ZMP

zgc:101130

Ensembl ID:

ENSDARG00000003102

ZFIN ID:

ZDB-GENE-040801-72

Description:

Novel protein containing zinc finger C2H2 type domain [Source:UniProtKB/TrEMBL;Acc:Q1LXM0]

Human Orthologues:

ZNF501, ZNF502

Human Descriptions:

zinc finger protein 501 [Source:HGNC Symbol;Acc:23717]
zinc finger protein 502 [Source:HGNC Symbol;Acc:23718]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43750	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa39356	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43750

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
ENSDART00000013201	Essential Splice Site	12	372	1	2

Genomic Location (Zv9):

Chromosome 22 (position 2591839)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	1404687
GRCz11	22	1421585

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTTCACTGAAGAGGATGGATCCATATGAAGATTTTGCAGAACAAAGAGG[T/C]TAGTGATTATTGATCATTCTTCGGTGGAATTAATCAAGTAGCCTAATAAT

Long Flanking Sequence:

ATGTTTCTATGACTGGTTATGTGTTTCTTTCTGTATGCTCTTATAAGAAATTAAATAAAAGTTGTGTAGAGCGAATGAACTCAGCTTTTTTACGCTGGAATGGGCGTGGCTTACGAAGAAAGCGCTTGTACTTCCGGAGCTGCCGCTTTTAGCAGTAGATAAATAGAATGGCGATATGATTGCTGCTTTGATCGTACGCGTTCGGAACGCTTCTTCTGTTCGATTGTTTGGAACGCGAGTTCTATTTTGCTGTTCACGCGGGTAAAACGGGAATAGCGGCGAAACGGACTCTCATTAGCAAATGTAAACAGCTCAATATAGAGGTCCGACTGTTTGTTAATCAGTACCTCGGGACTGCTGTTACGGATTGAGAATTGGTATTGTTAACCCTATTGGCGGTCAATACTAGTATACTCTACATGAGAAAATAGTAGAATATCCAGAGTTAAGAGTTCACTGAAGAGGATGGATCCATATGAAGATTTTGCAGAACAAAGAGG[T/C]TAGTGATTATTGATCATTCTTCGGTGGAATTAATCAAGTAGCCTAATAATTTCTGCACCACATGCTATATGAGAATAGTCATCTGTTTATAATGAAAACGACAGTAAATGTCATAAACAGAGTCTCAAATGTCTTCATGACAGATTTATTTTCAAAGTGTTTTCCTACTTTACGTAAATAAATCATGTGTTTATTAATGACTACTGATTAACCTTTAGTGTAATCGCTAAAAAGGTTAAACTGTTATTTGAACTAATGGAACTGATGTTCATTTTCGTGAGGAGTGTAGAGATAAACATTAAGAAATAATCGCAAAATCTTTCTCAAGGAAGGAAACTTACATTTTCATTCTATTACATTTAAAACGCTTCATTTGTTTATATTCAGGCACTTATTTGATTGCCAGCCCTTTTGATGATATACACTCACCGGCCACTTTATTAGGTACACCTTACTTGTACCGGGCTGGACCCCCTTTTGCCTTCAGAACTGCCTTAATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39356

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
ENSDART00000013201	Nonsense	358	372	2	2

Genomic Location (Zv9):

Chromosome 22 (position 2594059)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	1406907
GRCz11	22	1423805

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGGTGCTCGAAGAGTTTCAGGCGGGCGAGCCGTTTGTTGATTCATTTGAA[C/T]AAGCATCATTCGATGAATCTAACATTGTGGATTTTTCATGTTCATGAAAA

Long Flanking Sequence:

ACACCGGAGAGCGGCCTTTTATTTGCGACGAATGCGGGAAAAGTTTCCGACACGTCAATGGACTTCGCGATCATCAACTTTCGCACTCCGCCGTCAAATCCTTTCCGTGCGATCAATGCAATAAAGAGTTTATCACTCCATCTGCGCTGAAAAGACACCTCAGGGTTCACTCTGGCGAGAAGCCGTATTTGTGTACGCTGTGTGGGCGGAGTTTCTCTCGAGTGGATATTTTTAAAAGGCATCAGGAGGTCCATATTGGTGTGAAGGATCACGTCTGCTTCGAATGCGGGAAGGCGTTTATTACGTCCGACCAGCTCAAGCAGCACCAGAGGATTCACAGCGGAGAAAAACCCTACACGTGTTCGGTTTGCGCAAAGAGTTTCACGCAGTCGGCGCATCTGAAAGTACACGACAGAGTTCACCATAAGAAAACTGTGCAGCACTGTGATACGGTGCTCGAAGAGTTTCAGGCGGGCGAGCCGTTTGTTGATTCATTTGAA[C/T]AAGCATCATTCGATGAATCTAACATTGTGGATTTTTCATGTTCATGAAAATTATGTGTGTAGGCCAATATTATGGAATTATATATAAATATATATATACACAGTGGTCCCTCGTTATTCGCAGGAGTTACGTTCTAAAAATAACCTGTGATAGGCGAAATTCGCAAATGAGTCTGCTTTGTTTTACAATTATTATAAATAGTTTAAGGCTGTAAAACCCCTCACTGCACACGTTGTACACTTTTCTCTCAAAGTTGAAACCTTCATAGGAAAATTAGTCCAGTATTATAAAAAAAAAACCAAAGATCAAAACCATTTCATCTTCATTTGTTTATTACATAAGCCGGGTAACTTCTACCTTCCTTCTACCTAACTTTTTGTGCGATGGTTAGCATCTTGCCTTTTAGGTGCTACCACAGGTGCCTTTGACGGTGCAGAACGTTTAGTCGCTATTTTGGGAAGAAATCTTGGTACAGCACTTCAGAGTCACACTGCTAGCTA

Associated Phenotype:

Not determined