Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03198:Gm4297'

412905

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm4297

Ensembl Gene

ENSMUSG00000081218

Gene Name

predicted gene 4297

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL03198

Quality Score

Status

Chromosome

Chromosomal Location

24418489-24439544 bp(-) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

T to A at 24418810 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000112514 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000119285]

AlphaFold

D3YWB7

Predicted Effect

probably benign
Transcript: ENSMUST00000119285

SMART Domains

Protein: ENSMUSP00000112514
Gene: ENSMUSG00000081218

Domain	Start	End	E-Value	Type
low complexity region	15	26	N/A	INTRINSIC
Pfam:Cor1	128	209	3.8e-10	PFAM

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
Adhfe1	A	T	1: 9,620,177 (GRCm39)		probably benign	Het
Atp6v0a2	T	C	5: 124,789,425 (GRCm39)		probably null	Het
Brca1	G	T	11: 101,403,537 (GRCm39)		probably benign	Het
Cd55	A	T	1: 130,368,108 (GRCm39)	C372S	probably benign	Het
Clip2	A	T	5: 134,526,936 (GRCm39)		probably benign	Het
Dgkb	A	G	12: 38,186,615 (GRCm39)	N262D	probably damaging	Het
Fam227b	C	T	2: 125,966,499 (GRCm39)		probably null	Het
Foxj2	G	A	6: 122,809,966 (GRCm39)		probably null	Het
Grik3	A	G	4: 125,553,555 (GRCm39)	D429G	probably benign	Het
Hcfc1	T	C	X: 72,994,935 (GRCm39)	I924V	possibly damaging	Het
Lrrk1	A	G	7: 65,956,642 (GRCm39)	V411A	probably damaging	Het
Mdh1	A	T	11: 21,514,168 (GRCm39)	V83E	probably damaging	Het
Pa2g4	A	G	10: 128,401,647 (GRCm39)	V17A	probably damaging	Het
Podnl1	G	A	8: 84,858,818 (GRCm39)	V548I	probably benign	Het
Polg	A	G	7: 79,101,470 (GRCm39)	V1079A	probably damaging	Het
Polr2a	G	T	11: 69,638,107 (GRCm39)		probably null	Het
Ptk2	C	T	15: 73,108,065 (GRCm39)	S722N	probably damaging	Het
Rock2	A	G	12: 17,025,508 (GRCm39)	D1243G	probably benign	Het
Sirt4	T	C	5: 115,621,061 (GRCm39)	D37G	probably benign	Het
Slc35d1	T	C	4: 103,042,085 (GRCm39)	Y249C	probably damaging	Het
Snrnp27	A	T	6: 86,659,968 (GRCm39)		probably null	Het
Srek1	T	C	13: 103,881,443 (GRCm39)		probably null	Het
Sspo	A	T	6: 48,454,516 (GRCm39)	I2951F	probably benign	Het
Stxbp3	A	G	3: 108,734,405 (GRCm39)	F40L	probably damaging	Het
Sympk	T	C	7: 18,778,921 (GRCm39)	V604A	possibly damaging	Het
Tbc1d2b	T	C	9: 90,104,510 (GRCm39)	Y544C	probably damaging	Het
Tnpo2	C	T	8: 85,778,347 (GRCm39)	T592I	possibly damaging	Het
Txndc16	T	C	14: 45,388,941 (GRCm39)		probably benign	Het
Ubr5	A	T	15: 38,045,964 (GRCm39)	L120Q	probably damaging	Het
Wdfy4	A	T	14: 32,847,844 (GRCm39)	M836K	probably damaging	Het
Wdr48	A	G	9: 119,741,479 (GRCm39)	N141S	probably benign	Het
Zc3h7a	A	T	16: 10,980,528 (GRCm39)	Y28*	probably null	Het
Zfp423	T	C	8: 88,508,304 (GRCm39)	D659G	possibly damaging	Het

Other mutations in Gm4297

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01121:Gm4297	APN	X	24,418,854 (GRCm39)	missense	probably benign	0.03

Posted On

2016-08-02