Incidental Mutation 'IGL01616:Slc22a13b-ps'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc22a13b-ps
Ensembl Gene ENSMUSG00000092212
Gene Namesolute carrier family 22 (organic cation transporter), member 13b, pseudogene
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01616
Quality Score
Chromosomal Location119220488-119231692 bp(-) (GRCm38)
Type of Mutationcritical splice acceptor site
DNA Base Change (assembly) A to C at 119220928 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000170400] [ENSMUST00000173185]
Predicted Effect probably benign
Transcript: ENSMUST00000170400
SMART Domains Protein: ENSMUSP00000131982
Gene: ENSMUSG00000070280

transmembrane domain 68 90 N/A INTRINSIC
Pfam:Sugar_tr 150 555 1.2e-28 PFAM
Pfam:MFS_1 178 514 7.6e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000172684
SMART Domains Protein: ENSMUSP00000134179
Gene: ENSMUSG00000092212

Pfam:Sugar_tr 1 302 6e-27 PFAM
Pfam:MFS_1 141 318 3.7e-13 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000173185
SMART Domains Protein: ENSMUSP00000134667
Gene: ENSMUSG00000092212

transmembrane domain 22 44 N/A INTRINSIC
Pfam:MFS_1 141 349 3.4e-12 PFAM
Pfam:Sugar_tr 162 333 7e-9 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts5 T A 16: 85,887,814 probably null Het
Afg3l1 T A 8: 123,502,007 W771R probably damaging Het
Braf A G 6: 39,651,652 S348P probably damaging Het
Cd200 T C 16: 45,397,056 T112A possibly damaging Het
Cep350 T C 1: 155,953,247 I304V probably benign Het
Fry A G 5: 150,399,599 T1072A probably damaging Het
Fry A T 5: 150,438,811 probably null Het
Fuk G T 8: 110,890,476 H388N possibly damaging Het
Gcdh C T 8: 84,893,659 G8D probably damaging Het
Ivns1abp C A 1: 151,361,543 T486K possibly damaging Het
Mat1a G A 14: 41,109,479 V55M probably damaging Het
Olfr656 T C 7: 104,617,721 F22S probably damaging Het
Pcnx3 C T 19: 5,667,259 probably benign Het
Psrc1 C A 3: 108,386,692 S275Y possibly damaging Het
Ptpn21 A G 12: 98,680,013 L1062P probably damaging Het
Slc35b1 T A 11: 95,389,084 M178K probably benign Het
Slc6a11 A T 6: 114,134,868 Q132L possibly damaging Het
Slc9a8 C T 2: 167,424,166 T21I possibly damaging Het
Tox T C 4: 6,688,430 T526A probably damaging Het
Ubr3 C T 2: 70,020,484 P1749S probably benign Het
Wdfy3 C A 5: 101,913,260 A1363S probably damaging Het
Zdhhc23 T A 16: 43,973,480 H277L probably damaging Het
Posted On2013-12-09