Mutagenetix > Incidental Mutation

Incidental Mutation 'R1737:Sulf2'

199759

Institutional Source

Beutler Lab

Gene Symbol

Sulf2

Ensembl Gene

ENSMUSG00000006800

Gene Name

sulfatase 2

Synonyms

2010004N24Rik

MMRRC Submission

039769-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.313) question?

Stock #

R1737 (G1)

Quality Score

201

Status

Validated

Chromosome

Chromosomal Location

165915819-165997603 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 165924598 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 496 (V496E)

Ref Sequence

ENSEMBL: ENSMUSP00000154557 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000088086] [ENSMUST00000109249] [ENSMUST00000146497]

AlphaFold

Q8CFG0

Predicted Effect

probably benign
Transcript: ENSMUST00000088086
AA Change: V496E

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000085405
Gene: ENSMUSG00000006800
AA Change: V496E

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
Pfam:Sulfatase	44	375	2.8e-50	PFAM
low complexity region	512	523	N/A	INTRINSIC
Pfam:DUF3740	533	669	5.6e-47	PFAM
low complexity region	702	720	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000109249
AA Change: V496E

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000104872
Gene: ENSMUSG00000006800
AA Change: V496E

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
Pfam:Sulfatase	44	375	2.8e-50	PFAM
low complexity region	512	523	N/A	INTRINSIC
Pfam:DUF3740	532	670	1.3e-46	PFAM
low complexity region	702	720	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143996

Predicted Effect

probably benign
Transcript: ENSMUST00000146497
AA Change: V496E

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)

Meta Mutation Damage Score

0.0888

Coding Region Coverage

1x: 97.6%
3x: 96.9%
10x: 95.1%
20x: 91.4%

Validation Efficiency

100% (75/75)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Heparan sulfate proteoglycans (HSPGs) act as coreceptors for numerous heparin-binding growth factors and cytokines and are involved in cell signaling. Heparan sulfate 6-O-endosulfatases, such as SULF2, selectively remove 6-O-sulfate groups from heparan sulfate. This activity modulates the effects of heparan sulfate by altering binding sites for signaling molecules (Dai et al., 2005 [PubMed 16192265]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Homozygous disruption of this gene may lead to a partially penetrant, strain-dependent phenotype of embryonic lethality, reduced postnatal body weight, lung abnormalities, brain malformations, and reduced fertility. Mice homozygous for a hypomorphic gene-trap allele display skeletal defects. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts16	G	A	13: 70,927,637 (GRCm39)		probably benign	Het
Ak7	G	A	12: 105,708,591 (GRCm39)	V349M	probably damaging	Het
Aldh1a2	A	T	9: 71,192,453 (GRCm39)	E436V	possibly damaging	Het
Apc	C	A	18: 34,450,075 (GRCm39)	P2290T	probably damaging	Het
Atp10a	T	C	7: 58,476,986 (GRCm39)		probably benign	Het
Bahd1	T	C	2: 118,746,404 (GRCm39)	S8P	probably damaging	Het
BC049715	C	T	6: 136,817,306 (GRCm39)	P182L	probably damaging	Het
Capn10	T	C	1: 92,862,677 (GRCm39)	Y28H	probably benign	Het
Cdh10	A	T	15: 18,964,149 (GRCm39)	I104F	probably damaging	Het
Cep170b	A	G	12: 112,703,061 (GRCm39)	D508G	possibly damaging	Het
Ces2a	G	T	8: 105,467,456 (GRCm39)	A494S	probably damaging	Het
Ces4a	G	A	8: 105,864,729 (GRCm39)	G69S	probably damaging	Het
Cltc	G	A	11: 86,624,553 (GRCm39)	T123M	probably damaging	Het
Cnot1	A	G	8: 96,474,904 (GRCm39)	S1102P	probably damaging	Het
Col12a1	C	A	9: 79,610,733 (GRCm39)	D224Y	probably damaging	Het
Col14a1	T	A	15: 55,208,357 (GRCm39)		probably benign	Het
Cyp7a1	T	A	4: 6,272,848 (GRCm39)	T122S	probably benign	Het
Dock4	A	G	12: 40,857,000 (GRCm39)		probably null	Het
Eid2	T	C	7: 27,967,924 (GRCm39)	V182A	possibly damaging	Het
Eloa	A	T	4: 135,738,081 (GRCm39)	V293D	probably benign	Het
Enkur	G	A	2: 21,199,106 (GRCm39)	P143S	probably damaging	Het
Ep300	T	C	15: 81,510,548 (GRCm39)	Y99H	probably damaging	Het
Fbxw5	C	A	2: 25,393,596 (GRCm39)	L66I	probably benign	Het
Flg2	A	T	3: 93,110,928 (GRCm39)	R985S	unknown	Het
Fscb	A	T	12: 64,521,355 (GRCm39)	I37K	possibly damaging	Het
H2-M10.3	T	C	17: 36,679,296 (GRCm39)	N3S	probably benign	Het
H2-Q7	A	C	17: 35,658,602 (GRCm39)	Y80S	probably damaging	Het
H60c	A	T	10: 3,209,914 (GRCm39)	D124E	possibly damaging	Het
Hsd3b2	A	T	3: 98,618,862 (GRCm39)	V361E	probably damaging	Het
Ice1	A	C	13: 70,754,444 (GRCm39)	C547W	probably damaging	Het
Itprid1	A	T	6: 55,945,289 (GRCm39)	D670V	probably damaging	Het
Jmy	A	G	13: 93,635,303 (GRCm39)	V171A	probably damaging	Het
Klf7	C	A	1: 64,118,372 (GRCm39)	R75L	possibly damaging	Het
Klk1b1	A	T	7: 43,619,783 (GRCm39)	Q114L	probably benign	Het
Krt10	A	G	11: 99,278,213 (GRCm39)	M280T	possibly damaging	Het
Lama1	G	A	17: 68,109,916 (GRCm39)	R2179Q	probably benign	Het
Mbd3l1	C	T	9: 18,396,225 (GRCm39)	P117S	possibly damaging	Het
Med18	A	T	4: 132,187,420 (GRCm39)	S71R	probably damaging	Het
Mov10l1	T	A	15: 88,895,607 (GRCm39)	I643N	possibly damaging	Het
Nfib	T	C	4: 82,416,826 (GRCm39)	K70E	probably damaging	Het
Nr3c2	A	C	8: 77,634,958 (GRCm39)	S20R	probably benign	Het
Nr6a1	A	T	2: 38,628,955 (GRCm39)	F356L	probably benign	Het
Oca2	G	A	7: 55,978,533 (GRCm39)	R567H	probably damaging	Het
Or10k2	A	G	8: 84,268,045 (GRCm39)	S91G	probably benign	Het
Or1e35	T	A	11: 73,797,911 (GRCm39)	M136L	possibly damaging	Het
Or1p1	T	C	11: 74,179,637 (GRCm39)	L55P	probably damaging	Het
Or6c88	T	A	10: 129,406,697 (GRCm39)	Y58N	probably damaging	Het
Or8g33	T	C	9: 39,338,254 (GRCm39)	T38A	probably damaging	Het
Pcdhb10	A	G	18: 37,546,009 (GRCm39)	T362A	probably benign	Het
Pip5k1b	A	T	19: 24,374,404 (GRCm39)	V59E	probably damaging	Het
Pkhd1l1	G	A	15: 44,410,905 (GRCm39)		probably null	Het
Prr36	T	C	8: 4,264,370 (GRCm39)		probably benign	Het
Ptger2	A	G	14: 45,239,228 (GRCm39)	T289A	probably benign	Het
Rad18	A	G	6: 112,658,498 (GRCm39)	F136L	probably damaging	Het
Rhbg	T	A	3: 88,153,181 (GRCm39)	S258C	probably damaging	Het
Scgb2b27	T	C	7: 33,712,739 (GRCm39)	I34M	possibly damaging	Het
Senp7	C	A	16: 55,944,162 (GRCm39)	T135K	probably damaging	Het
Slc20a2	A	G	8: 23,035,582 (GRCm39)	I193M	probably damaging	Het
Slc27a1	G	A	8: 72,023,504 (GRCm39)	V47I	probably benign	Het
Slc9a5	G	A	8: 106,094,766 (GRCm39)	V786M	probably damaging	Het
Smyd1	A	G	6: 71,193,875 (GRCm39)	L350P	probably damaging	Het
Ston2	A	T	12: 91,614,681 (GRCm39)	F576I	probably damaging	Het
Tcl1b3	C	A	12: 105,157,481 (GRCm39)	S41Y	probably damaging	Het
Tulp2	A	T	7: 45,169,201 (GRCm39)	N256I	probably damaging	Het
Uspl1	T	A	5: 149,138,668 (GRCm39)	C349S	probably damaging	Het
Vcl	T	C	14: 21,070,604 (GRCm39)	I730T	probably damaging	Het
Vmn1r61	A	T	7: 5,614,060 (GRCm39)	F85I	probably benign	Het
Zfp318	A	G	17: 46,710,403 (GRCm39)	T709A	probably benign	Het
Zfr2	T	C	10: 81,077,919 (GRCm39)	S249P	probably damaging	Het

Other mutations in Sulf2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00844:Sulf2	APN	2	165,936,412 (GRCm39)	missense	possibly damaging	0.48
IGL01353:Sulf2	APN	2	165,929,015 (GRCm39)	missense	probably damaging	1.00
IGL02427:Sulf2	APN	2	165,931,218 (GRCm39)	missense	probably damaging	0.99
IGL02602:Sulf2	APN	2	165,923,220 (GRCm39)	missense	probably benign	0.32
IGL02681:Sulf2	APN	2	165,958,905 (GRCm39)	missense	probably benign	0.01
IGL03047:Sulf2	APN	2	165,922,814 (GRCm39)	splice site	probably null
PIT4468001:Sulf2	UTSW	2	165,922,720 (GRCm39)	missense	probably benign
R0029:Sulf2	UTSW	2	165,958,893 (GRCm39)	missense	possibly damaging	0.46
R0029:Sulf2	UTSW	2	165,958,893 (GRCm39)	missense	possibly damaging	0.46
R0233:Sulf2	UTSW	2	165,927,589 (GRCm39)	splice site	probably benign
R0332:Sulf2	UTSW	2	165,931,119 (GRCm39)	missense	probably benign	0.00
R0411:Sulf2	UTSW	2	165,935,436 (GRCm39)	missense	probably damaging	1.00
R0599:Sulf2	UTSW	2	165,925,799 (GRCm39)	missense	possibly damaging	0.53
R0694:Sulf2	UTSW	2	165,927,711 (GRCm39)	missense	probably damaging	1.00
R1594:Sulf2	UTSW	2	165,926,367 (GRCm39)	splice site	probably benign
R1710:Sulf2	UTSW	2	165,920,992 (GRCm39)	missense	probably benign
R1725:Sulf2	UTSW	2	165,923,281 (GRCm39)	missense	probably damaging	0.96
R1775:Sulf2	UTSW	2	165,921,532 (GRCm39)	missense	probably benign	0.07
R2001:Sulf2	UTSW	2	165,922,773 (GRCm39)	missense	probably benign	0.05
R2570:Sulf2	UTSW	2	165,927,721 (GRCm39)	missense	probably benign	0.21
R4052:Sulf2	UTSW	2	165,936,510 (GRCm39)	missense	probably damaging	1.00
R4357:Sulf2	UTSW	2	165,919,497 (GRCm39)	missense	probably benign	0.01
R4613:Sulf2	UTSW	2	165,974,525 (GRCm39)	missense	probably damaging	1.00
R4790:Sulf2	UTSW	2	165,931,215 (GRCm39)	missense	probably damaging	1.00
R4858:Sulf2	UTSW	2	165,923,524 (GRCm39)	missense	probably benign	0.00
R5033:Sulf2	UTSW	2	165,923,542 (GRCm39)	missense	probably benign	0.01
R5692:Sulf2	UTSW	2	165,923,426 (GRCm39)	missense	probably benign	0.03
R5695:Sulf2	UTSW	2	165,974,678 (GRCm39)	missense	probably benign	0.03
R6504:Sulf2	UTSW	2	165,925,841 (GRCm39)	missense	probably benign	0.00
R6816:Sulf2	UTSW	2	165,924,674 (GRCm39)	missense	probably benign
R6859:Sulf2	UTSW	2	165,929,039 (GRCm39)	missense	probably damaging	1.00
R6873:Sulf2	UTSW	2	165,931,195 (GRCm39)	missense	probably damaging	0.97
R7125:Sulf2	UTSW	2	165,917,448 (GRCm39)	nonsense	probably null
R7329:Sulf2	UTSW	2	165,959,008 (GRCm39)	missense	probably damaging	1.00
R7343:Sulf2	UTSW	2	165,919,536 (GRCm39)	missense	possibly damaging	0.69
R7669:Sulf2	UTSW	2	165,935,516 (GRCm39)	missense	possibly damaging	0.67
R7833:Sulf2	UTSW	2	165,921,456 (GRCm39)	missense	possibly damaging	0.92
R8421:Sulf2	UTSW	2	165,958,972 (GRCm39)	missense	probably benign	0.11
R8430:Sulf2	UTSW	2	165,916,736 (GRCm39)	missense	probably benign	0.03
R8861:Sulf2	UTSW	2	165,974,606 (GRCm39)	missense	possibly damaging	0.96
R9285:Sulf2	UTSW	2	165,935,435 (GRCm39)	missense	probably damaging	1.00
R9410:Sulf2	UTSW	2	165,936,444 (GRCm39)	missense
RF016:Sulf2	UTSW	2	165,924,523 (GRCm39)	missense	probably benign	0.01
X0063:Sulf2	UTSW	2	165,921,053 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AAAGTTCACATGGCCCAGCCAG -3'
(R):5'- TTAGCAGCTCAGATCCAAGGGAGG -3'

Sequencing Primer
(F):5'- TTAAAGAGCTTACGGCGTCC -3'
(R):5'- GGCATTTGCCAAGCTGAG -3'

Posted On

2014-05-23