Mutagenetix > Incidental Mutation

Incidental Mutation 'R0363:Flvcr1'

65701

Institutional Source

Beutler Lab

Gene Symbol

Flvcr1

Ensembl Gene

ENSMUSG00000066595

Gene Name

feline leukemia virus subgroup C cellular receptor 1

Synonyms

9630055N22Rik, Mfsd7b

MMRRC Submission

038569-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0363 (G1)

Quality Score

156

Status

Validated

Chromosome

Chromosomal Location

190738044-190758355 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 190744451 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000141985 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000085635] [ENSMUST00000192666]

AlphaFold

B2RXV4

Predicted Effect

probably benign
Transcript: ENSMUST00000085635

SMART Domains

Protein: ENSMUSP00000082777
Gene: ENSMUSG00000066595

Domain	Start	End	E-Value	Type
low complexity region	40	68	N/A	INTRINSIC
Pfam:MFS_1	100	483	1.5e-28	PFAM
transmembrane domain	498	517	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000192666

SMART Domains

Protein: ENSMUSP00000141985
Gene: ENSMUSG00000066595

Domain	Start	End	E-Value	Type
low complexity region	5	26	N/A	INTRINSIC
Pfam:MFS_1	54	198	3.1e-9	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000193399

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194589

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194917

Coding Region Coverage

1x: 98.9%
3x: 97.8%
10x: 94.7%
20x: 86.5%

Validation Efficiency

98% (78/80)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the major facilitator superfamily of transporter proteins. The encoded protein is a heme transporter that may play a critical role in erythropoiesis by protecting developing erythroid cells from heme toxicity. This gene may play a role in posterior column ataxia with retinitis pigmentosa and the hematological disorder Diamond-Blackfan syndrome. [provided by RefSeq, Jan 2011]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit runting, cardiomegaly and splenomegaly, lack definitive erythropoiesis, develop severe hyperchromic macrocytic anemia and reticulocytopenia, and show craniofacial and limb defects and intrauterine lethality modulated by genetic background. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930522H14Rik	T	A	4: 109,381,520 (GRCm39)	Q86L	probably null	Het
Abhd2	A	G	7: 79,000,561 (GRCm39)	D262G	possibly damaging	Het
Abhd5	T	C	9: 122,197,211 (GRCm39)	F133L	possibly damaging	Het
Agap2	T	A	10: 126,926,834 (GRCm39)	V957E	probably damaging	Het
Ankrd12	T	C	17: 66,292,676 (GRCm39)	K919R	probably damaging	Het
Ap1m1	T	C	8: 73,006,738 (GRCm39)	S245P	probably benign	Het
Ap1m1	T	C	8: 73,010,568 (GRCm39)		probably benign	Het
Apcdd1	A	G	18: 63,070,168 (GRCm39)	Y145C	possibly damaging	Het
Apob	A	T	12: 8,060,136 (GRCm39)	N2840Y	probably damaging	Het
Arel1	A	G	12: 84,981,027 (GRCm39)	S327P	probably damaging	Het
Arhgap21	C	A	2: 20,885,944 (GRCm39)	R421L	probably damaging	Het
Ccdc85a	A	T	11: 28,533,400 (GRCm39)	I48N	probably damaging	Het
Chd6	A	G	2: 160,856,244 (GRCm39)	S672P	probably damaging	Het
Ciz1	G	C	2: 32,267,375 (GRCm39)		probably null	Het
Cmbl	G	A	15: 31,585,588 (GRCm39)		probably null	Het
Cmya5	A	G	13: 93,231,377 (GRCm39)	V1237A	possibly damaging	Het
Cntnap4	A	T	8: 113,583,143 (GRCm39)	K1074*	probably null	Het
Cntnap5b	A	G	1: 100,202,193 (GRCm39)	M347V	probably benign	Het
Col1a2	G	A	6: 4,518,822 (GRCm39)		probably benign	Het
Cuzd1	A	T	7: 130,917,991 (GRCm39)	M203K	probably benign	Het
Cyp3a16	T	C	5: 145,392,689 (GRCm39)		probably benign	Het
Dlgap3	A	G	4: 127,129,314 (GRCm39)	E892G	probably damaging	Het
Dnah7b	T	C	1: 46,275,948 (GRCm39)	S2612P	probably damaging	Het
Epas1	T	G	17: 87,113,276 (GRCm39)		probably benign	Het
Etv5	G	A	16: 22,230,458 (GRCm39)	A192V	probably benign	Het
Fa2h	T	A	8: 112,075,921 (GRCm39)	H234L	probably damaging	Het
Fcho1	T	C	8: 72,170,134 (GRCm39)	Y47C	probably damaging	Het
Il1rl1	CTTGTTGTTGTTGTTGTTG	CTTGTTGTTGTTGTTGTTGTTG	1: 40,481,734 (GRCm39)		probably benign	Het
Ino80	G	A	2: 119,213,441 (GRCm39)	R1249C	probably damaging	Het
Inpp4b	T	C	8: 82,610,886 (GRCm39)		probably benign	Het
Isy1	G	A	6: 87,796,167 (GRCm39)	R257W	probably damaging	Het
Kmt2a	A	G	9: 44,721,010 (GRCm39)		probably null	Het
Krt4	G	A	15: 101,833,081 (GRCm39)	R9C	possibly damaging	Het
Map1a	T	C	2: 121,132,525 (GRCm39)	S876P	probably damaging	Het
Mettl21e	A	G	1: 44,250,190 (GRCm39)		probably null	Het
Msh2	C	T	17: 88,024,904 (GRCm39)	T594M	probably benign	Het
Mtmr3	A	G	11: 4,437,536 (GRCm39)	S973P	probably damaging	Het
Muc5ac	A	T	7: 141,354,697 (GRCm39)	M889L	probably benign	Het
Ntn1	A	G	11: 68,276,369 (GRCm39)	I193T	probably benign	Het
Nudt13	A	T	14: 20,359,851 (GRCm39)	I193F	probably damaging	Het
Or2n1	A	G	17: 38,486,338 (GRCm39)	D121G	probably damaging	Het
Or3a1	C	T	11: 74,225,925 (GRCm39)	G44D	probably damaging	Het
Or4b1b	A	T	2: 90,112,200 (GRCm39)	S240T	probably damaging	Het
Or5p73	A	T	7: 108,064,941 (GRCm39)	T137S	possibly damaging	Het
Otulin	A	G	15: 27,606,381 (GRCm39)	V344A	probably damaging	Het
P2rx7	C	T	5: 122,795,093 (GRCm39)	Q128*	probably null	Het
Pcdhb22	G	A	18: 37,652,213 (GRCm39)	R227H	probably benign	Het
Plekha5	G	A	6: 140,537,473 (GRCm39)	R646K	possibly damaging	Het
Pltp	C	T	2: 164,682,056 (GRCm39)	R394H	probably benign	Het
Ppip5k1	C	G	2: 121,177,836 (GRCm39)	A324P	probably damaging	Het
Pramel14	C	T	4: 143,718,221 (GRCm39)	M407I	probably benign	Het
Prdm13	A	C	4: 21,679,737 (GRCm39)	V251G	unknown	Het
Prkg1	T	C	19: 31,641,596 (GRCm39)	E29G	probably damaging	Het
Prrc2c	A	G	1: 162,525,380 (GRCm39)	S409P	unknown	Het
Rp1	T	A	1: 4,417,941 (GRCm39)	D1057V	probably damaging	Het
Rttn	G	A	18: 89,029,079 (GRCm39)	C599Y	probably damaging	Het
Shisa6	C	T	11: 66,416,153 (GRCm39)	R213Q	probably benign	Het
Slc3a1	T	C	17: 85,340,273 (GRCm39)	Y232H	probably damaging	Het
Slx4	G	A	16: 3,797,953 (GRCm39)	A1477V	probably damaging	Het
Ssrp1	T	G	2: 84,871,018 (GRCm39)	I218S	probably damaging	Het
St6galnac1	A	C	11: 116,659,756 (GRCm39)	S186A	probably benign	Het
Stab1	A	G	14: 30,880,965 (GRCm39)		probably benign	Het
Sycp2	T	C	2: 177,988,204 (GRCm39)		probably benign	Het
Syne2	T	A	12: 76,118,981 (GRCm39)	I5867N	probably damaging	Het
Taar7f	T	A	10: 23,925,839 (GRCm39)	D144E	probably damaging	Het
Tlcd5	A	T	9: 43,023,048 (GRCm39)	M84K	probably damaging	Het
Tmem87b	T	A	2: 128,673,153 (GRCm39)	S196T	probably damaging	Het
Tnfrsf21	A	G	17: 43,348,768 (GRCm39)	T127A	probably benign	Het
Trp73	A	G	4: 154,148,406 (GRCm39)	I336T	probably benign	Het
Ttl	A	G	2: 128,917,981 (GRCm39)	I148V	probably damaging	Het
Ttll7	T	C	3: 146,649,970 (GRCm39)	Y667H	probably benign	Het
Ubr4	A	G	4: 139,119,171 (GRCm39)	T152A	probably damaging	Het
Vmn1r58	A	T	7: 5,413,636 (GRCm39)	V198E	probably damaging	Het
Vps52	T	A	17: 34,181,091 (GRCm39)	F376L	probably benign	Het
Zfp1007	T	C	5: 109,824,754 (GRCm39)	E232G	probably benign	Het

Other mutations in Flvcr1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00093:Flvcr1	APN	1	190,747,686 (GRCm39)	nonsense	probably null
IGL01089:Flvcr1	APN	1	190,745,587 (GRCm39)	missense	probably damaging	0.98
IGL02572:Flvcr1	APN	1	190,757,843 (GRCm39)	missense	probably damaging	1.00
IGL03248:Flvcr1	APN	1	190,757,939 (GRCm39)	missense	probably damaging	1.00
R0009:Flvcr1	UTSW	1	190,740,388 (GRCm39)	missense	probably benign
R0122:Flvcr1	UTSW	1	190,753,423 (GRCm39)	missense	possibly damaging	0.79
R0417:Flvcr1	UTSW	1	190,743,416 (GRCm39)	missense	probably benign	0.05
R0718:Flvcr1	UTSW	1	190,757,779 (GRCm39)	missense	probably damaging	1.00
R1061:Flvcr1	UTSW	1	190,740,370 (GRCm39)	missense	probably benign	0.01
R1815:Flvcr1	UTSW	1	190,757,577 (GRCm39)	missense	probably damaging	1.00
R2029:Flvcr1	UTSW	1	190,753,353 (GRCm39)	missense	probably benign	0.01
R4590:Flvcr1	UTSW	1	190,744,343 (GRCm39)	missense	probably benign	0.05
R4766:Flvcr1	UTSW	1	190,753,303 (GRCm39)	missense	probably benign	0.00
R4889:Flvcr1	UTSW	1	190,757,764 (GRCm39)	missense	probably damaging	1.00
R4956:Flvcr1	UTSW	1	190,758,383 (GRCm39)	unclassified	probably benign
R4976:Flvcr1	UTSW	1	190,757,692 (GRCm39)	missense	probably damaging	1.00
R5434:Flvcr1	UTSW	1	190,758,206 (GRCm39)	missense	probably benign	0.07
R5508:Flvcr1	UTSW	1	190,757,656 (GRCm39)	missense	probably damaging	1.00
R5930:Flvcr1	UTSW	1	190,741,748 (GRCm39)	missense	probably damaging	1.00
R6698:Flvcr1	UTSW	1	190,757,929 (GRCm39)	missense	probably damaging	1.00
R6927:Flvcr1	UTSW	1	190,757,861 (GRCm39)	missense	possibly damaging	0.66
R7544:Flvcr1	UTSW	1	190,758,143 (GRCm39)	missense	probably damaging	0.99
R7654:Flvcr1	UTSW	1	190,743,802 (GRCm39)	missense	possibly damaging	0.83
R7853:Flvcr1	UTSW	1	190,757,843 (GRCm39)	missense	probably damaging	1.00
R8185:Flvcr1	UTSW	1	190,747,681 (GRCm39)	missense	probably damaging	1.00
R8387:Flvcr1	UTSW	1	190,743,731 (GRCm39)	critical splice donor site	probably null
R8995:Flvcr1	UTSW	1	190,743,817 (GRCm39)	missense	probably damaging	1.00
R9092:Flvcr1	UTSW	1	190,740,364 (GRCm39)	missense
R9202:Flvcr1	UTSW	1	190,744,351 (GRCm39)	missense	probably benign	0.04
R9448:Flvcr1	UTSW	1	190,744,406 (GRCm39)	missense	possibly damaging	0.65
R9487:Flvcr1	UTSW	1	190,743,829 (GRCm39)	missense	possibly damaging	0.79
X0064:Flvcr1	UTSW	1	190,757,644 (GRCm39)	missense	probably benign	0.08

Predicted Primers

PCR Primer
(F):5'- CCAGTAAGGCAGATCATTGCAAGCA -3'
(R):5'- ACTGTGCCTCAGCATTGCCC -3'

Sequencing Primer
(F):5'- agctgagttacctagtgaaacc -3'
(R):5'- gcagtcatctctccagcc -3'

Posted On

2013-08-08