ZMP
crtap
Ensembl ID:
ZFIN ID:
Description:
cartilage-associated protein [Source:RefSeq peptide;Acc:NP_001001406]
Human Orthologue:
CRTAP
Human Description:
cartilage associated protein [Source:HGNC Symbol;Acc:2379]
Mouse Orthologue:
Crtap
Mouse Description:
cartilage associated protein Gene [Source:MGI Symbol;Acc:MGI:1891221]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29258 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa36907 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29258
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010104 | Essential Splice Site | 153 | 396 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 44212399)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 43040167 |
| GRCz11 | 19 | 42609604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGATAAACGGGAGCCATACAAGTACCTGCAGTTCGCCTACTTCAAAG[T/C]GAGTAACGTAACGTTGCTGCTTTACTCACGTTTATTTAGTATACGTTTAT
Long Flanking Sequence:
CTGCTACTTTTTTGGGGGGGTTGCATCTCCATAAGCCACCATGGCTTCCTCATTCCATTGCATCCGAATTGCATTATTAATAATCTCCTTTTCCGTTTGCGTCCTCGCGCAGTATGAGAAATATAACTTTCGCAGTTTCCCACGACACGAGCTGATGCCGCTGGACTCCGCGTACCGACATGCGTTAGACCTGTACAGTGAGGAGAAGTGGAAGGAGAGCGTGGAGTTTCTGGAGGTCAGTCTGCGGCTCTACCGGCTGCTCCGGGACAGCGAGGCCTTCTGTAACCTCAACTGCAGCTCGGTCAGACTCGACGATGAGACCCGTTTCAGCGACTTTCCCGAGCTGCAGGCCTTCGGTAATGTGATGAAGAGAGCTCAGTGTTTGAAGAGGTGCAAACAGGGGCTACCAGCCTTCAGACAGACCCTCCCCAGCCGGGACACCGTCGATGAGTTTGATAAACGGGAGCCATACAAGTACCTGCAGTTCGCCTACTTCAAAG[T/C]GAGTAACGTAACGTTGCTGCTTTACTCACGTTTATTTAGTATACGTTTATTCATAATCAGGTAGCCTATTAATGTTAAGTTAAGTTAAGTTAATGTAAAGTTAACCATACATAATTTATGTATGGAATGATATGTATGGATCATGTTTCACACTTTACCTTAATGTTTCATAAATTAATGTATTTACTAACATGAACAAATTATGAATAATGTACAGCATTTATTAGTAATAGTTCAACATTTATAATGCATTATTAAAATCCAAATTTATGCTTGTTAACATTAGTAATGCACTGTGAGTTTACACGAACTTAACAAACAGCTGCTGTATTATCATCAACATTGACCAACATGAACAAATACTGTAATACATGTATTTTTCATTGTTTGTTCATGTTAGTAAATGCATGATTTAACATTAACTAATGAAACTTTATTGTAAAGTGTGACCCACTATGGTAACACTATAATAATGTTGCATTTGTTCATGTTAGTTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36907
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010104 | Nonsense | 221 | 396 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 44215129)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 43042897 |
| GRCz11 | 19 | 42612334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTTCATTCGGGCCGTGCGAGCGTATAATGGAGATAATTTCCGAACGT[C/A]GGTGTCAGATATGGAGCTGGCACTGAGAGACTTTTTTAAGGTATACGATG
Long Flanking Sequence:
TCCGCTGCACACACATTCCTGCTGAAGCATCCTGATGATGAGATGATGCAGAGAAACATGAACTACTACAAGAGTTTACCAGGAGCTGAGGACCATCTGAAAGACCTGGAGACCAAATCATACGAGGTGAGACCCCCATACACAAAACACTGGGCAGATCAGTCCTCATAATCATCTGCTGGATAATGCAACTTGAGAGGTACTGATATTAAAGAAAAATTATGACAGGGCAAATATTCGAGGTGTTTTACATTTTTAGCACTGTTGGCCCTTTTGGGTTAAATTGCTTAGGGCCCCAAAATGATTAAATCTGCCTCTGCCTTTAACTGTATATAAAATGTATCTACAATAATATTGCATTACTACATTTTTGCCTCGTATCAAGTATGAAATGACAGTAATAAACATGCTGTTTAAAGTCATGCTACTTCTTTATCTTCTGCTTCAGATGCTGTTCATTCGGGCCGTGCGAGCGTATAATGGAGATAATTTCCGAACGT[C/A]GGTGTCAGATATGGAGCTGGCACTGAGAGACTTTTTTAAGGTATACGATGAATGTATCGCCGCATCAGAAGGATCCAGACAGATTAAAGACTTTAAAGACTTTTACCCGTCCATCGCAGGTTGGCATGATAAACACACACTCTTTTATGTCCTCTGTAGCGTAAGATAAAACACACTGTAATAACATGCTTGTTTTTTGCCTTTAGATCATTACTCGGAGGTTCTGGAGAGGAAGGTTCGCTGTGAGAGCGAGCTTACGCCGGTTGTTGGAGGATTTGTTGTTGAGAAATTTGTGGCGACTATGTATCACTACCTGCAGTTTGCCTATTATAAATGTGAGTCAGCAAAGTTGTGCTTTTGAACTAATTTTGTGAGACATAACAGTGATGTGTGAAGATGTTTTGGTTCAGTAAGATCTATTTAAGATAATAGAGAAGCCTTTTATGCTTGCGAACATTAGATATATTTGATTATAATATATCAAAAACAGTAATACTGTG
Associated Phenotype:
Not determined