ZMP
clasp2
Ensembl ID:
ZFIN ID:
Description:
CLIP-associating protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q6NYW6]
Human Orthologue:
CLASP2
Human Description:
cytoplasmic linker associated protein 2 [Source:HGNC Symbol;Acc:17078]
Mouse Orthologue:
Clasp2
Mouse Description:
CLIP associating protein 2 Gene [Source:MGI Symbol;Acc:MGI:1923749]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13291 | Nonsense | Available for shipment | Available now |
sa36909 | Nonsense | Available for shipment | Available now |
sa16627 | Nonsense | Available for shipment | Available now |
sa18570 | Essential Splice Site | Available for shipment | Available now |
sa12804 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13291
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039871 | Nonsense | 174 | 1529 | 5 | 41 |
ENSDART00000076668 | None | None | 1287 | None | 35 |
ENSDART00000102499 | None | None | 1288 | None | 36 |
ENSDART00000136873 | Nonsense | 174 | 1476 | 5 | 37 |
ENSDART00000139109 | None | None | 1250 | None | 30 |
ENSDART00000144557 | None | None | 1288 | None | 36 |
The following transcripts of ENSDARG00000020345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 44308343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43136111 |
GRCz11 | 19 | 42705548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATACGGTGCTCAGCCCTTGAGTTTRAGTAAATTTGTTCCACATCTCTG[T/A]TCGCTAACAGGAGACCAAAACCCCCAGGTATGAATCTCTGTCTGTGTATG
Long Flanking Sequence:
CTGAGGATCGAACCAGCGATCTTCTTGCTGTGAGGCGACAACACTACCTACTGCGCCACTGTGTCGCCCTTTTCGGTTTTTATGTTAAACAAAAAATAAGATATTGTGAGGAATGTTAGAAACTGGGAACAACTGGTAACACAAATTACCGATTTCCAACATTTAAAAAAAAAAACTTTCTTGTTTTAAACAGAATAATAGAAACCAGTAAGAAATAATATGTAAATATTAAGTGTGTTTTTCTTAAAAAAAAAAAAAAAGGCATGTAATCTGCCAAATTAATCTTGTTTTTCCTTTTGACGTAATTTGATGTTGCTTACTCCATTGGCACATAATTTAACTTGTCTACCAGAAGTAAAGCTGTTGCACTGTTTTGTTTGATGCATGGAAACCTCTTGAACTTGCTGTGAGCGCTGCACTCAGTATTCCTTGTTTATTTTTCTTTCTCTTAGATACGGTGCTCAGCCCTTGAGTTTGAGTAAATTTGTTCCACATCTCTG[T/A]TCGCTAACAGGAGACCAAAACCCCCAGGTATGAATCTCTGTCTGTGTATGTAAGTAATGCCGGGAATGTGTGTGAAAAAGCAAAGTGAGTTGGACTTGCTCTTGCGTTCTGTCCTTTGTTTGTGTGTGAGGGAGGGAGGCTGTCTTCACTAATGTTAGGTTTCTAGACATGTACAGCTCTGCTCAAGCTCCCGCTGGGTGAATGGACCACTCGCAGAGATGAGCATTAGCGTTGGAGGTTGTCAAATGGAAGCAAGATTATTACATTCTATTAAAACTAAAACAAATATTTTTGTTGCTGAAATAATAATGTGACGTCATGTATTCTTGATTGTGAGGGGTTTTTACCTTTGGGAAGAGGTACTGTACTGTTGGTCATCAGTTGGCAGCAATAACCCTTTCGATAGGCCTGTGCAAAACAGTTTCAGGCTTTTATATGCAGTTCTATAGAGTAAAACAGCAGATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36909
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039871 | Nonsense | 360 | 1529 | 11 | 41 |
ENSDART00000076668 | Nonsense | 128 | 1287 | 6 | 35 |
ENSDART00000102499 | Nonsense | 128 | 1288 | 6 | 36 |
ENSDART00000136873 | Nonsense | 360 | 1476 | 11 | 37 |
ENSDART00000139109 | Nonsense | 121 | 1250 | 4 | 30 |
ENSDART00000144557 | Nonsense | 128 | 1288 | 6 | 36 |
The following transcripts of ENSDARG00000020345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 44345869)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43173637 |
GRCz11 | 19 | 42743074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACAGCTGAAGAAAATCCGATCTCTGCTGGTTGCCGGAGCAACAGACTA[T/A]GATTGTTTCTACCAGCACCTGCGCCTGTTGGATGGCGCCTTCAAGTTGTC
Long Flanking Sequence:
GTGGTGGTGATGATGATTATGGCGTCTCACATTTATTTTAATTTTAATTAACGTGCGCTTTGTTTCACAAACTGTAACATTGTAGCAAATTAAGAACAGAGCAAATAATCTACAGGGCTGGTGACTAGTAAAAAAAGCATGTGAGCAGCTCTCTATCAAGCTCATTAGCATTATCTCTGCATATTTCATTTACATGTGACCGAACTTGTTTCCTAAACCAATTTGGAGAAATTTAGTAGTATTAGTGTTTCCCATGGAAATCAGACAGTAGCATTAGGATGCACTAGACCTTGAGTTTTCTTTACATCGGGTTTGTTTTCATATTTAAATCCTCTATTCAATATTTTACAGACATGCCCAGAGTTTCTTGGCTTTTATGTTGTCCTCCTTATGCATTTGCATTCATTTGTGACATGCTCTCTCTGATGTGGTCTGGTTTCTCCTGTCGCTTCACAGCTGAAGAAAATCCGATCTCTGCTGGTTGCCGGAGCAACAGACTA[T/A]GATTGTTTCTACCAGCACCTGCGCCTGTTGGATGGCGCCTTCAAGTTGTCGGCTAAAGACCTGCGTTCCCAGGTGGTGCGGGAGGCTTGCATCACAGTGGCGTGAGTCACAACTTTAGCTCTGGTGTTAGAAAGATGTGTTTGCATTGTTTACATTTTATTAATCACATCACTGTGAACTGTACGCCAAAGCTGAGTGGACTTTTTTGAAGATGAGAAAGTACACCCATTGGATGACTCTTGTCTATTAGGCTGTTGTTGGTCTTTTGCTTTTATACATGCGGTGCTTTTATAAATGCGGTGCTTTTGTTGTGCTTTAGAATGCAATATTTAAATGTTTGTAAAAAAAAAAAGCCTATTGTACAATGCACTAATATTATGTGTTACCATAAACAATGGATTTGACCATACCATGAAATAAACGGTGGAGGATATTTTAAAATTATAGACTTTTTATTTTGGCTTTATGATATACAGTCAAAATTATTAGCCATTTTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16627
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039871 | Nonsense | 469 | 1529 | 14 | 41 |
ENSDART00000076668 | Nonsense | 237 | 1287 | 9 | 35 |
ENSDART00000102499 | Nonsense | 237 | 1288 | 9 | 36 |
ENSDART00000136873 | Nonsense | 469 | 1476 | 14 | 37 |
ENSDART00000139109 | Nonsense | 230 | 1250 | 7 | 30 |
ENSDART00000144557 | Nonsense | 237 | 1288 | 9 | 36 |
The following transcripts of ENSDARG00000020345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 44347361)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43175129 |
GRCz11 | 19 | 42744566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAGATCTCTTTCTTCTCTCWCCRTCTGTCAGGCGCTGTTATGAGTTCT[T/A]GGATCTKCTGCTGCAGGAATGGCAGACTCACTCTCTAGAGAGGTAAATMA
Long Flanking Sequence:
CGCGTCTAATTCCTCTCATCGCTAGTAACTGCACATCGAAATCTGTGGCCGTCCGGAGGTGAGACGTTTCATCTGTTTTTAAGGAGCACCATATATTTCTGTACACTGGGATATACAACAGGAATGTTTTGATTTTGTTTATTATCCACATATATGATGTGCATATATTCAATTCAAGTGTGTTTATATATCGATTTTTACAATAATTATTGTTTTAAAGCAGCTTTGCAGTATATATACTACAGCAAAACTAACAGATAAATCACTAGGATTTATCTTAACCTGGTTTTTAGCCTGCTATAGAGTAGGCTAGCTTCAGAGAGTAAGTCTCTGTCGTAAGTTCATTTATCCTGGTTTCATGCAACTCTATCAGGGCTAAATTCACCCAGGATATCTTGAAAACCCCCCAGTTTAATCCCCGATTGGATTTGCATACCTGTTCATTTATTTCTCAGATCTCTTTCTTCTCTCTCCATCTGTCAGGCGCTGTTATGAGTTCT[T/A]GGATCTTCTGCTGCAGGAATGGCAGACTCACTCTCTAGAGAGGTAAATCACAACACCCGCTAATCTAGCACTGCCTACTGATGCTGAAGGCCATGACTAGCAGCTGCTTTTCTCTCTTCTGTGTGTCAGGCATGCGGCTGTGCTGGTGGAGAGTATTAAGAAGGGAATCAGAGATGCCGACGCAGAGGCTCGAGTGGAGGCCAGGAAGTGAGTCCTCAGATTGTCTCATGTTTTTTTTCAGGGTTTCTTATTTCCTGCTCTTGGCGCATGTTCTACTGTAATCTGTTGTAGTCCTTTACTAATGCATGGAGGGCTGGTAATATAATCATCAATATCTATCAACAAACTGCATCACATGACCTCCCTTCCAAGCACACACACACTCTTGTTTTTGTCCTTAAAGCAGTCTGACTACAGTCGCACATCTGTTTGACTAGGGCCCTGTTTACCCTAATGCGTTTTAGTTTGAAAACGCATAAGATTTACTACGGTTACGCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18570
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039871 | Essential Splice Site | 938 | 1529 | 29 | 41 |
ENSDART00000076668 | Essential Splice Site | 677 | 1287 | 22 | 35 |
ENSDART00000102499 | Essential Splice Site | 677 | 1288 | 22 | 36 |
ENSDART00000136873 | Essential Splice Site | 885 | 1476 | 25 | 37 |
ENSDART00000139109 | Essential Splice Site | 659 | 1250 | 18 | 30 |
ENSDART00000144557 | Essential Splice Site | 677 | 1288 | 22 | 36 |
The following transcripts of ENSDARG00000020345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 44377533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43205301 |
GRCz11 | 19 | 42774738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAGTGAATGCATGTATKCAAGTTGAATTTGTCCTTWCTCTCTGTTTC[A/T]GTCGTGTTGAGCTGAARAGGCTGTGTGAAATCTTCACCAGGATGTTTGCA
Long Flanking Sequence:
CGACCCTGAATTAATAAAGGGACCAAGCCGACAAGAAAATGAATGAATGAATGAATATTTTAGTCAGTTTGACTGATTTAAGTTGAGATGACTAGAAAATTTTACGTGATTCAGACCCGGAAGGGACGTGATGGTGGAGAAAAAAAATGAGTGGGAGAAAAAAAGAGTGAAAGGTAAACATATTTTTGAAAGTTTTTGCGTTCCCTCGCAAAGATATTTTGCGATATCTCACAAAACTGTTGTTCGACAATTTCACCTCATACATGACAATCCTGTTTTTGCCGGGATTCTCCCATATTTTACCATTATATCCTAGTATTAGGTATTTTCCCATATTTCTCTCATATTTTAATTCTTGAAAGCTTATTGATATTAATATAAAAATGTCTGAATTCACTTTTTTTCCATTAAACCTGAGCGTCGATCAGCGCCCCTCATATGCAACCTCTGAATCAGTGAATGCATGTATTCAAGTTGAATTTGTCCTTTCTCTCTGTTTC[A/T]GTCGTGTTGAGCTGAAGAGGCTGTGTGAAATCTTCACCAGGATGTTTGCAGACCCACACAGCAAGGTACCCTCGCATGCCGCTTTCAGACACGCTGCAGAACAAACACACACACTTCTGCAGACATAACCCCGCATGATCTTCATGCATCACACAAAACCGCTTGACTGTATCGGATTCTGCCTCACCCACAGCCCGTGTTCTGGCCACAGACACACAGATCAACACTCTCAGGCATGTGCAGTGCACACTAACTCTCGGGTTAAAGACCATGGCTAATCGCATGGTTTGGTTTTGAGTGGATTTCTGATTTCAGGCTCGTTCGCTCGTCTTTTTTCCAACCATTGCAGCGCCGACTAAAACGTTTCTGGCATAGCTTTTCTCTCTTTCCTGCTTGCACTCACCTCACTCATATGCTGGGACTGTCACAAATCCTAAAATATAATAAATAGACAAACAGCTTAAAATTAGATCTGCATGATATTGGAAAAATGCTTACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12804
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 |
---|---|---|---|---|---|
ENSDART00000039871 | Nonsense | 1003 | 1529 | 30 | 41 |
ENSDART00000076668 | Nonsense | 761 | 1287 | 24 | 35 |
ENSDART00000102499 | Nonsense | 762 | 1288 | 25 | 36 |
ENSDART00000136873 | Nonsense | 950 | 1476 | 26 | 37 |
ENSDART00000139109 | Nonsense | 724 | 1250 | 19 | 30 |
ENSDART00000144557 | Nonsense | 762 | 1288 | 25 | 36 |
The following transcripts of ENSDARG00000020345 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 44385111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 43212879 |
GRCz11 | 19 | 42782316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTCACACAGCTGCTGAAGAAAATGGGAGCGGATCTGCTCGGCTCAGTA[C/T]AAGCCAAAGTACAGAAAGCCCTGGACGTCACAAGGTATGCTGTTTTCACA
Long Flanking Sequence:
GGTTTGCTAAATTTTATGCATATGCACACCCCAACAAAAGCTTCCCAATGTATCTAAAATTGCACTCATGTGGAGAAATTATACTTAATATTGAAATATACATCGCAGTAAAGTAAATCAGTGTCTTACAAATTTTTATGAAACAAAGTTTTTTTTCCCCCAATATCCTGCAGCCCTAGTGCCCTATACAGGGTTAGTGCATGTCACAATTCTCTGCCATTATATAAATGTATTTTCTTTTTGTGTTTCAAAAACAAAAGTAGCTTATGCAATATCAGAATAATGTTAGTGTGAGTAAATGATGACTGATTGAGAGTGGTACAGTGTGTACAGTATTTCTGATCTCCCTTGTGCCGCTGCTGTTTGTACAGGTGTTCAGCATGTTTCTGGAGACGCTGGTGGACTTCATTGCTGTTCATAAAGAGGATCTGCAGGACTGGCTCTTCGTGCTCCTCACACAGCTGCTGAAGAAAATGGGAGCGGATCTGCTCGGCTCAGTA[C/T]AAGCCAAAGTACAGAAAGCCCTGGACGTCACAAGGTATGCTGTTTTCACAAGAATGTTTTGATAATGAAACAGTGTTTCTTTGGACATATTGCCTGGTTAAGGCCTGTCATTAGCCATGTTTCCATCCAAAGATGTGAATTATAGCTCTTTTCCAGTGAGTGGTACAGTACAGTATGGTACGGTATGGGTCGATATGGATCACCTTTATCAAGCTTGCGTTTCCACTGCCAAAAGGGTACCAAACATTGAACAGGTTACAGTCTCTGATATGTTACCAATTACTGAAAATCTACACACAGCATACATTTAGTCCTTAATTGGGTTCAAAAACAACACACAACATATACCCCACAGTCAGTGCAAACCTCTCATCTGTTTCTTATATCTTCACCAGCACAAGTAACCTCTTGTTAGAAAGTAATTCTGTCATTCTGAGTTCATAATAGTCCAAAAGGCGATGACAATAAGGTTGAAGTCAGAATTATTAAACCCACTTTGT
Associated Phenotype:
Not determined