Mutagenetix > Incidental Mutation

Incidental Mutation 'R6114:Slc22a15'

485000

Institutional Source

Beutler Lab

Gene Symbol

Slc22a15

Ensembl Gene

ENSMUSG00000033147

Gene Name

solute carrier family 22 (organic anion/cation transporter), member 15

Synonyms

2610034P21Rik, A530052I06Rik

MMRRC Submission

044263-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

R6114 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

101763092-101831769 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 101768168 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 346 (Y346*)

Ref Sequence

ENSEMBL: ENSMUSP00000139518 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000106928] [ENSMUST00000183255] [ENSMUST00000190824]

AlphaFold

Q504N2

Predicted Effect

probably null
Transcript: ENSMUST00000106928
AA Change: Y501*

SMART Domains

Protein: ENSMUSP00000102541
Gene: ENSMUSG00000033147
AA Change: Y501*

Domain	Start	End	E-Value	Type
transmembrane domain	20	42	N/A	INTRINSIC
Pfam:Sugar_tr	58	495	6.9e-29	PFAM
Pfam:MFS_1	69	450	3.4e-24	PFAM
low complexity region	524	532	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182130

Predicted Effect

probably benign
Transcript: ENSMUST00000183255

SMART Domains

Protein: ENSMUSP00000138357
Gene: ENSMUSG00000033147

Domain	Start	End	E-Value	Type
transmembrane domain	20	42	N/A	INTRINSIC
Pfam:Sugar_tr	56	244	5.2e-13	PFAM
Pfam:MFS_1	69	244	7.6e-13	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183293

Predicted Effect

probably null
Transcript: ENSMUST00000190824
AA Change: Y346*

SMART Domains

Protein: ENSMUSP00000139518
Gene: ENSMUSG00000033147
AA Change: Y346*

Domain	Start	End	E-Value	Type
signal peptide	1	36	N/A	INTRINSIC
Pfam:Sugar_tr	88	341	3.3e-5	PFAM
low complexity region	369	377	N/A	INTRINSIC

Meta Mutation Damage Score

0.9707

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 94.0%

Validation Efficiency

94% (60/64)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Organic ion transporters, such as SLC22A15, transport various medically and physiologically important compounds, including pharmaceuticals, toxins, hormones, neurotransmitters, and cellular metabolites. These transporters are also referred to as amphiphilic solute facilitators (ASFs).[supplied by OMIM, Apr 2004]

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamdec1	C	A	14: 68,809,252 (GRCm39)	V237L	probably benign	Het
Aff1	T	C	5: 103,990,163 (GRCm39)	S878P	probably damaging	Het
Ahcy	A	C	2: 154,904,079 (GRCm39)	L386R	probably damaging	Het
Ank2	T	C	3: 126,804,700 (GRCm39)	N607D	probably damaging	Het
Arid5b	T	C	10: 67,933,574 (GRCm39)	D776G	possibly damaging	Het
Art4	T	A	6: 136,834,211 (GRCm39)	T11S	unknown	Het
Blm	T	C	7: 80,163,235 (GRCm39)	T39A	probably damaging	Het
Cabin1	T	A	10: 75,583,805 (GRCm39)	M221L	probably benign	Het
Cacna1c	T	C	6: 118,573,101 (GRCm39)	T1675A	probably benign	Het
Cacnb2	A	T	2: 14,980,012 (GRCm39)	H285L	possibly damaging	Het
Cchcr1	A	G	17: 35,836,227 (GRCm39)	E339G	probably damaging	Het
Cd14	A	G	18: 36,859,006 (GRCm39)	W150R	probably damaging	Het
Cep162	A	G	9: 87,085,763 (GRCm39)	I1187T	probably benign	Het
Cntnap4	A	G	8: 113,568,385 (GRCm39)	H807R	probably damaging	Het
Copb1	T	A	7: 113,846,036 (GRCm39)	H178L	probably benign	Het
Cpxm2	A	G	7: 131,756,035 (GRCm39)	V103A	probably benign	Het
Egfr	A	G	11: 16,854,374 (GRCm39)	T849A	possibly damaging	Het
Endou	T	A	15: 97,611,757 (GRCm39)	K294*	probably null	Het
Hoxd9	A	G	2: 74,529,709 (GRCm39)	N322D	probably damaging	Het
Hsph1	C	A	5: 149,550,852 (GRCm39)	V416L	possibly damaging	Het
Igkv4-78	T	A	6: 69,036,743 (GRCm39)	T97S	possibly damaging	Het
Itga10	G	T	3: 96,556,351 (GRCm39)	C162F	probably damaging	Het
Lmod2	A	G	6: 24,603,691 (GRCm39)	E222G	probably damaging	Het
Lpar5	A	G	6: 125,058,639 (GRCm39)	N120S	probably damaging	Het
Lrrc37	T	A	11: 103,508,617 (GRCm39)		probably benign	Het
Lrrk2	A	G	15: 91,632,029 (GRCm39)	I1318V	probably benign	Het
Lst1	T	C	17: 35,407,336 (GRCm39)	T11A	possibly damaging	Het
Mfn1	C	A	3: 32,617,985 (GRCm39)	A106D	probably damaging	Het
Ms4a12	G	T	19: 11,192,654 (GRCm39)	N227K	probably benign	Het
Nr1h4	T	A	10: 89,314,678 (GRCm39)	N273Y	possibly damaging	Het
Nrdc	A	T	4: 108,901,782 (GRCm39)	K617M	probably damaging	Het
Or10a3b	A	T	7: 108,444,593 (GRCm39)	M208K	possibly damaging	Het
Or1l8	A	T	2: 36,817,701 (GRCm39)	C142S	possibly damaging	Het
Or6c202	T	A	10: 128,996,202 (GRCm39)	H217L	probably benign	Het
Pcdhgc3	C	G	18: 37,940,925 (GRCm39)	T442R	probably benign	Het
Pcnx2	T	C	8: 126,500,686 (GRCm39)	N1468S	probably damaging	Het
Pde2a	A	T	7: 101,160,319 (GRCm39)		probably null	Het
Pitx2	C	G	3: 128,998,062 (GRCm39)		probably null	Het
Reck	T	A	4: 43,922,895 (GRCm39)	I390N	probably damaging	Het
Rora	A	G	9: 69,278,605 (GRCm39)	N254S	probably benign	Het
Samd4b	A	G	7: 28,222,217 (GRCm39)		probably null	Het
Scn8a	A	G	15: 100,938,477 (GRCm39)	T1949A	probably damaging	Het
Slc24a5	A	G	2: 124,925,012 (GRCm39)	T218A	probably benign	Het
Slc38a10	G	A	11: 120,020,138 (GRCm39)	Q305*	probably null	Het
Slc45a4	G	A	15: 73,477,453 (GRCm39)	P28S	probably damaging	Het
Smyd5	A	T	6: 85,417,244 (GRCm39)		probably benign	Het
Sox8	T	C	17: 25,786,494 (GRCm39)	D403G	probably damaging	Het
Stx7	A	G	10: 24,060,883 (GRCm39)		probably null	Het
Svil	T	C	18: 5,108,639 (GRCm39)	S1522P	probably damaging	Het
Sycp2	G	C	2: 177,990,038 (GRCm39)	R1403G	probably benign	Het
Tasor2	G	A	13: 3,640,081 (GRCm39)	T352M	probably damaging	Het
Tcf25	A	T	8: 124,111,114 (GRCm39)	K192M	probably damaging	Het
Tecpr1	C	T	5: 144,141,458 (GRCm39)	G804S	possibly damaging	Het
Teddm1a	C	G	1: 153,767,614 (GRCm39)	S26C	probably damaging	Het
Usp13	C	T	3: 32,908,818 (GRCm39)	P155S	probably damaging	Het
Usp17lb	T	A	7: 104,489,571 (GRCm39)	D451V	possibly damaging	Het
Vmn1r173	A	G	7: 23,402,254 (GRCm39)	N163S	possibly damaging	Het
Vmn2r103	G	T	17: 20,032,587 (GRCm39)	C787F	probably damaging	Het
Vmn2r106	G	A	17: 20,488,638 (GRCm39)	P587L	probably benign	Het
Wdr24	C	T	17: 26,043,579 (GRCm39)	H134Y	probably benign	Het
Zbtb40	T	A	4: 136,716,002 (GRCm39)	I988F	probably damaging	Het
Zbtb47	T	A	9: 121,594,661 (GRCm39)	F540Y	probably damaging	Het
Zfp536	A	T	7: 37,179,161 (GRCm39)	I84N	probably damaging	Het

Other mutations in Slc22a15

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00846:Slc22a15	APN	3	101,768,136 (GRCm39)	missense	probably benign	0.00
IGL01120:Slc22a15	APN	3	101,804,482 (GRCm39)	missense	probably damaging	1.00
IGL01345:Slc22a15	APN	3	101,787,492 (GRCm39)	missense	probably benign	0.00
IGL01871:Slc22a15	APN	3	101,768,110 (GRCm39)	splice site	probably benign
IGL01880:Slc22a15	APN	3	101,768,164 (GRCm39)	missense	probably benign	0.32
R0310:Slc22a15	UTSW	3	101,767,827 (GRCm39)	missense	probably benign	0.12
R1758:Slc22a15	UTSW	3	101,767,769 (GRCm39)	nonsense	probably null
R1937:Slc22a15	UTSW	3	101,787,505 (GRCm39)	critical splice acceptor site	probably null
R3804:Slc22a15	UTSW	3	101,804,590 (GRCm39)	missense	probably damaging	1.00
R4830:Slc22a15	UTSW	3	101,782,919 (GRCm39)	intron	probably benign
R5564:Slc22a15	UTSW	3	101,771,905 (GRCm39)	missense	probably benign	0.34
R5684:Slc22a15	UTSW	3	101,770,271 (GRCm39)	missense	probably damaging	1.00
R6034:Slc22a15	UTSW	3	101,770,235 (GRCm39)	missense	possibly damaging	0.80
R6034:Slc22a15	UTSW	3	101,770,235 (GRCm39)	missense	possibly damaging	0.80
R6481:Slc22a15	UTSW	3	101,790,899 (GRCm39)	missense	possibly damaging	0.88
R6641:Slc22a15	UTSW	3	101,783,022 (GRCm39)	missense	possibly damaging	0.52
R6945:Slc22a15	UTSW	3	101,831,430 (GRCm39)	missense	probably damaging	0.99
R7354:Slc22a15	UTSW	3	101,771,897 (GRCm39)	missense	probably benign	0.09
R7373:Slc22a15	UTSW	3	101,785,213 (GRCm39)	missense	possibly damaging	0.78
R7431:Slc22a15	UTSW	3	101,805,256 (GRCm39)	missense	probably benign	0.13
R7758:Slc22a15	UTSW	3	101,805,251 (GRCm39)	critical splice donor site	probably null
R8058:Slc22a15	UTSW	3	101,771,926 (GRCm39)	missense	probably benign
R8129:Slc22a15	UTSW	3	101,822,658 (GRCm39)	missense	possibly damaging	0.82
R8838:Slc22a15	UTSW	3	101,790,849 (GRCm39)	missense	probably damaging	1.00
R9652:Slc22a15	UTSW	3	101,790,848 (GRCm39)	missense	possibly damaging	0.94

Predicted Primers

PCR Primer
(F):5'- ATGAGAATTACCACCCAGGC -3'
(R):5'- CCTGCTGAGAAGCTGAATGG -3'

Sequencing Primer
(F):5'- TTTTGAGACAGGGACCCATGC -3'
(R):5'- CTGAGAAGCTGAATGGTTTGTTTG -3'

Posted On

2017-08-16