Mutagenetix > Incidental Mutation

Incidental Mutation 'R5294:Slc43a3'

405276

Institutional Source

Beutler Lab

Gene Symbol

Slc43a3

Ensembl Gene

ENSMUSG00000027074

Gene Name

solute carrier family 43, member 3

Synonyms

Eeg1, SEEEG-1

MMRRC Submission

042877-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5294 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

84936579-84958509 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 84956310 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 445 (V445A)

Ref Sequence

ENSEMBL: ENSMUSP00000088227 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000090726]

AlphaFold

A2AVZ9

Predicted Effect

probably benign
Transcript: ENSMUST00000090726
AA Change: V445A

PolyPhen 2 Score 0.127 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000088227
Gene: ENSMUSG00000027074
AA Change: V445A

Domain	Start	End	E-Value	Type
Pfam:MFS_1	12	457	1.2e-20	PFAM
transmembrane domain	470	487	N/A	INTRINSIC

Meta Mutation Damage Score

0.0773

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 96.0%

Validation Efficiency

97% (70/72)

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930579C12Rik	T	C	9: 89,152,003 (GRCm38)		noncoding transcript	Het
Acaca	A	G	11: 84,391,519 (GRCm38)	E2154G	probably benign	Het
Acacb	T	C	5: 114,241,952 (GRCm38)	F2056L	probably damaging	Het
Aff1	A	G	5: 103,811,157 (GRCm38)		probably benign	Het
Amn1	T	A	6: 149,185,124 (GRCm38)		probably benign	Het
Arid1a	C	A	4: 133,691,055 (GRCm38)		probably benign	Het
Aste1	T	A	9: 105,402,705 (GRCm38)		probably null	Het
Asxl3	T	A	18: 22,516,439 (GRCm38)	V495D	possibly damaging	Het
Atp1a3	T	A	7: 24,988,048 (GRCm38)	H688L	probably damaging	Het
B3gnt8	T	C	7: 25,628,766 (GRCm38)	L207P	probably damaging	Het
Baz2b	T	C	2: 59,978,602 (GRCm38)	H101R	probably benign	Het
Bicc1	G	A	10: 70,947,900 (GRCm38)	T387M	possibly damaging	Het
Champ1	A	C	8: 13,878,981 (GRCm38)	K380Q	probably damaging	Het
Cnst	A	G	1: 179,610,440 (GRCm38)	E523G	probably benign	Het
Cops6	G	C	5: 138,161,116 (GRCm38)		probably benign	Het
Cp	G	C	3: 19,966,316 (GRCm38)	V158L	probably benign	Het
Cyfip1	T	A	7: 55,873,483 (GRCm38)	M52K	possibly damaging	Het
Dars	A	T	1: 128,364,302 (GRCm38)	F480I	probably benign	Het
Diaph1	T	C	18: 37,897,580 (GRCm38)	M274V	unknown	Het
Diaph1	C	A	18: 37,897,550 (GRCm38)	E284*	probably null	Het
Dock8	G	A	19: 25,061,153 (GRCm38)	V68M	probably benign	Het
Elavl4	A	G	4: 110,211,430 (GRCm38)	F247L	possibly damaging	Het
Emc10	C	T	7: 44,496,439 (GRCm38)		probably benign	Het
Fbxw16	T	C	9: 109,436,644 (GRCm38)	D369G	probably benign	Het
Fgr	A	T	4: 132,997,500 (GRCm38)	D304V	probably benign	Het
Filip1l	G	A	16: 57,570,036 (GRCm38)	S91N	possibly damaging	Het
Gm884	A	G	11: 103,616,231 (GRCm38)		probably benign	Het
Haus8	A	G	8: 71,255,710 (GRCm38)	S103P	unknown	Het
Hscb	A	G	5: 110,834,792 (GRCm38)	L143P	probably damaging	Het
Hsd11b2	A	T	8: 105,523,297 (GRCm38)	M347L	probably benign	Het
Jrk	C	A	15: 74,707,336 (GRCm38)	E33D	possibly damaging	Het
Kbtbd8	T	A	6: 95,121,832 (GRCm38)	Y123*	probably null	Het
Mis18bp1	A	C	12: 65,157,043 (GRCm38)	M59R	probably damaging	Het
Mrps27	T	C	13: 99,409,873 (GRCm38)	V260A	probably damaging	Het
Ncapg2	G	T	12: 116,427,794 (GRCm38)	V488L	possibly damaging	Het
Nepn	A	T	10: 52,400,800 (GRCm38)	N211Y	probably benign	Het
Ntrk3	A	T	7: 78,517,506 (GRCm38)		probably null	Het
Olfr248	A	T	1: 174,391,225 (GRCm38)	Y52F	probably benign	Het
Olfr692	C	T	7: 105,368,413 (GRCm38)	T20I	probably benign	Het
Olfr748	A	G	14: 50,710,779 (GRCm38)	I150V	probably benign	Het
Olfr748	A	G	14: 50,710,443 (GRCm38)	T38A	possibly damaging	Het
Otud4	A	T	8: 79,672,892 (GRCm38)	Q744L	possibly damaging	Het
P2ry14	A	T	3: 59,115,568 (GRCm38)	I166N	possibly damaging	Het
Pak2	T	A	16: 32,021,830 (GRCm38)	N478Y	probably damaging	Het
Papss2	A	G	19: 32,639,000 (GRCm38)	D202G	probably benign	Het
Pcdh7	C	A	5: 57,728,111 (GRCm38)		probably null	Het
Peg3	C	A	7: 6,717,849 (GRCm38)	S19I	possibly damaging	Het
Prim2	G	T	1: 33,668,893 (GRCm38)	T40K	probably benign	Het
Ranbp2	T	C	10: 58,478,668 (GRCm38)	F1737L	probably benign	Het
Rex2	A	C	4: 147,057,985 (GRCm38)	N310T	probably benign	Het
Rnf123	AT	ATT	9: 108,064,003 (GRCm38)		probably null	Het
Rnf39	C	T	17: 36,947,200 (GRCm38)	A86V	probably damaging	Het
Ror1	A	T	4: 100,425,938 (GRCm38)	N400I	probably benign	Het
Slc38a8	C	T	8: 119,494,289 (GRCm38)	G177D	probably damaging	Het
Sptbn2	A	G	19: 4,718,908 (GRCm38)	N23S	possibly damaging	Het
Taf5l	A	G	8: 124,008,218 (GRCm38)	F74L	probably benign	Het
Trappc11	G	C	8: 47,530,731 (GRCm38)	A42G	possibly damaging	Het
Trim30d	T	C	7: 104,472,488 (GRCm38)	K350R	probably damaging	Het
Trnt1	T	C	6: 106,773,414 (GRCm38)	F93S	probably damaging	Het
Ube2c	T	C	2: 164,777,190 (GRCm38)	V161A	probably benign	Het
Usp24	A	G	4: 106,362,357 (GRCm38)	E555G	possibly damaging	Het
Vmn2r55	T	G	7: 12,651,864 (GRCm38)	S730R	probably damaging	Het
Vmn2r89	T	A	14: 51,455,113 (GRCm38)	N124K	probably benign	Het
Vmn2r98	T	A	17: 19,069,754 (GRCm38)	C517*	probably null	Het
Vps13a	A	T	19: 16,641,667 (GRCm38)	I2845N	probably damaging	Het
Vps51	T	G	19: 6,071,033 (GRCm38)	E283D	probably benign	Het
Xpo5	T	C	17: 46,236,922 (GRCm38)	V896A	probably benign	Het
Zfp2	T	C	11: 50,901,241 (GRCm38)		probably benign	Het
Zgrf1	G	A	3: 127,600,980 (GRCm38)	M1328I	probably benign	Het
Zswim5	A	G	4: 116,979,577 (GRCm38)	D686G	possibly damaging	Het

Other mutations in Slc43a3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02017:Slc43a3	APN	2	84,938,241 (GRCm38)	missense	probably damaging	1.00
IGL02405:Slc43a3	APN	2	84,938,241 (GRCm38)	missense	probably damaging	1.00
IGL02756:Slc43a3	APN	2	84,944,268 (GRCm38)	missense	probably benign	0.06
R0276:Slc43a3	UTSW	2	84,937,663 (GRCm38)	start gained	probably benign
R1158:Slc43a3	UTSW	2	84,937,796 (GRCm38)	missense	probably benign	0.27
R1865:Slc43a3	UTSW	2	84,946,901 (GRCm38)	missense	possibly damaging	0.90
R1992:Slc43a3	UTSW	2	84,957,740 (GRCm38)	missense	probably damaging	0.99
R2073:Slc43a3	UTSW	2	84,944,612 (GRCm38)	critical splice donor site	probably null
R2243:Slc43a3	UTSW	2	84,948,438 (GRCm38)	unclassified	probably benign
R3819:Slc43a3	UTSW	2	84,944,552 (GRCm38)	missense	probably damaging	1.00
R4758:Slc43a3	UTSW	2	84,944,525 (GRCm38)	missense	probably damaging	1.00
R5369:Slc43a3	UTSW	2	84,957,723 (GRCm38)	missense	probably damaging	0.98
R6516:Slc43a3	UTSW	2	84,957,761 (GRCm38)	missense	probably benign	0.00
R6729:Slc43a3	UTSW	2	84,938,285 (GRCm38)	missense	probably damaging	1.00
R7012:Slc43a3	UTSW	2	84,946,969 (GRCm38)	missense	probably damaging	0.99
R8358:Slc43a3	UTSW	2	84,950,516 (GRCm38)	missense	probably benign	0.38
R8391:Slc43a3	UTSW	2	84,937,807 (GRCm38)	missense	probably benign	0.32
R8711:Slc43a3	UTSW	2	84,938,327 (GRCm38)	missense	probably damaging	1.00
R9382:Slc43a3	UTSW	2	84,950,427 (GRCm38)	missense	probably benign	0.18
R9729:Slc43a3	UTSW	2	84,950,456 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TAGCTTAGCCTGGGCCTGAG -3'
(R):5'- GCCCTGTGCAATAGGTCCAG -3'

Sequencing Primer
(F):5'- TCTTGGGGTTAGAACTGAATAGAG -3'
(R):5'- TACACAGCGTTGCTCTCA -3'

Posted On

2016-07-22