Incidental Mutation 'IGL02930:Gm6878'
ID 364063
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 # IGL02930
Quality Score
Status
Chromosome 14
Chromosomal Location 67542337-67552160 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to G at 67548439 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: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A G 11: 9,328,226 (GRCm39) N3433S possibly damaging Het
Actl9 T C 17: 33,653,073 (GRCm39) S378P probably damaging Het
Aldh6a1 C A 12: 84,480,756 (GRCm39) L426F possibly damaging Het
Ankef1 T C 2: 136,392,245 (GRCm39) I478T possibly damaging Het
Cabs1 A G 5: 88,127,745 (GRCm39) D132G probably damaging Het
Ccdc39 T C 3: 33,879,643 (GRCm39) E475G probably damaging Het
Cmtm2b A C 8: 105,056,402 (GRCm39) M104L probably benign Het
Cops2 T C 2: 125,674,109 (GRCm39) probably benign Het
Dnajc4 C A 19: 6,966,801 (GRCm39) V176F possibly damaging Het
Eepd1 A G 9: 25,394,536 (GRCm39) N267D probably damaging Het
Elobl T G 11: 88,856,012 (GRCm39) D17A possibly damaging Het
Erich6 G A 3: 58,529,775 (GRCm39) probably benign Het
Flna G A X: 73,267,506 (GRCm39) R2548C probably damaging Het
Gpc1 G T 1: 92,785,021 (GRCm39) E355* probably null Het
Islr C T 9: 58,065,483 (GRCm39) probably benign Het
Mex3a A T 3: 88,443,532 (GRCm39) I203L probably benign Het
Or5p58 A T 7: 107,694,621 (GRCm39) I52N probably damaging Het
Or6c88 T C 10: 129,407,184 (GRCm39) I220T probably damaging Het
Or8g24 G T 9: 38,989,308 (GRCm39) H244Q probably damaging Het
Prokr2 T C 2: 132,215,394 (GRCm39) S195G probably benign Het
Pyroxd1 A T 6: 142,304,778 (GRCm39) D335V probably damaging Het
Rps6kl1 T C 12: 85,196,548 (GRCm39) T39A probably benign Het
Rusc2 G A 4: 43,416,376 (GRCm39) A561T probably damaging Het
Sel1l3 A C 5: 53,280,559 (GRCm39) V937G possibly damaging Het
Sh3pxd2b A G 11: 32,367,161 (GRCm39) T382A possibly damaging Het
Tbx21 A G 11: 96,990,865 (GRCm39) I271T probably damaging Het
Timeless T C 10: 128,083,060 (GRCm39) V632A probably benign Het
Tle3 A G 9: 61,301,981 (GRCm39) N67S possibly damaging Het
Tln2 G A 9: 67,300,944 (GRCm39) R95* probably null Het
Trim24 A G 6: 37,928,380 (GRCm39) probably benign Het
Uggt1 A T 1: 36,196,537 (GRCm39) D1253E probably benign Het
Vmn1r8 A G 6: 57,013,579 (GRCm39) K210R probably benign Het
Other mutations in Gm6878
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01991:Gm6878 APN 14 67,543,678 (GRCm39) intron probably benign
Posted On 2015-12-18