Incidental Mutation 'R3760:Ct45a'
ID 270524
Institutional Source Beutler Lab
Gene Symbol Ct45a
Ensembl Gene ENSMUSG00000064016
Gene Name cancer/testis antigen 45
Synonyms LOC270599, Gm648
MMRRC Submission 040740-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R3760 (G1)
Quality Score 222
Status Validated
Chromosome X
Chromosomal Location 55589234-55594966 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 55590568 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 78 (V78I)
Ref Sequence ENSEMBL: ENSMUSP00000079908 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081133]
AlphaFold Q3UJ22
Predicted Effect probably benign
Transcript: ENSMUST00000081133
AA Change: V78I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000079908
Gene: ENSMUSG00000064016
AA Change: V78I

DomainStartEndE-ValueType
Pfam:INT_SG_DDX_CT_C 136 198 4.9e-31 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency 100% (33/33)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl2 T C 3: 148,522,871 (GRCm39) E1448G probably damaging Het
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Ell2 A T 13: 75,910,281 (GRCm39) Q163L probably benign Het
Epha6 T A 16: 60,041,347 (GRCm39) T423S possibly damaging Het
Fhad1 T C 4: 141,637,124 (GRCm39) E1114G probably damaging Het
Gpr83 A T 9: 14,772,034 (GRCm39) T69S probably benign Het
Gramd1c A T 16: 43,818,154 (GRCm39) M342K probably damaging Het
H3c7 T C 13: 23,728,985 (GRCm39) C111R probably damaging Het
Idua T C 5: 108,817,978 (GRCm39) probably benign Het
Kcnh1 T C 1: 192,188,332 (GRCm39) L931P probably damaging Het
Map2 T A 1: 66,478,077 (GRCm39) S470T probably damaging Het
Map7 T C 10: 20,152,027 (GRCm39) probably benign Het
Obscn A G 11: 58,919,406 (GRCm39) L6213P probably damaging Het
Or5b109 T C 19: 13,212,250 (GRCm39) L212P probably damaging Het
Or8k38 G A 2: 86,488,232 (GRCm39) S190L possibly damaging Het
Pcnx4 C T 12: 72,613,780 (GRCm39) T575M probably damaging Het
Ppp1r12a A G 10: 108,100,595 (GRCm39) D348G probably damaging Het
Prrc2c T C 1: 162,520,420 (GRCm39) N730S probably damaging Het
Serpinb3d C T 1: 107,009,304 (GRCm39) probably benign Het
Skint6 T C 4: 112,794,655 (GRCm39) T705A possibly damaging Het
Slc6a20a A G 9: 123,492,054 (GRCm39) I50T probably damaging Het
Taf13 T C 3: 108,485,424 (GRCm39) probably benign Het
Tlr11 A T 14: 50,599,700 (GRCm39) E562V probably damaging Het
Uhrf2 T C 19: 30,051,331 (GRCm39) S302P probably benign Het
Ulk1 C T 5: 110,937,223 (GRCm39) R691Q probably benign Het
Unc79 T A 12: 103,058,964 (GRCm39) L1036Q probably damaging Het
Vmn1r85 A T 7: 12,818,932 (GRCm39) S71T probably damaging Het
Vmn2r-ps158 G A 7: 42,673,502 (GRCm39) E187K probably benign Het
Vps52 T C 17: 34,179,162 (GRCm39) F200L possibly damaging Het
Zfp521 T C 18: 13,977,686 (GRCm39) H909R possibly damaging Het
Other mutations in Ct45a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02889:Ct45a APN X 55,592,551 (GRCm39) missense probably damaging 1.00
R0626:Ct45a UTSW X 55,590,399 (GRCm39) missense probably benign 0.00
R3759:Ct45a UTSW X 55,590,568 (GRCm39) missense probably benign
R3761:Ct45a UTSW X 55,590,568 (GRCm39) missense probably benign
R3763:Ct45a UTSW X 55,590,568 (GRCm39) missense probably benign
R4212:Ct45a UTSW X 55,590,568 (GRCm39) missense probably benign
R4213:Ct45a UTSW X 55,590,568 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- ACTTACGTCGTCCAAAGCG -3'
(R):5'- TCAGAGCTCAGCCTTGTCAC -3'

Sequencing Primer
(F):5'- CAAAGCGTCGGATTTCTGTCATCAG -3'
(R):5'- AGCCTTGTCACAGCTCAGC -3'
Posted On 2015-03-18