ZMP
cspg4
Ensembl ID:
ZFIN ID:
Human Orthologues:
AC010724.5, AC011295.1, AC044860.1, AC135995.2, CSPG4, CSPG4P5
Human Descriptions:
chondroitin sulfate proteoglycan 4 [Source:HGNC Symbol;Acc:2466]
chondroitin sulfate proteoglycan 4 pseudogene 5 [Source:HGNC Symbol;Acc:29403]
chondroitin sulfate proteoglycan 4 pseudogene 5 [Source:HGNC Symbol;Acc:29403]
Mouse Orthologue:
Cspg4
Mouse Description:
chondroitin sulfate proteoglycan 4 Gene [Source:MGI Symbol;Acc:MGI:2153093]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37999 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39470 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14510 | Nonsense | Available for shipment | Available now |
sa24601 | Nonsense | Available for shipment | Available now |
sa15270 | Nonsense | Available for shipment | Available now |
sa12954 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37999
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112782 | Nonsense | 235 | 2305 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 6904698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6424140 |
GRCz11 | 25 | 6551542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACATGGACAAGACCTAACGTTGGAGCCCGTAGCCTGGAGATGTTAATC[A/T]AGACAACCATTGAGGATGCACTGTTGCTCTTCCATCCAGGACACCGAACA
Long Flanking Sequence:
GCTTAATGTGTGTTCATTTGTGTCTTTATATACAGGCTAGGATTGACATGGGATCTGGAGAAAAGGTTCTGGCCTCCTCTATGGGTCTCCAACTCAGTAACCTTCTTGACCACCATGTGTCTCTCCTTCTGAAAGACGGCAAACTCACTATGGCTGTGGACAACCTGTACACAACCTTCATCCAATTGGAGAATGCAGATGAGGACCTGAACATTGACCAGGGAGTGTTTCTTGGAGGAGTGAGAGATCTGGAAGTTGAGTACCTGAGCACGGCTGTTCCCTCCCTGCGCGGCTGCATGAGCGACGTTATGTTTGAGTCTCATGACTTTGATATTCTGTCCTTAGCCAATACAGTCTGCTATGACACCAAAGAGACATGCAGCAGTGAATTTGAGGCTGGAGATGGAGACTCTGTAAGCTTCATAAGCCCAGACTCGTTCATCTCTTTCCCTACATGGACAAGACCTAACGTTGGAGCCCGTAGCCTGGAGATGTTAATC[A/T]AGACAACCATTGAGGATGCACTGTTGCTCTTCCATCCAGGACACCGAACAGACTTCATTGCAATAGGAATGGTGGGAGGTTTCCTAAAAGGCATTATTGATCTGGGAGATGGGAAGTATATGCTGGACAATGTGGAAATAAAAATCGACGATGATCAGTGGCACAGAGTAAAAGTTCAGATTGAAAGCAACGAATTCCTGATAGCTGTGGATAGTCAACCGGTTTCACTTCGTCTTAATGAGACTGAAGGACAACTGGATCTAGTGGGGAATCTGTACCTAGGAGGTATTCAGAAGAAGATGAAGGATGTGTTTCAAGATGATTATCTGATTCGTGTTGAGGAGGAGATCACAACAGAGTCCTTCATCGGATGTTTAGGAGAGATCAAGGTGAATCAGAAAGGAAGAAGCCTCCAGGATGCTCTGATAACTAAAGACATTCATGTGAAATGTGAAGGGGAGTATGATTACTCATCTTATGATGATGATTTGGAGCCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39470
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112782 | Essential Splice Site | 1418 | 2305 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 6896022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6415464 |
GRCz11 | 25 | 6542866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGGTTTCAGGATGATGACGATCCGCTTGTCAGCTTCACCTGGGAGGAT[G/A]TGAGTATTAGCACATACACACTATTTTTATGGTTGCGCTTTGTTTTGATG
Long Flanking Sequence:
GCACTTGCTTGAACATCCTTTGGTCTTCTTAGGTGGAGCAGACAGACGTCCCACCCAAAGAGATGGTGTACTCGGTAAAAGACTTCCCTCGCCTTGGTCACGTGGTCAAACTCATCAATGACTCGGACAGCACCGCATCTCCCGTCCTGGACTACATTCATTCCTTCACACAGGAGGACATCAACCGGGGCAGGATCCTTTACGTCTCCGCTTCCCTGCAGGGCCGCGACCACTTCACCGCAGATGTCAGCAACGGCCTGACCACCATTGAAGACCTGGAGGTGCAGGTGGACATCGTTCCCCGAATCATACCTGTTCAGGTGGTCAATCTGACGGTGAGGGAAGGCGGATCAGTGCCGCTGACCCAAGACGTGCTCAATATCACACACCCCTACTACCGCTCCGTCAGCATTATGTTTATTATGGAGGAAGAACCTGAGCATGGAGATATCAGGTTTCAGGATGATGACGATCCGCTTGTCAGCTTCACCTGGGAGGAT[G/A]TGAGTATTAGCACATACACACTATTTTTATGGTTGCGCTTTGTTTTGATGGTTCGCTTTAGATGTGTGTTGATTTGAAAGCTAACTGTGTCAGAGCGTCTTAACTGTTTTAAAGCCTACTTCAAATGTATCTGTAGTACATGTAAGTGTCGACCCTCCTTTTTTTCCTGGGATTCTCCCGTATTTTACAGTTCTATCCTGCTATCATCCCGTAAAGGTATTGTCCCTTTTTTCTCTCGCATTTTCAATCTTTCTTTGCAATAAAGAGCCGATCCTCCCTATACGCAACCCATCCCGCCGGACCACCAGGGGACGTCCCTTGCTCTTAAATGTAAATCTGTTCTGTGCTTTTGCTTCATTTAGGCATGAAAACACTTTAAAATAAATATCAAAATGGACGGATTCCCTAACTTTCCATTACAAGCGCCATTGCCGCACCAATGCAATCATAATCATTAAAGTGAACATATTTAGTTATTGCAGTATAGTATTTAACACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14510
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 |
---|---|---|---|---|---|
ENSDART00000112782 | Nonsense | 1639 | 2305 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 6864143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6383585 |
GRCz11 | 25 | 6510987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATCAAACCTAACCAGCGTGGACAGTTTGAGGAGATCACCAGATTCACA[C/T]AAACTGAGGTAAATGTTGTASATTTSTAAATATGTCATAATGTACTAGCA
Long Flanking Sequence:
GCTTCAGCTTCACCGTGACTGATGGAGAACACACTTCACCTCTTTACCGCTTCTCTGTCAAAGCACGGCAGCTCACCATATCCATGGAAACAAAGGGCGAACTCATGGTCTTCCCAGGTGGGTTCCACACATCCCAGGCTTAAATCCAAATCCCTATCTCTATCTTTCTCTGGAGCAACAGAAAGATTTTTATCGGCAAAAGAGAGAAACTATTGCATTCAACTTCAAATAGGGAATAAATTTATTTTTTATTTTCCTCACCATTTGCATTATAATATCTGAATCAAATCTATTATGTCAGTGTAAATACATTTGAAGCAACATTATTTGTTTGATAATGTTTCCCAGGCACCAGGCAGGTGATCAGTAGAGATATTTTGCGGGCTATAACAAGTGAAGACGGTGATGTAATCACATACTCGCTGGTGAAACCTCCTCGCTTGGGACGTGTAATCAAACCTAACCAGCGTGGACAGTTTGAGGAGATCACCAGATTCACA[C/T]AAACTGAGGTAAATGTTGTAGATTTCTAAATATGTCATAATGTACTAGCAGCGGGAAACAGTAACACATACAGGTGCATTTCTAGAAAAGTTAGCTATAATTTTCTTATGCTAAATAGTTGCAGTATTGGAGTAAATTGTCTTAAAGCAGGCGTGACCAACCCTGTTCCTGGCGATCGACCTTCCTGCAGATTTCAGTTGCAACCCATATCAAACACACCTGCCTGTAATTATCAAGTGCTGTTCAGGTCCTAATTAATTGGTTCAGGTGTGTCTGATCAGGATTGGAGCTGAACTTTGCTGGAAGGTCGATCTCCAGGAACAAGGTTGAGCGCCACTGTCTTAAAGGGACAGTTCACCCAAAAAAGAAAATGTTCTCACTATTTAGTCACCCTCAGGTGGTTTCAAACTCTTTCTTCTGTTTAACATTAAGGAAGATCATTTCTAAAAAAAAAAAAAAGAAGTTGCAAATGTGTAGCAATTGACTTCCATAATAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24601
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 |
---|---|---|---|---|---|
ENSDART00000112782 | Nonsense | 1821 | 2305 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 6861801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6381243 |
GRCz11 | 25 | 6508645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGCCTGGTGCCGTGGTTTTAGAGGAGATCTTTTTGATCTCCCTCAGA[C/T]GACGAGACTCAAACCCGCCAGAGCTCGCAAGCTTGGACCTGCTTCTGGAA
Long Flanking Sequence:
TAAAACACAACAAGTAAATGATCGTTAGTTAAACTGTAAATGGTAGTGGCCCGATTGGGCTGCAATTGAGGAATCTTGTATGGTATTCTCTAGGCCAGCGGGTTGACTCTTAAAAGTAGTTTGATTGTTTTCTTTGGTGTATTACAGGTGTATCTGTGGTGCAGGGTCAGTCTAAAGTGATCGACAGCTCTGTTTTGGATGCCTCCAATCTGCTTGCTAGCTTGCCTGAGCAAAAGCGGGCAGGACAAGACATTGTCTACGAAGTACGCCGGTTCCCAGTTCATGGACGACTGTCTCTTGGAGGGTCAGATCTGCCACACGATGCTCCCCGTTTTATTCAGGAAGATGTGGCACGTGGGGATCTGGAGTACCATCACGATGACTCCGGAGCATCTTCGGATAGCTTCGCTTTCCGTGTCCATCTGAACCCCAGTGGTCGCACCCCGCAAGTCCAGCCTGGTGCCGTGGTTTTAGAGGAGATCTTTTTGATCTCCCTCAGA[C/T]GACGAGACTCAAACCCGCCAGAGCTCGCAAGCTTGGACCTGCTTCTGGAAGCACTGCAGGGCTCCACGACCATCATTTCCAAAAACTACCTCAACACAGTCGACCAAGACAGCACACCAGACGAAGTCCAATTCACCATCTCCAAGAGTCCTGCTAATGGATATCTCATCTACACAGACTCAGGAGACAGAATCAACAAGTTCAGCCAGGAAGATATCAACTCTGGGCGGGTGGCTTTTGTCAGTGATGGAAGCCTGTCTGATGGTTTCATGGAGTTTACAGTGTCAGATGGGAAACACCAAACAGACCCTCACACGCTGCATATTGGAATCCTGGCCAAATCCCTAATACTGAAGAAAGCTCCAGAGATCCAGGTAAAACAGGGTGATGATGAGACACTAATCACTGAGGACATGTTGAACGCTTCTACTGGAGGTCCCGTTGAGGAGGAGGTACTCTATAAAATAACCAACGTCCCAAAATATGCTGCTGTAATGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15270
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 |
---|---|---|---|---|---|
ENSDART00000112782 | Nonsense | 1982 | 2305 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 6861316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6380758 |
GRCz11 | 25 | 6508160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCCCGTTGAGGAGGAGGTACTCTATAAAATAACCAACGTMCCAAAATA[T/A]GCTGCTGTAATGGTAGACAGACAGCCAACCTCAGCTTTCACACAGARGCA
Long Flanking Sequence:
TTGATCTCCCTCAGACGACGAGACTCAAACCCGCCAGAGCTCGCAAGCTTGGACCTGCTTCTGGAAGCACTGCAGGGCTCCACGACCATCATTTCCAAAAACTACCTCAACACAGTCGACCAAGACAGCACACCAGACGAAGTCCAATTCACCATCTCCAAGAGTCCTGCTAATGGATATCTCATCTACACAGACTCAGGAGACAGAATCAACAAGTTCAGCCAGGAAGATATCAACTCTGGGCGGGTGGCTTTTGTCAGTGATGGAAGCCTGTCTGATGGTTTCATGGAGTTTACAGTGTCAGATGGGAAACACCAAACAGACCCTCACACGCTGCATATTGGAATCCTGGCCAAATCCCTAATACTGAAGAAAGCTCCAGAGATCCAGGTAAAACAGGGTGATGATGAGACACTAATCACTGAGGACATGTTGAACGCTTCTACTGGAGGTCCCGTTGAGGAGGAGGTACTCTATAAAATAACCAACGTCCCAAAATA[T/A]GCTGCTGTAATGGTAGACAGACAGCCAACCTCAGCTTTCACACAGAAGCAAATCAAGCAGGGAAGAGTAAGTGTCCGATTTGTGAAGTCCACCTCCCCAAGAGACAGCGTGGCCTTTGTTGCTCGAAGCAGGGCAGCGAATGTATCCTCAGTCCTCAACATTACTGTGAAACCACTGGCAAAGGTGGCACAAAATCCCCTGCTACCCAGAGGTGCTACTGTGCTTGTAGACAGAAAGTTGTTGGACGCTACTCCTCTGGCCAACAAAACCAGAACATCTCCAACCTTCAGCATGATTCAACAACCTCAAGGAGCTCGGTTTGTCAAAAGGGGTGGGCTCGATGACGGACAACCAGTGAGCTCTTTCACTCAGCAGGATCTGGATGAAGGCCGGGTAGCTTTGGAGATCTTAAACACAACCGGGGGCCAAAACGGTGGAGGTCAAAATCAAGATGAAGCACGGTTTCTCCTAAAGGCGCATGGCGTACCTCCTGCAGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12954
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 |
---|---|---|---|---|---|
ENSDART00000112782 | Nonsense | 2062 | 2305 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 6861077)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 6380519 |
GRCz11 | 25 | 6507921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAAAATCCCCTGCTACCCAGAGGTGCTACTGTGCTTGTARACAGAAAGT[T/A]GTTGGAYGCTWCTCCTCTGGCCAACAAAACCAGAACATCTCCAACCTTCA
Long Flanking Sequence:
TGGGCGGGTGGCTTTTGTCAGTGATGGAAGCCTGTCTGATGGTTTCATGGAGTTTACAGTGTCAGATGGGAAACACCAAACAGACCCTCACACGCTGCATATTGGAATCCTGGCCAAATCCCTAATACTGAAGAAAGCTCCAGAGATCCAGGTAAAACAGGGTGATGATGAGACACTAATCACTGAGGACATGTTGAACGCTTCTACTGGAGGTCCCGTTGAGGAGGAGGTACTCTATAAAATAACCAACGTCCCAAAATATGCTGCTGTAATGGTAGACAGACAGCCAACCTCAGCTTTCACACAGAAGCAAATCAAGCAGGGAAGAGTAAGTGTCCGATTTGTGAAGTCCACCTCCCCAAGAGACAGCGTGGCCTTTGTTGCTCGAAGCAGGGCAGCGAATGTATCCTCAGTCCTCAACATTACTGTGAAACCACTGGCAAAGGTGGCACAAAATCCCCTGCTACCCAGAGGTGCTACTGTGCTTGTAGACAGAAAGT[T/A]GTTGGACGCTACTCCTCTGGCCAACAAAACCAGAACATCTCCAACCTTCAGCATGATTCAACAACCTCAAGGAGCTCGGTTTGTCAAAAGGGGTGGGCTCGATGACGGACAACCAGTGAGCTCTTTCACTCAGCAGGATCTGGATGAAGGCCGGGTAGCTTTGGAGATCTTAAACACAACCGGGGGCCAAAACGGTGGAGGTCAAAATCAAGATGAAGCACGGTTTCTCCTAAAGGCGCATGGCGTACCTCCTGCAGAATGTGTCTTGCCCTTCCACGTGGTTCCTTATGATCCTTCCAAAGTTTATGGAGCCACATTGCTCAAGGTGCCACCGGTGTCGGTTTCTGACAGCAATGAAGCAGGTCAACCTGAGCCCCGGTGGAGGGGAGATGGTGACAAGACTTCAGGCAGCACTTCAGCAACTCCTGTGGTGTCTAGAAGGAATACTCTGTGGGCTATCCTTATTCCCATCCTTGTCATCCTCCTACTTGTGCTCCTGG
Associated Phenotype:
Not determined