Incidental Mutation 'IGL00432:Slc28a3'
ID4297
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc28a3
Ensembl Gene ENSMUSG00000021553
Gene Namesolute carrier family 28 (sodium-coupled nucleoside transporter), member 3
SynonymsCnt3
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL00432
Quality Score
Status
Chromosome13
Chromosomal Location58545399-58610877 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to T at 58569411 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000022036 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022036]
Predicted Effect probably null
Transcript: ENSMUST00000022036
SMART Domains Protein: ENSMUSP00000022036
Gene: ENSMUSG00000021553

DomainStartEndE-ValueType
transmembrane domain 119 141 N/A INTRINSIC
transmembrane domain 146 163 N/A INTRINSIC
transmembrane domain 184 206 N/A INTRINSIC
Pfam:Nucleos_tra2_N 221 292 3.5e-27 PFAM
Pfam:Gate 300 401 4.9e-11 PFAM
Pfam:Nucleos_tra2_C 403 627 4.1e-83 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Nucleoside transporters, such as SLC28A3, regulate multiple cellular processes, including neurotransmission, vascular tone, adenosine concentration in the vicinity of cell surface receptors, and transport and metabolism of nucleoside drugs. SLC28A3 shows broad specificity for pyrimidine and purine nucleosides (Ritzel et al., 2001 [PubMed 11032837]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AA986860 A T 1: 130,742,836 Q265L possibly damaging Het
Akr1c18 T A 13: 4,137,233 H168L probably damaging Het
Arid3b A G 9: 57,833,924 S80P possibly damaging Het
Barhl2 C T 5: 106,455,499 A265T possibly damaging Het
Brd1 A C 15: 88,730,158 V178G probably benign Het
Brd2 C T 17: 34,114,423 R26Q probably damaging Het
Ddr2 T C 1: 169,997,958 M358V probably benign Het
Dnajc14 A G 10: 128,806,332 D41G probably damaging Het
Erap1 T G 13: 74,673,659 V711G probably benign Het
Gchfr A G 2: 119,169,748 R37G probably damaging Het
Gm20518 T A 16: 17,858,498 N136I probably damaging Het
Grm6 A T 11: 50,863,297 probably benign Het
Hydin T A 8: 110,601,252 V4797E probably damaging Het
Iws1 C A 18: 32,084,688 N448K probably benign Het
Lin7c T C 2: 109,896,453 probably benign Het
Lrrc40 T A 3: 158,048,450 L196Q probably damaging Het
Lrrtm2 C T 18: 35,213,268 G327D probably benign Het
Masp1 C T 16: 23,513,851 C78Y probably damaging Het
Mmd C T 11: 90,264,534 R101W probably damaging Het
Myo1d A G 11: 80,601,740 Y730H probably benign Het
Pcdh15 A G 10: 74,291,082 probably benign Het
Pglyrp4 G A 3: 90,739,028 V290M probably damaging Het
Plxna2 G A 1: 194,644,096 V113I probably benign Het
Prkch T A 12: 73,702,589 probably benign Het
Rabgef1 G T 5: 130,208,724 E213* probably null Het
Rdh16f2 T A 10: 127,866,664 C37S probably damaging Het
Reln A G 5: 22,010,127 Y1109H probably damaging Het
Scn7a A T 2: 66,741,982 L215* probably null Het
Slc25a33 A T 4: 149,744,919 L261H probably damaging Het
Slc38a6 T C 12: 73,351,803 I369T probably benign Het
Tgm4 A T 9: 123,062,382 probably benign Het
Tnr A G 1: 159,861,245 I426V probably benign Het
Vmn1r216 A G 13: 23,099,404 I86V probably benign Het
Wwc1 G A 11: 35,844,202 P949S possibly damaging Het
Zfp326 A T 5: 105,896,533 I286F probably damaging Het
Other mutations in Slc28a3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00420:Slc28a3 APN 13 58574300 missense probably benign 0.05
IGL00553:Slc28a3 APN 13 58563009 splice site probably null
IGL01725:Slc28a3 APN 13 58578510 missense probably benign 0.30
IGL02068:Slc28a3 APN 13 58558597 missense probably damaging 1.00
IGL02270:Slc28a3 APN 13 58580584 missense probably benign 0.00
IGL02271:Slc28a3 APN 13 58558637 missense probably benign 0.21
IGL02373:Slc28a3 APN 13 58578404 critical splice donor site probably null
IGL02542:Slc28a3 APN 13 58573470 missense probably damaging 1.00
IGL03242:Slc28a3 APN 13 58574249 nonsense probably null
R0256:Slc28a3 UTSW 13 58573500 missense probably benign
R0323:Slc28a3 UTSW 13 58564052 nonsense probably null
R0391:Slc28a3 UTSW 13 58569415 splice site probably benign
R0838:Slc28a3 UTSW 13 58588269 missense probably benign 0.00
R1433:Slc28a3 UTSW 13 58563106 missense probably damaging 1.00
R1437:Slc28a3 UTSW 13 58558575 nonsense probably null
R3499:Slc28a3 UTSW 13 58573439 splice site probably benign
R3822:Slc28a3 UTSW 13 58558278 missense probably benign 0.00
R3948:Slc28a3 UTSW 13 58563010 splice site probably null
R4011:Slc28a3 UTSW 13 58566250 missense probably benign 0.06
R4028:Slc28a3 UTSW 13 58610756 missense probably benign 0.27
R4073:Slc28a3 UTSW 13 58559290 missense probably benign 0.01
R4745:Slc28a3 UTSW 13 58574263 missense possibly damaging 0.69
R4939:Slc28a3 UTSW 13 58558581 missense probably benign 0.44
R5416:Slc28a3 UTSW 13 58576793 missense probably damaging 0.99
R5421:Slc28a3 UTSW 13 58574265 missense possibly damaging 0.87
R5426:Slc28a3 UTSW 13 58563154 missense probably damaging 1.00
R5688:Slc28a3 UTSW 13 58558649 missense probably damaging 0.96
R6066:Slc28a3 UTSW 13 58578487 missense probably benign 0.00
R6790:Slc28a3 UTSW 13 58582650 missense probably benign 0.00
R6919:Slc28a3 UTSW 13 58573443 critical splice donor site probably null
R7009:Slc28a3 UTSW 13 58610804 missense probably benign 0.28
R7102:Slc28a3 UTSW 13 58588214 missense probably benign 0.04
R7305:Slc28a3 UTSW 13 58566231 missense possibly damaging 0.65
R7307:Slc28a3 UTSW 13 58563172 missense probably damaging 1.00
R7464:Slc28a3 UTSW 13 58563021 nonsense probably null
Posted On2012-04-20