Incidental Mutation 'IGL01991:Gm6878'
ID 182882
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6878
Ensembl Gene ENSMUSG00000075549
Gene Name predicted gene 6878
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01991
Quality Score
Status
Chromosome 14
Chromosomal Location 67542337-67552160 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) G to A at 67543678 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000135500 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022637] [ENSMUST00000176029] [ENSMUST00000176161]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000022637
SMART Domains Protein: ENSMUSP00000022637
Gene: ENSMUSG00000022053

DomainStartEndE-ValueType
IPT 252 336 9.09e-8 SMART
HLH 337 386 3.39e-1 SMART
internal_repeat_1 388 412 2.68e-6 PROSPERO
low complexity region 454 484 N/A INTRINSIC
low complexity region 512 531 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000100448
Predicted Effect probably benign
Transcript: ENSMUST00000176029
SMART Domains Protein: ENSMUSP00000135782
Gene: ENSMUSG00000022053

DomainStartEndE-ValueType
Pfam:COE1_DBD 16 246 2.3e-145 PFAM
IPT 252 336 9.09e-8 SMART
HLH 337 386 3.39e-1 SMART
internal_repeat_1 388 412 2.68e-6 PROSPERO
low complexity region 454 484 N/A INTRINSIC
low complexity region 512 531 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000176161
SMART Domains Protein: ENSMUSP00000135500
Gene: ENSMUSG00000022053

DomainStartEndE-ValueType
IPT 252 336 9.09e-8 SMART
HLH 337 386 3.39e-1 SMART
internal_repeat_1 388 412 2.68e-6 PROSPERO
low complexity region 454 484 N/A INTRINSIC
low complexity region 512 531 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700034J05Rik A T 6: 146,854,608 (GRCm39) F145I probably benign Het
Acot7 A G 4: 152,307,536 (GRCm39) K152E possibly damaging Het
Adamts13 G T 2: 26,880,610 (GRCm39) G731V probably damaging Het
Als2cl C T 9: 110,721,985 (GRCm39) R584C probably benign Het
Apba1 T A 19: 23,914,836 (GRCm39) S679T possibly damaging Het
Asxl3 G A 18: 22,649,219 (GRCm39) V403I probably damaging Het
Card11 T C 5: 140,899,133 (GRCm39) T14A possibly damaging Het
Creb1 T C 1: 64,598,913 (GRCm39) F97L probably benign Het
Crispld1 T A 1: 17,823,241 (GRCm39) H407Q probably benign Het
Crtac1 A T 19: 42,402,560 (GRCm39) L16Q possibly damaging Het
Cyp2c29 T C 19: 39,318,759 (GRCm39) I452T probably damaging Het
Dennd5b A T 6: 148,982,322 (GRCm39) D95E probably damaging Het
Dysf C T 6: 84,090,600 (GRCm39) P1002L probably damaging Het
Greb1 T C 12: 16,749,682 (GRCm39) Y1048C probably damaging Het
Iqcc T A 4: 129,511,582 (GRCm39) E105V probably benign Het
Lhx8 A G 3: 154,030,191 (GRCm39) L116P probably damaging Het
Lrrk2 A G 15: 91,664,149 (GRCm39) D1962G probably damaging Het
Map1b T A 13: 99,566,077 (GRCm39) M2215L unknown Het
Mapk8ip3 A T 17: 25,146,835 (GRCm39) L136Q possibly damaging Het
Mical3 T C 6: 120,912,172 (GRCm39) N1896D probably damaging Het
Mprip A G 11: 59,645,838 (GRCm39) E674G probably damaging Het
Or6b13 C T 7: 139,782,345 (GRCm39) E113K probably damaging Het
Or8j3 T C 2: 86,028,877 (GRCm39) N73S probably benign Het
Pdzrn4 T A 15: 92,299,807 (GRCm39) probably null Het
Pramel41 A T 5: 94,593,705 (GRCm39) Q10L probably benign Het
Prom1 T C 5: 44,204,848 (GRCm39) T209A probably benign Het
Prom2 C A 2: 127,371,142 (GRCm39) C785F probably damaging Het
Psg20 T C 7: 18,418,350 (GRCm39) Q139R probably benign Het
Rapgef6 T A 11: 54,443,695 (GRCm39) C93S probably benign Het
Rassf2 C T 2: 131,842,352 (GRCm39) probably null Het
Scn11a A G 9: 119,648,970 (GRCm39) I31T probably damaging Het
Slc4a5 A T 6: 83,240,525 (GRCm39) D164V possibly damaging Het
Slco3a1 T C 7: 73,934,144 (GRCm39) D676G possibly damaging Het
Tmcc2 T C 1: 132,288,830 (GRCm39) I208V probably benign Het
Traf4 T C 11: 78,050,872 (GRCm39) D428G possibly damaging Het
Trio T C 15: 27,871,360 (GRCm39) I586V possibly damaging Het
Unc80 T A 1: 66,508,668 (GRCm39) C46* probably null Het
Vmn2r89 A G 14: 51,689,676 (GRCm39) N60D probably benign Het
Wscd1 A T 11: 71,678,549 (GRCm39) K391* probably null Het
Wwc2 A T 8: 48,322,901 (GRCm39) L400* probably null Het
Other mutations in Gm6878
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02930:Gm6878 APN 14 67,548,439 (GRCm39) intron probably benign
Posted On 2014-05-07