ZMP
si:dkey-14d8.22
Ensembl ID:
ZFIN ID:
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
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]
RIKEN cDNA A430110N23 gene Gene [Source:MGI Symbol;Acc:MGI:3606211]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33374 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15366 | Nonsense | Available for shipment | Available now |
sa16960 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33374
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000008037 | Nonsense | 256 | 461 | 4 | 7 |
ENSDART00000133352 | Nonsense | 448 | 635 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 4 (position 5357160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5475341 |
GRCz11 | 4 | 5483911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATTTAGGCCCTATTAGGTTGGCAAATGGCCGTGACTCTTGTTCTGGG[C/T]GAGTGGAGTGGATTCATAATAAGACATGGGGAACAGTGAGTGATGATGGC
Long Flanking Sequence:
ACTGTAAGAGAAGCGCGTGGGGAATACATAACTGTGTGCATGGTGAAGATGCTGGAGTCATTTGTGAAGGTGAGTGAAGGCTGTATTTATTGAAATATACGGTCACACTTTATTTTGATGGTCCAATTGTTGAATTTAAGTCACATTGCATCTACATGCCAACTAATTCTCGTTAGATTGTAGGTAGACTGTTAGGTTGGGATTAGGGTTAATATAAGTTTACATTTACTTGCAAGGTTTTTTATAGTCAGTTAAATGTCTGTTGAAGGAGCATATCAACCAATATTAAGTGGACAATCTACTAATAGACCATCAAAATAAGGTGTTACCAAATATACAAATACTGTACACACTATGTCTGGAACTCTGTGTTATACTTCTATGTCTCTCTTTCTACATTTATACATTACATTCACCTCAAAAACTAAAGCTAAATCTATCAAATTTTATTATATTTAGGCCCTATTAGGTTGGCAAATGGCCGTGACTCTTGTTCTGGG[C/T]GAGTGGAGTGGATTCATAATAAGACATGGGGAACAGTGAGTGATGATGGCTGGGATCTGTCAGACGCTGCAGTGGTGTGTAGAGAACTGGACTGTGGGAATGTGATTGAGGCAAAGAGCGCTGCTTATTTTGGACAAGGAACAGGACCGGTATGGTTGGGCGCAGTGCAATGCTATGGGACCGAGGACTCGTTGATGAACTGTACATCCACAAAATGGGAAATACAGAGCGGTGACCATTCAAGAGATGCTGGAGTTATCTGTAACAGTGAGTAGCAAAGATGCAGATGCACTTTGCATGATGCCTTGTAAATTCCTTCAATAACTCATTACTTTATTGTGGTTTTTTATTTGTACTTTTATTTAGTGTGTATTTTAAATTGTTAAAGAACAATTTAGCAGACACTTTAGGACTAAACGTGCAGTACAACATGGTTTCATGAATTTTACATTAGTTTACCTTACATTAGCAAATTTGTTTTAACATTAGTTTACCACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15366
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008037 | Nonsense | 394 | 461 | 6 | 7 |
ENSDART00000133352 | Nonsense | 578 | 635 | 6 | 6 |
ENSDART00000008037 | Nonsense | 394 | 461 | 6 | 7 |
ENSDART00000133352 | Nonsense | 578 | 635 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 4 (position 5354784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5472965 |
GRCz11 | 4 | 5481535 |
KASP Assay ID:
2259-4441.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTGTGTTCCTCGGGCTGGGACRAAAAAGACGCTTCAGTGTTGTGTCAA[C/T]AGCTGGGTTGTGATGATACTGGACAGCCGAAGACATTCGCAAGTCCTTCA
Long Flanking Sequence:
TTTCCTTTTATTTAAAAGTTTGAAAACACTTTGATGGAGATTTTCTTTTATGATTTGAGCAAAAATATGTATTTGCACATTCACTGCTCTATAAGTTTACTACAACTATGATGAATTCCACTACTGAGATAACTAGAAATGTGAAAAGAGTGAATAGATAATAGATTTTCACATATAACCCTTTATTAATGACCTCATAAACACTGAAATGAGCTCAAACCAACAAATCCTTCAGGAGAATGTTTCATTGTTTTGTTTTTTACAATTTGTCATTGCATTCATTTCATGTGCATAAAGTGTTTTTTAGAAATTTCCTCATGCTTCAAATGTGACAATGAGTTTGTACAGTGTGGCTTGTGTGTGAACCTGTTTGATCAGATGTGAAGCTGGTGAACGGCTCCAGTGCGTGTGAGGGCAGATTTCAGATCCTGCATAATGATATCTGGGGCTCAGTGTGTTCCTCGGGCTGGGACGAAAAAGACGCTTCAGTGTTGTGTCAA[C/T]AGCTGGGTTGTGATGATACTGGACAGCCGAAGACATTCGCAAGTCCTTCAGTGGTGAATATCTGGATGAACAATGTGGCCTGTACAGGAGATGAGTTGTCACTGCAAACCTGTCCTTTTGCTGGATGGGGGTCAAGCTGTTTGACTGGACTTTCTGCAGGAGTGCTTTGCCAAAGTAAGATCATCTTACATGAGAGCATCACAAATGAAGGCATCATGATATCAAAACTGGTGTTTTATTGTGATACTAGAGTACAGATACACTGATACAGAGTTTGATTAACCAGCACAGTTGTGTCTGATTGGGTTGCAAATAAACTGTGCAGGCAGCCCCGCTGTAAAGCTTATCATGTCTATATTTCACTTGCAAAAATTAATTTTCTCTTGTGTTTTCAAGGACAATGCAGTTAAAAGATGCTAATGTGAAAAGTATTCCTCCTGTAATGCTTTTTGTGTCTGTATTTCACTTGTAGAAACTACAAAACAAGTTGTGGTGAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16960
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008037 | Nonsense | 394 | 461 | 6 | 7 |
ENSDART00000133352 | Nonsense | 578 | 635 | 6 | 6 |
ENSDART00000008037 | Nonsense | 394 | 461 | 6 | 7 |
ENSDART00000133352 | Nonsense | 578 | 635 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 4 (position 5354784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5472965 |
GRCz11 | 4 | 5481535 |
KASP Assay ID:
2259-4441.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTGTGTTCCTCGGGCTGGGACRAAAAAGACGCTTCAGTGTTGTGTCAA[C/T]AGCTGGGTTGTGATGATACTGGACAGCCGAAGACATTCGCAAGTCCTTCA
Long Flanking Sequence:
TTTCCTTTTATTTAAAAGTTTGAAAACACTTTGATGGAGATTTTCTTTTATGATTTGAGCAAAAATATGTATTTGCACATTCACTGCTCTATAAGTTTACTACAACTATGATGAATTCCACTACTGAGATAACTAGAAATGTGAAAAGAGTGAATAGATAATAGATTTTCACATATAACCCTTTATTAATGACCTCATAAACACTGAAATGAGCTCAAACCAACAAATCCTTCAGGAGAATGTTTCATTGTTTTGTTTTTTACAATTTGTCATTGCATTCATTTCATGTGCATAAAGTGTTTTTTAGAAATTTCCTCATGCTTCAAATGTGACAATGAGTTTGTACAGTGTGGCTTGTGTGTGAACCTGTTTGATCAGATGTGAAGCTGGTGAACGGCTCCAGTGCGTGTGAGGGCAGATTTCAGATCCTGCATAATGATATCTGGGGCTCAGTGTGTTCCTCGGGCTGGGACGAAAAAGACGCTTCAGTGTTGTGTCAA[C/T]AGCTGGGTTGTGATGATACTGGACAGCCGAAGACATTCGCAAGTCCTTCAGTGGTGAATATCTGGATGAACAATGTGGCCTGTACAGGAGATGAGTTGTCACTGCAAACCTGTCCTTTTGCTGGATGGGGGTCAAGCTGTTTGACTGGACTTTCTGCAGGAGTGCTTTGCCAAAGTAAGATCATCTTACATGAGAGCATCACAAATGAAGGCATCATGATATCAAAACTGGTGTTTTATTGTGATACTAGAGTACAGATACACTGATACAGAGTTTGATTAACCAGCACAGTTGTGTCTGATTGGGTTGCAAATAAACTGTGCAGGCAGCCCCGCTGTAAAGCTTATCATGTCTATATTTCACTTGCAAAAATTAATTTTCTCTTGTGTTTTCAAGGACAATGCAGTTAAAAGATGCTAATGTGAAAAGTATTCCTCCTGTAATGCTTTTTGTGTCTGTATTTCACTTGTAGAAACTACAAAACAAGTTGTGGTGAGCTT
Associated Phenotype:
Not determined