A T 10: 59,733,321 (GRCm39) K372N probably benign Het
Fhl5 A C 4: 25,200,118 (GRCm39) C239G probably benign Het
Gad2 G A 2: 22,575,422 (GRCm39) V509I probably benign Het
Glrb T A 3: 80,786,946 (GRCm39) R72S probably damaging Het
Hecw1 C T 13: 14,490,749 (GRCm39) D748N probably damaging Het
Hk2 A T 6: 82,712,322 (GRCm39) L542Q probably null Het
Iglc1 A T 16: 18,880,508 (GRCm39) C104* probably null Het
Kel T A 6: 41,675,334 (GRCm39) T306S probably benign Het
Lpo T C 11: 87,713,027 (GRCm39) D25G probably benign Het
Mboat7 T A 7: 3,691,545 (GRCm39) Y109F possibly damaging Het
Myh15 T G 16: 48,963,306 (GRCm39) N1082K probably benign Het
Nagk A G 6: 83,774,993 (GRCm39) E90G probably benign Het
Nagpa A T 16: 5,021,819 (GRCm39) F10I possibly damaging Het
Or9a4 T A 6: 40,548,998 (GRCm39) L226H probably damaging Het
Otog T A 7: 45,939,122 (GRCm39) C2051S probably damaging Het
Ptpn6 A G 6: 124,704,361 (GRCm39) V315A possibly damaging Het
Rbp3 G C 14: 33,677,253 (GRCm39) E400D probably benign Het
Rnf41 T C 10: 128,272,392 (GRCm39) S140P probably benign Het
Ros1 C T 10: 51,997,055 (GRCm39) V1206I possibly damaging Het
Scgb2b12 T A 7: 32,024,870 (GRCm39) E112D probably benign Het
Serpinb3b T A 1: 107,083,273 (GRCm39) M210L probably damaging Het
Sipa1l1 A G 12: 82,493,596 (GRCm39) R1672G possibly damaging Het
Smc5 A G 19: 23,246,210 (GRCm39) S70P probably benign Het
Spen C T 4: 141,200,450 (GRCm39) G2703S possibly damaging Het
Stard9 C G 2: 120,464,703 (GRCm39) A56G probably damaging Het
Wtap A G 17: 13,194,307 (GRCm39) S87P probably damaging Het
Zzef1 T G 11: 72,765,938 (GRCm39) S1488R probably benign Het
Other mutations in Gm6811
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03290:Gm6811 APN 17 21,314,311 (GRCm39) intron noncoding transcript
R1666:Gm6811 UTSW 17 21,314,529 (GRCm39) intron noncoding transcript
R1677:Gm6811 UTSW 17 21,314,185 (GRCm39) intron noncoding transcript
R4763:Gm6811 UTSW 17 21,314,109 (GRCm39) intron noncoding transcript
R4928:Gm6811 UTSW 17 21,314,893 (GRCm39) intron noncoding transcript
R6276:Gm6811 UTSW 17 21,314,952 (GRCm39) intron noncoding transcript
R6276:Gm6811 UTSW 17 21,314,245 (GRCm39) intron noncoding transcript
Predicted Primers PCR Primer
(F):5'- TTCAGGCCACACCAGATGAC -3'
(R):5'- ATTGCGTCTCTGCTGGGAAG -3'

Sequencing Primer
(F):5'- GATGACACCCACACAGGAC -3'
(R):5'- TCTCTGCTGGGAAGAGGAGAAATTC -3'
Posted On 2015-07-06