Mutagenetix > Incidental Mutation

Incidental Mutation 'R6989:Haao'

543174

Institutional Source

Beutler Lab

Gene Symbol

Haao

Ensembl Gene

ENSMUSG00000000673

Gene Name

3-hydroxyanthranilate 3,4-dioxygenase

Synonyms

3HAO, 0610012J07Rik, 3-HAOxase, 3-HAO, 0610007K21Rik

MMRRC Submission

045095-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6989 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

84138585-84155392 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 84139103 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Arginine at position 277 (Q277R)

Ref Sequence

ENSEMBL: ENSMUSP00000000687 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000000687]

AlphaFold

Q78JT3

Predicted Effect

probably damaging
Transcript: ENSMUST00000000687
AA Change: Q277R

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

SMART Domains

Protein: ENSMUSP00000000687
Gene: ENSMUSG00000000673
AA Change: Q277R

Domain	Start	End	E-Value	Type
Pfam:3-HAO	1	149	1e-78	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.3%
20x: 97.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] 3-Hydroxyanthranilate 3,4-dioxygenase is a monomeric cytosolic protein belonging to the family of intramolecular dioxygenases containing nonheme ferrous iron. It is widely distributed in peripheral organs, such as liver and kidney, and is also present in low amounts in the central nervous system. HAAO catalyzes the synthesis of quinolinic acid (QUIN) from 3-hydroxyanthranilic acid. QUIN is an excitotoxin whose toxicity is mediated by its ability to activate glutamate N-methyl-D-aspartate receptors. Increased cerebral levels of QUIN may participate in the pathogenesis of neurologic and inflammatory disorders. HAAO has been suggested to play a role in disorders associated with altered tissue levels of QUIN. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced LPS-induced depressive behaviors and altered kynurenine metabolism. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921536K21Rik	C	T	11: 3,840,076 (GRCm39)	R107H	probably damaging	Het
4930438A08Rik	T	C	11: 58,178,228 (GRCm39)	V96A	possibly damaging	Het
Abcc2	A	G	19: 43,820,611 (GRCm39)	D1370G	probably damaging	Het
Abcc9	T	A	6: 142,634,707 (GRCm39)	N186Y	probably damaging	Het
Adcy7	T	C	8: 89,035,414 (GRCm39)	V106A	probably benign	Het
Adgra3	A	G	5: 50,164,226 (GRCm39)	F251S	probably damaging	Het
Akr1c6	T	A	13: 4,499,045 (GRCm39)	I33N	probably damaging	Het
Alk	A	C	17: 72,204,947 (GRCm39)	M1075R	probably benign	Het
Amh	A	G	10: 80,641,338 (GRCm39)	Q86R	probably benign	Het
Aox1	T	C	1: 58,124,611 (GRCm39)	Y951H	probably damaging	Het
Arhgap26	G	T	18: 39,232,682 (GRCm39)	R119L	probably damaging	Het
Arl8a	A	G	1: 135,074,735 (GRCm39)	K7R	probably benign	Het
Birc6	T	G	17: 74,937,984 (GRCm39)	S2638A	probably benign	Het
Ccdc162	T	G	10: 41,457,349 (GRCm39)	Q256H	probably damaging	Het
Cenpe	T	A	3: 134,940,888 (GRCm39)	L679Q	probably damaging	Het
Cpa5	T	A	6: 30,625,891 (GRCm39)	H203Q	probably benign	Het
Cpne9	A	T	6: 113,277,544 (GRCm39)	D421V	possibly damaging	Het
Cux1	A	T	5: 136,308,502 (GRCm39)	C1212*	probably null	Het
Dock9	G	A	14: 121,864,791 (GRCm39)	H736Y	probably damaging	Het
Dpp3	A	T	19: 4,971,195 (GRCm39)	V214E	probably damaging	Het
Dtx3	T	C	10: 127,028,746 (GRCm39)	E161G	probably benign	Het
Ect2	A	T	3: 27,156,637 (GRCm39)	Y774*	probably null	Het
Enpep	G	T	3: 129,074,599 (GRCm39)	P717H	probably damaging	Het
Erich3	A	T	3: 154,469,314 (GRCm39)		probably benign	Het
Fbp2	C	T	13: 63,005,991 (GRCm39)	A41T	probably damaging	Het
Fbxl21	T	C	13: 56,674,874 (GRCm39)	V75A	probably damaging	Het
Fkbp5	C	T	17: 28,634,919 (GRCm39)	D197N	probably benign	Het
Fsip2	A	G	2: 82,807,298 (GRCm39)	T1206A	probably benign	Het
Ggt7	A	G	2: 155,345,380 (GRCm39)	V156A	probably benign	Het
Gpi1	T	C	7: 33,901,945 (GRCm39)	K156R	probably damaging	Het
Gpx5	T	C	13: 21,471,669 (GRCm39)	D178G	probably damaging	Het
Grm7	G	A	6: 111,184,766 (GRCm39)	E366K	probably damaging	Het
Lama1	T	C	17: 68,060,753 (GRCm39)	S694P		Het
Lrp10	A	G	14: 54,705,950 (GRCm39)	D380G	probably benign	Het
Lrp2	C	A	2: 69,302,799 (GRCm39)	D2977Y	probably damaging	Het
Map2	T	A	1: 66,454,065 (GRCm39)	M985K	probably benign	Het
Met	C	A	6: 17,535,927 (GRCm39)	N784K	possibly damaging	Het
Met	T	A	6: 17,535,928 (GRCm39)	Y65N	probably damaging	Het
Muc6	T	G	7: 141,226,246 (GRCm39)		probably benign	Het
Numbl	T	A	7: 26,980,265 (GRCm39)	W416R	probably damaging	Het
Nup160	G	A	2: 90,537,364 (GRCm39)	S746N	probably benign	Het
Pcca	G	A	14: 122,887,700 (GRCm39)	G102D	probably damaging	Het
Pira13	T	A	7: 3,825,163 (GRCm39)	Y493F	possibly damaging	Het
Psmc2	T	A	5: 22,006,217 (GRCm39)	F243L	possibly damaging	Het
Rictor	C	T	15: 6,801,635 (GRCm39)	S441L	probably benign	Het
Rpn1	G	T	6: 88,076,285 (GRCm39)	V357L	probably benign	Het
Rtn3	A	G	19: 7,433,856 (GRCm39)	F712S	possibly damaging	Het
Scgb1b10	T	A	7: 31,800,574 (GRCm39)	D54E	probably benign	Het
Scn5a	A	G	9: 119,315,395 (GRCm39)	I1771T	probably damaging	Het
Sec14l1	A	G	11: 117,047,220 (GRCm39)	I633V	probably damaging	Het
Slc17a6	T	C	7: 51,311,224 (GRCm39)	Y313H	possibly damaging	Het
Slc18a1	G	A	8: 69,491,514 (GRCm39)	T500I	probably benign	Het
Slx4	G	A	16: 3,813,702 (GRCm39)	A93V	probably damaging	Het
Stat4	T	C	1: 52,107,974 (GRCm39)	S148P	probably benign	Het
Tbc1d15	A	T	10: 115,045,474 (GRCm39)	C497S	probably damaging	Het
Ticam1	C	T	17: 56,576,900 (GRCm39)	E732K	probably benign	Het
Trav3-3	C	A	14: 53,903,802 (GRCm39)	P40Q	possibly damaging	Het
Trpv6	A	T	6: 41,602,390 (GRCm39)	L332Q	probably damaging	Het
Ube2t	T	G	1: 134,897,033 (GRCm39)	V55G	probably damaging	Het
Ufm1	T	C	3: 53,765,402 (GRCm39)	K69E	probably damaging	Het
Utp20	T	C	10: 88,614,102 (GRCm39)	D1284G	probably benign	Het
Vil1	C	T	1: 74,463,113 (GRCm39)	T432I	probably damaging	Het
Vps13b	T	A	15: 35,448,727 (GRCm39)	I567K	probably benign	Het
Zfp236	A	T	18: 82,646,488 (GRCm39)	V1023D	probably damaging	Het
Zfp429	A	G	13: 67,538,080 (GRCm39)	Y455H	probably benign	Het

Other mutations in Haao

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00580:Haao	APN	17	84,142,359 (GRCm39)	splice site	probably benign
IGL01728:Haao	APN	17	84,142,658 (GRCm39)	missense	probably damaging	1.00
IGL02603:Haao	APN	17	84,142,970 (GRCm39)	missense	probably benign	0.45
IGL03328:Haao	APN	17	84,154,078 (GRCm39)	missense	probably damaging	1.00
R0635:Haao	UTSW	17	84,146,003 (GRCm39)	missense	probably damaging	1.00
R1295:Haao	UTSW	17	84,146,267 (GRCm39)	missense	probably benign	0.38
R1296:Haao	UTSW	17	84,146,267 (GRCm39)	missense	probably benign	0.38
R1472:Haao	UTSW	17	84,146,267 (GRCm39)	missense	probably benign	0.38
R1563:Haao	UTSW	17	84,142,318 (GRCm39)	missense	probably benign	0.01
R2424:Haao	UTSW	17	84,142,991 (GRCm39)	missense	probably damaging	0.99
R3917:Haao	UTSW	17	84,146,228 (GRCm39)	critical splice donor site	probably null
R4657:Haao	UTSW	17	84,139,774 (GRCm39)	missense	possibly damaging	0.67
R4857:Haao	UTSW	17	84,146,009 (GRCm39)	critical splice acceptor site	probably null
R6475:Haao	UTSW	17	84,139,113 (GRCm39)	missense	possibly damaging	0.87
R7390:Haao	UTSW	17	84,154,081 (GRCm39)	missense	probably damaging	0.99
R8073:Haao	UTSW	17	84,142,649 (GRCm39)	missense	possibly damaging	0.86
R9309:Haao	UTSW	17	84,146,270 (GRCm39)	missense	probably damaging	1.00
R9718:Haao	UTSW	17	84,142,215 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCCAGTGACAGCTCTCAAC -3'
(R):5'- CCTCTAAGGTGACAATGGGAGG -3'

Sequencing Primer
(F):5'- GCTCTCAACCACTCAAGGGG -3'
(R):5'- TATAGCCCTGGCCCCAGATG -3'

Posted On

2018-11-28