Incidental Mutation 'IGL00503:Galnt15'
ID332502
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Galnt15
Ensembl Gene ENSMUSG00000021903
Gene Namepolypeptide N-acetylgalactosaminyltransferase 15
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.068) question?
Stock #IGL00503
Quality Score
Status
Chromosome14
Chromosomal Location32028989-32062197 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 32052356 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Methionine at position 359 (T359M)
Ref Sequence ENSEMBL: ENSMUSP00000131978 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022460] [ENSMUST00000164208]
Predicted Effect probably benign
Transcript: ENSMUST00000022460
AA Change: T483M

PolyPhen 2 Score 0.134 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000022460
Gene: ENSMUSG00000021903
AA Change: T483M

DomainStartEndE-ValueType
transmembrane domain 13 35 N/A INTRINSIC
low complexity region 105 116 N/A INTRINSIC
low complexity region 166 180 N/A INTRINSIC
Pfam:Glyco_tranf_2_3 191 436 2e-8 PFAM
Pfam:Glycos_transf_2 194 362 9e-32 PFAM
RICIN 505 630 1.19e-6 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000164208
AA Change: T359M

PolyPhen 2 Score 0.473 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000131978
Gene: ENSMUSG00000021903
AA Change: T359M

DomainStartEndE-ValueType
transmembrane domain 13 35 N/A INTRINSIC
low complexity region 105 116 N/A INTRINSIC
low complexity region 166 180 N/A INTRINSIC
low complexity region 228 248 N/A INTRINSIC
RICIN 381 506 1.19e-6 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930546C10Rik T A 18: 68,950,102 R14* probably null Het
Abcb5 A G 12: 118,907,601 S688P probably benign Het
Adgb T A 10: 10,406,099 Q597L possibly damaging Het
Aga G A 8: 53,518,921 V210I probably benign Het
Akap17b A G X: 36,612,310 S515P probably damaging Het
Brinp3 A T 1: 146,901,167 T451S probably benign Het
Cabcoco1 G T 10: 68,541,805 T18N possibly damaging Het
Ccar2 C T 14: 70,142,531 W402* probably null Het
Ccdc15 G A 9: 37,320,473 A185V probably damaging Het
Ccdc50 G A 16: 27,409,352 E90K probably damaging Het
Cckbr G A 7: 105,434,242 M217I probably benign Het
Clec16a A G 16: 10,694,649 T398A possibly damaging Het
Col4a1 A G 8: 11,240,076 probably benign Het
Cyp4v3 T A 8: 45,307,021 E498V probably damaging Het
Dgke T C 11: 89,041,501 I488V probably benign Het
Dip2c A G 13: 9,567,898 D443G probably damaging Het
Edem3 T G 1: 151,818,513 S852A probably benign Het
Fbxo8 T A 8: 56,588,023 M158K probably benign Het
Herc6 A G 6: 57,607,145 N330D probably benign Het
Kdf1 T C 4: 133,528,157 S62P probably damaging Het
Larp4 T A 15: 99,987,421 I51N probably damaging Het
Mfsd6l T A 11: 68,556,473 I50N probably damaging Het
Mroh2b A G 15: 4,899,197 Y4C probably benign Het
Muc3 G T 5: 137,137,123 Y343* probably null Het
Myom2 A C 8: 15,114,289 probably null Het
Npat A T 9: 53,572,649 probably benign Het
Pamr1 A T 2: 102,642,272 I639F possibly damaging Het
Pcsk2 A G 2: 143,793,239 S345G probably damaging Het
Pcyt1a A G 16: 32,467,101 T197A probably damaging Het
Pkd1 A G 17: 24,565,427 M316V probably benign Het
Plekhs1 T C 19: 56,464,599 probably null Het
Sema3e G T 5: 14,240,572 R557M probably damaging Het
Sgsm1 T C 5: 113,276,142 N154S probably benign Het
Smg1 A T 7: 118,185,483 probably benign Het
Sp110 A C 1: 85,577,329 F434C probably benign Het
Spats1 A T 17: 45,454,085 probably null Het
Tnfaip6 T G 2: 52,055,847 V235G probably damaging Het
Trim34a A T 7: 104,261,331 T447S probably damaging Het
Tut1 G A 19: 8,959,096 A95T probably damaging Het
Urgcp C T 11: 5,716,448 R630Q possibly damaging Het
Vmn1r125 G T 7: 21,272,181 M1I probably null Het
Vmn2r99 A G 17: 19,378,854 T267A probably benign Het
Wdr5 A G 2: 27,520,867 K162E probably benign Het
Zscan26 T G 13: 21,445,101 K285Q probably damaging Het
Other mutations in Galnt15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02491:Galnt15 APN 14 32056316 missense probably damaging 1.00
R0323:Galnt15 UTSW 14 32048085 missense probably damaging 0.99
R1900:Galnt15 UTSW 14 32049865 missense probably damaging 1.00
R4369:Galnt15 UTSW 14 32029539 missense possibly damaging 0.90
R4423:Galnt15 UTSW 14 32058269 missense possibly damaging 0.95
R4979:Galnt15 UTSW 14 32043290 missense probably damaging 0.99
R5093:Galnt15 UTSW 14 32049829 missense probably damaging 1.00
R5201:Galnt15 UTSW 14 32049865 missense probably damaging 1.00
R5254:Galnt15 UTSW 14 32058287 nonsense probably null
R5434:Galnt15 UTSW 14 32049843 missense possibly damaging 0.88
R5451:Galnt15 UTSW 14 32029911 missense probably benign 0.25
R5495:Galnt15 UTSW 14 32029817 missense probably damaging 0.97
R5874:Galnt15 UTSW 14 32052367 missense probably damaging 1.00
R6374:Galnt15 UTSW 14 32058159 missense probably damaging 0.96
R6444:Galnt15 UTSW 14 32040411 missense probably damaging 1.00
R7798:Galnt15 UTSW 14 32029905 missense possibly damaging 0.52
Z1177:Galnt15 UTSW 14 32052365 missense probably damaging 1.00
Posted On2015-08-05