ZMP

si:dkey-14d8.21

Ensembl ID:

ENSDARG00000045837

ZFIN ID:

ZDB-GENE-041210-147

Description:

Novel protein similar to vertebrate protein deleted in malignant brain tumors 1 [Source:UniProtKB/Tr

Human Orthologues:

AC008735.1, CD5L

Human Descriptions:

CD5 molecule-like [Source:HGNC Symbol;Acc:1690]
Scavenger receptor cysteine-rich domain-containing protein LOC284297 [Source:UniProtKB/Swiss-Prot;Ac

Mouse Orthologues:

A430110N23Rik, Cd5l

Mouse Descriptions:

CD5 antigen-like Gene [Source:MGI Symbol;Acc:MGI:1334419]
RIKEN cDNA A430110N23 gene Gene [Source:MGI Symbol;Acc:MGI:3606211]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa26211	Nonsense	Mutation detected in F1 DNA	Not yet available
sa40215	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa26211

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
ENSDART00000041166	Nonsense	357	665	4	8
ENSDART00000136960	Nonsense	381	940	4	9

The following transcripts of ENSDARG00000045837 do not overlap with this mutation:

ENSDART00000131902

Genomic Location (Zv9):

Chromosome 4 (position 5346880)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	5465061
GRCz11	4	5473631

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTCGAGAGCTTGGCTGTGGTCCTTTCAATAAGACATACAGTAGAGCTTA[T/A]CTTGGCCCCGGTTCCGGTAACATACTAATGGATAATCTACAGTGCAATGG

Long Flanking Sequence:

TGATGGTTATGGCTGGGGAACGGTTTATAATGATGGCTGGAATCTGCTGGGTGGAGATGTGATCTGCAAACAGCTCTCCTGTGGGACTGCATTGAGTGTCACGAATAGGTCTTTTTTAAAGAAGGGTAAAGGGAGCATTTGGACGTACAACAGTGCATGCACTGGCACTGAGATCTCTCTGAAAAGCTGCATTTCAGGGATCCAGAGTCAACAAGTTACCCACAACACTGATGCAGGAGTGATATGCAGAGGTAAGCGCCACCACAAACTAAACTACATCAATACTGCACGTCGATTGCAATGTGAATTCATACAAACTATTGTCTATTTTCAGAGGTGAGCTTGGTTAATGGTCCCAGCATGTGCTCTGGGACAGTGCAAGTTCGCTATAGTGGAAATTGGGGCACCGTGTGTGACAACAACTGGGGGGATCTGGATGGTCTTGTGTTGTGTCGAGAGCTTGGCTGTGGTCCTTTCAATAAGACATACAGTAGAGCTTA[T/A]CTTGGCCCCGGTTCCGGTAACATACTAATGGATAATCTACAGTGCAATGGGAGCGAGTCCTCGCTGAATCAATGCAGCTTCTCTGCCTCTATAAGCTCCTGTACACATTCACAAGATGCCGGAGTTGTCTGTGGAGGTAAATATAAACAAAGAGAGTTCTGAAATCAACAGATGTGCTTATGTACAATAGCTGCAATAGGATATATGCTAAAGAACTTTTAATTTTCAGTAATCCAGTTAAAACGCTTTCGGTGAACTGTATGCTGTTACAGAATTGCATTATTTAATGTCTGTTTTCATAACAAAATCAATGATCTTAACTGCCTCATTAATATATGATATAAAGTGGGTCTCAGACTGTAAAAGAAGAACTGCATTAAATTAAAATTTTCTGCACCATGTCTTATTTTATTGATCCTGATGGTGCGTGCGCTTAATTTTAATTACGTGACAGCCTAAATGCTCTAAAACAGGAGTGTCCAAACTCTGTCCTGGAGGGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40215

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000041166	Nonsense	394	665	4	8
ENSDART00000136960	Nonsense	418	940	4	9

The following transcripts of ENSDARG00000045837 do not overlap with this mutation:

ENSDART00000131902

Genomic Location (Zv9):

Chromosome 4 (position 5346990)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	5465171
GRCz11	4	5473741

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCGCTGAATCAATGCAGCTTCTCTGCCTCTATAAGCTCCTGTACACATT[C/A]ACAAGATGCCGGAGTTGTCTGTGGAGGTAAATATAAACAAAGAGAGTTCT

Long Flanking Sequence:

CTTTTTTAAAGAAGGGTAAAGGGAGCATTTGGACGTACAACAGTGCATGCACTGGCACTGAGATCTCTCTGAAAAGCTGCATTTCAGGGATCCAGAGTCAACAAGTTACCCACAACACTGATGCAGGAGTGATATGCAGAGGTAAGCGCCACCACAAACTAAACTACATCAATACTGCACGTCGATTGCAATGTGAATTCATACAAACTATTGTCTATTTTCAGAGGTGAGCTTGGTTAATGGTCCCAGCATGTGCTCTGGGACAGTGCAAGTTCGCTATAGTGGAAATTGGGGCACCGTGTGTGACAACAACTGGGGGGATCTGGATGGTCTTGTGTTGTGTCGAGAGCTTGGCTGTGGTCCTTTCAATAAGACATACAGTAGAGCTTATCTTGGCCCCGGTTCCGGTAACATACTAATGGATAATCTACAGTGCAATGGGAGCGAGTCCTCGCTGAATCAATGCAGCTTCTCTGCCTCTATAAGCTCCTGTACACATT[C/A]ACAAGATGCCGGAGTTGTCTGTGGAGGTAAATATAAACAAAGAGAGTTCTGAAATCAACAGATGTGCTTATGTACAATAGCTGCAATAGGATATATGCTAAAGAACTTTTAATTTTCAGTAATCCAGTTAAAACGCTTTCGGTGAACTGTATGCTGTTACAGAATTGCATTATTTAATGTCTGTTTTCATAACAAAATCAATGATCTTAACTGCCTCATTAATATATGATATAAAGTGGGTCTCAGACTGTAAAAGAAGAACTGCATTAAATTAAAATTTTCTGCACCATGTCTTATTTTATTGATCCTGATGGTGCGTGCGCTTAATTTTAATTACGTGACAGCCTAAATGCTCTAAAACAGGAGTGTCCAAACTCTGTCCTGGAGGGCCGGTGTCCTGCAGATTTTAGCTCCAACTTGCCTCAACACACCTGCAGGGATGTTTCTAGAAAGCCTAATAAGAGCTTGATAAGCTAGCCCAGGTGTGTCTGATTGGGGTT

Associated Phenotype:

Not determined