Incidental Mutation 'R6292:Ntng1'
| ID |
508488 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ntng1
|
| Ensembl Gene |
ENSMUSG00000059857 |
| Gene Name |
netrin G1 |
| Synonyms |
Lmnt1, A930010C08Rik |
| MMRRC Submission |
044461-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R6292 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
109687356-110051327 bp(-) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
T to C
at 110051202 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000119534
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000051253]
[ENSMUST00000128219]
[ENSMUST00000133268]
[ENSMUST00000156177]
|
| AlphaFold |
Q8R4G0 |
| Predicted Effect |
silent
Transcript: ENSMUST00000051253
|
| SMART Domains |
Protein: ENSMUSP00000052268
Gene: ENSMUSG00000059857
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
24 |
37 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000128219
|
| SMART Domains |
Protein: ENSMUSP00000116579
Gene: ENSMUSG00000059857
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
LamNT
|
59 |
295 |
1.5e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000133268
|
| SMART Domains |
Protein: ENSMUSP00000117371
Gene: ENSMUSG00000059857
| Domain | Start | End | E-Value | Type |
|---|
|
LamNT
|
59 |
295 |
3.22e-18 |
SMART |
|
EGF_Lam
|
297 |
354 |
6.86e-4 |
SMART |
|
EGF
|
365 |
397 |
5.12e-3 |
SMART |
|
low complexity region
|
421 |
436 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000156177
|
| SMART Domains |
Protein: ENSMUSP00000119534
Gene: ENSMUSG00000059857
| Domain | Start | End | E-Value | Type |
|---|
|
LamNT
|
59 |
295 |
3.22e-18 |
SMART |
|
EGF_Lam
|
297 |
354 |
6.86e-4 |
SMART |
|
EGF
|
387 |
419 |
5.12e-3 |
SMART |
|
low complexity region
|
443 |
458 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.2%
- 20x: 94.5%
|
| Validation Efficiency |
100% (50/50) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a preproprotein that is processed into a secreted protein containing eukaroytic growth factor (EGF)-like domains. This protein acts to guide axon growth during neuronal development. Polymorphisms in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for a null allele survive into adulthood with no major alterations in gross brain cytoarchitecture or axonal projection. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acacb |
T |
A |
5: 114,338,312 (GRCm39) |
V709E |
probably damaging |
Het |
| Ankrd33b |
C |
T |
15: 31,325,231 (GRCm39) |
|
probably null |
Het |
| Apaf1 |
T |
C |
10: 90,827,425 (GRCm39) |
T1202A |
possibly damaging |
Het |
| Apip |
G |
T |
2: 102,922,812 (GRCm39) |
C210F |
probably benign |
Het |
| Chd9 |
A |
T |
8: 91,659,550 (GRCm39) |
H170L |
probably benign |
Het |
| Clec16a |
T |
C |
16: 10,378,015 (GRCm39) |
|
probably null |
Het |
| Ep300 |
T |
A |
15: 81,500,935 (GRCm39) |
|
probably benign |
Het |
| Etl4 |
C |
T |
2: 20,748,384 (GRCm39) |
H39Y |
probably damaging |
Het |
| Gdap1l1 |
A |
T |
2: 163,293,427 (GRCm39) |
I218F |
probably damaging |
Het |
| Gm5141 |
A |
T |
13: 62,922,252 (GRCm39) |
C306S |
probably damaging |
Het |
| Gm9961 |
C |
T |
16: 11,748,336 (GRCm39) |
|
noncoding transcript |
Het |
| Gpr27 |
C |
T |
6: 99,670,619 (GRCm39) |
S327L |
possibly damaging |
Het |
| Hectd3 |
A |
C |
4: 116,856,005 (GRCm39) |
T435P |
probably damaging |
Het |
| Hs3st1 |
T |
A |
5: 39,772,133 (GRCm39) |
Q170L |
possibly damaging |
Het |
| Hykk |
T |
C |
9: 54,828,110 (GRCm39) |
|
probably null |
Het |
| Lilra5 |
T |
C |
7: 4,241,338 (GRCm39) |
S92P |
possibly damaging |
Het |
| Lrig1 |
A |
T |
6: 94,593,426 (GRCm39) |
N418K |
probably damaging |
Het |
| Miga1 |
A |
G |
3: 152,023,356 (GRCm39) |
F232L |
probably benign |
Het |
| Mkrn2 |
T |
A |
6: 115,590,295 (GRCm39) |
M217K |
probably damaging |
Het |
| Myh7b |
A |
T |
2: 155,474,316 (GRCm39) |
Q1677L |
probably damaging |
Het |
| N4bp1 |
T |
C |
8: 87,579,867 (GRCm39) |
E645G |
probably damaging |
Het |
| Nckap5 |
T |
C |
1: 125,842,752 (GRCm39) |
K1752E |
probably damaging |
Het |
| Nek1 |
A |
G |
8: 61,507,770 (GRCm39) |
|
probably null |
Het |
| Nup133 |
A |
G |
8: 124,644,176 (GRCm39) |
V730A |
probably benign |
Het |
| Or2t44 |
T |
A |
11: 58,677,063 (GRCm39) |
M1K |
probably null |
Het |
| Or51v14 |
T |
A |
7: 103,261,386 (GRCm39) |
H58L |
probably damaging |
Het |
| Paqr6 |
C |
T |
3: 88,275,205 (GRCm39) |
P213S |
probably damaging |
Het |
| Pign |
A |
T |
1: 105,512,802 (GRCm39) |
V627D |
possibly damaging |
Het |
| Rasal1 |
T |
A |
5: 120,797,685 (GRCm39) |
V139E |
probably damaging |
Het |
| Scgb1b24 |
G |
T |
7: 33,443,577 (GRCm39) |
A79S |
possibly damaging |
Het |
| Slc25a28 |
T |
C |
19: 43,653,031 (GRCm39) |
D210G |
probably benign |
Het |
| Slc38a3 |
A |
T |
9: 107,532,353 (GRCm39) |
I393N |
possibly damaging |
Het |
| Slc41a2 |
T |
C |
10: 83,090,790 (GRCm39) |
N465D |
probably damaging |
Het |
| Slc5a5 |
G |
A |
8: 71,343,822 (GRCm39) |
T160I |
probably damaging |
Het |
| Smarca2 |
C |
T |
19: 26,608,292 (GRCm39) |
A117V |
probably damaging |
Het |
| Sorcs2 |
C |
T |
5: 36,219,931 (GRCm39) |
R371H |
probably damaging |
Het |
| Taf4 |
A |
G |
2: 179,565,780 (GRCm39) |
S872P |
probably damaging |
Het |
| Tdrd3 |
G |
T |
14: 87,743,690 (GRCm39) |
C540F |
probably benign |
Het |
| Thumpd1 |
A |
T |
7: 119,319,897 (GRCm39) |
L23Q |
probably benign |
Het |
| Top1 |
A |
T |
2: 160,540,061 (GRCm39) |
Y213F |
probably benign |
Het |
| Txndc5 |
T |
C |
13: 38,712,160 (GRCm39) |
|
probably null |
Het |
| Unc79 |
C |
A |
12: 103,108,991 (GRCm39) |
A2005D |
possibly damaging |
Het |
| Upb1 |
T |
C |
10: 75,274,005 (GRCm39) |
L344P |
probably damaging |
Het |
| Vmn1r72 |
T |
A |
7: 11,403,579 (GRCm39) |
S290C |
probably benign |
Het |
| Vmn2r103 |
A |
G |
17: 20,013,866 (GRCm39) |
I219M |
possibly damaging |
Het |
| Wapl |
A |
G |
14: 34,451,152 (GRCm39) |
T729A |
probably damaging |
Het |
| Washc5 |
C |
T |
15: 59,227,783 (GRCm39) |
R393H |
probably damaging |
Het |
|
| Other mutations in Ntng1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02162:Ntng1
|
APN |
3 |
109,842,311 (GRCm39) |
nonsense |
probably null |
|
|
IGL02367:Ntng1
|
APN |
3 |
110,042,829 (GRCm39) |
splice site |
probably null |
|
|
IGL02448:Ntng1
|
APN |
3 |
109,841,875 (GRCm39) |
splice site |
probably benign |
|
|
IGL02487:Ntng1
|
APN |
3 |
109,842,363 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02500:Ntng1
|
APN |
3 |
110,042,646 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02578:Ntng1
|
APN |
3 |
110,042,710 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03009:Ntng1
|
APN |
3 |
109,842,018 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL03096:Ntng1
|
APN |
3 |
110,042,665 (GRCm39) |
missense |
probably benign |
0.19 |
|
R0108:Ntng1
|
UTSW |
3 |
109,759,071 (GRCm39) |
splice site |
probably benign |
|
|
R0326:Ntng1
|
UTSW |
3 |
110,042,819 (GRCm39) |
nonsense |
probably null |
|
|
R0403:Ntng1
|
UTSW |
3 |
109,841,927 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0699:Ntng1
|
UTSW |
3 |
109,779,611 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0702:Ntng1
|
UTSW |
3 |
109,779,570 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1981:Ntng1
|
UTSW |
3 |
109,842,326 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R2096:Ntng1
|
UTSW |
3 |
109,739,871 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3739:Ntng1
|
UTSW |
3 |
109,842,007 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3963:Ntng1
|
UTSW |
3 |
109,842,184 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4484:Ntng1
|
UTSW |
3 |
110,051,124 (GRCm39) |
unclassified |
probably benign |
|
|
R4516:Ntng1
|
UTSW |
3 |
109,842,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4518:Ntng1
|
UTSW |
3 |
109,842,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4520:Ntng1
|
UTSW |
3 |
109,842,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4523:Ntng1
|
UTSW |
3 |
109,842,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4524:Ntng1
|
UTSW |
3 |
109,842,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4776:Ntng1
|
UTSW |
3 |
109,842,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4817:Ntng1
|
UTSW |
3 |
109,842,184 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4827:Ntng1
|
UTSW |
3 |
110,042,727 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4990:Ntng1
|
UTSW |
3 |
110,042,577 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5067:Ntng1
|
UTSW |
3 |
110,042,661 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5087:Ntng1
|
UTSW |
3 |
110,042,645 (GRCm39) |
nonsense |
probably null |
|
|
R5196:Ntng1
|
UTSW |
3 |
109,842,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5263:Ntng1
|
UTSW |
3 |
109,842,188 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5743:Ntng1
|
UTSW |
3 |
110,042,736 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6268:Ntng1
|
UTSW |
3 |
109,842,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6419:Ntng1
|
UTSW |
3 |
109,690,169 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6898:Ntng1
|
UTSW |
3 |
109,779,534 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7081:Ntng1
|
UTSW |
3 |
109,759,105 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7090:Ntng1
|
UTSW |
3 |
109,842,496 (GRCm39) |
nonsense |
probably null |
|
|
R7134:Ntng1
|
UTSW |
3 |
109,842,445 (GRCm39) |
missense |
probably benign |
|
|
R7302:Ntng1
|
UTSW |
3 |
109,739,933 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7353:Ntng1
|
UTSW |
3 |
110,042,763 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7408:Ntng1
|
UTSW |
3 |
109,760,398 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7610:Ntng1
|
UTSW |
3 |
109,842,141 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7686:Ntng1
|
UTSW |
3 |
109,842,330 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7972:Ntng1
|
UTSW |
3 |
110,042,802 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9210:Ntng1
|
UTSW |
3 |
109,779,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9214:Ntng1
|
UTSW |
3 |
109,841,921 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9266:Ntng1
|
UTSW |
3 |
110,051,162 (GRCm39) |
missense |
unknown |
|
|
R9266:Ntng1
|
UTSW |
3 |
110,050,923 (GRCm39) |
unclassified |
probably benign |
|
|
R9364:Ntng1
|
UTSW |
3 |
110,042,680 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9593:Ntng1
|
UTSW |
3 |
109,842,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9596:Ntng1
|
UTSW |
3 |
110,042,956 (GRCm39) |
start gained |
probably benign |
|
|
| Predicted Primers |
|
| Posted On |
2018-03-15 |
Incidental Mutation