Incidental Mutation 'R5633:Slc41a1'
ID 439957
Institutional Source Beutler Lab
Gene Symbol Slc41a1
Ensembl Gene ENSMUSG00000013275
Gene Name solute carrier family 41, member 1
Synonyms B230315F01Rik
MMRRC Submission 043284-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5633 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 131755236-131776601 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 131774325 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 464 (H464R)
Ref Sequence ENSEMBL: ENSMUSP00000083747 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086559]
AlphaFold Q8BJA2
Predicted Effect possibly damaging
Transcript: ENSMUST00000086559
AA Change: H464R

PolyPhen 2 Score 0.675 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000083747
Gene: ENSMUSG00000013275
AA Change: H464R

DomainStartEndE-ValueType
transmembrane domain 97 119 N/A INTRINSIC
Pfam:MgtE 138 272 1.9e-25 PFAM
transmembrane domain 283 305 N/A INTRINSIC
transmembrane domain 314 336 N/A INTRINSIC
Pfam:MgtE 352 496 1.3e-32 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146360
Meta Mutation Damage Score 0.2309 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 96.0%
Validation Efficiency 98% (55/56)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4 T A 4: 144,344,598 (GRCm39) C125S probably benign Het
Abcb8 T C 5: 24,608,107 (GRCm39) L382P probably damaging Het
Acot3 A G 12: 84,105,724 (GRCm39) probably null Het
Acsl6 A T 11: 54,228,015 (GRCm39) Q345L probably benign Het
Adcy8 A G 15: 64,571,134 (GRCm39) S1170P probably damaging Het
Ankrd28 T G 14: 31,457,022 (GRCm39) D182A probably damaging Het
B3galt5 A T 16: 96,116,709 (GRCm39) H114L probably benign Het
Bcas2 T A 3: 103,085,740 (GRCm39) Y207* probably null Het
Best1 A G 19: 9,969,467 (GRCm39) L197P probably benign Het
Chil6 C A 3: 106,296,068 (GRCm39) C389F probably damaging Het
Chrna4 T C 2: 180,671,253 (GRCm39) T168A probably damaging Het
Ckmt1 C G 2: 121,194,110 (GRCm39) probably benign Het
Dhcr7 T C 7: 143,401,160 (GRCm39) L441P probably damaging Het
Dmtn T C 14: 70,842,419 (GRCm39) M365V probably benign Het
Dmxl1 T A 18: 50,010,764 (GRCm39) S974T probably damaging Het
Dnajb13 T C 7: 100,156,626 (GRCm39) D150G probably benign Het
Eef2k C A 7: 120,472,513 (GRCm39) probably benign Het
Elp2 T A 18: 24,748,267 (GRCm39) V213E probably damaging Het
Fbxo43 A T 15: 36,162,241 (GRCm39) probably null Het
Gm11559 C A 11: 99,755,412 (GRCm39) C20* probably null Het
Gnb2 T C 5: 137,527,454 (GRCm39) I213V probably benign Het
Gnb5 C T 9: 75,251,796 (GRCm39) T306I probably damaging Het
Ica1 A T 6: 8,667,257 (GRCm39) I303N possibly damaging Het
Idh1 A G 1: 65,204,295 (GRCm39) Y272H probably damaging Het
Ikzf2 G A 1: 69,578,256 (GRCm39) Q273* probably null Het
Itpkb A T 1: 180,154,790 (GRCm39) ⇒1 probably benign Het
Kntc1 C T 5: 123,957,120 (GRCm39) T2143I probably damaging Het
Lin9 T A 1: 180,496,763 (GRCm39) L351I probably benign Het
Lmbrd1 C A 1: 24,787,943 (GRCm39) D464E possibly damaging Het
Med13 A G 11: 86,169,757 (GRCm39) probably benign Het
Mn1 T C 5: 111,568,192 (GRCm39) F721L possibly damaging Het
Myo9a T A 9: 59,775,467 (GRCm39) L1026Q possibly damaging Het
Or6c204 A T 10: 129,022,718 (GRCm39) F191I probably benign Het
P4htm A C 9: 108,456,922 (GRCm39) D428E probably damaging Het
Parp8 C T 13: 117,013,116 (GRCm39) R602H probably damaging Het
Pkd2 T A 5: 104,646,372 (GRCm39) S726R probably damaging Het
Pla2g6 A T 15: 79,183,342 (GRCm39) I495N possibly damaging Het
Psmd5 A G 2: 34,746,500 (GRCm39) I359T probably benign Het
Rassf6 T C 5: 90,751,977 (GRCm39) H292R possibly damaging Het
Rnf145 T C 11: 44,450,915 (GRCm39) I413T probably damaging Het
Rpn2 T A 2: 157,125,516 (GRCm39) V9D possibly damaging Het
Rpp30 T C 19: 36,064,390 (GRCm39) L57P probably damaging Het
Slc47a1 G T 11: 61,260,087 (GRCm39) P163Q probably damaging Het
Smc4 T A 3: 68,915,443 (GRCm39) I165K probably damaging Het
Stra6l T A 4: 45,881,455 (GRCm39) I439K probably benign Het
Syt9 C T 7: 107,024,503 (GRCm39) T132I probably damaging Het
Timd6 C T 11: 46,465,433 (GRCm39) S9L unknown Het
Trpm2 T C 10: 77,774,187 (GRCm39) I471V possibly damaging Het
Uap1l1 A G 2: 25,253,361 (GRCm39) M358T probably benign Het
Vmn1r91 A T 7: 19,835,870 (GRCm39) H263L possibly damaging Het
Zfp407 T C 18: 84,579,169 (GRCm39) D648G probably benign Het
Zpbp2 T C 11: 98,445,584 (GRCm39) I150T probably damaging Het
Other mutations in Slc41a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00927:Slc41a1 APN 1 131,766,914 (GRCm39) missense probably damaging 1.00
IGL01368:Slc41a1 APN 1 131,766,862 (GRCm39) missense probably damaging 0.99
R0255:Slc41a1 UTSW 1 131,771,650 (GRCm39) splice site probably benign
R0737:Slc41a1 UTSW 1 131,768,690 (GRCm39) missense probably damaging 1.00
R1367:Slc41a1 UTSW 1 131,771,746 (GRCm39) missense probably benign
R1474:Slc41a1 UTSW 1 131,774,319 (GRCm39) missense probably damaging 0.98
R1927:Slc41a1 UTSW 1 131,768,938 (GRCm39) missense probably damaging 0.99
R4518:Slc41a1 UTSW 1 131,766,863 (GRCm39) missense probably damaging 0.99
R4790:Slc41a1 UTSW 1 131,758,690 (GRCm39) missense probably damaging 1.00
R4851:Slc41a1 UTSW 1 131,758,508 (GRCm39) missense probably benign 0.02
R5180:Slc41a1 UTSW 1 131,772,115 (GRCm39) missense probably damaging 0.99
R6060:Slc41a1 UTSW 1 131,767,972 (GRCm39) missense probably benign 0.04
R6526:Slc41a1 UTSW 1 131,768,887 (GRCm39) missense probably damaging 1.00
R6787:Slc41a1 UTSW 1 131,770,487 (GRCm39) splice site probably null
R7038:Slc41a1 UTSW 1 131,769,795 (GRCm39) missense possibly damaging 0.60
R7258:Slc41a1 UTSW 1 131,769,780 (GRCm39) missense probably benign 0.27
R7382:Slc41a1 UTSW 1 131,774,370 (GRCm39) missense probably damaging 1.00
R7405:Slc41a1 UTSW 1 131,766,884 (GRCm39) missense probably damaging 1.00
R7432:Slc41a1 UTSW 1 131,758,694 (GRCm39) missense probably damaging 1.00
R7574:Slc41a1 UTSW 1 131,766,889 (GRCm39) missense probably damaging 1.00
R7873:Slc41a1 UTSW 1 131,758,561 (GRCm39) missense possibly damaging 0.62
R7942:Slc41a1 UTSW 1 131,768,635 (GRCm39) missense probably damaging 0.99
R7956:Slc41a1 UTSW 1 131,771,766 (GRCm39) missense possibly damaging 0.53
R9040:Slc41a1 UTSW 1 131,768,623 (GRCm39) missense probably damaging 0.98
R9435:Slc41a1 UTSW 1 131,766,896 (GRCm39) missense probably damaging 1.00
R9723:Slc41a1 UTSW 1 131,772,103 (GRCm39) missense possibly damaging 0.94
Z1177:Slc41a1 UTSW 1 131,771,724 (GRCm39) missense probably benign
Z1189:Slc41a1 UTSW 1 131,767,972 (GRCm39) missense probably benign 0.04
Z1192:Slc41a1 UTSW 1 131,767,972 (GRCm39) missense probably benign 0.04
Predicted Primers PCR Primer
(F):5'- AAGGGCAGCCTTCCTGTAAG -3'
(R):5'- TATCAAAGTGAAATCCCAGAAAGGC -3'

Sequencing Primer
(F):5'- CAGGATTTAGTTTAGAAAGCCCCTGG -3'
(R):5'- TCCCAGAAAGGCATGGGAGTG -3'
Posted On 2016-11-08