ZMP

si:ch211-87h14.4

Ensembl ID:

ENSDARG00000092844

ZFIN ID:

ZDB-GENE-081104-241

Description:

Novel protein similar to H.sapiens CPAMD8, C3 and PZP-like, alpha-2-macroglobulin domain containing

Human Orthologue:

CPAMD8

Human Description:

C3 and PZP-like, alpha-2-macroglobulin domain containing 8 [Source:HGNC Symbol;Acc:23228]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37504	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa43829	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa43830	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37504

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000142419	None	None	216	None	5
ENSDART00000143592	Essential Splice Site	57	587	None	13

The following genes are also affected by this mutation:

ENSDARG00000056530

Genomic Location (Zv9):

Chromosome 22 (position 21582140)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	21235388
GRCz11	22	21260366

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGATGCAAGGCCACACGTACAACAAATCGTTTGAAGTGCAGAAGTACGG[T/G]AAGCATTTATGTATTAATATATACTGTAAAATGTAAATAGAAGTAGAAAT

Long Flanking Sequence:

ATGTGTTTGCTTAAGCTTGATTCTTTGCTGCCTTTTAACGAGTGTAAAGTGGCCTTCAGATTTAAGCAAAACAAATAAGCAAGAATGTGACTATTTGTACCACAAACTGTTTAAGATTACCACGTTGTTTACCCAGGACCCCAGAGGATCCCACATAGTCCATTGGAAAGATCTGAAGTCAATTTGTTGTGGTAAGGACTGTTACTATTATGTTCCTATGGATGTAGTCAGGATTTCAATTTTGTAATCTTTTTTCAATCATTGCATCATACTGTAAAACTTTTATGACAGTATTTATGATTTATAATATATTTTAACATTATGATGTGTGTACAGTGTGTATACATATAGTGTTAATATAAAAAATTATTATTGTCTCTATTAGGAATTGTCAATATGAGCTTTCCACTATCAGACCAACCAGTTTTTGGTGAATGGTTAGTCTTTGTCGAGATGCAAGGCCACACGTACAACAAATCGTTTGAAGTGCAGAAGTACGG[T/G]AAGCATTTATGTATTAATATATACTGTAAAATGTAAATAGAAGTAGAAATGCTTAGTTTTTCAGAAGTTCAGGTTTTTCCGAACAAGAAAGTTACAAGAGTTTTGTATGTGTTGTACGTTGTTTTCACAGTACATACAAAGTTTGTTTTTGAATAGACTGTTTTCATATTATCAAGTCAAATTTTAATGTTGATTTAAGAGCCCATATTATGCATTAAAATGGTTATATTTTGGTATAAGCCAACAACAGGCTTATATGCGTGCAAGGTCAAAACGTCAACAAAACGAACAACAAACGGCAGTGGATTGTGAGCTTACAAACGCATTTAAATTTATAAACAATGCGGCATGTGTCGCGTTTTCAACATGGCTTTAGATGCGAAATGAGAATATAAAGAGTTACCCAGAATCCAGATACAGTACAAGCAGTTACAAGTAACAAAACACTATTAAATACATAATTTGCAAGCTAGAGAAAACAACGAGGCAACCATTTTAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43829

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000142419	None	None	216	None	5
ENSDART00000143592	Essential Splice Site	520	587	None	13

The following genes are also affected by this mutation:

ENSDARG00000056530

Genomic Location (Zv9):

Chromosome 22 (position 21586645)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	21239893
GRCz11	22	21264871

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTTCCATGGCACTGGGACATCACTAAAGATGCCCGTTTTGCTTTTACGG[T/A]GAGGACATGACTTTCTCCACTTCCCCGTATTGTTTTAAGCTCAGGCAGCA

Long Flanking Sequence:

GTCCCGCTTCGAAAATGAGGTTGATTAATTTCAGTTCACCAATTGTCAATTCAGAAAATTCACCATAAAAAGAAAGTTCTGTCTTCTATTTGTTTAACAAACCTTCTTGTCTTCAGATCTCTGTGTCTTTGTCCACAAATGAGTCGATGCCAGGAAGCCCGATCAGTCTGAAGGTTAAAGCAGAAAGTGGCTCATGTGTATGTGTAGCTTCTGTGGACAAAAGCATGTACCTTCTCAAACCAGGCTTCCAGCTCACACCTGAAAAGGTTAGTCCTCGTTTGAACCTTCATATATCCTGTAAATAGCTGTAAAGTTGTTTAAACAGTTTGAGGGTTTCCAGGTGTTCAAGGATCTGGCCGAGTTTGATGTATCTGATGCCTTTGGGGTACCCAAAGATGAGGGACATTTTTGGTGGCCCGGATTGTCTTCACGAAGGCGACGTTCCTCCGTGTTTCCATGGCACTGGGACATCACTAAAGATGCCCGTTTTGCTTTTACGG[T/A]GAGGACATGACTTTCTCCACTTCCCCGTATTGTTTTAAGCTCAGGCAGCATAGTAGCTAAGTGGTTAGCACTCACAGTAAAGCTGCGGTCACAGTGCACTTTTCACCCCATAGACTTTCCTTCATAGGAACGAGAAACACCAGAAATGCAAGCTTGTGCAACAAGTTTCACAGTTTGCTAGTTGCGAAGTTCAAACTTGGTGAATTCTGACCTGCGAAATCGCTTCATGTGACTGCATGAGACCAAGAGAAGATCAGATGACCTCTCTGTACAGAAATGTAAAATATGGACCAACTGCATGCTTTTTCTAATCATCTTGTTTAATACCGCCCCTTTTCACAGCACCATACAACAGAATTTTGCATGCTAAAACTCTTGTGTGACCACGGTACTAAAAGTTTGCTGATTTGAGTCCCAGCTGGACCAGGACGTCATTCTGTGTGGAGTTTGCATGTTCTCCCTGTTTTTGAGTTGGTTTCCTCTGGGTGCTCCAATTGCCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43830

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
ENSDART00000142419	None	None	216	None	5
ENSDART00000143592	Nonsense	564	587	12	13

The following genes are also affected by this mutation:

ENSDARG00000056530

Genomic Location (Zv9):

Chromosome 22 (position 21587647)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	21240895
GRCz11	22	21265873

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACCTGCGTTTCAACCACACACCTCTACCCTGGTGGCAGCTATGCACTCC[C/T]GATCTGGGACACGGTACACATGCTCACAGTGTCTGAAATTTTAAGGTTAA

Long Flanking Sequence:

CTACATTCCAAAGACAGGCAGTATAGGTGAATTGAATAAACTGAATTGGCCATAGTGAATGAGTGTGTATGGATGATTTCCAGTAAAGGGTTGCAGCTGGAAGGGCATCCTCTGTGGCAACTCTTGATGGATAAAAGGACTGAATAAATGAAATTGACCACAGTGTGTGAATAGAAGAGTGTGGGGGTGTTTCTCAACACTGAGAGTTTTACTCAATGCTGGGTTGCGGTTGGAAAGGCATCTGTTGTTAAAACATATGATTGAGTAGTAGGTGGTGGTTTATTCCTCTTTGAAGACCACCAAATGAAGGGGGAAGCCGAAGTTAAGTAAATGAGTTCAAATTATAATATGCTTGTGTACCCGTGTTGTAGGAGACAGGGCTGGTGGTGATGACAGACATGGTGAGTCTCAATCACAGACAGAGTGGAGGGATGTACACAGACGAGGCCGTACCTGCGTTTCAACCACACACCTCTACCCTGGTGGCAGCTATGCACTCC[C/T]GATCTGGGACACGGTACACATGCTCACAGTGTCTGAAATTTTAAGGTTAATTTTACAGGCGATTATGGCTAACTTCAGTAAGGGACTTGTTTCTTATGTCAGTGTGTATTTTTCAGGGCAGAGAACCGTAGGCGTACATTCTTTCCAGAAACATGGATATGGCATTGCTTTAATGTCAGGTACTAAACTATTTCTATTATTCAATCAAATAGATAAATGATAATAAAAACATAGTAACCACAAACTTTTGAAGGGTAGTGTGTGTTTATATAGAGCAAGGATCACCAACCCTTCTCCTGAAGATTTCAGCTCCAACCCCAATTAAACACACCTTAAATAGATAATGAAGGGTTGCATGATAATTGTAGGCAGGTGTTCTGGAGCAGGGTTGGGACTGAAATCCGTAGGATAGTTGAACCTAAAGGCGGGCCTACACGATGCAAATTCTGATGGCTTAAAGATCATGAAAGATCAAGATCAGAAATCGCATACTTCCATAC

Associated Phenotype:

Not determined