Mutagenetix > Incidental Mutation

Incidental Mutation 'R5927:Slc16a14'

459920

Institutional Source

Beutler Lab

Gene Symbol

Slc16a14

Ensembl Gene

ENSMUSG00000026220

Gene Name

solute carrier family 16 (monocarboxylic acid transporters), member 14

Synonyms

1110004H10Rik

MMRRC Submission

044122-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.090) question?

Stock #

R5927 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

84883619-84912855 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 84889988 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 439 (H439R)

Ref Sequence

ENSEMBL: ENSMUSP00000027422 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027422]

AlphaFold

Q8K1C7

Predicted Effect

possibly damaging
Transcript: ENSMUST00000027422
AA Change: H439R

PolyPhen 2 Score 0.907 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000027422
Gene: ENSMUSG00000026220
AA Change: H439R

Domain	Start	End	E-Value	Type
Pfam:MFS_1	42	427	6.7e-42	PFAM
Pfam:MFS_1	419	509	7.9e-10	PFAM

Meta Mutation Damage Score

0.0985

Coding Region Coverage

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

Validation Efficiency

100% (73/73)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acadm	T	A	3: 153,644,745 (GRCm39)	I60F	probably damaging	Het
Ankrd26	A	G	6: 118,484,597 (GRCm39)		probably null	Het
Arhgdib	A	T	6: 136,901,136 (GRCm39)	W198R	probably damaging	Het
Atad5	T	A	11: 80,018,111 (GRCm39)	I1354N	probably damaging	Het
Ccdc146	T	A	5: 21,513,619 (GRCm39)	K500*	probably null	Het
Cdk11b	G	A	4: 155,732,697 (GRCm39)		probably benign	Het
Cmip	A	T	8: 117,984,048 (GRCm39)	T70S	possibly damaging	Het
Col22a1	G	T	15: 71,878,815 (GRCm39)	A114E	probably damaging	Het
Cpeb1	T	C	7: 81,011,428 (GRCm39)	D171G	possibly damaging	Het
Crebzf	C	T	7: 90,093,531 (GRCm39)		probably benign	Het
Cybb	C	G	X: 9,316,989 (GRCm39)	D246H	probably benign	Het
D630036H23Rik	C	A	12: 36,431,671 (GRCm39)		probably benign	Het
Dnah5	A	T	15: 28,335,864 (GRCm39)	T2277S	probably benign	Het
Dysf	T	A	6: 84,184,194 (GRCm39)	F2083Y	probably damaging	Het
Elavl4	T	A	4: 110,147,440 (GRCm39)		probably benign	Het
Elp3	A	G	14: 65,819,626 (GRCm39)	Y111H	probably damaging	Het
Eps8l2	A	T	7: 140,936,259 (GRCm39)	Q243L	probably benign	Het
Eri2	C	A	7: 119,385,291 (GRCm39)	L403F	probably damaging	Het
Fgfr4	T	A	13: 55,314,700 (GRCm39)	N614K	probably damaging	Het
Gm5108	T	G	5: 68,134,214 (GRCm39)	I74S	unknown	Het
Gpn1	T	C	5: 31,658,235 (GRCm39)	F130L	probably damaging	Het
Gpr176	T	A	2: 118,203,521 (GRCm39)	I50F	probably benign	Het
Gramd1a	A	G	7: 30,839,246 (GRCm39)	S221P	probably benign	Het
Hivep3	A	G	4: 119,954,305 (GRCm39)	T874A	possibly damaging	Het
Igkv12-40	A	G	6: 69,856,383 (GRCm39)		noncoding transcript	Het
Itgb2	C	A	10: 77,381,868 (GRCm39)	P57T	probably damaging	Het
Kcmf1	T	A	6: 72,819,988 (GRCm39)	D286V	possibly damaging	Het
Kcnt1	T	A	2: 25,799,388 (GRCm39)		probably benign	Het
Kif15	A	G	9: 122,846,326 (GRCm39)	S76G	probably benign	Het
Kpna3	C	T	14: 61,622,096 (GRCm39)	V223I	probably damaging	Het
Krt80	A	G	15: 101,262,089 (GRCm39)		probably benign	Het
Lama4	A	G	10: 38,948,808 (GRCm39)	Y857C	probably damaging	Het
Lcorl	G	T	5: 45,882,766 (GRCm39)		probably benign	Het
Map4k3	A	G	17: 80,921,348 (GRCm39)	V528A	probably benign	Het
Mmp8	T	A	9: 7,563,203 (GRCm39)	N255K	possibly damaging	Het
Npat	A	T	9: 53,473,521 (GRCm39)	K438*	probably null	Het
Or4a73	T	A	2: 89,421,444 (GRCm39)	N5I	possibly damaging	Het
P4htm	T	C	9: 108,474,582 (GRCm39)	Y61C	probably damaging	Het
Pgap6	T	C	17: 26,340,972 (GRCm39)	Y692H	probably benign	Het
Polr3h	G	T	15: 81,801,480 (GRCm39)		probably null	Het
Prlr	C	T	15: 10,322,532 (GRCm39)	T176I	probably benign	Het
Psme4	T	G	11: 30,754,294 (GRCm39)	F184V	possibly damaging	Het
Ptgfrn	A	T	3: 100,967,968 (GRCm39)	F542I	possibly damaging	Het
Rock1	T	C	18: 10,116,792 (GRCm39)	E448G	probably damaging	Het
Rpf1	A	T	3: 146,225,218 (GRCm39)		probably null	Het
Sectm1b	T	C	11: 120,946,500 (GRCm39)	I132V	probably benign	Het
Sestd1	T	A	2: 77,017,503 (GRCm39)	H688L	probably benign	Het
Sidt2	T	C	9: 45,855,752 (GRCm39)	Y530C	probably damaging	Het
Sin3a	A	T	9: 57,018,395 (GRCm39)	K938M	probably damaging	Het
Sin3b	C	A	8: 73,476,506 (GRCm39)	R647S	probably benign	Het
Stc1	T	C	14: 69,269,822 (GRCm39)	V134A	probably benign	Het
Stk11ip	G	A	1: 75,501,335 (GRCm39)	V24I	possibly damaging	Het
Tbx6	G	A	7: 126,384,025 (GRCm39)	A359T	possibly damaging	Het
Thra	G	A	11: 98,654,514 (GRCm39)	V295I	possibly damaging	Het
Tnr	T	C	1: 159,740,336 (GRCm39)	M1170T	probably damaging	Het
Tpcn2	T	A	7: 144,832,521 (GRCm39)	I112F	probably damaging	Het
Trdv2-2	T	C	14: 54,198,998 (GRCm39)	L96P	probably damaging	Het
Trim24	T	A	6: 37,935,504 (GRCm39)	W832R	probably damaging	Het
Usp4	T	G	9: 108,268,959 (GRCm39)	S891A	probably benign	Het
Vmn1r88	A	T	7: 12,912,440 (GRCm39)	R265S	probably benign	Het
Vmn2r118	A	G	17: 55,931,494 (GRCm39)	L60S	probably benign	Het
Wdr74	T	C	19: 8,717,197 (GRCm39)	C220R	possibly damaging	Het
Xpo1	A	T	11: 23,218,653 (GRCm39)		probably benign	Het
Xpo1	A	T	11: 23,218,656 (GRCm39)		probably benign	Het
Zfp850	C	A	7: 27,689,620 (GRCm39)	G196V	probably benign	Het

Other mutations in Slc16a14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00942:Slc16a14	APN	1	84,900,592 (GRCm39)	missense	probably damaging	0.99
IGL01563:Slc16a14	APN	1	84,889,908 (GRCm39)	splice site	probably benign
R0315:Slc16a14	UTSW	1	84,890,217 (GRCm39)	missense	possibly damaging	0.46
R0380:Slc16a14	UTSW	1	84,907,251 (GRCm39)	missense	possibly damaging	0.72
R1469:Slc16a14	UTSW	1	84,907,182 (GRCm39)	missense	probably damaging	1.00
R1469:Slc16a14	UTSW	1	84,907,182 (GRCm39)	missense	probably damaging	1.00
R1837:Slc16a14	UTSW	1	84,890,120 (GRCm39)	missense	probably benign	0.02
R2149:Slc16a14	UTSW	1	84,885,120 (GRCm39)	missense	probably damaging	1.00
R2293:Slc16a14	UTSW	1	84,890,564 (GRCm39)	missense	probably benign
R3790:Slc16a14	UTSW	1	84,907,001 (GRCm39)	unclassified	probably benign
R4016:Slc16a14	UTSW	1	84,890,228 (GRCm39)	nonsense	probably null
R4596:Slc16a14	UTSW	1	84,907,078 (GRCm39)	missense	probably damaging	1.00
R4637:Slc16a14	UTSW	1	84,885,003 (GRCm39)	missense	possibly damaging	0.86
R4723:Slc16a14	UTSW	1	84,890,741 (GRCm39)	missense	probably damaging	1.00
R5137:Slc16a14	UTSW	1	84,890,318 (GRCm39)	missense	probably damaging	1.00
R5262:Slc16a14	UTSW	1	84,890,612 (GRCm39)	missense	probably benign	0.00
R5410:Slc16a14	UTSW	1	84,885,145 (GRCm39)	missense	probably damaging	0.98
R5968:Slc16a14	UTSW	1	84,890,226 (GRCm39)	missense	possibly damaging	0.70
R6052:Slc16a14	UTSW	1	84,890,430 (GRCm39)	missense	possibly damaging	0.75
R6264:Slc16a14	UTSW	1	84,885,130 (GRCm39)	missense	probably benign	0.30
R6290:Slc16a14	UTSW	1	84,885,106 (GRCm39)	missense	probably benign	0.10
R7383:Slc16a14	UTSW	1	84,890,292 (GRCm39)	missense	probably damaging	1.00
R7390:Slc16a14	UTSW	1	84,907,187 (GRCm39)	missense	probably benign	0.25
R7535:Slc16a14	UTSW	1	84,890,843 (GRCm39)	missense	probably damaging	1.00
R8326:Slc16a14	UTSW	1	84,890,066 (GRCm39)	missense	possibly damaging	0.94
R8669:Slc16a14	UTSW	1	84,900,605 (GRCm39)	missense	probably benign	0.00
R8784:Slc16a14	UTSW	1	84,890,784 (GRCm39)	missense	probably benign	0.01
R9409:Slc16a14	UTSW	1	84,907,116 (GRCm39)	nonsense	probably null
R9469:Slc16a14	UTSW	1	84,900,612 (GRCm39)	missense	probably benign	0.05

Predicted Primers

PCR Primer
(F):5'- TTTGGACCAGTTTAGGCTGAC -3'
(R):5'- TGTATCAGCGTCTGGAATGTC -3'

Sequencing Primer
(F):5'- TCAAGCATGTGTCACCGTG -3'
(R):5'- GGAATGTCTTCCTCATCGCTAAC -3'

Posted On

2017-02-28