Incidental Mutation 'IGL03268:Rragb'
ID 415160
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rragb
Ensembl Gene ENSMUSG00000041658
Gene Name Ras-related GTP binding B
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # IGL03268
Quality Score
Status
Chromosome X
Chromosomal Location 151922977-151954939 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 151923493 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 5 (D5G)
Ref Sequence ENSEMBL: ENSMUSP00000134162 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039720] [ENSMUST00000144175]
AlphaFold Q6NTA4
Predicted Effect unknown
Transcript: ENSMUST00000039720
AA Change: D5G
SMART Domains Protein: ENSMUSP00000039013
Gene: ENSMUSG00000041658
AA Change: D5G

DomainStartEndE-ValueType
low complexity region 2 13 N/A INTRINSIC
Pfam:Arf 32 241 1.2e-6 PFAM
Pfam:Ras 42 238 3.8e-6 PFAM
Pfam:Gtr1_RagA 42 296 1.8e-107 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000144175
AA Change: D5G
SMART Domains Protein: ENSMUSP00000134162
Gene: ENSMUSG00000041658
AA Change: D5G

DomainStartEndE-ValueType
low complexity region 2 13 N/A INTRINSIC
Pfam:Gtr1_RagA 42 116 7.9e-39 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Ras-homologous GTPases constitute a large family of signal transducers that alternate between an activated, GTP-binding state and an inactivated, GDP-binding state. These proteins represent cellular switches that are operated by GTP-exchange factors and factors that stimulate their intrinsic GTPase activity. All GTPases of the Ras superfamily have in common the presence of six conserved motifs involved in GTP/GDP binding, three of which are phosphate-/magnesium-binding sites (PM1-PM3) and three of which are guanine nucleotide-binding sites (G1-G3). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1500002C15Rik G T 4: 155,818,648 (GRCm39) probably benign Het
Acvrl1 A T 15: 101,033,803 (GRCm39) I162F possibly damaging Het
Adprhl1 A G 8: 13,296,170 (GRCm39) probably benign Het
Anapc7 G A 5: 122,567,669 (GRCm39) probably null Het
Ankrd13a T C 5: 114,930,296 (GRCm39) L227P probably damaging Het
Anxa5 T C 3: 36,504,828 (GRCm39) I245V probably benign Het
Arf1 A T 11: 59,103,663 (GRCm39) V123E possibly damaging Het
Catsperg1 G A 7: 28,899,668 (GRCm39) R338C probably damaging Het
Cc2d1a A C 8: 84,860,154 (GRCm39) L855R probably damaging Het
Cdh18 G A 15: 23,366,953 (GRCm39) A220T probably damaging Het
Cep350 T C 1: 155,829,295 (GRCm39) H203R probably benign Het
Cep78 G T 19: 15,951,806 (GRCm39) S333* probably null Het
Chrna2 T A 14: 66,388,395 (GRCm39) probably benign Het
Dact1 T C 12: 71,364,257 (GRCm39) V346A probably damaging Het
Dcn A G 10: 97,319,240 (GRCm39) I6V probably benign Het
Dlg3 A G X: 99,853,493 (GRCm39) Y600C probably damaging Het
Dmd A G X: 82,849,814 (GRCm39) E1084G probably damaging Het
Epb41 A C 4: 131,655,806 (GRCm39) D825E probably damaging Het
Galc T A 12: 98,188,852 (GRCm39) probably benign Het
Hmcn1 T A 1: 150,648,261 (GRCm39) D675V probably damaging Het
Igkv2-137 A G 6: 67,533,092 (GRCm39) D85G probably benign Het
Kxd1 A G 8: 70,961,136 (GRCm39) I78T probably damaging Het
Lama1 G A 17: 68,111,531 (GRCm39) G2261R probably damaging Het
Lama2 A T 10: 27,298,649 (GRCm39) I149N probably damaging Het
Mbnl2 G T 14: 120,616,569 (GRCm39) C61F probably damaging Het
Mcts1 T C X: 37,690,859 (GRCm39) I22T possibly damaging Het
Or4k15b T C 14: 50,272,024 (GRCm39) T279A probably damaging Het
Or52e3 T G 7: 102,869,848 (GRCm39) F308V probably benign Het
Pde12 T A 14: 26,389,614 (GRCm39) E365V probably benign Het
Prl8a2 A G 13: 27,537,938 (GRCm39) K204R probably benign Het
Rnf25 A T 1: 74,638,217 (GRCm39) probably benign Het
Rsrc2 T A 5: 123,878,790 (GRCm39) K56* probably null Het
Scn5a T C 9: 119,350,297 (GRCm39) Q859R probably damaging Het
Septin4 G A 11: 87,480,529 (GRCm39) V388M probably damaging Het
Slc29a2 C T 19: 5,074,531 (GRCm39) probably benign Het
Slc30a5 G A 13: 100,943,211 (GRCm39) T549I probably damaging Het
Slc7a2 A G 8: 41,365,554 (GRCm39) T462A probably benign Het
Spsb2 A G 6: 124,786,450 (GRCm39) E61G probably damaging Het
Srr A G 11: 74,803,943 (GRCm39) Y5H probably benign Het
Suclg2 T C 6: 95,546,573 (GRCm39) D301G probably damaging Het
Syt14 A G 1: 192,669,142 (GRCm39) V37A probably benign Het
Syt9 A G 7: 107,035,612 (GRCm39) N210D probably benign Het
Tenm3 T C 8: 48,688,558 (GRCm39) D2343G probably damaging Het
Tma7 A G 9: 108,907,450 (GRCm39) probably benign Het
Tor3a T C 1: 156,497,020 (GRCm39) D175G probably damaging Het
Tpo G T 12: 30,144,964 (GRCm39) A595D possibly damaging Het
Tpst2 T C 5: 112,456,091 (GRCm39) V210A probably damaging Het
Uchl1 A T 5: 66,839,824 (GRCm39) E122V probably benign Het
Vmn1r210 A T 13: 23,011,405 (GRCm39) F294I probably benign Het
Other mutations in Rragb
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00514:Rragb APN X 151,954,294 (GRCm39) missense possibly damaging 0.75
R5398:Rragb UTSW X 151,923,550 (GRCm39) missense probably damaging 1.00
R5399:Rragb UTSW X 151,923,550 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02