Mutagenetix > Incidental Mutation

Incidental Mutation 'R4456:Fcer1g'

329175

Institutional Source

Beutler Lab

Gene Symbol

Fcer1g

Ensembl Gene

ENSMUSG00000058715

Gene Name

Fc receptor, IgE, high affinity I, gamma polypeptide

Synonyms

FcR-gamma, Fce1g, Ly-50, FcepsilonRI, FcRgamma, FcR[g]

MMRRC Submission

041716-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.257) question?

Stock #

R4456 (G1)

Quality Score

188

Status

Validated

Chromosome

Chromosomal Location

171057141-171061918 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 171061808 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 3 (S3P)

Ref Sequence

ENSEMBL: ENSMUSP00000141240 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000013737] [ENSMUST00000079957] [ENSMUST00000111318] [ENSMUST00000193973] [ENSMUST00000191871] [ENSMUST00000194778]

AlphaFold

P20491

Predicted Effect

probably benign
Transcript: ENSMUST00000013737

SMART Domains

Protein: ENSMUSP00000013737
Gene: ENSMUSG00000013593

Domain	Start	End	E-Value	Type
Pfam:Complex1_49kDa	193	463	1.1e-131	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000079957
AA Change: S3P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000078875
Gene: ENSMUSG00000058715
AA Change: S3P

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:TCR_zetazeta	21	51	3.7e-19	PFAM
ITAM	62	82	9.62e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000111318

SMART Domains

Protein: ENSMUSP00000106950
Gene: ENSMUSG00000013593

Domain	Start	End	E-Value	Type
Pfam:Complex1_49kDa	193	236	2e-21	PFAM
Pfam:Complex1_49kDa	232	437	1.7e-105	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000131286

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136976

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138069

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150108

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150997

Predicted Effect

probably benign
Transcript: ENSMUST00000193973
AA Change: S3P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000141240
Gene: ENSMUSG00000058715
AA Change: S3P

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:TCR_zetazeta	21	53	4.7e-19	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000191871

SMART Domains

Protein: ENSMUSP00000141942
Gene: ENSMUSG00000013593

Domain	Start	End	E-Value	Type
Pfam:Complex1_49kDa	114	146	5.3e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000194778

SMART Domains

Protein: ENSMUSP00000141370
Gene: ENSMUSG00000013593

Domain	Start	End	E-Value	Type
Pfam:Complex1_49kDa	166	231	3.4e-28	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.2%

Validation Efficiency

93% (42/45)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The high affinity IgE receptor is a key molecule involved in allergic reactions. It is a tetramer composed of 1 alpha, 1 beta, and 2 gamma chains. The gamma chains are also subunits of other Fc receptors. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for targeted null mutations exhibit impairments in macrophage phagocytosis, NK cell-mediated antibody-coated cytotoxicity, mast cell degranulation, IgE-mediated systemic anaphylaxis, and neutrophil recruitment and migration. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8b	A	G	11: 109,833,071 (GRCm39)	F1210L	probably benign	Het
Amfr	C	T	8: 94,711,568 (GRCm39)	A323T	possibly damaging	Het
Apob	T	A	12: 8,065,445 (GRCm39)	I4105N	probably damaging	Het
Bahd1	C	T	2: 118,746,887 (GRCm39)	P169S	probably damaging	Het
Cdc42ep1	A	G	15: 78,734,091 (GRCm39)	E397G	possibly damaging	Het
Cdkn2d	C	G	9: 21,202,185 (GRCm39)	V21L	probably benign	Het
Dnmt1	T	C	9: 20,821,138 (GRCm39)	T1250A	probably damaging	Het
Dst	A	T	1: 34,229,800 (GRCm39)	K2642N	probably benign	Het
Emcn	A	T	3: 137,085,608 (GRCm39)	K69*	probably null	Het
Eya1	C	T	1: 14,253,420 (GRCm39)	V519M	probably damaging	Het
Fbxo38	G	T	18: 62,659,320 (GRCm39)	R326S	probably damaging	Het
Glp1r	G	T	17: 31,137,949 (GRCm39)	E127*	probably null	Het
Gnmt	G	T	17: 47,039,910 (GRCm39)	H56Q	probably benign	Het
Hectd4	C	T	5: 121,446,334 (GRCm39)	T1513I	possibly damaging	Het
Hsd3b1	G	A	3: 98,763,459 (GRCm39)	T48I	probably benign	Het
Kmt2c	A	T	5: 25,515,210 (GRCm39)	C2878S	probably benign	Het
Loxhd1	A	G	18: 77,486,785 (GRCm39)	Y1290C	probably damaging	Het
Mkln1	A	G	6: 31,403,707 (GRCm39)	Y76C	probably damaging	Het
Mri1	C	A	8: 84,983,035 (GRCm39)	A129S	probably benign	Het
Mroh2b	A	T	15: 4,977,407 (GRCm39)	H1253L	probably benign	Het
Mslnl	G	A	17: 25,961,908 (GRCm39)	V128M	probably damaging	Het
Mthfsd	C	T	8: 121,832,504 (GRCm39)	V63I	possibly damaging	Het
Naip2	T	A	13: 100,291,419 (GRCm39)	H1173L	probably benign	Het
Nbea	A	G	3: 55,551,205 (GRCm39)	V2653A	probably benign	Het
Nckap5	A	T	1: 125,842,472 (GRCm39)		probably benign	Het
Notch4	G	A	17: 34,802,807 (GRCm39)	V1378M	probably damaging	Het
Or51a42	A	G	7: 103,708,507 (GRCm39)	S101P	possibly damaging	Het
Rab36	G	A	10: 74,880,328 (GRCm39)	V63I	probably damaging	Het
Rasl12	A	G	9: 65,305,866 (GRCm39)	K7R	probably null	Het
Rnf4	A	G	5: 34,508,705 (GRCm39)	Y189C	probably benign	Het
Shroom3	A	G	5: 93,088,858 (GRCm39)	H536R	probably benign	Het
Slc2a4	G	A	11: 69,834,148 (GRCm39)		probably benign	Het
Tbc1d5	A	C	17: 51,089,369 (GRCm39)	S604A	probably damaging	Het
Tcp11l1	A	T	2: 104,514,567 (GRCm39)	V400E	probably damaging	Het
Tom1l2	G	T	11: 60,243,641 (GRCm39)		probably benign	Het
Ttc28	AC	A	5: 111,371,924 (GRCm39)		probably null	Het
Txndc15	A	G	13: 55,865,977 (GRCm39)	D147G	possibly damaging	Het

Other mutations in Fcer1g

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02068:Fcer1g	APN	1	171,058,760 (GRCm39)	missense	probably damaging	1.00
R0219:Fcer1g	UTSW	1	171,058,795 (GRCm39)	missense	possibly damaging	0.71
R0734:Fcer1g	UTSW	1	171,058,748 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- ATTCAGAATCTGCTTCAGCCC -3'
(R):5'- GATCGTCCAGCTCCCCAAAATG -3'

Sequencing Primer
(F):5'- GAATCTGCTTCAGCCCTCCCTG -3'
(R):5'- CCAAAATGGCCCTTCCGG -3'

Posted On

2015-07-21