Mutagenetix > Incidental Mutation

Incidental Mutation 'R6086:Htr3b'

482488

Institutional Source

Beutler Lab

Gene Symbol

Htr3b

Ensembl Gene

ENSMUSG00000008590

Gene Name

5-hydroxytryptamine (serotonin) receptor 3B

Synonyms

5-HT3B, 5-HT3 receptor subunit B

MMRRC Submission

044427-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6086 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

48846308-48876290 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 48858598 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Glycine at position 94 (S94G)

Ref Sequence

ENSEMBL: ENSMUSP00000008734 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000008734]

AlphaFold

Q9JHJ5

Predicted Effect

probably benign
Transcript: ENSMUST00000008734
AA Change: S94G

PolyPhen 2 Score 0.163 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000008734
Gene: ENSMUSG00000008590
AA Change: S94G

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
Pfam:Neur_chan_LBD	28	235	1.5e-48	PFAM
Pfam:Neur_chan_memb	242	336	2.2e-15	PFAM
transmembrane domain	412	434	N/A	INTRINSIC

Meta Mutation Damage Score

0.2180

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.9%

Validation Efficiency

96% (65/68)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit B of the type 3 receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor causes fast, depolarizing responses in neurons after activation. It is not functional as a homomeric complex, but a pentaheteromeric complex with subunit A (HTR3A) displays the full functional features of this receptor. [provided by RefSeq, Aug 2011]

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Apob	G	T	12: 8,065,164 (GRCm39)	K4044N	probably benign	Het
Asic4	G	A	1: 75,449,887 (GRCm39)	V468I	possibly damaging	Het
Atf4	T	A	15: 80,141,654 (GRCm39)	V348D	probably benign	Het
Bcl9	A	G	3: 97,112,840 (GRCm39)	V1205A	possibly damaging	Het
Bora	A	T	14: 99,299,730 (GRCm39)	Q234L	possibly damaging	Het
Cap2	C	A	13: 46,789,188 (GRCm39)	P131Q	probably damaging	Het
Cdyl2	A	G	8: 117,316,035 (GRCm39)	S318P	probably damaging	Het
Ces1a	T	G	8: 93,753,981 (GRCm39)	N341H	probably benign	Het
Cimap2	T	C	4: 106,470,403 (GRCm39)	E218G	probably damaging	Het
Crlf3	C	T	11: 79,939,436 (GRCm39)	V352M	possibly damaging	Het
Cybb	C	G	X: 9,316,989 (GRCm39)	D246H	probably benign	Het
Cyren	A	G	6: 34,851,555 (GRCm39)	S127P	probably damaging	Het
Dnah2	T	C	11: 69,406,834 (GRCm39)	T529A	probably benign	Het
Dnah9	C	T	11: 65,880,741 (GRCm39)	D2619N	probably damaging	Het
Dnah9	A	C	11: 65,976,000 (GRCm39)	S1350A	probably benign	Het
Dnajc6	C	T	4: 101,455,004 (GRCm39)	S65L	probably benign	Het
Dnm3	C	A	1: 162,148,602 (GRCm39)	R256S	probably damaging	Het
Enpp2	T	C	15: 54,709,230 (GRCm39)	D795G	probably damaging	Het
Fah	A	T	7: 84,238,120 (GRCm39)	W367R	probably damaging	Het
Fam220a	T	A	5: 143,548,796 (GRCm39)	H69Q	probably benign	Het
Fgd3	T	A	13: 49,440,772 (GRCm39)	T220S	probably benign	Het
Furin	G	T	7: 80,045,179 (GRCm39)	H248Q	probably damaging	Het
Gabrg1	A	T	5: 70,911,396 (GRCm39)	L410Q	probably damaging	Het
Gm10801	AAGT	AAGTAGT	2: 98,494,148 (GRCm39)		probably null	Het
Gm9742	T	C	13: 8,080,069 (GRCm39)		noncoding transcript	Het
Gpcpd1	A	G	2: 132,380,034 (GRCm39)	S252P	probably damaging	Het
Hnrnpdl	C	T	5: 100,184,340 (GRCm39)	G398S	probably null	Het
Hspa1l	T	C	17: 35,197,131 (GRCm39)	V390A	possibly damaging	Het
Klf10	G	T	15: 38,297,181 (GRCm39)	S271R	probably benign	Het
Klk1b3	T	A	7: 43,851,158 (GRCm39)	L197Q	probably damaging	Het
Knl1	A	G	2: 118,924,549 (GRCm39)	R1861G	probably damaging	Het
Myo9a	C	T	9: 59,697,340 (GRCm39)	Q374*	probably null	Het
Myt1l	G	A	12: 29,882,331 (GRCm39)	G509R	unknown	Het
Ncapg	T	C	5: 45,850,578 (GRCm39)	L728P	probably damaging	Het
Nfxl1	A	C	5: 72,698,362 (GRCm39)	F228V	probably benign	Het
Ntaq1	C	A	15: 58,014,024 (GRCm39)	A71E	probably damaging	Het
Oc90	A	G	15: 65,761,560 (GRCm39)	S153P	probably damaging	Het
Or4c123	A	G	2: 89,127,198 (GRCm39)	C139R	probably damaging	Het
Or5b105	A	G	19: 13,079,745 (GRCm39)	*308Q	probably null	Het
Pbk	A	T	14: 66,052,702 (GRCm39)	K182*	probably null	Het
Piezo1	A	G	8: 123,228,396 (GRCm39)	F296S	possibly damaging	Het
Psmg1	T	A	16: 95,781,244 (GRCm39)	Y288F	probably damaging	Het
Rab11fip4	G	A	11: 79,574,306 (GRCm39)	D132N	probably damaging	Het
Recql4	T	C	15: 76,588,787 (GRCm39)	D1051G	probably damaging	Het
Reep5	A	C	18: 34,490,184 (GRCm39)	D104E	probably damaging	Het
Rnpepl1	T	C	1: 92,845,403 (GRCm39)	Y441H	probably damaging	Het
Scnm1	T	C	3: 95,037,596 (GRCm39)	I157V	probably benign	Het
Sema3b	T	C	9: 107,478,047 (GRCm39)	D446G	probably damaging	Het
Sema4d	C	T	13: 51,867,781 (GRCm39)	R190Q	probably damaging	Het
Slco3a1	G	A	7: 73,968,338 (GRCm39)	R461C	possibly damaging	Het
Spmap2l	T	A	5: 77,209,152 (GRCm39)	V458E	probably benign	Het
Tenm2	T	A	11: 35,899,473 (GRCm39)	I2562F	possibly damaging	Het
Tmem40	G	T	6: 115,710,628 (GRCm39)	N120K	possibly damaging	Het
Tmod3	T	C	9: 75,407,405 (GRCm39)	H351R	probably benign	Het
Tnn	C	T	1: 159,913,690 (GRCm39)	V1268M	probably damaging	Het
Tpmt	T	A	13: 47,188,506 (GRCm39)	D132V	probably damaging	Het
Trgc3	T	C	13: 19,447,454 (GRCm39)	S136P	probably damaging	Het
Trib1	G	A	15: 59,526,324 (GRCm39)	R298H	probably damaging	Het
Tsen2	A	G	6: 115,537,036 (GRCm39)	E264G	probably benign	Het
Urah	A	G	7: 140,416,711 (GRCm39)	I60M	probably benign	Het
Vmn2r26	T	A	6: 124,016,519 (GRCm39)	S328T	possibly damaging	Het
Vmn2r27	G	C	6: 124,168,958 (GRCm39)	T724R	probably damaging	Het
Washc2	A	G	6: 116,233,177 (GRCm39)		probably null	Het
Zfp955b	T	A	17: 33,521,478 (GRCm39)	W316R	probably benign	Het
Zranb2	T	C	3: 157,248,883 (GRCm39)		probably null	Het

Other mutations in Htr3b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01401:Htr3b	APN	9	48,858,934 (GRCm39)	missense	probably damaging	1.00
IGL02576:Htr3b	APN	9	48,856,804 (GRCm39)	missense	possibly damaging	0.67
space	UTSW	9	48,848,456 (GRCm39)	missense	probably damaging	1.00
stove	UTSW	9	48,847,343 (GRCm39)	splice site	probably null
thermador	UTSW	9	48,870,518 (GRCm39)	missense	possibly damaging	0.94
R0594:Htr3b	UTSW	9	48,858,931 (GRCm39)	missense	probably benign	0.09
R1158:Htr3b	UTSW	9	48,847,390 (GRCm39)	missense	possibly damaging	0.55
R1690:Htr3b	UTSW	9	48,848,394 (GRCm39)	missense	possibly damaging	0.51
R2184:Htr3b	UTSW	9	48,858,544 (GRCm39)	missense	probably damaging	1.00
R3441:Htr3b	UTSW	9	48,856,815 (GRCm39)	missense	probably benign	0.01
R3442:Htr3b	UTSW	9	48,856,815 (GRCm39)	missense	probably benign	0.01
R4334:Htr3b	UTSW	9	48,856,809 (GRCm39)	missense	probably damaging	1.00
R4906:Htr3b	UTSW	9	48,848,348 (GRCm39)	critical splice donor site	probably null
R4985:Htr3b	UTSW	9	48,847,241 (GRCm39)	missense	possibly damaging	0.95
R4992:Htr3b	UTSW	9	48,870,518 (GRCm39)	missense	possibly damaging	0.94
R5197:Htr3b	UTSW	9	48,856,815 (GRCm39)	missense	probably benign	0.01
R5238:Htr3b	UTSW	9	48,848,542 (GRCm39)	nonsense	probably null
R6328:Htr3b	UTSW	9	48,858,933 (GRCm39)	missense	probably damaging	1.00
R6412:Htr3b	UTSW	9	48,857,819 (GRCm39)	missense	possibly damaging	0.94
R7140:Htr3b	UTSW	9	48,848,441 (GRCm39)	missense	possibly damaging	0.52
R7349:Htr3b	UTSW	9	48,847,319 (GRCm39)	missense	probably benign	0.05
R7596:Htr3b	UTSW	9	48,847,361 (GRCm39)	missense	probably benign	0.31
R7815:Htr3b	UTSW	9	48,856,833 (GRCm39)	missense	probably benign	0.02
R7920:Htr3b	UTSW	9	48,848,456 (GRCm39)	missense	probably damaging	1.00
R7960:Htr3b	UTSW	9	48,856,852 (GRCm39)	missense	probably benign	0.08
R8103:Htr3b	UTSW	9	48,857,849 (GRCm39)	missense	possibly damaging	0.94
R8210:Htr3b	UTSW	9	48,847,343 (GRCm39)	splice site	probably null
R8318:Htr3b	UTSW	9	48,876,177 (GRCm39)	start gained	probably benign
R8359:Htr3b	UTSW	9	48,858,596 (GRCm39)	missense	probably damaging	0.99
R8507:Htr3b	UTSW	9	48,876,177 (GRCm39)	start gained	probably benign

Predicted Primers

PCR Primer
(F):5'- AGTGATGACCCCAGTGATTG -3'
(R):5'- GTACAGTCCCCTAACTCAGC -3'

Posted On

2017-07-14