ZMP
col9a3
Ensembl ID:
ZFIN ID:
Description:
Sb:cb367 protein [Source:UniProtKB/TrEMBL;Acc:A9JTG2]
Human Orthologue:
COL9A3
Human Description:
collagen, type IX, alpha 3 [Source:HGNC Symbol;Acc:2219]
Mouse Orthologue:
Col9a3
Mouse Description:
collagen, type IX, alpha 3 Gene [Source:MGI Symbol;Acc:MGI:894686]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16929 | Essential Splice Site | Available for shipment | Available now |
sa13060 | Essential Splice Site | Available for shipment | Available now |
sa13212 | Essential Splice Site | Available for shipment | Available now |
sa37580 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16929
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055139 | Essential Splice Site | 82 | 679 | 4 | 32 |
Genomic Location (Zv9):
Chromosome 23 (position 534142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 505133 |
GRCz11 | 23 | 517926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCGGGCRCTGCTGGAAGCCCAGGACTGCCAGGCCTGCCCGGTGTGGATG[T/C]AAGTCAACAWTGGAGGATTTTTCCCAATCTGGCAYCCTTTTAYTGTRTAA
Long Flanking Sequence:
TCACAGCAAGAAAGGTTTGAGTCCCAGCTGGGTCAGTTGGTGTTTCTGTATGGAGTTTGCATGTTCTCCCCATCCTCCGGGTGCTCCGGTTCCCCCCACAGTCCAAACACATGCACTATAGGGGAACTGATCAACTACACTGGCCGTAATGTATGAGTGTGTGTGTATATGAGTGTGTATGGTTGTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCGGCTGTGTAAAATATATGCCGGAATAGTTGGCGGTTCATTCCGCTGTGGCGAATTCTGTTGTGTAGATTCAGCACTGAATGATGCATGACTTCATTATTCATTATTAACGTGCAGCAGGTTTTAAAAGCTGGTTCTGAGATTAATAAGATGTGGATCTTGTGCACAGATCATGCTTTGACTTTAAAACTCTTTATTTTGTGACTGAAGGGTCCGAAAGGAAAAGCAGGTAAAGCGGGCGCTGCTGGAAGCCCAGGACTGCCAGGCCTGCCCGGTGTGGATG[T/C]AAGTCAACAATGGAGGATTTTTCCCAATCTGGCACCCTTTTACTGTGTAAATGAAATCTATTATGCATTAAAAAACTGCCTTCTGTAGGGTTTGACTGGTCCAGACGGTCCCGCTGGCAAAGATGGACCACCAGGAGCACCAGTAAGTCATTTATTTAACTTCATCACTCCTTAGCAATTAAATCCTAATCTAATAATGCCAGACGATCTGTCATTGGAAAGGTTTAAGTCTTCTGAACACACACGTTACCTTATGTAAAACACATTTACCCTCACTCTACATCCTGTGGAGCATTTACGGTTACATATTTAAAGCATAGTGTTATAATCTAAACATTAGGCAATCGTAACAAACTATACATCATTTAAAGGAAAAGCATTTCCAGGTTTCGTATCTGGGGATTTTTTCATGATAGATATCACTGAGCAACAGTCATTTATTCATTCACAACAAGAATACTCAGAGTGGTAAAGCATTACTTTGCTACAGCAATCCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13060
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055139 | Essential Splice Site | 261 | 679 | 15 | 32 |
ENSDART00000055139 | Essential Splice Site | 261 | 679 | 15 | 32 |
Genomic Location (Zv9):
Chromosome 23 (position 524008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 494999 |
GRCz11 | 23 | 507792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGGTTCCAGAGGAAAGCCTGGAATTGCTGGCATTATTGGGAAAACCG[T/G]GAGTRACTGCCCTTTGTTTTAAARGTTTATTCTCAAWAAGGTTTARRTCA
Long Flanking Sequence:
CAGATTGAGGAGTTGTTCACAGTGTTTCCTCTAATGTTTGTTCTTCTGGAGAAAGTCTGATTAGTTTTATTTGGGCTAGAATAAAAGCAGTTTTTAATAGTGTTAAAGTCATGTTAAGCTCAATATTATTCACCCCTTCAGCAATATTAGTGTTGGATTGTCTCCAGAACACACAACTGTTATACAATGACTTGCCTAATTACCCTAACTGTACCCTAATTACCCTAGTGAAGCCTTTACATGTCACTGTAAGCTGAACACTAGTGTCTTGAAGAATATCTAGTCTAATATTATGTGCTGTCATCATGCTGAAGAGAAAAGAAAATTATTAATGATTAAAACTACTACTGTATGTTGAAATATATTTTTAAATATTTATTTTGATATATTAAAACAGATTGAACAGTTAGATGCACTCACTGAATGATCTCCGCACTCTCTGTAGGGAATACCTGGTTCCAGAGGAAAGCCTGGAATTGCTGGCATTATTGGGAAAACCG[T/G]GAGTAACTGCCCTTTGTTTTAAAGGTTTATTCTCAATAAGGTTTAGGTCAGGGCTACGGTCTTTATGTTGTGAATAATATTTGCCCTGTGTATCTTAAATAGGGGGATGTTGGAGAAAAAGGACCTCAAGGTTTTAAAGGGCCCAAAGGAGAGATAGTAAGCACTTTTTATCATCAGATCCTTGTTCACACTGCAGACCTTTCCATTTCTGTAGTATAAGGTTGACTAACGTTATCAACATCATCCTCTAAACAGGGGAAAATAGGCCCCAAGGGCGTGCCTGGAGGTGCAGGACCTAAAGGAGAACCTGTGAGGAACATATTTACAGCTTATCATTATTCAAAATATTACATTTATGTCTGATAATAATGCTGTTGTGTTGCCTAATTGTAGGGGATCCCTGGCAGGGACGGGAAGGATGGAACTCAAGGCCTGGATGGTGAAAAGGTGATAATCAGTGTGTGTTTTAAATGCGAATGTCTTTATTTATGTATTAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13212
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055139 | Essential Splice Site | 261 | 679 | 15 | 32 |
ENSDART00000055139 | Essential Splice Site | 261 | 679 | 15 | 32 |
Genomic Location (Zv9):
Chromosome 23 (position 524008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 494999 |
GRCz11 | 23 | 507792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGGTTCCAGAGGAAAGCCTGGAATTGCTGGCATTATTGGGAAAACCG[T/G]GAGTRACTGCCCTTTGTTTTAAARGTTTATTCTCAAWAAGGTTTARRTCA
Long Flanking Sequence:
CAGATTGAGGAGTTGTTCACAGTGTTTCCTCTAATGTTTGTTCTTCTGGAGAAAGTCTGATTAGTTTTATTTGGGCTAGAATAAAAGCAGTTTTTAATAGTGTTAAAGTCATGTTAAGCTCAATATTATTCACCCCTTCAGCAATATTAGTGTTGGATTGTCTCCAGAACACACAACTGTTATACAATGACTTGCCTAATTACCCTAACTGTACCCTAATTACCCTAGTGAAGCCTTTACATGTCACTGTAAGCTGAACACTAGTGTCTTGAAGAATATCTAGTCTAATATTATGTGCTGTCATCATGCTGAAGAGAAAAGAAAATTATTAATGATTAAAACTACTACTGTATGTTGAAATATATTTTTAAATATTTATTTTGATATATTAAAACAGATTGAACAGTTAGATGCACTCACTGAATGATCTCCGCACTCTCTGTAGGGAATACCTGGTTCCAGAGGAAAGCCTGGAATTGCTGGCATTATTGGGAAAACCG[T/G]GAGTAACTGCCCTTTGTTTTAAAGGTTTATTCTCAATAAGGTTTAGGTCAGGGCTACGGTCTTTATGTTGTGAATAATATTTGCCCTGTGTATCTTAAATAGGGGGATGTTGGAGAAAAAGGACCTCAAGGTTTTAAAGGGCCCAAAGGAGAGATAGTAAGCACTTTTTATCATCAGATCCTTGTTCACACTGCAGACCTTTCCATTTCTGTAGTATAAGGTTGACTAACGTTATCAACATCATCCTCTAAACAGGGGAAAATAGGCCCCAAGGGCGTGCCTGGAGGTGCAGGACCTAAAGGAGAACCTGTGAGGAACATATTTACAGCTTATCATTATTCAAAATATTACATTTATGTCTGATAATAATGCTGTTGTGTTGCCTAATTGTAGGGGATCCCTGGCAGGGACGGGAAGGATGGAACTCAAGGCCTGGATGGTGAAAAGGTGATAATCAGTGTGTGTTTTAAATGCGAATGTCTTTATTTATGTATTAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37580
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055139 | Nonsense | 379 | 679 | 22 | 32 |
Genomic Location (Zv9):
Chromosome 23 (position 520626)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 491617 |
GRCz11 | 23 | 504410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTCCTCCCTCAGGGTGAGATCGGCATCCCTGGAGAGCGAGGAGAGGCC[G/T]GAGGCAGAGGTGTGGCTGTGAGTATACACTACTAAACTCTTTAAAGCTAG
Long Flanking Sequence:
TACAGCTCATGTGCTTTATTCAGTGTTAAATGCCAATAAAATCAGTGTGAATGCTGATTTACGTGATGTTTATTGCTGTACTTCTGACAGCAGCAGCAGCAGATAGTTCAGCTCAGATCTGGAGAATAAATGAAAGAGTCTGAAACTGAGCTGAGACTCAGAGCAAACCAACACATATCAGTGATTCAGCATCTACATTTAATCATGCTCCGGCATATAACGCACATGTTCACAGCAGAATATCTGACTTGAGCGTTGTTTTTCAGATAAACAGGAATGCTCACTAATTTTTAAATATCTGTCAATATTTTATGGTATTTTTATGTTTTAGTCAAAAACTTACATACAGCACCTTTAATGCATATATTAATGACTACCGGCCTCAGCTGTATCCCTTTTAGCACTATTCCCACATAATAAGTAAATTTTTGAAAAACGTTTAGTAAATGCGAGTCCTCCCTCAGGGTGAGATCGGCATCCCTGGAGAGCGAGGAGAGGCC[G/T]GAGGCAGAGGTGTGGCTGTGAGTATACACTACTAAACTCTTTAAAGCTAGGATTAATAAACTGCTTTAATCCTGAGTATTCTCATATGATATCTGCATGTTCATTAGGGTGGCGTTGGAGTACCTGGAAACACTGGACCACAAGGTGTGAAAGGATTCCAGGTGAGCTGCGCATGTGTGCATTACTGTACAACAGTGTGCGATACAACTGTTATCTCCTAATGAAGTGCAATGAACTCAATTGATTCAGTTAACTTGCGTTTGTATCTAGATATATTGCTAACTGGGGATTTAGTGAGCTTATACACACTGCAAATAATGCTTTACTTGTTTTTTACTTACTTCGTTTTTGTCTTTTTTATAGTCCAAATATCTACAAACTTTTAAATCAAGAAGCATTTTCTAGACGAGCAACACATATAGTCTTGTATGAGTAATAATGAGTCAAAATGAAGAGAGTTTTTTATTAAAACAAGCAGAATAATCTGACAATGGAGGATA
Associated Phenotype:
Not determined