Incidental Mutation 'IGL02563:Luc7l3'
ID 298762
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Luc7l3
Ensembl Gene ENSMUSG00000020863
Gene Name LUC7-like 3 (S. cerevisiae)
Synonyms 3300001P08Rik
Accession Numbers
Essential gene? Probably essential (E-score: 0.968) question?
Stock # IGL02563
Quality Score
Status
Chromosome 11
Chromosomal Location 94181899-94213196 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 94190894 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000129919 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021226] [ENSMUST00000107820] [ENSMUST00000107821] [ENSMUST00000107822] [ENSMUST00000166312]
AlphaFold Q5SUF2
Predicted Effect probably null
Transcript: ENSMUST00000021226
SMART Domains Protein: ENSMUSP00000021226
Gene: ENSMUSG00000020863

DomainStartEndE-ValueType
Pfam:LUC7 3 293 2.3e-89 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000107820
SMART Domains Protein: ENSMUSP00000103450
Gene: ENSMUSG00000020863

DomainStartEndE-ValueType
Pfam:LUC7 1 302 4.2e-72 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000107821
SMART Domains Protein: ENSMUSP00000103451
Gene: ENSMUSG00000020863

DomainStartEndE-ValueType
Pfam:LUC7 1 302 4.2e-72 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000107822
Predicted Effect probably null
Transcript: ENSMUST00000132623
SMART Domains Protein: ENSMUSP00000131166
Gene: ENSMUSG00000020863

DomainStartEndE-ValueType
coiled coil region 1 31 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135311
Predicted Effect noncoding transcript
Transcript: ENSMUST00000165620
Predicted Effect probably null
Transcript: ENSMUST00000166312
SMART Domains Protein: ENSMUSP00000129919
Gene: ENSMUSG00000020863

DomainStartEndE-ValueType
Pfam:LUC7 1 300 7.9e-72 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000171033
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein with an N-terminal half that contains cysteine/histidine motifs and leucine zipper-like repeats, and the C-terminal half is rich in arginine and glutamate residues (RE domain) and arginine and serine residues (RS domain). This protein localizes with a speckled pattern in the nucleus, and could be involved in the formation of splicesome via the RE and RS domains. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2009]
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930402F06Rik A T 2: 35,270,410 (GRCm39) V97E probably damaging Het
Abhd16a C T 17: 35,320,221 (GRCm39) T362M probably damaging Het
Adam23 T G 1: 63,607,136 (GRCm39) probably benign Het
Apeh C A 9: 107,970,908 (GRCm39) R87L possibly damaging Het
Arid3a T A 10: 79,786,717 (GRCm39) M490K probably damaging Het
Atp6v1b1 T A 6: 83,732,433 (GRCm39) V251D probably benign Het
Cog8 C T 8: 107,783,055 (GRCm39) R78Q possibly damaging Het
Cyld T C 8: 89,462,522 (GRCm39) I701T probably damaging Het
Dmgdh A G 13: 93,811,047 (GRCm39) probably benign Het
Dnm1 T C 2: 32,205,931 (GRCm39) probably null Het
Dop1b T A 16: 93,574,293 (GRCm39) V2D probably damaging Het
Dusp22 A T 13: 30,889,628 (GRCm39) S70C possibly damaging Het
Dync2h1 T C 9: 7,035,700 (GRCm39) Q3415R possibly damaging Het
Dysf T C 6: 84,163,498 (GRCm39) probably benign Het
Fam114a1 G A 5: 65,163,491 (GRCm39) probably null Het
Fam20a T A 11: 109,568,620 (GRCm39) Q302L possibly damaging Het
Fancm T A 12: 65,139,236 (GRCm39) L374H probably damaging Het
Fcgbpl1 G A 7: 27,857,317 (GRCm39) E2222K probably benign Het
Fgf17 G A 14: 70,874,178 (GRCm39) Q204* probably null Het
Gap43 T C 16: 42,112,495 (GRCm39) T89A probably benign Het
Gm5069 A G 1: 180,155,464 (GRCm39) probably benign Het
Gm9913 C T 2: 125,348,254 (GRCm39) probably benign Het
Gpr174 T C X: 106,336,854 (GRCm39) L222P probably benign Het
Grid2 A T 6: 64,322,857 (GRCm39) Q619L possibly damaging Het
Hoxc13 A G 15: 102,830,233 (GRCm39) D204G possibly damaging Het
Itgav T C 2: 83,601,580 (GRCm39) V317A probably benign Het
Keg1 A T 19: 12,696,521 (GRCm39) N288I probably damaging Het
Ksr1 C T 11: 78,935,684 (GRCm39) V234I possibly damaging Het
Lrp1 T A 10: 127,387,555 (GRCm39) D3365V probably damaging Het
Mta2 T C 19: 8,925,415 (GRCm39) I348T probably benign Het
Nphp4 A G 4: 152,640,677 (GRCm39) I1015V probably benign Het
Nup214 C T 2: 31,867,872 (GRCm39) S113F probably damaging Het
Or4f7 T C 2: 111,644,162 (GRCm39) K303R probably benign Het
Pabpn1l T A 8: 123,347,122 (GRCm39) T228S probably damaging Het
Paxx T C 2: 25,349,674 (GRCm39) *206W probably null Het
Pcdhb10 A G 18: 37,546,126 (GRCm39) T401A probably benign Het
Ppp1r3a A C 6: 14,719,761 (GRCm39) D384E probably benign Het
Rif1 T C 2: 51,967,077 (GRCm39) V122A probably damaging Het
Scn4b T C 9: 45,057,980 (GRCm39) L24P probably damaging Het
Sec22c T C 9: 121,513,716 (GRCm39) probably benign Het
Sh3rf2 A G 18: 42,289,207 (GRCm39) D676G probably damaging Het
Slc20a1 A G 2: 129,049,604 (GRCm39) T289A probably benign Het
Tekt2 T C 4: 126,218,418 (GRCm39) D84G possibly damaging Het
Tgfbr2 T A 9: 115,959,066 (GRCm39) N116I probably benign Het
Tmem196 A G 12: 119,910,209 (GRCm39) M1V probably null Het
Tnn A G 1: 159,942,123 (GRCm39) V1125A probably damaging Het
Vmn2r51 A T 7: 9,834,243 (GRCm39) M265K probably benign Het
Zfp319 T C 8: 96,050,362 (GRCm39) probably benign Het
Zfp65 A T 13: 67,856,184 (GRCm39) V365E possibly damaging Het
Zp3 T A 5: 136,016,464 (GRCm39) probably null Het
Other mutations in Luc7l3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00832:Luc7l3 APN 11 94,194,768 (GRCm39) missense probably benign 0.43
IGL02138:Luc7l3 APN 11 94,194,792 (GRCm39) missense probably benign 0.00
IGL02318:Luc7l3 APN 11 94,183,819 (GRCm39) missense probably benign 0.05
IGL02479:Luc7l3 APN 11 94,187,735 (GRCm39) unclassified probably benign
veritas UTSW 11 94,183,779 (GRCm39) missense probably damaging 0.98
R0096:Luc7l3 UTSW 11 94,192,320 (GRCm39) splice site probably benign
R0096:Luc7l3 UTSW 11 94,192,320 (GRCm39) splice site probably benign
R1706:Luc7l3 UTSW 11 94,188,582 (GRCm39) splice site probably benign
R3803:Luc7l3 UTSW 11 94,183,992 (GRCm39) utr 3 prime probably benign
R4260:Luc7l3 UTSW 11 94,186,876 (GRCm39) unclassified probably benign
R4647:Luc7l3 UTSW 11 94,200,467 (GRCm39) missense probably damaging 1.00
R5153:Luc7l3 UTSW 11 94,186,806 (GRCm39) unclassified probably benign
R5179:Luc7l3 UTSW 11 94,190,879 (GRCm39) missense possibly damaging 0.92
R5591:Luc7l3 UTSW 11 94,184,060 (GRCm39) unclassified probably benign
R6767:Luc7l3 UTSW 11 94,183,779 (GRCm39) missense probably damaging 0.98
R6912:Luc7l3 UTSW 11 94,200,462 (GRCm39) missense probably damaging 0.97
R7168:Luc7l3 UTSW 11 94,190,810 (GRCm39) missense unknown
R7541:Luc7l3 UTSW 11 94,186,791 (GRCm39) missense unknown
R9029:Luc7l3 UTSW 11 94,188,676 (GRCm39) missense unknown
R9154:Luc7l3 UTSW 11 94,190,793 (GRCm39) missense unknown
R9236:Luc7l3 UTSW 11 94,186,772 (GRCm39) missense unknown
R9620:Luc7l3 UTSW 11 94,212,545 (GRCm39) missense unknown
R9663:Luc7l3 UTSW 11 94,187,756 (GRCm39) missense unknown
Z1177:Luc7l3 UTSW 11 94,212,601 (GRCm39) frame shift probably null
Posted On 2015-04-16