ZMP
si:dkey-14d8.20
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate scavenger receptor protein [Source:UniProtKB/TrEMBL;Acc:Q5RHW7]
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 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6047 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14156 | Nonsense | Available for shipment | Available now |
sa13640 | Nonsense | Available for shipment | Available now |
sa13941 | Nonsense | Available for shipment | Available now |
sa15797 | Nonsense | Available for shipment | Available now |
sa10315 | Essential Splice Site | Available for shipment | Available now |
sa33373 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6047
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135122 | Nonsense | 525 | 1140 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 5271685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5389866 |
GRCz11 | 4 | 5398436 |
KASP Assay ID:
554-3721.1 (used for ordering genotyping assays)
KASP Sequence:
TCACTTAAGCCGAAAASTACTGACCATTCGAAGGACGCTGGGGTCATCTG[C/A]GACTGTAAGTCWTTTATATTTTATGCAAGTAAAAAGAGAAATGAAGGAAA
Long Flanking Sequence:
CAAAAGCATTAATAAACGTGGAAAAATTAAAACCTAAATCACAAATATGGAAAACTGCACATTTACGGATATTTTTTACAGTGTATTTTGGGTGGTTTAAAAAACAGTGAATAGCAGTAAACTGTATTTTCATTGTTGTGATGAACTATCTACGTTAATGTATCCATAAAAGTATCCGCTTATAACTCTCTAATCTTTCTAGCAAAAATGAGACTGGCGAGTGGTGACGGCTCCTGTTCTGGACGAGTGGAGGTTTTCCTCCACAGCCAGTGGGCAACAGTGTATGATGATGGCTGGGATCTGTCAGATGCTGCAGTGGTGTGTAGAGAGATGGGCTGTGGAGATGCTGCACAGGCAAAGAGTAATGCTTATTTCGGACAAGGAACTGGACAAACATACATGTCCAATGTAAACTGTGTTGGAAATGAGTCCTCACTGAGTGTCTGTGAATCACTTAAGCCGAAAAGTACTGACCATTCGAAGGACGCTGGGGTCATCTG[C/A]GACTGTAAGTCTTTTATATTTTATGCAAGTAAAAAGAGAAATGAAGGAAAATAGATATGCAGTTATTTATGTTTTACATTAAAAATGTTGGTAACTTTATTTGTATGTACAATGCAAGCTATTAACAAACCAGTAACAAAGGCTGCATTTATTATACTGCATGGTTCAAGTGACTCAGTTCCAATATTTTTCTCCCATGTGGCACAGATCAGATATGGCCCATGTACATATAAGCAGGAAGAAATCACATGGATTCAAATCAGATTTAGGCCTTATTCATATGTGGAAATATATTCGATTTAAATCGGATCTGTGCCCTCATGTCTGCAAAATGTTATATTTAATTTAATGTGTTGCTTTTTTCTAATTGTTTGTGATGTTTAGCCATTTCTGAGTGAAATTTGGTTTTGCACCAATTTATTACTAGTCATTATCACAATCCTAAACATGTTTTATTGTTCATTAATGTGGATTCAGCTCCTGTCAGGCTCATTAATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14156
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135122 | Nonsense | 538 | 1140 | 6 | 11 |
ENSDART00000135122 | Nonsense | 538 | 1140 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 5272197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5390378 |
GRCz11 | 4 | 5398948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTAATGTGGATTCAGCTCCTGTCAGGCTCATTAATGGAAATAACTCGTG[T/A]TCTGGAYGAGYGGAGGTTTTCTATAGTGGTCAGTGGGGAACAGTGTGTGG
Long Flanking Sequence:
TTTTATATTTTATGCAAGTAAAAAGAGAAATGAAGGAAAATAGATATGCAGTTATTTATGTTTTACATTAAAAATGTTGGTAACTTTATTTGTATGTACAATGCAAGCTATTAACAAACCAGTAACAAAGGCTGCATTTATTATACTGCATGGTTCAAGTGACTCAGTTCCAATATTTTTCTCCCATGTGGCACAGATCAGATATGGCCCATGTACATATAAGCAGGAAGAAATCACATGGATTCAAATCAGATTTAGGCCTTATTCATATGTGGAAATATATTCGATTTAAATCGGATCTGTGCCCTCATGTCTGCAAAATGTTATATTTAATTTAATGTGTTGCTTTTTTCTAATTGTTTGTGATGTTTAGCCATTTCTGAGTGAAATTTGGTTTTGCACCAATTTATTACTAGTCATTATCACAATCCTAAACATGTTTTATTGTTCATTAATGTGGATTCAGCTCCTGTCAGGCTCATTAATGGAAATAACTCGTG[T/A]TCTGGACGAGTGGAGGTTTTCTATAGTGGTCAGTGGGGAACAGTGTGTGGTGATGGCTGGGATCTGACAGATGCTGCAGTGCTGTGTAAAGATCTGGGATGTGGAGATGCCATTGAGGTCAAAAATGATAATTATTTTGGCCAGGGATCGGGGCCGGTATGGCTAAGTAATCTGCAGTGCTCTAGTACTGATACAAGGCTGCGAGACTGTAAATCAAGCGGATGGAGGATTGATAGCTGCGGACATGAGAACGATGCAGGAGTTATCTGTCATGGTGAGTGTAAACATTTAGTAATAATAATGTGATGTATTGGATTTCATGTGTAAGACAAAAAAATTTCCCCCTAAATATGTATTAAAATTATACAATAATTTAAGACATCAATTGACAAATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATAATAAATAATTTTATAATAAATTATATTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13640
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135122 | Nonsense | 538 | 1140 | 6 | 11 |
ENSDART00000135122 | Nonsense | 538 | 1140 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 5272197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5390378 |
GRCz11 | 4 | 5398948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTAATGTGGATTCAGCTCCTGTCAGGCTCATTAATGGAAATAACTCGTG[T/A]TCTGGAYGAGYGGAGGTTTTCTATAGTGGTCAGTGGGGAACAGTGTGTGG
Long Flanking Sequence:
TTTTATATTTTATGCAAGTAAAAAGAGAAATGAAGGAAAATAGATATGCAGTTATTTATGTTTTACATTAAAAATGTTGGTAACTTTATTTGTATGTACAATGCAAGCTATTAACAAACCAGTAACAAAGGCTGCATTTATTATACTGCATGGTTCAAGTGACTCAGTTCCAATATTTTTCTCCCATGTGGCACAGATCAGATATGGCCCATGTACATATAAGCAGGAAGAAATCACATGGATTCAAATCAGATTTAGGCCTTATTCATATGTGGAAATATATTCGATTTAAATCGGATCTGTGCCCTCATGTCTGCAAAATGTTATATTTAATTTAATGTGTTGCTTTTTTCTAATTGTTTGTGATGTTTAGCCATTTCTGAGTGAAATTTGGTTTTGCACCAATTTATTACTAGTCATTATCACAATCCTAAACATGTTTTATTGTTCATTAATGTGGATTCAGCTCCTGTCAGGCTCATTAATGGAAATAACTCGTG[T/A]TCTGGACGAGTGGAGGTTTTCTATAGTGGTCAGTGGGGAACAGTGTGTGGTGATGGCTGGGATCTGACAGATGCTGCAGTGCTGTGTAAAGATCTGGGATGTGGAGATGCCATTGAGGTCAAAAATGATAATTATTTTGGCCAGGGATCGGGGCCGGTATGGCTAAGTAATCTGCAGTGCTCTAGTACTGATACAAGGCTGCGAGACTGTAAATCAAGCGGATGGAGGATTGATAGCTGCGGACATGAGAACGATGCAGGAGTTATCTGTCATGGTGAGTGTAAACATTTAGTAATAATAATGTGATGTATTGGATTTCATGTGTAAGACAAAAAAATTTCCCCCTAAATATGTATTAAAATTATACAATAATTTAAGACATCAATTGACAAATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATAATAAATAATTTTATAATAAATTATATTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13941
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 |
---|---|---|---|---|---|
ENSDART00000135122 | Nonsense | 541 | 1140 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 5272204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5390385 |
GRCz11 | 4 | 5398955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGATTCAGCTCCTGTCAGGCTCATTAATGGAAATAACTCGTGWTCTGGA[C/T]GAGYGGAGGTTTTCTATAGTGGTCAGTGGGGAACAGTGTGTGGTGATGGC
Long Flanking Sequence:
TTTTATGCAAGTAAAAAGAGAAATGAAGGAAAATAGATATGCAGTTATTTATGTTTTACATTAAAAATGTTGGTAACTTTATTTGTATGTACAATGCAAGCTATTAACAAACCAGTAACAAAGGCTGCATTTATTATACTGCATGGTTCAAGTGACTCAGTTCCAATATTTTTCTCCCATGTGGCACAGATCAGATATGGCCCATGTACATATAAGCAGGAAGAAATCACATGGATTCAAATCAGATTTAGGCCTTATTCATATGTGGAAATATATTCGATTTAAATCGGATCTGTGCCCTCATGTCTGCAAAATGTTATATTTAATTTAATGTGTTGCTTTTTTCTAATTGTTTGTGATGTTTAGCCATTTCTGAGTGAAATTTGGTTTTGCACCAATTTATTACTAGTCATTATCACAATCCTAAACATGTTTTATTGTTCATTAATGTGGATTCAGCTCCTGTCAGGCTCATTAATGGAAATAACTCGTGTTCTGGA[C/T]GAGTGGAGGTTTTCTATAGTGGTCAGTGGGGAACAGTGTGTGGTGATGGCTGGGATCTGACAGATGCTGCAGTGCTGTGTAAAGATCTGGGATGTGGAGATGCCATTGAGGTCAAAAATGATAATTATTTTGGCCAGGGATCGGGGCCGGTATGGCTAAGTAATCTGCAGTGCTCTAGTACTGATACAAGGCTGCGAGACTGTAAATCAAGCGGATGGAGGATTGATAGCTGCGGACATGAGAACGATGCAGGAGTTATCTGTCATGGTGAGTGTAAACATTTAGTAATAATAATGTGATGTATTGGATTTCATGTGTAAGACAAAAAAATTTCCCCCTAAATATGTATTAAAATTATACAATAATTTAAGACATCAATTGACAAATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATAATAAATAATTTTATAATAAATTATATTATATTATATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15797
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135122 | Nonsense | 855 | 1140 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 5283418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5401599 |
GRCz11 | 4 | 5410169 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCGGCATCAACTCTTGTTCTGGACGAGTGGAGGTTTTCCATAACGGCT[T/G]ATGGGGAACAGTGTGTGATGATTACTGGGGTCTGACAAACGCTGCAGTGG
Long Flanking Sequence:
ATAACAACCAGCATAACAAAACATGTTTCTCAAGACAATCACCTACTGCTCCTTTATTGAAAAAAAAGTTCAATACAAATTATATTTTATTATTTTATTTTATAAATTGACATTTTATTAGTTAAAAATTATGTATAAGAAATAATATATAGAGAAATAAGCCTGTAGTAAGACAGAAAATGTACTGGAATGTTTGTAGTGTATTATACAACACCAACCCAACAATATATCACTTAAAACTATTAAAAATGTAAACAAAAGTCACTTTCATTGTTAAAAGTTGCTGGAAGAAGGATCAAGTTCTCGTAAAGCAATTCAAAAGCATAAATAAATGCAAAAAACTAAAAACATAATTCACAAAATATGGAAAACTGCTTATTTATGGATATTTTCACAGTGCATACCTAATGTTTTAATTCTTATGTCTTTATCAGCCAGAACTAGACTGGTGAGCGGCATCAACTCTTGTTCTGGACGAGTGGAGGTTTTCCATAACGGCT[T/G]ATGGGGAACAGTGTGTGATGATTACTGGGGTCTGACAAACGCTGCAGTGGTGTGTAGAGAGCTGGGATGTGGAGACGTGATTGAGGCAAAGAGTAATGCTTATTTTGCAGAAGGTTCAGGGCAAATATTGATGGATGATGTGAACTGCTCCAGAGATGATAATGCATTGAGTAAATGTGAATTTGCTGGATGGGGAGTGCACAACTGTGTTCATTCAGAGGACGCTGGAGTCGTCTGTCAGGGTGAGTGAACATTGCTCTGCATTTATTTGAGTATGATGACAGATTTAATGTACAGTCGAAGACAAAATTATTATTTTAATTGTAATTTTTGTAAGGGCATTAGGGAAAAAGCACAGTTTTAAACATAATAGTTTTAATAACTCATTTCTTTTGTCTTTGCCATGATGACAGTACATAATATTTTACTAGATAATTTTCATGATGCTAGTATTCAGCTTAAAGTGCAATTAAGGGTTAACTAAGCTAACTAGGTGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10315
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135122 | Essential Splice Site | 1039 | 1140 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 5288456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5406637 |
GRCz11 | 4 | 5415207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGTTAATCTCAGTTTTTTGTCTTTGTTTTTTCATTGGTGTCATCATCA[G/A]TCCCTGTCAGGCTGAYGGGTGGAMGAGACGCATGTTCTGGACTTGTGGAG
Long Flanking Sequence:
AAGGGGGGATTCTTCAACACGAAGATGGCTAAAGTAAGATGCTCTGGGGATTTATAGTGAGTTAGGCTTTATCTGACCGGTGGGTCATACATTAGCTAATGGAGCACGAGCTCCTCTTTAAATTAGTTTATAAATAAACTTCATTTAGATCATATAATTTTTACTATTTTTTTTTGTATAATCAGCTGAAAGTAATTAAATTAATAGTATATATAGCACTATCCTGAATAATGTCCATTGCATTTATTTTTGCTGTAAATTATTCTATTGAGAATTTATTTATTTATTTCAATTAAGACCTCTAACAGTAACACGTTTGTTTTACTCAGTTTGATTTAAGTTGAGATGACTAGAAAAGTTTGTTTGATTCAGCTAAAAAATTTAGGCAGCATGCTTTTTCCACTGTGCATTCATTTGTTATCATCCTTGTGGAAAATTCATTGTGCATAAGTTGTTAATCTCAGTTTTTTGTCTTTGTTTTTTCATTGGTGTCATCATCA[G/A]TCCCTGTCAGGCTGACGGGTGGAAGAGACGCATGTTCTGGACTTGTGGAGGTTTTTCATGACGGTCAGTGGGGGACGGTGAATGCTGATGGCTGGGATCTGGCAGACGCTGCAGTGGTGTGTAGAGAGATGGGATGTGGAGATGCTGTACAGGCAACGGGCGGTGCTTTTGGACGAGGAATTGGTCCAATATGGATGACTTTAGTCGACTGTGTTGGCAGTGAGTCTTCCCTAATACAATGTAGCTTAGATCGATGGCTGCCAAATCACGTCAACCATCTGAATGATGCTGGAGTCGTCTGCACTCGTGAGTGTCAATCACATTTAAATGTGCATACTATGAAATGTGCTATAAGTTAGTATTTCAAATACTTCCCAAATGATGTTTAACAGAGCAAAGAAATTTTCACAGCATTTGCCATTGTATTTTTCCTCCGGAGAAAGTCTTATTTGTTTTATTTCAGTTAGAATTAATTTATTTGTTTTTGAAATCATTTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33373
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 |
---|---|---|---|---|---|
ENSDART00000135122 | Nonsense | 1123 | 1140 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 4 (position 5288708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 5406889 |
GRCz11 | 4 | 5415459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTCGACTGTGTTGGCAGTGAGTCTTCCCTAATACAATGTAGCTTAGAT[C/T]GATGGCTGCCAAATCACGTCAACCATCTGAATGATGCTGGAGTCGTCTGC
Long Flanking Sequence:
CTGTAAATTATTCTATTGAGAATTTATTTATTTATTTCAATTAAGACCTCTAACAGTAACACGTTTGTTTTACTCAGTTTGATTTAAGTTGAGATGACTAGAAAAGTTTGTTTGATTCAGCTAAAAAATTTAGGCAGCATGCTTTTTCCACTGTGCATTCATTTGTTATCATCCTTGTGGAAAATTCATTGTGCATAAGTTGTTAATCTCAGTTTTTTGTCTTTGTTTTTTCATTGGTGTCATCATCAGTCCCTGTCAGGCTGACGGGTGGAAGAGACGCATGTTCTGGACTTGTGGAGGTTTTTCATGACGGTCAGTGGGGGACGGTGAATGCTGATGGCTGGGATCTGGCAGACGCTGCAGTGGTGTGTAGAGAGATGGGATGTGGAGATGCTGTACAGGCAACGGGCGGTGCTTTTGGACGAGGAATTGGTCCAATATGGATGACTTTAGTCGACTGTGTTGGCAGTGAGTCTTCCCTAATACAATGTAGCTTAGAT[C/T]GATGGCTGCCAAATCACGTCAACCATCTGAATGATGCTGGAGTCGTCTGCACTCGTGAGTGTCAATCACATTTAAATGTGCATACTATGAAATGTGCTATAAGTTAGTATTTCAAATACTTCCCAAATGATGTTTAACAGAGCAAAGAAATTTTCACAGCATTTGCCATTGTATTTTTCCTCCGGAGAAAGTCTTATTTGTTTTATTTCAGTTAGAATTAATTTATTTGTTTTTGAAATCATTTTAAGGTCAATATTTTAAGCAATATATTTTTTTTTCGGCTGTGTACTGAACAAACCAACGTTATACAATGACTTGCCTAATCACCCAATTAAGCCTTTAAATGTCACTTTAAGCTAAATACTAGTGTCTTGAAAAATATCTAGTCAAATCATGCTTGACAAATATACTGTCATCATGGCCAGGGGCGCCACTAAGGGGGGAAGTTATGATGATTCCAAGCGGCAACCTCCTGCTCTCTCTTGTGAGGGAAATACAGA
Associated Phenotype:
Not determined