ZMP
cotl1
Ensembl ID:
ZFIN ID:
Description:
coactosin-like protein [Source:RefSeq peptide;Acc:NP_956306]
Human Orthologue:
COTL1
Human Description:
coactosin-like 1 (Dictyostelium) [Source:HGNC Symbol;Acc:18304]
Mouse Orthologue:
Cotl1
Mouse Description:
coactosin-like 1 (Dictyostelium) Gene [Source:MGI Symbol;Acc:MGI:1919292]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39194 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45633 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43066 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39194
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 |
---|---|---|---|---|---|
ENSDART00000032151 | Nonsense | 4 | 142 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 12680773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13235585 |
GRCz11 | 18 | 13204097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTGCATTTAGACACATTATCTCCCTTTGCATCGTCGAAATGGCAACA[C/T]GAATTGACAAAGAGGCTTGCAGAGAGGCATACAATCTGGTGCGAGACGAC
Long Flanking Sequence:
TGTTTTTAATCGAGATTTGGACATATTTGTATTTTTAATTTACTTCTCAATTGTATCGTGTGTTTAATTTAGTTGAATCCTCGGGTGCGAAAATATTAAAAATAACAGCAAGTCATTGTTCTTATTCAAAAATTCAACGTGAACCCAACAAAGTCCACAAGATGGCAGAGTAATTCAAACCATCGATAGAACAGAACTGGGCGGATTTAATGTGACTCAATACCCAGGTTGGCCATTAGGAGGAGGTGAACCCGAGCTCTGCGATTCACTGGAACAGCAACCTGACAGACGAATATCACTAACGCCCATTAAGAGCAATAGGAAATGAATCGAGTCGTGAAATTAGTTGCCTCTCCATCCCACTGAGAGAAGAGACCTCTCCGGCACACCAGCAGCCCCTCTGTCGCACTTTGGGATTTATCTCGCTTTTTCTCTCATACCCCCGGCTTTGTTCTGCATTTAGACACATTATCTCCCTTTGCATCGTCGAAATGGCAACA[C/T]GAATTGACAAAGAGGCTTGCAGAGAGGCATACAATCTGGTGCGAGACGACAGCTCAGGTATATGCTGGTGAGTCAAGCCTTGATTTGCCGCACATCCACAGTATTCGATAACGGAACTCGTTACATTGTTTCAGAAAATAGACCGAATTCGAATTTAGAACGATACATTGTAGCGTTATTTCATTCATTGACACGGGATGTAGTGCAACATGTAGGGATGGGTCTTTTAACCCTTGGGTTGTGTTTCAAAATCTAGTTTGCTGCCTACCTAGGCGACAAAATAAATCTAGGGAGGCTGCTGGTTAGATTTTGACGCATTATAATAATTGTGTCCACTGTTAATAATGTCATATTTGATGTTTAAAGGGCATGTTTTAAGTATGACGGATCTACAATTGTACCAGGCGGGCATGGGTCCGACTATGAAGAATTCAAGAGCCAGTGTACAGGTGAGTGCTGTTTACCTGTCTTGTCTTGAATGTTGTTTAATATGCATTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45633
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032151 | Essential Splice Site | 26 | 142 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 12681138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13235950 |
GRCz11 | 18 | 13204462 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTATAATAATTGTGTCCACTGTTAATAATGTCATATTTGATGTTTAA[A/C]GGGCATGTTTTAAGTATGACGGATCTACAATTGTACCAGGCGGGCATGGG
Long Flanking Sequence:
AGAGAAGAGACCTCTCCGGCACACCAGCAGCCCCTCTGTCGCACTTTGGGATTTATCTCGCTTTTTCTCTCATACCCCCGGCTTTGTTCTGCATTTAGACACATTATCTCCCTTTGCATCGTCGAAATGGCAACACGAATTGACAAAGAGGCTTGCAGAGAGGCATACAATCTGGTGCGAGACGACAGCTCAGGTATATGCTGGTGAGTCAAGCCTTGATTTGCCGCACATCCACAGTATTCGATAACGGAACTCGTTACATTGTTTCAGAAAATAGACCGAATTCGAATTTAGAACGATACATTGTAGCGTTATTTCATTCATTGACACGGGATGTAGTGCAACATGTAGGGATGGGTCTTTTAACCCTTGGGTTGTGTTTCAAAATCTAGTTTGCTGCCTACCTAGGCGACAAAATAAATCTAGGGAGGCTGCTGGTTAGATTTTGACGCATTATAATAATTGTGTCCACTGTTAATAATGTCATATTTGATGTTTAA[A/C]GGGCATGTTTTAAGTATGACGGATCTACAATTGTACCAGGCGGGCATGGGTCCGACTATGAAGAATTCAAGAGCCAGTGTACAGGTGAGTGCTGTTTACCTGTCTTGTCTTGAATGTTGTTTAATATGCATTTCTGCAAAGCATAAAGGTGGAAAATTTCAAGTGGCATAATCTTTTCGCCACTTGTTTTTCCAAACATGTCTTCCTTCGATATTGAGAAATGACTCCATTCACCTAAATATTTTAAAGGGTGTCTAATCCTGCTCCCAATCCAATAGTTTGGATATTACCCGAATTAAACACACTTGAACCAGCAAATCTTACTAGAAACTTACTGATAGATTTATTGACGCAAGTTGGAGCTAAACTTTGCAAGTTAGTGGTCTTTCAGGACAAATTTTGGACTCTGGAAAATCAATAAGAGTGATCTGTGAGTTCCCCAGAAGAAATAAACAAGGTTTGAAACAGCAGTTTCATTTTTAAGTGAACTGTGCCTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43066
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 |
---|---|---|---|---|---|
ENSDART00000032151 | Nonsense | 137 | 142 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 12692618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 13247430 |
GRCz11 | 18 | 13215942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAAGAATACCTACGTACTGAGCTCAAGAAAGCTGGCGGCGCCAACTA[T/A]GATGCCCAGGCTGAATAAAACTTGGGGATGGGTTTCCACTGGGTTGAATG
Long Flanking Sequence:
AAACTTTTGACTGTCTAGAAATGTCAAATTCTCAAAAAAAGCTTGTTTTTCTGGCATTTAGCAAATGTAAATCATTAAGGTAATCCTAATTAACCTAAAATAGTAAACGTTTAGTATGATTTGCCATCAGACATTTTTTTAAAAATGGTAATGTTCCTTTTTTTAGAGTGTATGTAAACTTTTGGTTTCAACTGTAAGTGTTCGACTGAAATAGGAAAAAAGATTGACTTGTAAATAAAAAGTATTTTGATGTGAACTATATATTTAACCTTCTCTAACATGCAGATGAGAATTGTCCAGATTTCCTATAAAATTTAGCACACCCAGATACCAACCAAATCCGACTTTAACCAAATCTGTGCAAACAATCACTCAAGTTTTTGTATGTTGTTGTTTTTTAACATGCAGACCTTTGCCAAGGAGTTTATGATCAGCGACCCCAAAGAGCTGGAGGAAGAATACCTACGTACTGAGCTCAAGAAAGCTGGCGGCGCCAACTA[T/A]GATGCCCAGGCTGAATAAAACTTGGGGATGGGTTTCCACTGGGTTGAATGACATACACACACACACAAACATACACACACAGGGCAAATATCCATACCTCATTTTTCTCGTCAGTCTGGCTACGGTTGATTTATCTACTGTACTGTGCATCATCTCAGTGCTATAGTGCTCTCATCTCTTTTCTTCAGGGGCGTTTTGTAAGTCTTTTCTGAGAATGCTCTTTCGGTTCATCACTGTGATATGCTTTCAGAATCACTGGAGAGCATACGAGTCCAGCGTTGTTTTCTAAAGGGGGTTCTTGTGAATCGGATTCCTCCAAAACAGACCACTGTGTTTACGGTCTTGATCTTCTATAGAGAGCAAGACATTGTGGAATGTGTGCATTTGTGTATGTGTGCGTTTGCAGACACTGTACTGTGATTGGCTGACTTGCATGCAAGGGGGTGGGGCTTTAAATGAATCCCGTAGCCCCGATTGGCTGTTTCGCTATCTCTCCACCT
Associated Phenotype:
Not determined