Incidental Mutation 'RF044:Morn4'
ID 604980
Institutional Source Beutler Lab
Gene Symbol Morn4
Ensembl Gene ENSMUSG00000049670
Gene Name MORN repeat containing 4
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.196) question?
Stock # RF044 (G1)
Quality Score 217.554
Status Not validated
Chromosome 19
Chromosomal Location 42063378-42074796 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) GTGAG to GTGAGTCAAGCATTGAG at 42064553 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000062887 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051772]
AlphaFold Q6PGF2
Predicted Effect probably null
Transcript: ENSMUST00000051772
SMART Domains Protein: ENSMUSP00000062887
Gene: ENSMUSG00000049670

DomainStartEndE-ValueType
MORN 14 35 1.64e-5 SMART
MORN 37 58 4.15e-2 SMART
MORN 60 81 1.86e-4 SMART
MORN 83 104 1.84e0 SMART
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.7%
  • 10x: 99.3%
  • 20x: 98.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A030005L19Rik TG TGTGGCTGCCG 1: 82,891,310 (GRCm39) probably benign Het
Blm CTCC CTCCTCCTCCTCATCC 7: 80,162,678 (GRCm39) probably benign Het
Cacna1f GAG GAGTAG X: 7,486,296 (GRCm39) probably null Het
Ccdc85c GCC GCCACC 12: 108,240,871 (GRCm39) probably benign Het
Chga AGC AGCGGC 12: 102,527,655 (GRCm39) probably benign Het
Crtam TTCTTGATCTGAA T 9: 40,895,650 (GRCm39) probably null Het
Dspp TGACAGCAGCGACAGCAG TGACAGCAGCGACAGCAGAGACAGCAGCGACAGCAG 5: 104,326,290 (GRCm39) probably benign Het
Efhd2 CCGCCG CCGCCGACGCCG 4: 141,602,079 (GRCm39) probably benign Het
F830016B08Rik AAAAAA AAAAAAAAA 18: 60,433,010 (GRCm39) probably benign Het
Gab3 TCT TCTCCT X: 74,043,611 (GRCm39) probably benign Het
Gabre CTC CTCCGGATC X: 71,313,667 (GRCm39) probably benign Het
Gykl1 G A 18: 52,827,488 (GRCm39) R232Q probably benign Het
Haus4 AGGGCAGGCCGCTGGCCACACACCTGGGAGGGGGGCAGGCCGCTGGCCACACACCTGGGAGGGGGGCAGGCCGCTGGCCACACACCTGGGAG AGGGCAGGCCGCTGGCCACACACCTGGGAGGGGGGCAGGCCGCTGGCCACACACCTGGGAG 14: 54,781,577 (GRCm39) probably null Het
Igf1r GATGGAGC GATGGAGCTGGATATGGAGC 7: 67,875,927 (GRCm39) probably benign Het
Irag2 TG TGAGCACATCG 6: 145,119,516 (GRCm39) probably benign Het
Krtap28-10 CCACAG CCACAGACACAG 1: 83,019,852 (GRCm39) probably benign Het
Maml2 ACAGCAGCAGCAACAGCAGCAGCAGCAGCA ACAGCAACAGCAGCAGCAGCAGCA 9: 13,532,752 (GRCm39) probably benign Het
Map1a CAGCTCCAGCTCCAGCTCCAGCTCCA CAGCTCCAGCTCCAGCTCCAGCTCCAGCTCAAGCTCCAGCTCCAGCTCCAGCTCCA 2: 121,136,774 (GRCm39) probably benign Het
Mapk6 CCAC CCACCTCAC 9: 75,295,542 (GRCm39) probably null Het
Nefh CCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGG CCTCACCTGGGGACTTGGACTCACCTGGGGACTTGGCCTCACCTGGGGACTTGG 11: 4,891,021 (GRCm39) probably benign Het
Nefh CTTGGCCTCACCTGGGGACTTGGCCTCACCTGGGGA CTTGGCCTCACCTGGGGAATTGGCCTCACCTGGGGACTTGGCCTCACCTGGGGA 11: 4,891,016 (GRCm39) probably benign Het
Nefh TCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC TCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC 11: 4,891,023 (GRCm39) probably benign Het
Nolc1 CAGCAGC CAGCAGCAGAAGCAGC 19: 46,069,810 (GRCm39) probably benign Het
Or10n7-ps1 AAAATA AAAATAAATA 9: 39,598,043 (GRCm39) probably null Het
Phc1 TG TGCTGCGG 6: 122,300,559 (GRCm39) probably benign Het
Pla2g4e AGGG A 2: 120,075,205 (GRCm39) probably benign Het
Prr36 TGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGC TGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGC 8: 4,266,273 (GRCm39) probably benign Het
Ptdss1 G T 13: 67,093,412 (GRCm39) S84I possibly damaging Het
Ren1 ACCGC AC 1: 133,278,519 (GRCm39) probably benign Het
Rinl G T 7: 28,496,988 (GRCm39) G496V probably damaging Het
Ryr3 CTGA C 2: 112,740,869 (GRCm39) probably benign Het
Sbp A AAAAAGATGATGACAC 17: 24,164,340 (GRCm39) probably benign Het
Slc39a4 GTC GTCATCATGATCACCATGGTCACCATGATCACTGTGTTC 15: 76,499,070 (GRCm39) probably benign Het
Spaca1 TCTCGC TCTCGCGCTCGC 4: 34,049,846 (GRCm39) probably benign Het
Spaca1 TCGC TCGCTCGCGC 4: 34,049,854 (GRCm39) probably benign Het
Spmap2l ATCCTCCCCAGTCCCGCAAGGCCAG ATCCTCCCCAGTCCCGCAAGGCCAGCGCTCCTCCCCAGTCCCGCAAGGCCAG 5: 77,164,252 (GRCm39) probably benign Het
Strn C CCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCAGTA 17: 78,984,717 (GRCm39) probably null Het
Tmem59 T TGTTTGTTG 4: 107,047,729 (GRCm39) probably benign Het
Tob1 GCA GCAACA 11: 94,105,287 (GRCm39) probably benign Het
Zfp683 TGTGG TGTGGTGG 4: 133,786,185 (GRCm39) probably benign Het
Other mutations in Morn4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00971:Morn4 APN 19 42,064,559 (GRCm39) missense possibly damaging 0.53
IGL02572:Morn4 APN 19 42,064,886 (GRCm39) splice site probably benign
IGL02933:Morn4 APN 19 42,064,661 (GRCm39) missense probably benign 0.01
FR4449:Morn4 UTSW 19 42,064,548 (GRCm39) small insertion probably benign
FR4548:Morn4 UTSW 19 42,064,548 (GRCm39) small insertion probably benign
R1997:Morn4 UTSW 19 42,064,977 (GRCm39) missense possibly damaging 0.71
R2239:Morn4 UTSW 19 42,066,471 (GRCm39) missense possibly damaging 0.93
R4409:Morn4 UTSW 19 42,066,986 (GRCm39) missense possibly damaging 0.53
R5544:Morn4 UTSW 19 42,064,686 (GRCm39) missense possibly damaging 0.71
R5695:Morn4 UTSW 19 42,064,556 (GRCm39) missense possibly damaging 0.96
R6986:Morn4 UTSW 19 42,066,453 (GRCm39) missense possibly damaging 0.71
R7024:Morn4 UTSW 19 42,066,483 (GRCm39) missense possibly damaging 0.92
R8721:Morn4 UTSW 19 42,066,439 (GRCm39) missense possibly damaging 0.85
RF025:Morn4 UTSW 19 42,064,550 (GRCm39) nonsense probably null
RF030:Morn4 UTSW 19 42,064,550 (GRCm39) nonsense probably null
RF036:Morn4 UTSW 19 42,064,553 (GRCm39) nonsense probably null
RF040:Morn4 UTSW 19 42,064,550 (GRCm39) nonsense probably null
RF042:Morn4 UTSW 19 42,064,550 (GRCm39) nonsense probably null
RF057:Morn4 UTSW 19 42,064,545 (GRCm39) nonsense probably null
X0063:Morn4 UTSW 19 42,066,407 (GRCm39) missense possibly damaging 0.71
Predicted Primers PCR Primer
(F):5'- GAAGGACATAACTGCCGCAG -3'
(R):5'- CTGAGCGGAAACATTAATGCCC -3'

Sequencing Primer
(F):5'- CAAACCCCTCCACACTTTTCTG -3'
(R):5'- GCGGAAACATTAATGCCCTCTCC -3'
Posted On 2019-12-04