Incidental Mutation 'IGL01567:Map10'
ID 91027
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Map10
Ensembl Gene ENSMUSG00000050930
Gene Name microtubule-associated protein 10
Synonyms 4933403G14Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # IGL01567
Quality Score
Status
Chromosome 8
Chromosomal Location 125669818-125673359 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to A at 125671493 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 542 (Q542K)
Ref Sequence ENSEMBL: ENSMUSP00000061679 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053078]
AlphaFold Q8BJS7
Predicted Effect probably benign
Transcript: ENSMUST00000053078
AA Change: Q542K

PolyPhen 2 Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000061679
Gene: ENSMUSG00000050930
AA Change: Q542K

DomainStartEndE-ValueType
low complexity region 38 54 N/A INTRINSIC
low complexity region 68 91 N/A INTRINSIC
Pfam:HPHLAWLY 243 535 1.4e-130 PFAM
Pfam:HPHLAWLY 527 890 9.1e-133 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agbl1 A G 7: 76,421,880 (GRCm38) S317G probably benign Het
Akna T C 4: 63,381,850 (GRCm38) T652A probably benign Het
Anxa9 G A 3: 95,302,432 (GRCm38) probably benign Het
Bpifb4 T A 2: 153,947,278 (GRCm38) probably benign Het
Bptf A G 11: 107,058,774 (GRCm38) S2125P probably damaging Het
Capns2 C A 8: 92,902,006 (GRCm38) H174Q probably benign Het
Cd200 A C 16: 45,394,691 (GRCm38) L199R probably damaging Het
Clasp2 T C 9: 113,880,096 (GRCm38) V651A probably damaging Het
Cox18 G A 5: 90,217,588 (GRCm38) Q251* probably null Het
Depdc1a T C 3: 159,526,546 (GRCm38) S645P probably damaging Het
Dio3 T A 12: 110,279,427 (GRCm38) C66S possibly damaging Het
Dock9 A T 14: 121,653,084 (GRCm38) L258Q probably damaging Het
Ghrhr A G 6: 55,384,123 (GRCm38) D274G probably damaging Het
Gm5129 A G 5: 29,735,864 (GRCm38) probably benign Het
Grb7 A G 11: 98,454,950 (GRCm38) N518S probably damaging Het
Kdm5b G A 1: 134,602,540 (GRCm38) A430T probably damaging Het
Metap1 T C 3: 138,462,389 (GRCm38) T325A probably damaging Het
Ncan A T 8: 70,108,334 (GRCm38) M661K probably benign Het
Olfr38 T C 6: 42,762,727 (GRCm38) I225T probably benign Het
Olfr572 A G 7: 102,928,416 (GRCm38) I263V probably benign Het
Otog T C 7: 46,276,615 (GRCm38) probably benign Het
Pip4k2b T C 11: 97,729,561 (GRCm38) D116G probably damaging Het
Rps15 T A 10: 80,293,809 (GRCm38) L86Q probably benign Het
Sfxn4 G T 19: 60,853,898 (GRCm38) T122K probably damaging Het
Slc4a3 T C 1: 75,550,882 (GRCm38) V165A probably damaging Het
Spata48 A G 11: 11,515,015 (GRCm38) H122R possibly damaging Het
Synm A G 7: 67,735,232 (GRCm38) V452A probably damaging Het
Tdpoz1 T C 3: 93,670,706 (GRCm38) H257R possibly damaging Het
Tmem26 A G 10: 68,751,231 (GRCm38) T170A probably damaging Het
Wdfy4 T G 14: 33,151,661 (GRCm38) E230D probably benign Het
Other mutations in Map10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00813:Map10 APN 8 125,671,932 (GRCm38) missense probably benign 0.00
IGL02566:Map10 APN 8 125,671,755 (GRCm38) missense probably benign
IGL03088:Map10 APN 8 125,671,070 (GRCm38) missense probably benign 0.14
debauched UTSW 8 125,671,245 (GRCm38) missense probably damaging 1.00
R1083:Map10 UTSW 8 125,670,439 (GRCm38) nonsense probably null
R1543:Map10 UTSW 8 125,670,872 (GRCm38) missense probably benign 0.00
R3155:Map10 UTSW 8 125,671,574 (GRCm38) missense possibly damaging 0.79
R4076:Map10 UTSW 8 125,671,845 (GRCm38) missense probably benign 0.23
R4559:Map10 UTSW 8 125,671,814 (GRCm38) missense probably benign
R4856:Map10 UTSW 8 125,670,692 (GRCm38) missense probably damaging 1.00
R4886:Map10 UTSW 8 125,670,692 (GRCm38) missense probably damaging 1.00
R5412:Map10 UTSW 8 125,670,985 (GRCm38) missense probably damaging 1.00
R6034:Map10 UTSW 8 125,672,466 (GRCm38) missense probably damaging 1.00
R6034:Map10 UTSW 8 125,672,466 (GRCm38) missense probably damaging 1.00
R6150:Map10 UTSW 8 125,671,589 (GRCm38) missense probably damaging 0.96
R6351:Map10 UTSW 8 125,671,245 (GRCm38) missense probably damaging 1.00
R6466:Map10 UTSW 8 125,672,384 (GRCm38) nonsense probably null
R6544:Map10 UTSW 8 125,671,374 (GRCm38) missense probably benign 0.00
R6557:Map10 UTSW 8 125,670,252 (GRCm38) missense probably damaging 0.98
R6821:Map10 UTSW 8 125,670,399 (GRCm38) missense probably benign 0.01
R7096:Map10 UTSW 8 125,671,923 (GRCm38) missense probably damaging 0.99
R7128:Map10 UTSW 8 125,671,853 (GRCm38) missense probably benign
R7177:Map10 UTSW 8 125,671,845 (GRCm38) missense probably benign 0.23
R7237:Map10 UTSW 8 125,671,224 (GRCm38) missense probably benign 0.03
R7814:Map10 UTSW 8 125,671,611 (GRCm38) missense probably benign 0.14
R7819:Map10 UTSW 8 125,670,521 (GRCm38) frame shift probably null
R8202:Map10 UTSW 8 125,670,908 (GRCm38) missense possibly damaging 0.95
R8812:Map10 UTSW 8 125,669,925 (GRCm38) missense probably damaging 0.99
R8859:Map10 UTSW 8 125,670,552 (GRCm38) missense probably benign 0.04
R8947:Map10 UTSW 8 125,671,100 (GRCm38) missense probably benign 0.06
R9178:Map10 UTSW 8 125,670,910 (GRCm38) missense probably damaging 0.98
R9698:Map10 UTSW 8 125,671,984 (GRCm38) missense probably benign 0.16
Z1088:Map10 UTSW 8 125,671,931 (GRCm38) frame shift probably null
Z1177:Map10 UTSW 8 125,670,070 (GRCm38) missense probably damaging 1.00
Posted On 2013-12-09