Incidental Mutation 'IGL00953:Slc35g2'
ID 28216
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc35g2
Ensembl Gene ENSMUSG00000070287
Gene Name solute carrier family 35, member G2
Synonyms LOC245020, Tmem22
Accession Numbers
Essential gene? Probably non essential (E-score: 0.156) question?
Stock # IGL00953
Quality Score
Status
Chromosome 9
Chromosomal Location 100434241-100453143 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 100434516 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 385 (V385A)
Ref Sequence ENSEMBL: ENSMUSP00000091308 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000093792]
AlphaFold D3YVE8
Predicted Effect probably damaging
Transcript: ENSMUST00000093792
AA Change: V385A

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000091308
Gene: ENSMUSG00000070287
AA Change: V385A

DomainStartEndE-ValueType
Pfam:EamA 102 238 3.8e-12 PFAM
Pfam:EamA 255 390 5e-11 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189478
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aatk T C 11: 119,902,047 (GRCm39) E726G probably benign Het
Cdyl2 T A 8: 117,321,928 (GRCm39) probably benign Het
Cep41 T C 6: 30,660,966 (GRCm39) T109A probably benign Het
Clca3b C T 3: 144,552,972 (GRCm39) W84* probably null Het
Cyp27b1 A G 10: 126,885,551 (GRCm39) D130G probably benign Het
Cyp2f2 T C 7: 26,829,242 (GRCm39) V249A possibly damaging Het
Cyth3 G A 5: 143,692,920 (GRCm39) probably null Het
Dnah8 G T 17: 30,925,431 (GRCm39) E1289* probably null Het
Fam171a1 A T 2: 3,179,327 (GRCm39) D51V possibly damaging Het
Farp2 A G 1: 93,488,896 (GRCm39) R107G possibly damaging Het
Gemin6 T C 17: 80,535,294 (GRCm39) F85L possibly damaging Het
Hivep3 A C 4: 119,955,571 (GRCm39) T1296P probably damaging Het
Hnrnpm C A 17: 33,868,876 (GRCm39) R517L probably damaging Het
Htt T A 5: 34,976,021 (GRCm39) S670T probably benign Het
Klhl24 A T 16: 19,941,717 (GRCm39) N555I possibly damaging Het
Limd1 T A 9: 123,308,948 (GRCm39) S216T probably benign Het
Lmf2 A T 15: 89,238,102 (GRCm39) I234N probably damaging Het
Mrpl4 C A 9: 20,919,863 (GRCm39) D271E probably benign Het
Mydgf C T 17: 56,486,407 (GRCm39) G75R probably damaging Het
Nat1 A G 8: 67,943,630 (GRCm39) D5G possibly damaging Het
Or2t46 T C 11: 58,472,636 (GRCm39) V322A probably benign Het
Or5h22 A T 16: 58,895,052 (GRCm39) Y130* probably null Het
Or5k15 A C 16: 58,710,048 (GRCm39) H178Q probably damaging Het
Pla2g4c T A 7: 13,077,951 (GRCm39) M363K probably benign Het
Prex1 A G 2: 166,480,329 (GRCm39) F137S probably damaging Het
Rbm12b1 A G 4: 12,146,038 (GRCm39) D670G probably damaging Het
Rrp12 C A 19: 41,860,231 (GRCm39) M997I possibly damaging Het
Scn3a A G 2: 65,327,736 (GRCm39) V918A probably benign Het
Slit1 A T 19: 41,590,739 (GRCm39) I1311N probably damaging Het
Ube2j2 C T 4: 156,030,834 (GRCm39) probably benign Het
Ucp2 A G 7: 100,147,629 (GRCm39) T203A probably benign Het
Upk1b C T 16: 38,600,347 (GRCm39) G211D possibly damaging Het
Vmn1r220 A T 13: 23,367,935 (GRCm39) F254I probably benign Het
Zcchc4 T C 5: 52,965,638 (GRCm39) F314S probably damaging Het
Other mutations in Slc35g2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03264:Slc35g2 APN 9 100,434,699 (GRCm39) missense possibly damaging 0.93
R0127:Slc35g2 UTSW 9 100,435,170 (GRCm39) missense probably benign 0.12
R0626:Slc35g2 UTSW 9 100,435,495 (GRCm39) missense probably benign 0.00
R1123:Slc35g2 UTSW 9 100,435,047 (GRCm39) missense probably damaging 0.98
R2012:Slc35g2 UTSW 9 100,435,120 (GRCm39) missense possibly damaging 0.88
R2057:Slc35g2 UTSW 9 100,435,329 (GRCm39) missense probably damaging 1.00
R3922:Slc35g2 UTSW 9 100,434,780 (GRCm39) missense probably benign 0.20
R3924:Slc35g2 UTSW 9 100,434,780 (GRCm39) missense probably benign 0.20
R4561:Slc35g2 UTSW 9 100,435,287 (GRCm39) missense probably damaging 1.00
R4731:Slc35g2 UTSW 9 100,434,555 (GRCm39) missense probably benign 0.20
R4732:Slc35g2 UTSW 9 100,434,555 (GRCm39) missense probably benign 0.20
R4733:Slc35g2 UTSW 9 100,434,555 (GRCm39) missense probably benign 0.20
R4760:Slc35g2 UTSW 9 100,435,549 (GRCm39) missense probably benign 0.22
R8310:Slc35g2 UTSW 9 100,434,841 (GRCm39) missense probably damaging 1.00
R8420:Slc35g2 UTSW 9 100,435,224 (GRCm39) missense probably benign
X0020:Slc35g2 UTSW 9 100,435,069 (GRCm39) missense probably benign 0.30
Z1176:Slc35g2 UTSW 9 100,434,582 (GRCm39) missense probably damaging 1.00
Posted On 2013-04-17