ZMP
NP_001177685.1
Ensembl ID:
Description:
collagen type V alpha-3a [Source:RefSeq peptide;Acc:NP_001177685]
Human Orthologue:
COL5A3
Human Description:
collagen, type V, alpha 3 [Source:HGNC Symbol;Acc:14864]
Mouse Orthologue:
Col5a3
Mouse Description:
collagen, type V, alpha 3 Gene [Source:MGI Symbol;Acc:MGI:1858212]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26152 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40170 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20148 | Essential Splice Site | Available for shipment | Available now |
sa45158 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26152
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022993 | Nonsense | 603 | 1535 | 29 | 62 |
Genomic Location (Zv9):
Chromosome 3 (position 54743712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53638054 |
GRCz11 | 3 | 53892717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGTTTTGTATTTGTTGTTTGCAGGGTGCACGTGGGGGAAGAGGAGCA[C/T]GAGGTCCAACAGGGAAGCCTGGAGCCAAGGTAAGAAATCCATCCTTATAC
Long Flanking Sequence:
ATTTGGCTTATTTATGGTAATGGGACTTTAGAGGTTAATTTGTGGTTAATTAAATGTAGAGGTTGATTAATGAATGGAATGTGGTAATTGATTAACCTTCGTGATGGTCCACAGGGATCAGTGGGCTTTCCTGGAACAGCTGGGTTGGAAGGAGAGAAAGGAAAGAGGGTGAGAGGCCAGTGCCGAAGCACACTGTCCGAGGGATTACTTACAAACATACTGTTGAATCATTGCATTTGTGTTTCATTTTTAATATGTTTTCTTTACAGGGACCTGCTGGACAGGCTGGTGCAGATGGTGAAAGAGGTCCAAATGTAAGTCATAAGCTTGCTAGTAAAATAAAAGACCTCAGTGGTTTTACTACATACACATGCAAGGTTTAATGATGAAACAGCCAATAATAATTGATTGGACAATTAGTTTAATCATGCATACTTTATAAGCATATTTGCATGTTTTGTATTTGTTGTTTGCAGGGTGCACGTGGGGGAAGAGGAGCA[C/T]GAGGTCCAACAGGGAAGCCTGGAGCCAAGGTAAGAAATCCATCCTTATACAGATAAAGATCCTGTAGTATCCTTGTAAATAGGCTGCACTGTCTGTGTTTAAATTCATGTGACGTCTCTTTCTTTGTCTTTTGCTCAGGGCTCTGCTGGTCATGACGGCCCACCAGGTGCCACAGGAGAGAGAGTATGTGTTATCTATTACAATTCTCCTCATATCACACGGTCAATCTACCAGACTAATGTGAGATTTCACATTTCTTTTCATTGCTGGAGATAAATGAATAATCGCGTTACTTACTCTCACCTTCAGGGCCCTCAAGGACCGCAAGGGCGCAATGGAGAGGCTGGGCCAAAGGGACCAAATGTAAGTGACCATAAAATAAAATAAATTCTTTTGAGGGAGTGAAGGAATATATCTTAGTTTTTTTGTTCTTTCTTTTCAGGGCCCTCCTGGAAAAGATGGGTTGCCTGGTCACCCAGGTCAACGAGGAGAGCCAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40170
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022993 | Essential Splice Site | 682 | 1535 | 34 | 62 |
Genomic Location (Zv9):
Chromosome 3 (position 54746273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53640179 |
GRCz11 | 3 | 53894842 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACATTTTTGAGCTGGTTTAATAAAGCTCTCTAAATGATCTCTTATTCC[A/T]GGGCAAAACTGGGGAGACTGGACCCACCGGTGACAGGGGCCACCCAGGTG
Long Flanking Sequence:
GTTTATGAGCCATAATCAAGAAGGCGCGACCTCCTTTAGTAGCAATGATGACGTTTTTCATTTAATGGCTCAAAAATGCTTGTAAGTGCCACTTTGTGCCATCAGTACCAAGCTAGAGTAGTCCAGACAACCTATGCAGCAGCACCCAAGTGTGCGAAAAAAAAGGACTGAAGTATGCCTATAGGGGACTTTTTTAACTAACTAAATTAATTTACATAATTTGAAATACTGAAAACGAGATCTGATTTTATGAACAGTGGAAAAGCAATTCTGCAAAATAATTTCTGTTGGATTTATATAAAAATTACTTTTTCATACAGGGATTTCAAGGAAAGACTGGTCCCCCTGGGCCCGCAGGAGTGGTTGGACCACAGGTGGGTCAATCATACAGGCTTGGACGAACATTGCCTTTCTGGTTGCATGGTCTTCATTCACTCCTATGAAGCTATGTAACATTTTTGAGCTGGTTTAATAAAGCTCTCTAAATGATCTCTTATTCC[A/T]GGGCAAAACTGGGGAGACTGGACCCACCGGTGACAGGGGCCACCCAGGTGCCCCAGGACCTCCTGGAGAGCAAGGTCTGCCAGGAGCTGCAGGCAAAGAAGGGACCAAGGTTAGATATCAGCATTAAAATCATCATCATCATCATCATGAAACACACCAAACACATTCATCTAGTTATAACTTACATTGCTGATTACAAGCCATATGTTTCTGCTCATTCAATATGAATAGAGCTCCCAGCATGGCCCAGCGCCTATAAAGAGTGATGGATGACTGTTAATGAGTGAGAGAGTTGTGGAAACAGAGATCCATCTTTCTGTGTTCTCTGGTCTCCAGGGAGATCCAGGCCCCGCAGGGCAGCCCGGGAAGAGTGGTCCTGCTGGGCGACGTGGATTCAGAGGAGAAAGAGGCTTACCTGGCATTCTGGTAACACACCTCAAAGCATCTGAGAGAATATCTTCTTATAATCTCCGCTGTGATGGATGCTGCCTTTACATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20148
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022993 | Essential Splice Site | 718 | 1535 | 35 | 62 |
Genomic Location (Zv9):
Chromosome 3 (position 54746608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53640513 |
GRCz11 | 3 | 53895176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAGAGTTGTGGAAACAGAGATCCATCTTTCTGTGTTCTCTGGTCTCC[A/G]GGGAGATCCAGGCCCCGCAGGGCAGCCCGGGAAGAGTGGTCCTGCTGGGC
Long Flanking Sequence:
ACTGGTCCCCCTGGGCCCGCAGGAGTGGTTGGACCACAGGTGGGTCAATCATACAGGCTTGGACGAACATTGCCTTTCTGGTTGCATGGTCTTCATTCACTCCTATGAAGCTATGTAACATTTTTGAGCTGGTTTAATAAAGCTCTCTAAATGATCTCTTATTCCAGGGCAAAACTGGGGAGACTGGACCCACCGGTGACAGGGGCCACCCAGGTGCCCCAGGACCTCCTGGAGAGCAAGGTCTGCCAGGAGCTGCAGGCAAAGAAGGGACCAAGGTTAGATATCAGCATTAAAATCATCATCATCATCATCATGAAACACACCAAACACATTCATCTAGTTATAACTTACATTGCTGATTACAAGCCATATGTTTCTGCTCATTCAATATGAATAGAGCTCCCAGCATGGCCCAGCGCCTATAAAGAGTGATGGATGACTGTTAATGAGTGAGAGAGTTGTGGAAACAGAGATCCATCTTTCTGTGTTCTCTGGTCTCC[A/G]GGGAGATCCAGGCCCCGCAGGGCAGCCCGGGAAGAGTGGTCCTGCTGGGCGACGTGGATTCAGAGGAGAAAGAGGCTTACCTGGCATTCTGGTAACACACCTCAAAGCATCTGAGAGAATATCTTCTTATAATCTCCGCTGTGATGGATGCTGCCTTTACATAACCGTTAACTGTTCCAATATGAAAGCTGACTTTGTGCAAAAAAGGCAGATTGTGGTTGTATGATTTTTTAGCATGGATCCTTATATTTTTTTTCTTATTTTTGTGCATTAATAGGGCTCTTCTGGTCTGAAGGGTGGAGAGGGCCCCCTTGGTGTTGCAGGGCCAATTGTAAATGATTTTTCTATTGTCTTACACATTTTCCTGTTTGTATGGTTTAAAATATAGTTCACTTTACTAAAATGTTCTGCACAGGGTGCCACCGGAGAGAGGGGATCCTCTGGACCTGCTGGTGCCATTGGCCAGCCTGGTCGTCAGGGGGGTGTCGGCCCTGCTGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45158
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022993 | Nonsense | 1264 | 1535 | 58 | 62 |
Genomic Location (Zv9):
Chromosome 3 (position 54755502)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53649408 |
GRCz11 | 3 | 53904071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCCGCTATGATTGAGCCACTGCCAATCAGAGAGGGGCGCAAAAAG[C/T]GAAGGAGACACTCAAATCGACAAGGATCCGAGTCCAGGGCAGAGGCTGAG
Long Flanking Sequence:
AGGTGAGAAAGGATCTAAAGGAGACCAGGTTGGTATATATTTATATATATATATTTTCTTTGCAATCTTATTTTTCAGCCTCTCTCTGTCTATATGCTATTTGTTTGTTCTGATCTGAGCTCTCGCCTCTCTTATGAAACCTGAGTGAAATATATTGGCAGTGCTTGAGTTGTATCCTGCTGCTCCAACTTGGATAATCCCTCTGAACGAATCGCCATATGAAGCGCTGAGTTGGCAGGTGCCTTTGAGGGATGTGCCAAGTTTCGGGATGCCTGACTAAACTGTTTATGTTTCTCTCCCCTGAAAGGGAGCCATTGGTGCAAGAGGAGATACAGGACCTGCTGGGCCACCTGGACCACCTGTGAGCCATCATAAAGTCTCCTTACTTTTCCGTCCATTACTTTTTACCTTGTCTCCTCATATCTCCCATCACTCCATTTCATCAGGGCCCTCCAGCCGCTATGATTGAGCCACTGCCAATCAGAGAGGGGCGCAAAAAG[C/T]GAAGGAGACACTCAAATCGACAAGGATCCGAGTCCAGGGCAGAGGCTGAGGAAGAGGAAGCGGTTCAGCTCAACATGGAGGATTTCCTACAGGCAGATGAAGCTCTGGATGAGCCGGAAGGCATGGAGGAGGTGTTCGCTTCACTCAACTCAATGAAAACAGAGGTGGAGCTCATGAGGAAACCTCTCGGGACCTTTGAGAGTCCTGCCCGCACATGCAAGGAGCTGATGTTGTGTCACCCCGATTATAAAGACGGTGAGCGAATTTACACACATTTCCCTACAGCTAATGCAATGCTTTCATAGGGGGGATTCACTTAGAATGCCTGCTGATTGTGCCTGTGCTGGTTTATTTGCATACGCTGTCTGTTCACTAAAGGAATTATGCAGATCTAAGCTGAATGGAATTTGCACAATGCAATTCACCATCTTGCAGGCCAGTAATGAGGGTTTGGTTGTGGAAGACGCTATAGACTACCACTGTATGACAAACTTTCTTGA
Associated Phenotype:
Not determined