Incidental Mutation 'R5831:Morn1'
ID 449305
Institutional Source Beutler Lab
Gene Symbol Morn1
Ensembl Gene ENSMUSG00000029049
Gene Name MORN repeat containing 1
Synonyms 4930417P05Rik, 2900057D20Rik
MMRRC Submission 043220-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5831 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 155171034-155229962 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 155185733 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 183 (H183R)
Ref Sequence ENSEMBL: ENSMUSP00000030915 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030915] [ENSMUST00000132367]
AlphaFold A2RTS7
Predicted Effect probably benign
Transcript: ENSMUST00000030915
AA Change: H183R

PolyPhen 2 Score 0.022 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000030915
Gene: ENSMUSG00000029049
AA Change: H183R

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 noncoding transcript
Transcript: ENSMUST00000129180
Predicted Effect probably benign
Transcript: ENSMUST00000132367
AA Change: H183R

PolyPhen 2 Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000116794
Gene: ENSMUSG00000029049
AA Change: H183R

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: ENSMUST00000151710
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155375
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.8%
  • 20x: 96.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A T 11: 9,517,777 (GRCm39) K4460* probably null Het
Adam21 A G 12: 81,605,875 (GRCm39) V629A probably benign Het
Adamts5 C T 16: 85,665,006 (GRCm39) V653I probably damaging Het
Adarb2 G A 13: 8,609,169 (GRCm39) A44T probably benign Het
Ank2 T C 3: 127,132,808 (GRCm39) probably benign Het
Arhgap21 T C 2: 20,868,024 (GRCm39) Y833C probably damaging Het
Brwd1 A G 16: 95,820,636 (GRCm39) S1297P probably damaging Het
Cdc25b G T 2: 131,029,301 (GRCm39) probably null Het
Ciart A T 3: 95,786,214 (GRCm39) V287D probably damaging Het
Csf2ra A G 19: 61,213,650 (GRCm39) F353S probably damaging Het
D630045J12Rik C T 6: 38,119,592 (GRCm39) E1717K possibly damaging Het
Dhcr24 A G 4: 106,421,611 (GRCm39) K82R probably benign Het
Dnah9 T A 11: 65,998,947 (GRCm39) T1034S probably benign Het
Dock6 T C 9: 21,714,332 (GRCm39) E1837G probably damaging Het
Eeig2 A T 3: 108,900,019 (GRCm39) S110T possibly damaging Het
Flg2 G A 3: 93,107,541 (GRCm39) V9I probably damaging Het
Hif1a A T 12: 73,988,918 (GRCm39) T602S probably benign Het
Hip1 T C 5: 135,440,117 (GRCm39) E1015G probably benign Het
Iqgap2 C T 13: 95,811,880 (GRCm39) R707H probably damaging Het
Irgq C A 7: 24,232,763 (GRCm39) F201L probably damaging Het
Isoc2b C A 7: 4,854,023 (GRCm39) L116F probably null Het
Loxl3 A T 6: 83,025,999 (GRCm39) T416S probably benign Het
Map3k13 A G 16: 21,746,798 (GRCm39) *960W probably null Het
Mrc1 A T 2: 14,313,523 (GRCm39) N918I probably damaging Het
Nfxl1 A G 5: 72,679,540 (GRCm39) V763A probably benign Het
Or11g1 A G 14: 50,651,439 (GRCm39) probably null Het
Or4c100 G A 2: 88,356,824 (GRCm39) W299* probably null Het
Papola A G 12: 105,789,859 (GRCm39) K482E probably benign Het
Pck1 C T 2: 172,998,792 (GRCm39) T350I probably damaging Het
Peli2 G A 14: 48,405,727 (GRCm39) A51T probably damaging Het
Preb T C 5: 31,116,208 (GRCm39) H133R probably benign Het
Rpl36-ps4 T C 17: 88,228,685 (GRCm39) V73A probably benign Het
Scaf11 G A 15: 96,314,962 (GRCm39) P1240L probably benign Het
Selenom G T 11: 3,466,882 (GRCm39) E81* probably null Het
Serpinb1c T C 13: 33,081,081 (GRCm39) M1V probably null Het
Tanc1 T C 2: 59,615,685 (GRCm39) S231P possibly damaging Het
Trappc10 C T 10: 78,045,260 (GRCm39) R476Q probably damaging Het
Twf2 T A 9: 106,091,386 (GRCm39) D200E probably benign Het
Vmn1r17 T C 6: 57,337,999 (GRCm39) Y122C probably benign Het
Vmn2r71 G A 7: 85,272,922 (GRCm39) D579N probably benign Het
Vrtn A T 12: 84,695,349 (GRCm39) E33V probably damaging 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
IGL03112:Morn1 APN 4 155,177,601 (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
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
Predicted Primers PCR Primer
(F):5'- TTCAAGGGGAAAGCACTTAGC -3'
(R):5'- ATCCCAGCTTGGTCCAACAC -3'

Sequencing Primer
(F):5'- TAGCAAATTGAGCTGGACCCTTC -3'
(R):5'- AACACCTCCCATGTGGCTG -3'
Posted On 2016-12-20