ZMP
cltcb
Ensembl ID:
ZFIN ID:
Description:
clathrin, heavy polypeptide b (Hc) [Source:RefSeq peptide;Acc:NP_001181907]
Human Orthologue:
CLTC
Human Description:
clathrin, heavy chain (Hc) [Source:HGNC Symbol;Acc:2092]
Mouse Orthologue:
Cltc
Mouse Description:
clathrin, heavy polypeptide (Hc) Gene [Source:MGI Symbol;Acc:MGI:2388633]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22612 | Essential Splice Site | Available for shipment | Available now |
sa32024 | Nonsense | Available for shipment | Available now |
sa11813 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22612
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123172 | Essential Splice Site | 1154 | 1683 | 22 | 33 |
ENSDART00000130989 | Essential Splice Site | 1149 | 1678 | 21 | 32 |
ENSDART00000134512 | Essential Splice Site | 1148 | 1677 | 21 | 32 |
ENSDART00000140249 | None | None | 89 | None | 2 |
ENSDART00000143796 | None | None | 318 | None | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 16337623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17382586 |
GRCz11 | 15 | 17318608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGACCCTTCAGCCTACATGGAAGTGGGACAAGCTGCAGCCCAAAGCGG[T/C]AAGAACCAGTCCCCTGATTCACGACTATATCCACAGCATCCAAAGGTGTG
Long Flanking Sequence:
GATATTTCACTTTCATATGACCACAACTAAACAATTTCAGCTATTTCAAATTACTTCAAAGCCTAAAATGGATATGTAAAAAATAGGCTCATACAATTTTTATCAGGTGTGGTATAATTCGAATAATTGACTCCAATTCATTGTATTATTAGAAATTAATATACACAACCACTTTGTGTGCATTATTATAATAGTTTATATGATAAACTAATATAATATAACAACTAAATATTCTATTAAATTATGTTCATGTACTGCTTGAGTTGTTTCTCTATGGGCTCAAATCATTGTGTGTGTTGACCACAGGTTCTCATCGAGCACATTGGGAATCTGGACCGGGCTTATGAGTTTGCCGAGCGCTGCAATGAGCCAGCTGTGTGGAGTCAGTTGGCTAAAGCACAACTGCAGAAGGGGCTGGTGAAAGAGGCTATTGACTCTTACATCAAAGCTGATGACCCTTCAGCCTACATGGAAGTGGGACAAGCTGCAGCCCAAAGCGG[T/C]AAGAACCAGTCCCCTGATTCACGACTATATCCACAGCATCCAAAGGTGTGGGGGGTCATAAATACAGAAAATGGTTTGGTTGTTAGCTTAATGACGTTTTGTTTTCAGGAAACTGGGAGGATTTGGTCAAGTTTTTGCAGATGGCTCGTAAGAAGGCCCGTGAATCATATGTGGAGACTGAGCTGATCTTTGCCCTGGCCAAGACTAACCGTCTAGCTGAACTGGAGGAGTTTATCAACGGGCCAAACAACGCACACATTCAACAAGTATGCGTCTCTTACTTTTGATAATGTATTTTAAAAAATTATGAGGCCAACTATAGCAAGTATCATTTTATTTTTTATTTCATTTAATATATAATCATTTAAATGAAATAAAAAAAATATATTTTTATATTTTATTTGACTTTATTAACGTTTTTTATTTTATTTTTTTGATGCTTTAATTGTTGCCTGCTTAGCCTTTTAATGATGCATATTTTTGGTTATATTTATGCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32024
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123172 | Nonsense | 1377 | 1683 | 27 | 33 |
ENSDART00000130989 | Nonsense | 1372 | 1678 | 26 | 32 |
ENSDART00000134512 | Nonsense | 1371 | 1677 | 26 | 32 |
ENSDART00000140249 | None | None | 89 | None | 2 |
ENSDART00000143796 | Nonsense | 5 | 318 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 16340245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17385208 |
GRCz11 | 15 | 17321230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCATCTGTGGGGGGAGCTAGTCTTCCTGTATGATAAATATGAGGAGTA[C/A]GACAACGCCATCATCACCATGATGAACCATCCTGCAGATGCCTGGAAAGA
Long Flanking Sequence:
GCTCTCCCCAAGACTTTATCAGTAGTGCTGTTTGAGCTGTATGGTTTCTCCTTCAGGACCGTGGCTATTTCGAGGAGCTGATCACCATGCTGGAGGCGGCTCTGGGCTTGGAGCGCGCTCATATGGGCATGTTCACAGAACTGGCCATCCTCTACTCCAAATTTAAGCCACAGAAGATGAGGGAGCACCTGGAGCTCTTCTGGTCCAGAGTCAACATTCCCAAGGTCTGAGAGCTGAAACCATTCTCAACCATCTGTCTGAATATATATATTGACTAACGTAAATGGAGTTTTTTTTTATTCAGGCAAAACAAACATAATTTAAAATAGCAAATGCTTTGTATCCGTCTATTTAGGCACTTTGGTGTCTCTGTGCTTATTAATTGATGGAAGAAGTGAATGAGACAGTTCTTGTACTGTATGTGTTCAGGTTTTAAGGGCAGCAGAACAGGCTCATCTGTGGGGGGAGCTAGTCTTCCTGTATGATAAATATGAGGAGTA[C/A]GACAACGCCATCATCACCATGATGAACCATCCTGCAGATGCCTGGAAAGAGAGCCAGTTTAAAGACATCATAACTAAGGTTTTTATTTGCATCTCTTATTGAAATATGAAGTTGTTCTTATTATGTAATGTTTTTATGTATATCGATCTTGCCATAAGTTACTGATGTAGTAATAAATAAACTAAATAAATAAATTTCACCTAAAAGTCAACATGAAATAAAAATTTACTACTTATTTTGATGAAATATTACTGGAAATGGGTTGTCCTTGCTATTGACAAACCTGTATTTTCTTTTATGGCAATAAGCAGAGTATTAAGTAAAGATTATGTTTCATGAATACATTTAGCAAATTTCCTTCCATACATTTATTAAACTTTTTTTTTTAAATTAGAAATGCATATTAGGCATGTCCCAGTCAGGTTTTTTTGCCCTCGAGTCCGAGTCATTTGATTTTGAGTGTCTTCTGATACCGAAACTCGATCCGATACTTCTATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11813
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 |
---|---|---|---|---|---|
ENSDART00000123172 | Nonsense | 1424 | 1683 | 28 | 33 |
ENSDART00000130989 | Nonsense | 1419 | 1678 | 27 | 32 |
ENSDART00000134512 | Nonsense | 1418 | 1677 | 27 | 32 |
ENSDART00000140249 | None | None | 89 | None | 2 |
ENSDART00000143796 | Nonsense | 52 | 318 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 16342387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17387350 |
GRCz11 | 15 | 17323372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGCTGTATTACAGAGCCGTCCAGTTCTACCTGGAGTTCAAACCGCTGT[T/A]ACTGAATGACCTGCTGATCGTATTGTCTCCTCGTCTTGACCACACTCGTG
Long Flanking Sequence:
ACTTAAATTTGACAGCTTTAAAGGGGATTTTCTCAATATTATGAGTTTCCAGATTTAGTTCCAGAAATAGTTGCATCTCTGCCAGTTATTGTCTTATACTAACAACAAGCTTACAAAGCAAGCTTATGTATTCAGCTCTCAGATTATTGTAAAAAAAAATTACCCTTATGACTGGTTTTCTACTCCAGGCTCACAATTGTGGCCTTAGAATTGCATTTAAACTGTTAATGATCATGTGTTTTAAATTTTTTTTTATTTTATAACAGTTTTTTTTATAATCACAAATCAAAAACATTGTATACAATCTGTAATACTTTTTATACTGATGGTAATGATTATGCGCCTTGACTGTCCACTTTTGATTAGATCATTGGAAAATTATTATTTTTATCATACAAAGCTGAAAAGGAATTAACCTTTATGTTGATTTGTGTTGCAGGTGGCTAATGTTGAGCTGTATTACAGAGCCGTCCAGTTCTACCTGGAGTTCAAACCGCTGT[T/A]ACTGAATGACCTGCTGATCGTATTGTCTCCTCGTCTTGACCACACTCGTGCTGTCAACTTCTTCAGCAAGGTACTTCCCACATAACTTTTGCTTACCGTTAAGTTTTTTTGTTTTTATTCTGCAAAGATCCAACTATTTTGCTTTTTTAAAAAGTTTGTATGGGAGCTGGAAATTCTTGAAATTGCTTTGAGTTTGTAAAGTGCTCAGATTTTGGTTGAAGTGCTTGAACATGTAATCGTGTTGTTTTCATAATAATTTATCTTACTAAATAGGCAATGACAATGAACTATTGAAATAAAATGTATAATTTTTTGCTCAAACTCTAAAGTCTGCATTTGCACCTGTAGCATGATCTTATTATTTTTATTTGTATAAAGCTTTTTACTATAACTATTATTTCAAAGCAGCTTTACCGAAGGTTGGATATGCACATTATTGGATTACAATCAATATCAAAAAAGTTATGGTTATTAGTAACCATAACTTTATTACTTACTAA
Associated Phenotype:
Not determined