Incidental Mutation 'IGL02870:P3h1'
| ID |
362536 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
P3h1
|
| Ensembl Gene |
ENSMUSG00000028641 |
| Gene Name |
prolyl 3-hydroxylase 1 |
| Synonyms |
2410024C15Rik, Lepre1, Leprecan, Gros1 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02870
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
119090112-119106172 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 119104768 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Tryptophan
at position 684
(R684W)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000099723
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030393]
[ENSMUST00000081606]
[ENSMUST00000102662]
[ENSMUST00000121111]
[ENSMUST00000136278]
|
| AlphaFold |
Q3V1T4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000030393
AA Change: R691W
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000030393
Gene: ENSMUSG00000028641
AA Change: R691W
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
|
low complexity region
|
60 |
84 |
N/A |
INTRINSIC |
|
low complexity region
|
117 |
127 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
136 |
213 |
2.49e-12 |
PROSPERO |
|
internal_repeat_1
|
294 |
369 |
2.49e-12 |
PROSPERO |
|
Blast:P4Hc
|
419 |
462 |
2e-14 |
BLAST |
|
P4Hc
|
479 |
687 |
5.96e-53 |
SMART |
|
low complexity region
|
714 |
725 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000081606
AA Change: R505W
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000080312
Gene: ENSMUSG00000028641
AA Change: R505W
| Domain | Start | End | E-Value | Type |
|---|
|
SCOP:d1hxia_
|
80 |
195 |
4e-5 |
SMART |
|
Blast:P4Hc
|
125 |
206 |
2e-11 |
BLAST |
|
Blast:P4Hc
|
233 |
276 |
1e-14 |
BLAST |
|
P4Hc
|
293 |
501 |
5.96e-53 |
SMART |
|
low complexity region
|
528 |
539 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000102662
AA Change: R684W
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000099723
Gene: ENSMUSG00000028641
AA Change: R684W
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
|
low complexity region
|
60 |
84 |
N/A |
INTRINSIC |
|
low complexity region
|
117 |
127 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
136 |
213 |
1.9e-12 |
PROSPERO |
|
internal_repeat_1
|
294 |
369 |
1.9e-12 |
PROSPERO |
|
Blast:P4Hc
|
412 |
455 |
2e-14 |
BLAST |
|
P4Hc
|
472 |
680 |
5.96e-53 |
SMART |
|
low complexity region
|
707 |
718 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000121111
AA Change: R684W
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000112504
Gene: ENSMUSG00000028641
AA Change: R684W
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
|
low complexity region
|
60 |
84 |
N/A |
INTRINSIC |
|
low complexity region
|
117 |
127 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
136 |
213 |
2.32e-12 |
PROSPERO |
|
internal_repeat_1
|
294 |
369 |
2.32e-12 |
PROSPERO |
|
Blast:P4Hc
|
412 |
455 |
2e-14 |
BLAST |
|
P4Hc
|
472 |
680 |
5.96e-53 |
SMART |
|
low complexity region
|
707 |
718 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123963
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127087
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134548
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142361
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153940
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150252
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136278
|
| SMART Domains |
Protein: ENSMUSP00000119695
Gene: ENSMUSG00000028641
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
|
low complexity region
|
60 |
84 |
N/A |
INTRINSIC |
|
low complexity region
|
117 |
127 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
136 |
198 |
6.76e-13 |
PROSPERO |
|
internal_repeat_1
|
294 |
356 |
6.76e-13 |
PROSPERO |
|
| 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 an enzyme that is a member of the collagen prolyl hydroxylase family. These enzymes are localized to the endoplasmic reticulum and their activity is required for proper collagen synthesis and assembly. Mutations in this gene are associated with osteogenesis imperfecta type VIII. Three alternatively spliced transcript variants encoding different isoforms have been described. Other variants may exist, but their biological validity has not been determined. [provided by RefSeq, Aug 2011]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced size, disproportional reduction in long bone length, decreased bone density, decreased bone mineral density, reduced body fat, delayed ossification, and abnormal collagen networks in the skin and tendons. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 41 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrv1 |
C |
T |
13: 81,711,851 (GRCm39) |
V1042M |
probably benign |
Het |
| Agmat |
C |
A |
4: 141,474,253 (GRCm39) |
H45N |
probably benign |
Het |
| Akap13 |
T |
A |
7: 75,258,936 (GRCm39) |
V520D |
probably damaging |
Het |
| Ccser1 |
T |
A |
6: 61,288,276 (GRCm39) |
N146K |
probably damaging |
Het |
| Cdhr4 |
T |
A |
9: 107,875,263 (GRCm39) |
|
probably null |
Het |
| Col4a1 |
G |
A |
8: 11,271,375 (GRCm39) |
T753I |
probably benign |
Het |
| Cyp3a59 |
T |
C |
5: 146,034,994 (GRCm39) |
I224T |
probably benign |
Het |
| Ddx19a |
G |
T |
8: 111,710,258 (GRCm39) |
P114Q |
probably damaging |
Het |
| Eftud2 |
A |
G |
11: 102,753,452 (GRCm39) |
V275A |
probably damaging |
Het |
| Fgd6 |
T |
C |
10: 93,881,026 (GRCm39) |
S627P |
probably damaging |
Het |
| Flywch1 |
C |
T |
17: 23,974,876 (GRCm39) |
G541D |
probably damaging |
Het |
| Grk2 |
T |
C |
19: 4,340,430 (GRCm39) |
D317G |
probably damaging |
Het |
| H2-M5 |
T |
C |
17: 37,299,925 (GRCm39) |
E83G |
probably benign |
Het |
| Hltf |
T |
C |
3: 20,154,037 (GRCm39) |
F658L |
probably damaging |
Het |
| Hmmr |
G |
T |
11: 40,604,902 (GRCm39) |
Q390K |
possibly damaging |
Het |
| Lama1 |
G |
A |
17: 68,111,531 (GRCm39) |
G2261R |
probably damaging |
Het |
| Nsd1 |
A |
T |
13: 55,461,416 (GRCm39) |
T2548S |
probably benign |
Het |
| Or1j13 |
G |
A |
2: 36,370,043 (GRCm39) |
A33V |
probably benign |
Het |
| Peli2 |
G |
A |
14: 48,493,722 (GRCm39) |
V315M |
probably damaging |
Het |
| Pfkl |
T |
A |
10: 77,836,673 (GRCm39) |
K115* |
probably null |
Het |
| Plcxd1 |
A |
G |
5: 110,249,271 (GRCm39) |
T33A |
probably damaging |
Het |
| Ranbp17 |
A |
G |
11: 33,193,262 (GRCm39) |
S931P |
probably damaging |
Het |
| Retsat |
T |
C |
6: 72,584,007 (GRCm39) |
Y500H |
probably damaging |
Het |
| Rfx8 |
C |
T |
1: 39,722,871 (GRCm39) |
V249I |
possibly damaging |
Het |
| Runx1t1 |
A |
T |
4: 13,889,867 (GRCm39) |
I599L |
unknown |
Het |
| Sardh |
A |
T |
2: 27,125,503 (GRCm39) |
I337N |
possibly damaging |
Het |
| Serpinb7 |
A |
T |
1: 107,378,017 (GRCm39) |
M237L |
probably damaging |
Het |
| Slc35f1 |
A |
G |
10: 52,809,303 (GRCm39) |
S97G |
possibly damaging |
Het |
| Stab1 |
T |
C |
14: 30,861,354 (GRCm39) |
D2520G |
probably benign |
Het |
| Tnfrsf11b |
C |
T |
15: 54,119,423 (GRCm39) |
V184M |
probably benign |
Het |
| Trpv4 |
A |
T |
5: 114,763,117 (GRCm39) |
V764E |
probably damaging |
Het |
| Tsc22d1 |
C |
A |
14: 76,655,057 (GRCm39) |
A430E |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,580,949 (GRCm39) |
R23315G |
probably damaging |
Het |
| Txnrd1 |
A |
G |
10: 82,731,813 (GRCm39) |
I478M |
probably benign |
Het |
| Ush2a |
T |
C |
1: 188,410,555 (GRCm39) |
V2401A |
probably benign |
Het |
| Vill |
T |
C |
9: 118,890,967 (GRCm39) |
L191P |
probably damaging |
Het |
| Vmn1r30 |
A |
G |
6: 58,412,355 (GRCm39) |
V159A |
probably benign |
Het |
| Washc4 |
T |
A |
10: 83,421,740 (GRCm39) |
N939K |
probably benign |
Het |
| Wdfy3 |
A |
G |
5: 102,003,337 (GRCm39) |
V2926A |
probably damaging |
Het |
| Wdr7 |
T |
C |
18: 63,924,914 (GRCm39) |
S966P |
probably benign |
Het |
| Zfp12 |
C |
A |
5: 143,231,086 (GRCm39) |
T471N |
probably damaging |
Het |
|
| Other mutations in P3h1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01622:P3h1
|
APN |
4 |
119,092,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01623:P3h1
|
APN |
4 |
119,092,480 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01645:P3h1
|
APN |
4 |
119,093,980 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02140:P3h1
|
APN |
4 |
119,095,062 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02415:P3h1
|
APN |
4 |
119,105,152 (GRCm39) |
missense |
probably benign |
|
|
IGL02543:P3h1
|
APN |
4 |
119,095,053 (GRCm39) |
splice site |
probably benign |
|
|
IGL02972:P3h1
|
APN |
4 |
119,105,157 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
IGL03067:P3h1
|
APN |
4 |
119,092,477 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03077:P3h1
|
APN |
4 |
119,093,983 (GRCm39) |
missense |
probably damaging |
1.00 |
|
woohoo
|
UTSW |
4 |
119,098,329 (GRCm39) |
nonsense |
probably null |
|
|
R0194:P3h1
|
UTSW |
4 |
119,095,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0523:P3h1
|
UTSW |
4 |
119,098,727 (GRCm39) |
missense |
probably benign |
0.32 |
|
R0734:P3h1
|
UTSW |
4 |
119,095,885 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0944:P3h1
|
UTSW |
4 |
119,095,956 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1018:P3h1
|
UTSW |
4 |
119,095,104 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1978:P3h1
|
UTSW |
4 |
119,105,173 (GRCm39) |
missense |
probably null |
0.00 |
|
R2697:P3h1
|
UTSW |
4 |
119,104,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5668:P3h1
|
UTSW |
4 |
119,101,243 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5750:P3h1
|
UTSW |
4 |
119,095,863 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5965:P3h1
|
UTSW |
4 |
119,105,424 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5987:P3h1
|
UTSW |
4 |
119,103,862 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6111:P3h1
|
UTSW |
4 |
119,098,329 (GRCm39) |
nonsense |
probably null |
|
|
R6786:P3h1
|
UTSW |
4 |
119,095,151 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R7142:P3h1
|
UTSW |
4 |
119,104,358 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8068:P3h1
|
UTSW |
4 |
119,094,059 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8304:P3h1
|
UTSW |
4 |
119,104,402 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9502:P3h1
|
UTSW |
4 |
119,094,008 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R9680:P3h1
|
UTSW |
4 |
119,090,428 (GRCm39) |
missense |
probably benign |
0.17 |
|
| Posted On |
2015-12-18 |
Incidental Mutation