Incidental Mutation 'R3873:Arl8a'
ID 276647
Institutional Source Beutler Lab
Gene Symbol Arl8a
Ensembl Gene ENSMUSG00000026426
Gene Name ADP-ribosylation factor-like 8A
Synonyms 1110033P22Rik, Arl10b
MMRRC Submission 040791-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.557) question?
Stock # R3873 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 135074572-135084007 bp(+) (GRCm39)
Type of Mutation splice site (6 bp from exon)
DNA Base Change (assembly) T to C at 135080610 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000027684]
AlphaFold Q8VEH3
Predicted Effect probably null
Transcript: ENSMUST00000027684
SMART Domains Protein: ENSMUSP00000027684
Gene: ENSMUSG00000026426

DomainStartEndE-ValueType
ARF 1 185 2.25e-31 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123344
Predicted Effect probably null
Transcript: ENSMUST00000125774
SMART Domains Protein: ENSMUSP00000121545
Gene: ENSMUSG00000026426

DomainStartEndE-ValueType
Pfam:Roc 16 113 1e-12 PFAM
Pfam:Ras 18 162 4.2e-16 PFAM
Pfam:Arf 19 160 6.6e-41 PFAM
Pfam:Gtr1_RagA 26 155 3.7e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000125774
SMART Domains Protein: ENSMUSP00000121545
Gene: ENSMUSG00000026426

DomainStartEndE-ValueType
Pfam:Roc 16 113 1e-12 PFAM
Pfam:Ras 18 162 4.2e-16 PFAM
Pfam:Arf 19 160 6.6e-41 PFAM
Pfam:Gtr1_RagA 26 155 3.7e-9 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141177
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146700
Predicted Effect noncoding transcript
Transcript: ENSMUST00000157096
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 95.9%
Validation Efficiency 100% (50/50)
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 T A 11: 110,201,059 (GRCm39) Y447F probably damaging Het
Acaca A G 11: 84,203,547 (GRCm39) probably benign Het
Adam5 T C 8: 25,305,125 (GRCm39) T110A probably benign Het
Agtpbp1 T C 13: 59,608,410 (GRCm39) M175V possibly damaging Het
Akt1 T C 12: 112,622,967 (GRCm39) N367S probably benign Het
Ankrd61 T A 5: 143,828,646 (GRCm39) T67S probably damaging Het
Arvcf G A 16: 18,221,783 (GRCm39) R736Q probably damaging Het
Baz2a T A 10: 127,959,979 (GRCm39) M1419K probably damaging Het
Cep295 A T 9: 15,244,661 (GRCm39) V1265E probably damaging Het
Cfap299 A T 5: 98,885,482 (GRCm39) I130F probably damaging Het
Cyp2c29 A G 19: 39,317,588 (GRCm39) D397G probably damaging Het
Dlgap4 T C 2: 156,591,267 (GRCm39) S818P probably benign Het
Dnah2 A G 11: 69,320,174 (GRCm39) I3965T probably damaging Het
Dst A G 1: 34,328,701 (GRCm39) T4590A probably damaging Het
Eif1ad10 T C 12: 88,216,476 (GRCm39) D132G unknown Het
Fscb G T 12: 64,519,906 (GRCm39) P520Q unknown Het
Gli1 T A 10: 127,167,225 (GRCm39) N676I probably damaging Het
Hspg2 T C 4: 137,266,660 (GRCm39) I1916T probably damaging Het
Igfals G A 17: 25,100,579 (GRCm39) V557I possibly damaging Het
Il7 A T 3: 7,669,224 (GRCm39) V4D probably damaging Het
Itgae T A 11: 73,004,442 (GRCm39) I243N probably damaging Het
Itpa T G 2: 130,522,930 (GRCm39) S176A probably damaging Het
Klhl13 T C X: 23,151,415 (GRCm39) D21G probably benign Het
Krt26 T C 11: 99,225,570 (GRCm39) K304E probably damaging Het
Ly6g6e T C 17: 35,296,159 (GRCm39) V10A probably benign Het
Morc3 G A 16: 93,659,324 (GRCm39) V411I probably damaging Het
Mrpl32 G T 13: 14,787,630 (GRCm39) probably benign Het
Ncald G A 15: 37,397,497 (GRCm39) A61V probably damaging Het
Nek2 T C 1: 191,559,320 (GRCm39) V275A probably benign Het
Or12d12 T A 17: 37,610,870 (GRCm39) T148S probably benign Het
Or4f6 T C 2: 111,838,668 (GRCm39) T288A possibly damaging Het
Or5l13 T A 2: 87,779,874 (GRCm39) R234S probably damaging Het
Or5m10b T A 2: 85,699,306 (GRCm39) Y123* probably null Het
Pgam5 T C 5: 110,413,465 (GRCm39) Y210C probably damaging Het
Phf5a T C 15: 81,754,628 (GRCm39) N50D probably benign Het
Prl7d1 A G 13: 27,900,651 (GRCm39) M1T probably null Het
Sacs A G 14: 61,429,735 (GRCm39) K595R possibly damaging Het
Scyl3 A G 1: 163,778,206 (GRCm39) N448S probably benign Het
Serpinb9g A T 13: 33,670,518 (GRCm39) D2V probably benign Het
Sgsh A G 11: 119,241,773 (GRCm39) L111P probably damaging Het
Smg1 T C 7: 117,753,885 (GRCm39) probably benign Het
Taar1 T C 10: 23,796,482 (GRCm39) L60P probably damaging Het
Tmem51 T C 4: 141,759,059 (GRCm39) T230A probably damaging Het
Ubr4 T C 4: 139,151,301 (GRCm39) V623A probably damaging Het
Usp34 C T 11: 23,439,033 (GRCm39) P3532S possibly damaging Het
Vipr2 T C 12: 116,099,724 (GRCm39) probably benign Het
Vmn2r16 T C 5: 109,488,177 (GRCm39) M350T probably benign Het
Vmn2r22 T C 6: 123,614,339 (GRCm39) E417G possibly damaging Het
Vmn2r9 C A 5: 108,995,701 (GRCm39) V316F probably benign Het
Zfp53 C T 17: 21,728,893 (GRCm39) P309S probably damaging Het
Other mutations in Arl8a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01552:Arl8a APN 1 135,080,606 (GRCm39) critical splice donor site probably null
R0436:Arl8a UTSW 1 135,074,718 (GRCm39) start codon destroyed probably null 0.45
R1639:Arl8a UTSW 1 135,080,561 (GRCm39) nonsense probably null
R2393:Arl8a UTSW 1 135,080,604 (GRCm39) missense probably damaging 1.00
R2842:Arl8a UTSW 1 135,082,989 (GRCm39) missense probably damaging 0.98
R4764:Arl8a UTSW 1 135,074,837 (GRCm39) missense probably benign 0.04
R5736:Arl8a UTSW 1 135,082,458 (GRCm39) missense probably benign
R6007:Arl8a UTSW 1 135,080,606 (GRCm39) critical splice donor site probably null
R6989:Arl8a UTSW 1 135,074,735 (GRCm39) missense probably benign
R7036:Arl8a UTSW 1 135,082,206 (GRCm39) missense probably benign 0.19
R8758:Arl8a UTSW 1 135,082,189 (GRCm39) missense possibly damaging 0.90
Predicted Primers PCR Primer
(F):5'- AAGGAGCTGTGACCTTAGGG -3'
(R):5'- AGGCTGGCTGATCAGATCTG -3'

Sequencing Primer
(F):5'- CCCAATGGCTTTCAGTTG -3'
(R):5'- GGCTGATCAGATCTGTATATATATTA -3'
Posted On 2015-04-06