Mutagenetix > Incidental Mutation

Incidental Mutation 'R9268:Mfsd14b'

702700

Institutional Source

Beutler Lab

Gene Symbol

Mfsd14b

Ensembl Gene

ENSMUSG00000038212

Gene Name

major facilitator superfamily domain containing 14B

Synonyms

5730414C17Rik, Hiatl1

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.190) question?

Stock #

R9268 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

65212844-65260813 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 65222855 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 265 (L265P)

Ref Sequence

ENSEMBL: ENSMUSP00000118180 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054730] [ENSMUST00000155487]

AlphaFold

Q8CIA9

Predicted Effect

probably damaging
Transcript: ENSMUST00000054730
AA Change: L265P

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

SMART Domains

Protein: ENSMUSP00000062566
Gene: ENSMUSG00000038212
AA Change: L265P

Domain	Start	End	E-Value	Type
Pfam:MFS_1	50	396	4.5e-33	PFAM
transmembrane domain	428	450	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000155487
AA Change: L265P

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

SMART Domains

Protein: ENSMUSP00000118180
Gene: ENSMUSG00000038212
AA Change: L265P

Domain	Start	End	E-Value	Type
Pfam:MFS_1	50	396	4.6e-33	PFAM
transmembrane domain	428	450	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

100% (64/64)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933434E20Rik	A	G	3: 89,969,030 (GRCm39)	T218A	possibly damaging	Het
Acadsb	C	T	7: 131,033,763 (GRCm39)	T260I	probably damaging	Het
Acap2	A	T	16: 30,955,392 (GRCm39)	V161E	probably damaging	Het
Adnp	A	G	2: 168,031,233 (GRCm39)	I26T	possibly damaging	Het
Alk	T	C	17: 72,181,190 (GRCm39)	T1367A	probably damaging	Het
Apoa5	A	T	9: 46,181,719 (GRCm39)	D265V	probably benign	Het
Asb15	G	A	6: 24,566,298 (GRCm39)	R417H	probably benign	Het
Atg2a	A	C	19: 6,291,905 (GRCm39)	H27P	probably damaging	Het
Bace1	G	T	9: 45,767,282 (GRCm39)		probably benign	Het
Camk1d	A	G	2: 5,303,901 (GRCm39)	S351P	probably benign	Het
Carf	C	A	1: 60,148,558 (GRCm39)	Q85K	possibly damaging	Het
Cdh19	A	G	1: 110,877,111 (GRCm39)	F76S	probably damaging	Het
Ces1b	A	C	8: 93,798,583 (GRCm39)	V201G	probably damaging	Het
Clk1	A	G	1: 58,458,882 (GRCm39)	L133S	unknown	Het
Clstn3	G	A	6: 124,433,880 (GRCm39)	L427F	probably damaging	Het
Col15a1	G	C	4: 47,288,200 (GRCm39)		probably benign	Het
Cyp2j11	A	T	4: 96,207,781 (GRCm39)		probably benign	Het
Dctn4	T	A	18: 60,659,304 (GRCm39)	M1K	probably null	Het
Dnah12	A	G	14: 26,571,255 (GRCm39)	K2788R	possibly damaging	Het
Dtna	T	A	18: 23,702,643 (GRCm39)	V58D	possibly damaging	Het
Egfr	T	A	11: 16,855,410 (GRCm39)	D898E	probably damaging	Het
Eif2ak4	G	C	2: 118,271,701 (GRCm39)		probably null	Het
Enam	A	G	5: 88,640,778 (GRCm39)	M147V	probably benign	Het
Etaa1	A	T	11: 17,896,419 (GRCm39)	V566E	probably damaging	Het
F13a1	C	T	13: 37,076,910 (GRCm39)	G593D	probably benign	Het
Far2	C	T	6: 148,060,418 (GRCm39)	T257I	probably benign	Het
Fat4	C	T	3: 38,942,396 (GRCm39)	R430C	probably damaging	Het
Fhod3	T	C	18: 24,842,832 (GRCm39)		probably null	Het
Fuca2	G	A	10: 13,390,563 (GRCm39)	W453*	probably null	Het
Hjv	T	C	3: 96,435,881 (GRCm39)	F380L	probably benign	Het
Hycc2	T	C	1: 58,591,361 (GRCm39)	D94G	probably damaging	Het
Ift70a1	A	T	2: 75,811,279 (GRCm39)	V268E	probably benign	Het
Igkv4-72	A	T	6: 69,203,980 (GRCm39)	Y70*	probably null	Het
Kdm1b	A	C	13: 47,217,705 (GRCm39)	N388T	probably benign	Het
Klri2	A	T	6: 129,710,037 (GRCm39)	W188R	probably damaging	Het
Lama4	A	G	10: 38,950,688 (GRCm39)	Y997C	probably damaging	Het
Lrrc73	T	C	17: 46,565,535 (GRCm39)	S89P	probably benign	Het
Macf1	T	C	4: 123,367,582 (GRCm39)	E2393G	probably damaging	Het
Msantd5f3	T	C	4: 73,575,373 (GRCm39)	S351P	probably damaging	Het
Myo3b	A	C	2: 70,257,305 (GRCm39)	*1334C	probably null	Het
Nfatc4	A	T	14: 56,064,685 (GRCm39)	I391F	probably damaging	Het
Nlgn1	A	T	3: 25,490,548 (GRCm39)	M393K	probably damaging	Het
Or5h17	T	G	16: 58,820,083 (GRCm39)	F12V	probably damaging	Het
Or9i14	A	T	19: 13,792,388 (GRCm39)	C189S	probably damaging	Het
Otogl	A	T	10: 107,616,917 (GRCm39)	C1787S	probably damaging	Het
Papola	A	G	12: 105,766,032 (GRCm39)	E44G	probably benign	Het
Parp1	A	G	1: 180,415,509 (GRCm39)	K443E	possibly damaging	Het
Pcdh15	A	T	10: 74,479,455 (GRCm39)	E522V	probably benign	Het
Peli2	A	G	14: 48,518,927 (GRCm39)	E225G	probably benign	Het
Pus7l	T	C	15: 94,431,445 (GRCm39)	I395V	probably benign	Het
Rmi1	T	C	13: 58,555,853 (GRCm39)	I34T	probably damaging	Het
Rnf220	A	G	4: 117,346,833 (GRCm39)	I193T	probably benign	Het
Rpgrip1l	T	C	8: 92,007,355 (GRCm39)	T412A	probably benign	Het
Shisa7	T	G	7: 4,837,333 (GRCm39)	D244A	probably damaging	Het
Slco3a1	T	C	7: 73,952,946 (GRCm39)	T538A	probably benign	Het
Sptlc1	A	T	13: 53,512,872 (GRCm39)	I162N	probably damaging	Het
Ssrp1	C	A	2: 84,870,606 (GRCm39)		probably benign	Het
Sytl2	A	G	7: 90,034,359 (GRCm39)	N523S	probably benign	Het
Tcf20	A	G	15: 82,740,705 (GRCm39)	S249P	probably benign	Het
Thumpd3	T	A	6: 113,043,819 (GRCm39)	F411L	probably damaging	Het
Ttn	A	G	2: 76,768,079 (GRCm39)	W3007R	unknown	Het
Ulbp1	A	T	10: 7,396,392 (GRCm39)	L295Q	unknown	Het
Vmn1r29	T	A	6: 58,284,577 (GRCm39)	V99E	probably damaging	Het
Wdr47	T	C	3: 108,525,812 (GRCm39)	F112L	probably benign	Het
Wnk2	A	G	13: 49,235,507 (GRCm39)	V636A	possibly damaging	Het
Zswim8	T	C	14: 20,761,908 (GRCm39)	L227P	probably damaging	Het

Other mutations in Mfsd14b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00697:Mfsd14b	APN	13	65,214,515 (GRCm39)	missense	probably benign	0.00
IGL01935:Mfsd14b	APN	13	65,215,739 (GRCm39)	missense	probably benign
IGL01957:Mfsd14b	APN	13	65,234,907 (GRCm39)	missense	possibly damaging	0.90
R0555:Mfsd14b	UTSW	13	65,226,259 (GRCm39)	missense	probably benign	0.34
R0601:Mfsd14b	UTSW	13	65,234,964 (GRCm39)	missense	possibly damaging	0.88
R0988:Mfsd14b	UTSW	13	65,260,307 (GRCm39)	splice site	probably benign
R1136:Mfsd14b	UTSW	13	65,243,506 (GRCm39)	missense	probably benign	0.22
R1494:Mfsd14b	UTSW	13	65,243,485 (GRCm39)	missense	probably damaging	1.00
R2087:Mfsd14b	UTSW	13	65,215,796 (GRCm39)	missense	probably damaging	1.00
R4223:Mfsd14b	UTSW	13	65,214,422 (GRCm39)	utr 3 prime	probably benign
R5103:Mfsd14b	UTSW	13	65,234,907 (GRCm39)	missense	possibly damaging	0.56
R5568:Mfsd14b	UTSW	13	65,219,936 (GRCm39)	splice site	probably null
R5603:Mfsd14b	UTSW	13	65,221,420 (GRCm39)	missense	probably benign	0.00
R6181:Mfsd14b	UTSW	13	65,260,398 (GRCm39)	missense	probably benign	0.00
R6330:Mfsd14b	UTSW	13	65,243,500 (GRCm39)	missense	probably damaging	1.00
R6649:Mfsd14b	UTSW	13	65,214,599 (GRCm39)	missense	probably damaging	1.00
R7460:Mfsd14b	UTSW	13	65,219,837 (GRCm39)	missense	probably damaging	1.00
R7605:Mfsd14b	UTSW	13	65,214,591 (GRCm39)	missense	probably benign
R9034:Mfsd14b	UTSW	13	65,223,500 (GRCm39)	missense	probably damaging	1.00
R9545:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9597:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9598:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9598:Mfsd14b	UTSW	13	65,214,522 (GRCm39)	missense	probably benign	0.00
R9633:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9672:Mfsd14b	UTSW	13	65,260,320 (GRCm39)	missense	probably benign	0.00
R9696:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9698:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9702:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9755:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9756:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9783:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9801:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9802:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
R9803:Mfsd14b	UTSW	13	65,221,414 (GRCm39)	missense	probably benign	0.00
X0017:Mfsd14b	UTSW	13	65,219,867 (GRCm39)	missense	probably benign	0.08
X0027:Mfsd14b	UTSW	13	65,219,825 (GRCm39)	missense	probably benign	0.16
X0063:Mfsd14b	UTSW	13	65,226,299 (GRCm39)	splice site	probably null

Predicted Primers

PCR Primer
(F):5'- GGCCATCACTGAAATCACTGG -3'
(R):5'- TGCAGGCAGCTTGAATATCAAC -3'

Sequencing Primer
(F):5'- CTGAAATCACTGGACTATACAAAGTC -3'
(R):5'- GAATGTCAAGGTCATTCTCAGCTGC -3'

Posted On

2022-03-25