Incidental Mutation 'IGL01155:Mobp'
ID 52026
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mobp
Ensembl Gene ENSMUSG00000032517
Gene Name myelin-associated oligodendrocytic basic protein
Synonyms MOBP155
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.058) question?
Stock # IGL01155
Quality Score
Chromosome 9
Chromosomal Location 120149707-120181484 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to A at 120168234 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 73 (T73K)
Ref Sequence ENSEMBL: ENSMUSP00000071084 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000068698] [ENSMUST00000093773] [ENSMUST00000111627] [ENSMUST00000174193] [ENSMUST00000214943] [ENSMUST00000215512]
AlphaFold Q9D2P8
Predicted Effect probably benign
Transcript: ENSMUST00000068698
AA Change: T73K

PolyPhen 2 Score 0.081 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000071084
Gene: ENSMUSG00000032517
AA Change: T73K

Pfam:FYVE_2 1 75 6.4e-13 PFAM
low complexity region 82 99 N/A INTRINSIC
low complexity region 102 151 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000093773
SMART Domains Protein: ENSMUSP00000091287
Gene: ENSMUSG00000032517

Pfam:FYVE_2 1 77 3.8e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000111627
SMART Domains Protein: ENSMUSP00000107254
Gene: ENSMUSG00000032517

Pfam:FYVE_2 1 77 3.8e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000174193
SMART Domains Protein: ENSMUSP00000134410
Gene: ENSMUSG00000032517

Pfam:FYVE_2 1 77 3.8e-14 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214008
Predicted Effect probably benign
Transcript: ENSMUST00000214943
Predicted Effect probably benign
Transcript: ENSMUST00000215512
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for one null allele show abnormal myelin arrangements but do not exhibit an overt behavorial phenotype. Mice homozygous for another allele have normal myelin. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110038F14Rik G A 15: 76,950,275 V124I probably damaging Het
Adgrl3 T A 5: 81,560,893 I409N probably benign Het
Akap13 A G 7: 75,569,936 D29G probably damaging Het
Ap4e1 C A 2: 127,043,445 T322K probably damaging Het
Arfgef1 G A 1: 10,198,982 probably benign Het
Asic5 A G 3: 82,008,588 T282A probably benign Het
Bptf T C 11: 107,080,727 T985A probably damaging Het
Btnl9 A G 11: 49,175,691 F349L probably damaging Het
Bves T A 10: 45,353,859 I253K probably damaging Het
Cars T A 7: 143,569,849 Y455F probably benign Het
Cfap206 C T 4: 34,721,562 S162N probably damaging Het
Cuedc2 C A 19: 46,332,649 V15F probably damaging Het
Defa22 T A 8: 21,163,037 probably null Het
Fat1 G A 8: 45,023,949 A2011T probably damaging Het
Fyb2 C T 4: 104,999,386 T533I probably benign Het
Gm1043 T C 5: 37,187,089 L182P probably damaging Het
Ice1 A T 13: 70,604,082 V1295E possibly damaging Het
Il12b T A 11: 44,404,088 S18T probably benign Het
Iqcg A G 16: 33,040,875 V157A probably damaging Het
Itgax T A 7: 128,145,035 M937K probably benign Het
Large1 T C 8: 73,131,989 S84G probably benign Het
Lrp1b T C 2: 41,770,935 T54A probably benign Het
Mfn1 A G 3: 32,542,836 M148V probably damaging Het
Ms4a3 T C 19: 11,629,655 probably benign Het
Muc5ac C T 7: 141,806,943 probably benign Het
Mzt2 A C 16: 15,862,410 S104A possibly damaging Het
Naa16 T A 14: 79,384,715 K27N probably damaging Het
Nos1 T A 5: 117,945,926 I1267N probably damaging Het
Olfr16 T A 1: 172,956,924 I43N probably benign Het
Rara A G 11: 98,968,184 E153G possibly damaging Het
Scn2a T G 2: 65,717,748 S66A probably damaging Het
Slc6a1 A T 6: 114,314,465 probably null Het
Sorbs3 A G 14: 70,199,341 V136A probably damaging Het
Spink5 T A 18: 43,981,147 H143Q probably benign Het
Susd2 G A 10: 75,640,892 T99I possibly damaging Het
T C T 17: 8,441,745 probably null Het
Tac2 G A 10: 127,726,134 probably null Het
Tfap4 G T 16: 4,547,359 P180T probably damaging Het
Trap1 G A 16: 4,043,978 Q641* probably null Het
Unc119 A G 11: 78,348,609 N252S probably damaging Het
Other mutations in Mobp
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01730:Mobp APN 9 120167926 missense probably damaging 1.00
IGL02078:Mobp APN 9 120167914 missense probably damaging 1.00
IGL02470:Mobp APN 9 120168006 missense probably benign 0.18
P0041:Mobp UTSW 9 120168017 utr 3 prime probably benign
R3794:Mobp UTSW 9 120167967 nonsense probably null
R3890:Mobp UTSW 9 120167956 missense probably damaging 1.00
R5173:Mobp UTSW 9 120168245 missense possibly damaging 0.68
R5255:Mobp UTSW 9 120168353 unclassified probably benign
R5549:Mobp UTSW 9 120167810 missense probably damaging 1.00
R5870:Mobp UTSW 9 120167853 missense probably damaging 0.98
R6128:Mobp UTSW 9 120168326 unclassified probably benign
R7267:Mobp UTSW 9 120167848 missense probably damaging 1.00
R9260:Mobp UTSW 9 120168506 missense unknown
Posted On 2013-06-21