Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL02698:Gm17677'

304045

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm17677

Ensembl Gene

ENSMUSG00000091174

Gene Name

predicted gene, 17677

Synonyms

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

IGL02698

Quality Score

Status

Chromosome

Chromosomal Location

35741049-35742252 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 35741120 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000132657 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166746]

Predicted Effect

probably benign
Transcript: ENSMUST00000166746

SMART Domains

Protein: ENSMUSP00000132657
Gene: ENSMUSG00000091174

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arpp21	T	A	9: 112,185,744		probably benign	Het
Car8	A	T	4: 8,185,598	I186N	probably benign	Het
Ccdc174	G	A	6: 91,890,853	S183N	probably benign	Het
Ccdc66	T	A	14: 27,490,792	K525*	probably null	Het
Cebpz	A	G	17: 78,935,574	V217A	probably benign	Het
Cfap36	C	A	11: 29,247,014		probably null	Het
Cpne4	T	C	9: 105,032,785	V527A	probably damaging	Het
Crh	T	G	3: 19,694,190	D96A	possibly damaging	Het
Csgalnact1	C	A	8: 68,401,492	G219V	probably damaging	Het
Dcp1a	A	T	14: 30,505,542		probably benign	Het
Ddhd1	A	T	14: 45,605,206		probably benign	Het
Dis3l2	C	T	1: 87,048,829		probably benign	Het
Dopey1	T	C	9: 86,524,359		probably benign	Het
Etv3	A	G	3: 87,536,578	T490A	possibly damaging	Het
Fastkd2	A	G	1: 63,747,999	T531A	probably benign	Het
Fat1	C	T	8: 45,023,164	A1749V	probably benign	Het
Fgfr1	T	A	8: 25,573,608	L761*	probably null	Het
Gcc2	A	G	10: 58,271,290	K683E	possibly damaging	Het
Gm5117	C	T	8: 31,739,739		noncoding transcript	Het
Hif1a	T	C	12: 73,930,771		probably null	Het
Inha	A	G	1: 75,509,883	E274G	probably damaging	Het
Itih2	G	T	2: 10,130,501	P26H	probably damaging	Het
Kif23	G	A	9: 61,925,001	T620I	possibly damaging	Het
Klhl30	T	C	1: 91,353,707	F10S	probably damaging	Het
Kmt2b	T	C	7: 30,578,693		probably benign	Het
Lmf2	A	C	15: 89,354,154	L174R	probably damaging	Het
Med13l	T	C	5: 118,762,829	L2216P	probably damaging	Het
Mmp1b	T	A	9: 7,384,877	L257F	probably damaging	Het
Net1	A	G	13: 3,887,569		probably null	Het
Nfasc	A	G	1: 132,634,737	V100A	probably benign	Het
Nr4a2	A	G	2: 57,108,160	F535S	probably damaging	Het
Ntn4	G	T	10: 93,644,659	A45S	probably benign	Het
Olfr1141	T	A	2: 87,753,844	K50*	probably null	Het
Olfr1197	T	A	2: 88,729,471	I43F	probably damaging	Het
Olfr1386	T	A	11: 49,470,863	F237L	probably benign	Het
Olfr243	T	C	7: 103,717,278	V228A	probably damaging	Het
Olfr25	A	G	9: 38,330,210	T208A	probably benign	Het
Pappa	A	T	4: 65,181,020	E592V	probably damaging	Het
Pi4ka	A	T	16: 17,291,168	I1630N	probably damaging	Het
Ptprb	A	G	10: 116,363,280	D1997G	probably benign	Het
Rc3h2	A	T	2: 37,405,300	S235T	probably damaging	Het
S1pr1	T	A	3: 115,712,097	K283*	probably null	Het
Scn5a	T	A	9: 119,521,097	T904S	probably damaging	Het
Sema6d	T	C	2: 124,653,723	L30P	possibly damaging	Het
Slc26a7	A	C	4: 14,593,867	S83A	possibly damaging	Het
Slco1a6	C	A	6: 142,103,011	G348*	probably null	Het
Srgap3	C	T	6: 112,746,928	V524I	probably damaging	Het
Stxbp3-ps	A	T	19: 9,558,324		noncoding transcript	Het
Sv2b	C	T	7: 75,140,978		probably null	Het
Sympk	T	C	7: 19,045,634	I663T	probably benign	Het
Ttn	C	A	2: 76,944,771	V1976L	probably damaging	Het
Uqcrc1	T	C	9: 108,947,943		probably null	Het
Vmn2r111	T	C	17: 22,571,245	Y260C	probably damaging	Het

Other mutations in Gm17677

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02593:Gm17677	APN	9	35742142	missense	possibly damaging	0.92
IGL02612:Gm17677	APN	9	35742164	missense	possibly damaging	0.92
IGL02648:Gm17677	APN	9	35741109	missense	probably benign	0.14
R4240:Gm17677	UTSW	9	35742153	nonsense	probably null
R4983:Gm17677	UTSW	9	35742169	missense	probably benign	0.12
R5161:Gm17677	UTSW	9	35741588	nonsense	probably null
R5545:Gm17677	UTSW	9	35741644	missense	probably benign	0.10
R5980:Gm17677	UTSW	9	35741615	missense	probably damaging	0.99
R6131:Gm17677	UTSW	9	35741544	nonsense	probably null
R6147:Gm17677	UTSW	9	35742110	missense	possibly damaging	0.94
R6147:Gm17677	UTSW	9	35742232	missense	possibly damaging	0.66
X0066:Gm17677	UTSW	9	35742170	missense	possibly damaging	0.90

Posted On

2015-04-16