Incidental Mutation 'IGL01710:Tex28'
ID 104735
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tex28
Ensembl Gene ENSMUSG00000062564
Gene Name testis expressed 28
Synonyms LOC385380
Accession Numbers
Essential gene? Not available question?
Stock # IGL01710
Quality Score
Status
Chromosome X
Chromosomal Location 73194550-73211444 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 73195939 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 278 (K278*)
Ref Sequence ENSEMBL: ENSMUSP00000109967 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033771] [ENSMUST00000078060] [ENSMUST00000101457] [ENSMUST00000114328] [ENSMUST00000127445]
AlphaFold B1AYN9
Predicted Effect probably benign
Transcript: ENSMUST00000033771
SMART Domains Protein: ENSMUSP00000033771
Gene: ENSMUSG00000031394

DomainStartEndE-ValueType
Pfam:7tm_1 65 317 1.1e-46 PFAM
low complexity region 335 357 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000078060
AA Change: K278*
SMART Domains Protein: ENSMUSP00000077207
Gene: ENSMUSG00000062564
AA Change: K278*

DomainStartEndE-ValueType
Pfam:Tmemb_cc2 46 151 1.3e-28 PFAM
Pfam:Tmemb_cc2 131 380 2.3e-45 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000101457
SMART Domains Protein: ENSMUSP00000099000
Gene: ENSMUSG00000031394

DomainStartEndE-ValueType
Pfam:7tm_1 65 317 1.7e-46 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000114328
AA Change: K278*
SMART Domains Protein: ENSMUSP00000109967
Gene: ENSMUSG00000062564
AA Change: K278*

DomainStartEndE-ValueType
Pfam:Tmemb_cc2 44 382 6.8e-112 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123401
Predicted Effect probably benign
Transcript: ENSMUST00000127445
SMART Domains Protein: ENSMUSP00000118631
Gene: ENSMUSG00000031394

DomainStartEndE-ValueType
Pfam:7tm_1 1 159 3.6e-20 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim3 G A 18: 62,004,645 (GRCm39) T48I probably damaging Het
Ccpg1 T C 9: 72,904,723 (GRCm39) probably benign Het
Chkb G A 15: 89,310,843 (GRCm39) Q379* probably null Het
Chst15 T A 7: 131,872,236 (GRCm39) D15V probably benign Het
Cntn4 G A 6: 106,527,392 (GRCm39) V425I possibly damaging Het
Cpa6 T A 1: 10,395,497 (GRCm39) N390I probably damaging Het
Efhd2 A G 4: 141,587,872 (GRCm39) F193S probably damaging Het
Ell3 T C 2: 121,271,993 (GRCm39) H128R probably damaging Het
Ercc5 T G 1: 44,203,235 (GRCm39) L291V probably damaging Het
Eva1c A G 16: 90,701,235 (GRCm39) Y302C probably damaging Het
Fmo3 A C 1: 162,810,612 (GRCm39) L26R probably damaging Het
Galntl6 T A 8: 58,989,002 (GRCm39) D17V probably damaging Het
Gm6483 C T 8: 19,741,629 (GRCm39) P55S probably damaging Het
Gstt2 A G 10: 75,669,579 (GRCm39) probably benign Het
Hmcn2 T A 2: 31,233,114 (GRCm39) L221Q probably damaging Het
Hoxa3 T C 6: 52,147,554 (GRCm39) probably benign Het
Kctd12b T C X: 152,472,479 (GRCm39) D70G probably damaging Het
Kdm7a T A 6: 39,152,320 (GRCm39) E125D probably benign Het
Klk1b21 T A 7: 43,755,919 (GRCm39) F249L probably benign Het
Mrpl41 T C 2: 24,864,429 (GRCm39) D81G possibly damaging Het
Nomo1 T A 7: 45,687,980 (GRCm39) L82Q probably damaging Het
Or5p58 G T 7: 107,694,449 (GRCm39) F109L probably benign Het
Papolg A T 11: 23,814,026 (GRCm39) S718T probably damaging Het
Pex6 A G 17: 47,036,252 (GRCm39) probably benign Het
Pi4k2a T A 19: 42,093,418 (GRCm39) L253Q probably damaging Het
Prdx6b T A 2: 80,123,490 (GRCm39) F100I probably damaging Het
Prr36 G A 8: 4,265,243 (GRCm39) P169L probably damaging Het
Ptgfrn T C 3: 100,980,404 (GRCm39) E312G probably damaging Het
Rasgrf1 A G 9: 89,873,745 (GRCm39) I685V probably benign Het
Setdb1 T C 3: 95,246,164 (GRCm39) E586G probably damaging Het
Sez6l2 C A 7: 126,567,388 (GRCm39) T841K probably damaging Het
Slc25a17 A T 15: 81,211,527 (GRCm39) L163* probably null Het
Slc35f3 A T 8: 127,115,900 (GRCm39) I276F probably benign Het
Tcerg1l T A 7: 137,996,789 (GRCm39) K149N possibly damaging Het
Tmprss9 A G 10: 80,733,793 (GRCm39) probably benign Het
Tnfaip8l1 A G 17: 56,478,782 (GRCm39) K24R probably benign Het
Trim36 T C 18: 46,321,455 (GRCm39) probably benign Het
Uba1 C T X: 20,537,604 (GRCm39) T274I possibly damaging Het
Ubr2 T C 17: 47,254,335 (GRCm39) T1439A probably benign Het
Ubr4 A G 4: 139,145,772 (GRCm39) D1523G possibly damaging Het
Uchl4 A T 9: 64,142,788 (GRCm39) T90S probably benign Het
Other mutations in Tex28
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00535:Tex28 APN X 73,204,647 (GRCm39) missense probably damaging 0.99
IGL01139:Tex28 APN X 73,194,830 (GRCm39) missense possibly damaging 0.83
Z1176:Tex28 UTSW X 73,205,106 (GRCm39) missense probably damaging 1.00
Posted On 2014-01-21