Incidental Mutation 'R3926:Gal3st2b'
ID 308261
Institutional Source Beutler Lab
Gene Symbol Gal3st2b
Ensembl Gene ENSMUSG00000093805
Gene Name galactose-3-O-sulfotransferase 2B
Synonyms Gm9994
MMRRC Submission 040821-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.098) question?
Stock # R3926 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 93846159-93870367 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 93868512 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Leucine at position 246 (V246L)
Ref Sequence ENSEMBL: ENSMUSP00000136012 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000177958] [ENSMUST00000178757]
AlphaFold Q6XQH0
Predicted Effect probably benign
Transcript: ENSMUST00000177958
AA Change: V248L

PolyPhen 2 Score 0.060 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000136311
Gene: ENSMUSG00000093805
AA Change: V248L

DomainStartEndE-ValueType
Pfam:Gal-3-0_sulfotr 1 382 6.5e-151 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000178757
AA Change: V246L

PolyPhen 2 Score 0.060 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000136012
Gene: ENSMUSG00000093805
AA Change: V246L

DomainStartEndE-ValueType
Pfam:Gal-3-0_sulfotr 13 380 1.1e-151 PFAM
Meta Mutation Damage Score 0.1330 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.6%
Validation Efficiency 98% (55/56)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700012B07Rik G T 11: 109,684,980 (GRCm39) C172* probably null Het
Ahnak G A 19: 8,983,692 (GRCm39) D1659N probably benign Het
Arfgap2 C T 2: 91,105,150 (GRCm39) R405W probably damaging Het
Asb14 T C 14: 26,619,695 (GRCm39) I48T possibly damaging Het
Astn1 A T 1: 158,407,227 (GRCm39) I559F possibly damaging Het
Atg7 C T 6: 114,650,639 (GRCm39) T83M possibly damaging Het
Bco1 T C 8: 117,854,211 (GRCm39) S379P probably benign Het
Becn2 T C 1: 175,748,852 (GRCm39) V306A probably benign Het
Bst1 T C 5: 43,997,796 (GRCm39) V265A possibly damaging Het
Car11 T C 7: 45,349,915 (GRCm39) F45L probably benign Het
Cdkl2 T C 5: 92,180,998 (GRCm39) I214V possibly damaging Het
Cluap1 T A 16: 3,729,398 (GRCm39) S141T probably damaging Het
Col11a1 C T 3: 113,883,773 (GRCm39) probably benign Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Corin T G 5: 72,529,473 (GRCm39) D294A probably damaging Het
Crct1 C A 3: 92,922,014 (GRCm39) probably benign Het
Ddx41 A G 13: 55,679,083 (GRCm39) L559P probably damaging Het
Ddx59 T A 1: 136,344,482 (GRCm39) V51D probably benign Het
Dennd1b A G 1: 139,071,697 (GRCm39) N397D probably benign Het
Evc2 T A 5: 37,540,574 (GRCm39) L590Q probably damaging Het
Fhl5 A T 4: 25,214,790 (GRCm39) probably benign Het
Flg2 A G 3: 93,110,522 (GRCm39) Y850C unknown Het
Jam3 A T 9: 27,017,701 (GRCm39) I29K possibly damaging Het
Klhl1 A T 14: 96,584,316 (GRCm39) C305S possibly damaging Het
Lims2 A G 18: 32,090,996 (GRCm39) S327G probably benign Het
Lynx1 A G 15: 74,623,205 (GRCm39) Y76H probably damaging Het
Mycbp2 G A 14: 103,441,936 (GRCm39) P1943L probably damaging Het
Myo3a A G 2: 22,455,053 (GRCm39) D86G probably damaging Het
Nkx3-2 T A 5: 41,919,223 (GRCm39) Q255L probably damaging Het
Notch3 C T 17: 32,372,531 (GRCm39) R641H possibly damaging Het
Nr2c2 T A 6: 92,137,382 (GRCm39) M431K probably damaging Het
Ogfod3 T C 11: 121,074,255 (GRCm39) T265A probably damaging Het
Pcdh9 G T 14: 94,124,246 (GRCm39) Y641* probably null Het
Pcdha9 T A 18: 37,132,465 (GRCm39) D511E probably damaging Het
Pcdhgb8 A G 18: 37,895,443 (GRCm39) Y171C probably damaging Het
Pcnx1 T C 12: 82,005,505 (GRCm39) C1075R probably damaging Het
Pik3c3 C A 18: 30,444,382 (GRCm39) probably benign Het
Pkhd1 T C 1: 20,621,097 (GRCm39) T854A probably benign Het
Pycr1 T C 11: 120,532,961 (GRCm39) T100A probably benign Het
Rhof T C 5: 123,242,593 (GRCm39) probably null Het
Scn9a T A 2: 66,357,217 (GRCm39) D1028V possibly damaging Het
Serpina3f T C 12: 104,185,740 (GRCm39) I315T possibly damaging Het
Slc1a6 T A 10: 78,648,715 (GRCm39) S479T possibly damaging Het
Tmcc1 T C 6: 116,019,874 (GRCm39) D166G probably damaging Het
Trav3-3 A G 14: 53,903,828 (GRCm39) K49E probably benign Het
Usp28 T C 9: 48,942,223 (GRCm39) probably null Het
Utrn C T 10: 12,573,786 (GRCm39) V1095I probably benign Het
Zfp217 T C 2: 169,954,438 (GRCm39) D1038G probably damaging Het
Zfp709 A G 8: 72,644,397 (GRCm39) R609G probably damaging Het
Zfp729a T A 13: 67,768,310 (GRCm39) K640* probably null Het
Zfp986 A T 4: 145,619,090 (GRCm39) probably benign Het
Zkscan6 A T 11: 65,719,051 (GRCm39) H357L probably benign Het
Other mutations in Gal3st2b
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0593:Gal3st2b UTSW 1 93,868,549 (GRCm39) missense probably benign 0.05
R1631:Gal3st2b UTSW 1 93,868,505 (GRCm39) missense probably damaging 0.98
R1753:Gal3st2b UTSW 1 93,868,338 (GRCm39) missense probably damaging 1.00
R2354:Gal3st2b UTSW 1 93,867,508 (GRCm39) missense probably damaging 0.99
R4347:Gal3st2b UTSW 1 93,867,530 (GRCm39) missense probably damaging 1.00
R6132:Gal3st2b UTSW 1 93,867,688 (GRCm39) missense possibly damaging 0.57
R7069:Gal3st2b UTSW 1 93,868,341 (GRCm39) missense possibly damaging 0.95
R7116:Gal3st2b UTSW 1 93,868,498 (GRCm39) missense possibly damaging 0.58
R7662:Gal3st2b UTSW 1 93,868,614 (GRCm39) missense probably damaging 1.00
R7775:Gal3st2b UTSW 1 93,868,506 (GRCm39) missense probably damaging 1.00
R8669:Gal3st2b UTSW 1 93,868,764 (GRCm39) missense possibly damaging 0.90
R8924:Gal3st2b UTSW 1 93,868,653 (GRCm39) missense probably benign 0.18
R8937:Gal3st2b UTSW 1 93,868,570 (GRCm39) missense probably benign 0.15
R9635:Gal3st2b UTSW 1 93,868,777 (GRCm39) missense probably benign 0.12
R9645:Gal3st2b UTSW 1 93,866,328 (GRCm39) missense probably damaging 0.97
R9713:Gal3st2b UTSW 1 93,866,409 (GRCm39) missense probably benign
Z1176:Gal3st2b UTSW 1 93,866,407 (GRCm39) missense probably damaging 0.96
Predicted Primers PCR Primer
(F):5'- CTACAACGCTAGTGTGAGCC -3'
(R):5'- GCTCTGGATCCTGAAGACAC -3'

Sequencing Primer
(F):5'- GTGTGAGCCTGAAAAATGTCTATGC -3'
(R):5'- CTGAAGACACAGGGCCATG -3'
Posted On 2015-04-17