Busch Lab

ZMP

ENSDARG00000045752

Ensembl ID:
ENSDARG00000045752
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
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.
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.
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