Incidental Mutation 'R7398:Tagln3'
ID573989
Institutional Source Beutler Lab
Gene Symbol Tagln3
Ensembl Gene ENSMUSG00000022658
Gene Nametransgelin 3
Synonyms2700038H05Rik, 2900005O10Rik, Np25
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.247) question?
Stock #R7398 (G1)
Quality Score225.009
Status Not validated
Chromosome16
Chromosomal Location45711230-45724608 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 45723077 bp
ZygosityHeterozygous
Amino Acid Change Asparagine to Lysine at position 67 (N67K)
Ref Sequence ENSEMBL: ENSMUSP00000093762 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096057]
Predicted Effect probably damaging
Transcript: ENSMUST00000096057
AA Change: N67K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000093762
Gene: ENSMUSG00000022658
AA Change: N67K

DomainStartEndE-ValueType
CH 26 132 4.3e-24 SMART
Pfam:Calponin 174 198 2.6e-17 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abl1 T A 2: 31,790,799 S368T probably damaging Het
Acmsd A G 1: 127,729,435 probably benign Het
Arid3b A T 9: 57,796,212 S445T probably benign Het
Brinp1 A G 4: 68,841,354 V91A probably benign Het
Ccne1 A G 7: 38,106,277 probably null Het
Col3a1 A T 1: 45,327,813 I249F unknown Het
Crybg3 T C 16: 59,557,325 I1189V probably benign Het
Cyp2d34 A T 15: 82,616,763 D389E probably benign Het
D130043K22Rik A C 13: 24,893,377 I998L probably damaging Het
Dgkq A G 5: 108,655,190 I298T possibly damaging Het
Dnah17 T C 11: 118,080,724 E2161G probably damaging Het
Dnajc25 T C 4: 59,017,824 probably null Het
Dpp9 G A 17: 56,189,405 R768* probably null Het
Dusp27 A G 1: 166,100,475 S523P probably damaging Het
Dusp6 T A 10: 99,264,878 N245K probably damaging Het
E430018J23Rik C T 7: 127,393,324 C38Y probably null Het
Eea1 C A 10: 95,995,631 H195N probably benign Het
Efhc1 A G 1: 20,989,520 E598G probably benign Het
Epb41l1 T C 2: 156,534,762 V809A probably damaging Het
Gas8 T A 8: 123,518,951 M1K probably null Het
Gcm1 G A 9: 78,064,679 V301I probably benign Het
Gm11554 T A 11: 99,804,259 S43C unknown Het
Gm7298 A G 6: 121,781,953 I1177V probably benign Het
Gm8011 A G 14: 42,463,961 T27A Het
Hmcn1 A G 1: 150,646,670 I3493T probably benign Het
Insrr T G 3: 87,808,732 I578S probably damaging Het
Kif13b A G 14: 64,757,523 D908G probably null Het
Lhcgr G C 17: 88,772,046 Q71E probably benign Het
Lrrc34 T C 3: 30,643,342 D80G probably damaging Het
Lrrc7 C A 3: 158,291,958 E156* probably null Het
Lrrc9 A G 12: 72,500,816 D1255G probably damaging Het
Mcidas A G 13: 112,996,882 N116D probably benign Het
Mmp7 A G 9: 7,697,593 N210D probably damaging Het
Morc3 A G 16: 93,874,860 D926G probably damaging Het
Mrgpra9 A G 7: 47,235,637 I94T possibly damaging Het
Muc16 C A 9: 18,637,742 V5752F possibly damaging Het
Myo16 A T 8: 10,562,183 D1276V unknown Het
Nlrc4 T G 17: 74,446,542 E282A probably damaging Het
Nos2 T A 11: 78,936,471 Y227* probably null Het
Obox5 A C 7: 15,758,788 M223L probably benign Het
Olfr1337 C A 4: 118,781,699 L295F possibly damaging Het
Pygm G A 19: 6,385,936 R139H probably damaging Het
Ranbp2 C A 10: 58,467,277 P789T probably damaging Het
Riok2 T G 17: 17,387,239 S350A probably benign Het
Rnf214 C T 9: 45,867,547 V445I possibly damaging Het
Skida1 C T 2: 18,046,272 V603I unknown Het
Skint6 T A 4: 112,898,138 R747S probably benign Het
Slc24a5 G A 2: 125,085,774 W331* probably null Het
Slc5a10 A T 11: 61,673,579 C525S probably benign Het
Sult2b1 T C 7: 45,731,294 Y288C probably damaging Het
Trav21-dv12 A T 14: 53,876,705 H94L probably benign Het
Tshz2 A G 2: 169,884,174 E230G probably damaging Het
Usb1 T A 8: 95,345,303 H210Q probably damaging Het
Vill C T 9: 119,070,648 P767L probably benign Het
Vmn2r94 A T 17: 18,257,341 N269K probably benign Het
Other mutations in Tagln3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00816:Tagln3 APN 16 45724193 nonsense probably null
IGL02640:Tagln3 APN 16 45724233 missense probably benign 0.00
IGL02715:Tagln3 APN 16 45724225 missense probably benign
R0619:Tagln3 UTSW 16 45724272 missense probably damaging 0.99
R1118:Tagln3 UTSW 16 45724272 missense probably damaging 0.99
R1119:Tagln3 UTSW 16 45724272 missense probably damaging 0.99
R1865:Tagln3 UTSW 16 45711650 missense possibly damaging 0.89
R2111:Tagln3 UTSW 16 45711594 missense probably damaging 1.00
R6242:Tagln3 UTSW 16 45724338 start gained probably benign
R6329:Tagln3 UTSW 16 45713002 missense probably benign 0.03
R6857:Tagln3 UTSW 16 45724236 missense probably benign
R6995:Tagln3 UTSW 16 45722958 missense probably benign 0.01
X0026:Tagln3 UTSW 16 45723097 missense probably benign
Predicted Primers PCR Primer
(F):5'- CAGGAGGGCAGTTTACCTTC -3'
(R):5'- TCAAGGAGGGAACTAGGTTCTG -3'

Sequencing Primer
(F):5'- GGGCAGTTTACCTTCCCAGAGATC -3'
(R):5'- AACTAGGTTCTGGCTGCAAG -3'
Posted On2019-09-13