Mutagenetix > Incidental Mutation

Incidental Mutation 'R8688:Nmur2'

668258

Institutional Source

Beutler Lab

Gene Symbol

Nmur2

Ensembl Gene

ENSMUSG00000037393

Gene Name

neuromedin U receptor 2

Synonyms

MMRRC Submission

068543-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.211) question?

Stock #

R8688 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

55915816-55931813 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 55931654 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 19 (N19S)

Ref Sequence

ENSEMBL: ENSMUSP00000044718 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037682]

AlphaFold

Q8BZ39

Predicted Effect

probably damaging
Transcript: ENSMUST00000037682
AA Change: N19S

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

SMART Domains

Protein: ENSMUSP00000044718
Gene: ENSMUSG00000037393
AA Change: N19S

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srw	42	337	4.7e-7	PFAM
Pfam:7TM_GPCR_Srsx	48	334	1.8e-13	PFAM
Pfam:7tm_1	54	319	5.7e-51	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (55/55)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein from the G-protein coupled receptor 1 family. This protein is a receptor for neuromedin U, which is a neuropeptide that is widely distributed in the gut and central nervous system. This receptor plays an important role in the regulation of food intake and body weight. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for one knock-out allele exhibit increased chemical and thermal nociception thresholds, insensitivity to treatment with Nmu or Nms, and altered weight gain following a fast or when fed a high-fat diet that can be sex-dependent. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700018F24Rik	C	T	5: 144,982,183 (GRCm39)	T256I	probably damaging	Het
2700097O09Rik	C	T	12: 55,104,136 (GRCm39)	G161D	probably damaging	Het
Acvr1	G	A	2: 58,352,961 (GRCm39)	A333V	probably damaging	Het
Adamtsl1	A	C	4: 86,166,263 (GRCm39)	S209R		Het
Akr1c18	T	C	13: 4,187,194 (GRCm39)	K207E	possibly damaging	Het
Anapc1	T	G	2: 128,527,748 (GRCm39)	Q70P	probably benign	Het
Arhgef33	A	G	17: 80,680,615 (GRCm39)	E585G	probably damaging	Het
Baz1b	T	G	5: 135,271,343 (GRCm39)	S1309A	probably benign	Het
Bdp1	T	C	13: 100,240,307 (GRCm39)	R14G	probably damaging	Het
Bltp1	T	A	3: 37,090,066 (GRCm39)	Y745N		Het
Ccdc150	A	C	1: 54,407,132 (GRCm39)	Q1058H	probably damaging	Het
Cdk5rap2	A	G	4: 70,298,510 (GRCm39)	F74S	probably damaging	Het
CK137956	C	T	4: 127,844,739 (GRCm39)	E335K	possibly damaging	Het
Cyp2c66	A	T	19: 39,151,884 (GRCm39)	I200F	probably benign	Het
Dmbt1	T	A	7: 130,659,984 (GRCm39)	W412R	unknown	Het
Dsel	A	T	1: 111,790,468 (GRCm39)	C22*	probably null	Het
Ep400	A	G	5: 110,868,685 (GRCm39)	M949T	unknown	Het
Gcc1	A	T	6: 28,418,739 (GRCm39)	Y531*	probably null	Het
Gm10277	T	C	11: 77,676,405 (GRCm39)	R189G	unknown	Het
Gm17078	T	A	14: 51,848,687 (GRCm39)	R17*	probably null	Het
Gpr137b	T	C	13: 13,533,991 (GRCm39)	Y355C		Het
Grip1	A	G	10: 119,835,809 (GRCm39)	I502V	probably benign	Het
H2-M9	A	T	17: 36,953,034 (GRCm39)	V91D	probably damaging	Het
Hcls1	T	C	16: 36,781,821 (GRCm39)	L310P	probably benign	Het
Hsd17b11	T	A	5: 104,169,584 (GRCm39)	I8F	probably benign	Het
Iftap	T	C	2: 101,440,916 (GRCm39)	E29G	probably damaging	Het
Ildr2	A	T	1: 166,097,102 (GRCm39)	D107V	probably damaging	Het
Ivl	TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG	TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG	3: 92,479,608 (GRCm39)		probably benign	Het
Josd2	T	C	7: 44,120,640 (GRCm39)	W126R	probably damaging	Het
Ltbp2	T	A	12: 84,850,578 (GRCm39)	D912V	probably benign	Het
Mdc1	A	G	17: 36,161,383 (GRCm39)	I765M	probably benign	Het
Mroh1	A	G	15: 76,312,550 (GRCm39)	E579G	probably benign	Het
Obscn	T	C	11: 58,946,909 (GRCm39)	Y4075C	probably damaging	Het
Ogfr	AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG	AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG	2: 180,236,850 (GRCm39)		probably benign	Het
Or4k40	C	T	2: 111,250,958 (GRCm39)	V113I	probably benign	Het
Or8b51	T	A	9: 38,569,047 (GRCm39)	I214L	probably benign	Het
Orm1	G	A	4: 63,264,578 (GRCm39)	V167M	probably damaging	Het
Phf14	A	G	6: 11,990,034 (GRCm39)	N688D	probably damaging	Het
Phlpp2	A	G	8: 110,631,012 (GRCm39)	K219E	probably damaging	Het
Prdm2	T	C	4: 142,838,310 (GRCm39)	T1683A	probably benign	Het
Ptprh	T	A	7: 4,554,022 (GRCm39)	Q815L	probably benign	Het
Rag1	A	T	2: 101,472,968 (GRCm39)	Y725N	probably damaging	Het
Rp1	T	A	1: 4,416,628 (GRCm39)	I1495F	probably benign	Het
Scn3a	A	G	2: 65,356,047 (GRCm39)	V229A	possibly damaging	Het
Siglech	A	G	7: 55,418,362 (GRCm39)	D110G	probably benign	Het
St8sia2	A	T	7: 73,593,092 (GRCm39)	D321E	probably damaging	Het
Stxbp3	A	G	3: 108,709,425 (GRCm39)		probably benign	Het
Tbccd1	A	T	16: 22,641,208 (GRCm39)	S390T	possibly damaging	Het
Tg	T	A	15: 66,566,802 (GRCm39)		probably benign	Het
Trio	T	A	15: 27,748,324 (GRCm39)	N2443Y	possibly damaging	Het
Ube2s	C	T	7: 4,813,577 (GRCm39)	M62I	probably benign	Het
Ugt2b37	T	C	5: 87,390,240 (GRCm39)	D402G	possibly damaging	Het
Vmn2r80	A	G	10: 79,004,069 (GRCm39)	N94S	probably damaging	Het
Wapl	T	A	14: 34,414,549 (GRCm39)	S470R	possibly damaging	Het
Xrra1	A	G	7: 99,555,752 (GRCm39)	E373G	probably damaging	Het
Zfp335	A	G	2: 164,734,113 (GRCm39)	Y1329H	probably damaging	Het
Zfp689	C	A	7: 127,044,084 (GRCm39)	C182F	probably benign	Het
Zfp933	T	A	4: 147,911,249 (GRCm39)	S116C	probably benign	Het

Other mutations in Nmur2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00229:Nmur2	APN	11	55,931,603 (GRCm39)	missense	probably damaging	0.99
IGL01591:Nmur2	APN	11	55,917,825 (GRCm39)	missense	probably benign
IGL01960:Nmur2	APN	11	55,931,337 (GRCm39)	missense	probably damaging	0.99
IGL02108:Nmur2	APN	11	55,931,190 (GRCm39)	missense	probably benign	0.33
IGL02602:Nmur2	APN	11	55,917,889 (GRCm39)	missense	probably benign	0.19
PIT4677001:Nmur2	UTSW	11	55,923,835 (GRCm39)	missense	probably benign	0.00
R0324:Nmur2	UTSW	11	55,931,346 (GRCm39)	missense	probably damaging	1.00
R0458:Nmur2	UTSW	11	55,931,394 (GRCm39)	missense	possibly damaging	0.93
R0718:Nmur2	UTSW	11	55,920,324 (GRCm39)	splice site	probably benign
R1799:Nmur2	UTSW	11	55,920,447 (GRCm39)	missense	probably damaging	1.00
R2099:Nmur2	UTSW	11	55,931,589 (GRCm39)	missense	probably benign	0.00
R2263:Nmur2	UTSW	11	55,920,387 (GRCm39)	missense	probably damaging	0.97
R3701:Nmur2	UTSW	11	55,931,603 (GRCm39)	missense	probably damaging	0.99
R3705:Nmur2	UTSW	11	55,931,300 (GRCm39)	missense	probably damaging	1.00
R3951:Nmur2	UTSW	11	55,931,051 (GRCm39)	missense	probably damaging	1.00
R4083:Nmur2	UTSW	11	55,931,051 (GRCm39)	missense	probably damaging	1.00
R4744:Nmur2	UTSW	11	55,931,661 (GRCm39)	missense	probably benign	0.01
R4747:Nmur2	UTSW	11	55,931,105 (GRCm39)	missense	probably benign	0.05
R5288:Nmur2	UTSW	11	55,931,040 (GRCm39)	missense	probably damaging	1.00
R5384:Nmur2	UTSW	11	55,931,040 (GRCm39)	missense	probably damaging	1.00
R5579:Nmur2	UTSW	11	55,923,835 (GRCm39)	missense	probably benign	0.00
R6329:Nmur2	UTSW	11	55,920,411 (GRCm39)	missense	probably benign	0.30
R6477:Nmur2	UTSW	11	55,920,417 (GRCm39)	missense	probably damaging	1.00
R7445:Nmur2	UTSW	11	55,923,766 (GRCm39)	missense	probably damaging	0.97
R7580:Nmur2	UTSW	11	55,917,808 (GRCm39)	missense	probably benign	0.03
R7899:Nmur2	UTSW	11	55,931,161 (GRCm39)	missense	probably benign
R9090:Nmur2	UTSW	11	55,931,308 (GRCm39)	missense	probably benign	0.44
R9098:Nmur2	UTSW	11	55,920,408 (GRCm39)	missense	possibly damaging	0.93
R9271:Nmur2	UTSW	11	55,931,308 (GRCm39)	missense	probably benign	0.44
R9542:Nmur2	UTSW	11	55,931,649 (GRCm39)	missense	probably damaging	0.98
X0062:Nmur2	UTSW	11	55,931,675 (GRCm39)	missense	probably benign	0.01
Z1176:Nmur2	UTSW	11	55,917,927 (GRCm39)	missense	probably benign	0.12
Z1186:Nmur2	UTSW	11	55,931,104 (GRCm39)	missense	probably benign
Z1187:Nmur2	UTSW	11	55,931,104 (GRCm39)	missense	probably benign
Z1188:Nmur2	UTSW	11	55,931,104 (GRCm39)	missense	probably benign
Z1189:Nmur2	UTSW	11	55,931,104 (GRCm39)	missense	probably benign
Z1190:Nmur2	UTSW	11	55,931,104 (GRCm39)	missense	probably benign
Z1191:Nmur2	UTSW	11	55,931,104 (GRCm39)	missense	probably benign
Z1192:Nmur2	UTSW	11	55,931,104 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TCTGAGACTGCCAAGCTGAAG -3'
(R):5'- TCAAAAGGCATTAACAGCGTG -3'

Sequencing Primer
(F):5'- CTGCCAAGCTGAAGAGATAGTAGTTG -3'
(R):5'- AGAGGCTGATGCTATCCTTTCAC -3'

Posted On

2021-04-30