Busch Lab

ZMP

kcnip1b

Ensembl ID:
ENSDARG00000034808
ZFIN ID:
ZDB-GENE-041212-57
Description:
Kv channel interacting protein 1 b [Source:RefSeq peptide;Acc:NP_001008632]
Human Orthologue:
KCNIP1
Human Description:
Kv channel interacting protein 1 [Source:HGNC Symbol;Acc:15521]
Mouse Orthologue:
Kcnip1
Mouse Description:
Kv channel-interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1917607]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa12212 Essential Splice Site Available for shipment Available now
sa21722 Essential Splice Site Available for shipment Available now
sa27600 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15042 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12212
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035188 Essential Splice Site 62 215 3 8
ENSDART00000109420 Essential Splice Site 62 215 3 8
ENSDART00000035188 Essential Splice Site 62 215 3 8
ENSDART00000109420 Essential Splice Site 62 215 3 8
Genomic Location (Zv9):
Chromosome 10 (position 22226069)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 22056407
GRCz11 10 22025859
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/C]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACWTTTATG
Long Flanking Sequence:
TTAGATGTTACAGTACATAACAATATGTTTACTGCTTTTTTTCATTTTTTTATTTATTTTATACTAGTATTTTATTTACATTATCACATTTCTATTTATAAATGTAATTTTTTTTAGCATGAAAATACTAAAAAGTGGCATGTTTTCAGGCATGTTTATGTTATTTTTTAACACAATACAAATGTTTTAAATTTAGAAGGGTTAAGAAACTCTTGGTTGAATAAAACATTTTGTATTCTGTCATTTTCTTAAAAGAATTATCAAATAATAATAAATCAAATAATAAAATGAAAACAAATAATTATAACAATAATTGTGGTTGAAATTTTGACACCAGTAAAATAAATATAACAAATTCAGTCAAACACCTAAAAAAATCAATCCAAAACTATATTTATCAAGTGGTCTCCTAAATTGTTTCACATATTTCTATACTACTGGTTTGAAATATCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/C]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACATTTATGCACAATTTTTTCCACATGGAGGTACTTTCCAAACAATTCTTTAGTTAACACCAAAAAGAACACCTGTCATCACTTTGAGACCCTCATGTTTCTCCATTCCTATAAGAAATTTCTTCATCTTCAGTAGACAAATAAAAATATTTCAATCAAATCTGAAAGATTTCTGTCTCTCCCTTCAATGTGTTTTCAAAATATTTATAAAGATATTTTAAAAAATCCATATGAACTTCATGAGTTCACTCATGGACTCTCCTTCAGCATAGTCATTGATGTTACAGGGTTTGCCACAGCGGAATGAACCACCAATTACTCTGGAATTTGTTTTATGCAATGGATTAAAACATACAAAATATTCATTTGTGTTTAAGTTTATAAATTAACATGCACTGTAAAAAATTCTAGGTTCCACACAATGATTTGTGTTGGGACAACATGAAGGAATCAAGTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21722
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
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035188 Essential Splice Site 62 215 3 8
ENSDART00000109420 Essential Splice Site 62 215 3 8
ENSDART00000035188 Essential Splice Site 62 215 3 8
ENSDART00000109420 Essential Splice Site 62 215 3 8
Genomic Location (Zv9):
Chromosome 10 (position 22226069)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 22056407
GRCz11 10 22025859
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/T]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACATTTATG
Long Flanking Sequence:
TTAGATGTTACAGTACATAACAATATGTTTACTGCTTTTTTTCATTTTTTTATTTATTTTATACTAGTATTTTATTTACATTATCACATTTCTATTTATAAATGTAATTTTTTTTAGCATGAAAATACTAAAAAGTGGCATGTTTTCAGGCATGTTTATGTTATTTTTTAACACAATACAAATGTTTTAAATTTAGAAGGGTTAAGAAACTCTTGGTTGAATAAAACATTTTGTATTCTGTCATTTTCTTAAAAGAATTATCAAATAATAATAAATCAAATAATAAAATGAAAACAAATAATTATAACAATAATTGTGGTTGAAATTTTGACACCAGTAAAATAAATATAACAAATTCAGTCAAACACCTAAAAAAATCAATCCAAAACTATATTTATCAAGTGGTCTCCTAAATTGTTTCACATATTTCTATACTACTGGTTTGAAATATCCAAAAATGAGTCTCGTAGCAATATTATGACCTGTTTGTTTTCCCCCAC[A/T]GGAGTGTCCAAGTGGAGTGGTGAATGAGGACACTTTTAAACACATTTATGCACAATTTTTTCCACATGGAGGTACTTTCCAAACAATTCTTTAGTTAACACCAAAAAGAACACCTGTCATCACTTTGAGACCCTCATGTTTCTCCATTCCTATAAGAAATTTCTTCATCTTCAGTAGACAAATAAAAATATTTCAATCAAATCTGAAAGATTTCTGTCTCTCCCTTCAATGTGTTTTCAAAATATTTATAAAGATATTTTAAAAAATCCATATGAACTTCATGAGTTCACTCATGGACTCTCCTTCAGCATAGTCATTGATGTTACAGGGTTTGCCACAGCGGAATGAACCACCAATTACTCTGGAATTTGTTTTATGCAATGGATTAAAACATACAAAATATTCATTTGTGTTTAAGTTTATAAATTAACATGCACTGTAAAAAATTCTAGGTTCCACACAATGATTTGTGTTGGGACAACATGAAGGAATCAAGTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27600
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035188 Essential Splice Site 179 215 6 8
ENSDART00000109420 Essential Splice Site 179 215 6 8
Genomic Location (Zv9):
Chromosome 10 (position 22228685)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 22059023
GRCz11 10 22028475
KASP Assay ID:
2260-3186.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTTAAAAGGAGACGTACCAAAGGCGCATGTGGATGCTTTCTTTGAG[G/A]TCAGTCATTAGTCTGTTAATTATTCAGTCATTCTTGGAGGTTACATTAAA
Long Flanking Sequence:
AATATTACATACGATTTCAGAGAATTAACATATTTAATGTTTTCATCTGTCGCCACTCCTTTAACAGATGCCAGCACATATGCACATTATCTCTTCCATGCGTTCGACACCAGAAATAATGGATCAATAAAATTTGAGGTATGAAGCCTAGATGAGAGCAGAATTAAAATAATGACATCGCACAGAGAAATGATTTTCTCACTCTCTCAGGACTTTGTGATGGGACTATCCACTCTATTGCGGGGGACAGTCAGAGATAAGCTGGAATGGACATTTCATCTCTATGACATCAACAAAGATGGATTCATCAATAAGGAGGTATGTCATATTTAAAGGGCAGGTGTAAATGTCATTACTTGATTCAGTAACGAATTCATTCTTCATGTACCTTTCAGGAAATGACAGAGATAGTGAGAGCGATCTACGACATGATGGGGAAATACACATATCCAGCTTTAAAAGGAGACGTACCAAAGGCGCATGTGGATGCTTTCTTTGAG[G/A]TCAGTCATTAGTCTGTTAATTATTCAGTCATTCTTGGAGGTTACATTAAAATTTAAAAACATTGGATTTTTTGTATGCTTTTTTGTGCTTTTGAAAACTGCTTTCACTCAATTTAGTTGATTATAACAATGTAATCGAAATTCTGAGAAATTTTTCATGTTCCTTCTGTTTAATCCCTTCATTATCAGCAGTCACCACGGCAGAATAAACTGCCATTAACATATTAAATTATTAACATTTTTTTTAATCTCTGGTCTTGAGTGCCACATATTTCAGAAATCATTCTATAGTAGTGGTGAAGTACTGCTTAGTTATATTAAACTATTGCTGATGGTTAATTATTAAAATAGTTTTTGCTATTTTTTAAGTATTAGTGTGAACTGTTTTTGTTGCTTTTTTTTGGCTAAATTTTGTGAATGATTTTTATAGCACGAGCTGTCACAGCAAGCTAAATACACTTTCACTCTTTCACAGAAAATGGACAAAAACAAAGATGGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15042
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035188 Nonsense 187 215 7 8
ENSDART00000109420 Nonsense 187 215 7 8
Genomic Location (Zv9):
Chromosome 10 (position 22229181)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 22059519
GRCz11 10 22028971
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTAAATACAYTTTCACTCTTTCACAGAAAATGGACAAAAACAAAGAT[G/T]GAGTTGTAACATTGGAGGAGTTTGWCCTTGCCTGCCAAGAGGTACWTTCA
Long Flanking Sequence:
TGAGGTCAGTCATTAGTCTGTTAATTATTCAGTCATTCTTGGAGGTTACATTAAAATTTAAAAACATTGGATTTTTTGTATGCTTTTTTGTGCTTTTGAAAACTGCTTTCACTCAATTTAGTTGATTATAACAATGTAATCGAAATTCTGAGAAATTTTTCATGTTCCTTCTGTTTAATCCCTTCATTATCAGCAGTCACCACGGCAGAATAAACTGCCATTAACATATTAAATTATTAACATTTTTTTTAATCTCTGGTCTTGAGTGCCACATATTTCAGAAATCATTCTATAGTAGTGGTGAAGTACTGCTTAGTTATATTAAACTATTGCTGATGGTTAATTATTAAAATAGTTTTTGCTATTTTTTAAGTATTAGTGTGAACTGTTTTTGTTGCTTTTTTTTGGCTAAATTTTGTGAATGATTTTTATAGCACGAGCTGTCACAGCAAGCTAAATACACTTTCACTCTTTCACAGAAAATGGACAAAAACAAAGAT[G/T]GAGTTGTAACATTGGAGGAGTTTGTCCTTGCCTGCCAAGAGGTACATTCACATTATGTGCAATTTCATTAGTCTTTTGCTGGGGTGCCCAAACTCTGTCCTGAAGGGCTGTTGTCCGGCATAGTTTAGATCCAACCCCAATCAGACACACCTGGGATAGCTAATCAAGCTGCGGTCACACTGGACTTTTATTCCCATAGACTTCCATTCATATGCACGCAAATACGTCAGACTGGAAAGGCAAGCTCGTGCAAAAGGTTTCGCAGTTCGCTGCATTGCAAAGTTCAAGCTTGGTGAACTCTGACCTGCCAAATCACATCACTTGACTGCGTGACACCAACCATGGGGGTTAAAACATGACCTCTCTGGACAGAAATTTAAAATATGAACCAATCGCTTGCTTTTTAAATGTCTAATCATCTTGTTTAATCCCACCCCTTTTTACATCACCCTACAGAATTTCACACACACAAATTCTAGTGTGACCGCTGCTTTAATAGG
Associated Phenotype:
Not determined