Incidental Mutation 'R4350:Rpl7a-ps3'
ID 328481
Institutional Source Beutler Lab
Gene Symbol Rpl7a-ps3
Ensembl Gene ENSMUSG00000068579
Gene Name ribosomal protein L7A, pseudogene 3
Synonyms Gm5044
MMRRC Submission 041105-MU
Accession Numbers
Essential gene? Not available question?
Stock # R4350 (G1)
Quality Score 206
Status Not validated
Chromosome 15
Chromosomal Location 36308295-36309090 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 36308283 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000087632 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090170]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000090170
SMART Domains Protein: ENSMUSP00000087632
Gene: ENSMUSG00000068579

DomainStartEndE-ValueType
low complexity region 4 32 N/A INTRINSIC
Pfam:Ribosomal_L7Ae 126 220 1.6e-25 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 A G 17: 24,498,020 (GRCm39) probably null Het
Adamts1 T A 16: 85,599,234 (GRCm39) D122V probably benign Het
Ap3d1 T C 10: 80,555,119 (GRCm39) D402G probably benign Het
Ccdc88b T C 19: 6,827,640 (GRCm39) E954G probably damaging Het
Cdh20 A G 1: 104,906,814 (GRCm39) D547G probably damaging Het
Cst13 A G 2: 148,672,169 (GRCm39) M115V probably benign Het
Ctr9 T A 7: 110,648,525 (GRCm39) Y722N probably damaging Het
Dvl3 T C 16: 20,344,394 (GRCm39) Y257H possibly damaging Het
Dzip1 T C 14: 119,120,938 (GRCm39) D673G probably benign Het
Enah A T 1: 181,749,985 (GRCm39) S266T possibly damaging Het
Epha7 T C 4: 28,950,393 (GRCm39) V732A probably damaging Het
F13b A G 1: 139,444,036 (GRCm39) I457V probably benign Het
Fam98a A G 17: 75,848,220 (GRCm39) F165L probably damaging Het
Gcn1 G T 5: 115,741,389 (GRCm39) R1476L probably damaging Het
Gfy T C 7: 44,827,040 (GRCm39) E352G probably benign Het
Inava C T 1: 136,153,946 (GRCm39) V180I probably damaging Het
Lyn G A 4: 3,789,796 (GRCm39) R443H probably damaging Het
Mecom C A 3: 30,020,887 (GRCm39) V452L possibly damaging Het
Msh6 A G 17: 88,292,012 (GRCm39) S256G probably damaging Het
Ncor1 A G 11: 62,301,644 (GRCm39) probably null Het
Pabpc4 C T 4: 123,184,060 (GRCm39) T191I probably damaging Het
Ptch1 C T 13: 63,682,143 (GRCm39) R537H probably damaging Het
Rchy1 T C 5: 92,105,813 (GRCm39) D45G probably damaging Het
Rftn2 T C 1: 55,233,440 (GRCm39) T372A probably damaging Het
Rlf G A 4: 121,006,293 (GRCm39) P896S probably benign Het
Rnf31 AAC A 14: 55,838,555 (GRCm39) probably null Het
Sox7 A G 14: 64,185,995 (GRCm39) T344A probably benign Het
Sppl2b T C 10: 80,698,560 (GRCm39) Y127H probably benign Het
Srsf12 T C 4: 33,223,612 (GRCm39) V37A possibly damaging Het
Sst A G 16: 23,708,565 (GRCm39) S89P probably damaging Het
Svil T A 18: 5,118,154 (GRCm39) C1705S probably damaging Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Tubgcp3 T C 8: 12,691,117 (GRCm39) T474A probably benign Het
Tubgcp6 G A 15: 88,988,198 (GRCm39) P925L probably benign Het
Other mutations in Rpl7a-ps3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1659:Rpl7a-ps3 UTSW 15 36,308,309 (GRCm39) exon noncoding transcript
R3623:Rpl7a-ps3 UTSW 15 36,308,429 (GRCm39) exon noncoding transcript
R4387:Rpl7a-ps3 UTSW 15 36,308,429 (GRCm39) exon noncoding transcript
R4389:Rpl7a-ps3 UTSW 15 36,308,429 (GRCm39) exon noncoding transcript
R4486:Rpl7a-ps3 UTSW 15 36,308,429 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- CAAGGAACGTCATATATTAGTGAAGGC -3'
(R):5'- TCTGGCTAAGCTGGTGGAAG -3'

Sequencing Primer
(F):5'- CGTCATATATTAGTGAAGGCAGAGAC -3'
(R):5'- CTGGTGGAAGCTATTAGGACC -3'
Posted On 2015-07-07