Incidental Mutation 'IGL02576:Gm9945'
ID299218
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9945
Ensembl Gene ENSMUSG00000054450
Gene Namepredicted gene 9945
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.174) question?
Stock #IGL02576
Quality Score
Status
Chromosome11
Chromosomal Location53480166-53481097 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 53480351 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100561 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067523] [ENSMUST00000104955]
Predicted Effect unknown
Transcript: ENSMUST00000067523
AA Change: Y18C
Predicted Effect probably benign
Transcript: ENSMUST00000104955
SMART Domains Protein: ENSMUSP00000100561
Gene: ENSMUSG00000044352

DomainStartEndE-ValueType
low complexity region 2 14 N/A INTRINSIC
low complexity region 46 59 N/A INTRINSIC
low complexity region 81 100 N/A INTRINSIC
low complexity region 101 113 N/A INTRINSIC
low complexity region 157 168 N/A INTRINSIC
low complexity region 193 213 N/A INTRINSIC
low complexity region 295 308 N/A INTRINSIC
ANK 344 379 1.34e-1 SMART
ANK 383 413 5.84e-2 SMART
low complexity region 496 504 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 A G 7: 120,433,455 I232M probably benign Het
Ace G A 11: 105,974,111 V537M probably damaging Het
Alg1 A G 16: 5,244,529 E425G possibly damaging Het
Cacng3 G A 7: 122,671,910 S46N probably benign Het
Cdc45 C T 16: 18,798,729 M200I probably benign Het
Cfap65 A G 1: 74,903,458 S1646P probably damaging Het
Col20a1 C T 2: 181,013,405 Q1152* probably null Het
D130043K22Rik A C 13: 24,856,870 T92P possibly damaging Het
Drc3 T C 11: 60,370,551 M176T probably benign Het
Esyt3 T C 9: 99,315,225 R851G probably benign Het
Fbxo43 A G 15: 36,152,175 V496A probably benign Het
Fut4 T A 9: 14,751,405 M198L probably damaging Het
Galt C T 4: 41,755,953 probably benign Het
Glipr1l1 A G 10: 112,060,319 K4E possibly damaging Het
Hspa12a A C 19: 58,799,410 I660R possibly damaging Het
Htr3b T C 9: 48,945,504 I225V possibly damaging Het
Igf2r T C 17: 12,748,763 D23G possibly damaging Het
Igsf5 A G 16: 96,386,581 I158V probably benign Het
Itgae A G 11: 73,118,505 Y505C possibly damaging Het
Kif16b A G 2: 142,862,545 probably benign Het
Kif26b T C 1: 178,916,347 V1336A probably benign Het
Kmt2d A G 15: 98,864,120 S450P unknown Het
Lexm T C 4: 106,591,628 D411G possibly damaging Het
Lhfpl2 G A 13: 94,174,226 M1I probably null Het
Lig4 A G 8: 9,971,116 I888T probably damaging Het
Msh4 G A 3: 153,867,746 T563M probably damaging Het
Muc5ac C T 7: 141,817,044 A3238V probably benign Het
Myo15b A G 11: 115,890,053 S1246G probably null Het
Olfr193 T C 16: 59,109,771 I280V probably benign Het
Pecam1 G A 11: 106,671,774 T599M probably damaging Het
Phf3 G A 1: 30,830,036 P644S probably benign Het
Pkd1l1 A C 11: 8,844,560 F2317C possibly damaging Het
Prdm4 A G 10: 85,900,937 M613T possibly damaging Het
Prim2 A T 1: 33,484,717 I371N probably damaging Het
Ptprs T C 17: 56,414,958 D1316G probably damaging Het
Rnf19b C T 4: 129,073,522 R285* probably null Het
Secisbp2 A G 13: 51,670,858 N381D possibly damaging Het
Slc28a2 T C 2: 122,458,171 I586T probably damaging Het
Spef1 T C 2: 131,174,642 H11R possibly damaging Het
Taar4 T C 10: 23,961,011 L173S probably damaging Het
Tas2r123 T C 6: 132,847,740 F200S possibly damaging Het
Tex16 T A X: 112,118,956 L384Q probably benign Het
Tox2 A G 2: 163,276,180 Q168R probably damaging Het
Trim5 T A 7: 104,278,417 E172V probably damaging Het
Txndc11 G A 16: 11,075,017 probably benign Het
Vmn1r232 T A 17: 20,913,913 I142F probably benign Het
Zdhhc25 A T 15: 88,601,269 H269L probably benign Het
Znrf4 T C 17: 56,512,199 D36G probably damaging Het
Other mutations in Gm9945
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1130:Gm9945 UTSW 11 53480518 unclassified probably benign
R2518:Gm9945 UTSW 11 53480336 unclassified probably benign
R4665:Gm9945 UTSW 11 53480375 unclassified probably benign
Posted On2015-04-16