Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01469:Gal3st2c'

88223

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gal3st2c

Ensembl Gene

ENSMUSG00000073608

Gene Name

galactose-3-O-sulfotransferase 2C

Synonyms

Gm6086

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.068) question?

Stock #

IGL01469

Quality Score

Status

Chromosome

Chromosomal Location

93918227-93939261 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 93937039 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 328 (N328S)

Ref Sequence

ENSEMBL: ENSMUSP00000095234 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000097632]

AlphaFold

Q3ULK5

Predicted Effect

probably benign
Transcript: ENSMUST00000097632
AA Change: N328S

PolyPhen 2 Score 0.184 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000095234
Gene: ENSMUSG00000073608
AA Change: N328S

Domain	Start	End	E-Value	Type
Pfam:Gal-3-0_sulfotr	1	382	8.4e-150	PFAM

Meta Mutation Damage Score

0.0896

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4fm1	A	G	4: 144,255,192 (GRCm39)	Q204R	possibly damaging	Het
Actn2	C	T	13: 12,325,796 (GRCm39)	E60K	possibly damaging	Het
Alpk1	T	C	3: 127,471,401 (GRCm39)		probably null	Het
Ccdc107	A	G	4: 43,495,751 (GRCm39)	N218S	probably benign	Het
Cdh23	A	T	10: 60,433,504 (GRCm39)	M60K	probably benign	Het
Cenpe	A	G	3: 134,934,567 (GRCm39)	Q378R	probably damaging	Het
Dnaaf6rt	A	T	1: 31,262,510 (GRCm39)	D164V	probably damaging	Het
Dnah8	T	A	17: 30,902,688 (GRCm39)		probably benign	Het
Eif2b4	T	C	5: 31,345,111 (GRCm39)	D190G	probably benign	Het
Fmo5	A	G	3: 97,558,884 (GRCm39)	N448S	probably benign	Het
Gbf1	A	T	19: 46,267,803 (GRCm39)	E1271V	probably damaging	Het
Ifitm6	A	T	7: 140,596,725 (GRCm39)	V16D	probably damaging	Het
Ighv2-4	A	G	12: 113,616,966 (GRCm39)		probably null	Het
Kng2	T	A	16: 22,818,577 (GRCm39)	K305I	probably damaging	Het
Lrp1	C	T	10: 127,420,283 (GRCm39)	R900Q	probably damaging	Het
Maml1	A	G	11: 50,157,353 (GRCm39)	M274T	probably damaging	Het
Med23	A	G	10: 24,758,495 (GRCm39)	E278G	probably damaging	Het
Myo1h	A	G	5: 114,499,330 (GRCm39)	T164A	probably damaging	Het
Ncoa2	A	T	1: 13,257,093 (GRCm39)	S135R	probably benign	Het
Nrbf2	A	G	10: 67,105,919 (GRCm39)	L41P	probably damaging	Het
Or10a48	A	G	7: 108,424,534 (GRCm39)	V224A	probably benign	Het
Or1j13	T	C	2: 36,369,836 (GRCm39)	Y102C	probably benign	Het
Or1o11	T	A	17: 37,756,426 (GRCm39)	S5T	probably benign	Het
Or52e5	T	A	7: 104,719,595 (GRCm39)	M307K	probably benign	Het
Or6c6	A	G	10: 129,186,449 (GRCm39)	M6V	probably benign	Het
Otoa	T	C	7: 120,754,496 (GRCm39)		probably null	Het
Plxnb1	T	C	9: 108,934,483 (GRCm39)		probably benign	Het
Ppp1r42	A	T	1: 10,073,458 (GRCm39)		probably null	Het
Rad54l2	T	A	9: 106,599,957 (GRCm39)	K100M	probably damaging	Het
Rnf112	T	A	11: 61,342,167 (GRCm39)	T308S	possibly damaging	Het
Scaper	T	C	9: 55,767,051 (GRCm39)	D466G	probably damaging	Het
Sgsm2	T	A	11: 74,744,697 (GRCm39)	I796L	possibly damaging	Het
Shank3	T	C	15: 89,405,477 (GRCm39)	L476P	probably damaging	Het
Shkbp1	T	C	7: 27,055,366 (GRCm39)	T6A	probably benign	Het
Slc14a2	A	T	18: 78,198,781 (GRCm39)	I783N	probably damaging	Het
Stat1	A	G	1: 52,186,529 (GRCm39)	D447G	possibly damaging	Het
Tekt3	T	G	11: 62,964,294 (GRCm39)	I208S	probably damaging	Het
Tenm3	A	T	8: 48,689,458 (GRCm39)	V2043E	probably damaging	Het
Tgm3	T	C	2: 129,866,414 (GRCm39)	Y111H	probably damaging	Het
Tph2	T	A	10: 114,915,664 (GRCm39)	R459*	probably null	Het
Vmn2r109	T	C	17: 20,761,671 (GRCm39)	Y562C	probably damaging	Het

Other mutations in Gal3st2c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00468:Gal3st2c	APN	1	93,936,771 (GRCm39)	missense	probably benign	0.38
PIT4431001:Gal3st2c	UTSW	1	93,935,834 (GRCm39)	missense	probably damaging	1.00
R0110:Gal3st2c	UTSW	1	93,937,219 (GRCm39)	missense	probably benign	0.03
R0602:Gal3st2c	UTSW	1	93,936,901 (GRCm39)	missense	probably damaging	1.00
R0846:Gal3st2c	UTSW	1	93,934,669 (GRCm39)	missense	possibly damaging	0.51
R1577:Gal3st2c	UTSW	1	93,934,650 (GRCm39)	missense	probably damaging	0.98
R1900:Gal3st2c	UTSW	1	93,936,766 (GRCm39)	missense	probably damaging	1.00
R1902:Gal3st2c	UTSW	1	93,936,611 (GRCm39)	missense	probably damaging	1.00
R2143:Gal3st2c	UTSW	1	93,937,173 (GRCm39)	nonsense	probably null
R2846:Gal3st2c	UTSW	1	93,924,122 (GRCm39)	missense	possibly damaging	0.52
R3737:Gal3st2c	UTSW	1	93,937,050 (GRCm39)	missense	possibly damaging	0.79
R4236:Gal3st2c	UTSW	1	93,936,463 (GRCm39)	missense	probably damaging	1.00
R4623:Gal3st2c	UTSW	1	93,937,178 (GRCm39)	missense	possibly damaging	0.59
R5177:Gal3st2c	UTSW	1	93,936,930 (GRCm39)	nonsense	probably null
R5590:Gal3st2c	UTSW	1	93,936,023 (GRCm39)	critical splice donor site	probably null
R7529:Gal3st2c	UTSW	1	93,937,039 (GRCm39)	missense	probably benign	0.18
R7559:Gal3st2c	UTSW	1	93,937,075 (GRCm39)	missense	probably damaging	1.00
R9525:Gal3st2c	UTSW	1	93,935,928 (GRCm39)	missense	probably damaging	1.00
Z1088:Gal3st2c	UTSW	1	93,935,867 (GRCm39)	missense	probably benign	0.02

Posted On

2013-11-18