ZMP
cltca
Ensembl ID:
ZFIN ID:
Description:
clathrin, heavy polypeptide a [Source:RefSeq peptide;Acc:NP_001005391]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34925 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41680 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21757 | Nonsense | Available for shipment | Available now |
sa21756 | Essential Splice Site | Available for shipment | Available now |
sa16707 | Nonsense | Available for shipment | Available now |
sa14787 | Nonsense | Available for shipment | Available now |
sa31785 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34925
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063849 | Essential Splice Site | 15 | 1680 | 2 | 31 |
The following transcripts of ENSDARG00000043493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29037542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28469136 |
GRCz11 | 10 | 28355761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGTTTAGTGTGCTCATTCAAATGAAATAAAACTGTTCTCTTTTCCTA[G/T]CTCCAAAATTTGGGGATCAACCCAGCCAACATTGGGTTCAGCACCCTGAC
Long Flanking Sequence:
CTTGTGTCTGCTCTTTGTGTGTCCCTGAGATAAATTCCTCAAGGCTTTTTCAGATAGTAAAGCCATGTGGTTGACTCGGTGTAGGGAAAAAAGGATTTGCTGCTTCTATGCCACATTTAATTACTGTTCTTATTACTAGAAAGGCTGATCTCATAATACTCTTCAACACACACAATTACTGCTGAAATGTAGTGAAACTACAAAAATTATTTGCTGTTACGGTTTCATCTTTCTGCCTTGTAAATCATGTTTGAGATCCATTTAATCTTCAGTGTGGAACACTGTCATTGATTTTTATTAAAAGATTCATTCAGAAAGCAGTTCACAGGGTCAGAGAGACACCTGACCTGATATCACTTAAGAAATAAAATCAAATTATCTCAGTATTCTTGACTCTTAAAAAGGACGAAATGGAAATAAAAATGAGAATTGTATTAATTAGATAAAAAAAAGTGTTTAGTGTGCTCATTCAAATGAAATAAAACTGTTCTCTTTTCCTA[G/T]CTCCAAAATTTGGGGATCAACCCAGCCAACATTGGGTTCAGCACCCTGACAATGGAATCGGATAAGTTCATCTGTGTCCGGGAGAAGGTTGGAGAACAGGCGCAGGTGGTGATCATTGATATGGCGGACCCAAACACCCCCATCCGCAGGCCCATCTCTGCAGATAGTGCCATCATGAACCCTGCGAGCAAAGTCATTGCCCTCAAAGGTAGGAGATCTAGATTGTTAGTGCATTAGCTATTTGTAGTAACCTAATTGTAATGACTAGTTGACAACAGAATCATAGAACTGATCCAATTGTTGTTTTAAACTAGAATTTAAGTTGTCTTGTTTTCTTAGCCTCATTCATTCACCCAGAATCTCTTTTTAGTTAAAATTATGCTATACCTATTTCTTAAGCAAATGTTTTTGCATTTTCCCTCATTATAGGCTACATCTTATCTTAAAGTAACATGATATGTTGTGTATTTTTTGTCATGCAGCCATAATTGCTTTGTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41680
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 |
---|---|---|---|---|---|
ENSDART00000063849 | Nonsense | 221 | 1680 | 4 | 31 |
The following transcripts of ENSDARG00000043493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29032652)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28464246 |
GRCz11 | 10 | 28350871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAATGGAGGGAAACACTGAAGAATCCACTCTCTTCTGTTTCGCTGTG[C/T]GAGGTCAGGCAGGCGGAAAGGTGCGTTTCCATATGCATGCATACATTTGT
Long Flanking Sequence:
AATCATTTTAAAGAACCGTTCTGGATTGTTGGTCTAGAATTATTTTGGGTTACGCTTTAGTTTAGGTCACAGTTCACAGTATTAACAAACCATTAACTGACACTACTAGCTTAATAAACTACTTATAAGCTGTTTGTTAATAGTTAGTAAGGTAGAAGATGGGTAGGATTAGGAATTCAGAATAGTTTACAACTACTAATGAACTGTTAACATCCTAATAAAAGCCAGTAGTTAATAACACGAATAGTGACCTAAACTAAAGTGTACCTTATTTTACTTTGTCTGTCATTCAATTAAACGTTGGATATTGAATCAAAGACACCCCCCCCAAATCTCAAAACTGTTCTTTCATTTTGTAGCAAAACAGAGTTGTTGGAGCCATGCAGCTCTACTCTGTTGATAGGAAGGTGTCACAGCCTATTGAGGGGCACGCCGCTGGCTTTGGTCAATTCAAAATGGAGGGAAACACTGAAGAATCCACTCTCTTCTGTTTCGCTGTG[C/T]GAGGTCAGGCAGGCGGAAAGGTGCGTTTCCATATGCATGCATACATTTGTACATTTCACGAGTGCATCTAAGAATTGACATGCATTTTTTTTCGTTGCCGTAGTATTAAAAACTAATTTTTACTTTTAATCAAAGCAGAACAAGGAACTTTTACCTACATAAGGACATTGAAGCATCAGTCTGTTGCATGTTTTTTGTCATAAATGCAAGCACAAGCTTTTGTTCAAAGTGACTTACAATTGAGTTACTGCATATAATCACTTTGACCTGATATGTTTCAATCCAATAAAAAGACAAGTTATTTAGTTATCAGTATTCCCAAGACAGTTATCTAAGAAACAGTGGAAGTAGAGCTGGGCAATATGGCAAAAATTAAACCCTGATAAATTATTTTTCAAACTGAACAACAATATATATTTCGATATCAGTTGTTTATTCTTTCAGATTTAAAATAGTATCCCAACAGTGACTAAAGATGCAAATTAAAGGATCTGTTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21757
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 |
---|---|---|---|---|---|
ENSDART00000063849 | Nonsense | 603 | 1680 | 12 | 31 |
The following transcripts of ENSDARG00000043493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29014756)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28446350 |
GRCz11 | 10 | 28332975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCAAGCACAGTGGTCTCTTACAGGTTGCAGATGCCATCCTAGGAAAC[C/T]AGATGTTCACCAACTACGATCGTGCCCACATCGCCCAACTGTGTGAGAAA
Long Flanking Sequence:
TTTGCCTACCTTGTTTCGAGACTTCCGGTCTCATTCACTTCCATTGATTTCAGGCGTTAAAAACAGCTGGTTATGCTGCTTAATGATGCAAACTTGTATTTTCTTATTATTATTCTTTTTATAAATAGTCACAAACACACTTATGTGTAGAGCAAGTAATTTTACTGACATTTATTTTTCCTTGTCATTTCTCCTATAGGCAACTAAATAAGAAGTACTAAAACAATCGCAAAATACAAACACACTTCCGCATTGCAGAATACAGTCATTAATCTTGTGCTTTTGCCATGCCACTGCCTGAATCTCAGGTTGTTTTAAAATTGTTATTCTCAACATGTCCAGTTGTAATGTTGGCTAATATGTAATTACTGTGGTCAGCATTGTCCAAAATAAAAAACAGCAACACCCCAGTCCTCATCATCGCATTAGTTATTTTACCATTAGTCACTATTTTCAAGCACAGTGGTCTCTTACAGGTTGCAGATGCCATCCTAGGAAAC[C/T]AGATGTTCACCAACTACGATCGTGCCCACATCGCCCAACTGTGTGAGAAAGCAGGACTTCTTCAGAGAGCTTTAGAGCATTACACCGACTTGTATGACATCAAACGAGCTGTCGTGCACACACACCTGCTCAACCCGGAGGTACACAACAAGTCTTTACATTCATGCCCAATTAAAGTGCAACCACCTGCCTTTTCCTTTTGTTTCTCATGGTATTGGTCTCTGCTAATGTCTGCAGTGGCTGGTCAACTACTTTGGCTCTCTGTCAGTGGAGGACTCTCTGGAGTGTCTGAGGGCCATGCTGTCTGCTAACATCAGACAGAATCTCCAGATCTGCGTCCAGGTGGCGTCCAAGTATCACGAGCAGCTGAGCACACAGTCCCTCACCGAGCTCTTTGAGTCGTTCAAGAGTTTTGAGGGTAAGAAGTAGATCCAGCATGATTCAATTATTCTGTCTGTGTTATTGTCTGCTATCATGCAAAGCTTTCACATTCAAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21756
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 |
---|---|---|---|---|---|
ENSDART00000063849 | Essential Splice Site | 649 | 1680 | 12 | 31 |
The following transcripts of ENSDARG00000043493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29014614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28446208 |
GRCz11 | 10 | 28332833 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATGACATCAAACGAGCTGTCGTGCACACACACCTGCTCAACCCGGAGG[T/C]ACACAACAAGTCTTTACATTCATGCCCAATTAAAGTGCAACCACCTGCCT
Long Flanking Sequence:
ATGTGTAGAGCAAGTAATTTTACTGACATTTATTTTTCCTTGTCATTTCTCCTATAGGCAACTAAATAAGAAGTACTAAAACAATCGCAAAATACAAACACACTTCCGCATTGCAGAATACAGTCATTAATCTTGTGCTTTTGCCATGCCACTGCCTGAATCTCAGGTTGTTTTAAAATTGTTATTCTCAACATGTCCAGTTGTAATGTTGGCTAATATGTAATTACTGTGGTCAGCATTGTCCAAAATAAAAAACAGCAACACCCCAGTCCTCATCATCGCATTAGTTATTTTACCATTAGTCACTATTTTCAAGCACAGTGGTCTCTTACAGGTTGCAGATGCCATCCTAGGAAACCAGATGTTCACCAACTACGATCGTGCCCACATCGCCCAACTGTGTGAGAAAGCAGGACTTCTTCAGAGAGCTTTAGAGCATTACACCGACTTGTATGACATCAAACGAGCTGTCGTGCACACACACCTGCTCAACCCGGAGG[T/C]ACACAACAAGTCTTTACATTCATGCCCAATTAAAGTGCAACCACCTGCCTTTTCCTTTTGTTTCTCATGGTATTGGTCTCTGCTAATGTCTGCAGTGGCTGGTCAACTACTTTGGCTCTCTGTCAGTGGAGGACTCTCTGGAGTGTCTGAGGGCCATGCTGTCTGCTAACATCAGACAGAATCTCCAGATCTGCGTCCAGGTGGCGTCCAAGTATCACGAGCAGCTGAGCACACAGTCCCTCACCGAGCTCTTTGAGTCGTTCAAGAGTTTTGAGGGTAAGAAGTAGATCCAGCATGATTCAATTATTCTGTCTGTGTTATTGTCTGCTATCATGCAAAGCTTTCACATTCAAGGAAATGTAACTAAAAGGAAACATTTTAGTTTATTTTGCAATTTTGTAGGTTTTTCCAAATAAGATTTTTATGCACTTTAGTCTTTTTTTTTTGTTCGTTTTAAAGTTAAAATAAAAGTAGAAAATTTAAATATAAATTAAATGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16707
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 |
---|---|---|---|---|---|
ENSDART00000063849 | Nonsense | 943 | 1680 | 18 | 31 |
The following transcripts of ENSDARG00000043493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29004866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28436460 |
GRCz11 | 10 | 28323085 |
KASP Assay ID:
2260-3348.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTGATTTTTCTCTACAGGTTTGCAATGAGAACTCGCTGTTCAAGAGTT[T/A]GTCCCGCTATCTKGTGCGCCGCAGGGACCCYGAGCTMTGGGCCAGTGTGC
Long Flanking Sequence:
TTTGTGTTAACAAAAGTTTTTTTTTTTCTGTTATTTTAACCCAATGTTTACCTCCCTGTTTACATGTTTCAATTGAAATTAAGTTGCACATTGAACTAAGCTGCACATCGAAAGACGCTTTAGATTACTTTTACATGTTTTCTCTTTTGTAGACTGAAGCTGTTGTTGCCCTGGCTGGAGTCTCGTATCCACGAGGGCTGTGAGGAGCCAGCTACCCACAATGCCCTGGCCAAGATCTACATCGACAGCAACAACAACCCTGAACGCTTCCTGCGGGAGAACCCATACTACGATAGCCGCGTGGTGGGGAAATACTGCGAAAAACGAGACCCTCATCTGGCCTGTGTGGCCTATGAGAGAGGAACGTGTGACCAGGAGCTGATCAACGTCAGTAATGCTTCAGCATGCATGAGCTTAAGTGCAGCCATTCAGCATGAGAATTGATCTTGATTTTGATTTTTCTCTACAGGTTTGCAATGAGAACTCGCTGTTCAAGAGTT[T/A]GTCCCGCTATCTGGTGCGCCGCAGGGACCCTGAGCTATGGGCCAGTGTGCTTCTGGAGACCAACCCCTTCAGGAGGCCCCTTATTGACCAGGTACACAAATATGTTACATTCATCTCTTACAATAGATTAACATGGCTCATGCAGAAACATAATGATTATTCATCTCTTTCTATTCATTATTGGTGAAATGGACTATTTGCTGAATTAAATAGAATGTATTTATTATGACCAATAAACTTCTCCATCTGGAATTGACTTGAGTTTGTTACAATGCATTTTGTTATTTTTAATAATAATAAATAATAATAGTAATAGGGAAGAAATTACCAAGGTTTCTGCTGGGTCTTAAAATGAATTTCAAAAACTAAATTTTAGCCCTTAAAACGTCCTAATTTCACTGAAATATTGTCTTGTAGGTCTTAAATCCTTTTAAACAAGTTTTGATTTTCATCTATATCCATGTCTCCAATCAACATAAGTTCATCTCAAAAACACTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14787
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 |
---|---|---|---|---|---|
ENSDART00000063849 | Nonsense | 1043 | 1680 | 20 | 31 |
The following transcripts of ENSDARG00000043493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29002853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28434447 |
GRCz11 | 10 | 28321072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCTCATCCTAACAGCCATCAAAGCTGACCGTACTCGGGTCATGGAGTA[C/A]ATCAACCGCCTGGACAACTAYGATGCCCCAGACATCGCCAACATCGCCAT
Long Flanking Sequence:
TTTAGTATTTGTCTTTCCTAACAGCTTTAAGTAATTTAGTTCTGTTTATTTAGTTATTGTGAAGACCAAGCTCAAAACATAATTACATATTAATTTAAATAATGACACAGTCTGCAATTTAACAATAAATGATGAGGGAAAAATTCTTTGCCATAATAATATCAGAAACTTTATACATGACTGCATTCATTTTTATGGCTGCTCAAAAAAGGAAGTATTATATAGTATTAATAAAAGCTGGACATACTCCATTCGCCATATTGTCATTTTCATATGACCTACCAACATCGAAAAGAGTTTTATTAAAAACATCAGAGAGTTTTCATGACAGAAGTGTTCACAGAGAAATGACAGTGACCGGACAAAAACAAAGATGATAAAGGAATTAAAACTATAAATGGGGTTTAACTGACTTCCAATCTTCATCCCATACCCAGAAACCTGCAGAACCTGCTCATCCTAACAGCCATCAAAGCTGACCGTACTCGGGTCATGGAGTA[C/A]ATCAACCGCCTGGACAACTACGATGCCCCAGACATCGCCAACATCGCCATCAGCAGCGAGCTGTTTGAGGAGGCCTTCGCCATCTTCAAGAAATTCGATGTCAACACCTCTGCAGTGCAGGTTTGCTCTTCAGCCACAATATTTATACTAGATATCAGCTTATTATTAAAAGCGTTTTTTAATAGTACGTAATATTACAATATTTATTAATATCTCGAATTGTATCTTTATATTTCAGTTTTCATTTTAGCTAATGTTTATTATTTTAGTTTTGATACTATAATATTATCTTTATTTTAATAGAATATTTATAATTGCTTTGACTTTTTTTATTTATTAAACAGCAGTTAAAGAATGAGCTAATGCATCTTGTCATCCTCAGGTTCTGATCGAGCACATTGGTAATCTGGACCGGGCCTATGAGTTTGCGGAGCGCTGCAATGAACCTGCGGTGTGGAGTCAACTGGCCAAGGCTCAGCTTCAGAAGGGTCTCGTCAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31785
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063849 | Essential Splice Site | 1535 | 1680 | 28 | 31 |
The following transcripts of ENSDARG00000043493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 28997081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 28428675 |
GRCz11 | 10 | 28315300 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCTGGAAGCAGAGCGTGGAGCTGTGCAAGAAAGACAAGCTCTACAAG[G/A]TGAACCTTCACTCCTGTTACTCAAGCAATCAGTAAATGTGCATCTAATCA
Long Flanking Sequence:
ACTAAGGTCACCACATCAAATACTGGCTGGGGTATGTAAAACATAGTTTTTGGTTTTTACAAATGTGCAAATGCTGATCAGCATTGTCATGTAGGGAAAAACATTACTTTTTTTTCTTTTTCTTTTTTTGCTAGATTTTAGTTTGTTTGAAACTCAATATCAAATGAAAAAAAAAAGGTGGATAGAAAAAAACAGATTCACGACTTCTAAGAATCGATATAAAATCAACATTATTTTTTAAATACAATATACAGAGAAGTTTGTTTTTTTGGCTCAGCACTACTGTTACAGTCTAATATCTCATAACCCATTCCCCCATCTTATCGCAGGCCCTCAGGACGTCCATAGACGCGTACGATAACTTCGACAACATCTCTCTGGCTCAGCGTCTGGAGAAACACGAGTTAATTGAGTTCAGGAGAATCGCTGCTTACCTCTTCAAGGGGAACAACCGCTGGAAGCAGAGCGTGGAGCTGTGCAAGAAAGACAAGCTCTACAAG[G/A]TGAACCTTCACTCCTGTTACTCAAGCAATCAGTAAATGTGCATCTAATCATGGCCTTGACAGATATGTGTGTGTGTTTTCTCAGGATGCCATGCAATATGCATCGGAGTCAAAGGACACAGAGCTGGCCGAGGAGCTGCTGCAGTGGTTCCTGGATGAGAATAAGAAGGAGTGTTTTGCCGCCTGCCTCTTCACCTGCTACGATCTGCTCCGGCCTGACGTGGTGCTGGAGACATCCTGGAGGAACAACATCATGGACTTCGCCATGCCGTACTTCATCCAGGTCATGAGGGAATACCTCAGCAAGGTGAGGACAGGCTAAAAGAATGCATTATAAACCACACATTTTAAATAAGAAATCACTTCCAAATGTATTTTATTAACATTTACATATATTTAGTTATATATGAACAAGTATATTTATTGAATTTTTATTAACAAAACTTGGAGACCCCATTCAATGTTCGTACTGCACAACAATAAAACACATTTTACTGGACT
Associated Phenotype:
Not determined