Mutagenetix > Incidental Mutation

Incidental Mutation 'R8839:Mfsd9'

674303

Institutional Source

Beutler Lab

Gene Symbol

Mfsd9

Ensembl Gene

ENSMUSG00000041945

Gene Name

major facilitator superfamily domain containing 9

Synonyms

4931419K03Rik

MMRRC Submission

068667-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R8839 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

40811200-40829817 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 40813554 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 254 (T254A)

Ref Sequence

ENSEMBL: ENSMUSP00000035727 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039672] [ENSMUST00000131390]

AlphaFold

Q8C0T7

Predicted Effect

probably benign
Transcript: ENSMUST00000039672
AA Change: T254A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000035727
Gene: ENSMUSG00000041945
AA Change: T254A

Domain	Start	End	E-Value	Type
low complexity region	16	32	N/A	INTRINSIC
Pfam:Sugar_tr	39	301	4.7e-8	PFAM
Pfam:MFS_1	39	419	1.8e-42	PFAM
low complexity region	436	447	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000131390

SMART Domains

Protein: ENSMUSP00000137884
Gene: ENSMUSG00000041945

Domain	Start	End	E-Value	Type
low complexity region	16	32	N/A	INTRINSIC
low complexity region	36	46	N/A	INTRINSIC

Meta Mutation Damage Score

0.0936

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (51/51)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ace3	T	C	11: 105,889,194 (GRCm39)	Y475H	probably damaging	Het
Ankfy1	T	C	11: 72,621,392 (GRCm39)	I226T	probably benign	Het
Anln	G	A	9: 22,267,468 (GRCm39)	S825L	probably benign	Het
Aoc1l2	T	C	6: 48,907,974 (GRCm39)	Y325H	probably damaging	Het
Arb2a	A	T	13: 78,147,781 (GRCm39)	H283L	probably benign	Het
B3galt4	A	G	17: 34,169,867 (GRCm39)	S124P	possibly damaging	Het
Cabin1	T	C	10: 75,492,650 (GRCm39)	I1882V	probably benign	Het
Caprin2	A	T	6: 148,774,525 (GRCm39)	S262R	probably benign	Het
Csmd2	A	C	4: 128,336,681 (GRCm39)	I1420L		Het
Cyp2b9	T	G	7: 25,900,185 (GRCm39)	V331G	probably damaging	Het
Cyp3a59	A	T	5: 146,045,896 (GRCm39)	M433L	probably benign	Het
Edrf1	A	G	7: 133,255,644 (GRCm39)	D597G	probably benign	Het
Emc3	G	A	6: 113,496,931 (GRCm39)	R147C	possibly damaging	Het
Fkbp7	T	C	2: 76,497,581 (GRCm39)		probably benign	Het
Flii	T	C	11: 60,609,433 (GRCm39)	T665A	possibly damaging	Het
Fxr1	A	G	3: 34,100,831 (GRCm39)		probably benign	Het
Gpr37	T	G	6: 25,669,369 (GRCm39)	I492L	probably benign	Het
Hmg20b	A	C	10: 81,184,749 (GRCm39)	W108G	probably damaging	Het
Ighv9-3	G	A	12: 114,104,385 (GRCm39)	T93I	possibly damaging	Het
Inpp5a	T	C	7: 138,969,349 (GRCm39)	V15A	probably benign	Het
Inpp5d	T	A	1: 87,619,433 (GRCm39)	Y376N	probably damaging	Het
Ints6	A	G	14: 62,931,122 (GRCm39)	F854L	probably benign	Het
Ipo7	A	T	7: 109,641,223 (GRCm39)	K314N	probably damaging	Het
Ltn1	C	A	16: 87,215,390 (GRCm39)	C415F	probably damaging	Het
Musk	A	G	4: 58,286,151 (GRCm39)	T14A	probably benign	Het
Ncapd3	T	C	9: 27,005,730 (GRCm39)	V1438A		Het
Nnt	A	T	13: 119,494,173 (GRCm39)	V636D	unknown	Het
Or10ak14	A	G	4: 118,611,411 (GRCm39)	L110P	probably damaging	Het
Or11h23	A	T	14: 50,947,957 (GRCm39)	T57S	possibly damaging	Het
Or52ae9	A	G	7: 103,390,021 (GRCm39)	I142T	probably benign	Het
Ost4	T	C	5: 31,064,935 (GRCm39)		probably benign	Het
Pdzph1	T	C	17: 59,257,237 (GRCm39)	T934A	probably benign	Het
Plekhn1	T	A	4: 156,307,046 (GRCm39)		probably benign	Het
Prkd1	T	C	12: 50,389,616 (GRCm39)		probably benign	Het
Ptch1	A	T	13: 63,689,038 (GRCm39)	L413Q	probably damaging	Het
S100pbp	A	G	4: 129,076,000 (GRCm39)		probably null	Het
Sec23a	T	C	12: 59,037,781 (GRCm39)	K361E	possibly damaging	Het
Sema3b	C	T	9: 107,478,552 (GRCm39)		probably benign	Het
Serpina3g	A	G	12: 104,204,038 (GRCm39)		probably benign	Het
Slc23a2	C	T	2: 131,943,392 (GRCm39)		silent	Het
Smug1	T	C	15: 103,064,247 (GRCm39)	R225G	possibly damaging	Het
Srbd1	T	A	17: 86,295,849 (GRCm39)	I854L	probably benign	Het
Tbc1d16	G	A	11: 119,047,474 (GRCm39)	R417C	probably damaging	Het
Tiam1	A	G	16: 89,681,827 (GRCm39)	Y384H	probably damaging	Het
Trappc9	T	A	15: 72,930,087 (GRCm39)	K90*	probably null	Het
Tubgcp6	A	T	15: 88,987,681 (GRCm39)	H1097Q	possibly damaging	Het
Ugt2b37	A	G	5: 87,402,415 (GRCm39)	L72P	probably damaging	Het
Vmn2r20	A	T	6: 123,373,515 (GRCm39)	H442Q	possibly damaging	Het
Vmn2r65	A	T	7: 84,595,489 (GRCm39)	Y398*	probably null	Het
Zfhx4	A	G	3: 5,466,915 (GRCm39)	T2383A	probably benign	Het

Other mutations in Mfsd9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00946:Mfsd9	APN	1	40,812,940 (GRCm39)	missense	probably benign	0.22
IGL01453:Mfsd9	APN	1	40,829,638 (GRCm39)	splice site	probably benign
R0631:Mfsd9	UTSW	1	40,829,634 (GRCm39)	splice site	probably benign
R1644:Mfsd9	UTSW	1	40,812,958 (GRCm39)	missense	probably benign	0.39
R4204:Mfsd9	UTSW	1	40,820,670 (GRCm39)	missense	probably damaging	1.00
R4761:Mfsd9	UTSW	1	40,813,635 (GRCm39)	missense	possibly damaging	0.61
R4777:Mfsd9	UTSW	1	40,820,700 (GRCm39)	missense	possibly damaging	0.64
R5109:Mfsd9	UTSW	1	40,813,365 (GRCm39)	missense	probably damaging	0.98
R6712:Mfsd9	UTSW	1	40,825,601 (GRCm39)	splice site	probably null
R8776:Mfsd9	UTSW	1	40,812,915 (GRCm39)	makesense	probably null
R8776-TAIL:Mfsd9	UTSW	1	40,812,915 (GRCm39)	makesense	probably null
R9411:Mfsd9	UTSW	1	40,829,692 (GRCm39)	missense	probably damaging	0.98
R9478:Mfsd9	UTSW	1	40,812,941 (GRCm39)	missense	probably benign	0.00
R9499:Mfsd9	UTSW	1	40,813,152 (GRCm39)	missense	probably damaging	0.96
R9551:Mfsd9	UTSW	1	40,813,152 (GRCm39)	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- TAGCTGATGAGGTACCCTGTG -3'
(R):5'- CTGTGAGAATCCAGCACACTG -3'

Sequencing Primer
(F):5'- TACCCTGTGGTCTTGGGCC -3'
(R):5'- TGGCCACCTTAACAAGTCTC -3'

Posted On

2021-07-15