Incidental Mutation 'IGL01520:Hgs'
| ID |
90456 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Hgs
|
| Ensembl Gene |
ENSMUSG00000116045 |
| Gene Name |
HGF-regulated tyrosine kinase substrate |
| Synonyms |
Hrs, tn |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.800)
|
| Stock # |
IGL01520
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
120358461-120374805 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 120369174 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Threonine
at position 317
(P317T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000026900
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000026900]
[ENSMUST00000106203]
[ENSMUST00000106205]
[ENSMUST00000140862]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000026900
AA Change: P317T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000026900
Gene: ENSMUSG00000116045
AA Change: P317T
| Domain | Start | End | E-Value | Type |
|---|
|
VHS
|
8 |
139 |
6.97e-63 |
SMART |
|
FYVE
|
155 |
221 |
1.81e-31 |
SMART |
|
UIM
|
258 |
277 |
1.81e-1 |
SMART |
|
Pfam:Hrs_helical
|
406 |
500 |
1.2e-41 |
PFAM |
|
low complexity region
|
637 |
658 |
N/A |
INTRINSIC |
|
low complexity region
|
746 |
767 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000106203
AA Change: P317T
PolyPhen 2
Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000101809
Gene: ENSMUSG00000025793
AA Change: P317T
| Domain | Start | End | E-Value | Type |
|---|
|
VHS
|
8 |
139 |
6.97e-63 |
SMART |
|
FYVE
|
155 |
221 |
1.81e-31 |
SMART |
|
UIM
|
258 |
277 |
1.81e-1 |
SMART |
|
Pfam:Hrs_helical
|
405 |
500 |
2.2e-48 |
PFAM |
|
low complexity region
|
724 |
739 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000106205
AA Change: P317T
PolyPhen 2
Score 0.284 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000101811
Gene: ENSMUSG00000025793
AA Change: P317T
| Domain | Start | End | E-Value | Type |
|---|
|
VHS
|
8 |
139 |
6.97e-63 |
SMART |
|
FYVE
|
155 |
221 |
1.81e-31 |
SMART |
|
UIM
|
258 |
277 |
1.81e-1 |
SMART |
|
Pfam:Hrs_helical
|
404 |
499 |
2.2e-48 |
PFAM |
|
low complexity region
|
723 |
738 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000135231
AA Change: P38T
|
| SMART Domains |
Protein: ENSMUSP00000115037
Gene: ENSMUSG00000025793
AA Change: P38T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Hrs_helical
|
112 |
172 |
9.6e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140862
|
| SMART Domains |
Protein: ENSMUSP00000119396
Gene: ENSMUSG00000025793
| Domain | Start | End | E-Value | Type |
|---|
|
VHS
|
8 |
123 |
1.29e-48 |
SMART |
|
FYVE
|
139 |
205 |
1.81e-31 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141826
|
| 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 regulates endosomal sorting and plays a critical role in the recycling and degradation of membrane receptors. The encoded protein sorts monoubiquitinated membrane proteins into the multivesicular body, targeting these proteins for lysosome-dependent degradation. [provided by RefSeq, Dec 2010]
PHENOTYPE: Mice homozygous for disruptions in this gene display embryonic lethality during organogenesis with decreased size and no embryo turning. In addition, one allele shows cardia bifida, no foregut formation, failure of chorioallantoic fusion and neural tube,somite and allantois defects. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 48 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acan |
T |
A |
7: 78,734,318 (GRCm39) |
H58Q |
probably damaging |
Het |
| Atp6v1c2 |
A |
T |
12: 17,347,754 (GRCm39) |
L149Q |
probably damaging |
Het |
| Bltp1 |
T |
A |
3: 37,027,409 (GRCm39) |
Y2265* |
probably null |
Het |
| Cd40lg |
A |
G |
X: 56,265,148 (GRCm39) |
N132D |
probably benign |
Het |
| Cemip |
G |
T |
7: 83,597,830 (GRCm39) |
T1060K |
probably benign |
Het |
| Ces1a |
G |
T |
8: 93,771,726 (GRCm39) |
P24T |
probably damaging |
Het |
| Ces5a |
A |
T |
8: 94,246,206 (GRCm39) |
S328T |
probably benign |
Het |
| Cfap70 |
A |
G |
14: 20,470,755 (GRCm39) |
C497R |
probably benign |
Het |
| Cndp2 |
T |
C |
18: 84,686,732 (GRCm39) |
K430R |
probably benign |
Het |
| Cplane1 |
C |
A |
15: 8,251,395 (GRCm39) |
T1889K |
probably damaging |
Het |
| Crlf3 |
T |
C |
11: 79,950,972 (GRCm39) |
D126G |
probably benign |
Het |
| Cxcr1 |
A |
T |
1: 74,231,434 (GRCm39) |
L196Q |
probably damaging |
Het |
| E330013P04Rik |
A |
G |
19: 60,150,329 (GRCm39) |
|
noncoding transcript |
Het |
| Erbb2 |
C |
T |
11: 98,324,835 (GRCm39) |
H810Y |
probably benign |
Het |
| Fmn1 |
C |
A |
2: 113,274,713 (GRCm39) |
|
probably benign |
Het |
| Fpr3 |
A |
G |
17: 18,191,325 (GRCm39) |
T199A |
possibly damaging |
Het |
| Gcsh |
A |
G |
8: 117,710,688 (GRCm39) |
|
probably benign |
Het |
| Gm10073 |
T |
A |
8: 107,299,901 (GRCm39) |
I28F |
probably benign |
Het |
| Gucy1a2 |
C |
A |
9: 3,759,561 (GRCm39) |
Q456K |
probably damaging |
Het |
| Inmt |
C |
A |
6: 55,148,213 (GRCm39) |
V139F |
probably damaging |
Het |
| Kcnma1 |
C |
A |
14: 23,551,211 (GRCm39) |
M460I |
possibly damaging |
Het |
| Map9 |
A |
T |
3: 82,286,272 (GRCm39) |
N359I |
probably damaging |
Het |
| Mavs |
T |
C |
2: 131,087,263 (GRCm39) |
S254P |
probably benign |
Het |
| Mcts1 |
T |
A |
X: 37,700,636 (GRCm39) |
|
probably benign |
Het |
| Mecp2 |
C |
A |
X: 73,079,447 (GRCm39) |
R344L |
possibly damaging |
Het |
| Or1e32 |
T |
G |
11: 73,705,612 (GRCm39) |
T99P |
probably damaging |
Het |
| Or4z4 |
A |
G |
19: 12,077,000 (GRCm39) |
M1T |
probably null |
Het |
| Or5b3 |
G |
T |
19: 13,388,114 (GRCm39) |
M60I |
probably damaging |
Het |
| Or8g36 |
T |
C |
9: 39,422,342 (GRCm39) |
I225V |
possibly damaging |
Het |
| Or8g54 |
T |
G |
9: 39,706,674 (GRCm39) |
M1R |
probably null |
Het |
| Or9g4 |
T |
C |
2: 85,504,701 (GRCm39) |
T265A |
probably benign |
Het |
| Rasgrp1 |
T |
C |
2: 117,119,144 (GRCm39) |
I498V |
probably damaging |
Het |
| Rbbp6 |
T |
A |
7: 122,584,898 (GRCm39) |
S185T |
possibly damaging |
Het |
| Rd3 |
A |
T |
1: 191,717,283 (GRCm39) |
H251L |
possibly damaging |
Het |
| Rnf180 |
T |
A |
13: 105,386,864 (GRCm39) |
D148V |
probably damaging |
Het |
| Rnf43 |
C |
A |
11: 87,555,542 (GRCm39) |
A34E |
probably damaging |
Het |
| Rslcan18 |
A |
G |
13: 67,250,172 (GRCm39) |
V21A |
probably benign |
Het |
| Septin9 |
T |
C |
11: 117,243,469 (GRCm39) |
V128A |
probably damaging |
Het |
| Slc36a1 |
A |
G |
11: 55,110,482 (GRCm39) |
H103R |
probably benign |
Het |
| Spata6l |
A |
T |
19: 28,873,532 (GRCm39) |
|
probably null |
Het |
| Ssh2 |
A |
G |
11: 77,340,732 (GRCm39) |
D628G |
probably damaging |
Het |
| Tlcd3a |
T |
C |
11: 76,098,051 (GRCm39) |
|
probably null |
Het |
| Tmem119 |
A |
G |
5: 113,933,546 (GRCm39) |
F85S |
probably damaging |
Het |
| Tpp1 |
A |
T |
7: 105,396,936 (GRCm39) |
I398N |
probably benign |
Het |
| Ttc3 |
T |
C |
16: 94,191,066 (GRCm39) |
Y203H |
probably benign |
Het |
| Vars1 |
G |
T |
17: 35,232,849 (GRCm39) |
V898L |
probably benign |
Het |
| Vmn1r85 |
A |
C |
7: 12,819,081 (GRCm39) |
V21G |
probably damaging |
Het |
| Zfp521 |
T |
C |
18: 14,072,045 (GRCm39) |
H65R |
possibly damaging |
Het |
|
| Other mutations in Hgs |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01118:Hgs
|
APN |
11 |
120,366,040 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01532:Hgs
|
APN |
11 |
120,368,335 (GRCm39) |
splice site |
probably null |
|
|
IGL02346:Hgs
|
APN |
11 |
120,373,377 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02808:Hgs
|
APN |
11 |
120,360,492 (GRCm39) |
nonsense |
probably null |
|
|
LCD18:Hgs
|
UTSW |
11 |
120,360,404 (GRCm39) |
splice site |
probably benign |
|
|
R0100:Hgs
|
UTSW |
11 |
120,373,678 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R0462:Hgs
|
UTSW |
11 |
120,369,970 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R0653:Hgs
|
UTSW |
11 |
120,359,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0719:Hgs
|
UTSW |
11 |
120,362,431 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1482:Hgs
|
UTSW |
11 |
120,370,866 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1757:Hgs
|
UTSW |
11 |
120,370,889 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1782:Hgs
|
UTSW |
11 |
120,369,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2311:Hgs
|
UTSW |
11 |
120,370,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4077:Hgs
|
UTSW |
11 |
120,368,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4078:Hgs
|
UTSW |
11 |
120,373,874 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4079:Hgs
|
UTSW |
11 |
120,373,874 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4094:Hgs
|
UTSW |
11 |
120,359,859 (GRCm39) |
nonsense |
probably null |
|
|
R4204:Hgs
|
UTSW |
11 |
120,368,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4911:Hgs
|
UTSW |
11 |
120,368,028 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6477:Hgs
|
UTSW |
11 |
120,360,481 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6816:Hgs
|
UTSW |
11 |
120,362,397 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7264:Hgs
|
UTSW |
11 |
120,365,139 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7633:Hgs
|
UTSW |
11 |
120,365,128 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7807:Hgs
|
UTSW |
11 |
120,370,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8683:Hgs
|
UTSW |
11 |
120,366,044 (GRCm39) |
nonsense |
probably null |
|
|
R8733:Hgs
|
UTSW |
11 |
120,360,954 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8798:Hgs
|
UTSW |
11 |
120,370,938 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8866:Hgs
|
UTSW |
11 |
120,360,464 (GRCm39) |
missense |
probably benign |
0.10 |
|
R8910:Hgs
|
UTSW |
11 |
120,369,202 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9081:Hgs
|
UTSW |
11 |
120,366,076 (GRCm39) |
splice site |
probably benign |
|
|
X0024:Hgs
|
UTSW |
11 |
120,368,140 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Hgs
|
UTSW |
11 |
120,369,391 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2013-12-09 |
Incidental Mutation