Busch Lab

ZMP

fam32al

Ensembl ID:
ENSDARG00000042660
ZFIN ID:
ZDB-GENE-040704-44
Description:
Protein FAM32A-like [Source:UniProtKB/Swiss-Prot;Acc:Q6GQN4]
Human Orthologue:
FAM32A
Human Description:
family with sequence similarity 32, member A [Source:HGNC Symbol;Acc:24563]
Mouse Orthologues:
Fam32a, Gm5590
Mouse Descriptions:
family with sequence similarity 32, member A Gene [Source:MGI Symbol;Acc:MGI:1915172]
predicted gene 5590 Pseudogene [Source:MGI Symbol;Acc:MGI:3645451]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa11913 Nonsense Available for shipment Available now
sa12319 Nonsense Available for shipment Available now
sa37473 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa11913
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128149 Nonsense 51 109 2 4
ENSDART00000128149 Nonsense 51 109 2 4
Genomic Location (Zv9):
Chromosome 22 (position 15867117)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 15694687
GRCz11 22 15720957
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAACAAGTTTTGACCWCTGAAAACGAAGAAGGAACTAAAAAAGCTTA[T/A]GTTGACAAAAGGACACCAGCACAGATGGCATTCGACAAAATACAAGAGAA
Long Flanking Sequence:
GCGTATGAATTTATAACAAACGACTGGTTGGAAAAAGCAACTAAGCAGAAATAAATCGTTGTTTAAGAAACGAGTTTACTCCTGTTCTCTAGAGGGCAGTAAATCCGAGGAAAATTGATAAACAATCCTGTTGGGACGCAAGCTAGTCTGATACAGACAGAAGCTGAAATGTCGGAGTACAAGTCTGTCCAGAAAGGCTCTTTAAAACTGAAAGGGGTTTCTTTACCAAGTAAAAAGTGTGTATTTGTTTATGTTAGTTTTTAATATATCAAAACAACTATTACGATATTTATTTTGGAAATATTTTGTCATTGACTGACACGCCATCTGTTAGCTGTTATGCTAGCTCTGTGTTGTTGATCGACTTAACATCGTTGTTAATGTGATCAATTTTCATGTTGTGTTGTTTTTTTTAGGAAAAAGAAGAAGAATAAGGAAATGAAGCGTTTGGAGGAACAAGTTTTGACCTCTGAAAACGAAGAAGGAACTAAAAAAGCTTA[T/A]GTTGACAAAAGGACACCAGCACAGATGGCATTCGACAAAATACAAGAGAAAAGGGTGAGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCGACATTGCTCTTTAGCTTTCTGTGAGATTAACACACTATATTCTATCTTAAATATATTTTTCTCGTTAGCAAATGGAAAGAATCTTGAAGAAAGCCTCCAAAACACACAAGAGAAGAGTTGAGGTAAGCATCAGTATTGAGATTCATGTAAGTAACAAGTGGTTATTTGGTTATTAATGTGTAAATAAGTTATTTTTGTTGTGTTACAGGATTTCAACAGACACCTGGACACACTGACAGAGCATTATGACATTCCTAAAGTCAGCTGGACGAAATAAATATTTGTGGATTTTCAGTTTCATGCTTCAATAGCATATGGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12319
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128149 Nonsense 51 109 2 4
ENSDART00000128149 Nonsense 51 109 2 4
Genomic Location (Zv9):
Chromosome 22 (position 15867117)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 15694687
GRCz11 22 15720957
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAACAAGTTTTGACCWCTGAAAACGAAGAAGGAACTAAAAAAGCTTA[T/A]GTTGACAAAAGGACACCAGCACAGATGGCATTCGACAAAATACAAGAGAA
Long Flanking Sequence:
GCGTATGAATTTATAACAAACGACTGGTTGGAAAAAGCAACTAAGCAGAAATAAATCGTTGTTTAAGAAACGAGTTTACTCCTGTTCTCTAGAGGGCAGTAAATCCGAGGAAAATTGATAAACAATCCTGTTGGGACGCAAGCTAGTCTGATACAGACAGAAGCTGAAATGTCGGAGTACAAGTCTGTCCAGAAAGGCTCTTTAAAACTGAAAGGGGTTTCTTTACCAAGTAAAAAGTGTGTATTTGTTTATGTTAGTTTTTAATATATCAAAACAACTATTACGATATTTATTTTGGAAATATTTTGTCATTGACTGACACGCCATCTGTTAGCTGTTATGCTAGCTCTGTGTTGTTGATCGACTTAACATCGTTGTTAATGTGATCAATTTTCATGTTGTGTTGTTTTTTTTAGGAAAAAGAAGAAGAATAAGGAAATGAAGCGTTTGGAGGAACAAGTTTTGACCTCTGAAAACGAAGAAGGAACTAAAAAAGCTTA[T/A]GTTGACAAAAGGACACCAGCACAGATGGCATTCGACAAAATACAAGAGAAAAGGGTGAGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCGACATTGCTCTTTAGCTTTCTGTGAGATTAACACACTATATTCTATCTTAAATATATTTTTCTCGTTAGCAAATGGAAAGAATCTTGAAGAAAGCCTCCAAAACACACAAGAGAAGAGTTGAGGTAAGCATCAGTATTGAGATTCATGTAAGTAACAAGTGGTTATTTGGTTATTAATGTGTAAATAAGTTATTTTTGTTGTGTTACAGGATTTCAACAGACACCTGGACACACTGACAGAGCATTATGACATTCCTAAAGTCAGCTGGACGAAATAAATATTTGTGGATTTTCAGTTTCATGCTTCAATAGCATATGGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37473
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128149 Essential Splice Site 87 109 3 4
Genomic Location (Zv9):
Chromosome 22 (position 15867421)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 15694991
GRCz11 22 15721261
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAGAATCTTGAAGAAAGCCTCCAAAACACACAAGAGAAGAGTTGAGG[T/C]AAGCATCAGTATTGAGATTCATGTAAGTAACAAGTGGTTATTTGGTTATT
Long Flanking Sequence:
TTTGTCATTGACTGACACGCCATCTGTTAGCTGTTATGCTAGCTCTGTGTTGTTGATCGACTTAACATCGTTGTTAATGTGATCAATTTTCATGTTGTGTTGTTTTTTTTAGGAAAAAGAAGAAGAATAAGGAAATGAAGCGTTTGGAGGAACAAGTTTTGACCTCTGAAAACGAAGAAGGAACTAAAAAAGCTTATGTTGACAAAAGGACACCAGCACAGATGGCATTCGACAAAATACAAGAGAAAAGGGTGAGTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCGACATTGCTCTTTAGCTTTCTGTGAGATTAACACACTATATTCTATCTTAAATATATTTTTCTCGTTAGCAAATGGAAAGAATCTTGAAGAAAGCCTCCAAAACACACAAGAGAAGAGTTGAGG[T/C]AAGCATCAGTATTGAGATTCATGTAAGTAACAAGTGGTTATTTGGTTATTAATGTGTAAATAAGTTATTTTTGTTGTGTTACAGGATTTCAACAGACACCTGGACACACTGACAGAGCATTATGACATTCCTAAAGTCAGCTGGACGAAATAAATATTTGTGGATTTTCAGTTTCATGCTTCAATAGCATATGGGCTTGTTTTTGTTTTCTTGTAATTAGTGCTGCAGCAAAGTCCAGAGTGATTTTAAGTTTTCATTTAAAATTTTAAACCCTTTTGGATGCAGTCAACCTCTTTCTTTCTTTTTCTTTTCTTTTCTTTTTTAACACATTCAAGGTTCAAATGTTTGTGAAAATTACATTTTGTAACTTGTGGTTCAATTATGTATTTATGCTGTTGATTGGCTTTTGTTTATTGCAAGGCTTGACTGCCAAAAAAATAGTCCAAACATGTAAAGTGGCTTCAATTGCAATTTATGACAGAAAATGTTGATTCAAGAGT
Associated Phenotype:
Not determined