ZMP
cttnbp2
Ensembl ID:
ZFIN ID:
Description:
Novel protein containing ankyrin repeats [Source:UniProtKB/TrEMBL;Acc:Q1LX68]
Human Orthologue:
CTTNBP2
Human Description:
cortactin binding protein 2 [Source:HGNC Symbol;Acc:15679]
Mouse Orthologue:
Cttnbp2
Mouse Description:
cortactin binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:1353467]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11049 | Nonsense | Available for shipment | Available now |
sa17017 | Nonsense | Available for shipment | Available now |
sa10059 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11049
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 |
---|---|---|---|---|---|
ENSDART00000100743 | Nonsense | 201 | 1573 | 4 | 23 |
ENSDART00000143233 | Nonsense | 174 | 1427 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 18 (position 20549891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 20780114 |
GRCz11 | 18 | 20769180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGGTCGAAGAGAACCAGCGCTTTGAGGAACTTTCGTCCCRTACTGAG[C/T]AGGATGGTCGATCRGTGGGACGTCWGGAAGARGAACTGGCATCTGAACGA
Long Flanking Sequence:
GCATACTGTTAGAGTGGGAATTGCTTGATTACTTTTACACAAGCTGAAAATTACATAAAGTTAAATGAAAGTAACCTGAGATTTGAGGACTTATCCCCAAGTTTAGTTGTACTTGATTTAAAAATTACTGTCAAGGCATGGTTACATTGTAGAAGGAACTGTTGTACCTTTAATACCTTATGTAATTGTGTAGTAATCAGTGTCTTGCTCTATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTATTTACCCTCTGCGAGTCTCATTTTTGCCCTGCTGCTACTGTCTAGCTTGAAATGGAGAAACTGCAGCTGCAGAGCCTGGAGCAGGAACACAGGAAGCTGTCAGCTCAGCTGAAGGATGAGCGAGAGAAAAACAAACACGTGGTGATGTCACTGGTGCATGAATGCAAGCAGCTAGCTGCTCGTGTGGTCGAAGAGAACCAGCGCTTTGAGGAACTTTCGTCCCGTACTGAG[C/T]AGGATGGTCGATCGGTGGGACGTCTGGAAGAAGAACTGGCATCTGAACGACGTCGTAGCCAACAGATGGAAGCGGAGATGGAGAAACAGTTGGCTGAATTTGACACAGAGCGAGAGCAGCTACGTGCCAGGCTTAGCCGCGAGGAGACTCGTGCTGTGGAACTCCGGGCTGAAAGTGAGAATCTCCGCTTGCAGGTGGAGCAGCTAAGAACTGAAAGATGCAAAGATTCCCCACCACTGCCTTCTGTTACCCCAGCATCTGTCTCTGTTAAACCCAAGGCTATGGTGTCTGTGGCTGTGGGCACTGAAGCAACTGTTTGCAAGACTGTCTCTTCTCAGACAGATGCACCGCTGGAAAATGAAGGAGCTAAGAAAGTGCCACTTTCCATCCCTGTCAAGCCTAGTGGCTCCACCTATGCTAGCATGAACCTACCTAAGACCTCCAGTGCAGGACGGGGGCTACACCATGGGAGCTCACAGGCAGAAAATGGAGGGGACGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17017
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100743 | Nonsense | 502 | 1573 | 4 | 23 |
ENSDART00000143233 | Nonsense | 475 | 1427 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 18 (position 20548988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 20779211 |
GRCz11 | 18 | 20768277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACTGTGGCCCGAATCGAMAGGGRTAACCCACCCCCGATCCCACCAAAA[A/T]AACCTGGACTGTCCCAGACACCRTCCCCTCCACACCCACCAATTAAAGTA
Long Flanking Sequence:
GTGGCTCCACCTATGCTAGCATGAACCTACCTAAGACCTCCAGTGCAGGACGGGGGCTACACCATGGGAGCTCACAGGCAGAAAATGGAGGGGACGGTCAAACACATCTACATAGCTCACATTCACCTGGTGTATCTTCTACCTTGCCGACTGGGGTTAGTCCCCGCGTCCAGGCAGCCCGTTACAAATTCCAACCCTCTGCCTCAGAGCAGGACCAAAATGGAACCGCAAACCAGAGCCCCCCCTCGCGTGACCTGTCCCCCACAAATCGAGACAACTTTGCAGCTAAACAACAGGCTCGACACACTGTCACACAGGTTCTGTCCCGCTTCACAAGCCCTCCAGCAGGGGGACCCCCTGCAGCCCTTCGGCCCGGTCTGCCACATTCTACATCTGAGGGAGGACCCTTCACAGGACGTTTAGGCCACCCCCAGATAGGCCTTAAATCACCAACTGTGGCCCGAATCGACAGGGGTAACCCACCCCCGATCCCACCAAAA[A/T]AACCTGGACTGTCCCAGACACCATCCCCTCCACACCCACCAATTAAAGTAGTAGGTGAAGCTAGCAGGTCCCCAGGAACAGGACTTGGGGTGGGTCTTGCCAAATCAGCTACCACCCCTCAGCTTCCACCAAAACCCTCCTTAGATATGGGTGGTACAGTCCCAGCCATGACTGCGTCACAGGTGGGTGCATCCTGTTCTGGCTGGCCATGGGGGCAGCAGCCAACAGCAGCATGTGTGGAGTGTCCCCCTGTCATCACCTCCTCCACAGCTACCATTGTCAGTAGCCCCTCCATAAACCCATCTAGTCTTCCATCCCATAGCCCCCAGCACCTGGGCAGTCCCCTGGCAGCAGCATCAGGTAAAAGGGTGCTACGTTTTTCACCCTTGCTTTCACTACTTCTCTCTACTCCTCTCCCTTTTCCTACTTGATGCATTTATAAGTAAGTGCCAGCAGAGGAGGACATAGATGTGGAGTATCAAAGAGAGGAGTATTCATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10059
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 |
---|---|---|---|---|---|
ENSDART00000100743 | Essential Splice Site | 774 | 1573 | 7 | 23 |
ENSDART00000143233 | Essential Splice Site | 747 | 1427 | 6 | 19 |
Genomic Location (Zv9):
Chromosome 18 (position 20541044)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 20771267 |
GRCz11 | 18 | 20760333 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGAAAGTGTTGTTAGACGCAGGAGCAGACCGAACACACGTTACCACTG[T/C]GAGTTTGCAGCAGTGTTGCTCAAATGTCAATTACACACTGYGTTAGTGAG
Long Flanking Sequence:
TTGGGTTCATGCTGGTTCTGACAGGTCTTCTGCAGTGTTTGTGATGATTGGGATGCAGTTCAACAGATGATTCATCTGAAAATTCTACCGTCTGCCACTTTTCCAAATGATCAACTAGAAGTCAAGTTATTATTAGTTGCTCTTACAACTGAAATCGACAACATGAATTTTGTCAGTTAGTGTAGAAATCACATTTGATTTTGCTGTAGTATTTACTGTATTGCAGAATCACTGTTATCAGTGTAGTACCAGGTATAACCAGTATTCACCAGGTATACAGTATTTAGTCAGTTTAGTGTCTCTATTGTGTTTCTCAATGGAATGATAAAAAGTTTCTCTTATTGATAGGTGTGCGAGAGCTCTGGTGAACTGTGGTGCTGATTTGGAGAAGGAGTATTCACAGGGAAGGACCCCGCTGTACCTGGCCTGTGAACAGGGACATGTGCAGTGTGTGAAAGTGTTGTTAGACGCAGGAGCAGACCGAACACACGTTACCACTG[T/C]GAGTTTGCAGCAGTGTTGCTCAAATGTCAATTACACACTGCGTTAGTGAGCATGTTAAGAAAAACCACCCCTCTTTTCATCACCATGGTTACCTTAACAGCGTGGGCATTTCACTGTCTGTGTATGTTGCTCAGGGTGTAATTACGACCTCTATTTTAGAAACACTTAATTGTGCCTTGAATGTTTTCTCAGTTTGCTCTAATTGACTGGCCTGAAAAAAAGACCATGAATATCCTGGGAAATTCTTAAGGGCTAAATTAAATCTTTTTTTGTTTGGTTGGATTTTTCTTTTCGTGAGTTAGTTTTTTGTGATGTGCCTATATATTTTATTTATTATAATAATTTTTTTCACATTTTTTGCAATAAAAATTACTGATTTTGCGGTGGTAATGGTATATATATAGTACATATCTTTTTTACCATATTAGTTTGCCTACTATGTTAGGTGTGCAATCTGACAATAACAATAACACAAAACATAAAAATAAAGCTTCTTTATT
Associated Phenotype:
Not determined