Busch Lab

ZMP

si:ch1073-291c23.2

Ensembl ID:
ENSDARG00000074869
ZFIN ID:
ZDB-GENE-081107-2
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JMF6]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa2707 Essential Splice Site F2 line generated Not yet available
sa42104 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa44779 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa2707
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102941 None None 196 None 6
ENSDART00000109634 Essential Splice Site 84 204 4 7
ENSDART00000133731 None None 61 None 2
ENSDART00000140326 None None 85 None 3
ENSDART00000142695 None None 69 None 3
ENSDART00000147058 None None 110 None 3

The following transcripts of ENSDARG00000074869 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 235104)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 215123
GRCz11 13 345414
KASP Assay ID:
554-3209.1 (used for ordering genotyping assays)
KASP Sequence:
AGACTGANNNNNNNNTGATGTTGAATCACTAAGCATCTTGTCTTCTGTGC[A/T]GTTCTGTGTCTRTGGCRTTTTGTACATACTGTCTGAACGCAGCCCCWCCA
Long Flanking Sequence:
ACCACTGAGCCACCGTGCCGCACATATGTTGTGTTTGGTTATTTATTTAAATATAAAGCTTTCTCTGTTGTCGTTCTTCTTGCAGCATGTGCGAGTGATAATGTTTTGTAAAGCAATCGGTGTTGGTGAATCTAGCTCCTGTTTTTAGCACTGTTGTGATAGATATCCTTGTGAAAGGGTCCCAAAAAAGGGGGGCAGTGCAGTTTGCTATCTTGGTACTTTTGACAGTGAAAACTAAATGAAATGCATACCGTACTGTACTGAACCATACCTCTCTGTGGAAACAAGCCAAAAATATAGTCTATGGCATTAACTTTATCATGCCGTTTAGCTCACAACAATGTACACAATGCAGTTCAGGCTTTGTAGAAGCCTTAGATTAAAATAGCATGGTTTAATGAGGCTGTTTTAAGTGTTCTGGTTGTCAAGTCTTCACACACTGTTCACGTTAGACTGAGTATCTGATGATGTTGAATCACTAAGCATCTTGTCTTCTGTGC[A/T]GTTCTGTGTCTGTGGCGTTTTGTACATACTGTCTGAACGCAGCCCCTCCAAAAAGATCGTAAGTGTTTTATCCATCATCCAGATATTCAGTAAACGTTTTCTGCAATCAAAGTGTAATTCTGTGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGATTGTCCACAGATTACCGCTAGTTTTGCTCTGAGCATCATCTCCACCATTGGAGTGGTCAGCGCTTGTATGGACTTCATCAAATCAATGGTCATAATTGAACGTCAAGATGAGTACACCCATAACAACATCACAGAGGATGACTACGTTTATCTGAGACAACACTATGTGAGGGGTTTTATTCACTTATTCATTTGTGTTGCTTTCATGACATGCTTTTATTACGTTGAACTTGTTTCTAGTGCAAATATCAAAAAAAAAAAATACTTACGTTTAAGGGAGTTTTTCTTTAAAACAAGCAAAATAATCTGCCAATGAGGTAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42104
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
ENSDART00000102941 None None 196 None 6
ENSDART00000109634 Essential Splice Site 102 204 4 7
ENSDART00000133731 None None 61 None 2
ENSDART00000140326 None None 85 None 3
ENSDART00000142695 None None 69 None 3
ENSDART00000147058 None None 110 None 3

The following transcripts of ENSDARG00000074869 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 235044)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 215063
GRCz11 13 345354
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGGCGTTTTGTACATACTGTCTGAACGCAGCCCCTCCAAAAAGATCG[T/C]AAGTGTTTTATCCATCATCCAGATATTCAGTAAACGTTTTCTGCAATCAA
Long Flanking Sequence:
TTCTCTGTTGTCGTTCTTCTTGCAGCATGTGCGAGTGATAATGTTTTGTAAAGCAATCGGTGTTGGTGAATCTAGCTCCTGTTTTTAGCACTGTTGTGATAGATATCCTTGTGAAAGGGTCCCAAAAAAGGGGGGCAGTGCAGTTTGCTATCTTGGTACTTTTGACAGTGAAAACTAAATGAAATGCATACCGTACTGTACTGAACCATACCTCTCTGTGGAAACAAGCCAAAAATATAGTCTATGGCATTAACTTTATCATGCCGTTTAGCTCACAACAATGTACACAATGCAGTTCAGGCTTTGTAGAAGCCTTAGATTAAAATAGCATGGTTTAATGAGGCTGTTTTAAGTGTTCTGGTTGTCAAGTCTTCACACACTGTTCACGTTAGACTGAGTATCTGATGATGTTGAATCACTAAGCATCTTGTCTTCTGTGCAGTTCTGTGTCTGTGGCGTTTTGTACATACTGTCTGAACGCAGCCCCTCCAAAAAGATCG[T/C]AAGTGTTTTATCCATCATCCAGATATTCAGTAAACGTTTTCTGCAATCAAAGTGTAATTCTGTGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGATTGTCCACAGATTACCGCTAGTTTTGCTCTGAGCATCATCTCCACCATTGGAGTGGTCAGCGCTTGTATGGACTTCATCAAATCAATGGTCATAATTGAACGTCAAGATGAGTACACCCATAACAACATCACAGAGGATGACTACGTTTATCTGAGACAACACTATGTGAGGGGTTTTATTCACTTATTCATTTGTGTTGCTTTCATGACATGCTTTTATTACGTTGAACTTGTTTCTAGTGCAAATATCAAAAAAAAAAAATACTTACGTTTAAGGGAGTTTTTCTTTAAAACAAGCAAAATAATCTGCCAATGAGGTAAGAAAAACAGGTCACGCTTTATTCTGATGGTGTTTGTTGAATTTAAGTTACATTGCATCTACAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44779
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102941 None None 196 None 6
ENSDART00000109634 Nonsense 149 204 5 7
ENSDART00000133731 None None 61 None 2
ENSDART00000140326 None None 85 None 3
ENSDART00000142695 None None 69 None 3
ENSDART00000147058 None None 110 None 3

The following transcripts of ENSDARG00000074869 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 13 (position 234777)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 214796
GRCz11 13 345087
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCAAGATGAGTACACCCATAACAACATCACAGAGGATGACTACGTTTA[T/A]CTGAGACAACACTATGTGAGGGGTTTTATTCACTTATTCATTTGTGTTGC
Long Flanking Sequence:
TTAGCTCACAACAATGTACACAATGCAGTTCAGGCTTTGTAGAAGCCTTAGATTAAAATAGCATGGTTTAATGAGGCTGTTTTAAGTGTTCTGGTTGTCAAGTCTTCACACACTGTTCACGTTAGACTGAGTATCTGATGATGTTGAATCACTAAGCATCTTGTCTTCTGTGCAGTTCTGTGTCTGTGGCGTTTTGTACATACTGTCTGAACGCAGCCCCTCCAAAAAGATCGTAAGTGTTTTATCCATCATCCAGATATTCAGTAAACGTTTTCTGCAATCAAAGTGTAATTCTGTGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGATTGTCCACAGATTACCGCTAGTTTTGCTCTGAGCATCATCTCCACCATTGGAGTGGTCAGCGCTTGTATGGACTTCATCAAATCAATGGTCATAATTGAACGTCAAGATGAGTACACCCATAACAACATCACAGAGGATGACTACGTTTA[T/A]CTGAGACAACACTATGTGAGGGGTTTTATTCACTTATTCATTTGTGTTGCTTTCATGACATGCTTTTATTACGTTGAACTTGTTTCTAGTGCAAATATCAAAAAAAAAAAATACTTACGTTTAAGGGAGTTTTTCTTTAAAACAAGCAAAATAATCTGCCAATGAGGTAAGAAAAACAGGTCACGCTTTATTCTGATGGTGTTTGTTGAATTTAAGTTACATTGCATCTACATGCAGCCTAATTCTCATTAGATTATCAGTAGACTGTTCACATGCATAACACTACGCATATACACTGACATATACTCACAAAGCTTCTTATAGTAAGTTATATGTGTGTTGAAGGAGCGGTTTCAGCAGCTTTTAAGCAGACTAATACTCAAGTTTACCATCAAAATAAAGTGTTACTAAAAATAATCTGATCAAGAATAAATGTTGACTCATTATTTCTGACAATAAGAAACAAGACAAAGACAAAGACAGCAAGTGAGTGTAGAAGC
Associated Phenotype:
Not determined