Incidental Mutation 'IGL02899:Morn5'
ID 363523
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Morn5
Ensembl Gene ENSMUSG00000026894
Gene Name MORN repeat containing 5
Synonyms 1700010A17Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.150) question?
Stock # IGL02899
Quality Score
Status
Chromosome 2
Chromosomal Location 35939485-35969721 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 35945049 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 91 (F91S)
Ref Sequence ENSEMBL: ENSMUSP00000028256 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028256]
AlphaFold Q9DAI9
Predicted Effect probably damaging
Transcript: ENSMUST00000028256
AA Change: F91S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000028256
Gene: ENSMUSG00000026894
AA Change: F91S

DomainStartEndE-ValueType
MORN 6 27 1.24e1 SMART
MORN 29 50 3.61e-2 SMART
Pfam:MORN 54 75 2e-4 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arfgef2 A G 2: 166,710,971 (GRCm39) probably benign Het
Btbd7 A G 12: 102,803,921 (GRCm39) L373P probably damaging Het
Capn3 A G 2: 120,322,382 (GRCm39) N414S possibly damaging Het
Ccdc186 A T 19: 56,781,920 (GRCm39) I753N probably benign Het
Ccser2 G A 14: 36,662,716 (GRCm39) T156I probably benign Het
Celsr1 A G 15: 85,915,927 (GRCm39) M682T probably damaging Het
Cep97 C A 16: 55,738,903 (GRCm39) S267I probably damaging Het
Dhx35 A G 2: 158,643,370 (GRCm39) Y39C probably damaging Het
Dscam A T 16: 96,510,447 (GRCm39) D937E probably damaging Het
Elmod2 A G 8: 84,043,562 (GRCm39) Y202H probably damaging Het
Fyco1 T C 9: 123,659,396 (GRCm39) N260S possibly damaging Het
Gm5591 A G 7: 38,218,842 (GRCm39) L677P probably damaging Het
Gmppa A G 1: 75,418,474 (GRCm39) probably null Het
Hltf C T 3: 20,153,981 (GRCm39) T639I probably damaging Het
Inhca C A 9: 103,154,773 (GRCm39) V173L probably damaging Het
Kpnb1 T C 11: 97,066,612 (GRCm39) Y321C probably damaging Het
Lgr4 G A 2: 109,748,598 (GRCm39) G45R probably damaging Het
Ltn1 T C 16: 87,179,547 (GRCm39) D1538G probably benign Het
Maf1 T A 15: 76,237,220 (GRCm39) probably benign Het
Ncan C T 8: 70,567,698 (GRCm39) R138H possibly damaging Het
Or10ak7 A T 4: 118,791,859 (GRCm39) M62K probably damaging Het
Or5ac21 G T 16: 59,123,649 (GRCm39) L44F probably damaging Het
Parg T C 14: 31,960,531 (GRCm39) L82S probably damaging Het
Ppp2r2b A T 18: 42,778,874 (GRCm39) H417Q probably damaging Het
Rb1cc1 T C 1: 6,334,807 (GRCm39) L98P probably damaging Het
Ryr1 C A 7: 28,748,220 (GRCm39) V3752L possibly damaging Het
Slc25a12 A G 2: 71,109,979 (GRCm39) L489P probably damaging Het
Slc38a8 C T 8: 120,212,282 (GRCm39) V354M probably benign Het
Slf2 A G 19: 44,930,459 (GRCm39) E512G probably benign Het
Tarbp1 A G 8: 127,180,583 (GRCm39) M597T probably damaging Het
Tgfb3 G A 12: 86,116,550 (GRCm39) R163C probably damaging Het
Tmco5b A G 2: 113,127,265 (GRCm39) M279V probably benign Het
Ttll9 G A 2: 152,844,871 (GRCm39) G413D probably damaging Het
Tut1 A G 19: 8,939,751 (GRCm39) D245G probably damaging Het
Usf3 T A 16: 44,041,589 (GRCm39) V2023E probably damaging Het
Vps33a C T 5: 123,669,239 (GRCm39) G554D probably damaging Het
Zfp27 C A 7: 29,595,680 (GRCm39) R95M possibly damaging Het
Other mutations in Morn5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02158:Morn5 APN 2 35,947,088 (GRCm39) missense probably damaging 1.00
IGL02190:Morn5 APN 2 35,969,527 (GRCm39) missense probably benign 0.03
IGL02441:Morn5 APN 2 35,945,038 (GRCm39) nonsense probably null
R0306:Morn5 UTSW 2 35,944,986 (GRCm39) missense probably damaging 1.00
R1449:Morn5 UTSW 2 35,947,092 (GRCm39) nonsense probably null
R1803:Morn5 UTSW 2 35,943,089 (GRCm39) missense probably benign 0.03
R1819:Morn5 UTSW 2 35,942,987 (GRCm39) missense probably damaging 1.00
R2012:Morn5 UTSW 2 35,942,950 (GRCm39) missense probably benign 0.03
R3932:Morn5 UTSW 2 35,943,035 (GRCm39) missense probably damaging 0.99
R7078:Morn5 UTSW 2 35,944,990 (GRCm39) missense probably benign
R7681:Morn5 UTSW 2 35,947,156 (GRCm39) missense possibly damaging 0.95
R7938:Morn5 UTSW 2 35,947,082 (GRCm39) missense probably benign 0.03
R8438:Morn5 UTSW 2 35,945,076 (GRCm39) missense probably benign 0.03
R8805:Morn5 UTSW 2 35,969,533 (GRCm39) missense probably benign 0.28
R9153:Morn5 UTSW 2 35,942,993 (GRCm39) missense probably damaging 1.00
R9166:Morn5 UTSW 2 35,945,024 (GRCm39) missense probably damaging 1.00
R9256:Morn5 UTSW 2 35,939,553 (GRCm39) missense probably damaging 1.00
R9447:Morn5 UTSW 2 35,969,525 (GRCm39) critical splice acceptor site probably null
Posted On 2015-12-18