Busch Lab

ZMP

si:dkey-51p7.1

Ensembl ID:
ENSDARG00000075394
ZFIN ID:
ZDB-GENE-090312-28
Description:
Novel protein similar to H.sapiens CRTAC1, cartilage acidic protein 1 (CRTAC1) [Source:UniProtKB/TrE
Human Orthologue:
CRTAC1
Human Description:
cartilage acidic protein 1 [Source:HGNC Symbol;Acc:14882]
Mouse Orthologue:
Crtac1
Mouse Description:
cartilage acidic protein 1 Gene [Source:MGI Symbol;Acc:MGI:1920082]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa45499 Essential Splice Site, Splice Site Mutation detected in F1 DNA Not yet available
sa28184 Essential Splice Site, Missense Mutation detected in F1 DNA Not yet available
sa1879 Essential Splice Site Available for shipment Available now
sa5867 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45499
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:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115286 Splice Site None 644 None 14
ENSDART00000132048 Essential Splice Site 134 527 2 11
Genomic Location (Zv9):
Chromosome 13 (position 40979573)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 40010541
GRCz11 13 40136431
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGGAGGAAATTTACGTCCTCAACACTAATAATGCCTTTTCAGGTATG[T/A]AACGGTTTCACAAACAAGGCACTGAAGCAAATGCTACAGTAAATGGATTT
Long Flanking Sequence:
GTTTACGCTTTAACAACTAAATGAACACTGAAATCTATTTAACTGAGTATATCTTTAATAAATTACAGCATCGATGCTGTAAAAAGGAACCATAAAATTAAAAAAAGCCACATTAACTATTCACCTGAAGTTTATCAGTATGGGAAGAAACACTAGCTCGGCATATATCCTATCATATGAAATGAAATATTGCATTTTAATATAATGACTGATTAGAATATGTGGACTGTGTTAGTTTGCTTTAAATGCCTTACATGTGTTATGTATAAACTTATATGTACTTTTTCCCCCTCTTTAGCTACAATGGGCCAAATCTGGTGTTGAAGTATGACAAGTTTAAGAAGAGGCTTGTCAACATTGCTGTCGACAATCGCAGTTCTCCATATTACGCTCTCAGAGACCGACAGGGCAATGCCATTGGAGTGACAGCATGTGACATAGATGGTGACGGCAGGGAGGAAATTTACGTCCTCAACACTAATAATGCCTTTTCAGGTATG[T/A]AACGGTTTCACAAACAAGGCACTGAAGCAAATGCTACAGTAAATGGATTTTAGTTTCATGTAATTGTTTCTGTCATTTCATCCAGGGAGAGCGACATACACTGACAAGCTCTTTAAGTTTCGTAATGGCCGGTATGAGGATTTGCTGAATGATGACGTAAATGAACACAGAGATGTTGCCAATCGTGTGGCTGGCCGCTCTGTTGCATGCGTGGACAGAAAGGTGACAGCATTTACAGTTTTTATTGAATTGACCTGGTTTTATTGAATTGATTTATCTTTGTCCCAATGTGATCCCATACGGAAATCTGATGTTTATACAGTAACTATACATGAACTTGTATGTCATATATGTCATTTACATGCAGCATATTACCATACATTTGATTTCTATATGGTGAACTTCAATAACACAAACAGTATCATCTGTAAAAACCAAATAAGTACAAAAAGATATAGTTATGTGCAATGTTGTGCCACAAAATCTCACAGATCATCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28184
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:
A > G
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115286 Missense 146 644 3 14
ENSDART00000132048 Essential Splice Site 134 527 None 11
Genomic Location (Zv9):
Chromosome 13 (position 40979485)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 40010453
GRCz11 13 40136343
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAAATGGATTTTAGTTTCATGTAATTGTTTCTGTCATTTCATCCAGGG[A/G]GAGCGACATACACTGACAAGCTCTTTAAGTTTCGTAATGGCCGGTATGAG
Long Flanking Sequence:
ACCATAAAATTAAAAAAAGCCACATTAACTATTCACCTGAAGTTTATCAGTATGGGAAGAAACACTAGCTCGGCATATATCCTATCATATGAAATGAAATATTGCATTTTAATATAATGACTGATTAGAATATGTGGACTGTGTTAGTTTGCTTTAAATGCCTTACATGTGTTATGTATAAACTTATATGTACTTTTTCCCCCTCTTTAGCTACAATGGGCCAAATCTGGTGTTGAAGTATGACAAGTTTAAGAAGAGGCTTGTCAACATTGCTGTCGACAATCGCAGTTCTCCATATTACGCTCTCAGAGACCGACAGGGCAATGCCATTGGAGTGACAGCATGTGACATAGATGGTGACGGCAGGGAGGAAATTTACGTCCTCAACACTAATAATGCCTTTTCAGGTATGTAACGGTTTCACAAACAAGGCACTGAAGCAAATGCTACAGTAAATGGATTTTAGTTTCATGTAATTGTTTCTGTCATTTCATCCAGGG[A/G]GAGCGACATACACTGACAAGCTCTTTAAGTTTCGTAATGGCCGGTATGAGGATTTGCTGAATGATGACGTAAATGAACACAGAGATGTTGCCAATCGTGTGGCTGGCCGCTCTGTTGCATGCGTGGACAGAAAGGTGACAGCATTTACAGTTTTTATTGAATTGACCTGGTTTTATTGAATTGATTTATCTTTGTCCCAATGTGATCCCATACGGAAATCTGATGTTTATACAGTAACTATACATGAACTTGTATGTCATATATGTCATTTACATGCAGCATATTACCATACATTTGATTTCTATATGGTGAACTTCAATAACACAAACAGTATCATCTGTAAAAACCAAATAAGTACAAAAAGATATAGTTATGTGCAATGTTGTGCCACAAAATCTCACAGATCATCTGAAGTTCAGGATTTCCATTTATTTTATTGATGGGTTAAATGATTTCCAAGCCATGCTCAGACAAATGATATAAATATTAAATGTATATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1879
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000115286 Essential Splice Site 242 644 4 14
ENSDART00000132048 Essential Splice Site 230 527 4 11
Genomic Location (Zv9):
Chromosome 13 (position 40961133)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 39994205
GRCz11 13 40120095
KASP Assay ID:
554-1869.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCGYGCTGTCCAATGTGGCCGAGCAGGCCGGAGTCAACAAGTTCACAG[G/A]TGTGTGTCTACGTTATTTACAAATGCTTGAGTGTGTGTATACCTTCAATG
Long Flanking Sequence:
TGTGGGGATTTTCCCCTCTGATGACGTGCAAAGGGTGAATGTCAATCAAGTGTTTCTGCAGACTGTTTTTATAAAGTGTGATTATAAAAAAGAAAATTAAAAGATTTATTGTCATTAGAAGCTGGATATATTGACAGACTGTTGCCACACAACTATGTTTAAACCCCATGTAAAAGTGATTTTTACATAATAGATCCCCTGTTAAATTCTGTAAATAAAAATAAAGATATCCTAACCACTCTTATTAAGAGTATTATGATTATTTGTGATTATTTGTTTTCTCTATATAGTATACACACAAATTTTGTTGTTTATTTTGTATTTTTCTATTTTTCTATTTTAGGGTACAGGCCGTTACTCCATCTACATCGCCAACTATGCCAGCGGGACAGTAGGTCCACACGCTCTGATTGAAATGGATGAAAGTTCAAGTGACCCGTCCAAGGGAATTGTCGTGCTGTCCAATGTGGCCGAGCAGGCCGGAGTCAACAAGTTCACAG[G/A]TGTGTGTCTACGTTATTTACAAATGCTTGAGTGTGTGTATACCTTCAATGATGTCATGCAGTGTAAATAATAATGTTATTTTAATTAACATTTTCATTATTATGAGCTTAGAGGATGAATAGGATATAGAGTAGATTATTTATTGTTTTATGGAGAGGACAGATGAACAATGCGTGTCACGGTGGCGCAGAGGGTATCACGATCGCCTCATAGCAAGAAGGTCACTGGTTTAAACCACGGCCGGTTCAGTTGGCATTTCTGTGTGGTGTTTGCATGTTCTCCCCGTGTTCACGTGGGTTTCATTCATGTGCTCCAGTTTCTCCAACTAGTAGGGTAAATTGTCAGTAGTGTGTGTGAATGGGAGTGTATGGGTGTTTCCCAGTGATAGGTTGTGGCTGGAATGGCATCCGCTGCGTAAAACATATGCTGGATAAGTTGACGGTTCATTCCGCTGTTGCAACCCCAGAATAATAAAAGAATGAGAATGAACAATAATTGAA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa5867
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
ENSDART00000115286 Essential Splice Site 443 644 9 14
ENSDART00000132048 Essential Splice Site 431 527 9 11
Genomic Location (Zv9):
Chromosome 13 (position 40939426)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 39972498
GRCz11 13 40098388
KASP Assay ID:
554-3928.1 (used for ordering genotyping assays)
KASP Sequence:
ACATGGCGAAAGTGCAGCACAACCCATYTCTGTGTATCGAGTCACTCAGG[T/C]GAGAATGTGCGTCAGACACTTTTAAATTTGGGAGTTAAGTTCGATTATTT
Long Flanking Sequence:
AAATTTTAGAAAAAAAACATATTGTGATTTCTACATACACATTAATTGCTTTTAATGAAATAAGTAATTACAAAGCAGCCTATTAGACAAATTTCTGAAGGATATCACGTAACACTGAAAACTAGATTAATAGTGCTGGAAATTCAGGTTAACATACATTACTAAGTAATGTAATGACCTCCAAAGGTCCTGGAAATCCCCGGTCTGCCACTAGATGGCATTATAAATCCAGGTTTGCTGCGATTTACTGGCATTTATCATCGAGTTCTGTCACATCAGCACTAACAGATTCATCATATTATATGAAAGCCAATGTATTCTTGTAGAACTGGTTTAAGTTAAATGTGTTTGTATTAATGATAAGTGTTTCCAGCTGTCTGAGCAGATATGTGTTTTAGGAGCGGCTGTGACTGACTTTGATGGAGATGGACTGCTGGATCTTCTGGTCACACATGGCGAAAGTGCAGCACAACCCATCTCTGTGTATCGAGTCACTCAGG[T/C]GAGAATGTGCGTCAGACACTTTTAAATTTGGGAGTTAAGTTCGATTATTTACTTTATTTCATATGTTTTGTATTTATTTCATATGTACACCATCTTTATTTTTATTTCACGGCAAAAAGATATACCTTATTTTTTTAAGAGCGCGGCCATTTGTAAGCTAACTTGAATAAACTTGACGAGACTTCCGGTTTCATTTGTGTACCCGTTATTATTGCAAAAGCTACTTTATATTGTGACTTGATATTTGTTGTTACATTATTAAAATGTTTTATGTTTTTTTTTAAATTAGTTTACCTTTTATATTGTGTTAGCTATTAGGGGAATCAAAAGTAAGCACTTGCAAAGTAAACAAACTGTTGGCTTATGTTTAGCTACAAGGTTTGAAGTAGTTTTATAAGTTGAAGTTTAGAGTTTTGAGTTTTTTAATTTCTCAGTAAAAAGTGAATTTCTGACTTGGAGAGACTTGTTTAAAATATCAAATGTGTGTTTTTCTGATCTAG
Associated Phenotype:
Not determined