Incidental Mutation 'IGL01612:Rab3b'
ID 92178
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rab3b
Ensembl Gene ENSMUSG00000003411
Gene Name RAB3B, member RAS oncogene family
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01612
Quality Score
Status
Chromosome 4
Chromosomal Location 108736267-108800521 bp(+) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to A at 108781223 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000102262 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000003502] [ENSMUST00000106650] [ENSMUST00000106651]
AlphaFold Q9CZT8
Predicted Effect probably null
Transcript: ENSMUST00000003502
SMART Domains Protein: ENSMUSP00000003502
Gene: ENSMUSG00000003411

DomainStartEndE-ValueType
RAB 23 186 1.86e-96 SMART
Predicted Effect probably null
Transcript: ENSMUST00000106650
SMART Domains Protein: ENSMUSP00000102261
Gene: ENSMUSG00000003411

DomainStartEndE-ValueType
RAB 23 186 1.86e-96 SMART
Predicted Effect probably null
Transcript: ENSMUST00000106651
SMART Domains Protein: ENSMUSP00000102262
Gene: ENSMUSG00000003411

DomainStartEndE-ValueType
RAB 23 195 4.88e-91 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele are viable with no apparent decrease in weight or fertility. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik T C 14: 32,381,988 (GRCm39) T1326A possibly damaging Het
Afg3l1 C T 8: 124,221,592 (GRCm39) R484C probably benign Het
Atg2a C A 19: 6,302,514 (GRCm39) Q946K probably benign Het
Cdh20 T C 1: 104,921,895 (GRCm39) Y731H probably benign Het
Cdk15 A G 1: 59,328,932 (GRCm39) D282G possibly damaging Het
Ctnnd2 T C 15: 31,005,164 (GRCm39) S1073P probably damaging Het
Dnah2 T C 11: 69,355,889 (GRCm39) probably benign Het
Evi2a T A 11: 79,417,978 (GRCm39) R211W probably damaging Het
Fmo1 T A 1: 162,661,168 (GRCm39) I372F probably benign Het
Glyctk T C 9: 106,032,471 (GRCm39) D514G probably damaging Het
Gmnc G A 16: 26,779,069 (GRCm39) Q313* probably null Het
Grik1 T C 16: 87,743,623 (GRCm39) T520A probably damaging Het
Gtsf2 A T 15: 103,353,340 (GRCm39) C9S probably damaging Het
Ift80 T G 3: 68,870,996 (GRCm39) N200T possibly damaging Het
Ints1 A G 5: 139,742,047 (GRCm39) S1771P probably benign Het
Lrba A G 3: 86,683,484 (GRCm39) T2769A possibly damaging Het
Lrfn2 G T 17: 49,377,425 (GRCm39) V169L possibly damaging Het
Mei1 G A 15: 81,973,753 (GRCm39) R80H probably damaging Het
Nbeal2 A T 9: 110,473,746 (GRCm39) V31E probably damaging Het
Ncapd2 G T 6: 125,154,835 (GRCm39) P546T probably benign Het
Or52l1 A G 7: 104,829,929 (GRCm39) V212A probably damaging Het
Pan3 T C 5: 147,390,052 (GRCm39) probably benign Het
Rabl2 T C 15: 89,467,615 (GRCm39) K119E probably benign Het
Reln A G 5: 22,101,928 (GRCm39) V3334A probably damaging Het
Rfx1 A G 8: 84,819,601 (GRCm39) probably null Het
Rhod T C 19: 4,476,247 (GRCm39) Y168C probably damaging Het
Sag T C 1: 87,733,071 (GRCm39) I13T probably damaging Het
Sat2 T C 11: 69,513,789 (GRCm39) probably null Het
Scn5a A T 9: 119,315,091 (GRCm39) D1872E possibly damaging Het
Sh2b2 T G 5: 136,260,656 (GRCm39) I187L probably benign Het
Slit3 G A 11: 35,591,211 (GRCm39) G1341D possibly damaging Het
Tmed11 A T 5: 108,927,750 (GRCm39) S95T possibly damaging Het
Tmem186 A G 16: 8,453,733 (GRCm39) V176A possibly damaging Het
Trim12c A T 7: 103,997,422 (GRCm39) S45T possibly damaging Het
Ube4b C A 4: 149,468,275 (GRCm39) R167L probably damaging Het
Zfp335 A T 2: 164,752,540 (GRCm39) probably null Het
Other mutations in Rab3b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01391:Rab3b APN 4 108,797,999 (GRCm39) missense probably damaging 1.00
IGL01636:Rab3b APN 4 108,797,916 (GRCm39) missense possibly damaging 0.55
IGL01777:Rab3b APN 4 108,786,607 (GRCm39) missense probably damaging 1.00
R0601:Rab3b UTSW 4 108,747,586 (GRCm39) missense probably damaging 1.00
R1884:Rab3b UTSW 4 108,786,649 (GRCm39) missense probably damaging 1.00
R2302:Rab3b UTSW 4 108,786,640 (GRCm39) missense probably damaging 0.99
R2312:Rab3b UTSW 4 108,747,691 (GRCm39) missense probably damaging 1.00
R8744:Rab3b UTSW 4 108,781,184 (GRCm39) missense probably damaging 0.99
R8893:Rab3b UTSW 4 108,797,925 (GRCm39) missense probably benign 0.19
R9145:Rab3b UTSW 4 108,797,903 (GRCm39) missense probably benign 0.00
R9572:Rab3b UTSW 4 108,786,725 (GRCm39) critical splice donor site probably null
X0024:Rab3b UTSW 4 108,747,505 (GRCm39) start codon destroyed probably null 0.98
Posted On 2013-12-09