Busch Lab

ZMP

si:ch211-238g23.1

Ensembl ID:
ENSDARG00000055746
ZFIN ID:
ZDB-GENE-050420-173
Description:
Novel protein kinase domain containing protein [Source:UniProtKB/TrEMBL;Acc:A3KQ71]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa25070 Nonsense Mutation detected in F1 DNA Not yet available
sa25071 Essential Splice Site, Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25070
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000059289 Nonsense 26 287 1 6
ENSDART00000147656 Nonsense 426 693 4 9
Genomic Location (Zv9):
Chromosome 18 (position 35256984)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 36936140
GRCz11 18 36917148
KASP Assay ID:
554-7576.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGAGAAGGAGCGTTTGGCCAGGTGTTTGTGGCATCTTACAAACTTCGT[A/T]AAAGAGTAAAGGTAGAGAACTACTATTTACATTCAGTCAACATTTTCCTC
Long Flanking Sequence:
TGCAGCTCTGTTCATGTAGATGTTTCTGTTTGTTTTCTTCATTTTAGAAAAACCCAAGAAAGGAAGGAAAGGGAAAAGAGTCTCTGCTTTCTTTAAGAGAGTATGGAAGGCTATAACGCGCCCTTTCCTGTGCTGTGACACAGATATAGTCCAGCATCTTACGCCACATCCAGAGCTAGAGGAAGCTAACGAAGCTTCTGGACCCCCTGGTAGTAAGTCATCATTTTCTTCTATTTTCTGTAACTCATAATTATTATAAATTAGTGATCAATTTACGCCAGCAATTCTGATAGAAGTTATTGCTTTCAGCTCATTGCATTAAATCCAGATTCAAAGGATACGAGTTATTTATTTGATCCGTTTTATACCAGACAATCCAAGGAAATCTCCCTGCTTTTTTTCTGTGTTTTTCAGGATTAGATCTGTCTGATTTTAAAGTCGGAGCCGTGATTGGAGAAGGAGCGTTTGGCCAGGTGTTTGTGGCATCTTACAAACTTCGT[A/T]AAAGAGTAAAGGTAGAGAACTACTATTTACATTCAGTCAACATTTTCCTCCTGATTATTGAATATATTCAATTTGTTGGCTTTAATTTAATTTGTTGTTTTTTCTTCGCAGGTTGCCCTGAAGTTTATCTACAAGAGTTTCGACGACCGCTATCTTGACATTGTAAGTTGAATAAATCACACAACAGTGAAAATGTGCCGACCATTAACTCGTCTTTCACTTGTCCCGTACCTGTCTGGACCACTTTAAACTGAACTCAAGAGCAGATATGTTGGAAACAGGGAGCCACTGACTTCCATTGTAGAAACAGAAAATACTTGAAGTTTCTGCTTACTGGTTTTCAACATTAAATATCTTCTTTTGTGTTCAGCAGAAGAAATAAACCTGGAGACAAGTTTAGAACACATGAATGTAGGGCTGTGGAGTTAATGAAAACTCATTTGACATTATTGCAGATAAAAATGATCATTACGTCATATCCCGGCCCCTTGTAAAGCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25071
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, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000059289 Missense 47 287 2 6
ENSDART00000147656 Essential Splice Site 446 693 5 9
Genomic Location (Zv9):
Chromosome 18 (position 35257147)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 36936303
GRCz11 18 36917311
KASP Assay ID:
554-7857.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCCTGAAGTTTATCTACAAGAGTTTCGACGACCGCTATCTTGACATT[G/A]TAAGTTGAATAAATCACACAACAGTGAAAATGTGCCGACCATTAACTCGT
Long Flanking Sequence:
CCACATCCAGAGCTAGAGGAAGCTAACGAAGCTTCTGGACCCCCTGGTAGTAAGTCATCATTTTCTTCTATTTTCTGTAACTCATAATTATTATAAATTAGTGATCAATTTACGCCAGCAATTCTGATAGAAGTTATTGCTTTCAGCTCATTGCATTAAATCCAGATTCAAAGGATACGAGTTATTTATTTGATCCGTTTTATACCAGACAATCCAAGGAAATCTCCCTGCTTTTTTTCTGTGTTTTTCAGGATTAGATCTGTCTGATTTTAAAGTCGGAGCCGTGATTGGAGAAGGAGCGTTTGGCCAGGTGTTTGTGGCATCTTACAAACTTCGTAAAAGAGTAAAGGTAGAGAACTACTATTTACATTCAGTCAACATTTTCCTCCTGATTATTGAATATATTCAATTTGTTGGCTTTAATTTAATTTGTTGTTTTTTCTTCGCAGGTTGCCCTGAAGTTTATCTACAAGAGTTTCGACGACCGCTATCTTGACATT[G/A]TAAGTTGAATAAATCACACAACAGTGAAAATGTGCCGACCATTAACTCGTCTTTCACTTGTCCCGTACCTGTCTGGACCACTTTAAACTGAACTCAAGAGCAGATATGTTGGAAACAGGGAGCCACTGACTTCCATTGTAGAAACAGAAAATACTTGAAGTTTCTGCTTACTGGTTTTCAACATTAAATATCTTCTTTTGTGTTCAGCAGAAGAAATAAACCTGGAGACAAGTTTAGAACACATGAATGTAGGGCTGTGGAGTTAATGAAAACTCATTTGACATTATTGCAGATAAAAATGATCATTACGTCATATCCCGGCCCCTTGTAAAGCATTCTGCATTCATTTCTACGCAAAACTCAATTTCACGTTGACATCAGTGAAATCATGTAGCGTAACGTTTGCAGCATGGGATGTGCTTAATTAATTAGAGTGTATATGATTCATTCACGTCTTTAATAGTGCTTGTGCTGTTGTGTGCATGTGCTCAGCCACAAAG
Associated Phenotype:
Not determined