Mutagenetix > Incidental Mutation

Incidental Mutation 'R1445:Slc26a8'

158829

Institutional Source

Beutler Lab

Gene Symbol

Slc26a8

Ensembl Gene

ENSMUSG00000036196

Gene Name

solute carrier family 26, member 8

Synonyms

MMRRC Submission

039500-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.377) question?

Stock #

R1445 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

28856757-28909207 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 28867187 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 545 (V545M)

Ref Sequence

ENSEMBL: ENSMUSP00000110412 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000114764]

AlphaFold

Q8R0C3

Predicted Effect

possibly damaging
Transcript: ENSMUST00000114764
AA Change: V545M

PolyPhen 2 Score 0.719 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000110412
Gene: ENSMUSG00000036196
AA Change: V545M

Domain	Start	End	E-Value	Type
Pfam:Sulfate_transp	90	491	1.2e-72	PFAM
low complexity region	494	509	N/A	INTRINSIC
Pfam:STAS	542	792	7.3e-16	PFAM
low complexity region	881	896	N/A	INTRINSIC
low complexity region	923	958	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145224

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 98.8%
3x: 97.7%
10x: 93.9%
20x: 84.0%

Validation Efficiency

96% (101/105)

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 SLC26 gene family of anion transporters. Family members are well conserved in gene structure and protein length yet have markedly different tissue expression patterns. The expression of this gene appears to be restricted to spermatocytes. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jul 2010]
PHENOTYPE: Mice homozygous for a targeted allele exhibit male sterility associated with sperm immotility, abnormal flagella and reduced acrosomal reaction. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700061I17Rik	G	T	3: 116,861,385 (GRCm39)		noncoding transcript	Het
2300003K06Rik	G	T	11: 99,728,793 (GRCm39)	Q17K	probably benign	Het
Abca16	T	C	7: 120,119,256 (GRCm39)	V999A	probably benign	Het
Actn3	C	T	19: 4,915,483 (GRCm39)		probably benign	Het
Agap2	T	A	10: 126,926,981 (GRCm39)		probably benign	Het
Ago3	C	A	4: 126,265,580 (GRCm39)	R278L	probably benign	Het
Aldh1a2	T	C	9: 71,192,492 (GRCm39)	V449A	possibly damaging	Het
Alkbh2	C	T	5: 114,262,287 (GRCm39)	E148K	probably damaging	Het
Aplnr	A	G	2: 84,967,353 (GRCm39)	Y126C	probably damaging	Het
Apob	T	C	12: 8,066,084 (GRCm39)	I4351T	possibly damaging	Het
Ash1l	T	C	3: 88,914,659 (GRCm39)	L1763P	probably benign	Het
Aspn	T	C	13: 49,710,849 (GRCm39)	S165P	possibly damaging	Het
Atg13	A	T	2: 91,510,335 (GRCm39)	V349E	probably damaging	Het
Atp1b2	T	A	11: 69,493,309 (GRCm39)		probably null	Het
B3glct	A	T	5: 149,677,604 (GRCm39)	D411V	probably damaging	Het
Bcar3	A	T	3: 122,316,840 (GRCm39)	I255F	probably damaging	Het
Cacna1b	G	A	2: 24,608,148 (GRCm39)		probably benign	Het
Cep164	T	G	9: 45,690,198 (GRCm39)	E675A	possibly damaging	Het
Chd1l	C	T	3: 97,490,047 (GRCm39)	E503K	probably benign	Het
Chst8	C	A	7: 34,447,593 (GRCm39)	M8I	possibly damaging	Het
Clec4n	A	G	6: 123,212,475 (GRCm39)	E67G	probably benign	Het
Cobll1	A	T	2: 64,929,480 (GRCm39)	D653E	probably damaging	Het
Col9a1	T	C	1: 24,276,579 (GRCm39)		probably null	Het
Crip2	T	C	12: 113,107,124 (GRCm39)	L30P	probably damaging	Het
Ctbp1	C	T	5: 33,418,407 (GRCm39)	V22I	probably benign	Het
Cwc22	T	C	2: 77,747,521 (GRCm39)		probably benign	Het
Cyp4a32	C	A	4: 115,460,147 (GRCm39)	Y119*	probably null	Het
Dido1	G	T	2: 180,313,263 (GRCm39)	A463E	possibly damaging	Het
Dnah7a	G	A	1: 53,567,956 (GRCm39)	P1880L	probably benign	Het
Dock2	T	A	11: 34,189,705 (GRCm39)	T1489S	probably benign	Het
Dsp	A	G	13: 38,375,907 (GRCm39)	T1231A	probably damaging	Het
Eif2ak1	G	T	5: 143,810,717 (GRCm39)		probably benign	Het
Entrep1	G	A	19: 23,998,998 (GRCm39)	T140M	probably damaging	Het
Epc1	A	T	18: 6,452,360 (GRCm39)	M233K	probably damaging	Het
Gigyf2	A	G	1: 87,371,360 (GRCm39)		probably benign	Het
Greb1	T	G	12: 16,757,852 (GRCm39)	H58P	probably damaging	Het
Gtpbp1	T	C	15: 79,597,649 (GRCm39)	I348T	possibly damaging	Het
Hck	A	T	2: 152,970,192 (GRCm39)	N64Y	probably benign	Het
Herc2	T	C	7: 55,818,744 (GRCm39)	S2812P	probably damaging	Het
Inpp4b	T	A	8: 82,679,463 (GRCm39)		probably null	Het
Kcnq5	A	C	1: 21,475,248 (GRCm39)	S473A	probably benign	Het
Lrat	T	G	3: 82,810,676 (GRCm39)	D115A	probably damaging	Het
Lyst	A	G	13: 13,814,639 (GRCm39)	I1131M	possibly damaging	Het
Man2a2	T	C	7: 80,018,310 (GRCm39)	D160G	probably benign	Het
Marf1	C	T	16: 13,933,688 (GRCm39)	D1567N	probably benign	Het
Mars1	T	C	10: 127,133,857 (GRCm39)	D680G	possibly damaging	Het
Mat1a	T	C	14: 40,843,797 (GRCm39)	S339P	probably damaging	Het
Megf8	T	C	7: 25,042,081 (GRCm39)	S1300P	probably damaging	Het
Mga	T	C	2: 119,733,179 (GRCm39)	L9S	probably damaging	Het
Mllt6	T	C	11: 97,563,277 (GRCm39)		probably benign	Het
Mrpl37	A	G	4: 106,921,692 (GRCm39)	L179P	probably benign	Het
Mtnr1a	G	T	8: 45,540,782 (GRCm39)	V248L	probably benign	Het
Mylk	T	C	16: 34,635,835 (GRCm39)	S19P	possibly damaging	Het
Or11g1	A	G	14: 50,651,858 (GRCm39)	T286A	probably damaging	Het
Pacc1	A	G	1: 191,080,559 (GRCm39)		probably benign	Het
Parp8	A	T	13: 117,161,886 (GRCm39)		probably null	Het
Pcnx2	T	C	8: 126,479,023 (GRCm39)	D2075G	probably damaging	Het
Pigo	A	T	4: 43,021,460 (GRCm39)	I494K	probably benign	Het
Pkd1l1	A	T	11: 8,820,313 (GRCm39)	D1217E	probably benign	Het
Pkhd1l1	T	C	15: 44,369,040 (GRCm39)	V895A	probably benign	Het
Plcb4	A	T	2: 135,842,109 (GRCm39)	H1031L	possibly damaging	Het
Plxnb1	A	G	9: 108,937,989 (GRCm39)	K1245R	probably null	Het
Pold1	C	T	7: 44,192,181 (GRCm39)		probably benign	Het
Ptprq	T	C	10: 107,498,423 (GRCm39)	I885V	probably damaging	Het
Ptprz1	A	G	6: 23,050,473 (GRCm39)	D1398G	probably damaging	Het
Pygm	G	A	19: 6,439,917 (GRCm39)	A364T	probably benign	Het
Rbl1	T	C	2: 157,035,018 (GRCm39)	N354S	probably benign	Het
Scgb2b19	C	T	7: 32,979,037 (GRCm39)		probably null	Het
Slc27a1	T	A	8: 72,036,757 (GRCm39)		probably null	Het
Smpd1	A	G	7: 105,205,881 (GRCm39)	D416G	possibly damaging	Het
Sorbs3	A	G	14: 70,431,095 (GRCm39)	V284A	probably benign	Het
Stfa2l1	T	C	16: 35,982,154 (GRCm39)	V75A	probably damaging	Het
Syndig1	A	G	2: 149,772,841 (GRCm39)	D166G	probably damaging	Het
Tcp10a	G	A	17: 7,593,406 (GRCm39)		probably null	Het
Themis2	T	A	4: 132,510,212 (GRCm39)	I663F	possibly damaging	Het
Thrap3	T	C	4: 126,070,129 (GRCm39)	Q586R	probably damaging	Het
Tinag	C	A	9: 76,952,798 (GRCm39)	C62F	probably damaging	Het
Tmod1	T	C	4: 46,090,884 (GRCm39)	Y146H	probably damaging	Het
Tmprss4	T	A	9: 45,095,683 (GRCm39)	I54F	possibly damaging	Het
Tnks	A	C	8: 35,301,757 (GRCm39)		probably benign	Het
Trim43a	GATTTATTTATTTATTTATTTATTTATTTATTTATTTATT	GATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATT	9: 88,465,042 (GRCm39)		probably benign	Het
Trpc6	A	G	9: 8,680,538 (GRCm39)	E844G	probably benign	Het
Ubtd2	C	T	11: 32,466,125 (GRCm39)	R115W	probably damaging	Het
Ubxn6	T	C	17: 56,376,042 (GRCm39)	D373G	probably benign	Het
Upf1	T	A	8: 70,794,174 (GRCm39)	Q244L	probably benign	Het
Usp33	A	G	3: 152,074,271 (GRCm39)	I372M	probably damaging	Het
Usp34	A	G	11: 23,301,629 (GRCm39)	E351G	probably damaging	Het
Utrn	A	G	10: 12,554,318 (GRCm39)		probably benign	Het
Vmn1r78	A	G	7: 11,886,508 (GRCm39)	K40E	possibly damaging	Het
Vmn2r7	T	A	3: 64,632,223 (GRCm39)	M80L	probably benign	Het
Vps13a	G	T	19: 16,678,602 (GRCm39)	Y1126*	probably null	Het
Wfdc11	T	C	2: 164,506,366 (GRCm39)	N60S	probably benign	Het
Wnk2	C	T	13: 49,224,586 (GRCm39)	D992N	probably damaging	Het
Zpbp2	C	A	11: 98,444,670 (GRCm39)	T66K	probably damaging	Het

Other mutations in Slc26a8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01466:Slc26a8	APN	17	28,873,922 (GRCm39)	missense	probably benign	0.01
IGL02041:Slc26a8	APN	17	28,861,225 (GRCm39)	missense	probably damaging	1.00
IGL02389:Slc26a8	APN	17	28,857,624 (GRCm39)	missense	probably benign	0.00
E0370:Slc26a8	UTSW	17	28,861,361 (GRCm39)	missense	possibly damaging	0.77
FR4449:Slc26a8	UTSW	17	28,857,290 (GRCm39)	small deletion	probably benign
R1028:Slc26a8	UTSW	17	28,891,772 (GRCm39)	missense	probably damaging	1.00
R1501:Slc26a8	UTSW	17	28,857,536 (GRCm39)	missense	possibly damaging	0.73
R1606:Slc26a8	UTSW	17	28,857,455 (GRCm39)	missense	possibly damaging	0.73
R1819:Slc26a8	UTSW	17	28,903,808 (GRCm39)	missense	probably benign	0.31
R1950:Slc26a8	UTSW	17	28,863,614 (GRCm39)	missense	probably benign	0.06
R1973:Slc26a8	UTSW	17	28,882,579 (GRCm39)	missense	probably benign	0.01
R2203:Slc26a8	UTSW	17	28,866,981 (GRCm39)	missense	probably benign	0.06
R3912:Slc26a8	UTSW	17	28,863,753 (GRCm39)	missense	possibly damaging	0.92
R4176:Slc26a8	UTSW	17	28,866,973 (GRCm39)	missense	probably benign	0.04
R4539:Slc26a8	UTSW	17	28,878,591 (GRCm39)	missense	probably benign	0.00
R4661:Slc26a8	UTSW	17	28,857,658 (GRCm39)	missense	probably benign	0.04
R4766:Slc26a8	UTSW	17	28,857,635 (GRCm39)	missense	probably benign	0.01
R4850:Slc26a8	UTSW	17	28,873,857 (GRCm39)	missense	probably benign	0.01
R4867:Slc26a8	UTSW	17	28,882,608 (GRCm39)	missense	probably benign	0.05
R5521:Slc26a8	UTSW	17	28,873,833 (GRCm39)	missense	probably benign	0.10
R5713:Slc26a8	UTSW	17	28,880,853 (GRCm39)	missense	probably benign	0.01
R6092:Slc26a8	UTSW	17	28,867,129 (GRCm39)	missense	probably damaging	1.00
R6135:Slc26a8	UTSW	17	28,888,914 (GRCm39)	missense	probably benign	0.00
R6372:Slc26a8	UTSW	17	28,863,777 (GRCm39)	missense	probably benign	0.08
R6543:Slc26a8	UTSW	17	28,857,375 (GRCm39)	missense	possibly damaging	0.53
R6590:Slc26a8	UTSW	17	28,863,629 (GRCm39)	missense	possibly damaging	0.52
R6690:Slc26a8	UTSW	17	28,863,629 (GRCm39)	missense	possibly damaging	0.52
R6866:Slc26a8	UTSW	17	28,857,455 (GRCm39)	missense	probably benign	0.27
R7057:Slc26a8	UTSW	17	28,857,371 (GRCm39)	missense	possibly damaging	0.72
R7423:Slc26a8	UTSW	17	28,867,177 (GRCm39)	missense	probably benign	0.32
R7496:Slc26a8	UTSW	17	28,863,824 (GRCm39)	missense	probably benign	0.20
R8387:Slc26a8	UTSW	17	28,866,899 (GRCm39)	missense	probably benign	0.00
R9422:Slc26a8	UTSW	17	28,857,560 (GRCm39)	missense	possibly damaging	0.62
R9455:Slc26a8	UTSW	17	28,863,588 (GRCm39)	missense	probably damaging	1.00
RF015:Slc26a8	UTSW	17	28,857,315 (GRCm39)	small deletion	probably benign
Z1177:Slc26a8	UTSW	17	28,857,139 (GRCm39)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- TCACCATATTGACCTGGGAGACAGAAG -3'
(R):5'- TCCAACCTCTCACTGTGACTCAGAAG -3'

Sequencing Primer
(F):5'- TGGGAGACAGAAGAGGGGTC -3'
(R):5'- cagatagacagacagacagacag -3'

Posted On

2014-03-14