Incidental Mutation 'IGL02751:Gm1330'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm1330
Ensembl Gene ENSMUSG00000063507
Gene Namepredicted gene 1330
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.052) question?
Stock #IGL02751
Quality Score
Chromosomal Location148990343-149003251 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) G to A at 148990473 bp
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

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

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