Incidental Mutation 'R0306:Morn5'
ID 35779
Institutional Source Beutler Lab
Gene Symbol Morn5
Ensembl Gene ENSMUSG00000026894
Gene Name MORN repeat containing 5
Synonyms 1700010A17Rik
MMRRC Submission 038517-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.150) question?
Stock # R0306 (G1)
Quality Score 157
Status Validated
Chromosome 2
Chromosomal Location 35939485-35969721 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 35944986 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 70 (F70S)
Ref Sequence ENSEMBL: ENSMUSP00000028256 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028256]
AlphaFold Q9DAI9
Predicted Effect probably damaging
Transcript: ENSMUST00000028256
AA Change: F70S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000028256
Gene: ENSMUSG00000026894
AA Change: F70S

DomainStartEndE-ValueType
MORN 6 27 1.24e1 SMART
MORN 29 50 3.61e-2 SMART
Pfam:MORN 54 75 2e-4 PFAM
Meta Mutation Damage Score 0.5904 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.2%
Validation Efficiency 94% (61/65)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aoc1l1 T C 6: 48,953,020 (GRCm39) V315A probably damaging Het
BC028528 C T 3: 95,797,132 (GRCm39) probably benign Het
Bspry T C 4: 62,414,394 (GRCm39) F329S probably damaging Het
Cd209a A G 8: 3,795,535 (GRCm39) Y120H probably benign Het
Ces1f T C 8: 94,003,172 (GRCm39) probably benign Het
Cfap52 T C 11: 67,844,896 (GRCm39) N58D probably benign Het
Cfap74 G A 4: 155,549,896 (GRCm39) probably benign Het
Chst8 T C 7: 34,374,723 (GRCm39) E372G probably benign Het
Cplane1 T C 15: 8,209,373 (GRCm39) V270A probably damaging Het
Ddx49 A G 8: 70,747,322 (GRCm39) probably benign Het
Ddx52 G T 11: 83,835,474 (GRCm39) L133F probably benign Het
Defb26 T A 2: 152,349,888 (GRCm39) I131F unknown Het
Dip2c T A 13: 9,654,635 (GRCm39) S719T probably benign Het
Dnmt3a A G 12: 3,916,096 (GRCm39) S94G possibly damaging Het
Dytn G A 1: 63,724,272 (GRCm39) P3S possibly damaging Het
Fmn2 T C 1: 174,437,050 (GRCm39) probably benign Het
Gal3st1 T A 11: 3,948,546 (GRCm39) L251Q probably damaging Het
Gm19684 A T 17: 36,438,300 (GRCm39) probably benign Het
Il15 T A 8: 83,061,083 (GRCm39) probably benign Het
Jag1 C T 2: 136,927,855 (GRCm39) G852D probably damaging Het
Kbtbd4 A G 2: 90,744,530 (GRCm39) probably benign Het
Kdm3b C A 18: 34,937,070 (GRCm39) Q451K probably benign Het
Lrfn2 A T 17: 49,403,283 (GRCm39) I469F probably damaging Het
Mep1a A T 17: 43,813,534 (GRCm39) probably benign Het
Nav2 C A 7: 49,195,651 (GRCm39) P1009Q probably benign Het
Noc3l T C 19: 38,796,094 (GRCm39) Y334C probably damaging Het
Nsun4 A T 4: 115,910,019 (GRCm39) Y180* probably null Het
Nup210l T C 3: 90,114,675 (GRCm39) I1750T probably benign Het
Or51s1 A T 7: 102,559,010 (GRCm39) I12N probably benign Het
Or5p53 A T 7: 107,532,907 (GRCm39) Y60F probably damaging Het
Or8u9 T A 2: 86,002,060 (GRCm39) I34F possibly damaging Het
Parp14 A G 16: 35,676,944 (GRCm39) L1008P probably benign Het
Paxbp1 A G 16: 90,819,003 (GRCm39) V759A possibly damaging Het
Prdm10 C A 9: 31,227,520 (GRCm39) Q42K probably damaging Het
Prkcsh T C 9: 21,917,822 (GRCm39) probably benign Het
Psmg1 A G 16: 95,788,540 (GRCm39) C138R probably damaging Het
Ptprb T C 10: 116,179,893 (GRCm39) M1437T probably benign Het
Ryr3 A G 2: 112,606,000 (GRCm39) probably null Het
Serpinf1 T C 11: 75,304,761 (GRCm39) Y200C probably damaging Het
Shox2 T C 3: 66,881,167 (GRCm39) H130R probably damaging Het
Slc22a1 A G 17: 12,881,485 (GRCm39) F335L probably benign Het
Slc44a5 A G 3: 153,975,638 (GRCm39) N683S probably damaging Het
Slc9a9 A T 9: 95,019,987 (GRCm39) T519S probably benign Het
Smarca2 T A 19: 26,618,013 (GRCm39) L348Q probably damaging Het
Sorbs1 T C 19: 40,332,855 (GRCm39) D521G possibly damaging Het
Sorbs2 A T 8: 46,248,767 (GRCm39) T593S probably benign Het
Srp19 T C 18: 34,467,629 (GRCm39) probably benign Het
Stk35 T A 2: 129,643,683 (GRCm39) Y222* probably null Het
Syt10 T G 15: 89,711,191 (GRCm39) K114T probably benign Het
Tcam1 G A 11: 106,174,904 (GRCm39) E120K probably benign Het
Trpc4ap A G 2: 155,478,180 (GRCm39) V662A probably benign Het
Ttll4 G A 1: 74,735,916 (GRCm39) R1066Q probably benign Het
Tulp2 C T 7: 45,168,000 (GRCm39) probably benign Het
Unc5b C A 10: 60,615,437 (GRCm39) probably benign Het
Vmn1r230 T A 17: 21,066,895 (GRCm39) I28K possibly damaging Het
Vmn2r118 A C 17: 55,915,616 (GRCm39) F445V possibly damaging Het
Zfp142 C T 1: 74,609,341 (GRCm39) E1485K probably damaging Het
Zfp819 C A 7: 43,266,621 (GRCm39) A292E 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
IGL02899:Morn5 APN 2 35,945,049 (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
Predicted Primers PCR Primer
(F):5'- ACAACTGTGGCTTCTTTCCTGTTGG -3'
(R):5'- AGCACTGTTGTAGGTGCAAACTCTC -3'

Sequencing Primer
(F):5'- GCTGCGAGAAGCCAACTATTC -3'
(R):5'- ACCACTGCCATGATTTAGTAGGG -3'
Posted On 2013-05-09