Incidental Mutation 'IGL02119:Gm11146'
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ID280535
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11146
Ensembl Gene ENSMUSG00000079546
Gene Namepredicted gene 11146
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.103) question?
Stock #IGL02119
Quality Score
Status
Chromosome16
Chromosomal Location77588578-77602094 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to T at 77588610 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000109869 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114231]
Predicted Effect noncoding transcript
Transcript: ENSMUST00000068704
SMART Domains Protein: ENSMUSP00000070456
Gene: ENSMUSG00000052450

DomainStartEndE-ValueType
low complexity region 23 42 N/A INTRINSIC
low complexity region 105 116 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000114231
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170849
SMART Domains Protein: ENSMUSP00000127794
Gene: ENSMUSG00000090386

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182398
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182601
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182656
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182820
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183099
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183327
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 T A 2: 69,328,000 probably null Het
Acsbg2 T C 17: 56,868,459 probably benign Het
Ap3b1 T C 13: 94,462,403 V495A probably benign Het
Astn1 T C 1: 158,511,154 probably benign Het
Bora A G 14: 99,053,538 D94G probably damaging Het
Bpifb9b G T 2: 154,313,624 V348L possibly damaging Het
Cd160 A T 3: 96,808,823 I17N possibly damaging Het
Cyp2d11 A C 15: 82,390,064 I372S probably damaging Het
Dennd2c T A 3: 103,137,243 V380D probably damaging Het
Fat4 C T 3: 38,982,939 A3580V probably benign Het
Filip1 A G 9: 79,818,266 S1024P probably benign Het
Flnc G A 6: 29,447,512 E1105K probably damaging Het
Gbp4 T A 5: 105,121,042 E415V probably benign Het
Gdap1l1 T A 2: 163,453,668 F224Y probably damaging Het
Gsn G T 2: 35,302,495 R485L probably damaging Het
Havcr1 A G 11: 46,775,493 Y261C probably damaging Het
Maneal A T 4: 124,859,167 I229N probably benign Het
Med24 A T 11: 98,728,835 M27K probably benign Het
Nipsnap2 T A 5: 129,747,992 probably benign Het
Noa1 T A 5: 77,307,579 Q430L probably benign Het
Olfr1099 T C 2: 86,959,183 I92V probably benign Het
Olfr365 C A 2: 37,201,269 S9R possibly damaging Het
Olfr74 T A 2: 87,974,410 N85I probably benign Het
Olfr834 T C 9: 18,988,612 V208A probably benign Het
Pde3a T A 6: 141,459,803 S460R probably damaging Het
Pdzd8 T C 19: 59,300,490 Q826R possibly damaging Het
Pfkfb4 C T 9: 109,025,110 R351W probably damaging Het
Pikfyve T A 1: 65,272,571 I1989N probably damaging Het
Poldip2 T A 11: 78,517,908 F200I probably damaging Het
Prodh2 T C 7: 30,506,504 V208A probably damaging Het
Ranbp10 T C 8: 105,827,003 D89G probably damaging Het
Rbm33 T A 5: 28,339,017 S90R probably damaging Het
Slc44a4 A C 17: 34,928,661 D441A probably damaging Het
Slc4a10 A T 2: 62,228,670 I174F probably damaging Het
Smim17 T C 7: 6,427,161 probably benign Het
Tln1 T C 4: 43,546,760 E872G probably damaging Het
Tmem214 G A 5: 30,872,746 A296T probably benign Het
Top2b T C 14: 16,406,733 L625S probably damaging Het
Vmn2r59 A G 7: 42,046,169 V273A probably benign Het
Vmn2r9 G A 5: 108,843,636 L620F probably damaging Het
Whrn T G 4: 63,435,487 K348Q probably damaging Het
Zc3h14 T C 12: 98,763,895 V399A probably benign Het
Other mutations in Gm11146
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0392:Gm11146 UTSW 16 77597166 intron probably benign
R1302:Gm11146 UTSW 16 77602082 missense unknown
R2055:Gm11146 UTSW 16 77595081 intron probably benign
R4843:Gm11146 UTSW 16 77595256 intron probably benign
Posted On2015-04-16