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 |
---|---|---|---|
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:
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