ZMP
cttnl
Ensembl ID:
ZFIN IDs:
Description:
Cortactin, like [Source:UniProtKB/TrEMBL;Acc:Q7SXH4]
Human Orthologue:
CTTN
Human Description:
cortactin [Source:HGNC Symbol;Acc:3338]
Mouse Orthologue:
Cttn
Mouse Description:
cortactin Gene [Source:MGI Symbol;Acc:MGI:99695]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17004 | Essential Splice Site | Available for shipment | Available now |
sa23395 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17004
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 |
---|---|---|---|---|---|
ENSDART00000008696 | Essential Splice Site | 95 | 534 | 3 | 16 |
ENSDART00000017053 | Essential Splice Site | 28 | 206 | 2 | 9 |
ENSDART00000058468 | Essential Splice Site | 28 | 504 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 49870694)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50922504 |
GRCz11 | 18 | 50920068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCAGTGGATGAAGGAGCAGATGAYTGGGAAACTGACCCTGACTTTGAG[G/A]TACAAACCCCGACATTCCTCCTMCCCTTCATCTTCCTCTTCTCCTCCTCC
Long Flanking Sequence:
CCTAGATAGGTGTCTTGATTTGTGAGCGAGTGTGTATGGCAGATTATTAGTGCTGGATGGTGTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCTAATTTTGTTTTGCATTGTCCGATCATTTCTTTGTGTGTATGTGTGTGTTGTAATGGTGTGATGTGTGTGATCTGACAGTGTGTTATCAGATGGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTCTGATAGTGTGGTGTCAGATAATGTGTGTGTTGCGTGTAATTAAATGGTGTGTGTTTTGTCAGATAATGTGGGTGTGTTCTGATTGGCAGTTGGTTTGTGTGTGTGTGTTCTGCTGGTGTGTGTGTGTGTTCTGACGGTGTGTGTTGTGTGTTGTCAGATGTGGAAGGCAGCCGCTGGTCAGTCTGTCTCTATGTCAGTGGATGAAGGAGCAGATGACTGGGAAACTGACCCTGACTTTGAG[G/A]TACAAACCCCGACATTCCTCCTCCCCTTCATCTTCCTCTTCTCCTCCTCCTCTTCCTCCTCCTCCTCCTCATCATCTTCTCCTCCTGACTGAGCTGAAGCTGCAGATGCTCCTCGTGTGTGTCCCTGAGCGTGCCTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCCCTCCGCTCATGTTTCACTGTCTCCATCACACACAGAATGACGTGTCCGAGAAGGAGCAGCGATGGGGAGCCAAGACTGTGCAGGGGTCCGGACACCAGGAGCACATCAAGTCAGTCTGAGATGAATGTCCTGATCATGTTGAGCACGAGCGCGTGCAGAGCGGTTCAGTGTGGTGATGTCATCAGCCCATCAACATTTCCTGCTGGTTATCAGACTAGTTAATAACTGTGACGAGAGGCAGTTCAGTCATTACTCAATGTTTAAAGAGCGGTCACAACATGATTGATCAACATGCAGCTCTTATTCGACTCTCAGAAGCTCCAGAAATGACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23395
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 |
---|---|---|---|---|---|
ENSDART00000008696 | Nonsense | 237 | 534 | 8 | 16 |
ENSDART00000017053 | None | None | 206 | None | 9 |
ENSDART00000058468 | Nonsense | 170 | 504 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 49874011)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50925821 |
GRCz11 | 18 | 50917381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCACTGGTTTCGGGGGCCGGTACGGTGTTCAGGCTGACCGTGTGGAT[C/T]AGAGCGCGGTGGGCTTCGAGTATCAGGGGAAAACAGAGAAGCACGAGTCT
Long Flanking Sequence:
CTCACACTACTGCTGTTCTGCAGCCTCATTCACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTCTGCAGTCTGCTGTTGGTTTCGAGTATGTGGGAAAGACGGAGAAACACGCCTCTCAGAAAGGTGAATGGCAGTCTCTTACTCATTATAATATCGTGAGCCTCCTGCAGATGAACAACAGCTGTTTATATTTCACACTAAAGGTCATATTGTGTCTTGAATATCGAGAATAAGAGCTCTGATAAATGACCAAACACGTCAGAGTCCTCTGATGATGAGCATCTGCGCAGTTTTGTAAATATGGCTTCACTACTAGCTCTCAATATCAGCTGCTCATCCTGTGCGTGCGCGTGCGTGCGTTTGTGTGTGTGTGTGTGTGTGTGTGTGCAGATTACTCCACTGGTTTCGGGGGCCGGTACGGTGTTCAGGCTGACCGTGTGGAT[C/T]AGAGCGCGGTGGGCTTCGAGTATCAGGGGAAAACAGAGAAGCACGAGTCTCAGAAAGGTCAGTCCTCCTCGTCTGTGTCCTGCACGTCTCTGTGTTTCCGGATCTGTCTCTCATGCTGCTCCTCAATCTGCAGATTACGCTAAAGGCTTCGGGGGAAAGTTCGGCGTGGAGACGGATAAGGTGGACAAGAGTGCGATGGGCTTCGAGTATCAGGGGAAGACGGAGAAACACGAGTCTCAGAAAGGTCTGCGCTCTCACCACACACACACACACTCCACACAGCAGACAGACGCGGCTCAGCACAGGCTGCTGCACACTGATGATCAGCAGTACATGCGGGATTATGATGGAGTCAGTGCAGCAGAAACAGCCCACATCACCACACGGCAGTGAATCTGAAGCTGGAGATATTAACATCAGGGTCTTGTGTTCTTGTAGACTATGTGAAGGGCTTCGGAGGGAAGTTTGGTGTTCAGACGGACCGTCAGGATAAGTCTGCG
Associated Phenotype:
Not determined