Incidental Mutation 'IGL01587:Col24a1'
ID |
93368 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Col24a1
|
Ensembl Gene |
ENSMUSG00000028197 |
Gene Name |
collagen, type XXIV, alpha 1 |
Synonyms |
5430404K19Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL01587
|
Quality Score |
|
Status
|
|
Chromosome |
3 |
Chromosomal Location |
145292472-145552011 bp(+) (GRCm38) |
Type of Mutation |
splice site (4 bp from exon) |
DNA Base Change (assembly) |
A to G
at 145433355 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000029848
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029848]
|
AlphaFold |
Q30D77 |
Predicted Effect |
probably null
Transcript: ENSMUST00000029848
|
SMART Domains |
Protein: ENSMUSP00000029848 Gene: ENSMUSG00000028197
Domain | Start | End | E-Value | Type |
transmembrane domain
|
21 |
40 |
N/A |
INTRINSIC |
TSPN
|
41 |
230 |
2.7e-3 |
SMART |
LamG
|
106 |
229 |
8.07e-2 |
SMART |
Pfam:Collagen
|
506 |
565 |
9.6e-10 |
PFAM |
Pfam:Collagen
|
561 |
623 |
3.4e-10 |
PFAM |
Pfam:Collagen
|
604 |
678 |
2.3e-9 |
PFAM |
low complexity region
|
682 |
724 |
N/A |
INTRINSIC |
Pfam:Collagen
|
772 |
837 |
1.3e-10 |
PFAM |
Pfam:Collagen
|
865 |
938 |
6e-9 |
PFAM |
Pfam:Collagen
|
967 |
1042 |
3.1e-8 |
PFAM |
low complexity region
|
1056 |
1075 |
N/A |
INTRINSIC |
Pfam:Collagen
|
1107 |
1180 |
8e-9 |
PFAM |
Pfam:Collagen
|
1159 |
1218 |
4.2e-10 |
PFAM |
Pfam:Collagen
|
1218 |
1279 |
1.8e-10 |
PFAM |
Pfam:Collagen
|
1270 |
1334 |
3.1e-9 |
PFAM |
Pfam:Collagen
|
1378 |
1443 |
1.3e-9 |
PFAM |
Pfam:Collagen
|
1439 |
1500 |
1.8e-9 |
PFAM |
COLFI
|
1533 |
1733 |
9.34e-34 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This gene encodes the alpha-1 subunit of type XXIV collagen, one of the low abundance fibril-forming collagens found in cartilage. The encoded protein has structural features of invertebrate fibrillar collagens and is expressed predominantly in bone tissue. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 12 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acyp2 |
G |
A |
11: 30,506,362 |
S95F |
probably benign |
Het |
Casr |
A |
T |
16: 36,509,765 |
N402K |
probably benign |
Het |
Eps8 |
A |
G |
6: 137,514,713 |
F339S |
probably damaging |
Het |
Gnaz |
T |
A |
10: 74,991,944 |
L176Q |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,754,741 |
Y134* |
probably null |
Het |
Sall2 |
A |
G |
14: 52,314,571 |
I387T |
probably damaging |
Het |
Sh3rf1 |
A |
G |
8: 61,226,058 |
N45D |
probably damaging |
Het |
Simc1 |
A |
T |
13: 54,539,704 |
R95S |
probably damaging |
Het |
Tas1r3 |
C |
T |
4: 155,861,359 |
V527M |
probably damaging |
Het |
Tbx18 |
A |
G |
9: 87,724,408 |
V228A |
probably damaging |
Het |
Tenm4 |
G |
A |
7: 96,863,502 |
V1319I |
probably benign |
Het |
Utp20 |
C |
T |
10: 88,787,535 |
R1044Q |
probably damaging |
Het |
|
Other mutations in Col24a1 |
|
Posted On |
2013-12-09 |