Incidental Mutation 'IGL02648:Slc39a6'
ID |
302020 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Slc39a6
|
Ensembl Gene |
ENSMUSG00000024270 |
Gene Name |
solute carrier family 39 (metal ion transporter), member 6 |
Synonyms |
Ermelin, Zip6 |
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.641)
|
Stock # |
IGL02648
|
Quality Score |
|
Status
|
|
Chromosome |
18 |
Chromosomal Location |
24712938-24736874 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 24715424 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Valine
at position 699
(I699V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000064667
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000070726]
[ENSMUST00000154205]
|
AlphaFold |
Q8C145 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000070726
AA Change: I699V
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000064667 Gene: ENSMUSG00000024270 AA Change: I699V
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
low complexity region
|
94 |
141 |
N/A |
INTRINSIC |
low complexity region
|
187 |
198 |
N/A |
INTRINSIC |
Pfam:Zip
|
332 |
753 |
3e-104 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000154205
AA Change: I415V
PolyPhen 2
Score 0.778 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000122151 Gene: ENSMUSG00000024270 AA Change: I415V
Domain | Start | End | E-Value | Type |
Pfam:Zip
|
48 |
433 |
2e-94 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A6 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008] PHENOTYPE: Mice homozygous for a null allele do not display any gross skin abnormalities. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
A |
T |
4: 144,344,392 (GRCm39) |
|
probably null |
Het |
Acp4 |
A |
G |
7: 43,904,414 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,659,738 (GRCm39) |
M1997K |
probably benign |
Het |
Arhgdib |
T |
C |
6: 136,910,647 (GRCm39) |
D38G |
probably damaging |
Het |
Bbox1 |
T |
G |
2: 110,135,871 (GRCm39) |
D36A |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,734,457 (GRCm39) |
K104R |
probably damaging |
Het |
Cacna1i |
G |
A |
15: 80,182,839 (GRCm39) |
C75Y |
probably damaging |
Het |
Ccdc14 |
T |
C |
16: 34,517,528 (GRCm39) |
L70S |
probably damaging |
Het |
Ccdc88a |
T |
G |
11: 29,451,051 (GRCm39) |
V1580G |
probably benign |
Het |
Cdadc1 |
C |
A |
14: 59,823,812 (GRCm39) |
D227Y |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,242,976 (GRCm39) |
Y1415C |
probably damaging |
Het |
Cngb3 |
A |
G |
4: 19,428,489 (GRCm39) |
N493S |
probably benign |
Het |
Dock10 |
T |
A |
1: 80,551,840 (GRCm39) |
Y665F |
probably damaging |
Het |
Gm10549 |
C |
A |
18: 33,597,303 (GRCm39) |
|
probably benign |
Het |
Greb1 |
C |
T |
12: 16,758,683 (GRCm39) |
V678M |
probably damaging |
Het |
Gucy2c |
G |
A |
6: 136,706,211 (GRCm39) |
R497* |
probably null |
Het |
Itgad |
T |
C |
7: 127,782,546 (GRCm39) |
|
probably benign |
Het |
Lgr4 |
C |
A |
2: 109,842,718 (GRCm39) |
T877K |
probably damaging |
Het |
Lrig3 |
A |
G |
10: 125,802,463 (GRCm39) |
D40G |
probably benign |
Het |
Myo3b |
T |
C |
2: 69,935,716 (GRCm39) |
|
probably benign |
Het |
Neb |
A |
G |
2: 52,161,093 (GRCm39) |
Y2193H |
possibly damaging |
Het |
Or4b1 |
T |
A |
2: 89,979,697 (GRCm39) |
I218F |
possibly damaging |
Het |
Or8b3b |
T |
C |
9: 38,584,312 (GRCm39) |
M143V |
probably benign |
Het |
Pard6b |
A |
G |
2: 167,940,847 (GRCm39) |
Q278R |
probably benign |
Het |
Pate10 |
A |
T |
9: 35,652,405 (GRCm39) |
M21L |
probably benign |
Het |
Pkd2l1 |
T |
C |
19: 44,143,975 (GRCm39) |
Y366C |
possibly damaging |
Het |
Prl2c1 |
A |
G |
13: 28,041,542 (GRCm39) |
D188G |
probably benign |
Het |
Prl3a1 |
G |
T |
13: 27,454,218 (GRCm39) |
M65I |
probably benign |
Het |
Psg26 |
T |
A |
7: 18,216,691 (GRCm39) |
E49D |
probably benign |
Het |
Rapgef3 |
G |
A |
15: 97,656,273 (GRCm39) |
R38W |
probably damaging |
Het |
Rrn3 |
T |
C |
16: 13,629,453 (GRCm39) |
F590L |
probably benign |
Het |
Serpina12 |
T |
C |
12: 104,004,267 (GRCm39) |
K122E |
probably benign |
Het |
Tmem259 |
G |
A |
10: 79,813,651 (GRCm39) |
P443S |
probably damaging |
Het |
Vmn1r75 |
T |
A |
7: 11,615,091 (GRCm39) |
F274L |
probably benign |
Het |
|
Other mutations in Slc39a6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00943:Slc39a6
|
APN |
18 |
24,722,802 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01412:Slc39a6
|
APN |
18 |
24,718,413 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02182:Slc39a6
|
APN |
18 |
24,734,347 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02332:Slc39a6
|
APN |
18 |
24,722,880 (GRCm39) |
missense |
probably benign |
0.22 |
Lobar
|
UTSW |
18 |
24,729,386 (GRCm39) |
nonsense |
probably null |
|
R0066:Slc39a6
|
UTSW |
18 |
24,732,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Slc39a6
|
UTSW |
18 |
24,732,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Slc39a6
|
UTSW |
18 |
24,734,527 (GRCm39) |
missense |
probably benign |
0.00 |
R1128:Slc39a6
|
UTSW |
18 |
24,718,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R1621:Slc39a6
|
UTSW |
18 |
24,733,946 (GRCm39) |
missense |
probably benign |
0.08 |
R1799:Slc39a6
|
UTSW |
18 |
24,718,524 (GRCm39) |
missense |
probably benign |
0.00 |
R1800:Slc39a6
|
UTSW |
18 |
24,718,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:Slc39a6
|
UTSW |
18 |
24,734,539 (GRCm39) |
splice site |
probably null |
|
R4159:Slc39a6
|
UTSW |
18 |
24,730,885 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4809:Slc39a6
|
UTSW |
18 |
24,718,531 (GRCm39) |
nonsense |
probably null |
|
R4903:Slc39a6
|
UTSW |
18 |
24,730,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R4994:Slc39a6
|
UTSW |
18 |
24,729,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Slc39a6
|
UTSW |
18 |
24,734,093 (GRCm39) |
missense |
probably benign |
0.00 |
R5398:Slc39a6
|
UTSW |
18 |
24,730,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R5832:Slc39a6
|
UTSW |
18 |
24,734,669 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6182:Slc39a6
|
UTSW |
18 |
24,734,013 (GRCm39) |
missense |
probably benign |
0.16 |
R6853:Slc39a6
|
UTSW |
18 |
24,732,376 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7226:Slc39a6
|
UTSW |
18 |
24,717,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R7252:Slc39a6
|
UTSW |
18 |
24,734,442 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7263:Slc39a6
|
UTSW |
18 |
24,734,260 (GRCm39) |
missense |
probably benign |
|
R7328:Slc39a6
|
UTSW |
18 |
24,733,987 (GRCm39) |
missense |
probably benign |
0.00 |
R7388:Slc39a6
|
UTSW |
18 |
24,717,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Slc39a6
|
UTSW |
18 |
24,718,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R8393:Slc39a6
|
UTSW |
18 |
24,732,331 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8695:Slc39a6
|
UTSW |
18 |
24,736,811 (GRCm39) |
unclassified |
probably benign |
|
R8889:Slc39a6
|
UTSW |
18 |
24,729,386 (GRCm39) |
nonsense |
probably null |
|
R8892:Slc39a6
|
UTSW |
18 |
24,729,386 (GRCm39) |
nonsense |
probably null |
|
R9172:Slc39a6
|
UTSW |
18 |
24,715,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R9178:Slc39a6
|
UTSW |
18 |
24,733,970 (GRCm39) |
missense |
probably damaging |
0.99 |
R9215:Slc39a6
|
UTSW |
18 |
24,732,323 (GRCm39) |
missense |
probably benign |
0.04 |
R9349:Slc39a6
|
UTSW |
18 |
24,718,493 (GRCm39) |
missense |
probably benign |
|
X0065:Slc39a6
|
UTSW |
18 |
24,718,432 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Slc39a6
|
UTSW |
18 |
24,718,372 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-04-16 |