Incidental Mutation 'R1899:Nalcn'
ID |
214132 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nalcn
|
Ensembl Gene |
ENSMUSG00000000197 |
Gene Name |
sodium leak channel, non-selective |
Synonyms |
Vgcnl1, A530023G15Rik |
MMRRC Submission |
039919-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1899 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
123514046-123864556 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 123553538 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Lysine
at position 972
(M972K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000000201
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000201]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000000201
AA Change: M972K
PolyPhen 2
Score 0.503 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000000201 Gene: ENSMUSG00000000197 AA Change: M972K
Domain | Start | End | E-Value | Type |
Pfam:Ion_trans
|
35 |
333 |
2.8e-37 |
PFAM |
low complexity region
|
338 |
348 |
N/A |
INTRINSIC |
Pfam:Ion_trans
|
383 |
609 |
5.7e-34 |
PFAM |
coiled coil region
|
796 |
830 |
N/A |
INTRINSIC |
Pfam:Ion_trans
|
885 |
1166 |
2.4e-42 |
PFAM |
Pfam:Ion_trans
|
1209 |
1458 |
6.9e-30 |
PFAM |
low complexity region
|
1548 |
1560 |
N/A |
INTRINSIC |
low complexity region
|
1634 |
1649 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000227818
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000228860
|
Meta Mutation Damage Score |
0.4538 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.6%
- 20x: 93.4%
|
Validation Efficiency |
94% (94/100) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] NALCN forms a voltage-independent, nonselective, noninactivating cation channel permeable to Na+, K+, and Ca(2+). It is responsible for the neuronal background sodium leak conductance (Lu et al., 2007 [PubMed 17448995]).[supplied by OMIM, Mar 2008] PHENOTYPE: Mice homozygous for a null allele exhibit abnormal breathing at birth and die within 24 hours. Mice homozygous for a gain of function ENU mutation exhibit reduced the total amount and episode duration of REMS. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
T |
A |
5: 109,884,664 (GRCm39) |
Q398L |
probably benign |
Het |
4930596D02Rik |
T |
G |
14: 35,532,089 (GRCm39) |
K162T |
probably damaging |
Het |
Abca8b |
G |
T |
11: 109,828,744 (GRCm39) |
T1353K |
possibly damaging |
Het |
Abcg3 |
A |
C |
5: 105,086,065 (GRCm39) |
C565G |
probably damaging |
Het |
Actr3b |
G |
A |
5: 26,034,536 (GRCm39) |
V185I |
possibly damaging |
Het |
Akap6 |
A |
T |
12: 53,188,635 (GRCm39) |
E2016D |
possibly damaging |
Het |
Aldh3b2 |
T |
C |
19: 4,028,662 (GRCm39) |
V148A |
possibly damaging |
Het |
Ankfy1 |
C |
T |
11: 72,645,233 (GRCm39) |
Q771* |
probably null |
Het |
Anks1b |
A |
G |
10: 90,096,618 (GRCm39) |
D425G |
probably damaging |
Het |
Arrb1 |
T |
C |
7: 99,231,504 (GRCm39) |
|
probably benign |
Het |
Atg2a |
C |
A |
19: 6,295,097 (GRCm39) |
T170N |
probably damaging |
Het |
Atp8b5 |
C |
T |
4: 43,361,804 (GRCm39) |
R617C |
possibly damaging |
Het |
Bicra |
T |
C |
7: 15,721,676 (GRCm39) |
T614A |
possibly damaging |
Het |
Cacna1i |
A |
G |
15: 80,275,843 (GRCm39) |
D167G |
possibly damaging |
Het |
Calr4 |
T |
G |
4: 109,103,490 (GRCm39) |
|
probably null |
Het |
Camsap3 |
G |
T |
8: 3,653,922 (GRCm39) |
E515* |
probably null |
Het |
Casp8ap2 |
T |
C |
4: 32,643,647 (GRCm39) |
S907P |
probably damaging |
Het |
Cdk19 |
T |
A |
10: 40,355,776 (GRCm39) |
|
probably benign |
Het |
Chst14 |
A |
G |
2: 118,757,496 (GRCm39) |
M122V |
possibly damaging |
Het |
Cntn4 |
A |
G |
6: 106,652,774 (GRCm39) |
M748V |
probably benign |
Het |
Col7a1 |
A |
G |
9: 108,807,956 (GRCm39) |
D2552G |
unknown |
Het |
Cpeb2 |
C |
A |
5: 43,434,930 (GRCm39) |
P600Q |
probably damaging |
Het |
Cyp2a5 |
C |
T |
7: 26,538,458 (GRCm39) |
R274* |
probably null |
Het |
Dele1 |
T |
C |
18: 38,391,395 (GRCm39) |
W378R |
probably benign |
Het |
Dexi |
A |
G |
16: 10,360,382 (GRCm39) |
F58S |
probably damaging |
Het |
Dlg5 |
C |
A |
14: 24,198,368 (GRCm39) |
G1522W |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,244,286 (GRCm39) |
H1048R |
probably benign |
Het |
Dpp4 |
T |
C |
2: 62,175,394 (GRCm39) |
|
probably benign |
Het |
Dusp10 |
A |
T |
1: 183,801,377 (GRCm39) |
K381N |
possibly damaging |
Het |
Ercc4 |
A |
G |
16: 12,965,651 (GRCm39) |
E761G |
probably damaging |
Het |
Ern2 |
T |
C |
7: 121,783,065 (GRCm39) |
|
probably benign |
Het |
Fam83f |
A |
T |
15: 80,576,281 (GRCm39) |
T311S |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,153,004 (GRCm39) |
D3736G |
probably benign |
Het |
Fgf11 |
G |
T |
11: 69,692,279 (GRCm39) |
T58K |
probably benign |
Het |
Galntl5 |
C |
G |
5: 25,403,530 (GRCm39) |
S167* |
probably null |
Het |
Glg1 |
T |
G |
8: 111,892,306 (GRCm39) |
E846D |
probably benign |
Het |
Grm8 |
C |
A |
6: 28,125,894 (GRCm39) |
E77D |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,533,202 (GRCm39) |
D3028E |
probably damaging |
Het |
Htt |
A |
G |
5: 35,064,429 (GRCm39) |
I2943V |
probably benign |
Het |
Ift80 |
T |
C |
3: 68,825,846 (GRCm39) |
K498R |
probably benign |
Het |
Ipo9 |
A |
T |
1: 135,327,884 (GRCm39) |
M509K |
probably damaging |
Het |
Kcnj3 |
T |
C |
2: 55,327,256 (GRCm39) |
V15A |
probably damaging |
Het |
Kcnn3 |
A |
T |
3: 89,427,762 (GRCm39) |
|
probably benign |
Het |
Larp1b |
T |
A |
3: 40,918,519 (GRCm39) |
D53E |
probably benign |
Het |
Ltf |
T |
C |
9: 110,851,913 (GRCm39) |
F117L |
possibly damaging |
Het |
Maml1 |
A |
G |
11: 50,156,957 (GRCm39) |
L406P |
probably damaging |
Het |
Mnx1 |
G |
A |
5: 29,678,955 (GRCm39) |
A376V |
unknown |
Het |
Mroh2a |
G |
A |
1: 88,163,098 (GRCm39) |
R376H |
probably benign |
Het |
Mrpl4 |
A |
G |
9: 20,918,127 (GRCm39) |
Y111C |
probably damaging |
Het |
Mto1 |
T |
C |
9: 78,368,799 (GRCm39) |
|
probably benign |
Het |
Nemf |
T |
C |
12: 69,393,152 (GRCm39) |
I225V |
probably null |
Het |
Nipal4 |
T |
G |
11: 46,041,058 (GRCm39) |
D379A |
probably damaging |
Het |
Nktr |
A |
G |
9: 121,577,932 (GRCm39) |
|
probably benign |
Het |
Nlrp5 |
A |
G |
7: 23,104,222 (GRCm39) |
T28A |
probably benign |
Het |
Nxph1 |
T |
A |
6: 9,247,622 (GRCm39) |
Y198N |
probably damaging |
Het |
Or4c123 |
T |
C |
2: 89,127,014 (GRCm39) |
N200S |
probably damaging |
Het |
Or5an10 |
T |
C |
19: 12,275,707 (GRCm39) |
Y263C |
probably damaging |
Het |
Or8u10 |
A |
T |
2: 85,916,064 (GRCm39) |
V19D |
probably benign |
Het |
P2rx7 |
A |
G |
5: 122,811,799 (GRCm39) |
Y370C |
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,209,384 (GRCm39) |
|
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,216,305 (GRCm39) |
D1401G |
probably damaging |
Het |
Plxnd1 |
A |
G |
6: 115,946,324 (GRCm39) |
L879P |
probably benign |
Het |
Polr2a |
A |
T |
11: 69,634,772 (GRCm39) |
I636N |
probably damaging |
Het |
Prex2 |
G |
T |
1: 11,232,590 (GRCm39) |
E886* |
probably null |
Het |
Proca1 |
A |
T |
11: 78,095,847 (GRCm39) |
I73F |
probably damaging |
Het |
Prss55 |
A |
T |
14: 64,316,839 (GRCm39) |
V101E |
probably benign |
Het |
Psg26 |
T |
A |
7: 18,212,350 (GRCm39) |
H335L |
probably benign |
Het |
Rai1 |
A |
G |
11: 60,076,746 (GRCm39) |
E270G |
probably benign |
Het |
Reep1 |
A |
G |
6: 71,757,781 (GRCm39) |
N127D |
probably benign |
Het |
Rims1 |
G |
T |
1: 22,498,725 (GRCm39) |
P769Q |
probably damaging |
Het |
Robo4 |
A |
T |
9: 37,315,366 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,606,222 (GRCm39) |
D888E |
probably benign |
Het |
Scamp3 |
A |
G |
3: 89,087,567 (GRCm39) |
N135D |
probably damaging |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Sema4f |
A |
G |
6: 82,895,010 (GRCm39) |
M395T |
probably benign |
Het |
Sgip1 |
T |
C |
4: 102,825,534 (GRCm39) |
|
probably null |
Het |
Sik2 |
A |
T |
9: 50,906,974 (GRCm39) |
|
probably benign |
Het |
Smtn |
G |
T |
11: 3,481,326 (GRCm39) |
A223D |
possibly damaging |
Het |
Spen |
T |
C |
4: 141,197,654 (GRCm39) |
T3405A |
probably benign |
Het |
Srebf1 |
A |
G |
11: 60,094,312 (GRCm39) |
L601P |
probably damaging |
Het |
Srsf11 |
A |
T |
3: 157,737,217 (GRCm39) |
|
probably benign |
Het |
Tacc2 |
T |
G |
7: 130,225,932 (GRCm39) |
S891R |
possibly damaging |
Het |
Tbc1d17 |
T |
A |
7: 44,491,057 (GRCm39) |
|
probably benign |
Het |
Tgfbr3l |
C |
A |
8: 4,299,600 (GRCm39) |
R128S |
probably damaging |
Het |
Thsd1 |
G |
A |
8: 22,742,334 (GRCm39) |
|
probably benign |
Het |
Tlx3 |
T |
C |
11: 33,153,072 (GRCm39) |
S130G |
probably benign |
Het |
Tmem25 |
A |
T |
9: 44,709,513 (GRCm39) |
|
probably null |
Het |
Trak2 |
A |
T |
1: 58,985,495 (GRCm39) |
M1K |
probably null |
Het |
Trappc12 |
C |
T |
12: 28,796,984 (GRCm39) |
E183K |
probably damaging |
Het |
Ubl3 |
A |
G |
5: 148,446,090 (GRCm39) |
V71A |
possibly damaging |
Het |
Unc50 |
A |
G |
1: 37,477,880 (GRCm39) |
Y254C |
probably damaging |
Het |
Unkl |
T |
C |
17: 25,448,434 (GRCm39) |
|
probably null |
Het |
Uso1 |
T |
A |
5: 92,349,051 (GRCm39) |
S819T |
probably benign |
Het |
Yes1 |
A |
T |
5: 32,802,395 (GRCm39) |
R103S |
probably damaging |
Het |
Zfp131 |
A |
G |
13: 120,228,561 (GRCm39) |
V396A |
probably damaging |
Het |
Zfp553 |
T |
C |
7: 126,834,826 (GRCm39) |
I127T |
possibly damaging |
Het |
Zfp599 |
A |
T |
9: 22,162,845 (GRCm39) |
N102K |
probably benign |
Het |
Zmynd10 |
A |
T |
9: 107,427,236 (GRCm39) |
Q288L |
probably benign |
Het |
|
Other mutations in Nalcn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Nalcn
|
APN |
14 |
123,586,201 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00964:Nalcn
|
APN |
14 |
123,532,796 (GRCm39) |
splice site |
probably benign |
|
IGL01310:Nalcn
|
APN |
14 |
123,554,661 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01578:Nalcn
|
APN |
14 |
123,809,503 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01925:Nalcn
|
APN |
14 |
123,529,260 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02072:Nalcn
|
APN |
14 |
123,560,770 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02096:Nalcn
|
APN |
14 |
123,831,915 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02212:Nalcn
|
APN |
14 |
123,752,742 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02306:Nalcn
|
APN |
14 |
123,560,750 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02471:Nalcn
|
APN |
14 |
123,560,726 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02478:Nalcn
|
APN |
14 |
123,558,717 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02551:Nalcn
|
APN |
14 |
123,560,750 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02630:Nalcn
|
APN |
14 |
123,555,291 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02632:Nalcn
|
APN |
14 |
123,555,265 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02661:Nalcn
|
APN |
14 |
123,830,321 (GRCm39) |
splice site |
probably benign |
|
IGL02830:Nalcn
|
APN |
14 |
123,530,881 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02939:Nalcn
|
APN |
14 |
123,536,284 (GRCm39) |
missense |
probably null |
1.00 |
IGL03035:Nalcn
|
APN |
14 |
123,515,630 (GRCm39) |
nonsense |
probably null |
|
IGL03226:Nalcn
|
APN |
14 |
123,518,527 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03242:Nalcn
|
APN |
14 |
123,558,899 (GRCm39) |
missense |
possibly damaging |
0.91 |
Narnia
|
UTSW |
14 |
123,528,459 (GRCm39) |
missense |
probably benign |
0.11 |
R0019:Nalcn
|
UTSW |
14 |
123,744,901 (GRCm39) |
missense |
probably benign |
0.18 |
R0144:Nalcn
|
UTSW |
14 |
123,647,251 (GRCm39) |
splice site |
probably benign |
|
R0144:Nalcn
|
UTSW |
14 |
123,608,948 (GRCm39) |
missense |
probably damaging |
0.96 |
R0359:Nalcn
|
UTSW |
14 |
123,536,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Nalcn
|
UTSW |
14 |
123,744,971 (GRCm39) |
missense |
probably benign |
0.01 |
R0400:Nalcn
|
UTSW |
14 |
123,528,372 (GRCm39) |
splice site |
probably benign |
|
R0467:Nalcn
|
UTSW |
14 |
123,528,459 (GRCm39) |
missense |
probably benign |
0.11 |
R0506:Nalcn
|
UTSW |
14 |
123,834,026 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0583:Nalcn
|
UTSW |
14 |
123,531,755 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0620:Nalcn
|
UTSW |
14 |
123,536,553 (GRCm39) |
splice site |
probably benign |
|
R0624:Nalcn
|
UTSW |
14 |
123,607,444 (GRCm39) |
missense |
probably benign |
|
R0883:Nalcn
|
UTSW |
14 |
123,702,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1381:Nalcn
|
UTSW |
14 |
123,551,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Nalcn
|
UTSW |
14 |
123,702,068 (GRCm39) |
splice site |
probably benign |
|
R1689:Nalcn
|
UTSW |
14 |
123,522,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Nalcn
|
UTSW |
14 |
123,545,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Nalcn
|
UTSW |
14 |
123,515,678 (GRCm39) |
missense |
probably benign |
|
R1854:Nalcn
|
UTSW |
14 |
123,697,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R1869:Nalcn
|
UTSW |
14 |
123,831,965 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1871:Nalcn
|
UTSW |
14 |
123,831,965 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1873:Nalcn
|
UTSW |
14 |
123,521,013 (GRCm39) |
missense |
probably benign |
0.00 |
R1915:Nalcn
|
UTSW |
14 |
123,540,181 (GRCm39) |
missense |
probably benign |
0.08 |
R2016:Nalcn
|
UTSW |
14 |
123,831,993 (GRCm39) |
splice site |
probably null |
|
R2034:Nalcn
|
UTSW |
14 |
123,521,015 (GRCm39) |
missense |
probably benign |
0.01 |
R2087:Nalcn
|
UTSW |
14 |
123,518,557 (GRCm39) |
missense |
probably benign |
|
R2149:Nalcn
|
UTSW |
14 |
123,607,429 (GRCm39) |
missense |
probably benign |
0.01 |
R2157:Nalcn
|
UTSW |
14 |
123,647,164 (GRCm39) |
missense |
probably benign |
0.32 |
R2166:Nalcn
|
UTSW |
14 |
123,607,363 (GRCm39) |
missense |
probably benign |
0.00 |
R2932:Nalcn
|
UTSW |
14 |
123,830,430 (GRCm39) |
missense |
probably benign |
0.06 |
R3408:Nalcn
|
UTSW |
14 |
123,834,029 (GRCm39) |
missense |
probably null |
0.98 |
R3778:Nalcn
|
UTSW |
14 |
123,702,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Nalcn
|
UTSW |
14 |
123,515,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R3835:Nalcn
|
UTSW |
14 |
123,530,834 (GRCm39) |
splice site |
probably benign |
|
R3937:Nalcn
|
UTSW |
14 |
123,607,357 (GRCm39) |
missense |
probably benign |
0.00 |
R4001:Nalcn
|
UTSW |
14 |
123,834,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4015:Nalcn
|
UTSW |
14 |
123,723,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4033:Nalcn
|
UTSW |
14 |
123,837,401 (GRCm39) |
splice site |
probably benign |
|
R4231:Nalcn
|
UTSW |
14 |
123,837,325 (GRCm39) |
missense |
probably benign |
0.01 |
R4464:Nalcn
|
UTSW |
14 |
123,560,762 (GRCm39) |
missense |
probably benign |
|
R4512:Nalcn
|
UTSW |
14 |
123,532,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R4542:Nalcn
|
UTSW |
14 |
123,558,889 (GRCm39) |
synonymous |
silent |
|
R4557:Nalcn
|
UTSW |
14 |
123,558,647 (GRCm39) |
intron |
probably benign |
|
R4869:Nalcn
|
UTSW |
14 |
123,837,296 (GRCm39) |
missense |
probably benign |
0.44 |
R5083:Nalcn
|
UTSW |
14 |
123,560,706 (GRCm39) |
splice site |
probably null |
|
R5109:Nalcn
|
UTSW |
14 |
123,515,650 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5131:Nalcn
|
UTSW |
14 |
123,753,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R5158:Nalcn
|
UTSW |
14 |
123,753,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R5259:Nalcn
|
UTSW |
14 |
123,753,063 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5422:Nalcn
|
UTSW |
14 |
123,752,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R5514:Nalcn
|
UTSW |
14 |
123,521,123 (GRCm39) |
missense |
probably benign |
0.14 |
R5523:Nalcn
|
UTSW |
14 |
123,647,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R5551:Nalcn
|
UTSW |
14 |
123,515,698 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5667:Nalcn
|
UTSW |
14 |
123,532,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Nalcn
|
UTSW |
14 |
123,532,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Nalcn
|
UTSW |
14 |
123,809,450 (GRCm39) |
missense |
probably benign |
|
R5765:Nalcn
|
UTSW |
14 |
123,702,138 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6324:Nalcn
|
UTSW |
14 |
123,647,161 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6523:Nalcn
|
UTSW |
14 |
123,555,255 (GRCm39) |
missense |
probably benign |
0.00 |
R6558:Nalcn
|
UTSW |
14 |
123,723,919 (GRCm39) |
missense |
probably benign |
|
R6631:Nalcn
|
UTSW |
14 |
123,697,663 (GRCm39) |
missense |
probably benign |
0.17 |
R6667:Nalcn
|
UTSW |
14 |
123,558,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6670:Nalcn
|
UTSW |
14 |
123,702,084 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6724:Nalcn
|
UTSW |
14 |
123,535,479 (GRCm39) |
missense |
probably damaging |
0.99 |
R6731:Nalcn
|
UTSW |
14 |
123,837,346 (GRCm39) |
missense |
probably benign |
0.22 |
R6957:Nalcn
|
UTSW |
14 |
123,744,966 (GRCm39) |
missense |
probably damaging |
0.96 |
R6970:Nalcn
|
UTSW |
14 |
123,551,506 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7010:Nalcn
|
UTSW |
14 |
123,530,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R7018:Nalcn
|
UTSW |
14 |
123,647,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7040:Nalcn
|
UTSW |
14 |
123,525,267 (GRCm39) |
missense |
probably benign |
|
R7089:Nalcn
|
UTSW |
14 |
123,515,761 (GRCm39) |
missense |
probably benign |
0.01 |
R7128:Nalcn
|
UTSW |
14 |
123,831,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R7149:Nalcn
|
UTSW |
14 |
123,837,277 (GRCm39) |
missense |
probably benign |
0.02 |
R7361:Nalcn
|
UTSW |
14 |
123,529,251 (GRCm39) |
missense |
probably benign |
0.00 |
R7378:Nalcn
|
UTSW |
14 |
123,540,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7408:Nalcn
|
UTSW |
14 |
123,529,272 (GRCm39) |
missense |
probably benign |
0.00 |
R7470:Nalcn
|
UTSW |
14 |
123,809,456 (GRCm39) |
missense |
probably benign |
0.09 |
R7483:Nalcn
|
UTSW |
14 |
123,551,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R7521:Nalcn
|
UTSW |
14 |
123,530,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Nalcn
|
UTSW |
14 |
123,723,797 (GRCm39) |
critical splice donor site |
probably null |
|
R7585:Nalcn
|
UTSW |
14 |
123,753,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R7591:Nalcn
|
UTSW |
14 |
123,561,297 (GRCm39) |
missense |
probably benign |
0.01 |
R7761:Nalcn
|
UTSW |
14 |
123,531,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R7761:Nalcn
|
UTSW |
14 |
123,531,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Nalcn
|
UTSW |
14 |
123,536,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R7983:Nalcn
|
UTSW |
14 |
123,830,409 (GRCm39) |
missense |
probably benign |
0.17 |
R8089:Nalcn
|
UTSW |
14 |
123,537,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Nalcn
|
UTSW |
14 |
123,702,113 (GRCm39) |
missense |
probably benign |
0.00 |
R8190:Nalcn
|
UTSW |
14 |
123,837,351 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8273:Nalcn
|
UTSW |
14 |
123,554,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Nalcn
|
UTSW |
14 |
123,554,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8497:Nalcn
|
UTSW |
14 |
123,752,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R8544:Nalcn
|
UTSW |
14 |
123,608,935 (GRCm39) |
missense |
probably benign |
0.40 |
R8549:Nalcn
|
UTSW |
14 |
123,607,448 (GRCm39) |
missense |
probably benign |
0.01 |
R8731:Nalcn
|
UTSW |
14 |
123,837,266 (GRCm39) |
missense |
probably benign |
0.01 |
R8862:Nalcn
|
UTSW |
14 |
123,647,199 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8919:Nalcn
|
UTSW |
14 |
123,561,284 (GRCm39) |
missense |
probably benign |
0.00 |
R9072:Nalcn
|
UTSW |
14 |
123,532,863 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9073:Nalcn
|
UTSW |
14 |
123,532,863 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9182:Nalcn
|
UTSW |
14 |
123,834,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R9193:Nalcn
|
UTSW |
14 |
123,545,792 (GRCm39) |
nonsense |
probably null |
|
R9241:Nalcn
|
UTSW |
14 |
123,809,429 (GRCm39) |
missense |
probably benign |
0.00 |
R9267:Nalcn
|
UTSW |
14 |
123,518,567 (GRCm39) |
missense |
probably benign |
0.08 |
R9274:Nalcn
|
UTSW |
14 |
123,753,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R9277:Nalcn
|
UTSW |
14 |
123,518,523 (GRCm39) |
missense |
probably damaging |
0.98 |
R9376:Nalcn
|
UTSW |
14 |
123,515,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
X0060:Nalcn
|
UTSW |
14 |
123,522,653 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nalcn
|
UTSW |
14 |
123,831,980 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nalcn
|
UTSW |
14 |
123,531,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GATTGTCTCAAACATGAAGCAGGTG -3'
(R):5'- CCAACTCTCTGCAGGCATAG -3'
Sequencing Primer
(F):5'- TGGGTGGCAGCTTCACGTAC -3'
(R):5'- CTCTCTGCAGGCATAGAATATACTC -3'
|
Posted On |
2014-07-14 |