Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01590:Spopfm3'

91581

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Spopfm3

Ensembl Gene

ENSMUSG00000090268

Gene Name

speckle-type BTB/POZ protein family member 3

Synonyms

Gm5286

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01590

Quality Score

Status

Chromosome

Chromosomal Location

94104021-94107109 bp(+) (GRCm39)

Type of Mutation

utr 5 prime

DNA Base Change (assembly)

G to A at 94105674 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000125267 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000159524]

AlphaFold

E0CXI6

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159267

Predicted Effect

probably benign
Transcript: ENSMUST00000159524

SMART Domains

Protein: ENSMUSP00000125267
Gene: ENSMUSG00000090268

Domain	Start	End	E-Value	Type
MATH	17	126	7.18e-6	SMART
BTB	184	283	8.21e-26	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 33 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921504E06Rik	T	A	2: 19,482,590 (GRCm39)		probably benign	Het
Adgrb2	T	G	4: 129,907,606 (GRCm39)		probably benign	Het
Apcs	C	T	1: 172,722,034 (GRCm39)	G104D	probably damaging	Het
Atp10b	G	A	11: 43,063,548 (GRCm39)	R161H	probably benign	Het
Cep250	A	T	2: 155,834,237 (GRCm39)	Q2054L	possibly damaging	Het
Dennd6a	T	G	14: 26,340,507 (GRCm39)	V207G	probably benign	Het
Ehbp1	C	A	11: 22,045,611 (GRCm39)	D688Y	possibly damaging	Het
Fam83a	C	A	15: 57,873,173 (GRCm39)	S334Y	probably damaging	Het
Fam83e	T	A	7: 45,373,360 (GRCm39)	F242Y	probably null	Het
Fnip1	A	T	11: 54,384,126 (GRCm39)	D341V	probably damaging	Het
Gpatch3	A	G	4: 133,308,028 (GRCm39)		probably benign	Het
Gpc2	C	A	5: 138,272,640 (GRCm39)	V558F	probably damaging	Het
H2-M10.6	A	G	17: 37,123,641 (GRCm39)	N112D	probably benign	Het
Hs6st1	A	T	1: 36,142,785 (GRCm39)	D240V	probably damaging	Het
Inpp5f	T	A	7: 128,266,031 (GRCm39)		probably null	Het
Itga8	G	T	2: 12,165,144 (GRCm39)	H822N	probably damaging	Het
Kif20b	T	A	19: 34,932,126 (GRCm39)	N1263K	possibly damaging	Het
Krt28	A	G	11: 99,265,220 (GRCm39)		probably null	Het
Muc5ac	A	T	7: 141,352,630 (GRCm39)	M706L	probably benign	Het
Or1j12	A	T	2: 36,343,004 (GRCm39)	M136L	probably benign	Het
Or52h9	A	C	7: 104,202,782 (GRCm39)	I219L	probably benign	Het
Prox2	A	G	12: 85,134,845 (GRCm39)	W479R	probably damaging	Het
Rps19	A	T	7: 24,587,881 (GRCm39)	D152V	probably damaging	Het
Slc20a1	G	A	2: 129,051,146 (GRCm39)		probably benign	Het
Slc7a2	C	T	8: 41,367,137 (GRCm39)	P564S	probably damaging	Het
Slco1a5	C	A	6: 142,196,045 (GRCm39)	M319I	probably benign	Het
Spmip2	A	C	3: 79,356,647 (GRCm39)	N150T	probably damaging	Het
Tanc1	A	G	2: 59,615,817 (GRCm39)	T275A	probably benign	Het
Tenm3	A	G	8: 48,681,837 (GRCm39)	S2598P	probably damaging	Het
Tiparp	G	A	3: 65,439,397 (GRCm39)	E56K	probably benign	Het
Trpm5	G	A	7: 142,636,471 (GRCm39)	R489C	probably damaging	Het
Vmn2r84	C	A	10: 130,221,964 (GRCm39)	G752V	probably damaging	Het
Wnt5b	T	A	6: 119,417,515 (GRCm39)	T130S	possibly damaging	Het

Other mutations in Spopfm3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02603:Spopfm3	APN	3	94,105,744 (GRCm39)	missense	possibly damaging	0.53
R7130:Spopfm3	UTSW	3	94,105,834 (GRCm39)	missense	probably damaging	1.00
R7209:Spopfm3	UTSW	3	94,106,012 (GRCm39)	missense	probably benign
R7595:Spopfm3	UTSW	3	94,105,724 (GRCm39)	missense	probably benign	0.15
R7661:Spopfm3	UTSW	3	94,105,709 (GRCm39)	missense	probably damaging	0.98

Posted On

2013-12-09