Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01080:Gm8005'

52659

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm8005

Ensembl Gene

Gene Name

predicted gene 8005

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01080

Quality Score

Status

Chromosome

Chromosomal Location

42256113-42261630 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 42258971 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 119 (D119G)

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000167326
AA Change: D119G

SMART Domains

Protein: ENSMUSP00000129153
Gene: ENSMUSG00000092148
AA Change: D119G

Domain	Start	End	E-Value	Type
Pfam:Takusan	57	137	5.5e-26	PFAM
coiled coil region	164	186	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 25 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb4	A	T	5: 8,984,258 (GRCm39)	R663W	probably damaging	Het
Cacng5	A	T	11: 107,768,754 (GRCm39)	F179L	probably damaging	Het
Cacng5	C	T	11: 107,772,531 (GRCm39)	V106I	probably benign	Het
Cd96	T	C	16: 45,870,056 (GRCm39)	E471G	possibly damaging	Het
Cpt1c	T	C	7: 44,610,333 (GRCm39)	D621G	probably damaging	Het
Csmd3	T	C	15: 47,744,799 (GRCm39)	I1503V	probably benign	Het
Dmgdh	T	C	13: 93,840,286 (GRCm39)		probably benign	Het
Flg	A	T	3: 93,186,906 (GRCm39)	K119N	probably benign	Het
Gale	T	C	4: 135,693,389 (GRCm39)	Y104H	probably damaging	Het
Gstk1	A	T	6: 42,223,560 (GRCm39)	D50V	possibly damaging	Het
Kmt2a	T	C	9: 44,720,389 (GRCm39)	D3866G	unknown	Het
Mastl	A	G	2: 23,036,160 (GRCm39)	S119P	probably damaging	Het
Or2aj4	A	T	16: 19,384,958 (GRCm39)	V225E	probably damaging	Het
Phf11c	G	A	14: 59,630,648 (GRCm39)	T19I	probably benign	Het
Ppp1r16b	A	G	2: 158,599,092 (GRCm39)	T355A	probably damaging	Het
Prmt7	T	G	8: 106,963,846 (GRCm39)		probably benign	Het
Rad50	T	C	11: 53,596,895 (GRCm39)	T44A	probably damaging	Het
Rangap1	C	T	15: 81,589,953 (GRCm39)		probably benign	Het
Slc27a3	A	T	3: 90,292,767 (GRCm39)	V634E	probably benign	Het
Tbxas1	T	A	6: 38,998,115 (GRCm39)	L228I	probably damaging	Het
Tnfaip3	T	C	10: 18,887,403 (GRCm39)	K41E	probably benign	Het
Tti1	C	T	2: 157,824,379 (GRCm39)	V1025I	probably damaging	Het
Tyrobp	T	C	7: 30,116,841 (GRCm39)		probably null	Het
Wfdc16	A	T	2: 164,480,406 (GRCm39)	W30R	probably damaging	Het
Zyg11b	A	T	4: 108,094,613 (GRCm39)	L657Q	probably damaging	Het

Other mutations in Gm8005

Allele	Source	Chr	Coord	Type
R7564:Gm8005	UTSW	14	42,261,499 (GRCm39)	missense
R7652:Gm8005	UTSW	14	42,258,919 (GRCm39)	missense
R7945:Gm8005	UTSW	14	42,260,330 (GRCm39)	missense
R9291:Gm8005	UTSW	14	42,258,885 (GRCm39)	missense
R9612:Gm8005	UTSW	14	42,260,355 (GRCm39)	missense

Posted On

2013-06-21