Incidental Mutation 'R3951:Rtn4ip1'
ID307948
Institutional Source Beutler Lab
Gene Symbol Rtn4ip1
Ensembl Gene ENSMUSG00000019864
Gene Namereticulon 4 interacting protein 1
SynonymsNIMP, D10Ertd690e
MMRRC Submission 040828-MU
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.297) question?
Stock #R3951 (G1)
Quality Score225
Status Validated
Chromosome10
Chromosomal Location43901807-43957201 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to A at 43909897 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000060940 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054418]
Predicted Effect probably null
Transcript: ENSMUST00000054418
SMART Domains Protein: ENSMUSP00000060940
Gene: ENSMUSG00000019864

DomainStartEndE-ValueType
Pfam:ADH_N 71 168 5.8e-11 PFAM
Pfam:ADH_zinc_N 216 324 1.5e-16 PFAM
Pfam:ADH_zinc_N_2 247 393 1.3e-28 PFAM
Meta Mutation Damage Score 0.6308 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.9%
Validation Efficiency 100% (55/55)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a mitochondrial protein that interacts with reticulon 4, which is a potent inhibitor of regeneration following spinal cord injury. This interaction may be important for reticulon-induced inhibition of neurite growth. Mutations in this gene can cause optic atrophy 10, with or without ataxia, mental retardation, and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik T C 10: 100,615,296 probably benign Het
4932414N04Rik T C 2: 68,664,403 probably null Het
Akr1c18 C T 13: 4,135,285 V283I probably benign Het
Atp2b2 T A 6: 113,760,831 M861L possibly damaging Het
Cdh23 T C 10: 60,657,326 Y3C probably benign Het
Clspn A G 4: 126,576,379 E814G probably damaging Het
Csgalnact1 T C 8: 68,461,262 Q97R probably benign Het
Dera A G 6: 137,837,120 Y100C probably damaging Het
Ect2 A T 3: 27,130,120 D517E probably benign Het
Epha4 A T 1: 77,399,716 Y509N probably damaging Het
Fat2 T C 11: 55,296,382 T1213A probably benign Het
Fkbp8 T A 8: 70,532,661 L275Q probably damaging Het
Gabrb2 A G 11: 42,626,881 Y510C probably damaging Het
Gda T C 19: 21,472,445 T16A probably benign Het
Ggcx G A 6: 72,426,558 G363R probably benign Het
Gm527 T G 12: 64,923,502 probably benign Het
Hoxb2 A G 11: 96,353,175 E204G probably damaging Het
Hsd17b11 G A 5: 103,992,937 probably benign Het
Kat14 T C 2: 144,407,329 probably benign Het
Kif16b C T 2: 142,707,359 V1079I probably benign Het
Klhl29 T A 12: 5,140,660 S112C probably damaging Het
Lpcat2 G T 8: 92,864,903 M58I probably benign Het
Lrrc8d G T 5: 105,814,276 V851F probably benign Het
Ltbp3 T C 19: 5,756,001 V929A probably damaging Het
Map3k20 T G 2: 72,438,300 I550M probably damaging Het
Map3k9 T C 12: 81,722,521 M941V probably benign Het
Myom2 A T 8: 15,084,556 Y453F probably benign Het
Ncapd2 T C 6: 125,186,784 K78E probably damaging Het
Ncor2 G T 5: 125,032,256 D1496E possibly damaging Het
Ndnf T C 6: 65,703,141 Y135H possibly damaging Het
Ndst1 T C 18: 60,697,139 N633S probably benign Het
Nmur2 G C 11: 56,040,225 P220R probably damaging Het
Nsd1 G C 13: 55,268,454 E1438Q probably benign Het
Olfr1043 G T 2: 86,162,618 C110* probably null Het
Olfr1128 T C 2: 87,545,065 T160A probably damaging Het
Olfr1413 T A 1: 92,573,789 M206K possibly damaging Het
Olfr229 A T 9: 39,910,725 R307S probably benign Het
Pom121l2 T G 13: 21,982,128 S190A probably damaging Het
Prpmp5 G A 6: 132,312,694 P56S unknown Het
Scarb1 A C 5: 125,287,411 C85G probably damaging Het
Sh2d4b A G 14: 40,872,546 I159T probably damaging Het
Sntg1 C T 1: 8,782,901 probably benign Het
Sos1 G A 17: 80,424,181 T630I probably damaging Het
Spata7 T A 12: 98,669,473 D517E probably damaging Het
Tcaf1 T C 6: 42,679,059 T328A probably benign Het
Ticrr T C 7: 79,682,069 L776S probably damaging Het
Trpc2 T A 7: 102,093,574 M597K probably damaging Het
Ttc37 T G 13: 76,130,219 L551V probably damaging Het
Tubb3 C A 8: 123,421,264 T312N probably damaging Het
Ubr4 G A 4: 139,393,094 V277M probably damaging Het
Uhrf2 G A 19: 30,079,861 R473Q probably damaging Het
Vmn2r43 T A 7: 8,255,320 H298L probably benign Het
Other mutations in Rtn4ip1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01670:Rtn4ip1 APN 10 43928326 start codon destroyed probably null
R0005:Rtn4ip1 UTSW 10 43932478 missense probably benign 0.02
R0049:Rtn4ip1 UTSW 10 43921434 missense probably null 1.00
R0049:Rtn4ip1 UTSW 10 43921434 missense probably null 1.00
R1253:Rtn4ip1 UTSW 10 43910871 missense probably benign
R1756:Rtn4ip1 UTSW 10 43910830 missense probably damaging 1.00
R2104:Rtn4ip1 UTSW 10 43932406 missense probably benign 0.07
R2119:Rtn4ip1 UTSW 10 43935997 critical splice acceptor site probably null
R3950:Rtn4ip1 UTSW 10 43909897 splice site probably null
R3952:Rtn4ip1 UTSW 10 43909897 splice site probably null
R5283:Rtn4ip1 UTSW 10 43902465 missense probably damaging 0.99
R5345:Rtn4ip1 UTSW 10 43932470 missense probably damaging 1.00
R5503:Rtn4ip1 UTSW 10 43907883 missense probably benign
Predicted Primers PCR Primer
(F):5'- CCAGTGTGGTTTGAGTTCATAAC -3'
(R):5'- ATGAAGATGGCTGCTCTCGC -3'

Sequencing Primer
(F):5'- TTCATAACTCCAGAATCATACTCAAC -3'
(R):5'- TGGCTCTCTCTAAAACATGAAGC -3'
Posted On2015-04-17