ZMP

zgc:112982

Ensembl ID:

ENSDARG00000001829

ZFIN ID:

ZDB-GENE-050306-55

Description:

hypothetical protein LOC503771 [Source:RefSeq peptide;Acc:NP_001013367]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24506	Nonsense	Available for shipment	Available now
sa45013	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24506

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024606	None	None	271	None	9
ENSDART00000111096	Nonsense	231	763	3	13
ENSDART00000130038	Nonsense	247	779	3	13

The following transcripts of ENSDARG00000001829 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 24 (position 24723323)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	23970201
GRCz11	24	24115375

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCATCGCCAGGATGGAACAGAAATGAAGCTTTTGATAAGGACACCAATT[T/A]ACAGCACAGCCAAAGAGAGATGAGGGATAGGTCTTATCCAAGACATCAAG

Long Flanking Sequence:

ATTCAAGGTATTGAATTTAAATTAGATGTTTTGAGTGGGTGTTACACTTAAACATTATTTTGTTGTTGCGTTGCTGGTTATTAACTGCTTCTTGAACCTCTCGAATATCAACAGAATCCCAACCCTTCAGGGAAGAAGAGCGGAGGGATTATTTGGTAACCAGATGCGTTCATCAGTACAATCTGACACGTGGAGGAACCCTGAATATGTCAAAGTAGAAACTAACCCCCACTGGAACAAAGATTCCCACCAAGGAGAGCAAAATGTCGACCATTGGGCCAAATTTATCGATGCAATAGAGCATGCTCAACAAAGAGGGCCTTCGCCTATGGCCAGATATCCGATGCAGGCTGATGAAGATAGGCCATCCGATTCTCCGAGAAGGCTTCCGAGGGAGAGGTTACCTTCCCCTGAACACACACATTATGGTGTGGAAGAGCATTATAGGATGGCATCGCCAGGATGGAACAGAAATGAAGCTTTTGATAAGGACACCAATT[T/A]ACAGCACAGCCAAAGAGAGATGAGGGATAGGTCTTATCCAAGACATCAAGAGAGAAGAAGTCATGACAGGATGGATTATGAGTATCGTAATGAAGAACATGGCGATCAATATCATGAAAGAGGCTCCTATTCAGAGAGGTACAACAACGAAATTCTTTCCTTGCTTCATACCTCTGACGTGGAAGGAAAGGATCGACAAAAAGAAGAAAAGAGCTCATCACATTCTCCATCTCTTTTTGTGATGGATATAATTGGATCTGTTAGATTTTATGGCACAAATTTTTACAGTTTTATTAAGTCTAATCTTTAATTTTAGTTTTATTTTGTTCTTTGAGATTTGATTTCTGTCATTGTACCAACTTAAAATGTATAGATCCAGTTAAATATACCATTCACAAAAACCTTGGTTTTGTAGTTGATCTAATTTCATTCAGTCCTGTAGATTCAGCTTGTTAGGTATTGCTGTAATTTCATTCTAATCTCGGATAAATGTTACTTGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45013

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024606	Nonsense	89	271	2	9
ENSDART00000111096	Nonsense	581	763	6	13
ENSDART00000130038	Nonsense	597	779	6	13

The following transcripts of ENSDARG00000001829 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 24 (position 24718930)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	23965808
GRCz11	24	24110982

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTATTTTAGTGGCCAAGACATCCCACTCAATGAACGCTTTGCAAATGAA[C/T]AGTATTATTCAATCCCTGATGAGATTAAAGAAGAAGAAGAATATGAGGAT

Long Flanking Sequence:

AAAGGAAGTATACGAAAAGTTAAGGGACAACTGTCATATGTTAAAATGGGAATTGCGATGTCGATAAGAAAGAAGTGCTGCTTTTTACGGCTGATTTCATTCCAACAGGAGTACTACACTATCCTCACTTGGTTTATGTTTATTTCTTGTAAGTAATGATTCTTATATCTACACATACATGTTACCTCTTCTCCAGTTATTTAGGATATTCATCAGATAGGCAGTTATCACTGGACTTAGTCAATGTGGGTCGACAGCGTCTTGATTTCCTGCCCATGCTGGAGCATTCTGGCACTTACAAGGAATCAGCAGTACATTGTGGGACGTTTGCCCAAGAAATCATCACACTTGTACATCAGGTTAAAGGTGAGAAGAAAATGGATTAGCCTTGTAGTGTATTCTGGAGTTTGTGACATTTGATTAACTATTTGCTTTCTTGTTTTGCAGAAAATTATTTTAGTGGCCAAGACATCCCACTCAATGAACGCTTTGCAAATGAA[C/T]AGTATTATTCAATCCCTGATGAGATTAAAGAAGAAGAAGAATATGAGGATGAGCTGGAAATGGAAAACTTGAGAGCACTCATGAATAGGCATGCATGCTAATTATTTTAACAATTTCATAAGCCCTAATCCTTTGAAGTTCTTCATGTTGTTTGTGGTGCAAACTGAAATTTTGATTCTTTCATATTAGGCCTCAAAGAATGCCATCTTCAGGAGCTCTGGATCCAGTACGTTTGATTTTTTTTTTTCAGCTCTGTCACTTTCAAAAAGAGCATTTATGTATATTTGACTAAAATCTTTATGCTTTTGCTAGCTTCAGAGACAACAGCCAGTCCCTGACCCTGGTGACCTCAGGTATGACTTGGAGCGAAGACGACAGCAGAAACTGGAGGCTGTGAAGATCACCATTGCTGGCGCAAACTTTACTCAGATGCCTTCTGAGAGGTATGGGCTAAAAATTGTTTCAGCTGGCTTTTTCCATGTGAATATGAATTTCCATGT

Associated Phenotype:

Not determined