Busch Lab

ZMP

si:ch211-233h19.2

Ensembl ID:
ENSDARG00000042213
ZFIN ID:
ZDB-GENE-061009-14
Description:
hypothetical protein LOC565175 [Source:RefSeq peptide;Acc:NP_001082876]
Human Orthologue:
KIAA1324L
Human Description:
KIAA1324-like [Source:HGNC Symbol;Acc:21945]
Mouse Orthologue:
9330182L06Rik
Mouse Description:
RIKEN cDNA 9330182L06 gene Gene [Source:MGI Symbol;Acc:MGI:2443264]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa36574 Nonsense Mutation detected in F1 DNA Not yet available
sa43050 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa36574
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061900 Nonsense 223 1010 5 22
ENSDART00000145226 Nonsense 226 1013 5 22
Genomic Location (Zv9):
Chromosome 18 (position 8393715)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 8971093
GRCz11 18 8929112
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCAGGATTCAAGTAATAAATGGATCAAATTGACCAATCATGGAGAGTG[G/A]GGAGCACATAGTGTAAGTAAAAAAAAAATCTTATTTATTTGATGTATAAT
Long Flanking Sequence:
AATAAATACACAGCCTCAAACATTAACAAAAAAGATTGTCATAAGCTTTAAGAAACTTATTATTTTTCTTATTATTAATAAGCTTAAGAGATTCAATATTATACGAAATTTCAACAAGGAAAGTATTAAAAACAGGGTTTGTTTTTAGAAACTTATTTTTGTGTATAAAAAATTTACAGTGTAACACAAAAAATTTACAATAAGATCGAGAGCATGACCATCATCCGAGAAATACAGAAATATATCTTTTATAGACAAATTTAAATCATGTTTAAAAATGGATACCCCAATCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACCTAATCTACAATGTAAAAGCGCTATACAAATAAAGCTGAATTGAATTGAATTTTTGCATAATATGTCCCCTTCAAATGAACATTTTTTTGGACAGATTCAGAACGATCAGTGTCAAGAGATGGACCAGGATTCAAGTAATAAATGGATCAAATTGACCAATCATGGAGAGTG[G/A]GGAGCACATAGTGTAAGTAAAAAAAAAATCTTATTTATTTGATGTATAATTTTAGTTTTGTGTGCACTCATGCTTGCAAATTGCATACTTGTTGTCAAAAGTTTGAATTCTGTCAGATTTATAAAAATATTTTTAAATGAATGTGTGGTGTTTATCTGAAGGTTAAGTATGTAAGTTTGACACCTAGTGGATAAACTAGGTGTTGCACTTCTGGATCAAAACACATGCAAGTGTAGGTTGCCAGATTTATGCGAGTGTGCCTGACTATCGAGTCTAAAGGCTGATTTAAACCATTTTCTATCTAAAAGCAACGGCACACGATAAAAGGAATATTTTTCATACTAAAAGGAGTTTTTGTCCCTAACCAAGACCTGAAATCGTATTTTAGAAACAGCTATTTCTCAGCGTTGAAAACAGGATGAACTATGATCACCTCAGGTACACCTCATGTACTTTGTGTTAAATGCTAATATTGTGAATTTGAATGCCATTTTATATGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43050
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
ENSDART00000061900 Essential Splice Site 511 1010 12 22
ENSDART00000145226 Essential Splice Site 514 1013 12 22
Genomic Location (Zv9):
Chromosome 18 (position 8400575)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 8977953
GRCz11 18 8935972
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTTTGAAACCAGCTGTAAAGCCGACTGCGAGTTTTACTTTATGATGG[T/G]GAGTGTGTTCATATGGGATTGTGAAACTATTAATGTATATGGATATAGAG
Long Flanking Sequence:
AATATTTAAGATGTGGTTTCAGCTTCGGTGCACATTTGTGTTAAAGATCTTCATATCTTGTACATCTTGTGCGTTTTAGGTTGGGAAGTAGCCGGTGATCACATCCAATCAGGAGCAGGTCGTTCGGATAATGATTATCTCATATTAACTCTCAGAGTGCCCGGTTTCAAGTGAGTCTTCAAGCACTTGTCCACCTCCTCACAACTACACCGTTCAAGTGCTCATTAAAGCTCATTAAAGCCTTGTATGTTTAGCATGGTTAAGCCTTGTACATCACCTCTTCTGCTGCTTGCGATGGTATTAAAAGAATATATTAATTGAATAGTACGTTAGACTTGTTTATCATTACCCACGTCTCTCTGTGTAAAGAGGAATCTGTGTGGTTTATAATATCAGGTTGCCCTTGTCAGTTCGAGCCGCGTCCGGCAGCGAGTTTGGCCGGATCACGTTTGAGTTTGAAACCAGCTGTAAAGCCGACTGCGAGTTTTACTTTATGATGG[T/G]GAGTGTGTTCATATGGGATTGTGAAACTATTAATGTATATGGATATAGAGTTGAAATCAAAAGTTTTTTATTTTTTTATTTCCCAAATTATGTTTTACAAAGTATGGAATTTTTCACAGTATTTTTGATAATATTTTTTCTTCTGGAAAAAAAAATAAGATTATTATTATTTTTTTTAATCAATTTATGGTCAATATTATTAGCCCCCTTAAGCTATAATTGTTTTTGAACAAAGCATCTTTATACAATGACTTGCCTAATTACCCTAACTTGCCTAGTTAATCGAATTAATCTCGTTAAGTCTTTAAATGTCAGTTTAAGTCGAATACTATCATCTTTCAAAATAACTAGTAAAATGTTATTTACTGTCAACATGTTGAAGATAAAATAAATCGGATATTAGAAATTAGTTATTAAAACTATGATGTTTAGAAATGTTAATTTTCTGTTAAACCGAAAATGGGGATAATTACATACAGGGGGGCTAATAATTCTGACTT
Associated Phenotype:
Not determined