Incidental Mutation 'IGL01062:Tex21'
ID 52418
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tex21
Ensembl Gene ENSMUSG00000021056
Gene Name testis expressed gene 21
Synonyms 4931406F04Rik, tsec-2, 4931412D23Rik, 4931421K24Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.107) question?
Stock # IGL01062
Quality Score
Status
Chromosome 12
Chromosomal Location 76245460-76293520 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 76245718 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 526 (D526G)
Ref Sequence ENSEMBL: ENSMUSP00000021453 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021453]
AlphaFold Q9R0U9
Predicted Effect probably benign
Transcript: ENSMUST00000021453
AA Change: D526G

PolyPhen 2 Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000021453
Gene: ENSMUSG00000021056
AA Change: D526G

DomainStartEndE-ValueType
coiled coil region 83 190 N/A INTRINSIC
coiled coil region 308 356 N/A INTRINSIC
coiled coil region 409 447 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aen G A 7: 78,557,050 (GRCm39) M299I probably damaging Het
Amer3 A G 1: 34,625,820 (GRCm39) K20E probably damaging Het
Arhgap31 A G 16: 38,421,818 (GRCm39) L1416P probably damaging Het
Avpr1a G A 10: 122,285,434 (GRCm39) C242Y probably damaging Het
Bclaf3 T C X: 158,336,415 (GRCm39) Y281H probably benign Het
Cdc14a T A 3: 116,068,361 (GRCm39) probably benign Het
Cfap206 C T 4: 34,721,562 (GRCm39) S162N probably damaging Het
Cntn4 T C 6: 106,595,239 (GRCm39) probably benign Het
Cyp3a44 T A 5: 145,731,149 (GRCm39) D217V possibly damaging Het
Eprs1 A G 1: 185,111,812 (GRCm39) E274G probably benign Het
Ercc6l2 G T 13: 63,995,268 (GRCm39) Q354H probably null Het
Glb1l A T 1: 75,177,882 (GRCm39) I392N probably damaging Het
Gm3173 T C 14: 15,728,472 (GRCm39) probably null Het
Hadh C T 3: 131,034,640 (GRCm39) V219M probably damaging Het
Hspb9 A G 11: 100,604,761 (GRCm39) H29R possibly damaging Het
Iqgap3 G T 3: 88,017,429 (GRCm39) V240L probably benign Het
Jmjd1c T C 10: 67,062,494 (GRCm39) S1616P probably damaging Het
Knl1 A G 2: 118,907,461 (GRCm39) I1662V probably benign Het
Maco1 A T 4: 134,560,608 (GRCm39) V125E probably damaging Het
Mapre3 A G 5: 31,022,240 (GRCm39) I236V probably benign Het
Med17 T C 9: 15,190,917 (GRCm39) E58G probably benign Het
Myh6 T C 14: 55,189,749 (GRCm39) E1099G probably damaging Het
Myt1 T A 2: 181,439,522 (GRCm39) V348D probably damaging Het
Nat10 A T 2: 103,573,393 (GRCm39) I368N probably damaging Het
Nol6 T C 4: 41,118,205 (GRCm39) I811V probably benign Het
Oas1d C A 5: 121,057,127 (GRCm39) Y244* probably null Het
Or6e1 A T 14: 54,520,181 (GRCm39) M57K probably damaging Het
Osbpl1a A G 18: 13,038,132 (GRCm39) V273A probably benign Het
Pigw T C 11: 84,768,769 (GRCm39) R187G probably benign Het
Plekhg5 G A 4: 152,192,953 (GRCm39) D603N probably damaging Het
Ptprk T C 10: 28,456,414 (GRCm39) V1058A probably damaging Het
Robo4 G A 9: 37,317,296 (GRCm39) S537N probably benign Het
Rptn T A 3: 93,304,489 (GRCm39) F607L probably benign Het
Sall1 A G 8: 89,759,972 (GRCm39) V44A probably damaging Het
Sh3bp4 C A 1: 89,071,682 (GRCm39) Q177K probably benign Het
Skic3 T A 13: 76,303,581 (GRCm39) L1225* probably null Het
Spmip6 T A 4: 41,511,433 (GRCm39) E93D probably damaging Het
Srrt C A 5: 137,294,569 (GRCm39) G779V probably damaging Het
Tamalin A G 15: 101,126,777 (GRCm39) probably benign Het
Vmn1r10 A G 6: 57,090,821 (GRCm39) S138G possibly damaging Het
Yars2 C T 16: 16,124,406 (GRCm39) R338* probably null Het
Zfp454 T C 11: 50,765,033 (GRCm39) E22G probably benign Het
Zzef1 T A 11: 72,765,795 (GRCm39) C1441S probably benign Het
Other mutations in Tex21
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00472:Tex21 APN 12 76,253,571 (GRCm39) missense probably damaging 1.00
IGL00923:Tex21 APN 12 76,291,885 (GRCm39) missense probably damaging 1.00
IGL01063:Tex21 APN 12 76,245,592 (GRCm39) missense probably benign 0.34
IGL02624:Tex21 APN 12 76,261,398 (GRCm39) missense probably damaging 1.00
IGL03349:Tex21 APN 12 76,268,365 (GRCm39) missense probably benign 0.14
IGL03387:Tex21 APN 12 76,245,694 (GRCm39) missense probably damaging 1.00
IGL03412:Tex21 APN 12 76,291,780 (GRCm39) critical splice donor site probably null
ihop UTSW 12 76,286,229 (GRCm39) critical splice donor site probably null
R0189:Tex21 UTSW 12 76,286,307 (GRCm39) missense probably benign 0.13
R0730:Tex21 UTSW 12 76,250,940 (GRCm39) missense probably benign 0.25
R1521:Tex21 UTSW 12 76,251,044 (GRCm39) missense probably benign 0.38
R1572:Tex21 UTSW 12 76,253,665 (GRCm39) missense probably benign 0.03
R1700:Tex21 UTSW 12 76,268,446 (GRCm39) missense probably damaging 0.99
R1941:Tex21 UTSW 12 76,268,458 (GRCm39) missense possibly damaging 0.68
R4654:Tex21 UTSW 12 76,263,860 (GRCm39) missense probably benign 0.32
R4943:Tex21 UTSW 12 76,268,474 (GRCm39) missense probably damaging 1.00
R6175:Tex21 UTSW 12 76,245,707 (GRCm39) missense probably benign 0.00
R6262:Tex21 UTSW 12 76,259,306 (GRCm39) missense probably damaging 0.99
R6738:Tex21 UTSW 12 76,286,283 (GRCm39) missense probably benign 0.12
R6759:Tex21 UTSW 12 76,251,086 (GRCm39) critical splice acceptor site probably null
R6890:Tex21 UTSW 12 76,286,229 (GRCm39) critical splice donor site probably null
R8910:Tex21 UTSW 12 76,263,533 (GRCm39) unclassified probably benign
R9547:Tex21 UTSW 12 76,253,591 (GRCm39) missense probably damaging 0.99
Z1176:Tex21 UTSW 12 76,250,894 (GRCm39) missense probably damaging 1.00
Posted On 2013-06-21