Incidental Mutation 'IGL00401:Hspa9'
| ID |
3364 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Hspa9
|
| Ensembl Gene |
ENSMUSG00000024359 |
| Gene Name |
heat shock protein 9 |
| Synonyms |
Hsp74, mthsp70, GRP75, Hsc74, mot-2, Hspa9a, PBP74, CSA, C3H-specific antigen, mortalin, Hsp74a |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.971)
|
| Stock # |
IGL00401
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
18 |
| Chromosomal Location |
35070467-35087404 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
G to A
at 35071633 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000025217
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025217]
|
| AlphaFold |
P38647 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000025217
|
| SMART Domains |
Protein: ENSMUSP00000025217
Gene: ENSMUSG00000024359
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
3 |
26 |
N/A |
INTRINSIC |
|
Pfam:HSP70
|
55 |
653 |
2.7e-270 |
PFAM |
|
Pfam:FGGY_C
|
283 |
429 |
3e-8 |
PFAM |
|
low complexity region
|
657 |
679 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000083970
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000158614
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000172829
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173701
|
| 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 the heat shock protein 70 gene family. The encoded protein is primarily localized to the mitochondria but is also found in the endoplasmic reticulum, plasma membrane and cytoplasmic vesicles. This protein is a heat-shock cognate protein. This protein plays a role in cell proliferation, stress response and maintenance of the mitochondria. A pseudogene of this gene is found on chromosome 2.[provided by RefSeq, May 2010]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete embryonic lethality while heterozygotes display decreased pre-B cell number. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Alk |
T |
A |
17: 72,202,743 (GRCm39) |
D1164V |
probably damaging |
Het |
| Baiap3 |
T |
G |
17: 25,463,302 (GRCm39) |
L964F |
probably damaging |
Het |
| Cacna2d2 |
T |
A |
9: 107,392,072 (GRCm39) |
V471E |
probably damaging |
Het |
| Carmil3 |
C |
T |
14: 55,735,755 (GRCm39) |
T569M |
probably damaging |
Het |
| Dapk2 |
G |
T |
9: 66,176,060 (GRCm39) |
|
probably benign |
Het |
| Eps15l1 |
A |
T |
8: 73,138,682 (GRCm39) |
Y291* |
probably null |
Het |
| Fancd2 |
T |
C |
6: 113,541,357 (GRCm39) |
|
probably null |
Het |
| Fmnl2 |
T |
G |
2: 53,004,929 (GRCm39) |
D674E |
probably damaging |
Het |
| Foxq1 |
A |
T |
13: 31,743,260 (GRCm39) |
I121F |
probably damaging |
Het |
| Galnt13 |
C |
T |
2: 54,406,547 (GRCm39) |
|
probably benign |
Het |
| Git1 |
T |
C |
11: 77,389,782 (GRCm39) |
|
probably benign |
Het |
| Gm10220 |
A |
T |
5: 26,323,609 (GRCm39) |
F146Y |
possibly damaging |
Het |
| Gm7353 |
A |
G |
7: 3,160,630 (GRCm39) |
|
noncoding transcript |
Het |
| Kptn |
A |
G |
7: 15,854,050 (GRCm39) |
D56G |
possibly damaging |
Het |
| Krtap4-13 |
A |
T |
11: 99,700,543 (GRCm39) |
C39S |
unknown |
Het |
| Lgsn |
A |
G |
1: 31,242,647 (GRCm39) |
K243R |
possibly damaging |
Het |
| Lyz2 |
C |
T |
10: 117,118,090 (GRCm39) |
V20I |
probably benign |
Het |
| Mettl3 |
T |
A |
14: 52,534,424 (GRCm39) |
|
probably benign |
Het |
| Myh6 |
T |
A |
14: 55,190,874 (GRCm39) |
M934L |
probably benign |
Het |
| Nmnat2 |
A |
G |
1: 152,969,863 (GRCm39) |
|
probably null |
Het |
| Pias2 |
T |
A |
18: 77,220,907 (GRCm39) |
C381S |
probably damaging |
Het |
| Psme4 |
T |
C |
11: 30,771,079 (GRCm39) |
|
probably benign |
Het |
| Smc4 |
T |
A |
3: 68,937,712 (GRCm39) |
D887E |
probably damaging |
Het |
| Sorcs2 |
C |
A |
5: 36,194,745 (GRCm39) |
|
probably null |
Het |
| Tet2 |
T |
C |
3: 133,172,643 (GRCm39) |
E1873G |
possibly damaging |
Het |
| Txlng |
T |
A |
X: 161,565,305 (GRCm39) |
K341* |
probably null |
Het |
| Ugt2b37 |
T |
A |
5: 87,390,340 (GRCm39) |
T369S |
possibly damaging |
Het |
| Usp46 |
C |
A |
5: 74,163,832 (GRCm39) |
V302F |
probably damaging |
Het |
| Zfp292 |
A |
G |
4: 34,808,683 (GRCm39) |
C1454R |
probably benign |
Het |
|
| Other mutations in Hspa9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01939:Hspa9
|
APN |
18 |
35,071,761 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02008:Hspa9
|
APN |
18 |
35,081,028 (GRCm39) |
nonsense |
probably null |
|
|
IGL02604:Hspa9
|
APN |
18 |
35,087,266 (GRCm39) |
missense |
unknown |
|
|
Chiri-san
|
UTSW |
18 |
35,072,476 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0238:Hspa9
|
UTSW |
18 |
35,079,699 (GRCm39) |
nonsense |
probably null |
|
|
R0238:Hspa9
|
UTSW |
18 |
35,079,699 (GRCm39) |
nonsense |
probably null |
|
|
R0278:Hspa9
|
UTSW |
18 |
35,073,963 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R0613:Hspa9
|
UTSW |
18 |
35,081,033 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1414:Hspa9
|
UTSW |
18 |
35,071,644 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1454:Hspa9
|
UTSW |
18 |
35,071,659 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2013:Hspa9
|
UTSW |
18 |
35,079,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2014:Hspa9
|
UTSW |
18 |
35,079,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2015:Hspa9
|
UTSW |
18 |
35,079,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2936:Hspa9
|
UTSW |
18 |
35,081,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4261:Hspa9
|
UTSW |
18 |
35,072,476 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4622:Hspa9
|
UTSW |
18 |
35,082,090 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R4819:Hspa9
|
UTSW |
18 |
35,072,441 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5056:Hspa9
|
UTSW |
18 |
35,071,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5223:Hspa9
|
UTSW |
18 |
35,085,724 (GRCm39) |
splice site |
probably null |
|
|
R5666:Hspa9
|
UTSW |
18 |
35,087,300 (GRCm39) |
missense |
probably null |
|
|
R5820:Hspa9
|
UTSW |
18 |
35,076,227 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R5944:Hspa9
|
UTSW |
18 |
35,082,076 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6460:Hspa9
|
UTSW |
18 |
35,085,765 (GRCm39) |
missense |
probably benign |
|
|
R7404:Hspa9
|
UTSW |
18 |
35,076,329 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R7412:Hspa9
|
UTSW |
18 |
35,082,082 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7637:Hspa9
|
UTSW |
18 |
35,071,740 (GRCm39) |
missense |
not run |
|
|
R8524:Hspa9
|
UTSW |
18 |
35,087,297 (GRCm39) |
missense |
unknown |
|
|
R8830:Hspa9
|
UTSW |
18 |
35,081,157 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8987:Hspa9
|
UTSW |
18 |
35,080,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9028:Hspa9
|
UTSW |
18 |
35,075,084 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9184:Hspa9
|
UTSW |
18 |
35,082,168 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R9709:Hspa9
|
UTSW |
18 |
35,073,294 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
Z1177:Hspa9
|
UTSW |
18 |
35,076,198 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
| Posted On |
2012-04-20 |
Incidental Mutation