Incidental Mutation 'R6604:Gm5129'
ID 525533
Institutional Source Beutler Lab
Gene Symbol Gm5129
Ensembl Gene ENSMUSG00000053121
Gene Name predicted gene 5129
Synonyms ENSMUSG00000053121
MMRRC Submission 044727-MU
Accession Numbers
Essential gene? Not available question?
Stock # R6604 (G1)
Quality Score 225.009
Status Not validated
Chromosome 5
Chromosomal Location 29940332-29940934 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 29940765 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142783 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000008733] [ENSMUST00000012734] [ENSMUST00000065372] [ENSMUST00000114839] [ENSMUST00000196528] [ENSMUST00000196785] [ENSMUST00000198694]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000008733
SMART Domains Protein: ENSMUSP00000008733
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 4.64e-32 SMART
low complexity region 109 124 N/A INTRINSIC
low complexity region 125 158 N/A INTRINSIC
low complexity region 166 185 N/A INTRINSIC
low complexity region 249 261 N/A INTRINSIC
low complexity region 272 293 N/A INTRINSIC
low complexity region 339 363 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000012734
SMART Domains Protein: ENSMUSP00000012734
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 4.64e-32 SMART
low complexity region 111 124 N/A INTRINSIC
low complexity region 192 205 N/A INTRINSIC
coiled coil region 223 244 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000065372
AA Change: L57P
Predicted Effect probably benign
Transcript: ENSMUST00000114839
SMART Domains Protein: ENSMUSP00000110488
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 4.64e-32 SMART
low complexity region 109 124 N/A INTRINSIC
low complexity region 125 158 N/A INTRINSIC
low complexity region 166 185 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127753
Predicted Effect probably benign
Transcript: ENSMUST00000196528
SMART Domains Protein: ENSMUSP00000142878
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 3e-34 SMART
low complexity region 109 124 N/A INTRINSIC
low complexity region 125 158 N/A INTRINSIC
low complexity region 166 185 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000196785
Predicted Effect probably benign
Transcript: ENSMUST00000198694
SMART Domains Protein: ENSMUSP00000142783
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 1.4e-23 SMART
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930447A16Rik A G 15: 37,439,823 (GRCm39) probably benign Het
Abca13 T G 11: 9,328,384 (GRCm39) F3486V probably damaging Het
Adcy9 A G 16: 4,122,271 (GRCm39) L830P probably damaging Het
Aurkb T A 11: 68,939,388 (GRCm39) L157* probably null Het
Bbs10 T G 10: 111,136,965 (GRCm39) L693V possibly damaging Het
Dna2 G T 10: 62,803,522 (GRCm39) probably null Het
Efcab3 T A 11: 104,589,772 (GRCm39) L123* probably null Het
Ext1 A G 15: 52,946,555 (GRCm39) F550L probably damaging Het
Golm1 A G 13: 59,786,197 (GRCm39) Y332H probably damaging Het
Gpbp1l1 C T 4: 116,430,702 (GRCm39) P58S probably benign Het
Grk4 A T 5: 34,877,208 (GRCm39) D301V probably damaging Het
Haus1 T C 18: 77,851,797 (GRCm39) E106G probably damaging Het
Hpd T C 5: 123,318,964 (GRCm39) probably null Het
Kcnj6 C A 16: 94,563,504 (GRCm39) E313D probably damaging Het
Lmna A G 3: 88,395,589 (GRCm39) V57A probably damaging Het
Lrrtm1 T C 6: 77,221,221 (GRCm39) F226S possibly damaging Het
Otogl T C 10: 107,657,895 (GRCm39) probably null Het
Pgr A C 9: 8,946,867 (GRCm39) T703P possibly damaging Het
Ppig T C 2: 69,571,925 (GRCm39) S215P unknown Het
Pramel28 T C 4: 143,692,567 (GRCm39) R145G probably benign Het
Rasgrp3 A C 17: 75,810,110 (GRCm39) N270T probably benign Het
Rp1 C A 1: 4,089,351 (GRCm39) K1305N unknown Het
Shc1 A G 3: 89,329,186 (GRCm39) Y10C probably damaging Het
Slc12a1 G T 2: 125,026,735 (GRCm39) D457Y probably damaging Het
Sncaip A G 18: 53,038,918 (GRCm39) Q544R possibly damaging Het
Socs5 T C 17: 87,442,553 (GRCm39) Y498H probably damaging Het
Szt2 T C 4: 118,242,671 (GRCm39) D1472G probably benign Het
Tmem163 A G 1: 127,419,347 (GRCm39) M286T possibly damaging Het
Tmem236 A G 2: 14,179,512 (GRCm39) T38A probably benign Het
Vmn2r29 A T 7: 7,234,858 (GRCm39) V676E probably damaging Het
Vps13d A G 4: 144,907,694 (GRCm39) V56A probably damaging Het
Xirp2 T C 2: 67,340,189 (GRCm39) I810T possibly damaging Het
Zfp958 T C 8: 4,678,245 (GRCm39) L90P probably damaging Het
Other mutations in Gm5129
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01567:Gm5129 APN 5 29,940,862 (GRCm39) unclassified probably benign
IGL02437:Gm5129 APN 5 29,940,861 (GRCm39) unclassified probably benign
R1867:Gm5129 UTSW 5 29,940,654 (GRCm39) unclassified probably benign
R2026:Gm5129 UTSW 5 29,940,732 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- GGGACCACAATTCTCCAAGTCC -3'
(R):5'- CAACAAACAGGAAGTGCGTC -3'

Sequencing Primer
(F):5'- CTCCAAGTCCATAGGAGTGTGAGTC -3'
(R):5'- GGCGACGTCGACTTCCG -3'
Posted On 2018-06-22