Incidental Mutation 'IGL01368:Gm5039'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5039
Ensembl Gene ENSMUSG00000093847
Gene Namepredicted gene 5039
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.429) question?
Stock #IGL01368
Quality Score
Chromosomal Location88320122-88324026 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 88321088 bp
Amino Acid Change Aspartic acid to Asparagine at position 132 (D132N)
Ref Sequence ENSEMBL: ENSMUSP00000151971 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000177747] [ENSMUST00000218054]
Predicted Effect unknown
Transcript: ENSMUST00000177747
AA Change: D132N
SMART Domains Protein: ENSMUSP00000136949
Gene: ENSMUSG00000093847
AA Change: D132N

low complexity region 3 25 N/A INTRINSIC
eIF1a 28 110 4.9e-47 SMART
low complexity region 125 144 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000218054
AA Change: D132N
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222722
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acod1 T A 14: 103,051,334 D93E probably damaging Het
Adam22 T C 5: 8,127,411 Y566C probably damaging Het
Atp8b3 G A 10: 80,534,229 probably benign Het
Babam1 T A 8: 71,398,406 D104E probably damaging Het
Bcl2a1a T A 9: 88,957,447 W133R probably damaging Het
Ckm C T 7: 19,416,787 Q184* probably null Het
Clk4 T A 11: 51,281,172 Y246* probably null Het
Cyp3a57 T C 5: 145,369,068 S121P probably damaging Het
Gm5771 A G 6: 41,396,686 D161G possibly damaging Het
Gm8011 T C 14: 42,465,874 probably benign Het
Gpr153 T C 4: 152,282,994 F434S probably benign Het
Gpr158 G T 2: 21,827,098 W1003L probably damaging Het
Ighv5-9-1 T C 12: 113,736,390 E34G probably damaging Het
Igkv16-104 G T 6: 68,425,610 R2S possibly damaging Het
Map3k3 T C 11: 106,150,389 F395L probably benign Het
Myof T A 19: 37,936,457 T1161S probably damaging Het
Nlrp9a T C 7: 26,557,874 S217P probably damaging Het
Nol9 T A 4: 152,058,391 N687K probably benign Het
Olfr287 T C 15: 98,207,500 I295V probably damaging Het
Olfr697 T C 7: 106,741,622 E104G probably benign Het
Olfr748 T C 14: 50,710,993 V221A possibly damaging Het
Olfr952 A T 9: 39,426,180 V297D probably damaging Het
Rrh T C 3: 129,808,969 D229G probably benign Het
Sclt1 T C 3: 41,711,175 T153A probably damaging Het
Slc41a1 G A 1: 131,839,124 V127I probably damaging Het
Smarca2 C T 19: 26,774,294 S214L possibly damaging Het
Tmem63a T C 1: 180,970,232 V616A possibly damaging Het
Ubr1 A G 2: 120,941,131 probably benign Het
Vmn1r228 A G 17: 20,776,512 L248P probably benign Het
Zdhhc16 T A 19: 41,941,506 probably null Het
Other mutations in Gm5039
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02184:Gm5039 APN 12 88321181 missense probably benign 0.13
R2029:Gm5039 UTSW 12 88321421 missense unknown
R2943:Gm5039 UTSW 12 88321234 missense probably benign 0.04
R5022:Gm5039 UTSW 12 88321301 missense probably benign 0.08
R5054:Gm5039 UTSW 12 88321301 missense probably benign 0.08
R5988:Gm5039 UTSW 12 88321432 missense unknown
R6275:Gm5039 UTSW 12 88321225 missense possibly damaging 0.95
R6596:Gm5039 UTSW 12 88321287 missense possibly damaging 0.92
R6863:Gm5039 UTSW 12 88321198 missense probably damaging 1.00
Posted On2013-10-07