Incidental Mutation 'IGL02751:Gm1330'
ID306317
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm1330
Ensembl Gene ENSMUSG00000063507
Gene Namepredicted gene 1330
SynonymsLOC383753
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.052) question?
Stock #IGL02751
Quality Score
Status
Chromosome2
Chromosomal Location148990343-149003251 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) G to A at 148990473 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000105568 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081553] [ENSMUST00000109942]
Predicted Effect probably benign
Transcript: ENSMUST00000081553
SMART Domains Protein: ENSMUSP00000080268
Gene: ENSMUSG00000063507

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Blast:CY 34 162 3e-12 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000109942
SMART Domains Protein: ENSMUSP00000105568
Gene: ENSMUSG00000063507

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Blast:CY 34 162 1e-11 BLAST
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adra1a A T 14: 66,727,532 I324F possibly damaging Het
Ago2 G A 15: 73,130,897 A162V possibly damaging Het
Aox4 G T 1: 58,259,052 R1059I probably damaging Het
AU021092 C A 16: 5,212,619 V304L probably damaging Het
Bcs1l T G 1: 74,589,616 F20V probably damaging Het
Braf T C 6: 39,660,867 probably benign Het
Cacna1a T C 8: 84,569,952 C1200R probably damaging Het
Ccdc116 T A 16: 17,141,972 R284S probably benign Het
Cntnap5a T G 1: 116,184,457 probably null Het
Col12a1 A T 9: 79,613,859 probably benign Het
Cpa4 T A 6: 30,581,740 Y229N probably damaging Het
Fbp1 A C 13: 62,875,143 probably null Het
Gimap3 A T 6: 48,765,238 W253R probably benign Het
Gm4841 A G 18: 60,271,021 probably benign Het
Grip1 A G 10: 119,978,577 T338A probably benign Het
Hmg20b A T 10: 81,346,551 probably benign Het
Hnrnpdl A G 5: 100,037,974 F151L probably damaging Het
Klhl30 T A 1: 91,354,099 F141I probably damaging Het
Lamc3 T A 2: 31,920,704 F862Y probably benign Het
Lap3 T C 5: 45,504,796 C313R probably damaging Het
Lrp2 T C 2: 69,533,462 T344A possibly damaging Het
Mga A G 2: 119,947,770 E2023G possibly damaging Het
Mical2 A T 7: 112,332,036 K735N probably benign Het
Muc15 A G 2: 110,731,773 T185A probably benign Het
Olfr109 T C 17: 37,466,415 C70R probably damaging Het
Osbp2 T C 11: 3,863,434 K145R probably benign Het
Pde1c T C 6: 56,181,688 T52A probably damaging Het
Pidd1 A G 7: 141,439,163 S802P possibly damaging Het
Pip5k1c C A 10: 81,317,321 probably null Het
Prep T A 10: 45,115,186 I316N probably damaging Het
Prl3d2 G A 13: 27,126,031 probably null Het
Pygo1 A T 9: 72,945,037 I169F probably benign Het
Rnf10 G T 5: 115,242,666 A716E probably benign Het
Rtn4 G A 11: 29,706,409 probably null Het
Ryr1 A T 7: 29,078,774 V2099E probably damaging Het
Slc48a1 G A 15: 97,790,080 probably benign Het
Spag17 T A 3: 100,010,794 Y364* probably null Het
Syt3 A T 7: 44,386,062 D31V possibly damaging Het
Tango2 G T 16: 18,307,993 P143H probably benign Het
Tas2r104 A G 6: 131,685,144 S201P probably damaging Het
Tas2r107 G A 6: 131,659,484 L201F probably damaging Het
Vmn1r81 A T 7: 12,260,447 L78Q probably damaging Het
Vmn2r18 T A 5: 151,584,607 T351S probably benign Het
Other mutations in Gm1330
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02514:Gm1330 APN 2 148999385 splice site probably benign
R4463:Gm1330 UTSW 2 149003144 nonsense probably null
R5118:Gm1330 UTSW 2 149002986 intron probably benign
Posted On2015-04-16