Incidental Mutation 'R0134:Slc10a7'
ID 21826
Institutional Source Beutler Lab
Gene Symbol Slc10a7
Ensembl Gene ENSMUSG00000031684
Gene Name solute carrier family 10 (sodium/bile acid cotransporter family), member 7
Synonyms 2410193C02Rik
MMRRC Submission 038419-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.840) question?
Stock # R0134 (G1)
Quality Score 197
Status Validated
Chromosome 8
Chromosomal Location 79235975-79460632 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 79423787 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147659 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034111] [ENSMUST00000034111] [ENSMUST00000209490] [ENSMUST00000209490] [ENSMUST00000209992] [ENSMUST00000209992] [ENSMUST00000210515] [ENSMUST00000210630] [ENSMUST00000211286]
AlphaFold Q5PT53
Predicted Effect probably null
Transcript: ENSMUST00000034111
SMART Domains Protein: ENSMUSP00000034111
Gene: ENSMUSG00000031684

DomainStartEndE-ValueType
Pfam:SBF_like 10 324 1.9e-82 PFAM
Pfam:SBF 44 224 2.9e-17 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000034111
SMART Domains Protein: ENSMUSP00000034111
Gene: ENSMUSG00000031684

DomainStartEndE-ValueType
Pfam:SBF_like 10 324 1.9e-82 PFAM
Pfam:SBF 44 224 2.9e-17 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000209490
Predicted Effect probably null
Transcript: ENSMUST00000209490
Predicted Effect probably null
Transcript: ENSMUST00000209992
Predicted Effect probably null
Transcript: ENSMUST00000209992
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210132
Predicted Effect probably benign
Transcript: ENSMUST00000210515
Predicted Effect probably benign
Transcript: ENSMUST00000210630
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210703
Predicted Effect probably benign
Transcript: ENSMUST00000211286
Predicted Effect noncoding transcript
Transcript: ENSMUST00000211332
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.2%
  • 10x: 96.4%
  • 20x: 93.3%
Validation Efficiency 100% (59/59)
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110059E24Rik T C 19: 21,575,565 (GRCm39) probably benign Het
Abca16 T A 7: 120,139,378 (GRCm39) L1470Q probably damaging Het
Arhgap23 G T 11: 97,335,154 (GRCm39) V70L probably benign Het
Bicd1 T C 6: 149,414,448 (GRCm39) I387T probably benign Het
Btbd9 C T 17: 30,493,916 (GRCm39) D492N possibly damaging Het
Cd59b G A 2: 103,909,286 (GRCm39) probably null Het
Ddx50 A T 10: 62,457,156 (GRCm39) probably benign Het
Dele1 G A 18: 38,394,317 (GRCm39) V505I probably benign Het
Dnlz T C 2: 26,241,380 (GRCm39) N116S probably damaging Het
Efcab14 T C 4: 115,597,728 (GRCm39) F108L probably damaging Het
Esyt2 A G 12: 116,331,330 (GRCm39) N736S probably damaging Het
Exoc4 A G 6: 33,948,881 (GRCm39) D908G possibly damaging Het
Garnl3 T C 2: 32,896,816 (GRCm39) T608A possibly damaging Het
Hdac2 T A 10: 36,865,180 (GRCm39) D131E probably benign Het
Hes1 T C 16: 29,886,068 (GRCm39) V224A probably damaging Het
Hps1 G T 19: 42,754,619 (GRCm39) Q277K probably damaging Het
Ighv15-2 T G 12: 114,528,657 (GRCm39) probably benign Het
Il3 A G 11: 54,156,506 (GRCm39) probably null Het
Itgae A C 11: 73,002,168 (GRCm39) M91L probably benign Het
Kctd21 T A 7: 96,997,298 (GRCm39) I257N probably benign Het
Kif16b A T 2: 142,514,295 (GRCm39) S1215T probably benign Het
Lhx9 A T 1: 138,766,417 (GRCm39) C124S probably damaging Het
Lipo4 A G 19: 33,479,006 (GRCm39) V278A probably benign Het
Lrp1b T C 2: 40,486,995 (GRCm39) E142G probably damaging Het
Macf1 T C 4: 123,326,636 (GRCm39) M2835V possibly damaging Het
Map9 G A 3: 82,267,290 (GRCm39) probably benign Het
Miox C T 15: 89,218,657 (GRCm39) probably benign Het
Mndal A T 1: 173,685,079 (GRCm39) probably benign Het
Nanos3 C T 8: 84,902,763 (GRCm39) R133Q probably damaging Het
Nepn A T 10: 52,276,533 (GRCm39) T29S probably damaging Het
Nlgn1 C T 3: 25,490,089 (GRCm39) C546Y probably damaging Het
Or14a260 A G 7: 85,984,803 (GRCm39) I267T probably benign Het
Or8k53 T C 2: 86,178,072 (GRCm39) I13V possibly damaging Het
Pdgfra A G 5: 75,327,172 (GRCm39) D123G probably damaging Het
Plekhn1 T C 4: 156,312,700 (GRCm39) R53G probably benign Het
Pnp2 T C 14: 51,200,634 (GRCm39) F100S probably damaging Het
Prickle1 A G 15: 93,408,658 (GRCm39) L47P possibly damaging Het
Ptar1 T A 19: 23,695,459 (GRCm39) C309S probably benign Het
Rimoc1 T C 15: 4,015,776 (GRCm39) K263E probably damaging Het
Rxfp1 A G 3: 79,564,783 (GRCm39) S327P probably damaging Het
Siah2 A G 3: 58,583,536 (GRCm39) V250A probably damaging Het
Siglecg G A 7: 43,060,595 (GRCm39) G325D probably damaging Het
Slc9a1 A G 4: 133,147,916 (GRCm39) K645E probably benign Het
Smarca4 T C 9: 21,548,620 (GRCm39) L302P probably damaging Het
Smyd1 G T 6: 71,193,749 (GRCm39) T392N probably damaging Het
Snrnp40 C G 4: 130,271,836 (GRCm39) probably null Het
Tenm3 A T 8: 49,127,507 (GRCm39) L57Q probably damaging Het
Tep1 C T 14: 51,067,150 (GRCm39) V2269I possibly damaging Het
Tpd52l1 A G 10: 31,255,252 (GRCm39) S32P probably damaging Het
Tsfm A G 10: 126,858,798 (GRCm39) probably benign Het
Ttn T A 2: 76,540,468 (GRCm39) R34173W probably damaging Het
Ttn C A 2: 76,623,474 (GRCm39) V15368L possibly damaging Het
Vmn2r13 C A 5: 109,322,915 (GRCm39) V125L probably benign Het
Vps13b T C 15: 35,887,407 (GRCm39) I3272T probably benign Het
Zfp108 A G 7: 23,959,892 (GRCm39) H161R probably benign Het
Zfp518b A G 5: 38,832,002 (GRCm39) M1T probably null Het
Other mutations in Slc10a7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00802:Slc10a7 APN 8 79,425,209 (GRCm39) splice site probably benign
IGL01589:Slc10a7 APN 8 79,456,369 (GRCm39) missense probably damaging 0.98
IGL01868:Slc10a7 APN 8 79,423,965 (GRCm39) splice site probably null
IGL02197:Slc10a7 APN 8 79,242,292 (GRCm39) missense probably damaging 0.98
IGL02205:Slc10a7 APN 8 79,423,932 (GRCm39) missense probably benign 0.04
IGL03128:Slc10a7 APN 8 79,251,846 (GRCm39) missense probably damaging 1.00
R0123:Slc10a7 UTSW 8 79,423,787 (GRCm39) splice site probably null
R1973:Slc10a7 UTSW 8 79,423,962 (GRCm39) critical splice donor site probably null
R2266:Slc10a7 UTSW 8 79,236,264 (GRCm39) missense probably benign 0.02
R2362:Slc10a7 UTSW 8 79,236,261 (GRCm39) missense probably damaging 0.99
R4756:Slc10a7 UTSW 8 79,433,579 (GRCm39) critical splice donor site probably null
R5454:Slc10a7 UTSW 8 79,413,253 (GRCm39) missense possibly damaging 0.71
R5753:Slc10a7 UTSW 8 79,251,928 (GRCm39) critical splice donor site probably null
R6621:Slc10a7 UTSW 8 79,242,263 (GRCm39) missense probably damaging 1.00
R7814:Slc10a7 UTSW 8 79,425,202 (GRCm39) critical splice donor site probably null
R7977:Slc10a7 UTSW 8 79,423,843 (GRCm39) missense probably benign 0.13
R7987:Slc10a7 UTSW 8 79,423,843 (GRCm39) missense probably benign 0.13
R9141:Slc10a7 UTSW 8 79,236,241 (GRCm39) missense probably benign 0.12
R9586:Slc10a7 UTSW 8 79,456,266 (GRCm39) missense probably damaging 1.00
R9684:Slc10a7 UTSW 8 79,456,304 (GRCm39) missense possibly damaging 0.92
Predicted Primers PCR Primer
(F):5'- TTATGGACGCCCAGTGGAAGTTGC -3'
(R):5'- GAGCGTGGAATTGCTGCACAATG -3'

Sequencing Primer
(F):5'- TGGAAGTTGCACCACAAATACTG -3'
(R):5'- GCTGCACAATGCTGTGGG -3'
Posted On 2013-04-12