Mutagenetix > Incidental Mutation

Incidental Mutation 'R6370:Faah'

513461

Institutional Source

Beutler Lab

Gene Symbol

Faah

Ensembl Gene

ENSMUSG00000034171

Gene Name

fatty acid amide hydrolase

Synonyms

MMRRC Submission

044520-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.098) question?

Stock #

R6370 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

115853865-115876034 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 115860253 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 333 (D333G)

Ref Sequence

ENSEMBL: ENSMUSP00000041543 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049095]

AlphaFold

O08914

Predicted Effect

probably damaging
Transcript: ENSMUST00000049095
AA Change: D333G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000041543
Gene: ENSMUSG00000034171
AA Change: D333G

Domain	Start	End	E-Value	Type
transmembrane domain	7	29	N/A	INTRINSIC
low complexity region	74	87	N/A	INTRINSIC
Pfam:Amidase	95	562	1.4e-122	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125761

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133225

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143724

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150614

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150668

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154249

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156126

Meta Mutation Damage Score

0.9375

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 94.1%

Validation Efficiency

95% (54/57)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that is responsible for the hydrolysis of a number of primary and secondary fatty acid amides, including the neuromodulatory compounds anandamide and oleamide. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a null allele show high brain anandamide (AEA) levels, reduced pain sensation, altered behavioral responses to AEA, and sex-specific changes in ethanol intake and sensitivity. Homozygotes for the C385A variant show enhanced cued fear extinction and reduced anxiety-like behavior. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Asb6	A	G	2: 30,717,024 (GRCm39)	V67A	probably damaging	Het
Atic	T	A	1: 71,617,819 (GRCm39)	F590I	probably damaging	Het
Atxn10	T	C	15: 85,277,586 (GRCm39)	F351S	probably damaging	Het
Bcl2l13	A	G	6: 120,842,583 (GRCm39)	N92S	probably benign	Het
Carm1	G	T	9: 21,498,815 (GRCm39)	A518S	probably benign	Het
Ccar1	C	T	10: 62,600,308 (GRCm39)	R541H	probably damaging	Het
Cfhr2	A	T	1: 139,750,065 (GRCm39)	L96Q	probably damaging	Het
Chrnb4	A	G	9: 54,942,143 (GRCm39)	L377S	probably benign	Het
Clcn3	A	G	8: 61,376,058 (GRCm39)	Y639H	probably damaging	Het
Cngb1	C	T	8: 95,991,050 (GRCm39)	M717I	probably benign	Het
Ctcf	T	C	8: 106,390,852 (GRCm39)	M153T	probably benign	Het
Cyp2b19	T	C	7: 26,462,783 (GRCm39)	S222P	probably benign	Het
Dixdc1	A	T	9: 50,593,523 (GRCm39)		probably null	Het
Entpd2	G	A	2: 25,287,429 (GRCm39)	G47S	probably damaging	Het
Erbb3	A	G	10: 128,405,943 (GRCm39)	M1158T	possibly damaging	Het
Foxred2	T	A	15: 77,827,506 (GRCm39)	T618S	probably benign	Het
Gm2381	G	A	7: 42,470,010 (GRCm39)	A38V	probably benign	Het
Gpx5	A	T	13: 21,472,872 (GRCm39)		probably null	Het
Gtdc1	A	G	2: 44,646,334 (GRCm39)	V98A	probably damaging	Het
Hal	T	C	10: 93,333,368 (GRCm39)	I312T	probably damaging	Het
Krtap21-1	T	C	16: 89,200,519 (GRCm39)	Y41C	unknown	Het
Larp6	A	G	9: 60,644,646 (GRCm39)	E262G	probably damaging	Het
Lrrn1	A	G	6: 107,546,185 (GRCm39)	Y661C	probably damaging	Het
Lsm14a	A	G	7: 34,056,906 (GRCm39)	V244A	probably benign	Het
Mfrp	T	C	9: 44,017,558 (GRCm39)	C517R	probably damaging	Het
Mtarc1	T	C	1: 184,527,689 (GRCm39)	D257G	probably damaging	Het
Ncoa3	T	C	2: 165,907,825 (GRCm39)	S1145P	probably benign	Het
Nosip	G	T	7: 44,726,164 (GRCm39)		probably null	Het
Or4c100	T	A	2: 88,329,712 (GRCm39)	C94*	probably null	Het
Or51f2	A	T	7: 102,526,377 (GRCm39)	T17S	probably benign	Het
Or52n1	T	C	7: 104,383,124 (GRCm39)	K149R	probably benign	Het
Phykpl	T	C	11: 51,477,543 (GRCm39)	S112P	probably damaging	Het
Pik3cb	A	T	9: 98,922,987 (GRCm39)	I1015K	probably damaging	Het
Pomt2	A	G	12: 87,155,973 (GRCm39)	W818R	probably damaging	Het
Ptpn21	A	T	12: 98,655,293 (GRCm39)	M558K	possibly damaging	Het
Rnf213	T	A	11: 119,367,904 (GRCm39)	N4647K	probably damaging	Het
Rsf1	GCG	GCGACGGCGACG	7: 97,229,114 (GRCm39)		probably benign	Homo
Rxrg	T	C	1: 167,462,006 (GRCm39)	V227A	probably damaging	Het
Satb1	A	T	17: 52,089,825 (GRCm39)	S341T	possibly damaging	Het
Skint5	T	G	4: 113,471,307 (GRCm39)	Q983P	unknown	Het
Slc6a18	G	A	13: 73,816,278 (GRCm39)	T367I	probably benign	Het
Slc7a1	A	G	5: 148,277,483 (GRCm39)	L344P	probably damaging	Het
Slc7a6	T	A	8: 106,922,069 (GRCm39)	F399I	probably benign	Het
St3gal1	A	G	15: 66,983,195 (GRCm39)	V187A	possibly damaging	Het
Sugt1	T	C	14: 79,847,774 (GRCm39)	V208A	probably benign	Het
Syt3	A	G	7: 44,045,107 (GRCm39)	K480E	probably damaging	Het
Thop1	C	T	10: 80,913,817 (GRCm39)	T186I	probably benign	Het
Trim55	G	A	3: 19,745,650 (GRCm39)	E509K	possibly damaging	Het
Upf2	A	G	2: 5,980,821 (GRCm39)	N469S	unknown	Het
Usp24	G	T	4: 106,237,718 (GRCm39)	K1125N	probably null	Het
Usp5	A	T	6: 124,797,391 (GRCm39)	D494E	probably benign	Het
Vmn2r51	T	C	7: 9,832,143 (GRCm39)	K481R	probably damaging	Het
Vps16	C	A	2: 130,285,304 (GRCm39)	A787D	probably damaging	Het
Washc4	C	T	10: 83,407,226 (GRCm39)	H488Y	possibly damaging	Het
Wdfy4	C	A	14: 32,790,807 (GRCm39)	A2053S	probably benign	Het
Zfp74	A	T	7: 29,631,835 (GRCm39)	D136E	probably damaging	Het

Other mutations in Faah

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00679:Faah	APN	4	115,865,480 (GRCm39)	missense	possibly damaging	0.85
IGL03355:Faah	APN	4	115,859,725 (GRCm39)	missense	probably benign	0.28
R0013:Faah	UTSW	4	115,861,588 (GRCm39)	missense	probably damaging	1.00
R0387:Faah	UTSW	4	115,862,889 (GRCm39)	nonsense	probably null
R0727:Faah	UTSW	4	115,862,257 (GRCm39)	missense	probably damaging	1.00
R1405:Faah	UTSW	4	115,858,345 (GRCm39)	missense	probably damaging	1.00
R1405:Faah	UTSW	4	115,858,345 (GRCm39)	missense	probably damaging	1.00
R1465:Faah	UTSW	4	115,856,755 (GRCm39)	missense	probably damaging	1.00
R1465:Faah	UTSW	4	115,856,755 (GRCm39)	missense	probably damaging	1.00
R1861:Faah	UTSW	4	115,865,432 (GRCm39)	missense	probably benign	0.45
R2062:Faah	UTSW	4	115,855,770 (GRCm39)	missense	probably damaging	1.00
R4926:Faah	UTSW	4	115,856,823 (GRCm39)	intron	probably benign
R5162:Faah	UTSW	4	115,857,938 (GRCm39)	intron	probably benign
R5425:Faah	UTSW	4	115,857,993 (GRCm39)	missense	probably null	0.47
R5449:Faah	UTSW	4	115,856,692 (GRCm39)	splice site	probably null
R6236:Faah	UTSW	4	115,856,786 (GRCm39)	missense	probably benign	0.03
R6569:Faah	UTSW	4	115,874,829 (GRCm39)	missense	probably benign
R7384:Faah	UTSW	4	115,862,364 (GRCm39)	missense	probably damaging	1.00
R9432:Faah	UTSW	4	115,874,772 (GRCm39)	missense	probably benign
X0024:Faah	UTSW	4	115,860,176 (GRCm39)	missense	possibly damaging	0.77

Predicted Primers

PCR Primer
(F):5'- TTTAGACTGGTCTTACACAGCC -3'
(R):5'- TGGTCTGTGGCTCCTACAAC -3'

Sequencing Primer
(F):5'- TGGTCTTACACAGCCAAAGTTC -3'
(R):5'- GGTCTGTGGCTCCTACAACAATAG -3'

Posted On

2018-04-27