ZMP

si:dkey-179j5.5

Ensembl ID:

ENSDARG00000074538

ZFIN ID:

ZDB-GENE-070705-320

Description:

hypothetical protein LOC100007187 [Source:RefSeq peptide;Acc:NP_001098618]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29798	Nonsense	Mutation detected in F1 DNA	Not yet available
sa24184	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa29798

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
ENSDART00000102751	Nonsense	43	127	3	6
ENSDART00000125831	Nonsense	75	159	3	5

Genomic Location (Zv9):

Chromosome 22 (position 25464354)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	24964260
GRCz11	22	24991884

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCTCAGACGTCGTAACTGCATGCGAGGGGTTTCTCCTGTATCTGACCTG[T/A]CCAAGTAAGATGAAGCGTCAATCTACTAAAGCTCTTGACTACATAATACT

Long Flanking Sequence:

TCTGATTAGCAATGCACAGGTGTCTTAATCAGTTCTTATCTGTATTTTCAGTAATGCTTATGAACTGCAGTCTGCTGATATCTGCAGATGATTGTGATGGACCAACTGGTACATTTGATGACTTCAGACCATTTATTTATTTATTTACTTATTTATTTATTGATTGCAACGTAGGAATGCTTGACACTTAATTGGTCTTTTGCTCCGTATTTGCTAAAATCTAAATGTGGATAGTAATATTGAGATGAGTGTTTACAAATAGTCTGATACCTTGTGAATCTATTGATATGAACGGGCAAAGTGCACTCATGCACTGTCAGGACCCTGAACAACTCTGTGCGTTAAAGAGTAGATGAGTGAATGTGTTTCTGTACCAAACTTATTCAGAGCCCTTATCTCAATCGCGGACCAGTTTAAGTGATGATTAATGCCCTAAAGCTGGTCTTTCTTTTCTCAGACGTCGTAACTGCATGCGAGGGGTTTCTCCTGTATCTGACCTG[T/A]CCAAGTAAGATGAAGCGTCAATCTACTAAAGCTCTTGACTACATAATACTGCTGTTTTATTCATGTTGCATAGTAAATCTAAAATCGTTCATCATGTCACACGCAGTCTCTTTATTAACTTCTGTACTCTTGTTCTACATATAGAACATCATAAGATCACGATAATTGATGCACTCTATGGGCGTAAAACTAAAGCAATCTGCTATGATCAACCTCAAGACCAGCTCCAGAACACCAACTGCTATTCTCCTCACGCACTGCACATTGTGTCAGAAAGGTATAGATTACAGCAATTTGCTTTATAATTCTAATACTTGGGCTTATTTTTATATTGATGGTTTTCAAATACTAGAGGAGATGCCAGTAGGTTGGGTTAAGGGTTGTGGTAAATGTTAATAAAACAATATTTCCTGTAAGGTGTTGGTTTAGGGTTGTGGTAAGTGTTATTGAAACTAAACAGGTTACTGTGAGATTGTGTTTAGGATTGGTGGGACATTAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24184

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

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000102751	Essential Splice Site	89	127	4	6
ENSDART00000125831	Essential Splice Site	121	159	4	5

Genomic Location (Zv9):

Chromosome 22 (position 25464075)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	24963981
GRCz11	22	24991605

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAACACCAACTGCTATTCTCCTCACGCACTGCACATTGTGTCAGAAAGG[T/C]ATAGATTACAGCAATTTGCTTTATAATTCTAATACTTGGGCTTATTTTTA

Long Flanking Sequence:

CTATTGATATGAACGGGCAAAGTGCACTCATGCACTGTCAGGACCCTGAACAACTCTGTGCGTTAAAGAGTAGATGAGTGAATGTGTTTCTGTACCAAACTTATTCAGAGCCCTTATCTCAATCGCGGACCAGTTTAAGTGATGATTAATGCCCTAAAGCTGGTCTTTCTTTTCTCAGACGTCGTAACTGCATGCGAGGGGTTTCTCCTGTATCTGACCTGTCCAAGTAAGATGAAGCGTCAATCTACTAAAGCTCTTGACTACATAATACTGCTGTTTTATTCATGTTGCATAGTAAATCTAAAATCGTTCATCATGTCACACGCAGTCTCTTTATTAACTTCTGTACTCTTGTTCTACATATAGAACATCATAAGATCACGATAATTGATGCACTCTATGGGCGTAAAACTAAAGCAATCTGCTATGATCAACCTCAAGACCAGCTCCAGAACACCAACTGCTATTCTCCTCACGCACTGCACATTGTGTCAGAAAGG[T/C]ATAGATTACAGCAATTTGCTTTATAATTCTAATACTTGGGCTTATTTTTATATTGATGGTTTTCAAATACTAGAGGAGATGCCAGTAGGTTGGGTTAAGGGTTGTGGTAAATGTTAATAAAACAATATTTCCTGTAAGGTGTTGGTTTAGGGTTGTGGTAAGTGTTATTGAAACTAAACAGGTTACTGTGAGATTGTGTTTAGGATTGGTGGGACATTAATAAAACACAATAGGTTGAATCCTATGTAATTTACTCAAATCAATGGAATCTACAGGAGGTTTGTATAGCCGAGTTGCACCACAAGCCACCCACTTGGGGTTGACCTGCCCATTTGGAGCTGGCTTCTATACCTCAGTTTATACCCTTCTTTGATAATGGGGAATTTTTTTATTTATTTATTTTTTTAATATAAATCAAATGTTGGTTTTAGACTCAAACTTAGTTGATGTGTGATCTGCATAATTAATATGGTTAATTTAAAATTTGTCATTTTCATGCT

Associated Phenotype:

Not determined