Mutagenetix > Incidental Mutation

Incidental Mutation 'R9484:Slc22a14'

716453

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

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.060) question?

Stock #

R9484 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

119169455-119365553 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 119180549 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 160 (Y160C)

Ref Sequence

ENSEMBL: ENSMUSP00000091289 (fasta)

Gene Model

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

AlphaFold

Q497L9

Predicted Effect

probably damaging
Transcript: ENSMUST00000093775
AA Change: Y160C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000091289
Gene: ENSMUSG00000070280
AA Change: Y160C

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

probably benign
Transcript: ENSMUST00000127794

Predicted Effect

probably damaging
Transcript: ENSMUST00000170400
AA Change: Y160C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000131982
Gene: ENSMUSG00000070280
AA Change: Y160C

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

Coding Region Coverage

1x: 99.9%
3x: 99.8%
10x: 99.2%
20x: 97.1%

Validation Efficiency

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: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acads	A	T	5: 115,112,786	C151S	probably damaging	Het
Actr8	T	C	14: 29,986,344	I193T	probably benign	Het
Btbd2	T	C	10: 80,644,269	N419S	probably benign	Het
Cacna2d1	T	A	5: 16,356,833	W821R	probably damaging	Het
Cadps2	T	C	6: 23,626,647	Y214C	probably benign	Het
Calu	T	A	6: 29,366,163	L180Q	probably damaging	Het
Corin	C	T	5: 72,339,937	V615I	probably damaging	Het
Cyp8b1	A	T	9: 121,915,917	D116E	probably benign	Het
D630036H23Rik	C	A	12: 36,381,712	A96S	unknown	Het
Ddx24	A	T	12: 103,411,296	Y717N	probably damaging	Het
Dmap1	G	T	4: 117,676,111	Q249K	probably benign	Het
Dnah10	T	A	5: 124,823,444	W3922R	probably damaging	Het
Dnah14	T	C	1: 181,690,208	F2036L	probably benign	Het
Dnah14	T	C	1: 181,797,746	I4064T	probably benign	Het
Dock9	A	C	14: 121,581,432	V1546G	probably damaging	Het
Eif3a	A	T	19: 60,766,568	S1059T	unknown	Het
Ep300	A	G	15: 81,636,825	E1262G	unknown	Het
Evl	T	A	12: 108,686,457	I387N	probably damaging	Het
Fat2	A	C	11: 55,309,926	V774G	probably damaging	Het
Fez1	T	A	9: 36,843,797	Y31N	probably benign	Het
Fkbp10	A	G	11: 100,423,134	I435V	probably damaging	Het
Flnb	A	G	14: 7,929,004	D1911G	probably benign	Het
Fnbp1	T	C	2: 31,083,026	Y154C	probably benign	Het
Fndc10	T	C	4: 155,695,039	I180T	possibly damaging	Het
Frmd4a	G	A	2: 4,604,215	V965I	possibly damaging	Het
Gabrr2	A	G	4: 33,071,352	H64R	possibly damaging	Het
Glis3	T	C	19: 28,531,003	D527G	probably damaging	Het
Gm2022	A	T	12: 87,895,479	Q37L	possibly damaging	Het
H2-Ob	T	A	17: 34,241,015	F33L	probably damaging	Het
Hbb-bh1	C	T	7: 103,843,032	E27K	probably benign	Het
Ifnb1	T	A	4: 88,522,678	T33S	probably benign	Het
Igkv4-80	T	A	6: 69,016,782	T42S	probably damaging	Het
Irs2	C	T	8: 11,007,334	G366D	probably damaging	Het
Kcnk2	CAAA	CAA	1: 189,256,694		probably null	Het
Krtap5-3	T	A	7: 142,202,331	C302S	unknown	Het
Lgi1	A	G	19: 38,306,309	K510E	probably benign	Het
Lgi2	T	A	5: 52,538,594	D341V	probably benign	Het
Lin7c	T	C	2: 109,894,468	I14T	probably benign	Het
Lrrc19	A	T	4: 94,643,336	M13K	probably benign	Het
Lrrc69	T	C	4: 14,666,012	I315M	probably benign	Het
Myo5c	A	T	9: 75,297,488	D1541V	probably damaging	Het
Mypn	T	G	10: 63,167,240	M373L	probably benign	Het
Nckipsd	C	A	9: 108,812,638	H333N	probably damaging	Het
Nrg2	A	T	18: 36,024,348	L428Q	probably null	Het
Olfr1367	C	A	13: 21,347,417	T163K	probably damaging	Het
Olfr235	T	C	19: 12,268,371	I47T	possibly damaging	Het
Olfr53	T	C	7: 140,651,991	L4S	probably benign	Het
Otogl	T	A	10: 107,822,033		probably null	Het
Otogl	C	T	10: 107,901,295	G86D	probably damaging	Het
Papln	A	T	12: 83,791,844	Q1249L	probably benign	Het
Plxna2	G	T	1: 194,644,894	G379C	probably damaging	Het
Pofut2	T	C	10: 77,259,426	I35T	probably benign	Het
Pros1	A	G	16: 62,924,524	T501A	possibly damaging	Het
Rapgef1	T	C	2: 29,735,809	S1042P	possibly damaging	Het
Rps6kb1	C	T	11: 86,517,617	E185K	probably damaging	Het
Slc13a2	A	T	11: 78,403,407	L216Q	probably damaging	Het
Slc22a4	T	A	11: 53,988,947	I429F	possibly damaging	Het
Slc26a3	A	G	12: 31,461,786	K457E	probably damaging	Het
Slc47a2	T	C	11: 61,336,234	I169M	possibly damaging	Het
Slco1a1	C	T	6: 141,908,946	V660I	probably benign	Het
Smyd1	A	G	6: 71,225,466	Y252H	probably damaging	Het
Soga3	G	A	10: 29,196,973	D754N	probably damaging	Het
Spp2	A	T	1: 88,406,973		probably benign	Het
Stra8	T	A	6: 34,934,186	W250R	probably damaging	Het
Syne1	A	C	10: 5,220,359	L5183R	probably damaging	Het
Tdrd9	T	C	12: 112,046,250	S1203P	probably damaging	Het
Th	C	A	7: 142,899,883	E27*	probably null	Het
Thada	C	A	17: 84,429,191	L887F	probably damaging	Het
Timm23	T	C	14: 32,180,629	T186A	probably benign	Het
Tmem132b	A	T	5: 125,783,356	E555V	probably damaging	Het
Tnik	A	T	3: 28,594,944	Q457L	unknown	Het
Uba7	C	A	9: 107,983,838	H942Q	probably benign	Het
Upf2	T	C	2: 5,961,267	S233P	unknown	Het
Urm1	T	A	2: 29,842,748	N72K	probably damaging	Het
Usp10	T	C	8: 119,948,765	S508P	possibly damaging	Het
Usp37	G	A	1: 74,459,922	P632S	probably damaging	Het
Wdr77	T	A	3: 105,965,088	N209K	probably benign	Het
Zbtb24	C	T	10: 41,451,433	T105M	probably benign	Het
Zfp341	T	A	2: 154,643,843	I671N	probably damaging	Het
Zfp414	A	G	17: 33,630,010	T73A	probably benign	Het
Zfp574	A	T	7: 25,081,979	I809F	possibly damaging	Het
Zfp62	T	C	11: 49,217,281	I733T	probably damaging	Het
Zfp719	A	G	7: 43,590,157	I390V	possibly damaging	Het

Other mutations in Slc22a14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00338:Slc22a14	APN	9	119178513	missense	possibly damaging	0.58
R0086:Slc22a14	UTSW	9	119222738	critical splice donor site	probably benign
R0505:Slc22a14	UTSW	9	119172034	splice site	probably benign
R0593:Slc22a14	UTSW	9	119169851	missense	probably benign	0.15
R0597:Slc22a14	UTSW	9	119172124	missense	probably damaging	0.99
R0674:Slc22a14	UTSW	9	119178542	missense	probably damaging	1.00
R1290:Slc22a14	UTSW	9	119178452	missense	probably damaging	1.00
R1459:Slc22a14	UTSW	9	119223761	missense	possibly damaging	0.70
R1706:Slc22a14	UTSW	9	119180984	missense	probably benign	0.06
R3980:Slc22a14	UTSW	9	119178486	missense	probably benign	0.02
R4166:Slc22a14	UTSW	9	119178432	missense	probably benign	0.00
R4166:Slc22a14	UTSW	9	119179868	missense	possibly damaging	0.53
R4574:Slc22a14	UTSW	9	119179495	missense	probably damaging	0.99
R4959:Slc22a14	UTSW	9	119174035	small deletion	probably benign
R4973:Slc22a14	UTSW	9	119174035	small deletion	probably benign
R5273:Slc22a14	UTSW	9	119170638	missense	probably benign	0.08
R5330:Slc22a14	UTSW	9	119230596	missense	probably damaging	1.00
R5331:Slc22a14	UTSW	9	119230596	missense	probably damaging	1.00
R5543:Slc22a14	UTSW	9	119173608	missense	probably benign	0.01
R5801:Slc22a14	UTSW	9	119172083	missense	probably benign	0.01
R6521:Slc22a14	UTSW	9	119220769	splice site	probably null
R6622:Slc22a14	UTSW	9	119170577	missense	possibly damaging	0.81
R6948:Slc22a14	UTSW	9	119231416	missense	probably damaging	1.00
R7027:Slc22a14	UTSW	9	119231215	splice site	probably null
R7731:Slc22a14	UTSW	9	119170611	missense	possibly damaging	0.95
R7985:Slc22a14	UTSW	9	119170638	missense	probably benign	0.01
R8412:Slc22a14	UTSW	9	119180856	missense	probably benign	0.00
R8508:Slc22a14	UTSW	9	119180585	missense	probably damaging	1.00
R8674:Slc22a14	UTSW	9	119178401	missense	probably null	1.00
R8773:Slc22a14	UTSW	9	119230224	intron	probably benign
R8950:Slc22a14	UTSW	9	119169710	missense	possibly damaging	0.71
R9633:Slc22a14	UTSW	9	119179462	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AAATGCATGCTCATTTCCTGGC -3'
(R):5'- TCAGAGGCCCTACTGTAACAC -3'

Sequencing Primer
(F):5'- TTCCTGGCTTAAGAAAATCAGGGC -3'
(R):5'- TGTAACACCAGCTGGATCCTG -3'

Posted On

2022-07-18