Mutagenetix > Incidental Mutation

Incidental Mutation 'R5976:Mfsd2b'

471788

Institutional Source

Beutler Lab

Gene Symbol

Mfsd2b

Ensembl Gene

ENSMUSG00000037336

Gene Name

MFSD2 lysolipid transporter B, sphingolipid

Synonyms

Gm1964, major facilitator superfamily domain containing 2B

MMRRC Submission

044158-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5976 (G1)

Quality Score

170

Status

Not validated

Chromosome

Chromosomal Location

4912440-4924359 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 4916522 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Aspartic acid at position 216 (A216D)

Ref Sequence

ENSEMBL: ENSMUSP00000117057 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045921] [ENSMUST00000085790] [ENSMUST00000137337] [ENSMUST00000147241]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000045921
AA Change: A319D

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

SMART Domains

Protein: ENSMUSP00000045315
Gene: ENSMUSG00000037336
AA Change: A319D

Domain	Start	End	E-Value	Type
Pfam:MFS_2	33	472	4.6e-74	PFAM
low complexity region	476	490	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000085790
AA Change: A319D

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

SMART Domains

Protein: ENSMUSP00000082945
Gene: ENSMUSG00000037336
AA Change: A319D

Domain	Start	End	E-Value	Type
Pfam:MFS_2	32	346	2.2e-56	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125344

Predicted Effect

probably damaging
Transcript: ENSMUST00000137337
AA Change: A216D

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

SMART Domains

Protein: ENSMUSP00000117057
Gene: ENSMUSG00000037336
AA Change: A216D

Domain	Start	End	E-Value	Type
Pfam:MFS_2	1	368	1.1e-59	PFAM
low complexity region	373	387	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143446

Predicted Effect

probably benign
Transcript: ENSMUST00000147241

SMART Domains

Protein: ENSMUSP00000114977
Gene: ENSMUSG00000037336

Domain	Start	End	E-Value	Type
Pfam:MFS_2	33	110	3.1e-13	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150764

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153676

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 94.2%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Homozygous KO reduces sphingosine-1-phosphate export from, and increases its accumulation in, red blood cells and platelets, and leads to reduced leukocyte, reticulocyte, and erythrocyte cell numbers. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ankar	T	C	1: 72,682,450 (GRCm39)	T1154A	probably benign	Het
Ankrd26	A	T	6: 118,494,855 (GRCm39)		probably null	Het
Arih2	A	T	9: 108,485,172 (GRCm39)	*54R	probably null	Het
AW146154	T	G	7: 41,129,721 (GRCm39)	K465T	probably damaging	Het
Bend3	A	G	10: 43,386,540 (GRCm39)	Y311C	probably benign	Het
Bltp2	G	A	11: 78,174,955 (GRCm39)	A1697T	probably benign	Het
Ccdc110	A	T	8: 46,396,536 (GRCm39)	Y809F	possibly damaging	Het
Ccnh	C	T	13: 85,338,982 (GRCm39)	P76L	probably damaging	Het
Chaf1a	T	A	17: 56,371,115 (GRCm39)	C667S	probably damaging	Het
Clca3a1	A	T	3: 144,452,636 (GRCm39)	Y616N	probably damaging	Het
Cldn4	A	G	5: 134,975,410 (GRCm39)	C64R	probably damaging	Het
Crybg2	TGGAGGAGGAGGAGGAGGAG	TGGAGGAGGAGGAGGAG	4: 133,801,837 (GRCm39)		probably benign	Het
Dclk2	C	A	3: 86,694,532 (GRCm39)	R752L	possibly damaging	Het
Dzank1	C	A	2: 144,343,409 (GRCm39)	G318W	probably damaging	Het
Edem1	T	A	6: 108,819,923 (GRCm39)	I236K	probably damaging	Het
Eif4e1b	T	C	13: 54,932,635 (GRCm39)	F75L	probably damaging	Het
Elmo3	A	G	8: 106,034,279 (GRCm39)	Y266C	probably damaging	Het
Enpep	A	G	3: 129,092,773 (GRCm39)	S509P	probably damaging	Het
Exoc8	A	G	8: 125,623,392 (GRCm39)	M325T	probably benign	Het
Fah	A	G	7: 84,243,949 (GRCm39)	M270T	probably benign	Het
Gabbr1	T	C	17: 37,378,754 (GRCm39)	L532P	probably damaging	Het
Gm10770	T	A	2: 150,021,320 (GRCm39)	K66*	probably null	Het
Gprc5c	A	T	11: 114,755,313 (GRCm39)	Q330L	possibly damaging	Het
Grin3a	T	A	4: 49,792,602 (GRCm39)	H377L	probably damaging	Het
Hipk3	T	C	2: 104,301,529 (GRCm39)	E221G	probably damaging	Het
Hsd17b6	T	A	10: 127,827,308 (GRCm39)	M255L	probably benign	Het
Ighv1-7	T	A	12: 114,502,379 (GRCm39)	E29D	probably benign	Het
Ing3	T	A	6: 21,971,173 (GRCm39)	S326T	probably benign	Het
Ipo7	T	C	7: 109,648,014 (GRCm39)	L632P	probably damaging	Het
Kdm6b	A	G	11: 69,294,614 (GRCm39)		probably null	Het
Kif21a	T	G	15: 90,820,015 (GRCm39)	D1583A	probably damaging	Het
Lama2	C	T	10: 27,066,672 (GRCm39)	V1070I	probably benign	Het
Lrp1	A	T	10: 127,419,770 (GRCm39)	S946R	probably damaging	Het
Lrrc37a	A	G	11: 103,389,897 (GRCm39)	S1843P	possibly damaging	Het
Ltbp1	T	C	17: 75,597,078 (GRCm39)	Y517H	probably damaging	Het
Map2k4	T	A	11: 65,600,778 (GRCm39)	N51I	probably benign	Het
Nbea	T	C	3: 55,761,268 (GRCm39)	T2025A	probably benign	Het
Neb	A	G	2: 52,106,928 (GRCm39)	V4162A	possibly damaging	Het
Nr3c1	A	T	18: 39,554,602 (GRCm39)	F599I	probably damaging	Het
Nsun2	T	G	13: 69,771,271 (GRCm39)		probably null	Het
Or10ab4	T	A	7: 107,655,005 (GRCm39)	M272K	possibly damaging	Het
Or8b37	G	T	9: 37,958,997 (GRCm39)	V160F	possibly damaging	Het
Otoa	T	A	7: 120,726,936 (GRCm39)	W524R	probably benign	Het
Paip1	T	A	13: 119,593,533 (GRCm39)	D182E	probably damaging	Het
Pde1a	G	A	2: 79,698,586 (GRCm39)	Q415*	probably null	Het
Pfkfb2	T	A	1: 130,635,816 (GRCm39)	K72*	probably null	Het
Pigg	A	G	5: 108,480,057 (GRCm39)	E444G	probably null	Het
Plec	T	C	15: 76,073,237 (GRCm39)	Y669C	probably damaging	Het
Ptp4a3	T	C	15: 73,627,885 (GRCm39)	V94A	possibly damaging	Het
Ptprg	A	G	14: 12,211,625 (GRCm38)	E969G	probably damaging	Het
R3hcc1l	T	A	19: 42,551,789 (GRCm39)	V262E	probably benign	Het
Ranbp3l	T	G	15: 9,030,916 (GRCm39)	F65C	possibly damaging	Het
Rbm19	T	A	5: 120,278,372 (GRCm39)	S718R	probably benign	Het
Recql4	C	A	15: 76,593,624 (GRCm39)	R162L	probably benign	Het
Rest	T	C	5: 77,416,119 (GRCm39)	L111P	probably benign	Het
Rgma	T	C	7: 73,059,216 (GRCm39)	S13P	probably damaging	Het
Rogdi	T	A	16: 4,831,175 (GRCm39)	I31F	probably benign	Het
Serpinb9e	T	A	13: 33,439,112 (GRCm39)	D179E	probably benign	Het
Slc1a5	T	C	7: 16,529,807 (GRCm39)	C409R	probably damaging	Het
Slc25a38	A	G	9: 119,945,613 (GRCm39)	T38A	probably damaging	Het
Spag17	C	T	3: 100,003,107 (GRCm39)	Q1897*	probably null	Het
St7	C	A	6: 17,694,221 (GRCm39)	A4E	possibly damaging	Het
Tbcel	T	A	9: 42,350,499 (GRCm39)	I263F	possibly damaging	Het
Tmtc3	A	G	10: 100,312,534 (GRCm39)	V103A	probably benign	Het
Tnc	G	A	4: 63,936,403 (GRCm39)	P178S	probably benign	Het
Vwf	A	G	6: 125,580,426 (GRCm39)	D558G		Het
Zfp541	A	G	7: 15,810,344 (GRCm39)	K127R	probably benign	Het

Other mutations in Mfsd2b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01810:Mfsd2b	APN	12	4,916,469 (GRCm39)	missense	possibly damaging	0.63
IGL03188:Mfsd2b	APN	12	4,916,538 (GRCm39)	splice site	probably null
IGL03339:Mfsd2b	APN	12	4,924,335 (GRCm39)	start codon destroyed	probably null
R0142:Mfsd2b	UTSW	12	4,916,234 (GRCm39)	missense	probably benign	0.11
R1468:Mfsd2b	UTSW	12	4,920,536 (GRCm39)	nonsense	probably null
R1468:Mfsd2b	UTSW	12	4,920,536 (GRCm39)	nonsense	probably null
R1535:Mfsd2b	UTSW	12	4,920,605 (GRCm39)	missense	probably damaging	1.00
R1718:Mfsd2b	UTSW	12	4,919,037 (GRCm39)	missense	probably damaging	1.00
R1894:Mfsd2b	UTSW	12	4,919,155 (GRCm39)	missense	probably damaging	0.99
R2127:Mfsd2b	UTSW	12	4,917,659 (GRCm39)	missense	probably benign	0.01
R2392:Mfsd2b	UTSW	12	4,915,164 (GRCm39)	missense	possibly damaging	0.73
R3737:Mfsd2b	UTSW	12	4,920,578 (GRCm39)	missense	probably damaging	1.00
R3738:Mfsd2b	UTSW	12	4,920,578 (GRCm39)	missense	probably damaging	1.00
R3739:Mfsd2b	UTSW	12	4,920,578 (GRCm39)	missense	probably damaging	1.00
R3956:Mfsd2b	UTSW	12	4,916,848 (GRCm39)	missense	probably damaging	1.00
R4035:Mfsd2b	UTSW	12	4,920,578 (GRCm39)	missense	probably damaging	1.00
R4244:Mfsd2b	UTSW	12	4,924,356 (GRCm39)	utr 5 prime	probably benign
R4595:Mfsd2b	UTSW	12	4,915,807 (GRCm39)	missense	possibly damaging	0.87
R4667:Mfsd2b	UTSW	12	4,917,636 (GRCm39)	missense	probably benign	0.01
R4723:Mfsd2b	UTSW	12	4,918,992 (GRCm39)	missense	probably benign	0.03
R5126:Mfsd2b	UTSW	12	4,916,183 (GRCm39)	missense	probably benign	0.30
R5145:Mfsd2b	UTSW	12	4,915,908 (GRCm39)	unclassified	probably benign
R5890:Mfsd2b	UTSW	12	4,917,651 (GRCm39)	missense	probably damaging	1.00
R6753:Mfsd2b	UTSW	12	4,917,358 (GRCm39)	missense	possibly damaging	0.90
R6912:Mfsd2b	UTSW	12	4,920,611 (GRCm39)	nonsense	probably null
R7182:Mfsd2b	UTSW	12	4,916,157 (GRCm39)	critical splice donor site	probably null
R7472:Mfsd2b	UTSW	12	4,916,481 (GRCm39)	missense	probably damaging	1.00
R8429:Mfsd2b	UTSW	12	4,916,487 (GRCm39)	missense	possibly damaging	0.90
R8559:Mfsd2b	UTSW	12	4,921,471 (GRCm39)	missense	possibly damaging	0.63
R8992:Mfsd2b	UTSW	12	4,921,490 (GRCm39)	missense	probably benign
R9410:Mfsd2b	UTSW	12	4,915,747 (GRCm39)	missense	probably damaging	1.00
R9474:Mfsd2b	UTSW	12	4,916,820 (GRCm39)	missense	possibly damaging	0.91
X0062:Mfsd2b	UTSW	12	4,915,170 (GRCm39)	missense	probably benign	0.01
Z1176:Mfsd2b	UTSW	12	4,916,530 (GRCm39)	critical splice acceptor site	probably null
Z1177:Mfsd2b	UTSW	12	4,915,794 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TTAGGAAGCTCAGCCCTGTAC -3'
(R):5'- TGAGCTGAGAACCTCAAGGG -3'

Sequencing Primer
(F):5'- GTACCTGGTCCCATGCTCG -3'
(R):5'- CCTCAAGGGCTAAAGTTTTAATAGTC -3'

Posted On

2017-03-31