Incidental Mutation 'R0317:Rab11a'
ID 25467
Institutional Source Beutler Lab
Gene Symbol Rab11a
Ensembl Gene ENSMUSG00000004771
Gene Name RAB11A, member RAS oncogene family
MMRRC Submission 038527-MU
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock # R0317 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 64715299-64737758 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 64725553 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 24 (S24P)
Ref Sequence ENSEMBL: ENSMUSP00000125755 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000004892] [ENSMUST00000167569] [ENSMUST00000169058] [ENSMUST00000171100] [ENSMUST00000172298]
AlphaFold P62492
Predicted Effect probably benign
Transcript: ENSMUST00000004892
SMART Domains Protein: ENSMUSP00000004892
Gene: ENSMUSG00000004771

RAB 12 153 1.47e-85 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000165083
Predicted Effect noncoding transcript
Transcript: ENSMUST00000166857
Predicted Effect probably damaging
Transcript: ENSMUST00000167569
AA Change: S24P

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000125755
Gene: ENSMUSG00000004771
AA Change: S24P

Pfam:Ras 5 44 1e-6 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000168366
AA Change: S39P
SMART Domains Protein: ENSMUSP00000128150
Gene: ENSMUSG00000004771
AA Change: S39P

Pfam:Ras 1 59 2.5e-17 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000169058
SMART Domains Protein: ENSMUSP00000129729
Gene: ENSMUSG00000004771

RAB 12 153 5.11e-85 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000171100
AA Change: S35P

PolyPhen 2 Score 0.904 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000127968
Gene: ENSMUSG00000004771
AA Change: S35P

Pfam:Ras 1 55 1e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000172298
AA Change: S154P

PolyPhen 2 Score 0.357 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000129163
Gene: ENSMUSG00000004771
AA Change: S154P

RAB 12 175 1.01e-115 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000172444
Predicted Effect noncoding transcript
Transcript: ENSMUST00000197528
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 96.1%
  • 20x: 92.8%
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 belongs to the Rab family of the small GTPase superfamily. It is associated with both constitutive and regulated secretory pathways, and may be involved in protein transport. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011]
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T C 11: 9,293,459 V1774A probably damaging Het
Adam34 G A 8: 43,652,251 P119L probably benign Het
Ap3b2 T C 7: 81,463,681 probably null Het
Arfip2 G A 7: 105,637,223 T124M probably damaging Het
Arhgef26 T C 3: 62,423,544 S560P probably damaging Het
Bcl11a A T 11: 24,172,697 probably null Het
Cab39 A G 1: 85,849,160 E322G probably damaging Het
Cad C A 5: 31,072,321 P1382Q probably benign Het
Cc2d2a T C 5: 43,706,901 probably null Het
Cela2a A T 4: 141,821,700 probably null Het
Ces1e A C 8: 93,224,039 I38S probably benign Het
Ces1f A T 8: 93,263,391 F364I probably benign Het
Chgb A G 2: 132,793,811 T558A probably benign Het
Cnpy4 C T 5: 138,192,812 Q217* probably null Het
Col4a3bp C T 13: 96,634,121 R487* probably null Het
Crlf1 A G 8: 70,498,599 T43A probably benign Het
Dnah7b T A 1: 46,134,656 M707K probably damaging Het
Ets2 G A 16: 95,712,149 S123N probably damaging Het
Fam196b C A 11: 34,402,826 D289E possibly damaging Het
Fry T C 5: 150,471,468 F304S probably damaging Het
Gadd45gip1 G A 8: 84,834,116 R120H probably benign Het
Gbf1 A G 19: 46,254,020 T96A probably benign Het
Ggn T A 7: 29,171,090 M1K probably null Het
Gm5239 A G 18: 35,536,916 T112A probably benign Het
Kif1bp A T 10: 62,578,082 probably null Het
Lrrc15 A T 16: 30,273,743 H259Q probably benign Het
Lysmd4 A G 7: 67,226,297 Y236C probably damaging Het
Med29 T C 7: 28,386,859 T175A possibly damaging Het
Mfsd12 G T 10: 81,357,799 D68Y probably damaging Het
Myh1 T C 11: 67,217,512 L1308P probably damaging Het
Nphp4 T A 4: 152,551,931 probably null Het
Olfr948 A G 9: 39,319,461 I51T probably benign Het
Pdhx A G 2: 103,028,280 V393A probably benign Het
Pgm5 A G 19: 24,824,399 I155T possibly damaging Het
Pgr A T 9: 8,965,022 I889F probably benign Het
Phactr4 T A 4: 132,386,930 K51I probably damaging Het
Pum2 T A 12: 8,728,754 I468K possibly damaging Het
Rasef T C 4: 73,748,562 Q160R probably damaging Het
Rbl2 A G 8: 91,087,144 D339G probably benign Het
Recql5 A G 11: 115,894,673 S666P probably benign Het
Rfc1 A T 5: 65,296,052 probably null Het
Scarb1 A G 5: 125,289,692 V59A probably damaging Het
Slc2a4 C T 11: 69,946,356 V85M probably damaging Het
Slc6a12 A G 6: 121,358,625 I291V possibly damaging Het
Slco3a1 A C 7: 74,504,426 Y104D probably damaging Het
Suz12 T A 11: 79,999,078 D13E probably damaging Het
Tlr1 G T 5: 64,925,967 C422* probably null Het
Tmco1 T C 1: 167,325,893 V114A probably damaging Het
Trpa1 T C 1: 14,881,632 T948A probably benign Het
Tub A T 7: 109,020,927 N93Y probably damaging Het
Ufsp2 G A 8: 45,992,233 probably null Het
Veph1 T C 3: 66,171,975 D373G probably benign Het
Vmn1r206 A G 13: 22,620,960 S26P possibly damaging Het
Vmn2r1 T C 3: 64,081,819 S60P possibly damaging Het
Wdcp A G 12: 4,851,583 S480G probably benign Het
Wnk4 T C 11: 101,268,804 S612P probably benign Het
Zfp503 T C 14: 21,986,459 K130E probably benign Het
Zkscan16 G A 4: 58,957,602 C628Y possibly damaging Het
Other mutations in Rab11a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02474:Rab11a APN 9 64726647 missense possibly damaging 0.89
IGL02687:Rab11a APN 9 64726698 missense probably damaging 1.00
R4527:Rab11a UTSW 9 64725568 missense probably benign 0.38
R7860:Rab11a UTSW 9 64728331 nonsense probably null
R8848:Rab11a UTSW 9 64716982 missense probably damaging 1.00
Predicted Primers PCR Primer

Sequencing Primer
(R):5'- gaggcagaggcaggcag -3'
Posted On 2013-04-16