Incidental Mutation 'IGL00943:Slc39a6'
| ID |
29426 |
| 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 # |
IGL00943
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
18 |
| Chromosomal Location |
24712938-24736874 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
A to G
at 24722802 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000122151
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000070726]
[ENSMUST00000154205]
|
| AlphaFold |
Q8C145 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000070726
|
| SMART Domains |
Protein: ENSMUSP00000064667
Gene: ENSMUSG00000024270
| 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 |
probably null
Transcript: ENSMUST00000154205
|
| SMART Domains |
Protein: ENSMUSP00000122151
Gene: ENSMUSG00000024270
| 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: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abl1 |
A |
G |
2: 31,680,824 (GRCm39) |
Y372C |
probably damaging |
Het |
| Carmil1 |
C |
T |
13: 24,295,869 (GRCm39) |
V382M |
possibly damaging |
Het |
| Chkb |
A |
T |
15: 89,312,951 (GRCm39) |
V138E |
probably damaging |
Het |
| Col7a1 |
G |
T |
9: 108,806,765 (GRCm39) |
G2434* |
probably null |
Het |
| Cpa3 |
A |
G |
3: 20,282,979 (GRCm39) |
V156A |
possibly damaging |
Het |
| Dicer1 |
A |
C |
12: 104,663,031 (GRCm39) |
S1517A |
possibly damaging |
Het |
| Dnajc14 |
T |
G |
10: 128,652,675 (GRCm39) |
S578A |
possibly damaging |
Het |
| Dse |
A |
G |
10: 34,038,801 (GRCm39) |
Y201H |
probably damaging |
Het |
| Fam114a2 |
A |
T |
11: 57,405,099 (GRCm39) |
M1K |
probably null |
Het |
| Gm4847 |
A |
T |
1: 166,469,922 (GRCm39) |
S50R |
probably benign |
Het |
| Gpr156 |
A |
G |
16: 37,808,938 (GRCm39) |
Y220C |
probably damaging |
Het |
| Grxcr1 |
T |
C |
5: 68,189,638 (GRCm39) |
|
probably benign |
Het |
| Hspg2 |
T |
C |
4: 137,289,512 (GRCm39) |
V3824A |
probably benign |
Het |
| Ino80b |
A |
T |
6: 83,101,129 (GRCm39) |
L116Q |
probably damaging |
Het |
| Inpp5e |
A |
G |
2: 26,290,163 (GRCm39) |
|
probably benign |
Het |
| Lrrc8e |
T |
C |
8: 4,285,658 (GRCm39) |
C628R |
probably damaging |
Het |
| Maml1 |
A |
G |
11: 50,149,541 (GRCm39) |
V733A |
probably damaging |
Het |
| Mcm9 |
A |
G |
10: 53,424,685 (GRCm39) |
L635P |
probably damaging |
Het |
| Myh15 |
A |
T |
16: 48,986,176 (GRCm39) |
I1549F |
probably damaging |
Het |
| Myo1b |
T |
A |
1: 51,823,646 (GRCm39) |
I414F |
probably damaging |
Het |
| Nlrc3 |
T |
A |
16: 3,782,981 (GRCm39) |
I159F |
possibly damaging |
Het |
| Nvl |
A |
T |
1: 180,929,199 (GRCm39) |
D727E |
possibly damaging |
Het |
| Or1l4 |
T |
C |
2: 37,092,183 (GRCm39) |
V310A |
probably benign |
Het |
| Pgs1 |
A |
G |
11: 117,896,366 (GRCm39) |
I348V |
probably benign |
Het |
| Pkp1 |
A |
T |
1: 135,805,922 (GRCm39) |
V592E |
probably damaging |
Het |
| Setd7 |
T |
A |
3: 51,440,459 (GRCm39) |
D194V |
probably damaging |
Het |
| Slc26a7 |
T |
C |
4: 14,506,477 (GRCm39) |
D624G |
probably benign |
Het |
| Sorbs1 |
T |
C |
19: 40,283,484 (GRCm39) |
|
probably benign |
Het |
| Tnfrsf19 |
A |
T |
14: 61,261,631 (GRCm39) |
M56K |
possibly damaging |
Het |
| Togaram2 |
C |
T |
17: 72,031,999 (GRCm39) |
R873C |
probably damaging |
Het |
| Tubgcp6 |
G |
A |
15: 89,006,600 (GRCm39) |
R141* |
probably null |
Het |
| Vill |
A |
G |
9: 118,892,380 (GRCm39) |
E337G |
probably damaging |
Het |
| Vmn1r17 |
A |
G |
6: 57,338,185 (GRCm39) |
L11S |
possibly damaging |
Het |
|
| Other mutations in Slc39a6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
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 |
|
IGL02648:Slc39a6
|
APN |
18 |
24,715,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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 |
2013-04-17 |
Incidental Mutation