Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02458:Mfsd13a'

294524

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Mfsd13a

Ensembl Gene

ENSMUSG00000025227

Gene Name

major facilitator superfamily domain containing 13a

Synonyms

4930538D17Rik, 4930449A08Rik, Tmem180

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.477) question?

Stock #

IGL02458

Quality Score

Status

Chromosome

Chromosomal Location

46345315-46363693 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 46360686 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 388 (E388G)

Ref Sequence

ENSEMBL: ENSMUSP00000119072 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000040270] [ENSMUST00000086969] [ENSMUST00000128041] [ENSMUST00000128455] [ENSMUST00000142994]

AlphaFold

Q6PDE8

Predicted Effect

probably benign
Transcript: ENSMUST00000040270

SMART Domains

Protein: ENSMUSP00000039844
Gene: ENSMUSG00000025228

Domain	Start	End	E-Value	Type
ACTIN	9	376	4.18e-203	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000086969
AA Change: E388G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000084189
Gene: ENSMUSG00000025227
AA Change: E388G

Domain	Start	End	E-Value	Type
Pfam:MFS_2	15	441	6.2e-23	PFAM
low complexity region	453	463	N/A	INTRINSIC
transmembrane domain	470	492	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000128041
AA Change: E388G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000119072
Gene: ENSMUSG00000025227
AA Change: E388G

Domain	Start	End	E-Value	Type
Pfam:MFS_2	9	441	1.1e-26	PFAM
low complexity region	453	463	N/A	INTRINSIC
transmembrane domain	470	492	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000128455

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000137143

Predicted Effect

probably benign
Transcript: ENSMUST00000142994

SMART Domains

Protein: ENSMUSP00000122944
Gene: ENSMUSG00000025227

Domain	Start	End	E-Value	Type
Pfam:MFS_2	8	318	7.8e-17	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam25	A	T	8: 41,206,844 (GRCm39)	I37L	probably benign	Het
Alpk1	A	G	3: 127,474,968 (GRCm39)		probably null	Het
Ankrd33	T	C	15: 101,014,488 (GRCm39)	F8L	probably damaging	Het
Avil	A	G	10: 126,852,222 (GRCm39)	K669R	probably benign	Het
Bcor	G	T	X: 11,914,749 (GRCm39)	L1165I	probably damaging	Het
C7	A	G	15: 5,088,871 (GRCm39)		probably benign	Het
Cc2d2a	A	G	5: 43,875,896 (GRCm39)	I958V	probably benign	Het
Cenpe	A	T	3: 134,935,869 (GRCm39)	K435*	probably null	Het
Chrna7	G	A	7: 62,755,842 (GRCm39)	L235F	probably damaging	Het
Col6a3	C	A	1: 90,706,919 (GRCm39)	V2065L	unknown	Het
Copb1	A	T	7: 113,846,020 (GRCm39)	N183K	probably benign	Het
Cpn2	G	A	16: 30,079,653 (GRCm39)	A16V	probably benign	Het
Cul1	A	G	6: 47,502,542 (GRCm39)	K769E	possibly damaging	Het
Deup1	C	T	9: 15,503,656 (GRCm39)	V302M	probably benign	Het
Dnah17	T	C	11: 117,927,176 (GRCm39)	K3871E	probably damaging	Het
Dnah6	A	G	6: 73,004,431 (GRCm39)	V3844A	probably benign	Het
Dnah7a	A	T	1: 53,657,487 (GRCm39)	L763*	probably null	Het
Donson	A	T	16: 91,478,064 (GRCm39)	W461R	probably damaging	Het
Dpp10	T	C	1: 123,269,418 (GRCm39)	I664V	probably benign	Het
Dusp8	T	A	7: 141,636,484 (GRCm39)	T369S	probably benign	Het
Dync2h1	A	T	9: 7,117,422 (GRCm39)	L56Q	probably damaging	Het
Ecd	A	T	14: 20,374,545 (GRCm39)	S532T	probably benign	Het
Frg2f1	G	A	4: 119,388,154 (GRCm39)	T115I	probably damaging	Het
Gpatch2l	A	G	12: 86,335,735 (GRCm39)		probably benign	Het
Gtf3c2	T	A	5: 31,316,867 (GRCm39)		probably null	Het
Haghl	T	C	17: 26,002,470 (GRCm39)		probably benign	Het
Hoxc8	A	T	15: 102,901,181 (GRCm39)	N208I	probably damaging	Het
Igf2	T	C	7: 142,207,785 (GRCm39)	D115G	probably benign	Het
Jag2	T	A	12: 112,879,613 (GRCm39)	D385V	probably damaging	Het
Laptm4b	A	G	15: 34,258,888 (GRCm39)	H54R	probably benign	Het
Lrp2	A	G	2: 69,352,117 (GRCm39)	S640P	probably damaging	Het
Map3k8	A	C	18: 4,334,660 (GRCm39)	V328G	probably damaging	Het
Ms4a13	G	A	19: 11,149,292 (GRCm39)	T168I	probably benign	Het
Mtg1	C	A	7: 139,730,085 (GRCm39)	Q294K	probably benign	Het
Myh3	C	T	11: 66,987,766 (GRCm39)	A1413V	possibly damaging	Het
Neo1	A	T	9: 58,801,150 (GRCm39)		probably benign	Het
Ogfod3	T	C	11: 121,091,749 (GRCm39)	E119G	probably benign	Het
Or10ak9	A	G	4: 118,726,497 (GRCm39)	N173S	possibly damaging	Het
Or2t49	A	T	11: 58,393,073 (GRCm39)	M109K	probably benign	Het
Or4a77	A	G	2: 89,487,692 (GRCm39)	L31P	probably damaging	Het
Or5ak20	G	A	2: 85,184,006 (GRCm39)	T88I	probably benign	Het
Or6c210	A	T	10: 129,496,475 (GRCm39)	I267F	probably benign	Het
Parvb	G	T	15: 84,187,635 (GRCm39)	D248Y	probably damaging	Het
Pcdh11x	A	T	X: 119,310,315 (GRCm39)	H586L	possibly damaging	Het
Phactr2	T	C	10: 13,137,572 (GRCm39)	E120G	probably damaging	Het
Ppfibp2	A	T	7: 107,342,171 (GRCm39)	Q775L	probably damaging	Het
Rcbtb1	A	G	14: 59,467,443 (GRCm39)	Y427C	probably damaging	Het
Rftn2	A	T	1: 55,250,351 (GRCm39)	C131*	probably null	Het
Rigi	A	G	4: 40,229,536 (GRCm39)	S83P	probably damaging	Het
Rps6ka2	A	G	17: 7,556,402 (GRCm39)	D474G	probably benign	Het
Rsbn1l	T	C	5: 21,156,734 (GRCm39)	E17G	probably damaging	Het
Ryr2	T	C	13: 11,720,585 (GRCm39)	M2688V	probably benign	Het
Slc22a18	C	A	7: 143,046,574 (GRCm39)		probably benign	Het
Smarcc1	A	G	9: 109,961,194 (GRCm39)		probably benign	Het
Soat2	T	C	15: 102,070,550 (GRCm39)	V451A	probably damaging	Het
Sptlc2	A	T	12: 87,356,667 (GRCm39)		probably benign	Het
Tada1	C	T	1: 166,220,203 (GRCm39)	L308F	probably damaging	Het
Tango2	A	T	16: 18,128,731 (GRCm39)		probably null	Het
Tbc1d15	A	T	10: 115,065,111 (GRCm39)	V158D	probably damaging	Het
Tmx2	A	T	2: 84,503,588 (GRCm39)		probably benign	Het
Tpte	T	A	8: 22,795,874 (GRCm39)	I79K	probably benign	Het
Trav6-1	A	G	14: 52,876,199 (GRCm39)	I40V	probably benign	Het
Trgv3	A	G	13: 19,427,423 (GRCm39)	Y102C	probably damaging	Het
Ubash3a	T	C	17: 31,450,455 (GRCm39)	S377P	possibly damaging	Het
Vmn2r7	T	C	3: 64,600,446 (GRCm39)	D575G	probably damaging	Het
Vps41	A	G	13: 19,037,649 (GRCm39)	D704G	possibly damaging	Het
Vwa5a	T	C	9: 38,638,259 (GRCm39)	S261P	possibly damaging	Het
Zc3hav1	A	G	6: 38,317,264 (GRCm39)	V112A	probably damaging	Het

Other mutations in Mfsd13a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00232:Mfsd13a	APN	19	46,354,958 (GRCm39)	missense	probably damaging	1.00
IGL01380:Mfsd13a	APN	19	46,356,347 (GRCm39)	missense	probably damaging	1.00
IGL01773:Mfsd13a	APN	19	46,357,733 (GRCm39)	missense	possibly damaging	0.60
IGL02955:Mfsd13a	APN	19	46,356,192 (GRCm39)	missense	possibly damaging	0.81
R0057:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R0113:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R0114:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R0115:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R0361:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R0656:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R1174:Mfsd13a	UTSW	19	46,363,125 (GRCm39)	missense	probably benign	0.13
R1210:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R1251:Mfsd13a	UTSW	19	46,360,492 (GRCm39)	missense	probably damaging	1.00
R1364:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R1365:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R1366:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R1367:Mfsd13a	UTSW	19	46,354,943 (GRCm39)	missense	probably benign	0.22
R1692:Mfsd13a	UTSW	19	46,360,515 (GRCm39)	missense	probably benign	0.00
R1852:Mfsd13a	UTSW	19	46,360,619 (GRCm39)	critical splice acceptor site	probably null
R1968:Mfsd13a	UTSW	19	46,360,492 (GRCm39)	missense	probably damaging	1.00
R2846:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R2985:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R3415:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R3416:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R3431:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R3432:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R3735:Mfsd13a	UTSW	19	46,356,767 (GRCm39)	missense	probably damaging	1.00
R4393:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R4394:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R4396:Mfsd13a	UTSW	19	46,360,431 (GRCm39)	missense	probably damaging	1.00
R4920:Mfsd13a	UTSW	19	46,355,655 (GRCm39)	missense	probably damaging	1.00
R5289:Mfsd13a	UTSW	19	46,356,719 (GRCm39)	missense	probably benign	0.00
R5806:Mfsd13a	UTSW	19	46,354,849 (GRCm39)	missense	probably benign	0.01
R6153:Mfsd13a	UTSW	19	46,356,321 (GRCm39)	missense	probably damaging	1.00
R6514:Mfsd13a	UTSW	19	46,363,064 (GRCm39)	splice site	probably null
R6558:Mfsd13a	UTSW	19	46,354,917 (GRCm39)	missense	probably damaging	1.00
R6649:Mfsd13a	UTSW	19	46,360,704 (GRCm39)	missense	probably benign
R6649:Mfsd13a	UTSW	19	46,356,305 (GRCm39)	missense	probably damaging	0.99
R6653:Mfsd13a	UTSW	19	46,356,305 (GRCm39)	missense	probably damaging	0.99
R6911:Mfsd13a	UTSW	19	46,357,716 (GRCm39)	missense	probably damaging	1.00
R7022:Mfsd13a	UTSW	19	46,356,763 (GRCm39)	nonsense	probably null
R7334:Mfsd13a	UTSW	19	46,356,809 (GRCm39)	missense	probably damaging	1.00
R7525:Mfsd13a	UTSW	19	46,357,716 (GRCm39)	missense	probably damaging	1.00
R7976:Mfsd13a	UTSW	19	46,360,446 (GRCm39)	missense	probably benign	0.03
R8696:Mfsd13a	UTSW	19	46,356,557 (GRCm39)	missense	probably benign
R8771:Mfsd13a	UTSW	19	46,360,668 (GRCm39)	missense	probably damaging	0.99
R8857:Mfsd13a	UTSW	19	46,356,567 (GRCm39)	missense	probably benign	0.00
R9056:Mfsd13a	UTSW	19	46,354,900 (GRCm39)	missense	probably benign	0.04
R9432:Mfsd13a	UTSW	19	46,354,868 (GRCm39)	missense	probably benign	0.05

Posted On

2015-04-16