Incidental Mutation 'IGL01696:Gm15737'
ID 104274
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm15737
Ensembl Gene ENSMUSG00000079462
Gene Name predicted gene 15737
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01696
Quality Score
Status
Chromosome 6
Chromosomal Location 92846338-92861392 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to A at 92856802 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000126498 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113434] [ENSMUST00000113438] [ENSMUST00000167391]
AlphaFold D3YZR0
Predicted Effect unknown
Transcript: ENSMUST00000113434
AA Change: I77K
Predicted Effect probably benign
Transcript: ENSMUST00000113438
SMART Domains Protein: ENSMUSP00000109065
Gene: ENSMUSG00000030022

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:Pep_M12B_propep 49 207 1.8e-37 PFAM
low complexity region 234 247 N/A INTRINSIC
Pfam:Reprolysin_5 291 476 7.6e-17 PFAM
Pfam:Reprolysin_4 291 495 2e-11 PFAM
Pfam:Reprolysin 293 499 7.4e-29 PFAM
Pfam:Reprolysin_2 310 489 1e-13 PFAM
Pfam:Reprolysin_3 314 445 1.7e-14 PFAM
TSP1 591 643 2.15e-9 SMART
Pfam:ADAM_spacer1 753 871 7.3e-35 PFAM
TSP1 881 936 1.14e0 SMART
Blast:TSP1 938 993 2e-28 BLAST
TSP1 1000 1054 3.78e-5 SMART
TSP1 1055 1109 5.64e-4 SMART
TSP1 1110 1166 1.25e-5 SMART
TSP1 1186 1240 1.45e-6 SMART
TSP1 1242 1296 4.41e-6 SMART
TSP1 1328 1380 7.06e-5 SMART
TSP1 1381 1436 4.24e-8 SMART
TSP1 1440 1495 8.23e-6 SMART
TSP1 1496 1551 1.23e-4 SMART
TSP1 1552 1609 2e-4 SMART
TSP1 1611 1672 1.25e-5 SMART
TSP1 1676 1730 3.47e-4 SMART
Pfam:GON 1732 1930 1.6e-85 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000167391
SMART Domains Protein: ENSMUSP00000126498
Gene: ENSMUSG00000030022

DomainStartEndE-ValueType
TSP1 10 62 2.15e-9 SMART
Pfam:ADAM_spacer1 172 290 6.1e-35 PFAM
TSP1 300 355 1.14e0 SMART
Blast:TSP1 357 412 3e-28 BLAST
TSP1 419 473 3.78e-5 SMART
TSP1 474 528 5.64e-4 SMART
TSP1 529 585 1.25e-5 SMART
TSP1 605 659 1.45e-6 SMART
TSP1 661 715 4.41e-6 SMART
TSP1 747 799 7.06e-5 SMART
TSP1 800 855 4.24e-8 SMART
TSP1 859 914 8.23e-6 SMART
TSP1 915 970 1.23e-4 SMART
TSP1 971 1028 2e-4 SMART
TSP1 1030 1091 1.25e-5 SMART
TSP1 1095 1149 3.47e-4 SMART
Pfam:GON 1150 1350 2.1e-86 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam1b A G 5: 121,638,856 (GRCm39) S730P possibly damaging Het
Ano3 T G 2: 110,498,082 (GRCm39) D753A probably damaging Het
Apoc4 C T 7: 19,412,109 (GRCm39) C113Y probably damaging Het
Arhgdia A G 11: 120,471,202 (GRCm39) probably benign Het
Ccdc171 A G 4: 83,573,815 (GRCm39) T459A possibly damaging Het
Ccdc190 A C 1: 169,761,393 (GRCm39) K165T probably damaging Het
Dop1b T C 16: 93,567,128 (GRCm39) V1185A probably benign Het
Ednrb C T 14: 104,060,625 (GRCm39) V223I probably benign Het
Ermp1 T C 19: 29,623,538 (GRCm39) I151V possibly damaging Het
Herc3 A G 6: 58,837,371 (GRCm39) H348R possibly damaging Het
Immp2l G T 12: 41,675,590 (GRCm39) A95S probably damaging Het
Invs A G 4: 48,425,997 (GRCm39) Y928C probably damaging Het
Itprid1 A G 6: 55,874,680 (GRCm39) H210R probably benign Het
Or1l4 A G 2: 37,091,523 (GRCm39) E90G probably benign Het
Or7g17 A T 9: 18,768,352 (GRCm39) I135L probably benign Het
Or8c15 A C 9: 38,120,345 (GRCm39) probably benign Het
Pkd1l2 G T 8: 117,783,126 (GRCm39) S731R probably benign Het
Pkhd1l1 T C 15: 44,392,747 (GRCm39) M1694T possibly damaging Het
Pld2 C A 11: 70,433,606 (GRCm39) R212S probably damaging Het
Plekhg6 A G 6: 125,355,793 (GRCm39) F4L probably benign Het
Rps6ka6 T C X: 110,317,214 (GRCm39) Q634R probably benign Het
Slc1a3 T C 15: 8,671,822 (GRCm39) E378G probably benign Het
Tmem184b T C 15: 79,262,729 (GRCm39) T43A possibly damaging Het
Ttn A G 2: 76,577,132 (GRCm39) V24587A probably damaging Het
Uba7 T A 9: 107,854,547 (GRCm39) L262Q probably damaging Het
Zfp954 G T 7: 7,118,397 (GRCm39) H382Q probably damaging Het
Other mutations in Gm15737
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03052:Gm15737 APN 6 92,846,481 (GRCm39) intron probably benign
R0892:Gm15737 UTSW 6 92,856,721 (GRCm39) intron probably benign
R2566:Gm15737 UTSW 6 92,856,701 (GRCm39) nonsense probably null
R9198:Gm15737 UTSW 6 92,856,640 (GRCm39) missense unknown
Z1177:Gm15737 UTSW 6 92,856,872 (GRCm39) missense unknown
Posted On 2014-01-21