Incidental Mutation 'R7427:Slc35f4'
ID576206
Institutional Source Beutler Lab
Gene Symbol Slc35f4
Ensembl Gene ENSMUSG00000021852
Gene Namesolute carrier family 35, member F4
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.149) question?
Stock #R7427 (G1)
Quality Score225.009
Status Validated
Chromosome14
Chromosomal Location49298519-49526046 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 49298898 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 427 (I427F)
Ref Sequence ENSEMBL: ENSMUSP00000073972 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074368] [ENSMUST00000138884]
Predicted Effect probably damaging
Transcript: ENSMUST00000074368
AA Change: I427F

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000073972
Gene: ENSMUSG00000021852
AA Change: I427F

DomainStartEndE-ValueType
low complexity region 22 30 N/A INTRINSIC
transmembrane domain 123 145 N/A INTRINSIC
transmembrane domain 160 182 N/A INTRINSIC
Pfam:SLC35F 216 435 7.6e-8 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000138884
AA Change: I277F

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000119007
Gene: ENSMUSG00000021852
AA Change: I277F

DomainStartEndE-ValueType
Pfam:EmrE 18 143 1e-12 PFAM
Pfam:EamA 57 135 8.4e-9 PFAM
Pfam:DUF914 68 314 4.8e-8 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.4%
Validation Efficiency 100% (78/78)
Allele List at MGI
Other mutations in this stock
Total: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931423N10Rik C T 2: 23,256,994 R337C probably benign Het
Adck5 T A 15: 76,594,385 C318S possibly damaging Het
Aspm T A 1: 139,457,616 C333S probably benign Het
B3gnt4 A G 5: 123,510,731 N53S probably damaging Het
Bpifb5 G A 2: 154,225,122 M98I probably benign Het
Cacna2d3 A G 14: 29,064,275 M585T probably damaging Het
Cbarp T C 10: 80,131,304 D701G probably damaging Het
Cntrl T A 2: 35,170,534 W1913R probably benign Het
Cry2 T C 2: 92,413,047 D483G possibly damaging Het
Csmd1 A G 8: 16,023,850 F2044L possibly damaging Het
Ctgf T G 10: 24,597,499 M312R probably damaging Het
Cxcl16 A G 11: 70,458,804 V78A possibly damaging Het
Cxcr6 A T 9: 123,810,240 Y109F probably benign Het
Cyb5b A G 8: 107,170,416 D106G probably benign Het
D630036H23Rik T C 12: 36,381,538 R154G unknown Het
Dnah9 T C 11: 65,955,219 T2998A probably benign Het
Focad T C 4: 88,368,751 S1254P unknown Het
Gm21886 A T 18: 80,089,652 L97Q probably damaging Het
Gm6614 T G 6: 142,003,508 probably null Het
Gpr158 A C 2: 21,827,318 L1076F probably benign Het
Hivep2 T C 10: 14,133,741 M1714T possibly damaging Het
Hlcs A G 16: 94,267,899 V154A probably benign Het
Hpdl A T 4: 116,820,865 L133Q probably damaging Het
Il1rn C A 2: 24,349,542 T150K probably benign Het
Il6st A G 13: 112,488,560 I237V probably benign Het
Inpp5f A G 7: 128,679,805 D510G probably damaging Het
Ism2 G T 12: 87,286,995 T92K possibly damaging Het
Kif13b T C 14: 64,788,460 I1422T probably benign Het
Kit G A 5: 75,645,847 V671I possibly damaging Het
Klhdc8a A T 1: 132,302,967 N190I probably damaging Het
Lad1 C T 1: 135,825,838 T41I probably damaging Het
Lrrc7 G T 3: 158,198,141 T294K probably benign Het
Megf8 C T 7: 25,338,371 R771C probably benign Het
Micu3 A C 8: 40,378,914 N440T possibly damaging Het
Mnx1 T C 5: 29,474,213 N291D unknown Het
Mthfr A G 4: 148,051,603 M378V probably benign Het
Mup2 A T 4: 60,138,454 D79E probably benign Het
Myzap T C 9: 71,505,183 T451A probably benign Het
Nlrp9c T C 7: 26,371,435 D907G probably benign Het
Nr1h4 T C 10: 89,498,405 E41G probably benign Het
Nup98 A T 7: 102,135,001 probably null Het
Nxpe5 A C 5: 138,239,760 Y194S probably damaging Het
Olfr1024 T A 2: 85,904,131 R308* probably null Het
Olfr1032 A T 2: 86,008,219 I148L probably benign Het
Olfr105-ps T C 17: 37,383,299 V244A probably damaging Het
Olfr1121 G T 2: 87,371,690 V53L probably benign Het
Olfr332 A G 11: 58,489,780 I325T probably benign Het
Olfr466 A G 13: 65,153,052 Y276C probably damaging Het
Olfr554 A G 7: 102,640,326 I27V probably benign Het
Omd A T 13: 49,592,269 E385V possibly damaging Het
Pcdh9 G T 14: 93,887,111 T541K probably damaging Het
Pdia6 T C 12: 17,278,545 V167A probably damaging Het
Phf7 C T 14: 31,240,413 R145Q possibly damaging Het
Pitx3 T C 19: 46,137,424 D20G possibly damaging Het
Plxnb1 T C 9: 109,108,168 V1139A probably benign Het
Pon2 A T 6: 5,268,995 N226K probably damaging Het
Ppp1r10 T A 17: 35,930,133 H642Q possibly damaging Het
Prom2 A G 2: 127,539,811 L195P probably damaging Het
Psg23 C T 7: 18,611,983 probably null Het
Rfx4 C A 10: 84,896,012 Q618K probably benign Het
Rhobtb1 T A 10: 69,248,824 I15N probably damaging Het
Rhot2 A T 17: 25,841,609 V233E probably damaging Het
Ripply2 T C 9: 87,019,756 S112P possibly damaging Het
Slc12a1 C A 2: 125,214,132 T861N probably benign Het
Slc35f1 T A 10: 53,089,414 S308R probably damaging Het
Sned1 G A 1: 93,289,358 V1322I probably benign Het
Sprr2f G A 3: 92,365,944 V17M unknown Het
Srd5a3 A G 5: 76,154,643 H285R probably benign Het
Stab1 T C 14: 31,159,259 T605A probably benign Het
Syne1 T C 10: 5,273,718 Q3054R probably damaging Het
Tas1r1 T C 4: 152,038,308 T27A probably benign Het
Tmem150b A T 7: 4,716,210 V237E probably benign Het
Trpv6 C T 6: 41,625,153 M407I probably benign Het
Ttn T G 2: 76,720,354 D31528A probably damaging Het
Uroc1 A T 6: 90,346,362 D354V possibly damaging Het
Vmn2r69 T C 7: 85,411,259 I372M probably benign Het
Vmn2r93 A T 17: 18,326,410 H848L probably benign Het
Zfp971 T A 2: 178,033,174 C189S probably damaging Het
Other mutations in Slc35f4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01511:Slc35f4 APN 14 49298877 missense probably benign 0.15
IGL01640:Slc35f4 APN 14 49318768 missense probably damaging 0.99
IGL01942:Slc35f4 APN 14 49525505 splice site probably benign
IGL01990:Slc35f4 APN 14 49304169 critical splice donor site probably null
IGL02097:Slc35f4 APN 14 49306246 missense probably damaging 1.00
IGL02803:Slc35f4 APN 14 49304257 missense probably benign 0.00
R0005:Slc35f4 UTSW 14 49322486 splice site probably benign
R0238:Slc35f4 UTSW 14 49304256 missense possibly damaging 0.78
R0238:Slc35f4 UTSW 14 49304256 missense possibly damaging 0.78
R0239:Slc35f4 UTSW 14 49304256 missense possibly damaging 0.78
R0239:Slc35f4 UTSW 14 49304256 missense possibly damaging 0.78
R0764:Slc35f4 UTSW 14 49306339 splice site probably benign
R1884:Slc35f4 UTSW 14 49313634 missense probably damaging 1.00
R1916:Slc35f4 UTSW 14 49303923 intron probably benign
R2047:Slc35f4 UTSW 14 49303572 intron probably benign
R2239:Slc35f4 UTSW 14 49306203 critical splice donor site probably null
R2380:Slc35f4 UTSW 14 49306203 critical splice donor site probably null
R4273:Slc35f4 UTSW 14 49304301 missense possibly damaging 0.81
R4420:Slc35f4 UTSW 14 49313577 unclassified probably benign
R4425:Slc35f4 UTSW 14 49318850 missense possibly damaging 0.85
R5261:Slc35f4 UTSW 14 49303489 intron probably benign
R5398:Slc35f4 UTSW 14 49298847 missense probably damaging 1.00
R5402:Slc35f4 UTSW 14 49318874 missense probably damaging 1.00
R6310:Slc35f4 UTSW 14 49322457 missense probably damaging 1.00
R6596:Slc35f4 UTSW 14 49525600 missense probably damaging 1.00
R6729:Slc35f4 UTSW 14 49318960 missense probably benign 0.16
R6864:Slc35f4 UTSW 14 49318853 missense possibly damaging 0.55
R7428:Slc35f4 UTSW 14 49298898 missense probably damaging 0.99
R7559:Slc35f4 UTSW 14 49304275 missense probably benign 0.03
R7596:Slc35f4 UTSW 14 49306209 missense probably damaging 1.00
R7722:Slc35f4 UTSW 14 49306274 missense probably benign 0.22
R8263:Slc35f4 UTSW 14 49313627 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGGTCGTTCCGTTTCAAGCC -3'
(R):5'- TGTGATTTACAGCAAAGGAACG -3'

Sequencing Primer
(F):5'- TTTCAAGCCAGCGGTATGGAC -3'
(R):5'- TGATTTACAGCAAAGGAACGGGAAG -3'
Posted On2019-10-07