Mutagenetix > Incidental Mutation

Incidental Mutation 'R1706:Slc22a14'

190082

Institutional Source

Beutler Lab

Gene Symbol

Slc22a14

Ensembl Gene

ENSMUSG00000070280

Gene Name

solute carrier family 22 (organic cation transporter), member 14

Synonyms

LOC382113

MMRRC Submission

039739-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.050) question?

Stock #

R1706 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

118998521-119019496 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 119010050 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 15 (N15S)

Ref Sequence

ENSEMBL: ENSMUSP00000131982 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000093775] [ENSMUST00000127794] [ENSMUST00000170400]

AlphaFold

Q497L9

Predicted Effect

probably benign
Transcript: ENSMUST00000093775
AA Change: N15S

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000091289
Gene: ENSMUSG00000070280
AA Change: N15S

Domain	Start	End	E-Value	Type
transmembrane domain	68	90	N/A	INTRINSIC
Pfam:Sugar_tr	156	556	1.3e-28	PFAM
Pfam:MFS_1	178	514	7.8e-28	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000127794
AA Change: N15S

Predicted Effect

probably benign
Transcript: ENSMUST00000170400
AA Change: N15S

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000131982
Gene: ENSMUSG00000070280
AA Change: N15S

Domain	Start	End	E-Value	Type
transmembrane domain	68	90	N/A	INTRINSIC
Pfam:Sugar_tr	150	555	1.2e-28	PFAM
Pfam:MFS_1	178	514	7.6e-28	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 96.7%
20x: 93.6%

Validation Efficiency

100% (60/60)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 3. The encoded protein is a transmembrane protein which is thought to transport small molecules and since this protein is conserved among several species, it is suggested to have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921524L21Rik	T	C	18: 6,624,059 (GRCm39)		probably benign	Het
4931406C07Rik	G	A	9: 15,209,153 (GRCm39)	T47I	probably damaging	Het
Adcy2	T	A	13: 68,868,865 (GRCm39)	N558I	probably damaging	Het
Ago3	G	A	4: 126,264,085 (GRCm39)	P374S	probably damaging	Het
Ak8	T	C	2: 28,650,007 (GRCm39)	C345R	possibly damaging	Het
Akap8l	C	T	17: 32,551,457 (GRCm39)	R511H	probably damaging	Het
BC005624	T	C	2: 30,868,922 (GRCm39)	E84G	possibly damaging	Het
Cav1	T	C	6: 17,339,181 (GRCm39)	F89L	probably damaging	Het
Cfap206	G	A	4: 34,688,875 (GRCm39)	P593L	probably damaging	Het
Clcn6	G	A	4: 148,102,025 (GRCm39)	T353I	probably benign	Het
Cstl1	G	A	2: 148,593,079 (GRCm39)		probably null	Het
Cyp2d10	A	C	15: 82,289,783 (GRCm39)	S140A	probably damaging	Het
D130052B06Rik	G	A	11: 33,566,230 (GRCm39)	R18H	unknown	Het
Ddi2	A	G	4: 141,411,308 (GRCm39)	F535L	probably benign	Het
Dop1a	C	T	9: 86,436,133 (GRCm39)	T2383M	possibly damaging	Het
Duox1	A	G	2: 122,149,953 (GRCm39)	T115A	probably benign	Het
Ercc6l2	T	A	13: 64,020,272 (GRCm39)		probably benign	Het
Gm7052	A	G	17: 22,258,823 (GRCm39)		probably benign	Het
Gm9925	G	A	18: 74,198,573 (GRCm39)		probably benign	Het
Gnas	T	A	2: 174,141,768 (GRCm39)	S646T	possibly damaging	Het
Gpatch3	T	A	4: 133,302,484 (GRCm39)	C138*	probably null	Het
Igsf8	C	T	1: 172,144,972 (GRCm39)	R100C	probably damaging	Het
Kcnh3	A	G	15: 99,135,959 (GRCm39)	K652R	possibly damaging	Het
Kcnn4	T	A	7: 24,074,167 (GRCm39)	V77E	probably damaging	Het
Kif13b	T	A	14: 64,998,115 (GRCm39)		probably benign	Het
Lca5l	T	C	16: 95,977,164 (GRCm39)	N214S	probably benign	Het
Luc7l3	T	C	11: 94,188,582 (GRCm39)		probably benign	Het
Lypd3	T	C	7: 24,339,755 (GRCm39)	I274T	probably benign	Het
Macf1	A	G	4: 123,264,377 (GRCm39)		probably null	Het
Mchr1	A	G	15: 81,121,364 (GRCm39)	Y38C	probably damaging	Het
Mia2	T	A	12: 59,191,552 (GRCm39)	L716*	probably null	Het
Mki67	A	G	7: 135,302,295 (GRCm39)	L913P	probably benign	Het
Mug2	T	A	6: 122,013,191 (GRCm39)		probably benign	Het
Neu3	A	G	7: 99,472,563 (GRCm39)	L58P	probably damaging	Het
Or4p23	G	A	2: 88,576,482 (GRCm39)	P250L	probably damaging	Het
Or8h9	A	T	2: 86,789,424 (GRCm39)	I126N	probably damaging	Het
Pak1ip1	T	C	13: 41,166,164 (GRCm39)	V363A	probably benign	Het
Pcdhb16	A	G	18: 37,612,705 (GRCm39)	D555G	probably benign	Het
Pygb	G	A	2: 150,669,067 (GRCm39)	G671D	probably damaging	Het
Rab30	A	T	7: 92,478,875 (GRCm39)	I79L	possibly damaging	Het
Rab44	C	A	17: 29,357,080 (GRCm39)	T70K	probably damaging	Het
Rccd1	C	G	7: 79,970,411 (GRCm39)	G69R	possibly damaging	Het
Sema5b	T	C	16: 35,470,125 (GRCm39)	V329A	probably damaging	Het
Setd2	A	G	9: 110,378,932 (GRCm39)	S632G	probably benign	Het
Smurf2	G	A	11: 106,715,573 (GRCm39)	H632Y	probably damaging	Het
Syt10	C	T	15: 89,674,979 (GRCm39)	D456N	probably damaging	Het
Tex10	C	T	4: 48,456,800 (GRCm39)	R637Q	probably benign	Het
Tgm6	T	C	2: 129,987,079 (GRCm39)	C516R	possibly damaging	Het
Tmprss9	T	C	10: 80,734,021 (GRCm39)		probably benign	Het
Trim67	A	G	8: 125,521,160 (GRCm39)	N174S	probably damaging	Het
Ttc8	C	A	12: 98,910,142 (GRCm39)	T123K	probably benign	Het
Ugt1a7c	T	A	1: 88,023,447 (GRCm39)	M202K	probably damaging	Het
Vmn2r7	T	A	3: 64,598,880 (GRCm39)	H559L	possibly damaging	Het
Zfp511	A	G	7: 139,617,192 (GRCm39)	D96G	probably benign	Het
Zfp868	A	G	8: 70,065,060 (GRCm39)	Y92H	probably benign	Het
Zzz3	T	A	3: 152,154,735 (GRCm39)	D633E	probably damaging	Het

Other mutations in Slc22a14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00338:Slc22a14	APN	9	119,007,579 (GRCm39)	missense	possibly damaging	0.58
R0086:Slc22a14	UTSW	9	119,051,804 (GRCm39)	critical splice donor site	probably benign
R0505:Slc22a14	UTSW	9	119,001,100 (GRCm39)	splice site	probably benign
R0593:Slc22a14	UTSW	9	118,998,919 (GRCm39)	missense	probably benign	0.15
R0597:Slc22a14	UTSW	9	119,001,190 (GRCm39)	missense	probably damaging	0.99
R0674:Slc22a14	UTSW	9	119,007,608 (GRCm39)	missense	probably damaging	1.00
R1290:Slc22a14	UTSW	9	119,007,518 (GRCm39)	missense	probably damaging	1.00
R1459:Slc22a14	UTSW	9	119,052,827 (GRCm39)	missense	possibly damaging	0.70
R3980:Slc22a14	UTSW	9	119,007,552 (GRCm39)	missense	probably benign	0.02
R4166:Slc22a14	UTSW	9	119,008,934 (GRCm39)	missense	possibly damaging	0.53
R4166:Slc22a14	UTSW	9	119,007,498 (GRCm39)	missense	probably benign	0.00
R4574:Slc22a14	UTSW	9	119,008,561 (GRCm39)	missense	probably damaging	0.99
R4959:Slc22a14	UTSW	9	119,003,101 (GRCm39)	small deletion	probably benign
R4973:Slc22a14	UTSW	9	119,003,101 (GRCm39)	small deletion	probably benign
R5273:Slc22a14	UTSW	9	118,999,704 (GRCm39)	missense	probably benign	0.08
R5330:Slc22a14	UTSW	9	119,059,662 (GRCm39)	missense	probably damaging	1.00
R5331:Slc22a14	UTSW	9	119,059,662 (GRCm39)	missense	probably damaging	1.00
R5543:Slc22a14	UTSW	9	119,002,674 (GRCm39)	missense	probably benign	0.01
R5801:Slc22a14	UTSW	9	119,001,149 (GRCm39)	missense	probably benign	0.01
R6521:Slc22a14	UTSW	9	119,049,835 (GRCm39)	splice site	probably null
R6622:Slc22a14	UTSW	9	118,999,643 (GRCm39)	missense	possibly damaging	0.81
R6948:Slc22a14	UTSW	9	119,060,482 (GRCm39)	missense	probably damaging	1.00
R7027:Slc22a14	UTSW	9	119,060,281 (GRCm39)	splice site	probably null
R7731:Slc22a14	UTSW	9	118,999,677 (GRCm39)	missense	possibly damaging	0.95
R7985:Slc22a14	UTSW	9	118,999,704 (GRCm39)	missense	probably benign	0.01
R8412:Slc22a14	UTSW	9	119,009,922 (GRCm39)	missense	probably benign	0.00
R8508:Slc22a14	UTSW	9	119,009,651 (GRCm39)	missense	probably damaging	1.00
R8674:Slc22a14	UTSW	9	119,007,467 (GRCm39)	missense	probably null	1.00
R8773:Slc22a14	UTSW	9	119,059,290 (GRCm39)	intron	probably benign
R8950:Slc22a14	UTSW	9	118,998,778 (GRCm39)	missense	possibly damaging	0.71
R9484:Slc22a14	UTSW	9	119,009,615 (GRCm39)	missense	probably damaging	1.00
R9633:Slc22a14	UTSW	9	119,008,528 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CTGGAATGTGCCAAATTCCCCAATG -3'
(R):5'- CCAGAGATGCCTCAGATGTGTGAAC -3'

Sequencing Primer
(F):5'- TGGCATCCATAACACTGGC -3'
(R):5'- AGCTCCTGGCATTCATGCAG -3'

Posted On

2014-05-14