Mutagenetix > Incidental Mutation

Incidental Mutation 'R4607:Gna14'

346108

Institutional Source

Beutler Lab

Gene Symbol

Gna14

Ensembl Gene

ENSMUSG00000024697

Gene Name

guanine nucleotide binding protein, alpha 14

Synonyms

G alpha 14

MMRRC Submission

041818-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.110) question?

Stock #

R4607 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

16413126-16588184 bp(+) (GRCm39)

Type of Mutation

critical splice acceptor site

DNA Base Change (assembly)

A to G at 16511075 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000025602 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025602]

AlphaFold

P30677

Predicted Effect

probably null
Transcript: ENSMUST00000025602

SMART Domains

Protein: ENSMUSP00000025602
Gene: ENSMUSG00000024697

Domain	Start	End	E-Value	Type
G_alpha	15	354	9.68e-201	SMART

Meta Mutation Damage Score

0.9488

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

97% (65/67)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the guanine nucleotide-binding, or G protein family. G proteins are heterotrimers consisting of alpha, beta and gamma subunits. The encoded protein is a member of the alpha family of G proteins, more specifically the alpha q subfamily of G proteins. The encoded protein may play a role in pertussis-toxin resistant activation of phospholipase C-beta and its downstream effectors.[provided by RefSeq, Feb 2009]

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acss3	T	A	10: 106,802,890 (GRCm39)	I452F	possibly damaging	Het
Adgra3	A	C	5: 50,128,081 (GRCm39)	V800G	probably damaging	Het
Aldh1a1	A	T	19: 20,599,051 (GRCm39)	Y154F	probably benign	Het
Bbs10	T	G	10: 111,136,681 (GRCm39)	I598S	probably damaging	Het
Bbs10	A	G	10: 111,136,995 (GRCm39)	K703E	probably benign	Het
Ccnl1	C	T	3: 65,854,131 (GRCm39)		probably benign	Het
Chrna9	A	G	5: 66,134,078 (GRCm39)	I310V	possibly damaging	Het
Cpeb3	A	G	19: 37,152,239 (GRCm39)	S46P	possibly damaging	Het
Dab1	C	T	4: 104,588,948 (GRCm39)	A524V	probably benign	Het
Dlgap5	A	G	14: 47,650,475 (GRCm39)	I151T	possibly damaging	Het
Dsg4	C	T	18: 20,604,302 (GRCm39)	T923M	probably damaging	Het
Eif4g3	G	T	4: 137,853,769 (GRCm39)	R618L	probably benign	Het
Erlin1	C	T	19: 44,051,474 (GRCm39)	V76M	probably damaging	Het
Fam161a	G	A	11: 22,970,710 (GRCm39)	S296N	probably benign	Het
Fam187b	T	A	7: 30,677,170 (GRCm39)	N226K	probably benign	Het
Fes	G	A	7: 80,036,959 (GRCm39)	R42W	probably damaging	Het
Fmnl2	T	A	2: 52,993,728 (GRCm39)	N374K	possibly damaging	Het
Fpgt	G	A	3: 154,792,333 (GRCm39)	Q565*	probably null	Het
Gm26657	C	A	4: 56,741,114 (GRCm39)	H100N	probably benign	Het
Gsg1l	T	A	7: 125,557,721 (GRCm39)	I136F	probably damaging	Het
Hhip	C	T	8: 80,724,192 (GRCm39)	R350Q	probably damaging	Het
Ints10	G	A	8: 69,263,271 (GRCm39)	R394Q	probably damaging	Het
Ipo11	A	G	13: 107,037,319 (GRCm39)	S175P	probably damaging	Het
Klk13	C	A	7: 43,363,284 (GRCm39)	C10*	probably null	Het
Leng8	T	A	7: 4,147,796 (GRCm39)	I607N	probably damaging	Het
Map3k2	T	C	18: 32,333,030 (GRCm39)	L68P	probably damaging	Het
Memo1	G	A	17: 74,565,456 (GRCm39)	Q36*	probably null	Het
Mink1	A	G	11: 70,496,893 (GRCm39)	E417G	possibly damaging	Het
Myrf	G	T	19: 10,206,431 (GRCm39)	D29E	probably damaging	Het
Nelfcd	T	A	2: 174,264,955 (GRCm39)	D215E	probably benign	Het
Nostrin	G	A	2: 69,014,243 (GRCm39)	V400M	possibly damaging	Het
Nrip1	T	C	16: 76,089,920 (GRCm39)	T546A	probably benign	Het
Or13a24	A	G	7: 140,154,554 (GRCm39)	M163V	probably benign	Het
Or1l4	T	A	2: 37,092,094 (GRCm39)	Y280*	probably null	Het
Or2h2b-ps1	A	T	17: 37,481,173 (GRCm39)	V20E	probably damaging	Het
Or4c114	G	T	2: 88,904,656 (GRCm39)	P260T	probably benign	Het
Or6aa1	A	T	7: 86,043,718 (GRCm39)		probably null	Het
Or8g32	T	C	9: 39,306,031 (GRCm39)	*312Q	probably null	Het
P2ry6	A	G	7: 100,587,511 (GRCm39)	Y283H	probably damaging	Het
Pcdh9	T	A	14: 93,253,009 (GRCm39)	N1218I	probably benign	Het
Pcdhga6	A	G	18: 37,841,671 (GRCm39)	N464D	probably damaging	Het
Pramel52-ps	G	T	5: 94,531,387 (GRCm39)	R90S	probably benign	Het
Rdx	T	A	9: 51,980,137 (GRCm39)	S243R	probably damaging	Het
Rxfp1	T	C	3: 79,594,196 (GRCm39)	N66S	probably damaging	Het
Slit1	C	A	19: 41,605,232 (GRCm39)	R873L	probably benign	Het
Spata31e3	G	A	13: 50,399,542 (GRCm39)	T928I	possibly damaging	Het
Strc	T	A	2: 121,203,426 (GRCm39)	I1130F	probably benign	Het
Tlk2	T	A	11: 105,145,844 (GRCm39)	L350Q	probably damaging	Het
Tmem74	G	T	15: 43,730,554 (GRCm39)	T163K	probably damaging	Het
Trav15-1-dv6-1	T	A	14: 53,797,511 (GRCm39)	H53Q	probably benign	Het
Trbv24	T	C	6: 41,195,335 (GRCm39)		probably benign	Het
Uba2	T	C	7: 33,854,021 (GRCm39)	D307G	probably damaging	Het
Uty	C	T	Y: 1,131,134 (GRCm39)	R924Q	probably damaging	Het
Wdr7	C	T	18: 63,910,651 (GRCm39)	T681I	probably benign	Het
Zbtb42	C	T	12: 112,646,976 (GRCm39)	R384W	probably damaging	Het
Zfand4	T	A	6: 116,305,195 (GRCm39)	C207*	probably null	Het
Zfp512b	C	A	2: 181,230,567 (GRCm39)	R441L	probably damaging	Het

Other mutations in Gna14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02545:Gna14	APN	19	16,511,090 (GRCm39)	missense	probably damaging	1.00
IGL03331:Gna14	APN	19	16,586,832 (GRCm39)	missense	probably damaging	1.00
R0563:Gna14	UTSW	19	16,585,483 (GRCm39)	missense	probably benign	0.04
R1479:Gna14	UTSW	19	16,511,133 (GRCm39)	missense	possibly damaging	0.50
R2058:Gna14	UTSW	19	16,585,505 (GRCm39)	splice site	probably benign
R3016:Gna14	UTSW	19	16,580,746 (GRCm39)	missense	probably benign	0.00
R4703:Gna14	UTSW	19	16,576,344 (GRCm39)	missense	possibly damaging	0.95
R4948:Gna14	UTSW	19	16,580,656 (GRCm39)	missense	probably benign	0.00
R5027:Gna14	UTSW	19	16,580,636 (GRCm39)	missense	probably benign	0.03
R5512:Gna14	UTSW	19	16,585,492 (GRCm39)	missense	probably benign	0.07
R5629:Gna14	UTSW	19	16,414,097 (GRCm39)	missense	possibly damaging	0.71
R5895:Gna14	UTSW	19	16,580,692 (GRCm39)	missense	possibly damaging	0.92
R6108:Gna14	UTSW	19	16,580,707 (GRCm39)	missense	probably damaging	0.98
R7037:Gna14	UTSW	19	16,511,128 (GRCm39)	missense
R7310:Gna14	UTSW	19	16,511,113 (GRCm39)	missense
R7403:Gna14	UTSW	19	16,576,445 (GRCm39)	missense
R8155:Gna14	UTSW	19	16,576,338 (GRCm39)	missense	probably benign	0.02
R8750:Gna14	UTSW	19	16,585,458 (GRCm39)	missense
R9687:Gna14	UTSW	19	16,582,350 (GRCm39)	missense
R9752:Gna14	UTSW	19	16,586,781 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CTGTTTCAGGACTTGAGGAAAGG -3'
(R):5'- GGAAGGCGTACATTCTGACAC -3'

Sequencing Primer
(F):5'- GAAGATGGACGGGCACTACCTC -3'
(R):5'- AAGTACAGTACCTTATTCTGCTCAC -3'

Posted On

2015-09-25