Incidental Mutation 'IGL03112:Morn1'
ID 419239
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Morn1
Ensembl Gene ENSMUSG00000029049
Gene Name MORN repeat containing 1
Synonyms 4930417P05Rik, 2900057D20Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03112
Quality Score
Status
Chromosome 4
Chromosomal Location 155171034-155229962 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 155177601 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 178 (Y178N)
Ref Sequence ENSEMBL: ENSMUSP00000116794 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030915] [ENSMUST00000127457] [ENSMUST00000132367] [ENSMUST00000155775]
AlphaFold A2RTS7
Predicted Effect probably damaging
Transcript: ENSMUST00000030915
AA Change: Y178N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000030915
Gene: ENSMUSG00000029049
AA Change: Y178N

DomainStartEndE-ValueType
Pfam:MORN 23 35 1.4e-3 PFAM
MORN 37 58 4.11e-6 SMART
MORN 60 81 2.41e-1 SMART
MORN 84 105 1.43e-1 SMART
MORN 107 128 8.05e0 SMART
MORN 130 151 2.06e-6 SMART
MORN 153 174 7.56e-5 SMART
MORN 176 197 1.2e0 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000127457
AA Change: Y178N

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000116690
Gene: ENSMUSG00000029049
AA Change: Y178N

DomainStartEndE-ValueType
Pfam:MORN 23 35 5.5e-4 PFAM
MORN 37 58 4.11e-6 SMART
MORN 60 81 2.41e-1 SMART
MORN 84 105 1.43e-1 SMART
MORN 107 128 8.05e0 SMART
MORN 130 151 2.06e-6 SMART
MORN 153 174 7.56e-5 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129180
Predicted Effect probably damaging
Transcript: ENSMUST00000132367
AA Change: Y178N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000116794
Gene: ENSMUSG00000029049
AA Change: Y178N

DomainStartEndE-ValueType
Pfam:MORN 23 35 6.8e-4 PFAM
MORN 37 58 4.11e-6 SMART
MORN 60 81 2.41e-1 SMART
MORN 84 105 1.43e-1 SMART
MORN 107 128 8.05e0 SMART
MORN 130 151 2.06e-6 SMART
MORN 153 174 7.56e-5 SMART
MORN 176 197 1.2e0 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155375
Predicted Effect probably benign
Transcript: ENSMUST00000155775
SMART Domains Protein: ENSMUSP00000123207
Gene: ENSMUSG00000029049

DomainStartEndE-ValueType
Pfam:MORN 23 35 2.7e-4 PFAM
MORN 37 58 4.11e-6 SMART
MORN 60 81 2.41e-1 SMART
MORN 93 114 2.06e-6 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam26b T C 8: 43,974,549 (GRCm39) N151S probably benign Het
Adgre1 G A 17: 57,755,029 (GRCm39) probably null Het
Apol11a T A 15: 77,401,509 (GRCm39) L332Q probably damaging Het
B430306N03Rik C T 17: 48,623,834 (GRCm39) S45L probably benign Het
Cend1 G A 7: 141,007,640 (GRCm39) T60M probably benign Het
Col6a3 C A 1: 90,739,242 (GRCm39) E329* probably null Het
Col9a3 A G 2: 180,249,435 (GRCm39) R266G possibly damaging Het
Defb48 C T 14: 63,221,854 (GRCm39) probably benign Het
Eps8l2 T G 7: 140,941,649 (GRCm39) L640R probably damaging Het
Exoc2 T A 13: 31,090,570 (GRCm39) probably benign Het
Fam149a C T 8: 45,801,580 (GRCm39) V514M possibly damaging Het
Fbxo25 A T 8: 13,971,034 (GRCm39) D74V probably benign Het
Gm11733 A G 11: 117,377,966 (GRCm39) *126W probably null Het
Grm8 C T 6: 27,363,262 (GRCm39) C751Y probably damaging Het
Kctd16 A T 18: 40,391,853 (GRCm39) D147V probably benign Het
Lclat1 A T 17: 73,546,742 (GRCm39) T220S probably damaging Het
Lgi1 T A 19: 38,272,478 (GRCm39) H116Q possibly damaging Het
Lrrc40 G A 3: 157,747,302 (GRCm39) probably benign Het
Lsm4 T A 8: 71,130,656 (GRCm39) I60N probably damaging Het
Mybl2 A G 2: 162,904,456 (GRCm39) E89G probably damaging Het
Myo18b T C 5: 113,021,856 (GRCm39) E512G probably benign Het
Myrfl A T 10: 116,639,311 (GRCm39) S583T probably benign Het
Nek6 A G 2: 38,450,914 (GRCm39) I106V probably damaging Het
Oas1a A T 5: 121,036,412 (GRCm39) D338E possibly damaging Het
Or10ag52 T A 2: 87,043,944 (GRCm39) I236N probably damaging Het
Or4a76 G A 2: 89,460,678 (GRCm39) T188I probably benign Het
Or6c1 A G 10: 129,517,792 (GRCm39) V272A probably benign Het
Pitrm1 C A 13: 6,615,044 (GRCm39) Q508K probably benign Het
S100b A G 10: 76,095,808 (GRCm39) D62G probably damaging Het
Sesn3 A G 9: 14,221,557 (GRCm39) H119R probably damaging Het
Sez6l T A 5: 112,621,333 (GRCm39) E247V probably damaging Het
Shoc1 G T 4: 59,049,355 (GRCm39) Q1069K probably benign Het
Shq1 C A 6: 100,550,574 (GRCm39) E455* probably null Het
Slc9b1 T A 3: 135,103,433 (GRCm39) M521K probably damaging Het
Supt16 A G 14: 52,413,855 (GRCm39) F543L probably damaging Het
Tcf25 T C 8: 124,109,258 (GRCm39) probably benign Het
Usp48 C A 4: 137,335,375 (GRCm39) Q183K probably damaging Het
Vmn1r178 G A 7: 23,593,086 (GRCm39) G45S probably damaging Het
Vmn1r237 T A 17: 21,534,368 (GRCm39) Y30* probably null Het
Other mutations in Morn1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00471:Morn1 APN 4 155,176,785 (GRCm39) missense possibly damaging 0.81
IGL01143:Morn1 APN 4 155,176,761 (GRCm39) missense probably damaging 1.00
IGL02214:Morn1 APN 4 155,176,776 (GRCm39) missense probably damaging 1.00
R0091:Morn1 UTSW 4 155,229,629 (GRCm39) missense probably damaging 1.00
R0573:Morn1 UTSW 4 155,195,473 (GRCm39) missense possibly damaging 0.87
R0639:Morn1 UTSW 4 155,173,960 (GRCm39) missense possibly damaging 0.92
R0918:Morn1 UTSW 4 155,171,928 (GRCm39) missense probably damaging 1.00
R2041:Morn1 UTSW 4 155,175,399 (GRCm39) missense probably damaging 1.00
R2360:Morn1 UTSW 4 155,176,770 (GRCm39) missense probably damaging 0.98
R5831:Morn1 UTSW 4 155,185,733 (GRCm39) missense probably benign 0.02
R6897:Morn1 UTSW 4 155,171,112 (GRCm39) missense probably benign 0.06
R8178:Morn1 UTSW 4 155,213,160 (GRCm39) missense probably benign 0.00
R8505:Morn1 UTSW 4 155,177,792 (GRCm39) missense unknown
Posted On 2016-08-02