Mutagenetix > Incidental Mutation

Incidental Mutation 'R7747:Mfsd6'

596871

Institutional Source

Beutler Lab

Gene Symbol

Mfsd6

Ensembl Gene

ENSMUSG00000041439

Gene Name

major facilitator superfamily domain containing 6

Synonyms

MMR2, 9630025I22Rik, 2210010L05Rik

MMRRC Submission

Accession Numbers

Ncbi RefSeq: NM_133829.2, NM_178081.4; MGI:1922925

Essential gene?

Probably non essential (E-score: 0.143) question?

Stock #

R7747 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

52656286-52727462 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 52676547 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 524 (T524A)

Ref Sequence

ENSEMBL: ENSMUSP00000084991 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087701] [ENSMUST00000156876]

AlphaFold

Q8CBH5

Predicted Effect

probably benign
Transcript: ENSMUST00000087701
AA Change: T524A

PolyPhen 2 Score 0.054 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000084991
Gene: ENSMUSG00000041439
AA Change: T524A

Domain	Start	End	E-Value	Type
low complexity region	33	48	N/A	INTRINSIC
Pfam:MFS_1_like	68	144	4.8e-19	PFAM
Pfam:MFS_1	70	162	7e-11	PFAM
Pfam:MFS_2	72	571	3.8e-13	PFAM
Pfam:Nuc_H_symport	424	628	1.1e-11	PFAM
Pfam:MFS_1	453	708	6.3e-18	PFAM

Predicted Effect

SMART Domains

Protein: ENSMUSP00000115398
Gene: ENSMUSG00000041439
AA Change: T354A

Domain	Start	End	E-Value	Type
low complexity region	89	101	N/A	INTRINSIC
transmembrane domain	120	142	N/A	INTRINSIC
transmembrane domain	163	185	N/A	INTRINSIC
transmembrane domain	200	219	N/A	INTRINSIC
Pfam:Nuc_H_symport	255	459	1.4e-11	PFAM
Pfam:MFS_1	284	539	6.8e-18	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000156876
AA Change: T524A

PolyPhen 2 Score 0.950 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000122881
Gene: ENSMUSG00000041439
AA Change: T524A

Domain	Start	End	E-Value	Type
low complexity region	33	48	N/A	INTRINSIC
Pfam:MFS_1_like	68	144	6.2e-20	PFAM
Pfam:MFS_1	70	162	1.8e-10	PFAM
low complexity region	258	270	N/A	INTRINSIC
transmembrane domain	289	311	N/A	INTRINSIC
transmembrane domain	332	354	N/A	INTRINSIC
transmembrane domain	369	388	N/A	INTRINSIC
Pfam:Nuc_H_symport	424	628	2.6e-11	PFAM
Pfam:MFS_1	453	707	1.7e-17	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (89/89)

Allele List at MGI

All alleles(4) : Targeted(4)

Other mutations in this stock

Total: 91 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010109A12Rik	G	A	5: 93,206,557		probably null	Het
2410004P03Rik	C	T	12: 17,007,148	S116N	probably damaging	Het
3425401B19Rik	T	C	14: 32,663,069	D313G	possibly damaging	Het
AA986860	A	G	1: 130,743,547	E502G	possibly damaging	Het
Adamts20	T	A	15: 94,291,587	K1462*	probably null	Het
Adgrg6	A	C	10: 14,450,577		probably null	Het
Ankrd13d	G	A	19: 4,280,985	H165Y	probably damaging	Het
Arap3	T	C	18: 37,988,888		probably null	Het
Arhgap33	A	G	7: 30,524,135	V823A	probably damaging	Het
Aup1	C	A	6: 83,054,795	P34T	unknown	Het
Bcl2l2	C	T	14: 54,884,379		probably benign	Het
Bicc1	T	C	10: 70,946,993	T515A	probably benign	Het
Ccdc73	A	C	2: 104,929,556	K106Q	probably damaging	Het
Celsr3	G	A	9: 108,829,978	R1220Q	possibly damaging	Het
Cep290	C	T	10: 100,558,176	Q2082*	probably null	Het
Cercam	A	G	2: 29,871,286	D104G	probably benign	Het
Champ1	A	G	8: 13,879,990	H716R	probably damaging	Het
Cntrl	A	T	2: 35,116,798	I159F	probably damaging	Het
Col11a1	T	C	3: 114,102,572	I507T	unknown	Het
Cped1	T	C	6: 22,143,974	I573T	probably damaging	Het
Crot	C	T	5: 8,968,869		probably null	Het
D1Pas1	T	A	1: 186,968,677	S268T	probably benign	Het
Erich6	A	G	3: 58,618,928	V551A	probably damaging	Het
Fbxo32	T	C	15: 58,191,361	N192S	probably damaging	Het
Fgd6	T	C	10: 94,044,916	V544A	probably damaging	Het
Fnbp1	C	T	2: 31,036,147	G552E	probably damaging	Het
Gjb5	A	T	4: 127,356,162	V63D	probably damaging	Het
Gm10053	T	C	19: 24,876,039	I96T	probably benign	Het
Gm11639	T	G	11: 104,842,603	I2011S	probably damaging	Het
Gm38119	T	C	3: 92,738,021	S89G	unknown	Het
Gm884	A	T	11: 103,614,255	S2296T	probably damaging	Het
Gpn2	A	G	4: 133,586,045	I183V	probably benign	Het
Greb1	C	T	12: 16,674,795	V1793M	probably benign	Het
H2-Q7	A	G	17: 35,440,061	I163V	probably benign	Het
Hrh2	T	C	13: 54,214,530	V175A	possibly damaging	Het
Hsd3b3	C	T	3: 98,743,898	V79I	possibly damaging	Het
Itgb7	T	C	15: 102,216,604	I727M	possibly damaging	Het
Kcnj16	T	A	11: 111,024,743	F77Y	probably damaging	Het
Lilra6	T	A	7: 3,912,996	Q288L	probably benign	Het
Malrd1	G	A	2: 16,074,835	V1788M	unknown	Het
Mau2	T	C	8: 70,026,723	I349V	possibly damaging	Het
Mbnl3	C	T	X: 51,130,334	R181H	probably damaging	Het
Mical2	G	T	7: 112,333,839	R740L	probably benign	Het
Mknk1	G	A	4: 115,878,072	C379Y	possibly damaging	Het
Mta3	A	T	17: 83,791,736	K410*	probably null	Het
Myb	A	C	10: 21,156,425	I19S	possibly damaging	Het
Ncor2	A	G	5: 125,027,038	F996S		Het
Nlrp1a	T	C	11: 71,123,408	M339V	possibly damaging	Het
Olfr136	C	T	17: 38,335,394	P79L	probably benign	Het
Olfr689	A	G	7: 105,314,447	K148E	probably damaging	Het
Pcdhga5	C	T	18: 37,696,782	T761I	possibly damaging	Het
Pcmtd2	T	C	2: 181,851,659	L219P	possibly damaging	Het
Pfdn1	C	T	18: 36,432,305		probably null	Het
Pkn3	G	A	2: 30,090,584	C829Y	probably benign	Het
Pld1	T	C	3: 28,087,189	S634P	possibly damaging	Het
Pofut2	T	G	10: 77,262,470	V139G	possibly damaging	Het
Prdm12	C	A	2: 31,653,871		probably null	Het
Prkar2b	C	A	12: 32,060,938	A49S	probably benign	Het
Prmt1	A	T	7: 44,984,136		probably null	Het
Rab39	A	T	9: 53,686,400	D188E	probably benign	Het
Repin1	G	T	6: 48,597,345	E403*	probably null	Het
Scgb1b19	A	G	7: 33,287,498	I25V	probably benign	Het
Scn9a	A	T	2: 66,484,298	I1692N	probably damaging	Het
Sdk1	G	T	5: 142,084,491	G1137V	probably damaging	Het
Sec16b	A	G	1: 157,565,472	T950A	possibly damaging	Het
Senp2	G	T	16: 22,038,622	R398L	probably damaging	Het
Sfswap	G	T	5: 129,550,593		probably null	Het
Sh3rf1	A	G	8: 61,353,753	T362A	probably damaging	Het
Slc17a1	A	T	13: 23,888,052	I418F	probably benign	Het
Slc1a4	A	T	11: 20,308,587	M284K	probably damaging	Het
Slc5a2	A	T	7: 128,266,395		probably null	Het
Slco5a1	A	G	1: 12,990,122	V125A	probably benign	Het
Smu1	A	G	4: 40,748,600	V230A	probably benign	Het
Sp4	A	G	12: 118,254,404		probably null	Het
Stbd1	A	G	5: 92,605,557	K302R	probably damaging	Het
Stx2	A	T	5: 128,986,417	V268D	probably benign	Het
Tbc1d9b	G	A	11: 50,161,620	A885T	probably benign	Het
Tbce	T	A	13: 14,006,478	D267V	possibly damaging	Het
Tert	T	C	13: 73,627,606	Y159H	probably damaging	Het
Thbs2	T	A	17: 14,670,039	I1102F	possibly damaging	Het
Tmprss7	G	C	16: 45,683,510	A183G	probably benign	Het
Top3b	C	A	16: 16,887,721	P450Q	probably benign	Het
Trpm6	A	T	19: 18,750,045		probably null	Het
Ube4a	T	C	9: 44,925,973	D988G	probably damaging	Het
Vmn1r158	A	T	7: 22,790,300	S161R	probably benign	Het
Vps41	T	C	13: 18,841,252		probably null	Het
Zfp354c	TCACACTCGGCACA	TCACA	11: 50,815,240		probably benign	Het
Zfp617	T	A	8: 71,928,189		probably null	Het
Zfp808	C	T	13: 62,171,505	H183Y	probably benign	Het
Zfy1	A	T	Y: 725,496	C756*	probably null	Het
Zswim2	A	T	2: 83,915,607	Y496N	probably damaging	Het

Other mutations in Mfsd6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00490:Mfsd6	APN	1	52708254	missense	probably damaging	1.00
IGL00820:Mfsd6	APN	1	52708306	missense	probably damaging	1.00
IGL01518:Mfsd6	APN	1	52709322	missense	probably damaging	1.00
IGL02111:Mfsd6	APN	1	52708344	missense	probably damaging	1.00
IGL02517:Mfsd6	APN	1	52663277	splice site	probably benign
IGL02687:Mfsd6	APN	1	52708675	missense	probably damaging	0.99
IGL02887:Mfsd6	APN	1	52708878	missense	probably benign	0.19
IGL02901:Mfsd6	APN	1	52708473	missense	probably benign	0.07
IGL03030:Mfsd6	APN	1	52709703	start codon destroyed	probably null	1.00
PIT4280001:Mfsd6	UTSW	1	52660880	missense	probably benign	0.00
PIT4466001:Mfsd6	UTSW	1	52708897	missense	probably benign	0.03
R0043:Mfsd6	UTSW	1	52708652	nonsense	probably null
R0113:Mfsd6	UTSW	1	52709189	missense	probably damaging	1.00
R0226:Mfsd6	UTSW	1	52658690	intron	probably benign
R0302:Mfsd6	UTSW	1	52709457	missense	probably damaging	1.00
R0613:Mfsd6	UTSW	1	52658696	intron	probably benign
R1126:Mfsd6	UTSW	1	52709511	missense	probably benign	0.16
R1368:Mfsd6	UTSW	1	52708605	missense	possibly damaging	0.49
R1471:Mfsd6	UTSW	1	52709557	missense	probably benign	0.32
R1733:Mfsd6	UTSW	1	52709365	missense	probably damaging	1.00
R1768:Mfsd6	UTSW	1	52660805	critical splice donor site	probably null
R1951:Mfsd6	UTSW	1	52709358	missense	probably damaging	1.00
R2031:Mfsd6	UTSW	1	52708854	missense	probably benign	0.04
R2116:Mfsd6	UTSW	1	52660975	missense	probably benign	0.21
R2240:Mfsd6	UTSW	1	52660819	missense	probably damaging	0.97
R2242:Mfsd6	UTSW	1	52709598	missense	probably benign	0.03
R2303:Mfsd6	UTSW	1	52676513	missense	probably damaging	0.98
R2382:Mfsd6	UTSW	1	52708410	missense	probably benign	0.10
R4568:Mfsd6	UTSW	1	52663289	nonsense	probably null
R4801:Mfsd6	UTSW	1	52709596	missense	probably benign	0.08
R4802:Mfsd6	UTSW	1	52709596	missense	probably benign	0.08
R4958:Mfsd6	UTSW	1	52661024	missense	probably damaging	1.00
R5134:Mfsd6	UTSW	1	52708356	missense	possibly damaging	0.80
R5827:Mfsd6	UTSW	1	52662392	missense	probably damaging	1.00
R5844:Mfsd6	UTSW	1	52658383	missense	probably benign
R6124:Mfsd6	UTSW	1	52708252	missense	probably damaging	1.00
R6435:Mfsd6	UTSW	1	52709444	nonsense	probably null
R6515:Mfsd6	UTSW	1	52660961	missense	probably damaging	1.00
R6874:Mfsd6	UTSW	1	52660709	missense	probably benign	0.02
R6878:Mfsd6	UTSW	1	52708753	missense	probably damaging	0.98
R7111:Mfsd6	UTSW	1	52709758	splice site	probably null
R7170:Mfsd6	UTSW	1	52662388	critical splice donor site	probably null
R7242:Mfsd6	UTSW	1	52709474	missense	probably damaging	0.98
R7548:Mfsd6	UTSW	1	52663287	missense	possibly damaging	0.79
R7664:Mfsd6	UTSW	1	52709053	missense	probably benign	0.00
R7686:Mfsd6	UTSW	1	52662395	missense	probably benign	0.00
R7763:Mfsd6	UTSW	1	52708640	missense	probably benign
R8138:Mfsd6	UTSW	1	52709512	missense	probably benign
R8150:Mfsd6	UTSW	1	52708641	missense	probably benign	0.00
R8807:Mfsd6	UTSW	1	52658547	critical splice acceptor site	probably benign
R8938:Mfsd6	UTSW	1	52709295	missense	probably damaging	1.00
R9229:Mfsd6	UTSW	1	52708744	missense	probably damaging	1.00
R9276:Mfsd6	UTSW	1	52708355	nonsense	probably null
R9480:Mfsd6	UTSW	1	52660676	missense	unknown
Z1177:Mfsd6	UTSW	1	52658501	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TTTGGCTCAGCACAAGACGG -3'
(R):5'- TCCATGAGGTATCCTGTTCCTAAG -3'

Sequencing Primer
(F):5'- ACGGCATTCAGAGCAGCTG -3'
(R):5'- AGGTATCCTGTTCCTAAGTTTGGAAC -3'

Posted On

2019-11-26