ZMP
ENSDARG00000039462
Ensembl ID:
Human Orthologues:
COL9A1, COL9A2, COL9A3
Human Descriptions:
collagen, type IX, alpha 1 [Source:HGNC Symbol;Acc:2217]
collagen, type IX, alpha 2 [Source:HGNC Symbol;Acc:2218]
collagen, type IX, alpha 3 [Source:HGNC Symbol;Acc:2219]
collagen, type IX, alpha 2 [Source:HGNC Symbol;Acc:2218]
collagen, type IX, alpha 3 [Source:HGNC Symbol;Acc:2219]
Mouse Orthologues:
Col9a1, Col9a2, Col9a3
Mouse Descriptions:
collagen, type IX, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:88465]
collagen, type IX, alpha 2 Gene [Source:MGI Symbol;Acc:MGI:88466]
collagen, type IX, alpha 3 Gene [Source:MGI Symbol;Acc:MGI:894686]
collagen, type IX, alpha 2 Gene [Source:MGI Symbol;Acc:MGI:88466]
collagen, type IX, alpha 3 Gene [Source:MGI Symbol;Acc:MGI:894686]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43205 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43205
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057652 | Nonsense | 183 | 347 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 4514037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN150230.1 | 9084 |
GRCz11 | KN150230.1 | 9084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCGTCACCTTCCCAGGCCTTTCCGTGCTCTTCAACACCAAATGGCAC[A/T]AAGTGATGGTGGGCGTGGAGAAGGAGCTGGTGACGCTGTATGTGGACTGT
Long Flanking Sequence:
CAGTGGTAAGCAATGTCGCCTCACAGCAAGAAGGTCGCTGGTTCAAATTCCTGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGGATGTTCTCTCCATGTTGGCGTGGGTTTCCTCGGGTTTCCCCCACAGTCCAAACACATGCGCTATAGGTGAATTGGATGATCTAAATTGGCCGTAGTGTATGAGTGTGCATGAGAAACAGCCACTGCATCACTTTATACAACCATATTGAACTGTATGTGTTTTCCACTAGGCTGAACTTTCCCAGAGGCTTCCCAGATGAGTATTCCTTCATGACCACCTTCCGCATGATCAAGAACACCGTGAACAAGGTGTGGAACCTGTGGCAGGTGGTGGACGAGGATGGACTGAAGCAGGCCGGGATGCGTCTTAACGGGGATCAGCAGGCTCTGGAGTTCTTCCTCACCACCCTGGAGGGAGATGTGCAGACCGTCACCTTCCCAGGCCTTTCCGTGCTCTTCAACACCAAATGGCAC[A/T]AAGTGATGGTGGGCGTGGAGAAGGAGCTGGTGACGCTGTATGTGGACTGTCACCAGGTTGACCAGAAGGAGATCAAGAGGAAAGGTTACGTCAACACAGAGGGAGACACTCTGATCGGGAGGCTGGATTCGGACCCCAACACTTCTGTAGTGGTGAGACTCCACACTCTGAGCTTCAGGATTTCTCTAGGTTTTTTTTTTTTAAATCAGTTTGTTTGGTTATAATGTGTTACCGGCAGCACTTTAAGATCTTTTTGAGTTTTCTGTTTTAATTATAATGTATAGAAAAAAGGTCAGACATAAGTTAAATTTATAATTACATTTAGTCAATTTGCAGAATCTTTTTATCCAAAGGGATGTACAAATGAGGATAATAGAAGCACTTTAGGTCATTTAATTTATTGATTTAAAAAAAAATTAATAAATAAATAAAATTTAATAAAATAAAATAAAACTGAATTAAATTAAATTAACTTTTAATTTAATTTAATTTAATTTAAT
Associated Phenotype:
Not determined