Incidental Mutation 'IGL01080:Gm8005'
ID52659
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm8005
Ensembl Gene ENSMUSG00000092148
Gene Namepredicted gene 8005
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01080
Quality Score
Status
Chromosome14
Chromosomal Location42434156-42439673 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 42437014 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glycine at position 119 (D119G)
Gene Model predicted gene model for transcript(s):
Predicted Effect unknown
Transcript: ENSMUST00000167326
AA Change: D119G
SMART Domains Protein: ENSMUSP00000129153
Gene: ENSMUSG00000092148
AA Change: D119G

DomainStartEndE-ValueType
Pfam:Takusan 57 137 5.5e-26 PFAM
coiled coil region 164 186 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 A T 5: 8,934,258 R663W probably damaging Het
Cacng5 A T 11: 107,877,928 F179L probably damaging Het
Cacng5 C T 11: 107,881,705 V106I probably benign Het
Cd96 T C 16: 46,049,693 E471G possibly damaging Het
Cpt1c T C 7: 44,960,909 D621G probably damaging Het
Csmd3 T C 15: 47,881,403 I1503V probably benign Het
Dmgdh T C 13: 93,703,778 probably benign Het
Flg A T 3: 93,279,599 K119N probably benign Het
Gale T C 4: 135,966,078 Y104H probably damaging Het
Gstk1 A T 6: 42,246,626 D50V possibly damaging Het
Kmt2a T C 9: 44,809,092 D3866G unknown Het
Mastl A G 2: 23,146,148 S119P probably damaging Het
Olfr169 A T 16: 19,566,208 V225E probably damaging Het
Phf11c G A 14: 59,393,199 T19I probably benign Het
Ppp1r16b A G 2: 158,757,172 T355A probably damaging Het
Prmt7 T G 8: 106,237,214 probably benign Het
Rad50 T C 11: 53,706,068 T44A probably damaging Het
Rangap1 C T 15: 81,705,752 probably benign Het
Slc27a3 A T 3: 90,385,460 V634E probably benign Het
Tbxas1 T A 6: 39,021,181 L228I probably damaging Het
Tnfaip3 T C 10: 19,011,655 K41E probably benign Het
Tti1 C T 2: 157,982,459 V1025I probably damaging Het
Tyrobp T C 7: 30,417,416 probably null Het
Wfdc16 A T 2: 164,638,486 W30R probably damaging Het
Zyg11b A T 4: 108,237,416 L657Q probably damaging Het
Other mutations in Gm8005
AlleleSourceChrCoordTypePredicted EffectPPH Score
R7564:Gm8005 UTSW 14 42439542 missense
R7652:Gm8005 UTSW 14 42436962 missense
Posted On2013-06-21