Mutagenetix > Incidental Mutation

Incidental Mutation 'R7462:Slc38a6'

578519

Institutional Source

Beutler Lab

Gene Symbol

Slc38a6

Ensembl Gene

ENSMUSG00000044712

Gene Name

solute carrier family 38, member 6

Synonyms

EG625098

MMRRC Submission

045536-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R7462 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

73333553-73400823 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 73397351 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 331 (M331K)

Ref Sequence

ENSEMBL: ENSMUSP00000120810 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000140523]

AlphaFold

G3UVW3

Predicted Effect

probably benign
Transcript: ENSMUST00000140523
AA Change: M331K

PolyPhen 2 Score 0.150 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000120810
Gene: ENSMUSG00000044712
AA Change: M331K

Domain	Start	End	E-Value	Type
Pfam:Aa_trans	44	452	2.5e-77	PFAM

Meta Mutation Damage Score

0.2076

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

98% (60/61)

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ank2	G	C	3: 126,736,683 (GRCm39)	T3067S	unknown	Het
Ankrd28	T	C	14: 31,500,886 (GRCm39)	N35S	probably benign	Het
Bicra	A	T	7: 15,713,060 (GRCm39)	S996T	possibly damaging	Het
Btbd7	T	C	12: 102,803,981 (GRCm39)	E353G	possibly damaging	Het
Cdhr2	A	T	13: 54,874,552 (GRCm39)	I875F	probably damaging	Het
Ceacam5	A	T	7: 17,494,764 (GRCm39)	Y924F	probably damaging	Het
Clca4b	A	G	3: 144,628,621 (GRCm39)	I362T	probably benign	Het
Dchs2	A	G	3: 83,253,462 (GRCm39)		probably null	Het
Dlc1	T	A	8: 37,405,118 (GRCm39)	T224S	unknown	Het
Dmxl2	T	C	9: 54,273,916 (GRCm39)		probably null	Het
Dnajc1	A	G	2: 18,313,710 (GRCm39)	F137S	probably damaging	Het
E130311K13Rik	T	C	3: 63,836,722 (GRCm39)	T24A	probably benign	Het
Eya1	T	C	1: 14,301,638 (GRCm39)	E317G	probably null	Het
Fpr-rs6	A	G	17: 20,402,485 (GRCm39)	L292P	probably damaging	Het
Gca	G	T	2: 62,502,753 (GRCm39)	D54Y	possibly damaging	Het
Gm45861	G	A	8: 28,024,517 (GRCm39)		probably null	Het
Gm57858	T	A	3: 36,080,055 (GRCm39)		probably null	Het
Gtf2a1l	A	G	17: 89,001,566 (GRCm39)	T141A	possibly damaging	Het
Hgsnat	T	C	8: 26,447,241 (GRCm39)	N351S	probably benign	Het
Htr1f	A	T	16: 64,746,383 (GRCm39)	V303E	probably damaging	Het
Iars2	C	A	1: 185,055,063 (GRCm39)	W302L	probably damaging	Het
Igkv4-74	T	A	6: 69,162,100 (GRCm39)	Q23L	possibly damaging	Het
Il18	A	T	9: 50,476,673 (GRCm39)		probably benign	Het
Ints4	A	G	7: 97,155,335 (GRCm39)	D329G	probably benign	Het
Itsn1	T	C	16: 91,650,073 (GRCm39)	F249S	possibly damaging	Het
Ktn1	A	G	14: 47,932,089 (GRCm39)	E672G	probably null	Het
Lhx6	A	G	2: 35,974,083 (GRCm39)	I359T	possibly damaging	Het
Lrp1b	T	C	2: 41,003,041 (GRCm39)	E2030G		Het
Macf1	T	A	4: 123,386,556 (GRCm39)	K1114N	probably damaging	Het
Mbd5	A	G	2: 49,147,892 (GRCm39)	M701V	possibly damaging	Het
Mcemp1	A	T	8: 3,717,065 (GRCm39)	M69L	probably benign	Het
Mfsd4b2	T	A	10: 39,797,877 (GRCm39)	K159N	probably benign	Het
Mroh2b	T	A	15: 4,938,109 (GRCm39)	D243E	probably damaging	Het
Muc21	T	C	17: 35,931,568 (GRCm39)	S873G	unknown	Het
Mug1	A	T	6: 121,852,399 (GRCm39)	Q829L	probably benign	Het
Nav3	A	T	10: 109,659,439 (GRCm39)	V726E	probably damaging	Het
Nfib	T	C	4: 82,271,826 (GRCm39)	Q247R	probably benign	Het
Npbwr1	T	C	1: 5,987,151 (GRCm39)	N121S	probably damaging	Het
Or1e19	T	C	11: 73,316,296 (GRCm39)	D171G	probably benign	Het
Or52b2	T	A	7: 104,986,707 (GRCm39)	D72V	probably damaging	Het
Or5h19	A	T	16: 58,856,379 (GRCm39)	C240*	probably null	Het
Pkd1l3	A	G	8: 110,355,409 (GRCm39)	S726G	probably benign	Het
Ppip5k1	A	T	2: 121,167,232 (GRCm39)	V847D	probably damaging	Het
Ptpn18	G	A	1: 34,512,445 (GRCm39)	D417N	possibly damaging	Het
Ripor2	G	A	13: 24,880,290 (GRCm39)	V385M	unknown	Het
Rufy1	C	T	11: 50,298,655 (GRCm39)	V379M	possibly damaging	Het
S100a5	A	G	3: 90,517,207 (GRCm39)	K26R	probably damaging	Het
Sin3a	T	C	9: 57,002,809 (GRCm39)	S234P	probably benign	Het
Sirt7	G	A	11: 120,511,618 (GRCm39)	T225I	probably benign	Het
Slc34a1	A	T	13: 24,006,401 (GRCm39)	T476S	probably damaging	Het
Spam1	T	C	6: 24,796,907 (GRCm39)	I286T	probably damaging	Het
Syne1	T	A	10: 5,002,793 (GRCm39)	I214F	possibly damaging	Het
Tmtc1	A	G	6: 148,226,643 (GRCm39)	L427P	probably damaging	Het
Tpbg	G	A	9: 85,726,903 (GRCm39)	A291T	possibly damaging	Het
Zfp40	A	G	17: 23,397,362 (GRCm39)	F45S	possibly damaging	Het
Zfp451	C	T	1: 33,816,094 (GRCm39)	V619M	probably damaging	Het
Zim1	A	G	7: 6,680,811 (GRCm39)	L284P	probably damaging	Het
Zkscan4	A	G	13: 21,668,044 (GRCm39)	E165G	probably benign	Het
Zmynd11	T	A	13: 9,748,720 (GRCm39)	N154Y	probably benign	Het
Zscan12	A	T	13: 21,553,457 (GRCm39)	H427L	possibly damaging	Het

Other mutations in Slc38a6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00432:Slc38a6	APN	12	73,398,577 (GRCm39)	missense	probably benign	0.00
IGL01083:Slc38a6	APN	12	73,335,267 (GRCm39)	missense	possibly damaging	0.94
IGL01302:Slc38a6	APN	12	73,335,299 (GRCm39)	critical splice donor site	probably null
IGL02106:Slc38a6	APN	12	73,397,320 (GRCm39)	missense	possibly damaging	0.84
IGL02429:Slc38a6	APN	12	73,397,342 (GRCm39)	missense	probably benign	0.18
IGL02815:Slc38a6	APN	12	73,338,979 (GRCm39)	missense	probably damaging	1.00
IGL03001:Slc38a6	APN	12	73,383,827 (GRCm39)	missense	probably benign	0.03
IGL03167:Slc38a6	APN	12	73,397,311 (GRCm39)	nonsense	probably null
R0394:Slc38a6	UTSW	12	73,399,304 (GRCm39)	missense	probably benign
R0918:Slc38a6	UTSW	12	73,391,559 (GRCm39)	splice site	probably null
R1377:Slc38a6	UTSW	12	73,397,345 (GRCm39)	missense	probably damaging	0.98
R1533:Slc38a6	UTSW	12	73,391,626 (GRCm39)	missense	probably benign	0.11
R4171:Slc38a6	UTSW	12	73,397,326 (GRCm39)	missense	probably benign	0.21
R4579:Slc38a6	UTSW	12	73,335,298 (GRCm39)	critical splice donor site	probably null
R4864:Slc38a6	UTSW	12	73,390,424 (GRCm39)	splice site	probably null
R5162:Slc38a6	UTSW	12	73,376,759 (GRCm39)	missense	possibly damaging	0.70
R5627:Slc38a6	UTSW	12	73,390,457 (GRCm39)	missense	possibly damaging	0.59
R6189:Slc38a6	UTSW	12	73,356,970 (GRCm39)	missense	probably damaging	1.00
R6302:Slc38a6	UTSW	12	73,383,849 (GRCm39)	missense	probably damaging	1.00
R6407:Slc38a6	UTSW	12	73,356,949 (GRCm39)	missense	probably damaging	1.00
R7289:Slc38a6	UTSW	12	73,333,786 (GRCm39)	missense	probably benign
R8031:Slc38a6	UTSW	12	73,397,377 (GRCm39)	missense	probably benign	0.39
R8074:Slc38a6	UTSW	12	73,391,658 (GRCm39)	missense	possibly damaging	0.84
R9091:Slc38a6	UTSW	12	73,398,544 (GRCm39)	missense	probably benign	0.01
R9190:Slc38a6	UTSW	12	73,388,526 (GRCm39)	missense	possibly damaging	0.84
R9270:Slc38a6	UTSW	12	73,398,544 (GRCm39)	missense	probably benign	0.01
R9406:Slc38a6	UTSW	12	73,376,767 (GRCm39)	nonsense	probably null
R9587:Slc38a6	UTSW	12	73,388,513 (GRCm39)	missense	probably benign	0.18

Predicted Primers

PCR Primer
(F):5'- GCCTAGTATAAACCAGTAATGCAACAG -3'
(R):5'- GGGACCATGTGCTAGTATGAGG -3'

Sequencing Primer
(F):5'- AGTAATGCAACAGAAAATAACTTTGG -3'
(R):5'- GAGGTCTTGGATCAATTACCTGAC -3'

Posted On

2019-10-07