ZMP
si:ch211-106n13.3
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC563353 [Source:RefSeq peptide;Acc:NP_001038479]
Human Orthologue:
COL21A1
Human Description:
collagen, type XXI, alpha 1 [Source:HGNC Symbol;Acc:17025]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15157 | Nonsense | Available for shipment | Available now |
sa39942 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33044 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14259 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15157
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083654 | Nonsense | 567 | 873 | 14 | 24 |
ENSDART00000140294 | None | None | 195 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 50589056)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50284588 |
GRCz11 | 2 | 50018818 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TKGGATTCAAAACTGTACTTAAAGTGTGTSTTTGTGGTTTTAGGGTAWAC[G/T]AGGGCTTCCTGGAGAGATGGGGCCTGCWGGAGCTCAAGTAAGAACCYARA
Long Flanking Sequence:
ACTGAAAGTTAACTCTACTCATTTGAAAAGAGTTTTGAACTCAGTGTTAAAGGTAATGAGTTAATTAAATACCTCATTACTTCAACTTAAATGGAGTGAGTTCACTGTACTCATATAGATAAGGTTTTTTTTTTAACTCAAATGGTTTGTTGCAATCGGTTTCCTGAAACAGTTTGGTCCACTGGGTTTTACAGTACTCAGTTGGTTTGAGTTCTCTTCATTCATTGGATTTTACTGTACTCAACTTGTTTTTGCAAATGGGTAAGTTCACAGTACTCATTAGGATTAATTTTTGAACTTAAATGGTTTGAGTTACCTTAACTTTATGGGTTTTAAAGTGTACAAATTTTAACAAGTTTGCCACTAGATCAAAAAGTTAAAAACTGACAAGACATTGTTGATATTTGATGGTAATTTGACGTTTTATTTTGTGCAATCGGGAAAGTATTATGGGATTCAAAACTGTACTTAAAGTGTGTGTTTGTGGTTTTAGGGTATAC[G/T]AGGGCTTCCTGGAGAGATGGGGCCTGCTGGAGCTCAAGTAAGAACCCAAAATATAACTGAAAATATTAAGTATACATACAATTGCTGTTAATATTGCTTAATAATTATGTACAGGATGTCTTTAATTGCAATACCATTAAAAAAACTAGCAGAAAATGATCAGTTTTCAACTTTCTACATGATAATATTTGTAATTGAATTTGGGATGAATTGCTCTTATACATTTAGAATGAAACAAACATTAGCATTTTACTCAAATCCATATCTAATAATCCAGGGGTGTCAAACTCTGGAGGGCCGCAGCTCTGCACAGTTTAGTTTCTGCCCTGCTTCAACACAATTATCTGTAGGCATCTGTTACAAAGCCCTGATGTTAGTCGAGGGTTGTGGGGTTTGACATTTATTTAATTAAAATATATTTATATAAACAGTGAATGAGTGGAAAGACAACCAACGTAATGCCAAAAAATGTGTGCTTTTATTTACAATCCCAAAGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39942
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083654 | Nonsense | 645 | 873 | 18 | 24 |
ENSDART00000140294 | None | None | 195 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 50571048)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50266580 |
GRCz11 | 2 | 50000810 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGGTTAAATGCCATCATTTTATATTTGCAGGGTGAATCCGGATCATTG[G/A]GACCGAAAGGAAGTCAGGTATAGTGTGATCGACATCTGTGACATTTAATT
Long Flanking Sequence:
CATTCACACTAATTTTTATAATCACATGATGTCTTAAAACAAAATCACATCACCTTTTTAATGCACATACTGGAATTTGTTCAGTAAAAGTGTTTCCATTATAGTTTATGCGCATCTTTTCTTATCAAATAAGCAAATAAGACGTTTATCCTACTCATTTATGCGCATACGTTTTAGGCACATTTTAAAAATATATGCGCATCTTGACGTTTCCATAAGCCGTTTTTTTATGTGCATCACCAAAATGCACATAACGATAGGTGGATGGAAAATAGCTAGTGAGAAAGCATCTTTAGGCAAAGAAAATGGGCAATATTTTTTTCAGAATAAGCATTGAGCGTGCATATTTTAAATTAAAATTTGCCAAATTACTGTTAATTATTGCAATCTCGACAAAATCTTTGCATTTGATAGTTTTATTCAAAATACTTTATTATTTTTTTTCTTCTGCATGGTTAAATGCCATCATTTTATATTTGCAGGGTGAATCCGGATCATTG[G/A]GACCGAAAGGAAGTCAGGTATAGTGTGATCGACATCTGTGACATTTAATTTCCCTTTGTTGAAAAGAAACATGTTCTGAGAGAGAAAAGAGGAAGTGAAAAAAAAAAGGTGTTACTGCCGTTGCGTTTTCCATAACATGAATTATTATGACATACCAGCTGTTCTACATTGGTTTTACTTGTAAAAGCTGACCTATTCTGGAACTGCACACTCTGTTGTAGTAAGAAAGCGAAGCAGACTGGTTGATCTTGTGTTTTTTTTAATAAGACTAATTATTGCATGCTTGTTTTTCCCCATTATAATACTGTACTGTATATTTTAAAGCATGACAACACTTAAAACTCTTATTTCAGGGCGAGAAAGGAAACCAAGGAGAACCTGGAGTCAATGGAAAACATGTATGTATTTATTCTTCCTTAGTGATGTTGGTAATGCAAGCATACTATTAGATATGAGTTTGAATATCTTTGTAAAACCTACGCCTTAAGCTTTGATGCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33044
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 |
---|---|---|---|---|---|
ENSDART00000083654 | Nonsense | 725 | 873 | 22 | 24 |
ENSDART00000140294 | Nonsense | 47 | 195 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 50560418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50255950 |
GRCz11 | 2 | 49990180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGAACTGTCTCTTTAAGAAGCGATATTCCCTTAACAGCCCAGCTGCCA[C/T]AGCTCCTGCAGGCAATGGAGCAAAGAAGCTGCCAGCACTGTGAGACCAAA
Long Flanking Sequence:
TGAATGAATGATTATGGAAATTAGCTTCTTTGTTGCAGTTCTTTAATTTGTACATTGTCAGCAGAAATACTCATAGATCTTGGCACCCATCTGCTCTTTTATACAATTGCAGTCTCTCGCTATTTATTTTGCCCCGTTTAGCAAATCTGTTTGCTATTCTAATGCCAGATACCAGTCAAAAAGGGATAAGTCACCCAAAAATGTAAATGACCTCATCATCTGATATGTTTTTTTTCTTCTGTTGAACACAAAAGAAGATACTGTAAGTACTGTATGCTTGTATCTGGCGCCCATTGACTTCCATAGTAGGAAACATATTACATAGCAAGTCAATATGTACCAACATCAACCAGCATTCTTCAAAATATCTTATTTTGAGTCCAATGGAAGAAAGAAACTCAAATAGGTAATAGGGGAAGGGTGAGTAAATGATGACAGATTTGACTTTTGGGTGAACTGTCTCTTTAAGAAGCGATATTCCCTTAACAGCCCAGCTGCCA[C/T]AGCTCCTGCAGGCAATGGAGCAAAGAAGCTGCCAGCACTGTGAGACCAAACGAGGGCCAGCAGGCGATCCAGGTCCCCCAGGCCCAACGGGCCCATCTGGACCACCAGGGTATCCTGGCAGGGCAGGGTCTCCAGGATATCCAGGACCTCCGGGCAGCAGAGGGCCTGAGGGAGTCAAAGGTGATTATACTGTGATTATAAATTCACAGGAAGATTAGAGACAAGTACTAAAACGATTTGATGTTTTTCTTATAGGTGATATTGGTCCGATGGGTATAAAAGGTGCTAAAGGACAGGGTGAAATTGGGTTGCCAGGTCCACCTGGCCAACAAGGTAAAAAAATAAATAGAAAATACTAATGCATGACAGTAGTTATTTATTATTATTATTATGGTCACTTTATTTTAAGGTACAGTTCTCGCTTCATAACAAACCATTAACTAATGCTGCGTCCCAATTCGCATACACATACTAAGCCCTAAAAGTATGTACTTTTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14259
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 |
---|---|---|---|---|---|
ENSDART00000083654 | Essential Splice Site | 785 | 873 | 22 | 24 |
ENSDART00000140294 | Essential Splice Site | 107 | 195 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 50560236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50255768 |
GRCz11 | 2 | 49989998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGGATATCCAGGACCTCCGGGCAGCAGAGGGCCTGAGGGAGTCAAAGG[T/G]GATTATACTGYGATTATAAATTSACAGGAAGATTAGAGACAAGTACTAAA
Long Flanking Sequence:
GGGATAAGTCACCCAAAAATGTAAATGACCTCATCATCTGATATGTTTTTTTTCTTCTGTTGAACACAAAAGAAGATACTGTAAGTACTGTATGCTTGTATCTGGCGCCCATTGACTTCCATAGTAGGAAACATATTACATAGCAAGTCAATATGTACCAACATCAACCAGCATTCTTCAAAATATCTTATTTTGAGTCCAATGGAAGAAAGAAACTCAAATAGGTAATAGGGGAAGGGTGAGTAAATGATGACAGATTTGACTTTTGGGTGAACTGTCTCTTTAAGAAGCGATATTCCCTTAACAGCCCAGCTGCCACAGCTCCTGCAGGCAATGGAGCAAAGAAGCTGCCAGCACTGTGAGACCAAACGAGGGCCAGCAGGCGATCCAGGTCCCCCAGGCCCAACGGGCCCATCTGGACCACCAGGGTATCCTGGCAGGGCAGGGTCTCCAGGATATCCAGGACCTCCGGGCAGCAGAGGGCCTGAGGGAGTCAAAGG[T/G]GATTATACTGTGATTATAAATTCACAGGAAGATTAGAGACAAGTACTAAAACGATTTGATGTTTTTCTTATAGGTGATATTGGTCCGATGGGTATAAAAGGTGCTAAAGGACAGGGTGAAATTGGGTTGCCAGGTCCACCTGGCCAACAAGGTAAAAAAATAAATAGAAAATACTAATGCATGACAGTAGTTATTTATTATTATTATTATGGTCACTTTATTTTAAGGTACAGTTCTCGCTTCATAACAAACCATTAACTAATGCTGCGTCCCAATTCGCATACACATACTAAGCCCTAAAAGTATGTACTTTTTTGTGAAGGAAAAATATTTACTTTTGAATGTGTAACAAGAATATGCTAGCTTTGGGACATACTACTTCCTCGTTAACAGATCGCTACGTTGCTTAGTTATGAGCCCTGTCAATCATCCACATTTCTGTCATATTTCATTTCCTACCTTATTGGAGAAGCAGCAGCAGGTTAATCTGCCATTCACAA
Associated Phenotype:
Not determined