Incidental Mutation 'R5653:Capza2'
Institutional Source Beutler Lab
Gene Symbol Capza2
Ensembl Gene ENSMUSG00000015733
Gene Namecapping protein (actin filament) muscle Z-line, alpha 2
Synonyms1110053K06Rik, Cappa2
MMRRC Submission 043299-MU
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.364) question?
Stock #R5653 (G1)
Quality Score225
Status Not validated
Chromosomal Location17636234-17666972 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 17654113 bp
Amino Acid Change Alanine to Threonine at position 55 (A55T)
Ref Sequence ENSEMBL: ENSMUSP00000145159 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000015877] [ENSMUST00000130606] [ENSMUST00000152005]
Predicted Effect possibly damaging
Transcript: ENSMUST00000015877
AA Change: A55T

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000015877
Gene: ENSMUSG00000015733
AA Change: A55T

Pfam:F-actin_cap_A 14 282 3.2e-109 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000130606
AA Change: A55T

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000123398
Gene: ENSMUSG00000015733
AA Change: A55T

Pfam:F-actin_cap_A 12 173 1.3e-52 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136771
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148694
Predicted Effect probably damaging
Transcript: ENSMUST00000152005
AA Change: A55T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000145159
Gene: ENSMUSG00000015733
AA Change: A55T

Pfam:F-actin_cap_A 14 145 2.1e-42 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156701
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the F-actin capping protein alpha subunit family. It is the alpha subunit of the barbed-end actin binding protein Cap Z. By capping the barbed end of actin filaments, Cap Z regulates the growth of the actin filaments at the barbed end. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim2 T C 5: 35,883,412 L663P probably damaging Het
Atp10d A T 5: 72,264,067 Q682L probably benign Het
Atp8b1 A G 18: 64,545,197 V876A probably damaging Het
Bard1 A T 1: 71,031,429 V632E probably benign Het
Baz1b A T 5: 135,209,097 E209V probably benign Het
Bmp1 T A 14: 70,490,094 Y683F probably benign Het
Cacnb1 A T 11: 98,009,279 probably null Het
Cc2d2a A G 5: 43,722,462 N1127S possibly damaging Het
Ccdc13 A G 9: 121,798,787 *255R probably null Het
Ddias G T 7: 92,858,729 N659K probably damaging Het
Ddr1 C T 17: 35,686,508 A531T probably benign Het
Dnah9 T C 11: 65,849,980 T4127A probably damaging Het
Dnajc10 T A 2: 80,349,368 Y749N probably damaging Het
Dnm1l A G 16: 16,319,489 L422P probably damaging Het
Edil3 A T 13: 89,131,812 N203I probably damaging Het
Egfr C T 11: 16,911,617 A1132V probably benign Het
Entpd7 C T 19: 43,691,157 R50* probably null Het
Fam160a1 A T 3: 85,722,501 L40Q probably damaging Het
Fat2 T C 11: 55,310,316 D644G probably damaging Het
Galnt11 T A 5: 25,248,858 D27E probably damaging Het
Gm10801 T A 2: 98,664,051 F158I probably damaging Het
Gm37240 A G 3: 84,497,795 F234L probably damaging Het
Gtf2ird1 A T 5: 134,410,967 F136L probably damaging Het
Hspa1l T C 17: 34,977,420 V145A probably damaging Het
Ice2 A G 9: 69,428,380 T882A probably benign Het
Itgb4 C T 11: 115,984,157 R447W probably benign Het
Kat6b A G 14: 21,669,372 N1264S probably benign Het
Kcnq4 C A 4: 120,702,411 V531L probably benign Het
Kif9 A T 9: 110,524,931 K790N probably damaging Het
Lipe T A 7: 25,398,408 I37L probably benign Het
Lrrc43 A G 5: 123,499,580 D270G probably damaging Het
Mon2 A G 10: 123,026,094 Y782H probably damaging Het
Mrpl52 T C 14: 54,427,229 S49P probably damaging Het
Olfr132 T A 17: 38,131,184 T3S possibly damaging Het
Olfr177 A G 16: 58,872,484 L222P probably damaging Het
Olfr318 G A 11: 58,720,251 H266Y probably damaging Het
Olfr477 A T 7: 107,990,385 T7S probably benign Het
Park2 C T 17: 11,237,649 A119V probably damaging Het
Pcbp2 C T 15: 102,487,089 A141V probably damaging Het
Pcsk9 T A 4: 106,458,916 Y110F probably damaging Het
Plxna4 A G 6: 32,517,616 S22P possibly damaging Het
Polq T A 16: 37,040,534 L506Q probably damaging Het
Prx C T 7: 27,517,604 P510L probably damaging Het
Ptpre T C 7: 135,653,943 F54L probably damaging Het
Rspry1 T G 8: 94,636,611 probably null Het
Tnfrsf11b A T 15: 54,259,866 L113Q probably damaging Het
Tnk1 C T 11: 69,853,585 G411S probably damaging Het
Tor3a A G 1: 156,656,510 L290S probably damaging Het
Tril T C 6: 53,817,985 T751A probably benign Het
Tubgcp6 C T 15: 89,108,612 V547I possibly damaging Het
Txnrd3 T C 6: 89,654,085 L121P probably benign Het
Vmn1r210 T A 13: 22,827,208 R303* probably null Het
Vmn2r38 T C 7: 9,097,765 M1V probably null Het
Other mutations in Capza2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01115:Capza2 APN 6 17654123 missense probably damaging 1.00
IGL01330:Capza2 APN 6 17654171 critical splice donor site probably null
IGL02692:Capza2 APN 6 17654116 nonsense probably null
R0086:Capza2 UTSW 6 17660774 missense probably damaging 1.00
R0302:Capza2 UTSW 6 17648524 missense probably benign 0.01
R0331:Capza2 UTSW 6 17665103 missense probably benign 0.09
R1466:Capza2 UTSW 6 17657159 intron probably benign
R2036:Capza2 UTSW 6 17660778 missense probably damaging 1.00
R4395:Capza2 UTSW 6 17656450 splice site probably null
R4978:Capza2 UTSW 6 17662115 missense probably null 0.69
R5734:Capza2 UTSW 6 17660765 missense probably damaging 1.00
R7190:Capza2 UTSW 6 17654121 nonsense probably null
Predicted Primers PCR Primer

Sequencing Primer
Posted On2016-11-09