Incidental Mutation 'R5832:Slc39a6'
| ID |
449386 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Slc39a6
|
| Ensembl Gene |
ENSMUSG00000024270 |
| Gene Name |
solute carrier family 39 (metal ion transporter), member 6 |
| Synonyms |
Ermelin, Zip6 |
| MMRRC Submission |
044054-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.585)
|
| Stock # |
R5832 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
18 |
| Chromosomal Location |
24712938-24736874 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 24734669 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Leucine
at position 7
(V7L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000120247
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025120]
[ENSMUST00000070726]
[ENSMUST00000152504]
[ENSMUST00000154205]
|
| AlphaFold |
Q8C145 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000025120
|
| SMART Domains |
Protein: ENSMUSP00000025120
Gene: ENSMUSG00000024271
| Domain | Start | End | E-Value | Type |
|---|
|
WD40
|
47 |
91 |
1.06e-3 |
SMART |
|
WD40
|
94 |
143 |
2.24e-2 |
SMART |
|
WD40
|
196 |
237 |
4.69e-5 |
SMART |
|
WD40
|
271 |
319 |
2.44e-3 |
SMART |
|
Blast:WD40
|
329 |
368 |
1e-20 |
BLAST |
|
WD40
|
376 |
415 |
2.12e-3 |
SMART |
|
WD40
|
429 |
467 |
1.71e1 |
SMART |
|
WD40
|
556 |
600 |
7.43e-1 |
SMART |
|
WD40
|
603 |
642 |
1.93e-6 |
SMART |
|
WD40
|
661 |
697 |
1.55e-5 |
SMART |
|
Blast:WD40
|
709 |
753 |
7e-21 |
BLAST |
|
WD40
|
766 |
825 |
1.92e0 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000070726
AA Change: V7L
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000064667
Gene: ENSMUSG00000024270
AA Change: V7L
| 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 |
noncoding transcript
Transcript: ENSMUST00000128106
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000152504
AA Change: V7L
PolyPhen 2
Score 0.805 (Sensitivity: 0.84; Specificity: 0.93)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000154205
|
| SMART Domains |
Protein: ENSMUSP00000122151
Gene: ENSMUSG00000024270
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Zip
|
48 |
433 |
2e-94 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.8%
- 20x: 96.7%
|
| 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: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
| Adgrv1 |
G |
A |
13: 81,251,421 (GRCm39) |
S6232F |
possibly damaging |
Het |
| Alox12 |
T |
C |
11: 70,144,106 (GRCm39) |
E129G |
probably damaging |
Het |
| Anxa13 |
C |
A |
15: 58,205,389 (GRCm39) |
|
noncoding transcript |
Het |
| Arfgef3 |
C |
T |
10: 18,506,168 (GRCm39) |
G878D |
probably damaging |
Het |
| Asnsd1 |
T |
C |
1: 53,386,634 (GRCm39) |
D331G |
probably damaging |
Het |
| Crisp1 |
A |
G |
17: 40,612,208 (GRCm39) |
|
probably null |
Het |
| Eml5 |
T |
C |
12: 98,842,447 (GRCm39) |
N217S |
probably benign |
Het |
| Fat1 |
A |
T |
8: 45,470,460 (GRCm39) |
Y1463F |
possibly damaging |
Het |
| Fhod3 |
T |
C |
18: 25,223,752 (GRCm39) |
W1033R |
probably damaging |
Het |
| Galr2 |
T |
A |
11: 116,172,457 (GRCm39) |
L49Q |
probably damaging |
Het |
| Gstm5 |
T |
C |
3: 107,804,853 (GRCm39) |
V115A |
probably benign |
Het |
| Gtpbp2 |
C |
T |
17: 46,478,788 (GRCm39) |
T535I |
probably damaging |
Het |
| Hk1 |
T |
C |
10: 62,128,144 (GRCm39) |
E326G |
probably benign |
Het |
| Igfn1 |
A |
G |
1: 135,902,533 (GRCm39) |
V388A |
probably damaging |
Het |
| Iqgap2 |
C |
T |
13: 95,811,880 (GRCm39) |
R707H |
probably damaging |
Het |
| Kitl |
C |
A |
10: 99,915,882 (GRCm39) |
P137H |
probably damaging |
Het |
| Lamp3 |
A |
T |
16: 19,520,070 (GRCm39) |
Y38N |
probably damaging |
Het |
| Lmo7 |
A |
T |
14: 102,121,649 (GRCm39) |
N5I |
probably damaging |
Het |
| Mc3r |
T |
A |
2: 172,091,350 (GRCm39) |
C191S |
probably benign |
Het |
| Mep1a |
G |
A |
17: 43,789,055 (GRCm39) |
H574Y |
probably benign |
Het |
| Mybpc3 |
A |
G |
2: 90,949,520 (GRCm39) |
|
probably null |
Het |
| Nav2 |
A |
T |
7: 49,197,817 (GRCm39) |
|
probably null |
Het |
| Patz1 |
C |
T |
11: 3,256,277 (GRCm39) |
P521L |
probably benign |
Het |
| Pramel14 |
A |
G |
4: 143,718,532 (GRCm39) |
S304P |
probably damaging |
Het |
| Prkcd |
T |
C |
14: 30,327,778 (GRCm39) |
T103A |
probably damaging |
Het |
| Pttg1ip |
T |
C |
10: 77,419,859 (GRCm39) |
|
probably null |
Het |
| Rcbtb2 |
C |
A |
14: 73,404,262 (GRCm39) |
Q85K |
possibly damaging |
Het |
| Rdh16f1 |
T |
A |
10: 127,624,618 (GRCm39) |
V152E |
probably damaging |
Het |
| Rsph4a |
A |
G |
10: 33,785,498 (GRCm39) |
I470V |
probably benign |
Het |
| Sarnp |
T |
C |
10: 128,684,181 (GRCm39) |
|
probably null |
Het |
| Slco1a4 |
A |
G |
6: 141,765,270 (GRCm39) |
I324T |
probably benign |
Het |
| Spata31d1a |
A |
T |
13: 59,849,380 (GRCm39) |
V916E |
probably damaging |
Het |
| Srgap1 |
T |
G |
10: 121,676,819 (GRCm39) |
T392P |
probably damaging |
Het |
| Tbc1d20 |
A |
T |
2: 152,153,282 (GRCm39) |
M271L |
possibly damaging |
Het |
| Tbc1d22b |
T |
C |
17: 29,789,621 (GRCm39) |
I161T |
possibly damaging |
Het |
| Tcof1 |
G |
T |
18: 60,952,611 (GRCm39) |
N918K |
unknown |
Het |
| Tnr |
A |
G |
1: 159,713,692 (GRCm39) |
T707A |
probably benign |
Het |
| Trim66 |
A |
G |
7: 109,054,409 (GRCm39) |
F1267S |
probably damaging |
Het |
| Trpm6 |
A |
G |
19: 18,764,183 (GRCm39) |
H263R |
possibly damaging |
Het |
| Tshz2 |
T |
A |
2: 169,725,965 (GRCm39) |
V187D |
possibly damaging |
Het |
| Ube2f |
T |
G |
1: 91,213,046 (GRCm39) |
V176G |
possibly damaging |
Het |
| Vmn2r109 |
C |
T |
17: 20,761,318 (GRCm39) |
A680T |
probably benign |
Het |
| Vmn2r77 |
T |
A |
7: 86,460,670 (GRCm39) |
C665* |
probably null |
Het |
| Zfp954 |
A |
G |
7: 7,118,389 (GRCm39) |
V385A |
probably damaging |
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 |
|
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 |
|
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 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGGAATCATTCTCTCCGTAGCG -3'
(R):5'- TGCATCTGCTTCAGGAGACC -3'
Sequencing Primer
(F):5'- CATTCTCTCCGTAGCGGTAGAATAG -3'
(R):5'- TCTGCTTCAGGAGACCACAAG -3'
|
| Posted On |
2016-12-20 |
Incidental Mutation