Mutagenetix > Incidental Mutation

Incidental Mutation 'R2090:Slc2a13'

231738

Institutional Source

Beutler Lab

Gene Symbol

Slc2a13

Ensembl Gene

ENSMUSG00000036298

Gene Name

solute carrier family 2 (facilitated glucose transporter), member 13

Synonyms

A630029G22Rik

MMRRC Submission

040095-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2090 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

91151899-91457464 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 91400695 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 176 (I176F)

Ref Sequence

ENSEMBL: ENSMUSP00000104906 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109283]

AlphaFold

Q3UHK1

Predicted Effect

probably benign
Transcript: ENSMUST00000109283
AA Change: I176F

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000104906
Gene: ENSMUSG00000036298
AA Change: I176F

Domain	Start	End	E-Value	Type
low complexity region	36	54	N/A	INTRINSIC
Pfam:Sugar_tr	73	412	2e-87	PFAM
Pfam:MFS_1	77	411	6.6e-23	PFAM
Pfam:Sugar_tr	487	598	8.1e-28	PFAM

Meta Mutation Damage Score

0.1333

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.5%

Validation Efficiency

100% (67/67)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam32	A	G	8: 25,391,456 (GRCm39)		probably null	Het
Adcy7	A	T	8: 89,042,485 (GRCm39)	T451S	probably damaging	Het
Adgrg3	A	T	8: 95,766,558 (GRCm39)	T410S	possibly damaging	Het
Alg11	G	T	8: 22,555,646 (GRCm39)	L302F	possibly damaging	Het
Ankrd17	A	G	5: 90,445,905 (GRCm39)	V310A	possibly damaging	Het
Atg16l2	C	T	7: 100,942,575 (GRCm39)		probably null	Het
B3gnt2	A	G	11: 22,786,291 (GRCm39)	V299A	probably benign	Het
Birc6	A	G	17: 74,969,791 (GRCm39)	N4258S	probably benign	Het
C2cd4d	A	G	3: 94,271,321 (GRCm39)	K196E	probably benign	Het
Calhm6	A	G	10: 34,002,358 (GRCm39)	S242P	probably damaging	Het
Cdr2l	A	G	11: 115,281,827 (GRCm39)	K111E	probably damaging	Het
Crtam	T	C	9: 40,895,612 (GRCm39)	Q41R	possibly damaging	Het
Cspp1	A	G	1: 10,160,493 (GRCm39)	K560R	possibly damaging	Het
Dcaf15	A	T	8: 84,824,400 (GRCm39)	Y571*	probably null	Het
Defa39	A	T	8: 22,192,805 (GRCm39)	W64R	possibly damaging	Het
Dpy19l4	T	C	4: 11,304,344 (GRCm39)	Y99C	probably benign	Het
Edem3	C	T	1: 151,680,577 (GRCm39)		probably benign	Het
Enpp6	A	T	8: 47,518,405 (GRCm39)		probably null	Het
Foxf2	T	A	13: 31,810,824 (GRCm39)	D254E	probably benign	Het
Gjb5	T	C	4: 127,249,794 (GRCm39)	N117D	probably benign	Het
Glmn	G	A	5: 107,709,794 (GRCm39)	L337F	probably damaging	Het
Gsdmc2	T	A	15: 63,698,675 (GRCm39)	Y307F	probably benign	Het
Gsdmc3	T	A	15: 63,738,631 (GRCm39)	M144L	probably benign	Het
Ibtk	A	G	9: 85,603,046 (GRCm39)	I653T	probably benign	Het
Il24	T	G	1: 130,812,574 (GRCm39)	D99A	possibly damaging	Het
Intu	A	G	3: 40,637,966 (GRCm39)	Q484R	probably benign	Het
Iqca1l	A	G	5: 24,755,674 (GRCm39)	S283P	probably benign	Het
Lsp1	T	C	7: 142,045,544 (GRCm39)		probably benign	Het
Mad1l1	A	G	5: 139,995,011 (GRCm39)	S672P	probably benign	Het
Man2a2	A	T	7: 80,013,858 (GRCm39)		probably benign	Het
Morc3	C	A	16: 93,663,341 (GRCm39)	H515N	probably benign	Het
Nav1	T	C	1: 135,534,903 (GRCm39)		probably benign	Het
Ndor1	A	G	2: 25,139,230 (GRCm39)	L247P	probably damaging	Het
Nfkbiz	A	T	16: 55,636,818 (GRCm39)	F494L	probably benign	Het
Nr1d1	G	A	11: 98,661,436 (GRCm39)	P277S	probably damaging	Het
Nrg2	T	C	18: 36,151,496 (GRCm39)	D682G	probably benign	Het
Nrros	C	T	16: 31,962,975 (GRCm39)	W311*	probably null	Het
Oasl1	G	A	5: 115,073,993 (GRCm39)	D301N	probably damaging	Het
Or10ag56	A	T	2: 87,139,762 (GRCm39)	I230F	probably benign	Het
Or14a258	A	T	7: 86,035,289 (GRCm39)	I193N	probably benign	Het
Or5h26	A	G	16: 58,988,503 (GRCm39)	M1T	probably null	Het
Palmd	A	G	3: 116,721,083 (GRCm39)	S123P	probably damaging	Het
Patj	A	G	4: 98,325,560 (GRCm39)		probably benign	Het
Pcsk4	T	C	10: 80,161,655 (GRCm39)	D162G	probably benign	Het
Plppr5	A	G	3: 117,369,520 (GRCm39)	D59G	possibly damaging	Het
Pmvk	A	C	3: 89,369,189 (GRCm39)	R11S	possibly damaging	Het
Pnliprp1	A	G	19: 58,728,901 (GRCm39)	T363A	probably benign	Het
Poll	A	T	19: 45,547,277 (GRCm39)	I65N	probably benign	Het
Prox1	T	A	1: 189,893,009 (GRCm39)	S479C	probably damaging	Het
Prss50	A	T	9: 110,691,361 (GRCm39)	S222C	probably damaging	Het
Rasa3	A	C	8: 13,632,381 (GRCm39)		probably benign	Het
Sec14l3	T	C	11: 4,025,481 (GRCm39)	V335A	probably benign	Het
Setbp1	C	T	18: 78,899,935 (GRCm39)	S1244N	probably benign	Het
Sgcg	A	T	14: 61,483,213 (GRCm39)	F63I	probably damaging	Het
Skp2	C	A	15: 9,113,786 (GRCm39)	G376C	probably damaging	Het
Smc6	A	G	12: 11,339,987 (GRCm39)	T432A	probably benign	Het
Snx25	G	A	8: 46,509,150 (GRCm39)	P478L	probably damaging	Het
Taf2	A	T	15: 54,879,882 (GRCm39)	H1151Q	probably damaging	Het
Thsd1	A	G	8: 22,749,673 (GRCm39)	K795R	possibly damaging	Het
Tmem108	G	A	9: 103,361,976 (GRCm39)	L537F	possibly damaging	Het
Ubr3	T	C	2: 69,766,361 (GRCm39)	Y410H	probably damaging	Het
Vav3	T	C	3: 109,555,055 (GRCm39)		probably null	Het
Vmn1r224	T	C	17: 20,639,524 (GRCm39)	Y34H	probably benign	Het
Zeb1	T	C	18: 5,766,458 (GRCm39)	V323A	possibly damaging	Het
Zfp652	A	G	11: 95,644,834 (GRCm39)	D240G	probably benign	Het
Zfp963	A	T	8: 70,195,996 (GRCm39)	C152*	probably null	Het

Other mutations in Slc2a13

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00899:Slc2a13	APN	15	91,381,602 (GRCm39)	missense	probably benign
IGL01295:Slc2a13	APN	15	91,234,335 (GRCm39)	critical splice acceptor site	probably null
IGL01863:Slc2a13	APN	15	91,400,695 (GRCm39)	missense	probably benign	0.00
IGL02149:Slc2a13	APN	15	91,227,924 (GRCm39)	missense	probably benign
IGL02670:Slc2a13	APN	15	91,381,712 (GRCm39)	missense	probably damaging	0.99
IGL02692:Slc2a13	APN	15	91,205,861 (GRCm39)	missense	probably benign	0.23
IGL03307:Slc2a13	APN	15	91,160,317 (GRCm39)	missense	probably damaging	0.98
R0394:Slc2a13	UTSW	15	91,400,595 (GRCm39)	missense	probably damaging	1.00
R0624:Slc2a13	UTSW	15	91,234,215 (GRCm39)	missense	possibly damaging	0.89
R0698:Slc2a13	UTSW	15	91,205,870 (GRCm39)	missense	probably benign
R0702:Slc2a13	UTSW	15	91,205,870 (GRCm39)	missense	probably benign
R1052:Slc2a13	UTSW	15	91,296,363 (GRCm39)	missense	probably damaging	0.96
R2118:Slc2a13	UTSW	15	91,400,679 (GRCm39)	missense	probably damaging	0.99
R4445:Slc2a13	UTSW	15	91,234,223 (GRCm39)	missense	possibly damaging	0.46
R4896:Slc2a13	UTSW	15	91,296,415 (GRCm39)	missense	probably benign	0.20
R6028:Slc2a13	UTSW	15	91,160,319 (GRCm39)	missense	probably damaging	1.00
R6414:Slc2a13	UTSW	15	91,228,008 (GRCm39)	missense	probably benign	0.00
R6836:Slc2a13	UTSW	15	91,205,835 (GRCm39)	missense	probably benign	0.00
R6928:Slc2a13	UTSW	15	91,160,382 (GRCm39)	missense	probably damaging	1.00
R7353:Slc2a13	UTSW	15	91,205,807 (GRCm39)	missense	probably benign
R7423:Slc2a13	UTSW	15	91,456,883 (GRCm39)	missense	probably damaging	1.00
R7458:Slc2a13	UTSW	15	91,296,390 (GRCm39)	missense	probably benign	0.04
R7641:Slc2a13	UTSW	15	91,156,359 (GRCm39)	makesense	probably null
R7993:Slc2a13	UTSW	15	91,296,356 (GRCm39)	nonsense	probably null
R8057:Slc2a13	UTSW	15	91,400,619 (GRCm39)	missense	probably damaging	0.99
R8164:Slc2a13	UTSW	15	91,160,281 (GRCm39)	missense	probably damaging	0.96
R8520:Slc2a13	UTSW	15	91,457,105 (GRCm39)	missense	probably damaging	1.00
R8794:Slc2a13	UTSW	15	91,234,302 (GRCm39)	missense	probably damaging	1.00
R9061:Slc2a13	UTSW	15	91,234,333 (GRCm39)	missense	possibly damaging	0.85
R9185:Slc2a13	UTSW	15	91,227,906 (GRCm39)	missense	probably damaging	0.99
R9396:Slc2a13	UTSW	15	91,227,915 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TTGTAGCGCCTCAAAGTCATAGC -3'
(R):5'- TGTTCAGAGATCAGAACCTCAC -3'

Sequencing Primer
(F):5'- GTAGCGCCTCAAAGTCATAGCTTATC -3'
(R):5'- TTCAGAGATCAGAACCTCACATACTG -3'

Posted On

2014-09-18