Incidental Mutation 'R3690:Tex47'
ID 269717
Institutional Source Beutler Lab
Gene Symbol Tex47
Ensembl Gene ENSMUSG00000040514
Gene Name testis expressed 47
Synonyms 4921511H03Rik
MMRRC Submission 040685-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # R3690 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 7354119-7361491 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to G at 7354777 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000143568 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088796] [ENSMUST00000159546] [ENSMUST00000160634] [ENSMUST00000200317]
AlphaFold Q9D5W8
Predicted Effect probably benign
Transcript: ENSMUST00000088796
SMART Domains Protein: ENSMUSP00000086176
Gene: ENSMUSG00000040514

DomainStartEndE-ValueType
Blast:BLUF 47 146 2e-20 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000159546
SMART Domains Protein: ENSMUSP00000124368
Gene: ENSMUSG00000040514

DomainStartEndE-ValueType
Blast:BLUF 47 146 2e-20 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000160634
SMART Domains Protein: ENSMUSP00000125471
Gene: ENSMUSG00000040514

DomainStartEndE-ValueType
Blast:BLUF 47 146 2e-20 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196680
Predicted Effect probably benign
Transcript: ENSMUST00000200317
SMART Domains Protein: ENSMUSP00000143568
Gene: ENSMUSG00000092094

DomainStartEndE-ValueType
ZnF_C2H2 56 80 2e-2 SMART
low complexity region 958 970 N/A INTRINSIC
low complexity region 1155 1179 N/A INTRINSIC
low complexity region 1196 1207 N/A INTRINSIC
low complexity region 1215 1234 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency 98% (54/55)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aass T A 6: 23,091,328 (GRCm39) Y629F probably benign Het
Abcb5 T A 12: 118,836,668 (GRCm39) D1081V probably damaging Het
Afdn A G 17: 14,108,671 (GRCm39) E1398G probably damaging Het
Atp8b5 T C 4: 43,368,055 (GRCm39) C893R probably damaging Het
Avl9 C T 6: 56,713,812 (GRCm39) H357Y probably benign Het
Bclaf1 C T 10: 20,201,143 (GRCm39) T423I possibly damaging Het
Btbd19 A T 4: 116,977,789 (GRCm39) probably benign Het
Cap1 A G 4: 122,758,419 (GRCm39) S254P probably damaging Het
Cdc42ep1 T C 15: 78,731,629 (GRCm39) S25P probably benign Het
Cln6 T C 9: 62,754,252 (GRCm39) I98T possibly damaging Het
Cul9 T C 17: 46,814,957 (GRCm39) probably null Het
Dcx T C X: 142,660,240 (GRCm39) E268G possibly damaging Het
Ddias G A 7: 92,509,366 (GRCm39) P183L probably benign Het
Dnase2b A T 3: 146,299,326 (GRCm39) Y42* probably null Het
Dusp16 C T 6: 134,738,082 (GRCm39) probably benign Het
Egfr T C 11: 16,821,881 (GRCm39) probably benign Het
Fam171a1 T C 2: 3,227,393 (GRCm39) V842A probably benign Het
Folr1 T C 7: 101,507,745 (GRCm39) S232G probably benign Het
Foxj3 T C 4: 119,473,839 (GRCm39) probably benign Het
Fpr-rs6 T C 17: 20,403,137 (GRCm39) M75V probably benign Het
Fxyd5 G T 7: 30,735,864 (GRCm39) L128M possibly damaging Het
Gigyf2 T C 1: 87,349,238 (GRCm39) S500P possibly damaging Het
Inppl1 A G 7: 101,481,275 (GRCm39) L268P probably damaging Het
Klk1b24 A T 7: 43,841,243 (GRCm39) H192L probably benign Het
Llgl1 T G 11: 60,597,828 (GRCm39) Y316D probably damaging Het
Lmbrd1 T A 1: 24,801,374 (GRCm39) *143R probably null Het
Map3k15 T A X: 158,905,568 (GRCm39) N1295K possibly damaging Het
Mcm3ap A G 10: 76,318,513 (GRCm39) E678G probably damaging Het
Mrpl44 T A 1: 79,757,366 (GRCm39) Y270* probably null Het
Nav1 T A 1: 135,395,382 (GRCm39) I996L probably benign Het
Neb T C 2: 52,027,397 (GRCm39) E6868G probably damaging Het
Nexmif A T X: 103,131,213 (GRCm39) Y235N probably damaging Het
Nup50 C T 15: 84,823,994 (GRCm39) T449M probably damaging Het
Or14a256 G A 7: 86,265,686 (GRCm39) P56S probably damaging Het
Or2b6 A G 13: 21,823,508 (GRCm39) F62L probably damaging Het
Or51aa2 T C 7: 103,188,274 (GRCm39) T56A probably benign Het
Or52e8b A G 7: 104,673,902 (GRCm39) L95P probably damaging Het
Or52n2 T C 7: 104,542,724 (GRCm39) Y37C possibly damaging Het
Pald1 A T 10: 61,191,587 (GRCm39) probably null Het
Pde11a T A 2: 76,121,510 (GRCm39) K357I probably damaging Het
Ric3 A G 7: 108,637,817 (GRCm39) V312A possibly damaging Het
Scaper C T 9: 55,791,205 (GRCm39) G231D probably benign Het
Smc1b T A 15: 85,001,464 (GRCm39) probably benign Het
Smcr8 A G 11: 60,668,854 (GRCm39) M1V probably null Het
Smtn T C 11: 3,477,687 (GRCm39) probably benign Het
Spatc1 A T 15: 76,152,495 (GRCm39) K42* probably null Het
Taf7l A T X: 133,365,074 (GRCm39) I449K probably damaging Het
Tram2 T A 1: 21,075,824 (GRCm39) Y198F probably damaging Het
Ttn C G 2: 76,629,588 (GRCm39) W14284C probably damaging Het
Ube3a A G 7: 58,926,547 (GRCm39) K442E probably damaging Het
Vmn2r116 T A 17: 23,603,798 (GRCm39) F8I unknown Het
Vmn2r59 A G 7: 41,661,370 (GRCm39) F815S possibly damaging Het
Zap70 T C 1: 36,820,493 (GRCm39) C563R probably damaging Het
Zfp579 T C 7: 4,997,719 (GRCm39) H64R probably damaging Het
Other mutations in Tex47
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00163:Tex47 APN 5 7,355,468 (GRCm39) nonsense probably null
IGL00673:Tex47 APN 5 7,355,211 (GRCm39) missense probably damaging 1.00
PIT4495001:Tex47 UTSW 5 7,355,011 (GRCm39) missense probably benign 0.34
R0648:Tex47 UTSW 5 7,355,215 (GRCm39) missense probably benign 0.04
R1911:Tex47 UTSW 5 7,355,022 (GRCm39) missense probably damaging 0.98
R2163:Tex47 UTSW 5 7,355,022 (GRCm39) missense probably damaging 0.98
R3762:Tex47 UTSW 5 7,355,529 (GRCm39) missense probably benign 0.01
R4423:Tex47 UTSW 5 7,355,364 (GRCm39) missense probably benign 0.10
R4424:Tex47 UTSW 5 7,355,364 (GRCm39) missense probably benign 0.10
R5107:Tex47 UTSW 5 7,354,842 (GRCm39) missense probably benign 0.01
R5379:Tex47 UTSW 5 7,354,843 (GRCm39) missense probably null 0.01
R5589:Tex47 UTSW 5 7,354,834 (GRCm39) missense probably benign
R6265:Tex47 UTSW 5 7,355,461 (GRCm39) missense probably damaging 1.00
R6325:Tex47 UTSW 5 7,354,935 (GRCm39) nonsense probably null
R6580:Tex47 UTSW 5 7,355,212 (GRCm39) missense probably damaging 1.00
R8390:Tex47 UTSW 5 7,355,301 (GRCm39) missense probably benign 0.00
R8889:Tex47 UTSW 5 7,355,115 (GRCm39) missense probably damaging 0.99
R8892:Tex47 UTSW 5 7,355,115 (GRCm39) missense probably damaging 0.99
R9416:Tex47 UTSW 5 7,355,194 (GRCm39) missense possibly damaging 0.48
Predicted Primers PCR Primer
(F):5'- TTGTGAACTCAGAAGCAATGGC -3'
(R):5'- GTAGCCCACTAGAAACATCCTG -3'

Sequencing Primer
(F):5'- AATGGCTGCATTTGTTTCACATC -3'
(R):5'- ACATCCTGTGAAGGAGGAATTTC -3'
Posted On 2015-02-19