Mutagenetix > Incidental Mutation

Incidental Mutation 'R5387:Slc45a1'

425324

Institutional Source

Beutler Lab

Gene Symbol

Slc45a1

Ensembl Gene

ENSMUSG00000039838

Gene Name

solute carrier family 45, member 1

Synonyms

Dnb5

MMRRC Submission

042959-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.137) question?

Stock #

R5387 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

150713052-150736631 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

T to A at 150728366 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000112737 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037827] [ENSMUST00000117997]

AlphaFold

Q8BIV7

Predicted Effect

probably benign
Transcript: ENSMUST00000037827

SMART Domains

Protein: ENSMUSP00000036774
Gene: ENSMUSG00000039838

Domain	Start	End	E-Value	Type
low complexity region	58	69	N/A	INTRINSIC
Pfam:MFS_2	86	310	7.3e-11	PFAM
Pfam:MFS_1	92	356	1.4e-12	PFAM
transmembrane domain	529	551	N/A	INTRINSIC
transmembrane domain	575	597	N/A	INTRINSIC
transmembrane domain	604	626	N/A	INTRINSIC
transmembrane domain	631	653	N/A	INTRINSIC
transmembrane domain	680	702	N/A	INTRINSIC
transmembrane domain	712	734	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000117997

SMART Domains

Protein: ENSMUSP00000112737
Gene: ENSMUSG00000039838

Domain	Start	End	E-Value	Type
low complexity region	58	69	N/A	INTRINSIC
Pfam:MFS_2	87	307	1.6e-12	PFAM
Pfam:MFS_1	92	362	2.4e-12	PFAM
transmembrane domain	529	551	N/A	INTRINSIC
transmembrane domain	575	597	N/A	INTRINSIC
transmembrane domain	604	626	N/A	INTRINSIC
transmembrane domain	631	653	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147706

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.6%
20x: 96.0%

Validation Efficiency

99% (80/81)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene was isolated initially from a region on chromosome 1p that is frequently deleted in human neuroblastoma, although no causal relationship has since been demonstrated. The encoded protein belongs to the glycoside-pentoside-hexuronide cation symporter transporter family and may play a role in glucose uptake. [provided by RefSeq, Mar 2014]

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210408I21Rik	T	A	13: 77,408,092 (GRCm39)	S140T	probably benign	Het
Ahnak	T	C	19: 8,981,055 (GRCm39)	S780P	probably damaging	Het
Ankhd1	C	A	18: 36,767,697 (GRCm39)	H1205N	probably damaging	Het
Ano1	T	C	7: 144,202,356 (GRCm39)	K139R	probably benign	Het
Anp32b	T	G	4: 46,468,573 (GRCm39)	C114W	probably damaging	Het
Ascl1	C	T	10: 87,328,551 (GRCm39)	A134T	probably damaging	Het
Atl2	C	T	17: 80,160,229 (GRCm39)	E453K	probably benign	Het
Aup1	C	T	6: 83,032,005 (GRCm39)	A84V	probably damaging	Het
Btbd7	A	T	12: 102,804,044 (GRCm39)	M332K	probably damaging	Het
Cacna1d	A	G	14: 29,822,708 (GRCm39)	V1107A	probably damaging	Het
Cd33	G	A	7: 43,181,477 (GRCm39)	Q114*	probably null	Het
Cdhr18	C	A	14: 13,914,438 (GRCm38)	M1I	probably null	Het
Col4a4	C	T	1: 82,471,312 (GRCm39)	G681E	unknown	Het
Defb22	C	A	2: 152,327,826 (GRCm39)	A120S	unknown	Het
Dnah7b	A	G	1: 46,227,819 (GRCm39)	I1347M	probably damaging	Het
Efcab5	A	G	11: 77,025,668 (GRCm39)	I549T	possibly damaging	Het
Esp15	T	A	17: 39,955,468 (GRCm39)		probably null	Het
Fbxo7	A	G	10: 85,860,518 (GRCm39)	T42A	probably benign	Het
Filip1	A	G	9: 79,725,556 (GRCm39)	I1021T	probably benign	Het
Gad1	C	A	2: 70,394,195 (GRCm39)	S7*	probably null	Het
H2ac7	T	A	13: 23,758,841 (GRCm39)		probably null	Het
H2-Q7	C	T	17: 35,658,518 (GRCm39)	T52M	probably damaging	Het
H2-T3	C	T	17: 36,497,594 (GRCm39)	G28R	probably benign	Het
Idh2	TCCCAGG	T	7: 79,748,079 (GRCm39)		probably benign	Het
Ift81	A	G	5: 122,693,598 (GRCm39)	Y604H	probably damaging	Het
Igsf11	A	G	16: 38,842,785 (GRCm39)	Y154C	probably damaging	Het
Kif26b	G	T	1: 178,742,441 (GRCm39)	A846S	probably benign	Het
Lnx2	G	A	5: 146,964,964 (GRCm39)	P420S	probably benign	Het
Lrit2	A	G	14: 36,794,216 (GRCm39)	T427A	probably damaging	Het
Lrrc43	G	T	5: 123,637,734 (GRCm39)		probably null	Het
Mettl25b	A	T	3: 87,837,318 (GRCm39)		probably benign	Het
Mug1	T	C	6: 121,861,353 (GRCm39)	Y1325H	probably damaging	Het
Naglu	A	T	11: 100,967,550 (GRCm39)	Y500F	probably damaging	Het
Npy4r	A	G	14: 33,868,940 (GRCm39)	M116T	probably benign	Het
Nrdc	A	G	4: 108,896,959 (GRCm39)	Y526C	probably damaging	Het
Nrp2	T	C	1: 62,801,972 (GRCm39)	S472P	probably benign	Het
Or12d2	T	A	17: 37,625,183 (GRCm39)	T31S	probably benign	Het
Or12k8	T	C	2: 36,975,731 (GRCm39)	T10A	possibly damaging	Het
Otogl	T	A	10: 107,616,794 (GRCm39)	T1828S	probably benign	Het
Pank2	C	T	2: 131,116,182 (GRCm39)	T200I	probably benign	Het
Pbrm1	A	G	14: 30,804,567 (GRCm39)	Y946C	probably damaging	Het
Pde12	A	T	14: 26,387,608 (GRCm39)	S437T	probably benign	Het
Pikfyve	A	G	1: 65,304,427 (GRCm39)	K1710E	possibly damaging	Het
Plcd3	A	G	11: 102,969,281 (GRCm39)	S229P	probably damaging	Het
Polr3a	T	C	14: 24,505,009 (GRCm39)	I1084V	possibly damaging	Het
Prkaa2	C	A	4: 104,897,374 (GRCm39)	D280Y	probably damaging	Het
Ptprg	T	A	14: 12,153,873 (GRCm38)	S531R	probably damaging	Het
R3hdm2	T	C	10: 127,321,303 (GRCm39)	S620P	probably damaging	Het
Rab33b	A	G	3: 51,400,876 (GRCm39)	T117A	probably damaging	Het
Rasal2	T	C	1: 156,985,335 (GRCm39)	D804G	possibly damaging	Het
Rbp3	A	G	14: 33,678,370 (GRCm39)	T773A	possibly damaging	Het
Rspry1	A	G	8: 95,364,914 (GRCm39)	T185A	possibly damaging	Het
Sec61a2	G	T	2: 5,887,356 (GRCm39)		probably benign	Het
Setx	C	T	2: 29,037,606 (GRCm39)	R1364C	probably benign	Het
Shtn1	G	T	19: 59,026,801 (GRCm39)	L97M	probably damaging	Het
Slc35f1	T	C	10: 52,984,260 (GRCm39)	L340P	probably damaging	Het
Slmap	T	C	14: 26,181,088 (GRCm39)	E386G	probably benign	Het
Smc2	C	T	4: 52,475,096 (GRCm39)	A924V	probably benign	Het
Sp110	C	G	1: 85,516,839 (GRCm39)	E219D	probably damaging	Het
Tecta	G	A	9: 42,286,359 (GRCm39)	L766F	probably damaging	Het
Tle3	C	T	9: 61,314,771 (GRCm39)		probably null	Het
Top3a	A	G	11: 60,653,316 (GRCm39)	F53L	probably damaging	Het
Trappc2b	A	T	11: 51,576,801 (GRCm39)	D32E	probably benign	Het
Trem1	T	C	17: 48,548,541 (GRCm39)	I26T	possibly damaging	Het
Ttc7b	G	T	12: 100,413,222 (GRCm39)	Q199K	possibly damaging	Het
Ubap2l	T	C	3: 89,913,903 (GRCm39)	Y975C	probably benign	Het
Ubxn11	C	A	4: 133,850,737 (GRCm39)	D196E	probably damaging	Het
Unc80	A	G	1: 66,569,180 (GRCm39)	H945R	possibly damaging	Het
Usp15	A	G	10: 122,967,191 (GRCm39)	I405T	probably damaging	Het
Uty	C	T	Y: 1,189,339 (GRCm39)	E138K	probably damaging	Het
Wapl	A	G	14: 34,399,252 (GRCm39)	E107G	probably benign	Het
Wbp1l	T	C	19: 46,632,896 (GRCm39)		probably null	Het
Zfp184	T	G	13: 22,133,810 (GRCm39)		probably benign	Het
Zfp36	A	C	7: 28,077,293 (GRCm39)	L205R	possibly damaging	Het

Other mutations in Slc45a1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01796:Slc45a1	APN	4	150,728,426 (GRCm39)	missense	probably damaging	1.00
IGL02009:Slc45a1	APN	4	150,722,447 (GRCm39)	missense	probably damaging	1.00
IGL02251:Slc45a1	APN	4	150,723,176 (GRCm39)	splice site	probably benign
IGL02752:Slc45a1	APN	4	150,722,478 (GRCm39)	missense	probably benign	0.01
IGL02881:Slc45a1	APN	4	150,722,987 (GRCm39)	missense	probably benign	0.36
PIT4508001:Slc45a1	UTSW	4	150,722,892 (GRCm39)	missense	probably benign	0.00
R0017:Slc45a1	UTSW	4	150,714,023 (GRCm39)	missense	possibly damaging	0.56
R0017:Slc45a1	UTSW	4	150,714,023 (GRCm39)	missense	possibly damaging	0.56
R0449:Slc45a1	UTSW	4	150,727,762 (GRCm39)	missense	probably damaging	1.00
R0756:Slc45a1	UTSW	4	150,727,054 (GRCm39)	frame shift	probably null
R1435:Slc45a1	UTSW	4	150,728,505 (GRCm39)	missense	probably damaging	1.00
R1837:Slc45a1	UTSW	4	150,722,916 (GRCm39)	missense	probably benign	0.00
R1943:Slc45a1	UTSW	4	150,728,734 (GRCm39)	missense	probably benign	0.02
R2186:Slc45a1	UTSW	4	150,722,708 (GRCm39)	missense	probably benign	0.01
R3766:Slc45a1	UTSW	4	150,722,517 (GRCm39)	missense	probably damaging	1.00
R4689:Slc45a1	UTSW	4	150,722,996 (GRCm39)	missense	probably benign	0.31
R4697:Slc45a1	UTSW	4	150,722,741 (GRCm39)	missense	probably damaging	1.00
R4709:Slc45a1	UTSW	4	150,722,697 (GRCm39)	missense	probably benign	0.04
R5253:Slc45a1	UTSW	4	150,722,727 (GRCm39)	missense	probably damaging	0.98
R5914:Slc45a1	UTSW	4	150,713,997 (GRCm39)	missense	possibly damaging	0.57
R6259:Slc45a1	UTSW	4	150,722,817 (GRCm39)	missense	possibly damaging	0.63
R6290:Slc45a1	UTSW	4	150,727,096 (GRCm39)	missense	probably damaging	1.00
R6961:Slc45a1	UTSW	4	150,714,110 (GRCm39)	missense	probably damaging	0.99
R6981:Slc45a1	UTSW	4	150,723,051 (GRCm39)	missense	possibly damaging	0.48
R7099:Slc45a1	UTSW	4	150,714,030 (GRCm39)	missense	probably benign	0.00
R7209:Slc45a1	UTSW	4	150,719,669 (GRCm39)	splice site	probably null
R7601:Slc45a1	UTSW	4	150,713,994 (GRCm39)	missense	possibly damaging	0.78
R7615:Slc45a1	UTSW	4	150,723,002 (GRCm39)	missense	probably benign	0.01
R7730:Slc45a1	UTSW	4	150,715,397 (GRCm39)	missense	probably damaging	1.00
R7750:Slc45a1	UTSW	4	150,728,498 (GRCm39)	missense	probably damaging	1.00
R8022:Slc45a1	UTSW	4	150,722,766 (GRCm39)	missense	possibly damaging	0.71
R8768:Slc45a1	UTSW	4	150,714,206 (GRCm39)	missense	probably damaging	0.98
R9006:Slc45a1	UTSW	4	150,722,731 (GRCm39)	missense	probably damaging	1.00
R9258:Slc45a1	UTSW	4	150,723,071 (GRCm39)	missense	possibly damaging	0.88
R9388:Slc45a1	UTSW	4	150,727,067 (GRCm39)	missense	probably damaging	1.00
R9768:Slc45a1	UTSW	4	150,722,982 (GRCm39)	missense	probably benign
X0026:Slc45a1	UTSW	4	150,728,507 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAGATTATGCACTGCCAGC -3'
(R):5'- TGGGAACTGCTCTTCAATGGC -3'

Sequencing Primer
(F):5'- CAGATTATGCACTGCCAGCTTGATG -3'
(R):5'- AACTGCTCTTCAATGGCTGCATTC -3'

Posted On

2016-08-04