Incidental Mutation 'IGL03263:Marchf6'
| ID |
414949 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Marchf6
|
| Ensembl Gene |
ENSMUSG00000039100 |
| Gene Name |
membrane associated ring-CH-type finger 6 |
| Synonyms |
March6, F830029L24Rik |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.374)
|
| Stock # |
IGL03263
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
15 |
| Chromosomal Location |
31456045-31531172 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 31486508 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 349
(I349T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000087694
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090227]
|
| AlphaFold |
Q6ZQ89 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090227
AA Change: I349T
PolyPhen 2
Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000087694
Gene: ENSMUSG00000039100
AA Change: I349T
| Domain | Start | End | E-Value | Type |
|---|
|
RINGv
|
8 |
56 |
1.13e-21 |
SMART |
|
transmembrane domain
|
92 |
114 |
N/A |
INTRINSIC |
|
transmembrane domain
|
141 |
163 |
N/A |
INTRINSIC |
|
low complexity region
|
223 |
259 |
N/A |
INTRINSIC |
|
transmembrane domain
|
290 |
312 |
N/A |
INTRINSIC |
|
transmembrane domain
|
332 |
354 |
N/A |
INTRINSIC |
|
transmembrane domain
|
367 |
389 |
N/A |
INTRINSIC |
|
transmembrane domain
|
420 |
442 |
N/A |
INTRINSIC |
|
transmembrane domain
|
480 |
502 |
N/A |
INTRINSIC |
|
transmembrane domain
|
522 |
540 |
N/A |
INTRINSIC |
|
low complexity region
|
574 |
599 |
N/A |
INTRINSIC |
|
transmembrane domain
|
633 |
655 |
N/A |
INTRINSIC |
|
transmembrane domain
|
675 |
697 |
N/A |
INTRINSIC |
|
transmembrane domain
|
720 |
742 |
N/A |
INTRINSIC |
|
transmembrane domain
|
762 |
784 |
N/A |
INTRINSIC |
|
transmembrane domain
|
805 |
827 |
N/A |
INTRINSIC |
|
transmembrane domain
|
847 |
866 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000227757
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of a family of membrane-associated E3 ubiquitin ligases containing RING-CH-type zinc finger motifs. Ubiquitination of type II deiodinase by the encoded protein is an important regulatory step in thyroid hormone signalling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 48 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700123K08Rik |
T |
A |
5: 138,562,499 (GRCm39) |
I81F |
probably damaging |
Het |
| Acacb |
C |
T |
5: 114,351,754 (GRCm39) |
H1164Y |
probably damaging |
Het |
| Adamts5 |
A |
T |
16: 85,666,830 (GRCm39) |
V554E |
probably damaging |
Het |
| Asns |
G |
A |
6: 7,689,404 (GRCm39) |
R33C |
probably benign |
Het |
| BC051076 |
T |
G |
5: 88,111,977 (GRCm39) |
|
noncoding transcript |
Het |
| Bcas3 |
C |
T |
11: 85,712,948 (GRCm39) |
|
probably benign |
Het |
| Bpifb1 |
A |
G |
2: 154,057,226 (GRCm39) |
M395V |
probably benign |
Het |
| Cdcp1 |
C |
A |
9: 123,009,152 (GRCm39) |
V509L |
probably benign |
Het |
| Cdhr2 |
A |
G |
13: 54,865,926 (GRCm39) |
T277A |
possibly damaging |
Het |
| Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
| Clca4a |
T |
A |
3: 144,672,192 (GRCm39) |
E250V |
probably damaging |
Het |
| Cplx4 |
T |
C |
18: 66,100,559 (GRCm39) |
D79G |
probably benign |
Het |
| Dcaf11 |
A |
G |
14: 55,802,949 (GRCm39) |
D246G |
probably damaging |
Het |
| Dnah2 |
A |
T |
11: 69,420,207 (GRCm39) |
|
probably null |
Het |
| Dock3 |
A |
T |
9: 106,807,330 (GRCm39) |
|
probably benign |
Het |
| Fam170a |
T |
C |
18: 50,413,588 (GRCm39) |
|
probably benign |
Het |
| Fgfr2 |
T |
A |
7: 129,782,149 (GRCm39) |
M423L |
probably benign |
Het |
| Gabra2 |
A |
G |
5: 71,130,836 (GRCm39) |
F331L |
probably damaging |
Het |
| Galnt18 |
C |
T |
7: 111,119,321 (GRCm39) |
R400Q |
probably damaging |
Het |
| H2-M11 |
A |
T |
17: 36,859,805 (GRCm39) |
Q266L |
probably damaging |
Het |
| Igf2bp1 |
A |
T |
11: 95,857,499 (GRCm39) |
V502D |
probably damaging |
Het |
| Ik |
A |
G |
18: 36,881,699 (GRCm39) |
N111S |
probably damaging |
Het |
| Intu |
T |
A |
3: 40,627,027 (GRCm39) |
Y269* |
probably null |
Het |
| Krt82 |
T |
C |
15: 101,450,307 (GRCm39) |
Y463C |
probably benign |
Het |
| Lrig1 |
A |
G |
6: 94,588,628 (GRCm39) |
M507T |
probably benign |
Het |
| Lrrc37 |
A |
G |
11: 103,504,525 (GRCm39) |
V2481A |
possibly damaging |
Het |
| Mag |
T |
G |
7: 30,598,953 (GRCm39) |
|
probably null |
Het |
| Map7 |
T |
A |
10: 20,121,068 (GRCm39) |
Y121* |
probably null |
Het |
| Mas1 |
A |
G |
17: 13,060,451 (GRCm39) |
V324A |
possibly damaging |
Het |
| Nckap1l |
T |
C |
15: 103,372,832 (GRCm39) |
W259R |
probably damaging |
Het |
| Nhsl1 |
T |
A |
10: 18,373,827 (GRCm39) |
Y164* |
probably null |
Het |
| Or52e5 |
T |
A |
7: 104,719,209 (GRCm39) |
H178Q |
probably damaging |
Het |
| Or8b38 |
A |
T |
9: 37,973,009 (GRCm39) |
Y131F |
probably damaging |
Het |
| Pcdhb2 |
A |
G |
18: 37,429,059 (GRCm39) |
D344G |
probably damaging |
Het |
| Pclo |
T |
C |
5: 14,731,824 (GRCm39) |
V3442A |
unknown |
Het |
| Polr3c |
C |
T |
3: 96,621,567 (GRCm39) |
|
probably benign |
Het |
| Ppp2r2d |
C |
T |
7: 138,474,651 (GRCm39) |
R11* |
probably null |
Het |
| Ptgfr |
T |
A |
3: 151,541,500 (GRCm39) |
M3L |
probably benign |
Het |
| Rfx6 |
A |
G |
10: 51,601,903 (GRCm39) |
S741G |
probably benign |
Het |
| Rif1 |
T |
C |
2: 51,980,273 (GRCm39) |
V490A |
probably damaging |
Het |
| Samd7 |
T |
A |
3: 30,816,302 (GRCm39) |
H349Q |
probably damaging |
Het |
| Sh3pxd2a |
T |
C |
19: 47,302,482 (GRCm39) |
N199S |
probably damaging |
Het |
| Spef2 |
T |
A |
15: 9,667,305 (GRCm39) |
K794N |
possibly damaging |
Het |
| Spta1 |
C |
T |
1: 174,041,484 (GRCm39) |
A1316V |
probably damaging |
Het |
| Vwa7 |
A |
G |
17: 35,240,575 (GRCm39) |
E410G |
probably benign |
Het |
| Washc2 |
T |
A |
6: 116,215,084 (GRCm39) |
|
probably benign |
Het |
| Wdr72 |
A |
C |
9: 74,064,711 (GRCm39) |
Y581S |
probably damaging |
Het |
| Zdhhc17 |
T |
C |
10: 110,796,877 (GRCm39) |
D298G |
probably damaging |
Het |
|
| Other mutations in Marchf6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00479:Marchf6
|
APN |
15 |
31,475,909 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00902:Marchf6
|
APN |
15 |
31,485,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02352:Marchf6
|
APN |
15 |
31,509,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02359:Marchf6
|
APN |
15 |
31,509,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02565:Marchf6
|
APN |
15 |
31,490,712 (GRCm39) |
splice site |
probably benign |
|
|
IGL02735:Marchf6
|
APN |
15 |
31,486,266 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02808:Marchf6
|
APN |
15 |
31,478,552 (GRCm39) |
missense |
probably benign |
0.32 |
|
IGL03122:Marchf6
|
APN |
15 |
31,478,439 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03235:Marchf6
|
APN |
15 |
31,486,141 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03238:Marchf6
|
APN |
15 |
31,462,087 (GRCm39) |
critical splice donor site |
probably benign |
|
|
ideation
|
UTSW |
15 |
31,482,650 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0003:Marchf6
|
UTSW |
15 |
31,469,678 (GRCm39) |
splice site |
probably benign |
|
|
R0056:Marchf6
|
UTSW |
15 |
31,467,880 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R0115:Marchf6
|
UTSW |
15 |
31,475,958 (GRCm39) |
missense |
probably benign |
|
|
R0126:Marchf6
|
UTSW |
15 |
31,462,151 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0148:Marchf6
|
UTSW |
15 |
31,490,758 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0744:Marchf6
|
UTSW |
15 |
31,480,437 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0833:Marchf6
|
UTSW |
15 |
31,480,437 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1205:Marchf6
|
UTSW |
15 |
31,469,819 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1339:Marchf6
|
UTSW |
15 |
31,486,548 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1485:Marchf6
|
UTSW |
15 |
31,498,839 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1885:Marchf6
|
UTSW |
15 |
31,502,952 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1889:Marchf6
|
UTSW |
15 |
31,459,339 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1984:Marchf6
|
UTSW |
15 |
31,469,792 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2007:Marchf6
|
UTSW |
15 |
31,462,087 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2046:Marchf6
|
UTSW |
15 |
31,486,580 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2135:Marchf6
|
UTSW |
15 |
31,509,910 (GRCm39) |
nonsense |
probably null |
|
|
R3116:Marchf6
|
UTSW |
15 |
31,486,265 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3710:Marchf6
|
UTSW |
15 |
31,509,972 (GRCm39) |
splice site |
probably benign |
|
|
R3715:Marchf6
|
UTSW |
15 |
31,465,405 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3749:Marchf6
|
UTSW |
15 |
31,462,160 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3944:Marchf6
|
UTSW |
15 |
31,488,960 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4327:Marchf6
|
UTSW |
15 |
31,498,887 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4329:Marchf6
|
UTSW |
15 |
31,498,887 (GRCm39) |
missense |
probably benign |
0.17 |
|
R5001:Marchf6
|
UTSW |
15 |
31,465,468 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5149:Marchf6
|
UTSW |
15 |
31,462,140 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R5654:Marchf6
|
UTSW |
15 |
31,486,082 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6163:Marchf6
|
UTSW |
15 |
31,465,497 (GRCm39) |
missense |
probably benign |
|
|
R6172:Marchf6
|
UTSW |
15 |
31,483,013 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6381:Marchf6
|
UTSW |
15 |
31,467,838 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6888:Marchf6
|
UTSW |
15 |
31,459,379 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7347:Marchf6
|
UTSW |
15 |
31,486,505 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8029:Marchf6
|
UTSW |
15 |
31,496,148 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8316:Marchf6
|
UTSW |
15 |
31,482,650 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8342:Marchf6
|
UTSW |
15 |
31,494,262 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8431:Marchf6
|
UTSW |
15 |
31,505,892 (GRCm39) |
nonsense |
probably null |
|
|
R8437:Marchf6
|
UTSW |
15 |
31,482,695 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R8554:Marchf6
|
UTSW |
15 |
31,482,976 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8893:Marchf6
|
UTSW |
15 |
31,498,850 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9523:Marchf6
|
UTSW |
15 |
31,498,845 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation