Incidental Mutation 'IGL02222:Fetub'
| ID |
285181 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Fetub
|
| Ensembl Gene |
ENSMUSG00000022871 |
| Gene Name |
fetuin beta |
| Synonyms |
2310011O17Rik, D17980 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
IGL02222
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
16 |
| Chromosomal Location |
22737132-22758518 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 22751078 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Phenylalanine
at position 62
(L62F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112324
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023587]
[ENSMUST00000116625]
[ENSMUST00000167399]
[ENSMUST00000170805]
[ENSMUST00000231768]
[ENSMUST00000231880]
[ENSMUST00000232097]
|
| AlphaFold |
Q9QXC1 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000023587
AA Change: L142F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000023587
Gene: ENSMUSG00000022871
AA Change: L142F
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
CY
|
28 |
129 |
1.05e-2 |
SMART |
|
CY
|
153 |
255 |
1.77e-11 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000116625
AA Change: L62F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000112324
Gene: ENSMUSG00000022871
AA Change: L62F
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:CY
|
1 |
61 |
4e-33 |
BLAST |
|
CY
|
73 |
175 |
1.77e-11 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000167399
AA Change: L142F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000128745
Gene: ENSMUSG00000022871
AA Change: L142F
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
CY
|
28 |
129 |
1.05e-2 |
SMART |
|
CY
|
153 |
255 |
1.77e-11 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000170805
AA Change: L142F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000128989
Gene: ENSMUSG00000022871
AA Change: L142F
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
CY
|
28 |
129 |
1.05e-2 |
SMART |
|
CY
|
153 |
255 |
1.77e-11 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000231768
AA Change: L142F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000231880
AA Change: L62F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000232097
AA Change: L142F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the fetuin family, part of the cystatin superfamily of cysteine protease inhibitors. Fetuins have been implicated in several diverse functions, including osteogenesis and bone resorption, regulation of the insulin and hepatocyte growth factor receptors, and response to systemic inflammation. This protein may be secreted by cells. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit female infertility due to premature hardening of the zona pellucida. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 31 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca12 |
T |
A |
1: 71,322,045 (GRCm39) |
R1682W |
probably benign |
Het |
| Angptl6 |
A |
T |
9: 20,785,203 (GRCm39) |
M450K |
probably damaging |
Het |
| Armc12 |
C |
A |
17: 28,757,694 (GRCm39) |
N275K |
probably damaging |
Het |
| Cd27 |
T |
C |
6: 125,211,495 (GRCm39) |
H144R |
probably damaging |
Het |
| Cenpf |
T |
C |
1: 189,386,641 (GRCm39) |
K1880E |
probably benign |
Het |
| Dchs1 |
A |
T |
7: 105,414,094 (GRCm39) |
I907N |
probably damaging |
Het |
| Dpy19l4 |
A |
C |
4: 11,281,116 (GRCm39) |
F443C |
possibly damaging |
Het |
| Eif3i |
C |
T |
4: 129,485,881 (GRCm39) |
D315N |
possibly damaging |
Het |
| Fam217a |
A |
G |
13: 35,095,102 (GRCm39) |
L128P |
probably damaging |
Het |
| Fmn1 |
A |
T |
2: 113,423,454 (GRCm39) |
I1047F |
probably damaging |
Het |
| G2e3 |
A |
G |
12: 51,410,016 (GRCm39) |
H267R |
probably damaging |
Het |
| Gigyf2 |
A |
G |
1: 87,338,585 (GRCm39) |
|
probably null |
Het |
| Gm10650 |
T |
C |
3: 127,833,789 (GRCm39) |
|
noncoding transcript |
Het |
| Grip1 |
C |
T |
10: 119,835,714 (GRCm39) |
T470I |
probably damaging |
Het |
| Hmcn1 |
T |
G |
1: 150,682,152 (GRCm39) |
D466A |
probably benign |
Het |
| Lrrc63 |
T |
C |
14: 75,323,580 (GRCm39) |
Y548C |
probably damaging |
Het |
| Naaa |
T |
C |
5: 92,407,409 (GRCm39) |
|
probably benign |
Het |
| Parpbp |
T |
A |
10: 87,975,947 (GRCm39) |
E55D |
possibly damaging |
Het |
| Pnpt1 |
A |
T |
11: 29,109,327 (GRCm39) |
D691V |
possibly damaging |
Het |
| Pnpt1 |
G |
A |
11: 29,080,842 (GRCm39) |
A29T |
probably benign |
Het |
| Pramel11 |
A |
G |
4: 143,622,416 (GRCm39) |
M313T |
possibly damaging |
Het |
| Psg25 |
T |
C |
7: 18,263,652 (GRCm39) |
N57S |
probably damaging |
Het |
| Selenbp2 |
T |
A |
3: 94,607,269 (GRCm39) |
V168E |
probably damaging |
Het |
| Syne2 |
G |
A |
12: 75,999,617 (GRCm39) |
E2337K |
probably damaging |
Het |
| Synj2 |
A |
G |
17: 6,087,755 (GRCm39) |
T1269A |
probably benign |
Het |
| Tent5b |
T |
C |
4: 133,213,864 (GRCm39) |
V245A |
probably damaging |
Het |
| Tnfrsf13c |
C |
A |
15: 82,107,364 (GRCm39) |
V144L |
probably damaging |
Het |
| Uspl1 |
G |
T |
5: 149,130,854 (GRCm39) |
V132L |
probably benign |
Het |
| Vmn2r58 |
T |
A |
7: 41,513,449 (GRCm39) |
Y398F |
possibly damaging |
Het |
| Vps13a |
T |
A |
19: 16,659,539 (GRCm39) |
T1663S |
probably benign |
Het |
| Ythdc1 |
G |
A |
5: 86,975,902 (GRCm39) |
R503H |
possibly damaging |
Het |
|
| Other mutations in Fetub |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00706:Fetub
|
APN |
16 |
22,754,446 (GRCm39) |
missense |
probably benign |
0.29 |
|
IGL00843:Fetub
|
APN |
16 |
22,748,379 (GRCm39) |
splice site |
probably benign |
|
|
IGL01450:Fetub
|
APN |
16 |
22,747,986 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01522:Fetub
|
APN |
16 |
22,748,391 (GRCm39) |
start codon destroyed |
probably null |
0.10 |
|
IGL02745:Fetub
|
APN |
16 |
22,756,676 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0062:Fetub
|
UTSW |
16 |
22,747,836 (GRCm39) |
intron |
probably benign |
|
|
R0310:Fetub
|
UTSW |
16 |
22,748,506 (GRCm39) |
splice site |
probably benign |
|
|
R0508:Fetub
|
UTSW |
16 |
22,748,045 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0604:Fetub
|
UTSW |
16 |
22,754,410 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1560:Fetub
|
UTSW |
16 |
22,758,117 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1844:Fetub
|
UTSW |
16 |
22,754,419 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1896:Fetub
|
UTSW |
16 |
22,751,045 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3716:Fetub
|
UTSW |
16 |
22,754,443 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3717:Fetub
|
UTSW |
16 |
22,754,443 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4274:Fetub
|
UTSW |
16 |
22,754,429 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4751:Fetub
|
UTSW |
16 |
22,756,645 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4941:Fetub
|
UTSW |
16 |
22,756,624 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5468:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5470:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5690:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5692:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5781:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6038:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6038:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6039:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6039:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6193:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6195:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6244:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6245:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6273:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6274:Fetub
|
UTSW |
16 |
22,751,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7134:Fetub
|
UTSW |
16 |
22,748,007 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R7698:Fetub
|
UTSW |
16 |
22,758,059 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7969:Fetub
|
UTSW |
16 |
22,748,449 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8437:Fetub
|
UTSW |
16 |
22,752,985 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R8788:Fetub
|
UTSW |
16 |
22,758,182 (GRCm39) |
nonsense |
probably null |
|
|
R8855:Fetub
|
UTSW |
16 |
22,758,321 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R8866:Fetub
|
UTSW |
16 |
22,758,321 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
| Posted On |
2015-04-16 |
Incidental Mutation