Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01898:F830104G03Rik'

179455

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

F830104G03Rik

Ensembl Gene

Gene Name

RIKEN cDNA F830104G03 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01898

Quality Score

Status

Chromosome

Chromosomal Location

56795483-56798749 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 56797637 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 97 (Q97*)

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000099093
AA Change: Q97*

SMART Domains

Protein: ENSMUSP00000096691
Gene: ENSMUSG00000074592
AA Change: Q97*

Domain	Start	End	E-Value	Type
coiled coil region	28	56	N/A	INTRINSIC
low complexity region	73	84	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 23 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actl10	A	T	2: 154,394,633 (GRCm39)	D195V	probably damaging	Het
Aqp11	A	G	7: 97,375,870 (GRCm39)	W260R	probably benign	Het
Atp8a2	T	C	14: 60,260,962 (GRCm39)	T390A	probably damaging	Het
Atp8b4	T	C	2: 126,231,281 (GRCm39)	N431S	probably benign	Het
Ccdc110	T	G	8: 46,395,161 (GRCm39)	S351A	possibly damaging	Het
Cntnap4	T	C	8: 113,582,939 (GRCm39)	F1006L	possibly damaging	Het
Ddr2	A	G	1: 169,825,725 (GRCm39)	F292L	possibly damaging	Het
Fam171a2	T	C	11: 102,330,582 (GRCm39)	T267A	possibly damaging	Het
Gm10718	A	T	9: 3,025,118 (GRCm39)	Y194F	probably benign	Het
Gm21738	G	A	14: 19,416,979 (GRCm38)	S144L	probably benign	Het
Igkv5-43	T	A	6: 69,752,876 (GRCm39)	K69*	probably null	Het
Mios	T	C	6: 8,222,668 (GRCm39)	I534T	probably benign	Het
Nus1	A	G	10: 52,306,163 (GRCm39)	D185G	probably benign	Het
Proc	A	G	18: 32,266,198 (GRCm39)		probably null	Het
Psma3	T	A	12: 71,031,448 (GRCm39)	H36Q	probably benign	Het
Sh3rf3	G	T	10: 58,885,352 (GRCm39)	A412S	probably damaging	Het
Smgc	A	T	15: 91,728,727 (GRCm39)		probably null	Het
Sp140l2	A	G	1: 85,231,907 (GRCm39)		probably benign	Het
Spta1	T	A	1: 174,041,428 (GRCm39)	S1297R	probably benign	Het
Steap3	T	C	1: 120,169,304 (GRCm39)	D293G	probably benign	Het
Tbx18	A	T	9: 87,589,912 (GRCm39)	M342K	possibly damaging	Het
Trip11	T	C	12: 101,851,935 (GRCm39)	M425V	probably benign	Het
Vmn2r129	C	T	4: 156,690,549 (GRCm39)		noncoding transcript	Het

Other mutations in F830104G03Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
R1669:F830104G03Rik	UTSW	3	56,797,998 (GRCm39)	missense	unknown
R4479:F830104G03Rik	UTSW	3	56,797,634 (GRCm39)	missense	unknown
R4877:F830104G03Rik	UTSW	3	56,797,917 (GRCm39)	missense	unknown

Posted On

2014-05-07