ZMP
si:ch211-212d10.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate cartilage intermediate layer protein, nucleotide pyrophosphohydr
Human Orthologue:
CILP2
Human Description:
cartilage intermediate layer protein 2 [Source:HGNC Symbol;Acc:24213]
Mouse Orthologue:
Cilp2
Mouse Description:
cartilage intermediate layer protein 2 Gene [Source:MGI Symbol;Acc:MGI:1915959]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24147 | Nonsense | Available for shipment | Available now |
sa43811 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37492 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15010 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24147
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061430 | Nonsense | 213 | 1255 | 5 | 10 |
ENSDART00000132684 | Nonsense | 99 | 1141 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 18705011)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 18455946 |
GRCz11 | 22 | 18480924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCACTGAAATCTTGACTTAATAGCCATGTGGAGCCAGTGGGGTTCATG[G/A]GGAGCTTGCTCAGTAACCTGTGGAAAGGGACGGAGGACAAGACGTAGGAC
Long Flanking Sequence:
ATAAGGTATTTGTGCATACAGATTTGCTGCTCACTGGATATTTTCTCTTTTTGTACCATTCTCTGTAAACCCTAGAGATGGTTGTGCATGAAAATCCCAGTAGATTAGAAGTTTCTGAAATACTCAGAGCAGCCCATCTGGCACCAACAACCATGCCACATACTGATACTCGGTTTGAACTGCTGCAGATCGTCTTGACCACGTGTACATGCCTAAATGCATTTAGTTGCTGCTAATTAAAAATTTGCATTGACAAACAGATGGACAGTACCTTATAAAGTGGCCAGTGAGTGTATATAAAAGTATGTTATGTATGAGTGTATTTTAGTATGACATTTGCATAAATTTGATCAGGCTTTTTTTCTAGCATCTACTGTAATTTACACCATAAACCTGATATATTAAAGAGGTGCAAATTTTACTAACACAACAATAGTTAACTGCTCCTATTTTCACTGAAATCTTGACTTAATAGCCATGTGGAGCCAGTGGGGTTCATG[G/A]GGAGCTTGCTCAGTAACCTGTGGAAAGGGACGGAGGACAAGACGTAGGACATGCCACAGATCTTCTACTAAGATTCAGTGTACAGGACGACCCATAGAGGTGCAAAAGTGTGGAAATCCATGCCCAGGTGAGGTGTATTAAAACAAATATGTTTTGTCAACCTACAATAGTTCTCTTGACTACATAGAAATCAAAAATTATTTTACAGTGAAATGCAAACGTGTCTGTCCTGGGGGACGTCCCGATAAGAGCTGCAGCTACTGTATCTGCGATGGACAGGCACTACATGGGGAAGTCTTCAGCATTACAGGGGTCCCAGTGATGAATGCCACGGTGGCTTTGGCCAGCCAAGCCAAGATTATCCGTGCCCACACTGATGCCAAGGGTCAGTTCAAGATGGATGGGCTGTGCATCAGTCCTCAGACCCAAATTGTCATTAGAAAGGATAAATTTGCACCTGCCACTCTCCCAGTGTCCAACAACAGTACTGATGAACTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43811
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 |
---|---|---|---|---|---|
ENSDART00000061430 | Nonsense | 424 | 1255 | 8 | 10 |
ENSDART00000132684 | Nonsense | 310 | 1141 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 18705891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 18456826 |
GRCz11 | 22 | 18481804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACAATTTTCAAATATGACGAAGATTTGATATTGCGAGACCTCAAACCA[G/T]AGCAGTCTGGGCAATATCACTGCAAAGCAACTAGTCTGACAGGCAGCATC
Long Flanking Sequence:
CCAAGGGTCAGTTCAAGATGGATGGGCTGTGCATCAGTCCTCAGACCCAAATTGTCATTAGAAAGGATAAATTTGCACCTGCCACTCTCCCAGTGTCCAACAACAGTACTGATGAACTTTGGGTACGGGCTATCTTGCAATCATCAGGTAAAAAGGACAATTTTAAAAAGTTGAATAATTTCATGTACATTTGAACAAAGCTCACTATGTGATGGATTGTGCTGTTTTATGTCTGACAGAAAAGCCATATATTGAGAAGCATCCTGAAGACAAAGTACGTTACGAGGGACAACGTGCAACTCTTTGCTGTAGAGCAACAGGATCACCAAAACCTGACAAATATTACTGGTAAAAACAATGAATTTGACAGTTTTTTGACAAATAGTGGTAATGTCCTAGTAATTATCATTTGTTTATTGCAAAGGTACCACAATGGAACCTTACTGAATCGTACAATTTTCAAATATGACGAAGATTTGATATTGCGAGACCTCAAACCA[G/T]AGCAGTCTGGGCAATATCACTGCAAAGCAACTAGTCTGACAGGCAGCATCAAGTCTACTTCAGCGGTCCTCACTGTTTTCAGTAAGTGCAAAACCATTTTAACAGTCAAGAGGGATTTGCCATTATACTATTTTTGCAAATGTCCCTAAAGTACTCTATTAAATATTGAAGGCTTCGATTAAATATTAAAGCCTATAATGTCAAGTGACATGTGGTGAACAATATTTTATTATGTTTAAGTTGGTAGAAATTACCACTTTCTAAACAAGGAATGACTGGCAAAAAGTTGTGGTGGGCAGAATAAAGTTCCTAAATCCCAACCGCTTTTTATATTAAAGTGAAATCCAAGCTTGTCGATAAATCCTATTTTTTCATTCTCGGACAAGTATGCATTTCCACATTCGCCGACATAACTACACATTGTAAAAATTCCCATGATGCTTATTATCCAAGATATAGATTGTCAGAAATAGTCTGCCGAAATGTGTGCTAAAGCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37492
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061430 | Nonsense | 982 | 1255 | 9 | 10 |
ENSDART00000132684 | Nonsense | 868 | 1141 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 18708727)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 18459662 |
GRCz11 | 22 | 18484640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTTGATGCCAACCACTTTCGTTTTTTCCGTGTTGAAAAAGATAAATA[T/A]GAATACAATGTGGTACCCTTTCAGGAAAGTGACCTTACATCTTGGACTGG
Long Flanking Sequence:
GTTAGGGCATACATGAGTGACAAGTTCTTGCCCAACGAGCAACTCGAAGGAGTTGTAATAAACTTGATTAACCTGGAACCTAAACCTGGTTACTCGTCAAATCCGCGAGCCTGGGGTCGCTTTGATAGCGTGATAACAGGACCAAACGGTGCTTGTCTTCCAGCTTTCTGTGATGCTCAGAGGGCTGATGCTTACACAGCTTATGTAACGGCTATAATGGGAGGAGAGGAACTAGAAGCAGCTCCCTCAATGCCAAAAATGAACCCAAACATTATTGGTGTGTCTCAGCCATATTTAGGGAAGTTAGATTACCAGCGTTCAGATCATGAGGACTCAGCACTCAAAAAAACAGCCTTCCGAATAAACCTGGCCAAACCAAACCCTAACAATTTTGATGAAACAAATGGACCCATCTATCCTTTCCAGAGTTTAATTGCATGTGAAAATGCACCTGTTGATGCCAACCACTTTCGTTTTTTCCGTGTTGAAAAAGATAAATA[T/A]GAATACAATGTGGTACCCTTTCAGGAAAGTGACCTTACATCTTGGACTGGAGACTACCTTTCCTGGTGGCCAAATCCACAAGAGTTCAGAGCTTGCTTCATTAAAGTTAAGATTCATGGAGCTACAGAAATTATGGTAAGGTCAAGAAATCTTGGTGGGACTCATCCTCAAACAAGAGGTCAGTTGTATGGTATTAGAGACATTCGCAGTACTCGAGACTTACACCATCCCAACACCTCTGCTGCTTGTCTTGAATTTAAGTGCAGCGGGATGCTCTTTGATCAAGGTAGTGTAGACAGGTCACTCATTTCTGTGATCCCACAGGCCAACTGCCGTCGTATAGGCATTAACAGTCTCCTGCAAGAGTATCTGATAAAGCATCCCCCTGTTCTTCAGAATAATGAGTCACATGCATTCAATATGTTAGCACCCGTTGATCCCCTTGGACACAATTATGGAATATACACCGTCACGGACCAGAACCCACGCGTTGCCAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15010
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061430 | Nonsense | 1114 | 1255 | 9 | 10 |
ENSDART00000132684 | Nonsense | 1000 | 1141 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 18709121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 18460056 |
GRCz11 | 22 | 18485034 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATTAACAGTCTCCTGCAAGAGTATCWGATAAAGCATCCCCCTGTTCTT[C/T]AGAATAATGAGTCACATGCATTCAATATGTTAGCACCCGTTGATCCCCTT
Long Flanking Sequence:
ATGAAACAAATGGACCCATCTATCCTTTCCAGAGTTTAATTGCATGTGAAAATGCACCTGTTGATGCCAACCACTTTCGTTTTTTCCGTGTTGAAAAAGATAAATATGAATACAATGTGGTACCCTTTCAGGAAAGTGACCTTACATCTTGGACTGGAGACTACCTTTCCTGGTGGCCAAATCCACAAGAGTTCAGAGCTTGCTTCATTAAAGTTAAGATTCATGGAGCTACAGAAATTATGGTAAGGTCAAGAAATCTTGGTGGGACTCATCCTCAAACAAGAGGTCAGTTGTATGGTATTAGAGACATTCGCAGTACTCGAGACTTACACCATCCCAACACCTCTGCTGCTTGTCTTGAATTTAAGTGCAGCGGGATGCTCTTTGATCAAGGTAGTGTAGACAGGTCACTCATTTCTGTGATCCCACAGGCCAACTGCCGTCGTATAGGCATTAACAGTCTCCTGCAAGAGTATCTGATAAAGCATCCCCCTGTTCTT[C/T]AGAATAATGAGTCACATGCATTCAATATGTTAGCACCCGTTGATCCCCTTGGACACAATTATGGAATATACACCGTCACGGACCAGAACCCACGCGTTGCCAAAGAGATCGCCATTGGCCGCTGCTTTGATGGAACTTCAGATGGTTTTTCCAGGGAGATGAAGTCAGATTCTGGAGTGGCACTGACGTTCAGCTGCCCTAAAAGAACTGTGAATCGCGAGAGCTTATTCCAACGCTTGCAAACAAATCCAGGCCTAACACTAACACAGATGGCACGGGAGATGAGGGAGTCCCAGGGATTACAAGTCAGAAGAGGGTCAACTCAAATGGTGGCCTACCCCTTTGGCCAACAGGGCAGGAGCCAGAACCGCAGAGCCACGAACACTAACAGAAGGAGACCTGCTTCAAGGACACAACCAAGACAGTAGATCTTTAGGTGAGTTCATTGAGTGCACTTTAAAATAAAAAGATGAACAAAAACAAGATTTTTATGAAAATAA
Associated Phenotype:
Not determined