ZMP
ENSDARG00000045752
Ensembl ID:
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26241 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45168 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26241
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102496 | Essential Splice Site | 451 | 1318 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 10016512)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10953139 |
GRCz11 | 4 | 10951988 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAACATGACTGTCGACACAAGGAGGATGTAGGAGTCGTCTGCTCTGG[T/C]GAACAATATACTTCATATGCAGTTTATGTAACATCCAGTGTATAAAACAA
Long Flanking Sequence:
TGATGGGCTTCCAGTGCTCTGGGAGTGAAGCTCATCTGGGGAACTGCAGCTCTCCACAAACTCTCAACTGCAGCTCCACACAACAGCTGTCAATCACCTGCCTTGGTGAGAACAACAACATCTTGGCAGATTCTGGAGTTGTTCCTGATCAATAATGTGTTTCTCTTTCTCTGAATATCAGGCCGCGGGTCCATCAGGCTGGTGGGTTCTGGGGGAGACTGTGCAGGGAGGCTGGAGGTTTTTCACAGCGGCTCATGGGGGACAGTGTGTGACGACTCCTGGGATATTAAAGATGCCCATGTGGTGTGCAGACAGCTGCAGTGTGGAGTGGCCCTCAGTAACCAGCAGGTACCAGCCTGGTTTGGTCCTGGTTCTGGACCCATATGGCTGGATGAGGTGGAGTGTGAGGGGAATGAGACGTCCCTGTGGAGCTGCTCTTCTCCAGGCTGGGGAAAACATGACTGTCGACACAAGGAGGATGTAGGAGTCGTCTGCTCTGG[T/C]GAACAATATACTTCATATGCAGTTTATGTAACATCCAGTGTATAAAACAAATGTTTGGTTTTAAGTTATCCCATGTTTCCATCCAGCGTTTAAAGAGATCAGGTTAACTGAAGGCTGTGAAGGGAATGTGGAGGTTTTCTACAATGGATCCTGGGGAAATGTGTGCTGGAATCAGATGGAAATAGACACAGTGAGTATTATTTGTCAAGAGCTGAACTGTGGAAGATCTGGTGTTTTGTCTGTTTCTACATCAAGACTGAAATCAGCTCCTAACTGGCTGGACAAAGTAACATGTCGATCACATGATTCACATCTTTTGCAATGTCCGTCTTCAATTTGGGGACAAAATGACTGTAATACAGATGAAGTGGCCAAAGTTACCTGCTCAGGTAAAATTATAGAATATTGTTCACTACACAATACAGAAATATTGCTTTAATACTTTGAGTATACATAGAAAAAGACACATTGCATATATTACTGTATCTGATGATTACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45168
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 |
---|---|---|---|---|---|
ENSDART00000102496 | Nonsense | 506 | 1318 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 10016260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10952887 |
GRCz11 | 4 | 10951736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCAAGAGCTGAACTGTGGAAGATCTGGTGTTTTGTCTGTTTCTACAT[C/A]AAGACTGAAATCAGCTCCTAACTGGCTGGACAAAGTAACATGTCGATCAC
Long Flanking Sequence:
TCATGGGGGACAGTGTGTGACGACTCCTGGGATATTAAAGATGCCCATGTGGTGTGCAGACAGCTGCAGTGTGGAGTGGCCCTCAGTAACCAGCAGGTACCAGCCTGGTTTGGTCCTGGTTCTGGACCCATATGGCTGGATGAGGTGGAGTGTGAGGGGAATGAGACGTCCCTGTGGAGCTGCTCTTCTCCAGGCTGGGGAAAACATGACTGTCGACACAAGGAGGATGTAGGAGTCGTCTGCTCTGGTGAACAATATACTTCATATGCAGTTTATGTAACATCCAGTGTATAAAACAAATGTTTGGTTTTAAGTTATCCCATGTTTCCATCCAGCGTTTAAAGAGATCAGGTTAACTGAAGGCTGTGAAGGGAATGTGGAGGTTTTCTACAATGGATCCTGGGGAAATGTGTGCTGGAATCAGATGGAAATAGACACAGTGAGTATTATTTGTCAAGAGCTGAACTGTGGAAGATCTGGTGTTTTGTCTGTTTCTACAT[C/A]AAGACTGAAATCAGCTCCTAACTGGCTGGACAAAGTAACATGTCGATCACATGATTCACATCTTTTGCAATGTCCGTCTTCAATTTGGGGACAAAATGACTGTAATACAGATGAAGTGGCCAAAGTTACCTGCTCAGGTAAAATTATAGAATATTGTTCACTACACAATACAGAAATATTGCTTTAATACTTTGAGTATACATAGAAAAAGACACATTGCATATATTACTGTATCTGATGATTACAGAAAAGGAGAGTCCTGCATCCCCCAGAAGTTATCTTACTATTTCCACATCTCCTCACCAAAGACAATGTTTTGGTAAGTGTATTTCATAGAAACACAAATTAAGAGAGCTGTATACAGGGTAAGGTCATACAAGTAACCGTTATGACCCCTATATACAGTAGGTGTCTCTGTTGTGACAGTACTCTGCTTTCTTTTTGTGTGAGATGTGTGTGTTTTAGCTCACGTTCCTCTCAGACTGCGTGGAGGGCACAAC
Associated Phenotype:
Not determined