Mutagenetix > Incidental Mutation

Incidental Mutation 'R7506:Negr1'

581778

Institutional Source

Beutler Lab

Gene Symbol

Negr1

Ensembl Gene

ENSMUSG00000040037

Gene Name

neuronal growth regulator 1

Synonyms

neurotractin, Ntra, 5330422G01Rik

MMRRC Submission

045579-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7506 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

156267431-157022082 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to G at 156774870 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 195 (Y195*)

Ref Sequence

ENSEMBL: ENSMUSP00000073664 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041425] [ENSMUST00000074015] [ENSMUST00000106065]

AlphaFold

Q80Z24

Predicted Effect

probably null
Transcript: ENSMUST00000041425
AA Change: Y195*

SMART Domains

Protein: ENSMUSP00000041132
Gene: ENSMUSG00000040037
AA Change: Y195*

Domain	Start	End	E-Value	Type
signal peptide	1	31	N/A	INTRINSIC
IG	39	130	2.52e-9	SMART
IGc2	145	204	3.22e-16	SMART
IGc2	230	298	3.82e-9	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000074015
AA Change: Y195*

SMART Domains

Protein: ENSMUSP00000073664
Gene: ENSMUSG00000040037
AA Change: Y195*

Domain	Start	End	E-Value	Type
signal peptide	1	31	N/A	INTRINSIC
IG	39	130	2.52e-9	SMART
IGc2	145	204	3.22e-16	SMART
IGc2	230	298	3.82e-9	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000106065
AA Change: Y195*

SMART Domains

Protein: ENSMUSP00000101680
Gene: ENSMUSG00000040037
AA Change: Y195*

Domain	Start	End	E-Value	Type
signal peptide	1	31	N/A	INTRINSIC
IG	39	130	2.52e-9	SMART
IGc2	145	204	3.22e-16	SMART
IGc2	230	298	3.82e-9	SMART

Coding Region Coverage

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

Validation Efficiency

98% (58/59)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out or ENU-induced allele exhibit reduced body weight. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931406C07Rik	C	T	9: 15,209,202 (GRCm39)	V31I	probably benign	Het
4933430I17Rik	T	C	4: 62,450,498 (GRCm39)	V24A	possibly damaging	Het
Adamtsl3	A	T	7: 82,164,186 (GRCm39)	R334W	probably damaging	Het
Aox1	G	A	1: 58,088,562 (GRCm39)	C116Y	probably damaging	Het
B3gntl1	A	T	11: 121,561,740 (GRCm39)	I74N	probably damaging	Het
Bicra	C	T	7: 15,722,138 (GRCm39)	V460M	possibly damaging	Het
Ccdc18	G	A	5: 108,311,605 (GRCm39)	C437Y	possibly damaging	Het
Cdh6	A	G	15: 13,034,396 (GRCm39)	S755P	probably damaging	Het
Crtc2	G	T	3: 90,166,519 (GRCm39)	A165S	probably damaging	Het
Cwf19l2	C	T	9: 3,456,775 (GRCm39)	H703Y	probably damaging	Het
Cyc1	C	A	15: 76,227,885 (GRCm39)	T41K	probably benign	Het
Defb28	A	T	2: 152,360,221 (GRCm39)	H12L	possibly damaging	Het
Dsg3	T	A	18: 20,666,521 (GRCm39)	C577S	probably benign	Het
Ggt6	G	T	11: 72,328,724 (GRCm39)	C408F	possibly damaging	Het
Gm3278	T	A	14: 16,080,479 (GRCm39)	Y97N	probably damaging	Het
Gpr155	A	G	2: 73,198,683 (GRCm39)	L412P	probably damaging	Het
Gucd1	T	C	10: 75,347,019 (GRCm39)	H77R	probably benign	Het
H2bc8	G	A	13: 23,755,658 (GRCm39)	A18T	unknown	Het
Hat1	T	A	2: 71,250,691 (GRCm39)	I158N	probably damaging	Het
Hhla1	C	T	15: 65,808,231 (GRCm39)	W271*	probably null	Het
Igsf10	T	A	3: 59,226,775 (GRCm39)	L2299F	probably damaging	Het
Iqsec1	A	G	6: 90,644,891 (GRCm39)	S914P	probably damaging	Het
Iqsec1	G	T	6: 90,639,788 (GRCm39)	H983Q	possibly damaging	Het
Irx2	G	T	13: 72,777,328 (GRCm39)	G50C	probably damaging	Het
Kif26b	T	C	1: 178,357,064 (GRCm39)		probably benign	Het
Lmo7	A	G	14: 102,157,045 (GRCm39)	E1405G	unknown	Het
Mdm2	T	C	10: 117,526,596 (GRCm39)	D330G	possibly damaging	Het
Mgat5	A	C	1: 127,294,192 (GRCm39)	D178A	probably benign	Het
Mier2	C	A	10: 79,386,176 (GRCm39)	R25L	probably benign	Het
Mlip	T	C	9: 77,072,085 (GRCm39)	K257E	probably damaging	Het
Mtfr2	T	C	10: 20,229,131 (GRCm39)	S80P	probably benign	Het
Ndst2	A	G	14: 20,780,153 (GRCm39)	V29A	probably benign	Het
Nptn	T	C	9: 58,526,156 (GRCm39)	L101P	probably damaging	Het
Nrip1	G	A	16: 76,091,347 (GRCm39)	T70I	probably damaging	Het
Nrtn	C	T	17: 57,058,633 (GRCm39)	V123M	probably damaging	Het
Onecut1	T	A	9: 74,770,522 (GRCm39)	F315Y	possibly damaging	Het
Or1p1	A	T	11: 74,179,949 (GRCm39)	H159L	possibly damaging	Het
P4htm	A	G	9: 108,460,878 (GRCm39)	L198S	probably damaging	Het
Pappa	A	C	4: 65,149,419 (GRCm39)	I920L	probably benign	Het
Pcdhgb5	A	C	18: 37,865,525 (GRCm39)	D440A	probably damaging	Het
Ppard	A	T	17: 28,517,735 (GRCm39)	N268Y	possibly damaging	Het
Rapgef6	T	A	11: 54,526,997 (GRCm39)	S563T	probably benign	Het
Rtn3	T	A	19: 7,407,118 (GRCm39)	E949D	probably benign	Het
Sf3a1	T	C	11: 4,127,561 (GRCm39)	M629T	probably benign	Het
Slc39a8	T	C	3: 135,590,067 (GRCm39)	I319T	probably benign	Het
Sorcs1	C	T	19: 50,171,112 (GRCm39)	W925*	probably null	Het
Spag9	G	A	11: 93,999,290 (GRCm39)	D1069N	probably damaging	Het
Taar7a	A	G	10: 23,868,892 (GRCm39)	V163A	possibly damaging	Het
Tmem150a	G	A	6: 72,333,753 (GRCm39)		probably null	Het
Tnxb	G	A	17: 34,934,665 (GRCm39)	V2425I	possibly damaging	Het
Tppp2	A	G	14: 52,158,058 (GRCm39)	K168E	possibly damaging	Het
Ttn	T	A	2: 76,719,812 (GRCm39)	D7099V	unknown	Het
Vmn1r41	A	T	6: 89,724,159 (GRCm39)	R50*	probably null	Het
Vmn1r60	T	C	7: 5,547,861 (GRCm39)	K80E		Het
Vmn2r18	A	G	5: 151,508,485 (GRCm39)	F213S	possibly damaging	Het
Vmn2r26	G	A	6: 124,016,700 (GRCm39)	S388N	probably benign	Het
Vmn2r63	A	T	7: 42,576,391 (GRCm39)	F474Y	probably damaging	Het
Zc3hav1	G	A	6: 38,309,875 (GRCm39)	R316*	probably null	Het
Zfp654	A	T	16: 64,612,211 (GRCm39)	I225N	probably damaging	Het
Zfp97	A	G	17: 17,365,542 (GRCm39)	E347G	probably damaging	Het

Other mutations in Negr1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01284:Negr1	APN	3	156,851,854 (GRCm39)	missense	probably damaging	1.00
IGL01635:Negr1	APN	3	156,267,929 (GRCm39)	missense	probably benign	0.00
IGL02006:Negr1	APN	3	156,721,810 (GRCm39)	splice site	probably benign
IGL02427:Negr1	APN	3	156,267,827 (GRCm39)	start gained	probably benign
IGL02542:Negr1	APN	3	156,267,862 (GRCm39)	missense	probably damaging	1.00
PIT4466001:Negr1	UTSW	3	156,565,235 (GRCm39)	missense	probably benign	0.44
R0241:Negr1	UTSW	3	156,914,036 (GRCm39)	intron	probably benign
R0496:Negr1	UTSW	3	156,721,904 (GRCm39)	missense	probably damaging	1.00
R0506:Negr1	UTSW	3	156,866,385 (GRCm39)	splice site	probably benign
R0507:Negr1	UTSW	3	156,267,862 (GRCm39)	missense	probably damaging	0.97
R0634:Negr1	UTSW	3	156,721,903 (GRCm39)	missense	possibly damaging	0.51
R1324:Negr1	UTSW	3	156,774,860 (GRCm39)	missense	probably damaging	1.00
R1923:Negr1	UTSW	3	156,267,836 (GRCm39)	missense	probably benign	0.06
R4569:Negr1	UTSW	3	156,914,013 (GRCm39)	intron	probably benign
R4592:Negr1	UTSW	3	156,914,023 (GRCm39)	intron	probably benign
R4874:Negr1	UTSW	3	156,565,082 (GRCm39)	missense	probably damaging	0.98
R5137:Negr1	UTSW	3	156,721,833 (GRCm39)	missense	probably damaging	0.99
R5330:Negr1	UTSW	3	156,774,913 (GRCm39)	nonsense	probably null
R5331:Negr1	UTSW	3	156,774,913 (GRCm39)	nonsense	probably null
R5974:Negr1	UTSW	3	156,774,923 (GRCm39)	missense	probably damaging	1.00
R6560:Negr1	UTSW	3	157,018,494 (GRCm39)	missense	probably benign
R7677:Negr1	UTSW	3	156,774,823 (GRCm39)	nonsense	probably null
R8080:Negr1	UTSW	3	156,866,357 (GRCm39)	missense	probably damaging	1.00
R8523:Negr1	UTSW	3	156,866,297 (GRCm39)	missense	probably damaging	1.00
R8950:Negr1	UTSW	3	156,721,906 (GRCm39)	missense	probably damaging	1.00
R8997:Negr1	UTSW	3	156,721,918 (GRCm39)	missense	probably damaging	1.00
R9082:Negr1	UTSW	3	156,774,876 (GRCm39)	nonsense	probably null
R9317:Negr1	UTSW	3	156,904,081 (GRCm39)	missense	probably benign	0.00
R9691:Negr1	UTSW	3	156,267,898 (GRCm39)	missense	probably damaging	0.98
R9715:Negr1	UTSW	3	156,774,936 (GRCm39)	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TGGATAGTAATGTCTGGTAGGAAC -3'
(R):5'- GATCTGCTAAGGCCATGGTAC -3'

Sequencing Primer
(F):5'- GGAACCACTAAGTTTGTTGTTTTCC -3'
(R):5'- CACATATAAACGTGTGTGTGTGTG -3'

Posted On

2019-10-17