Busch Lab

ZMP

accn4b

Ensembl ID:
ENSDARG00000004243
ZFIN ID:
ZDB-GENE-040513-6
Description:
Amiloride-sensitive cation channel 4-B [Source:UniProtKB/Swiss-Prot;Acc:Q708S3]
Human Orthologue:
ACCN4
Human Description:
amiloride-sensitive cation channel 4, pituitary [Source:HGNC Symbol;Acc:21263]
Mouse Orthologue:
Accn4
Mouse Description:
amiloride-sensitive cation channel 4, pituitary Gene [Source:MGI Symbol;Acc:MGI:2652846]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa33831 Nonsense Mutation detected in F1 DNA Not yet available
sa44632 Nonsense Mutation detected in F1 DNA Not yet available
sa14893 Nonsense Available for shipment Available now
sa40654 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16524 Nonsense Available for shipment Available now
sa12799 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa33831
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104716 Nonsense 111 558 1 10
Genomic Location (Zv9):
Chromosome 6 (position 13516249)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 13373528
GRCz11 6 13607063
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTATCTGGAGCGTCCCCACCTCGCAGCTCTAAGGGAAGAAACCCGCCGA[G/T]AGCTCACCTTTCCGGCCATCACGCTCTGTAACGTCAACAGATTCCGCTTC
Long Flanking Sequence:
AGGAGAGACTCACTGGGAGTAGATGGAGAGAGCAGAAAAAGTTGAGCAATATTTGTTAATGATTAACAAGATTTGAGAAAGAAGATTTAGGAAAGGAGGAAAATCTCAGCCGAAGGAAGGATCAGAATACATTTGCAAAGGGCTCTTCACACGGAGCCCTGGCCAACCACATGCCCATCGAATTTGTTTGTAAAATCAAGTTCGCTGAGGGCGAAGAAGCCAAGGGGGCCTCGACAGAAGGAGGAGGAACCGGCATGCTAGATGAAGGCCTTCGGCGGCAAAAAGAAGGCATGGCTGACCTGGCATCCTTTGCAAGCTCCTCTTCACTTCACGGTTTGGCTCGGGCACTAGGGACCTCGGAGCGCTTGGGTTTCAGACAGACTCTTTGGGGACTGGCACTGCTGGTCTCGCTTGGTCTCTTCCTGTACCAGGCGACATGGAGTGCGGCGACTTATCTGGAGCGTCCCCACCTCGCAGCTCTAAGGGAAGAAACCCGCCGA[G/T]AGCTCACCTTTCCGGCCATCACGCTCTGTAACGTCAACAGATTCCGCTTCTCTGCCCTCACAGATGCGGACATCTACCACTTGGCTAACCTCACCGGCCTTCCGCCCAAGAGCCGTAAAGGACACCGGCCAAGCGAGCTCCAGTACCCACCCCCAAACATGCTAGACATTTTCCAGAGGACTGGCCACCAGCTGGAAGACATGCTGAAGAGCTGCAACTTCAGCGGGCAGAACTGCTCAAGCGAAGACTTCAGCGTGGTGAGTAGCACTGGCTTTGATTGGCTTCCAGGCGCAAGAAAGATATGATTGTTAGGGGCTCTTTTTGTTTGGTGACTGTGGGCAAAGTGTTGTACAATGCCTCCCTCAGCCGTTTCCTTTATTAGAGACAGATAACAGCTAAATAATGTGTGTGGAAAAAGGAAATTAAGCCCCATCCATCTGTGTCTAACCTCCATGCTGGGGCAACAGACAGTAAAACAGTGCAGTTATTTGCTCAGTTCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44632
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
ENSDART00000104716 Nonsense 293 558 4 10
Genomic Location (Zv9):
Chromosome 6 (position 13578511)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 13435790
GRCz10 6 13540025
GRCz11 6 13669325
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTCTTTCTCTAAATGTCTCCTGTTTTTATAGCTAACATACCTGCCA[C/T]AGCCGTGGGGAAACTGTCGGGCTTCATCCGAGCCTGTGATCCCAGGATAC
Long Flanking Sequence:
TAGAATATTGAATTACTTGTGCAAGCTGTTAGTTTTACTTACACAGTATGATCTGTCCATCTTCAGACGAGACTACGCTGGAAGCAGGTATTCGGGTTCAGATACACAGTCAGAATGAACCCCCGTACATCCACCAGCTGGGCTTTGGAGTCTCACCAGGATTCCAAACATTTGTTTCCTGCCAGGAACAGAGGGTAAGTTTAAACTCATTGCTTTTTGCATGGCAGAAAGGCTGTTATGCATCTGAATTCAACACCAAGCTGTTATACATCTGAATTTAACACCGGGCTGTTCTCAACTCTCGAATTTCAGACATTTAAAATTAGGAGCTAATTTACAAAATGTCAAACAGATTTCAAGGCTGACTGGAATATTTTCTAATTGAGACTGCATGTGCTATTTCACGGCCATAGGGTGCACTCAGGCAGACAAAGAAGCAGAGAGACGCCGGTTTTTCTTTCTCTAAATGTCTCCTGTTTTTATAGCTAACATACCTGCCA[C/T]AGCCGTGGGGAAACTGTCGGGCTTCATCCGAGCCTGTGATCCCAGGATACGACACCTACAGCGTCAGCGCCTGCAGACTGCACTGTGAGAGCACACAGGTGCAGAGAGAGTGCAACTGCAGGATGGTGCATATGCCAGGTGCGAGCTGTAGTATGAGAGCTGTCATAATAATAAAAAAAACTGTCCGTATCAGTGAGAACAAATGTGTCGTTGTTACTTGAGGGGTTACAGCCGAGGCCGGAAGTTAAAATAAATTATTTTTATATTATTTATTAAATGACCTATTAATTGTATTTTATTAATGTATTTTTCTTACCCCTCACTCTAATGTAAAAATTATAAAGATAATTATTTTTATTATTCATAAAATTACCAATTAATTGTATTTTATAAATGCACTGTTAACAATTTCCTGTTTGCCAGTAACTTACTGTAAATCAAACAGAGCAAAACTACTGTATTTACATATACAGCACTAATTATTTTGCTGTTCATTTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14893
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104716 Nonsense 309 558 4 10
Genomic Location (Zv9):
Chromosome 6 (position 13578561)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 13435840
GRCz10 6 13540075
GRCz11 6 13669375
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCRTGGGGAAACTGTCGGGCTTCATCCGAGCCTGTGATCCCAGGWTA[C/A]GACACCTACAGCGTCAGCGCCTGCAGACTGCACTGTGAGAGCACACAGGT
Long Flanking Sequence:
ATCTGTCCATCTTCAGACGAGACTACGCTGGAAGCAGGTATTCGGGTTCAGATACACAGTCAGAATGAACCCCCGTACATCCACCAGCTGGGCTTTGGAGTCTCACCAGGATTCCAAACATTTGTTTCCTGCCAGGAACAGAGGGTAAGTTTAAACTCATTGCTTTTTGCATGGCAGAAAGGCTGTTATGCATCTGAATTCAACACCAAGCTGTTATACATCTGAATTTAACACCGGGCTGTTCTCAACTCTCGAATTTCAGACATTTAAAATTAGGAGCTAATTTACAAAATGTCAAACAGATTTCAAGGCTGACTGGAATATTTTCTAATTGAGACTGCATGTGCTATTTCACGGCCATAGGGTGCACTCAGGCAGACAAAGAAGCAGAGAGACGCCGGTTTTTCTTTCTCTAAATGTCTCCTGTTTTTATAGCTAACATACCTGCCACAGCCGTGGGGAAACTGTCGGGCTTCATCCGAGCCTGTGATCCCAGGATA[C/A]GACACCTACAGCGTCAGCGCCTGCAGACTGCACTGTGAGAGCACACAGGTGCAGAGAGAGTGCAACTGCAGGATGGTGCATATGCCAGGTGCGAGCTGTAGTATGAGAGCTGTCATAATAATAAAAAAAACTGTCCGTATCAGTGAGAACAAATGTGTCGTTGTTACTTGAGGGGTTACAGCCGAGGCCGGAAGTTAAAATAAATTATTTTTATATTATTTATTAAATGACCTATTAATTGTATTTTATTAATGTATTTTTCTTACCCCTCACTCTAATGTAAAAATTATAAAGATAATTATTTTTATTATTCATAAAATTACCAATTAATTGTATTTTATAAATGCACTGTTAACAATTTCCTGTTTGCCAGTAACTTACTGTAAATCAAACAGAGCAAAACTACTGTATTTACATATACAGCACTAATTATTTTGCTGTTCATTTATATTTACAGAATTGTATGTGTATATCTTTACAGTTAAGTACTATGTAATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40654
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104716 Essential Splice Site 439 558 8 10
Genomic Location (Zv9):
Chromosome 6 (position 13596749)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 13454028
GRCz10 6 13558263
GRCz11 6 13687563
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGCTTTAGTTGCCCATTTTGATGTCATCACAGTGTGGTTTCTATTTTC[A/G]GGAGACATTGGTGGACAGATGGGCCTCTTCATTGGAGCCAGTATTCTTAC
Long Flanking Sequence:
AATCTTTTATATGGTTGTTTGCATGCGTCATCAAGAAATTAAACATTGATAACATGCAGAAAATTACTCACAAAAGGAAAATGGCAACTATGAACTTCGGCAACTGTAGGTGGTGGGCTTAAATGTCCTTTTTATCATAAGGAAATGTCACTTTTTCAAAAAGAATGTACAAAATACACCACTTTATATCTGTCTCAGGTCATTTTTGATTGACAAAGCATAATATGTTTGCTGGGTGACAATCACTACTTTGAGTATCACTACTTTTTTTGCAATAATGAGTTGGTTTGTGCATATATGAAGCATTTTTGTAATTTTAAAGCAAACTGAATGTAAAATGAAATTCTGTGGCAAACTGCAAGGAGAACTTCTGAAAAATGGCTGACCTCAAAAATAAATAATTAAAATGTAGTGTTTGTTGGGTAATTATGATAGATCAACTTGATTTGAAATGCTTTAGTTGCCCATTTTGATGTCATCACAGTGTGGTTTCTATTTTC[A/G]GGAGACATTGGTGGACAGATGGGCCTCTTCATTGGAGCCAGTATTCTTACCATACTGGAAATACTCGACTACATCTATGAGGTACCTTCACTTCACTGAGAAAATATTTATACAGTTGAAGTCAGAATTACTAGCCCACCTGTTTATTTTTCCCCCCAATTTCTGTTTAATGGAGAGAAGATTTTTTTCAACACGTTTTAAACATAATAGTTTTAATAACTCATTTCTAATAGCTAATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTTACTAGAATTTTTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAACTAGGCAGGTTAGGGTAATTAAGCAAGGTATTGTATATTGATGGTTTGTTTTGTCGACTATCGAAAAAAATATATAGCTTAAAGGGGCTAATAATTTTGTCCTTAAAATGGTGTTTAAAAAATAAAAATAAAAATGCTTTTATTCTAGCCGAAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16524
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
ENSDART00000104716 Nonsense 508 558 9 10
Genomic Location (Zv9):
Chromosome 6 (position 13597570)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 13454849
GRCz10 6 13559084
GRCz11 6 13688384
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGCAGATCCAGAGAACCAAGAACCTGCGGGAGCAGAACCTRAAAGCT[C/T]AGCTAACTGCCGGAGCAATAGCTACAGTCARGTTTGAAGAAGTCAAAGTC
Long Flanking Sequence:
TTTAAAGGCTTAACTAGGTTAACTAGGCAGGTTAGGGTAATTAAGCAAGGTATTGTATATTGATGGTTTGTTTTGTCGACTATCGAAAAAAATATATAGCTTAAAGGGGCTAATAATTTTGTCCTTAAAATGGTGTTTAAAAAATAAAAATAAAAATGCTTTTATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATTAGACATACTGTAAAAATTTCCTTGCTCTGTTAAACATCATTTTGGAAATATTAAAATAAAAAAAATTATTTAAAGGGGGGCTAATAATTCTGACTTCAACTATATATAAACAAACAAATACACAACATCCCATAACATTTTAATCATTGCCTCTACAGGTAGCCAAAAACAAAATCAAGCAACTCCTGAAACCAAAGAAGAGCCAGAAACAAACCAACCAACGGAACTTGATCCAAGAGCAGATCCAGAGAACCAAGAACCTGCGGGAGCAGAACCTGAAAGCT[C/T]AGCTAACTGCCGGAGCAATAGCTACAGTCAGGTTTGAAGAAGTCAAAGTCAAGGTGAGTCGGGGAAATAAAGTGTATTCCAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTGCACCTAGTAATTAATGATGTGATTTGTTTGTCAACAGGCAGCTAATGATGTGGCTCAACCACACAGCGCACATCCAACTTCGGTATTACCAAATCATCACAATGCACAACAAGCCGTACAGCAGGACTTTGCTTGTTAAAGGACGACTTCTGTCTGTTCATTTTTTCATATCACCGAACTTGACGTTGGGGTCTTGGATGGATCCTGTACACATTTCTCCTTTTTTCACTTATAAAAGCTACAGCCAAAGCATAATCCAGGACCTCATGTGAAACCGGTTCAAACTAGTCACAATGAAAAAACCACATGTTTTTTTAGATTTTTTTTTTCCTCTCTCTGGATGGACAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12799
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000104716 Essential Splice Site 525 558 9 10
Genomic Location (Zv9):
Chromosome 6 (position 13597624)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 13454903
GRCz11 6 13688438
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACTGCCGGAGCAATAGCTACAGTCARGTTTGAAGAAGTCAAAGTCAAG[G/A]TGAGTCRGGGAAATAAAGTGTATTCCAAACAMAMACACACACACACACAC
Long Flanking Sequence:
GTATATTGATGGTTTGTTTTGTCGACTATCGAAAAAAATATATAGCTTAAAGGGGCTAATAATTTTGTCCTTAAAATGGTGTTTAAAAAATAAAAATAAAAATGCTTTTATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATTAGACATACTGTAAAAATTTCCTTGCTCTGTTAAACATCATTTTGGAAATATTAAAATAAAAAAAATTATTTAAAGGGGGGCTAATAATTCTGACTTCAACTATATATAAACAAACAAATACACAACATCCCATAACATTTTAATCATTGCCTCTACAGGTAGCCAAAAACAAAATCAAGCAACTCCTGAAACCAAAGAAGAGCCAGAAACAAACCAACCAACGGAACTTGATCCAAGAGCAGATCCAGAGAACCAAGAACCTGCGGGAGCAGAACCTGAAAGCTCAGCTAACTGCCGGAGCAATAGCTACAGTCAGGTTTGAAGAAGTCAAAGTCAAG[G/A]TGAGTCGGGGAAATAAAGTGTATTCCAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTGCACCTAGTAATTAATGATGTGATTTGTTTGTCAACAGGCAGCTAATGATGTGGCTCAACCACACAGCGCACATCCAACTTCGGTATTACCAAATCATCACAATGCACAACAAGCCGTACAGCAGGACTTTGCTTGTTAAAGGACGACTTCTGTCTGTTCATTTTTTCATATCACCGAACTTGACGTTGGGGTCTTGGATGGATCCTGTACACATTTCTCCTTTTTTCACTTATAAAAGCTACAGCCAAAGCATAATCCAGGACCTCATGTGAAACCGGTTCAAACTAGTCACAATGAAAAAACCACATGTTTTTTTAGATTTTTTTTTTCCTCTCTCTGGATGGACATATCATGGACTGCATAAAAGAAAATGACCAAGGCGCCACTTGAATTTGGCATATA
Associated Phenotype:
Not determined