Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02589:Gm5796'

299647

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5796

Ensembl Gene

ENSMUSG00000096775

Gene Name

predicted gene 5796

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02589

Quality Score

Status

Chromosome

Chromosomal Location

18428405-18445832 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 15379030 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Stop codon at position 24 (K24*)

Ref Sequence

ENSEMBL: ENSMUSP00000093898 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096184]

AlphaFold

E9Q7M8

Predicted Effect

probably null
Transcript: ENSMUST00000096184
AA Change: K24*

SMART Domains

Protein: ENSMUSP00000093898
Gene: ENSMUSG00000096775
AA Change: K24*

Domain	Start	End	E-Value	Type
Pfam:Takusan	46	129	7.9e-32	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2ml1	T	G	6: 128,558,463 (GRCm39)	I5L	probably benign	Het
Ang6	A	G	14: 44,239,419 (GRCm39)	I103T	possibly damaging	Het
Arhgdib	A	G	6: 136,910,576 (GRCm39)		probably benign	Het
Atp13a2	C	T	4: 140,733,722 (GRCm39)	T1037M	probably damaging	Het
Bptf	T	C	11: 107,002,357 (GRCm39)	N252D	possibly damaging	Het
Capn2	T	C	1: 182,311,913 (GRCm39)	Y387C	probably damaging	Het
Cdc27	T	G	11: 104,396,470 (GRCm39)	D817A	probably benign	Het
Cdc45	C	T	16: 18,617,479 (GRCm39)	M200I	probably benign	Het
Cntnap3	T	G	13: 64,940,244 (GRCm39)	I318L	probably benign	Het
Cog6	A	T	3: 52,914,691 (GRCm39)	L255Q	probably damaging	Het
Ect2l	T	A	10: 18,016,342 (GRCm39)		probably benign	Het
Ercc5	T	C	1: 44,203,209 (GRCm39)	V282A	probably damaging	Het
Fras1	A	G	5: 96,917,372 (GRCm39)	D3464G	probably damaging	Het
Gabrg1	A	T	5: 70,999,495 (GRCm39)	L18*	probably null	Het
Ggcx	T	C	6: 72,406,131 (GRCm39)	Y586H	probably damaging	Het
Gnb4	C	T	3: 32,643,998 (GRCm39)	V187M	probably damaging	Het
Gpt2	C	T	8: 86,242,795 (GRCm39)	Q276*	probably null	Het
Idnk	G	T	13: 58,311,239 (GRCm39)		probably benign	Het
Igkv3-9	A	G	6: 70,565,683 (GRCm39)	D94G	possibly damaging	Het
Ipo8	C	A	6: 148,711,405 (GRCm39)	L294F	probably damaging	Het
Itgad	A	T	7: 127,780,883 (GRCm39)	D157V	probably damaging	Het
Kcnab3	A	T	11: 69,222,928 (GRCm39)	I392L	probably benign	Het
Kdm3b	A	G	18: 34,945,471 (GRCm39)	S761G	possibly damaging	Het
Kif21a	G	A	15: 90,869,489 (GRCm39)	T454M	probably damaging	Het
Lta4h	A	G	10: 93,310,793 (GRCm39)	N441S	probably benign	Het
Man2a1	A	G	17: 64,986,773 (GRCm39)	E595G	probably benign	Het
Micos13	T	C	17: 56,915,856 (GRCm39)	E66G	probably benign	Het
Mvd	T	C	8: 123,164,773 (GRCm39)		probably benign	Het
Notch2	A	G	3: 98,011,663 (GRCm39)		probably null	Het
Phf20l1	G	T	15: 66,487,481 (GRCm39)		probably benign	Het
Rdm1	A	G	11: 101,518,831 (GRCm39)	S13G	possibly damaging	Het
Rnf123	G	A	9: 107,945,501 (GRCm39)	R390*	probably null	Het
Scn4a	G	T	11: 106,218,958 (GRCm39)	D953E	probably benign	Het
Sh2b1	A	G	7: 126,068,440 (GRCm39)	I457T	probably benign	Het
Srrm1	G	A	4: 135,052,415 (GRCm39)	P658L	unknown	Het
Tagap	C	A	17: 8,152,504 (GRCm39)	T563K	possibly damaging	Het
Ugt1a7c	T	C	1: 88,023,360 (GRCm39)	I173T	probably benign	Het
Unc79	C	T	12: 103,139,755 (GRCm39)	A2370V	probably damaging	Het
Vmn2r102	T	A	17: 19,901,480 (GRCm39)	C536S	probably damaging	Het
Vmn2r53	G	A	7: 12,315,872 (GRCm39)	T649I	possibly damaging	Het
Whrn	G	A	4: 63,336,334 (GRCm39)	Q301*	probably null	Het
Zfp1007	T	A	5: 109,826,386 (GRCm39)	H62L	possibly damaging	Het
Zfp518a	G	A	19: 40,903,061 (GRCm39)	G997R	probably damaging	Het

Other mutations in Gm5796

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R7712:Gm5796	UTSW	14	15,379,960 (GRCm39)	missense	probably damaging	1.00

Posted On

2015-04-16