Incidental Mutation 'IGL01861:Hpx'
| ID |
178329 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Hpx
|
| Ensembl Gene |
ENSMUSG00000030895 |
| Gene Name |
hemopexin |
| Synonyms |
Hpxn, hx |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01861
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
105240818-105249323 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
A to T
at 105241393 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 339
(Y339*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000033185
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000033185]
[ENSMUST00000210531]
|
| AlphaFold |
Q91X72 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000033185
AA Change: Y339*
|
| SMART Domains |
Protein: ENSMUSP00000033185
Gene: ENSMUSG00000030895
AA Change: Y339*
| Domain | Start | End | E-Value | Type |
|---|
|
HX
|
56 |
93 |
1.29e0 |
SMART |
|
HX
|
97 |
140 |
5.52e-8 |
SMART |
|
Blast:HX
|
143 |
186 |
3e-7 |
BLAST |
|
HX
|
187 |
230 |
3.48e-5 |
SMART |
|
HX
|
261 |
304 |
1.07e-5 |
SMART |
|
HX
|
306 |
351 |
5.49e-3 |
SMART |
|
Blast:HX
|
358 |
403 |
2e-17 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000210531
|
| 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 plasma glycoprotein that binds heme with high affinity. The encoded protein is an acute phase protein that transports heme from the plasma to the liver and may be involved in protecting cells from oxidative stress. [provided by RefSeq, Apr 2009]
PHENOTYPE: Mice homozygous for disruptions in this gene display an essentially normal phenotype. However, they have increased susceptiblity to induced hemolytic stress. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arrdc5 |
T |
C |
17: 56,607,144 (GRCm39) |
T34A |
possibly damaging |
Het |
| Atm |
C |
A |
9: 53,405,912 (GRCm39) |
R1252L |
probably null |
Het |
| Cd34 |
T |
C |
1: 194,640,888 (GRCm39) |
|
probably benign |
Het |
| Cmya5 |
A |
G |
13: 93,226,256 (GRCm39) |
V2944A |
probably damaging |
Het |
| Cntnap3 |
C |
T |
13: 64,946,922 (GRCm39) |
G169D |
probably damaging |
Het |
| Dnah7a |
T |
A |
1: 53,679,508 (GRCm39) |
T326S |
probably benign |
Het |
| Dnah7a |
C |
T |
1: 53,623,608 (GRCm39) |
|
probably benign |
Het |
| Fam133b |
A |
G |
5: 3,614,242 (GRCm39) |
|
probably benign |
Het |
| Fhod1 |
A |
G |
8: 106,057,808 (GRCm39) |
S906P |
probably damaging |
Het |
| Gli3 |
A |
G |
13: 15,899,910 (GRCm39) |
Y1099C |
probably damaging |
Het |
| Gpr63 |
C |
T |
4: 25,008,545 (GRCm39) |
T423M |
probably damaging |
Het |
| Lingo2 |
A |
T |
4: 35,709,526 (GRCm39) |
D151E |
probably benign |
Het |
| Mill2 |
A |
T |
7: 18,590,565 (GRCm39) |
Q215L |
probably damaging |
Het |
| Naf1 |
T |
C |
8: 67,317,185 (GRCm39) |
|
probably benign |
Het |
| Ndufv1 |
A |
G |
19: 4,058,803 (GRCm39) |
V235A |
probably benign |
Het |
| Or8b41 |
T |
C |
9: 38,055,046 (GRCm39) |
I205T |
probably damaging |
Het |
| Pafah1b1 |
A |
T |
11: 74,581,403 (GRCm39) |
N22K |
possibly damaging |
Het |
| Prune1 |
G |
T |
3: 95,172,868 (GRCm39) |
R66S |
probably damaging |
Het |
| Ptcd1 |
A |
T |
5: 145,095,587 (GRCm39) |
I291N |
possibly damaging |
Het |
| Ptprk |
A |
G |
10: 28,259,441 (GRCm39) |
I294V |
possibly damaging |
Het |
| Rfx6 |
G |
A |
10: 51,597,675 (GRCm39) |
V471M |
probably damaging |
Het |
| Rnase6 |
C |
A |
14: 51,367,748 (GRCm39) |
Q47K |
probably benign |
Het |
| Skint5 |
T |
C |
4: 113,417,021 (GRCm39) |
|
probably benign |
Het |
| Srcap |
T |
A |
7: 127,124,457 (GRCm39) |
|
probably benign |
Het |
| Stap1 |
A |
G |
5: 86,244,383 (GRCm39) |
I217V |
possibly damaging |
Het |
| Taf1d |
T |
C |
9: 15,220,035 (GRCm39) |
|
probably null |
Het |
| Tecta |
T |
C |
9: 42,284,658 (GRCm39) |
H809R |
probably benign |
Het |
| Tex15 |
A |
G |
8: 34,060,717 (GRCm39) |
N49S |
probably damaging |
Het |
| Tubb4b-ps1 |
A |
G |
5: 7,229,374 (GRCm39) |
|
probably benign |
Het |
| Uhrf2 |
A |
G |
19: 30,063,804 (GRCm39) |
Y589C |
probably damaging |
Het |
| Zfp616 |
A |
T |
11: 73,973,742 (GRCm39) |
T4S |
possibly damaging |
Het |
| Zfp687 |
A |
T |
3: 94,919,171 (GRCm39) |
F200L |
probably damaging |
Het |
|
| Other mutations in Hpx |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00337:Hpx
|
APN |
7 |
105,240,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02441:Hpx
|
APN |
7 |
105,241,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03117:Hpx
|
APN |
7 |
105,249,278 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL03230:Hpx
|
APN |
7 |
105,248,519 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL03376:Hpx
|
APN |
7 |
105,241,458 (GRCm39) |
unclassified |
probably benign |
|
|
IGL03392:Hpx
|
APN |
7 |
105,241,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4520001:Hpx
|
UTSW |
7 |
105,241,341 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0138:Hpx
|
UTSW |
7 |
105,241,445 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0364:Hpx
|
UTSW |
7 |
105,245,471 (GRCm39) |
missense |
probably benign |
0.18 |
|
R1195:Hpx
|
UTSW |
7 |
105,248,856 (GRCm39) |
splice site |
probably benign |
|
|
R1195:Hpx
|
UTSW |
7 |
105,248,856 (GRCm39) |
splice site |
probably benign |
|
|
R1958:Hpx
|
UTSW |
7 |
105,245,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2007:Hpx
|
UTSW |
7 |
105,244,781 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2025:Hpx
|
UTSW |
7 |
105,244,311 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2173:Hpx
|
UTSW |
7 |
105,241,290 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2207:Hpx
|
UTSW |
7 |
105,241,633 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3162:Hpx
|
UTSW |
7 |
105,248,847 (GRCm39) |
intron |
probably benign |
|
|
R3849:Hpx
|
UTSW |
7 |
105,245,498 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4206:Hpx
|
UTSW |
7 |
105,244,354 (GRCm39) |
missense |
probably null |
0.01 |
|
R4510:Hpx
|
UTSW |
7 |
105,241,295 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4511:Hpx
|
UTSW |
7 |
105,241,295 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4709:Hpx
|
UTSW |
7 |
105,249,243 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5029:Hpx
|
UTSW |
7 |
105,240,971 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5540:Hpx
|
UTSW |
7 |
105,241,119 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R5631:Hpx
|
UTSW |
7 |
105,244,808 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5664:Hpx
|
UTSW |
7 |
105,244,355 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5820:Hpx
|
UTSW |
7 |
105,240,995 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5922:Hpx
|
UTSW |
7 |
105,244,831 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6707:Hpx
|
UTSW |
7 |
105,244,682 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6714:Hpx
|
UTSW |
7 |
105,244,302 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7356:Hpx
|
UTSW |
7 |
105,240,917 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7425:Hpx
|
UTSW |
7 |
105,241,068 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8048:Hpx
|
UTSW |
7 |
105,244,685 (GRCm39) |
missense |
probably benign |
|
|
R8184:Hpx
|
UTSW |
7 |
105,241,352 (GRCm39) |
missense |
probably damaging |
0.99 |
|
X0066:Hpx
|
UTSW |
7 |
105,245,594 (GRCm39) |
missense |
probably benign |
0.17 |
|
| Posted On |
2014-05-07 |
Incidental Mutation