Mutagenetix > Incidental Mutation

Incidental Mutation 'R9786:Slc7a15'

734350

Institutional Source

Beutler Lab

Gene Symbol

Slc7a15

Ensembl Gene

ENSMUSG00000020600

Gene Name

solute carrier family 7 (cationic amino acid transporter, y+ system), member 15

Synonyms

Arpat, 9030221C07Rik, 2010001P20Rik

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.133) question?

Stock #

R9786 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

8578483-8649066 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 8580280 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 384 (F384S)

Ref Sequence

ENSEMBL: ENSMUSP00000093548 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036938] [ENSMUST00000095863] [ENSMUST00000165657]

AlphaFold

Q50E62

Predicted Effect

probably benign
Transcript: ENSMUST00000036938
AA Change: F124S

PolyPhen 2 Score 0.310 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000047873
Gene: ENSMUSG00000020600
AA Change: F124S

Domain	Start	End	E-Value	Type
Pfam:AA_permease_2	1	197	2.6e-20	PFAM
Pfam:AA_permease	1	221	1.5e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000095863
AA Change: F384S

PolyPhen 2 Score 0.310 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000093548
Gene: ENSMUSG00000020600
AA Change: F384S

Domain	Start	End	E-Value	Type
Pfam:AA_permease_2	31	453	2.6e-57	PFAM
Pfam:AA_permease	35	480	2.2e-21	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000165657
AA Change: F124S

PolyPhen 2 Score 0.310 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000129806
Gene: ENSMUSG00000020600
AA Change: F124S

Domain	Start	End	E-Value	Type
Pfam:AA_permease_2	1	197	2.6e-20	PFAM
Pfam:AA_permease	1	221	1.5e-9	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.8%
10x: 99.2%
20x: 97.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A4gnt	T	A	9: 99,502,536 (GRCm39)	M232K	possibly damaging	Het
Abcc1	T	C	16: 14,222,927 (GRCm39)	S243P	probably damaging	Het
Acsl1	T	C	8: 46,974,486 (GRCm39)	Y320H	probably damaging	Het
Adam11	A	G	11: 102,653,090 (GRCm39)	S61G	probably benign	Het
Adamts1	G	A	16: 85,592,302 (GRCm39)	T965I	probably benign	Het
Adcyap1r1	T	A	6: 55,456,182 (GRCm39)	M190K	probably damaging	Het
Ankrd2	T	A	19: 42,033,358 (GRCm39)	L300Q		Het
Ankrd27	A	T	7: 35,291,294 (GRCm39)	Q30L	possibly damaging	Het
Atp8b5	T	A	4: 43,305,798 (GRCm39)	I114K	probably damaging	Het
Atrn	A	T	2: 130,786,809 (GRCm39)	I205F	probably damaging	Het
BC035947	A	G	1: 78,488,561 (GRCm39)		probably benign	Het
Boc	C	T	16: 44,311,692 (GRCm39)	R677H		Het
Calhm6	A	G	10: 34,003,643 (GRCm39)	F88S	probably benign	Het
Ccdc121rt3	T	A	5: 112,502,939 (GRCm39)	E255V	probably benign	Het
Dpysl3	G	T	18: 43,462,922 (GRCm39)	T485K	probably damaging	Het
Esyt3	T	C	9: 99,194,038 (GRCm39)	D867G	possibly damaging	Het
Fam178b	G	A	1: 36,603,517 (GRCm39)	T478I	probably damaging	Het
Foxd2	G	T	4: 114,764,850 (GRCm39)	T390K	possibly damaging	Het
Furin	A	G	7: 80,040,645 (GRCm39)	V731A	probably benign	Het
Grin2a	T	A	16: 9,471,466 (GRCm39)	I601F	possibly damaging	Het
Hat1	G	A	2: 71,250,959 (GRCm39)	R169Q	possibly damaging	Het
Ighe	G	C	12: 113,236,851 (GRCm39)	Q6E		Het
Ighv8-2	T	C	12: 114,426,179 (GRCm39)	I31V	probably benign	Het
Klk1	A	G	7: 43,878,104 (GRCm39)	D120G	probably damaging	Het
Kmt2e	A	G	5: 23,702,982 (GRCm39)	D1054G	probably benign	Het
Lamp5	A	T	2: 135,910,998 (GRCm39)	I244F	probably damaging	Het
Maco1	A	T	4: 134,557,993 (GRCm39)	Y173*	probably null	Het
Mcm5	C	T	8: 75,844,168 (GRCm39)	S313F	probably benign	Het
Mfsd4b1	T	C	10: 39,878,865 (GRCm39)	E344G	probably damaging	Het
Mns1	A	G	9: 72,346,556 (GRCm39)	K13R	probably benign	Het
Mrpl43	C	T	19: 44,994,346 (GRCm39)	S91N	probably benign	Het
Mtbp	T	C	15: 55,481,032 (GRCm39)	S706P	probably benign	Het
Nelfb	A	T	2: 25,095,145 (GRCm39)	V348D	probably damaging	Het
Or1l8	T	A	2: 36,817,416 (GRCm39)	K237*	probably null	Het
Or5p72	A	T	7: 108,021,924 (GRCm39)	I49F	probably benign	Het
Or7g20	C	T	9: 18,947,241 (GRCm39)	A274V	possibly damaging	Het
Or8k18	G	A	2: 86,085,428 (GRCm39)	S203L	probably benign	Het
Or8s8	T	C	15: 98,354,713 (GRCm39)	I174T	possibly damaging	Het
Pde6c	T	C	19: 38,140,009 (GRCm39)	I324T	possibly damaging	Het
Phlpp2	T	A	8: 110,660,655 (GRCm39)	L770*	probably null	Het
Pik3c2b	T	A	1: 133,019,338 (GRCm39)	F1029I	possibly damaging	Het
Rfx2	A	T	17: 57,087,890 (GRCm39)	S500R	probably benign	Het
Sarm1	T	C	11: 78,365,743 (GRCm39)	M761V	probably benign	Het
Serpina1a	A	G	12: 103,822,140 (GRCm39)	L264P	possibly damaging	Het
Slc37a1	G	T	17: 31,556,965 (GRCm39)	G377V	probably damaging	Het
Slc38a4	T	A	15: 96,906,378 (GRCm39)	M364L	probably damaging	Het
Smyd4	T	C	11: 75,281,625 (GRCm39)	V366A	probably benign	Het
Spata31d1b	T	A	13: 59,866,155 (GRCm39)	V1101D	possibly damaging	Het
Spata31d1e	C	T	13: 59,890,498 (GRCm39)	D441N	possibly damaging	Het
Stab2	C	A	10: 86,757,997 (GRCm39)	M1090I	probably benign	Het
Tex15	C	T	8: 34,062,457 (GRCm39)	T903I	probably damaging	Het
Tgds	A	T	14: 118,368,049 (GRCm39)	Y41*	probably null	Het
Tle4	G	T	19: 14,495,304 (GRCm39)	H142N	probably benign	Het
Tlx2	T	C	6: 83,046,274 (GRCm39)		probably null	Het
Tmem151a	C	G	19: 5,131,869 (GRCm39)	A446P	probably damaging	Het
Tmem205	A	T	9: 21,832,496 (GRCm39)	D138E	probably damaging	Het
Tmprss9	A	G	10: 80,734,042 (GRCm39)	K1009E	unknown	Het
Tnk2	T	A	16: 32,498,875 (GRCm39)	C729*	probably null	Het
Trim46	T	A	3: 89,142,399 (GRCm39)	D696V	probably damaging	Het
Tuba3b	G	A	6: 145,564,482 (GRCm39)	R84Q	probably benign	Het
Unc119b	C	T	5: 115,263,521 (GRCm39)	D228N	probably damaging	Het
Usp17la	A	G	7: 104,510,864 (GRCm39)	T490A	probably benign	Het
Zfp267	T	A	3: 36,219,853 (GRCm39)	C625*	probably null	Het
Zfp687	C	T	3: 94,919,768 (GRCm39)	M1I	probably null	Het
Zfp729a	T	C	13: 67,768,628 (GRCm39)	T534A	possibly damaging	Het
Zfp985	A	T	4: 147,668,047 (GRCm39)	H305L	probably benign	Het
Zscan10	C	T	17: 23,828,330 (GRCm39)	Q291*	probably null	Het

Other mutations in Slc7a15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00310:Slc7a15	APN	12	8,589,121 (GRCm39)	missense	probably damaging	1.00
IGL00507:Slc7a15	APN	12	8,585,474 (GRCm39)	missense	probably damaging	1.00
IGL01839:Slc7a15	APN	12	8,589,365 (GRCm39)	missense	probably damaging	1.00
IGL02006:Slc7a15	APN	12	8,585,508 (GRCm39)	critical splice acceptor site	probably null
IGL02201:Slc7a15	APN	12	8,589,023 (GRCm39)	missense	possibly damaging	0.93
R0422:Slc7a15	UTSW	12	8,584,400 (GRCm39)	missense	probably benign	0.17
R0794:Slc7a15	UTSW	12	8,589,278 (GRCm39)	missense	probably benign	0.19
R1194:Slc7a15	UTSW	12	8,585,772 (GRCm39)	missense	probably damaging	1.00
R1420:Slc7a15	UTSW	12	8,584,442 (GRCm39)	missense	probably benign	0.01
R2696:Slc7a15	UTSW	12	8,579,345 (GRCm39)	makesense	probably null
R4809:Slc7a15	UTSW	12	8,589,002 (GRCm39)	missense	probably benign	0.10
R5236:Slc7a15	UTSW	12	8,589,005 (GRCm39)	missense	probably benign	0.38
R5579:Slc7a15	UTSW	12	8,589,344 (GRCm39)	missense	probably benign	0.00
R6453:Slc7a15	UTSW	12	8,584,490 (GRCm39)	missense	possibly damaging	0.77
R7136:Slc7a15	UTSW	12	8,588,895 (GRCm39)	missense	probably damaging	0.98
R8005:Slc7a15	UTSW	12	8,589,395 (GRCm39)	missense	probably damaging	0.97
R8910:Slc7a15	UTSW	12	8,589,117 (GRCm39)	start gained	probably benign
R9474:Slc7a15	UTSW	12	8,588,794 (GRCm39)	missense	probably damaging	0.99
X0027:Slc7a15	UTSW	12	8,589,350 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCAGCCATTGATATATGCCTTGTC -3'
(R):5'- ACTCACTGGGTCATCTTTAAGC -3'

Sequencing Primer
(F):5'- TAGGCTGGCAGTTCTCAAC -3'
(R):5'- TCAGCAGGAGTAGTCAGATCTC -3'

Posted On

2022-11-14