Incidental Mutation 'R5577:Lgalsl'
ID 437264
Institutional Source Beutler Lab
Gene Symbol Lgalsl
Ensembl Gene ENSMUSG00000042363
Gene Name galectin like
Synonyms 1110067D22Rik
MMRRC Submission 043132-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.144) question?
Stock # R5577 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 20773576-20781056 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 20779316 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 110 (Q110*)
Ref Sequence ENSEMBL: ENSMUSP00000044342 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047028]
AlphaFold Q8VED9
Predicted Effect probably null
Transcript: ENSMUST00000047028
AA Change: Q110*
SMART Domains Protein: ENSMUSP00000044342
Gene: ENSMUSG00000042363
AA Change: Q110*

DomainStartEndE-ValueType
GLECT 38 172 2.16e-18 SMART
Gal-bind_lectin 44 172 1.05e-45 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123160
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132928
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144441
Predicted Effect noncoding transcript
Transcript: ENSMUST00000154300
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130023H24Rik A C 7: 127,835,826 (GRCm39) Y256D probably damaging Het
Acr C A 15: 89,458,441 (GRCm39) T374K probably benign Het
Akt2 G A 7: 27,335,731 (GRCm39) G335R probably damaging Het
Ccn3 T A 15: 54,615,897 (GRCm39) I354N possibly damaging Het
Cd177 A T 7: 24,444,562 (GRCm39) F673Y probably damaging Het
Clmn G T 12: 104,743,329 (GRCm39) S879R probably damaging Het
Csrp3 T C 7: 48,489,225 (GRCm39) H19R possibly damaging Het
Dmkn T C 7: 30,463,971 (GRCm39) S137P probably damaging Het
Eno1 C A 4: 150,331,067 (GRCm39) Y236* probably null Het
Enpp7 T A 11: 118,882,953 (GRCm39) N342K probably benign Het
Fancm T A 12: 65,177,185 (GRCm39) probably benign Het
Fshr A T 17: 89,293,351 (GRCm39) D442E probably benign Het
Gm3898 T A 9: 43,741,362 (GRCm39) noncoding transcript Het
Hdac7 A T 15: 97,709,336 (GRCm39) S43T probably benign Het
Herc1 T C 9: 66,389,263 (GRCm39) C3927R probably damaging Het
Klc4 G T 17: 46,946,355 (GRCm39) A490D probably damaging Het
Lcn9 T A 2: 25,713,663 (GRCm39) I63N probably damaging Het
Lrp1b A T 2: 40,765,135 (GRCm39) M2783K possibly damaging Het
Lrrk2 A T 15: 91,649,948 (GRCm39) Y1695F probably damaging Het
Myo1e G A 9: 70,277,753 (GRCm39) E817K probably benign Het
Nav3 A T 10: 109,605,264 (GRCm39) D936E probably damaging Het
Necab3 T C 2: 154,387,076 (GRCm39) probably null Het
Nlrp1a T A 11: 70,990,400 (GRCm39) I951F probably damaging Het
Or5v1 T A 17: 37,810,493 (GRCm39) I317K probably benign Het
Or8b52 A G 9: 38,576,297 (GRCm39) I281T possibly damaging Het
Ppp2r5d T C 17: 46,998,901 (GRCm39) S54G probably benign Het
Prdx6 A G 1: 161,071,255 (GRCm39) S146P probably damaging Het
Sec24a A T 11: 51,625,448 (GRCm39) H258Q probably benign Het
Sec31a T C 5: 100,550,133 (GRCm39) T194A possibly damaging Het
Sqstm1 T C 11: 50,098,266 (GRCm39) I167V probably benign Het
Tas1r3 T C 4: 155,946,522 (GRCm39) E361G probably benign Het
Tlr1 T A 5: 65,083,428 (GRCm39) Q383L possibly damaging Het
Trappc8 G C 18: 20,969,836 (GRCm39) Y1051* probably null Het
Vmn2r2 T A 3: 64,024,416 (GRCm39) M722L probably benign Het
Vmn2r43 T C 7: 8,247,811 (GRCm39) H784R probably damaging Het
Zfp534 T G 4: 147,759,173 (GRCm39) K499Q probably damaging Het
Other mutations in Lgalsl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00970:Lgalsl APN 11 20,776,493 (GRCm39) missense probably benign 0.01
IGL02706:Lgalsl APN 11 20,780,090 (GRCm39) missense probably damaging 1.00
R1434:Lgalsl UTSW 11 20,776,418 (GRCm39) missense possibly damaging 0.93
R1748:Lgalsl UTSW 11 20,776,491 (GRCm39) missense probably benign 0.16
R1858:Lgalsl UTSW 11 20,779,420 (GRCm39) missense probably benign 0.03
R3153:Lgalsl UTSW 11 20,776,487 (GRCm39) missense probably damaging 1.00
R6207:Lgalsl UTSW 11 20,779,382 (GRCm39) nonsense probably null
R8364:Lgalsl UTSW 11 20,781,009 (GRCm39) start codon destroyed possibly damaging 0.75
R9226:Lgalsl UTSW 11 20,779,306 (GRCm39) missense possibly damaging 0.91
R9498:Lgalsl UTSW 11 20,779,439 (GRCm39) missense possibly damaging 0.84
R9688:Lgalsl UTSW 11 20,779,442 (GRCm39) missense probably benign 0.15
Predicted Primers PCR Primer
(F):5'- AAGGCAAGCATTAACATCTATCAGC -3'
(R):5'- CTGACTCCTGGCTAAGTGAC -3'

Sequencing Primer
(F):5'- CAGCAAACAGACTTCTTTTGTTG -3'
(R):5'- CTGGCTAAGTGACACTGTTTTC -3'
Posted On 2016-10-26