Incidental Mutation 'IGL01368:Gm5039'
ID76005
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5039
Ensembl Gene ENSMUSG00000093847
Gene Namepredicted gene 5039
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.429) question?
Stock #IGL01368
Quality Score
Status
Chromosome12
Chromosomal Location88320122-88324026 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 88321088 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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