Incidental Mutation 'R0040:Rpl14'
Institutional Source Beutler Lab
Gene Symbol Rpl14
Ensembl Gene ENSMUSG00000025794
Gene Nameribosomal protein L14
Synonyms3100001N19Rik, CTG-B33, CAG-ISL-7, L14
MMRRC Submission 038334-MU
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.939) question?
Stock #R0040 (G1)
Quality Score
Status Validated
Chromosomal Location120571444-120574654 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to G at 120572101 bp
Amino Acid Change Phenylalanine to Leucine at position 3 (F3L)
Ref Sequence ENSEMBL: ENSMUSP00000131489 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047687] [ENSMUST00000165532]
Predicted Effect probably benign
Transcript: ENSMUST00000047687
SMART Domains Protein: ENSMUSP00000036830
Gene: ENSMUSG00000041608

transmembrane domain 21 43 N/A INTRINSIC
Pfam:GDA1_CD39 49 483 4.3e-102 PFAM
transmembrane domain 486 508 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000165532
AA Change: F3L

PolyPhen 2 Score 0.772 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000131489
Gene: ENSMUSG00000025794
AA Change: F3L

Blast:KOW 6 33 1e-7 BLAST
Pfam:Ribosomal_L14e 46 120 3.8e-35 PFAM
low complexity region 137 217 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213310
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215063
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216628
Predicted Effect unknown
Transcript: ENSMUST00000216990
AA Change: F2L
Meta Mutation Damage Score 0.3468 question?
Coding Region Coverage
  • 1x: 84.2%
  • 3x: 77.3%
  • 10x: 61.4%
  • 20x: 43.8%
Validation Efficiency 96% (74/77)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L14E family of ribosomal proteins. It contains a basic region-leucine zipper (bZIP)-like domain. The protein is located in the cytoplasm. This gene contains a trinucleotide (GCT) repeat tract whose length is highly polymorphic; these triplet repeats result in a stretch of alanine residues in the encoded protein. Transcript variants utilizing alternative polyA signals and alternative 5'-terminal exons exist but all encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m T G 6: 121,645,206 L356R possibly damaging Het
Antxr2 G A 5: 97,938,425 T441I possibly damaging Het
Apcs A G 1: 172,894,456 Y108H probably benign Het
Arpp21 T C 9: 112,147,409 probably benign Het
Atcay C T 10: 81,210,519 probably null Het
Bahcc1 A G 11: 120,268,370 D141G probably damaging Het
Cacng5 A T 11: 107,884,510 L11Q probably damaging Het
Ccdc73 T C 2: 104,992,084 S793P probably damaging Het
Ceacam10 A G 7: 24,778,264 Y68C probably damaging Het
Csmd3 G A 15: 47,633,816 P3062S probably damaging Het
Dctn4 A G 18: 60,544,042 N145D possibly damaging Het
Dusp12 A G 1: 170,880,657 Y164H probably damaging Het
Fat1 A G 8: 45,026,404 D2829G probably damaging Het
Fbxl13 T C 5: 21,486,373 T671A probably damaging Het
Fndc3b T A 3: 27,556,117 probably null Het
Gprc6a T A 10: 51,614,984 K819* probably null Het
Gucy2g T A 19: 55,217,302 T709S possibly damaging Het
Gxylt1 A T 15: 93,254,555 probably benign Het
Idh2 A G 7: 80,097,822 S317P probably damaging Het
Ifi30 T C 8: 70,763,776 probably null Het
Ifna16 G A 4: 88,676,630 A76V probably benign Het
Itpr2 C T 6: 146,345,140 E1127K probably damaging Het
Kank4 A G 4: 98,779,220 V330A probably benign Het
Kri1 T C 9: 21,281,105 Y131C probably damaging Het
Krt71 T A 15: 101,738,433 H280L possibly damaging Het
Lox A T 18: 52,520,826 H399Q possibly damaging Het
Mapt A G 11: 104,305,398 M446V probably damaging Het
Mpp7 A T 18: 7,403,180 probably benign Het
Mycbp2 A G 14: 103,224,272 V1447A probably benign Het
Myl3 A C 9: 110,767,929 D119A probably damaging Het
Myo1b A T 1: 51,781,989 I451N probably damaging Het
Nubp1 A G 16: 10,421,117 T199A probably damaging Het
Olfml2b A G 1: 170,668,751 H317R probably benign Het
Pard3b A T 1: 62,637,820 Y1170F probably damaging Het
Pear1 T C 3: 87,754,358 D536G probably damaging Het
Pira6 A G 7: 4,281,483 noncoding transcript Het
Pkhd1l1 T A 15: 44,573,625 Y3460N probably damaging Het
Plxna2 G T 1: 194,643,896 R46L probably benign Het
Rnf168 T A 16: 32,278,173 probably null Het
Scara5 C T 14: 65,762,717 probably benign Het
Sh3rf1 T A 8: 61,329,252 Y143N possibly damaging Het
Slc4a8 T A 15: 100,789,846 I288N probably damaging Het
Synpr G A 14: 13,563,024 A86T probably damaging Het
Ttc38 C A 15: 85,841,489 F184L probably damaging Het
Wdpcp A G 11: 21,711,638 I303M probably damaging Het
Zc3h12d G A 10: 7,867,914 A483T probably benign Het
Zfp106 C A 2: 120,531,613 K1008N probably damaging Het
Zfp68 G A 5: 138,607,779 T94I probably benign Het
Zfp867 C T 11: 59,463,865 A213T possibly damaging Het
Zkscan3 A T 13: 21,394,920 probably null Het
Other mutations in Rpl14
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02701:Rpl14 APN 9 120573573 splice site probably benign
IGL03061:Rpl14 APN 9 120572127 missense probably damaging 0.98
R0040:Rpl14 UTSW 9 120572101 missense possibly damaging 0.77
R0494:Rpl14 UTSW 9 120574362 utr 3 prime probably benign
R1984:Rpl14 UTSW 9 120572187 missense possibly damaging 0.81
R5169:Rpl14 UTSW 9 120572188 missense possibly damaging 0.66
R5895:Rpl14 UTSW 9 120574174 utr 3 prime probably benign
R6970:Rpl14 UTSW 9 120574227 utr 3 prime probably benign
R7311:Rpl14 UTSW 9 120574105 missense probably damaging 0.96
Posted On2012-12-21