Busch Lab

ZMP

cttnbp2

Ensembl ID:
ENSDARG00000040991
ZFIN ID:
ZDB-GENE-030131-8134
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
sa43092 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43091 Nonsense Mutation detected in F1 DNA Not yet available
sa8747 Nonsense Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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

Mutation Details

Allele Name:
sa43092
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100743 Essential Splice Site 1064 1573 13 23
ENSDART00000143233 Essential Splice Site 1037 1427 12 19
Genomic Location (Zv9):
Chromosome 18 (position 20527856)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20758079
GRCz11 18 20747145
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAAGCTTTCAGGAGTACATCGCCAACCAGATATCTCATTATATCAAGG[T/G]AATTATCATAAATATTAGAGTCTATGTGCAACACTATTGCTTTGTCAACT
Long Flanking Sequence:
AAAAGTTTCATTTTTTCACATTTTCACTCTTAGCATGTCTGATCTACTCTGAGTGATCTTAATAGTTTGTATAAAGAGAGCTGAGAGAAAGCTAAAACTCTTACAAAACATCTGGACTTTAAACATCATTCACCGAGCCTACAAAACTAGTTTGGCACCTTGGAGCAACTGATACTATTTGTGTTTTGAATGTTGTAACAGAAGACACATTGCAGTGCAACAAGCAGTAACTTAAGACTAGAAAACACCCTCCAAAACACACTTGAGTAATCAGCCAGCATGAATAAAATATTTGGCACGAGTGATAAAATGAAGAAGGTCAAAATGAATAGTGCATGTGCTGTTGTTTGTGATGTTTACCAGCGTGATGAACTTGATTGGGTTATTTGTTTTTTTTTTTTCTGGTGATCAGGTGGAACAGTACCATAATGTTATTTTCCATGGGCTGGAGGGAAGCTTTCAGGAGTACATCGCCAACCAGATATCTCATTATATCAAGG[T/G]AATTATCATAAATATTAGAGTCTATGTGCAACACTATTGCTTTGTCAACTGTCAAGTTCGTATGTTATTTAAAGTTTCATCACAAAAAAAAGTTTAAAAGGAAATGTAACAAATGAAGAAAAATTGTAATTAGGGGGCAAGCTCCAAAGATTTGAGCCATAAGGGCTAGCAACAAAATAGTGGATTTAATTATGATTGTTATGATGTCATTAACTTTCATTAAAAAAAAAAAAATGTCTGTCGGCTCCAGTGGTGTAGTGGTTAGTGCGTCGACACATGCACTCTGGTGCTCGCGGCCACCTGGGTTCGATTCCGCCTCGTGGTCCTGTGCCGATCCTTCCCCTCTCTCTCTGCTCCCCATACTTTCCTGTCAATTCTCTCTACTGTCCTATCAAAAATAAAGGTGAAAACCCCGAAAAAATTATATAAAAATATATATATATATGTCTTTCCGATATCATGCTTTTTAATAAACTGATATATTCTCTAATAACATATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43091
Status:
Mutation detected in F1 DNA
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
ENSDART00000100743 Nonsense 1189 1573 16 23
ENSDART00000143233 Nonsense 1162 1427 15 19
Genomic Location (Zv9):
Chromosome 18 (position 20520038)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20750261
GRCz11 18 20739327
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGGGTGCTGAGCTGCGATTACAGCAGCACTTCCGCTGGGTTCAGCTG[C/T]GATGGGACAGCGAGCCCCTCAATGGCATGCTGGGACGGCATATGCGCAGA
Long Flanking Sequence:
TTGGATATGGCCTGATAAAAATAAATAAATAATAACAATATTAATGATAATAATAATAATTATGATTTCTGGGTCATGTGATTGAAGACTAAGGTAATAATGCTAAAATTCAGCTTTATGTTGCAGTAATTACAATTAATAATAATAATAATAATAATAATAATAAATATGAAAACTGTTACATTAGGTTAAATAATATTTTACAATTTTTGCTGAATTTTTTTTATTAAATAGAGATCGTCTTGGTGAGCAGAATAGGCTTCTTTTAAAAAAGAAAAAAGATCAAACAGATCCCAGATGATTGAAAGATCATTTATAGCAGAGCTGGAATAGCCAATGCTCCTGTAATAATATCTGGAATCAACTATTTCTTTTGCTGGGCAGGTCATGATGGGCTGTACTATTTCCGGGAAGGGAGTTTTTTAATGGGAACTCTGGCCAAGCCTCGTCTGCAGGGTGCTGAGCTGCGATTACAGCAGCACTTCCGCTGGGTTCAGCTG[C/T]GATGGGACAGCGAGCCCCTCAATGGCATGCTGGGACGGCATATGCGCAGAAAGTTGCTCCACAAGGTCAGCACTGCTTATTATGTAATAAGCTACAGGGATGACCACCAGAATAGCCTTTCAGCACTAAATTTAGTTCAGATCGTTTAGTATATTTAGTCAATGGTTGCTGCATCATTCCAGCAAACACTGAGTGATCTACATATAAATAATGATTTCAGCATTTAGTTTTTTTTTTCTATTTGTGTGTTCATAGATACAGTTAAAGTCAGAAATATTAGAAATATATATATTTTTTATTTCCCGAATTATGTTTACAGAGCATTGAAATGTTCACAGTATGTCTTACAATATTTTTTCTTCTGGAGAACGTCTTTGTTTTATTTTGGCTAGAATAAAAGCAGTTTTCAATTTTTTTAAAACAATTTTAAGTTCAAAATTATTAGCCCCTTTAAGCTACATTTTTCCGATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8747
Status:
Mutation detected in F1 DNA
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
ENSDART00000100743 Nonsense 1300 1573 18 23
ENSDART00000143233 Nonsense 1269 1427 17 19
Genomic Location (Zv9):
Chromosome 18 (position 20516123)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 20746346
GRCz11 18 20735412
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTYGAGGACGCTGTTATATCGAGAGTAACAGCCAAACGCTCTCCCTCR[C/T]AGCGACGGTCCCCCAACAGCAAAGCTCTGACCCCGGGCCARAGAGCAGTG
Long Flanking Sequence:
TAAAAATTTGGACCAATCGCTCTCTTTTATAAATGTCTAATCATCTTGTTTTATCCCGCCCTTTTTCTCTTCGCCATACAACAGAATTTTGCATGCTCAAACTCTAGTGTGACCACAGCATAATTCATCATTGACAATCATTCTATTATCCGATCAGCATAAGACCAAACCCCTATAAATAAGAGCCGACATTTAATCAAAATTCTATTGGCTGTTTTTTTAAAGCGGGAGGAGCTACTTAGTATGTCATGCTGTGTTATGTTTTAGTTGTAATTATGCCACACTTTAAACCCAACTATGCATTTCAAGGCACTTCAGGGTACACTATCCTAGATAGATTATTTTTCATTGTTTTCTTTTTTATCTGCACAGGCAGTGTTTTGTACTAACACTGGTCAATGTGTCTGTTCAGGTGGTTGGTGAGGCTTTGGAATGCAGTGATTGTTCCACGAGTCGAGGACGCTGTTATATCGAGAGTAACAGCCAAACGCTCTCCCTCG[C/T]AGCGACGGTCCCCCAACAGCAAAGCTCTGACCCCGGGCCAGAGAGCAGTGGTCAAAGCTGCTCTCAATATCCTGCTCAATAAAGCTGTTCTGCAAGGTTGCCCACTGCCCAGACCAGGTACAGCATTATCAGAACTGATGGGGAACGCATGGAAATAATAGTAACTACTGATGCGATTACATTCATGAGTAGCGTGACAGAAGCTCAGCTGATTTCACTATGAAGGGCCTTTTTCAAGCGCAAGAACAAACAAAAAGATTTAAACAAAATGTAATTAGTCTTGAGTTTGTGTCAGTGGTTTATCAAATCTAATTTACCTCAGCTAGTAAACAAACAATTACATAATAGATGAGTATGACTGTGATGGGGCTCCACTTTCTTTGATTTGAACATCCTTTCTAGTTCATTTCCTCTGTTCAGTTTTTCAAGTAAAAACCTTAAGAGATGCTTAAAGGGACCGTTCACCCTCAAATGAACATTTACTCTCCCTTAAATGGTTG
Associated Phenotype:
Not determined