Incidental Mutation 'R3154:Rnf126'
ID 263416
Institutional Source Beutler Lab
Gene Symbol Rnf126
Ensembl Gene ENSMUSG00000035890
Gene Name ring finger protein 126
Synonyms 2610010O19Rik
MMRRC Submission 040605-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.706) question?
Stock # R3154 (G1)
Quality Score 209
Status Not validated
Chromosome 10
Chromosomal Location 79594349-79602786 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 79597465 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 149 (I149N)
Ref Sequence ENSEMBL: ENSMUSP00000039486 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020577] [ENSMUST00000047203] [ENSMUST00000219228] [ENSMUST00000219981]
AlphaFold Q91YL2
PDB Structure Solution structure of the Zinc finger, C3HC4 type (RING finger) domain of RING finger protein 126 [SOLUTION NMR]
Predicted Effect probably benign
Transcript: ENSMUST00000020577
SMART Domains Protein: ENSMUSP00000020577
Gene: ENSMUSG00000020327

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
FGF 30 159 1.73e-62 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000047203
AA Change: I149N

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000039486
Gene: ENSMUSG00000035890
AA Change: I149N

DomainStartEndE-ValueType
Pfam:zinc_ribbon_9 9 40 5e-11 PFAM
low complexity region 109 121 N/A INTRINSIC
low complexity region 124 139 N/A INTRINSIC
RING 231 271 5.68e-9 SMART
low complexity region 293 313 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218770
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219189
Predicted Effect probably benign
Transcript: ENSMUST00000219228
Predicted Effect probably benign
Transcript: ENSMUST00000219981
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.5%
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 contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6820408C15Rik A C 2: 152,282,744 (GRCm39) N200H probably damaging Het
Abca17 T A 17: 24,547,720 (GRCm39) D218V probably damaging Het
Ap1b1 T C 11: 4,973,135 (GRCm39) V326A possibly damaging Het
Bdp1 A T 13: 100,186,322 (GRCm39) V1710E probably damaging Het
Chrna3 C T 9: 54,923,334 (GRCm39) C158Y probably damaging Het
Cnnm3 T A 1: 36,560,303 (GRCm39) S608T probably damaging Het
Cnot1 T C 8: 96,470,906 (GRCm39) E1314G possibly damaging Het
Cobll1 A T 2: 64,937,394 (GRCm39) M406K probably benign Het
Cyp2d34 T C 15: 82,501,767 (GRCm39) K248E probably benign Het
Dcdc2a A C 13: 25,286,340 (GRCm39) I125L probably benign Het
Dgat1 G A 15: 76,386,721 (GRCm39) L439F probably benign Het
Disc1 T A 8: 125,862,043 (GRCm39) S472T probably damaging Het
Dnajb3 C A 1: 88,132,773 (GRCm39) V210F probably benign Het
Fancd2 A G 6: 113,570,230 (GRCm39) S1394G possibly damaging Het
Fasn A T 11: 120,698,765 (GRCm39) L2475Q probably damaging Het
Fn1 A T 1: 71,632,242 (GRCm39) C2335S probably damaging Het
Gpld1 T C 13: 25,127,603 (GRCm39) S2P unknown Het
Gpld1 G T 13: 25,140,146 (GRCm39) probably null Het
Gsc2 G A 16: 17,732,364 (GRCm39) R137W probably damaging Het
Gsdme T C 6: 50,228,343 (GRCm39) R42G probably damaging Het
Gtf3c5 T C 2: 28,469,548 (GRCm39) T119A probably damaging Het
Hs6st3 T C 14: 120,106,389 (GRCm39) S266P probably damaging Het
Htr2a T C 14: 74,943,262 (GRCm39) F281L probably benign Het
Hus1b T C 13: 31,131,236 (GRCm39) K141R probably benign Het
Ireb2 T C 9: 54,793,230 (GRCm39) probably null Het
Klhdc7a T A 4: 139,693,024 (GRCm39) Y641F probably benign Het
Kri1 T C 9: 21,193,190 (GRCm39) E57G possibly damaging Het
Map4 A G 9: 109,828,860 (GRCm39) T82A probably benign Het
Mthfr T G 4: 148,136,061 (GRCm39) M353R probably benign Het
Mtus2 A G 5: 148,240,083 (GRCm39) probably benign Het
Muc5ac T A 7: 141,346,473 (GRCm39) probably null Het
Myo15a T A 11: 60,370,186 (GRCm39) probably null Het
Nynrin A T 14: 56,101,044 (GRCm39) Q278L possibly damaging Het
Pced1b T G 15: 97,282,423 (GRCm39) probably null Het
Penk T C 4: 4,134,152 (GRCm39) D165G probably damaging Het
Pfkm T A 15: 98,016,090 (GRCm39) V90D probably damaging Het
Pgk2 T A 17: 40,519,134 (GRCm39) D98V probably damaging Het
Psg28 C A 7: 18,160,348 (GRCm39) A283S possibly damaging Het
Rgl3 A G 9: 21,892,070 (GRCm39) L338P probably damaging Het
Ros1 T C 10: 51,927,077 (GRCm39) H2181R probably benign Het
Slc38a11 C T 2: 65,160,679 (GRCm39) C305Y probably damaging Het
Speg T A 1: 75,378,186 (GRCm39) V798E probably damaging Het
Spesp1 G A 9: 62,189,376 (GRCm39) probably benign Het
Styk1 A T 6: 131,286,975 (GRCm39) Y84* probably null Het
Syt2 T C 1: 134,669,599 (GRCm39) L80P possibly damaging Het
Tra2a C T 6: 49,222,446 (GRCm39) probably benign Het
Trim10 T A 17: 37,182,580 (GRCm39) C149S probably damaging Het
Vmn2r38 T C 7: 9,097,689 (GRCm39) T135A probably benign Het
Wipf1 A G 2: 73,267,834 (GRCm39) V188A possibly damaging Het
Yipf2 G A 9: 21,501,197 (GRCm39) A67V probably benign Het
Zfp759 A G 13: 67,286,719 (GRCm39) E96G probably benign Het
Zic3 G A X: 57,076,838 (GRCm39) V100M possibly damaging Het
Other mutations in Rnf126
AlleleSourceChrCoordTypePredicted EffectPPH Score
BB007:Rnf126 UTSW 10 79,596,726 (GRCm39) missense probably damaging 1.00
BB017:Rnf126 UTSW 10 79,596,726 (GRCm39) missense probably damaging 1.00
R0087:Rnf126 UTSW 10 79,595,068 (GRCm39) missense probably damaging 0.97
R0302:Rnf126 UTSW 10 79,595,057 (GRCm39) missense probably damaging 1.00
R0418:Rnf126 UTSW 10 79,598,477 (GRCm39) unclassified probably benign
R0671:Rnf126 UTSW 10 79,597,441 (GRCm39) missense possibly damaging 0.83
R1403:Rnf126 UTSW 10 79,596,702 (GRCm39) missense probably benign 0.00
R1449:Rnf126 UTSW 10 79,597,448 (GRCm39) missense probably benign 0.31
R2058:Rnf126 UTSW 10 79,594,971 (GRCm39) unclassified probably benign
R3153:Rnf126 UTSW 10 79,597,465 (GRCm39) missense probably damaging 1.00
R5535:Rnf126 UTSW 10 79,598,533 (GRCm39) missense probably damaging 1.00
R5815:Rnf126 UTSW 10 79,602,603 (GRCm39) missense probably benign 0.03
R6622:Rnf126 UTSW 10 79,597,397 (GRCm39) critical splice donor site probably null
R6748:Rnf126 UTSW 10 79,597,970 (GRCm39) missense probably benign 0.00
R7930:Rnf126 UTSW 10 79,596,726 (GRCm39) missense probably damaging 1.00
R9439:Rnf126 UTSW 10 79,597,465 (GRCm39) missense probably damaging 1.00
RF022:Rnf126 UTSW 10 79,594,977 (GRCm39) frame shift probably null
RF023:Rnf126 UTSW 10 79,594,977 (GRCm39) frame shift probably null
RF056:Rnf126 UTSW 10 79,594,976 (GRCm39) frame shift probably null
Predicted Primers PCR Primer
(F):5'- ACCTGCGTGATGATGGTGTC -3'
(R):5'- AATCCCTGTGAAATAGTTGTACCC -3'

Sequencing Primer
(F):5'- ATGATGGTGTCCAGGCCG -3'
(R):5'- CCCTGTGAAATAGTTGTACCCAATGG -3'
Posted On 2015-02-05