Mutagenetix > Incidental Mutation

Incidental Mutation 'R6920:Slc38a9'

539600

Institutional Source

Beutler Lab

Gene Symbol

Slc38a9

Ensembl Gene

ENSMUSG00000047789

Gene Name

solute carrier family 38, member 9

Synonyms

9430067K09Rik, 9130023D20Rik, 4833412L08Rik, 6720411P22Rik

MMRRC Submission

045040-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.233) question?

Stock #

R6920 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

112797285-112875283 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 112838060 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 275 (T275I)

Ref Sequence

ENSEMBL: ENSMUSP00000052172 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052514]

AlphaFold

Q8BGD6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000052514
AA Change: T275I

PolyPhen 2 Score 0.635 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000052172
Gene: ENSMUSG00000047789
AA Change: T275I

Domain	Start	End	E-Value	Type
Pfam:Aa_trans	114	253	4.5e-17	PFAM
Pfam:Aa_trans	266	560	2.5e-16	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.1%
20x: 97.2%

Validation Efficiency

100% (65/65)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	A	T	3: 137,773,811 (GRCm39)	Y1000F	probably damaging	Het
1700018B08Rik	A	G	8: 122,262,160 (GRCm39)		probably null	Het
Aadat	T	C	8: 60,982,467 (GRCm39)	F245L	probably damaging	Het
Adcy10	T	G	1: 165,403,227 (GRCm39)	L1575W	probably damaging	Het
Anks4b	A	T	7: 119,782,231 (GRCm39)	T421S	probably damaging	Het
Anpep	A	T	7: 79,475,097 (GRCm39)	I155N	probably damaging	Het
Arnt	T	C	3: 95,397,932 (GRCm39)	F572L	probably damaging	Het
Brip1	G	A	11: 86,039,362 (GRCm39)	Q391*	probably null	Het
Brpf3	C	A	17: 29,042,970 (GRCm39)	H1004N	probably benign	Het
Cand2	T	A	6: 115,768,250 (GRCm39)	V465D	possibly damaging	Het
Card10	G	T	15: 78,686,609 (GRCm39)	Y69*	probably null	Het
Catsperd	A	T	17: 56,962,175 (GRCm39)	K450*	probably null	Het
Ccdc137	T	C	11: 120,351,009 (GRCm39)	L137P	probably damaging	Het
Cic	T	C	7: 24,990,107 (GRCm39)	S1905P	probably damaging	Het
Csmd3	C	T	15: 47,507,601 (GRCm39)	G2971S	probably damaging	Het
Dmxl2	A	G	9: 54,379,496 (GRCm39)	Y183H	probably damaging	Het
Drosha	T	C	15: 12,834,396 (GRCm39)	Y167H	unknown	Het
E330034G19Rik	A	G	14: 24,358,310 (GRCm39)	K214R	unknown	Het
Fam180a	T	G	6: 35,290,765 (GRCm39)	I73L	possibly damaging	Het
Fbxo28	G	T	1: 182,168,986 (GRCm39)	H51N	probably benign	Het
Gm12728	T	G	4: 105,647,533 (GRCm39)		probably null	Het
Gm973	T	C	1: 59,591,620 (GRCm39)	C335R	possibly damaging	Het
Gpx8	A	G	13: 113,179,770 (GRCm39)	V177A	probably damaging	Het
Hdlbp	A	G	1: 93,340,083 (GRCm39)		probably null	Het
Htt	T	G	5: 35,034,444 (GRCm39)	Y1972D	probably null	Het
Igkv6-14	T	C	6: 70,412,116 (GRCm39)	Y56C	possibly damaging	Het
Kcnma1	A	G	14: 23,576,602 (GRCm39)		probably null	Het
Klc1	T	C	12: 111,754,019 (GRCm39)	S105P	probably damaging	Het
Klhl20	T	C	1: 160,921,266 (GRCm39)	D63G	possibly damaging	Het
Lamc3	A	G	2: 31,798,701 (GRCm39)	D469G	probably damaging	Het
Lrit1	G	C	14: 36,782,052 (GRCm39)	V242L	probably damaging	Het
Mboat4	G	A	8: 34,591,865 (GRCm39)	R434H	probably benign	Het
Mttp	T	C	3: 137,821,043 (GRCm39)	K270E	possibly damaging	Het
Muc5ac	G	A	7: 141,347,035 (GRCm39)	C337Y	possibly damaging	Het
Nars1	A	G	18: 64,634,471 (GRCm39)	V484A	probably damaging	Het
Noxa1	G	T	2: 24,981,844 (GRCm39)		probably null	Het
Or14c45	A	G	7: 86,176,522 (GRCm39)	T186A	probably benign	Het
Or7g18	T	A	9: 18,786,821 (GRCm39)	L63H	probably damaging	Het
Osbpl7	G	A	11: 96,941,584 (GRCm39)	G36S	probably damaging	Het
P4htm	C	T	9: 108,460,812 (GRCm39)	G220D	probably benign	Het
Pcdhga7	A	G	18: 37,848,199 (GRCm39)	I69V	probably benign	Het
Pla2g4e	C	T	2: 120,015,795 (GRCm39)	E250K	possibly damaging	Het
Plcd4	A	G	1: 74,604,994 (GRCm39)		probably benign	Het
Ppfia3	C	A	7: 45,008,231 (GRCm39)	G213V	possibly damaging	Het
Ppp1r1a	A	G	15: 103,441,513 (GRCm39)	S67P	probably damaging	Het
Prss43	T	C	9: 110,657,680 (GRCm39)	F193S	probably benign	Het
Rfx1	A	G	8: 84,822,117 (GRCm39)	Y872C	probably damaging	Het
Rhot1	T	A	11: 80,132,921 (GRCm39)	N218K	probably benign	Het
Sall1	A	G	8: 89,757,021 (GRCm39)	F1028L	probably damaging	Het
Siglec1	G	A	2: 130,919,997 (GRCm39)	Q845*	probably null	Het
Slc39a4	A	T	15: 76,497,470 (GRCm39)	S481T	probably damaging	Het
Ssr1	A	T	13: 38,169,998 (GRCm39)	N191K	probably damaging	Het
Tenm4	A	T	7: 96,544,757 (GRCm39)	S2258C	probably damaging	Het
Tm7sf3	T	G	6: 146,507,645 (GRCm39)	R472S	possibly damaging	Het
Tmprss11a	G	A	5: 86,576,494 (GRCm39)	T119M	probably benign	Het
Traip	C	T	9: 107,838,240 (GRCm39)	R142*	probably null	Het
Utrn	T	C	10: 12,626,214 (GRCm39)	N100D	probably damaging	Het
Vmn1r74	T	C	7: 11,581,575 (GRCm39)	S292P	probably benign	Het
Vmn2r71	A	T	7: 85,273,108 (GRCm39)	I641F	probably damaging	Het
Vmn2r9	T	A	5: 108,996,912 (GRCm39)	Y119F	possibly damaging	Het
Vmn2r98	A	G	17: 19,285,510 (GRCm39)	N110S	probably damaging	Het
Vwce	A	G	19: 10,642,057 (GRCm39)	T928A	probably benign	Het
Zfp608	T	A	18: 55,121,337 (GRCm39)	K83N	probably damaging	Het
Zfp808	A	G	13: 62,320,982 (GRCm39)	H737R	probably benign	Het
Zswim4	T	C	8: 84,940,714 (GRCm39)	N795S	probably benign	Het

Other mutations in Slc38a9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00427:Slc38a9	APN	13	112,838,152 (GRCm39)	missense	probably damaging	1.00
IGL01950:Slc38a9	APN	13	112,831,787 (GRCm39)	missense	probably damaging	1.00
IGL01955:Slc38a9	APN	13	112,831,952 (GRCm39)	splice site	probably benign
IGL02352:Slc38a9	APN	13	112,826,720 (GRCm39)	missense	probably benign	0.10
IGL02359:Slc38a9	APN	13	112,826,720 (GRCm39)	missense	probably benign	0.10
IGL02407:Slc38a9	APN	13	112,826,777 (GRCm39)	missense	probably benign
IGL02511:Slc38a9	APN	13	112,834,541 (GRCm39)	missense	possibly damaging	0.47
IGL02588:Slc38a9	APN	13	112,834,511 (GRCm39)	splice site	probably null
IGL03278:Slc38a9	APN	13	112,826,052 (GRCm39)	splice site	probably benign
R0126:Slc38a9	UTSW	13	112,865,791 (GRCm39)	missense	possibly damaging	0.52
R0553:Slc38a9	UTSW	13	112,850,732 (GRCm39)	missense	probably damaging	1.00
R0558:Slc38a9	UTSW	13	112,865,730 (GRCm39)	critical splice acceptor site	probably null
R0699:Slc38a9	UTSW	13	112,859,823 (GRCm39)	missense	probably damaging	1.00
R1036:Slc38a9	UTSW	13	112,838,193 (GRCm39)	splice site	probably benign
R1142:Slc38a9	UTSW	13	112,850,744 (GRCm39)	missense	probably damaging	1.00
R1344:Slc38a9	UTSW	13	112,826,714 (GRCm39)	missense	probably benign	0.20
R1418:Slc38a9	UTSW	13	112,826,714 (GRCm39)	missense	probably benign	0.20
R4223:Slc38a9	UTSW	13	112,850,782 (GRCm39)	critical splice donor site	probably null
R4344:Slc38a9	UTSW	13	112,865,749 (GRCm39)	missense	probably benign	0.02
R4824:Slc38a9	UTSW	13	112,859,832 (GRCm39)	missense	probably damaging	0.98
R4872:Slc38a9	UTSW	13	112,826,098 (GRCm39)	missense	probably damaging	1.00
R5841:Slc38a9	UTSW	13	112,831,856 (GRCm39)	missense	possibly damaging	0.76
R5844:Slc38a9	UTSW	13	112,868,035 (GRCm39)	missense	probably damaging	1.00
R6039:Slc38a9	UTSW	13	112,806,231 (GRCm39)	missense	probably damaging	1.00
R6039:Slc38a9	UTSW	13	112,806,231 (GRCm39)	missense	probably damaging	1.00
R6151:Slc38a9	UTSW	13	112,825,910 (GRCm39)	missense	probably damaging	1.00
R6166:Slc38a9	UTSW	13	112,831,801 (GRCm39)	missense	possibly damaging	0.96
R6175:Slc38a9	UTSW	13	112,840,093 (GRCm39)	nonsense	probably null
R6324:Slc38a9	UTSW	13	112,862,634 (GRCm39)	missense	probably benign	0.01
R6747:Slc38a9	UTSW	13	112,826,714 (GRCm39)	missense	probably benign	0.20
R7342:Slc38a9	UTSW	13	112,806,125 (GRCm39)	start gained	probably benign
R7592:Slc38a9	UTSW	13	112,831,889 (GRCm39)	missense	probably damaging	0.99
R7787:Slc38a9	UTSW	13	112,825,880 (GRCm39)	missense	probably damaging	0.99
R7860:Slc38a9	UTSW	13	112,868,148 (GRCm39)	missense	probably benign
R8742:Slc38a9	UTSW	13	112,865,818 (GRCm39)	missense	probably damaging	1.00
R8799:Slc38a9	UTSW	13	112,840,136 (GRCm39)	missense	probably damaging	1.00
R8824:Slc38a9	UTSW	13	112,838,021 (GRCm39)	missense	probably benign
R8846:Slc38a9	UTSW	13	112,859,814 (GRCm39)	nonsense	probably null
R9112:Slc38a9	UTSW	13	112,850,777 (GRCm39)	missense	probably damaging	0.99
R9221:Slc38a9	UTSW	13	112,825,910 (GRCm39)	missense	probably damaging	1.00
R9780:Slc38a9	UTSW	13	112,862,591 (GRCm39)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- AAGTATGCATACGCTTCCAAGAAG -3'
(R):5'- CAAGTTAAGCAGCTCAGAACAGTAG -3'

Sequencing Primer
(F):5'- TCCAAGAAGGGAGCCTGCATTC -3'
(R):5'- CTCAGAACAGTAGGAGGTGACTGTC -3'

Posted On

2018-11-06