ZMP
ctgf
Ensembl ID:
ZFIN ID:
Description:
connective tissue growth factor [Source:RefSeq peptide;Acc:NP_001015041]
Human Orthologue:
CTGF
Human Description:
connective tissue growth factor [Source:HGNC Symbol;Acc:2500]
Mouse Orthologue:
Ctgf
Mouse Description:
connective tissue growth factor Gene [Source:MGI Symbol;Acc:MGI:95537]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25135 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11839 | Nonsense | Available for shipment | Available now |
sa13699 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25135
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 |
---|---|---|---|---|---|
ENSDART00000063028 | Nonsense | 184 | 345 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 25371609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 25442912 |
GRCz11 | 20 | 25342002 |
KASP Assay ID:
554-7641.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGTAACATCTTATTGCTTCTTGTAGCTTACAGAGAGGAGGAGACATA[C/A]GGTCCCGATCCCTCCATGATGAGAGAGAACTGCCTGGTTCAGACTACAGA
Long Flanking Sequence:
AACAATCTTCCATCTCCGTCCCACAGCCAGAGATGGTGCCACTTGTGTGTTTGGTGGAATGGTGTACCGCAGTGGAGAGTCTTTCCAGAGCAGTTGTAAATACCAGTGCACGTGTCTGGACGGTGCTGTAGGTTGCGTGCCCCTCTGTGGAATGGACATCAGGCTCCCCAGCCCAGACTGCCCAATGCCCCGCAGGGTGAAAGTGCCTGGGAAGTGCTGCGAGGAGTGGGTGTGTGACTCCCCTCGTCAAAACACCTTTGTGGGATCAGCTTTAGCAGGTGAGCATTTCTCAATCTTAAAAGCCAAACTGTGATGGAAAAATTACTCCTAAAGAATGTATTTAGACAAAGTAATGGTCTTGGTATTAGGGGGTTTAGAATGAATATCAGTATAACATCAGATGTAACAATAAGAATAGCAGGATGACATCATGCTGTTGGATGGAATGTGTTGAGTAACATCTTATTGCTTCTTGTAGCTTACAGAGAGGAGGAGACATA[C/A]GGTCCCGATCCCTCCATGATGAGAGAGAACTGCCTGGTTCAGACTACAGAATGGAGCGCATGCTCAAAAACCTGTGGCTTGGGAATCTCTACTCGTGTGACCAATGACAACCGTGAGTGCCGCCTTGAGAAGCAGTCTCGCCTTTGCATGGTCCGCCCTTGCGAGTCACACCTGGAGGAGAAAATAAGGGTAAGGGGCTATCTACCGATAAAATGAAATCATGCCACAGCTTCAATCTTGCTTTCACCGTGATGTAACTGAGCTTTATGGTTAACCTTCATTTTTTATCTTTCCAGAAAGGGAAAAAGTGCATCCGCACACCACGAGTCTCCAAACCCATGAAGTTTGAGATTTCCGGCTGTACCACTACCAAGTCTTACAGACCCAAGTTCTGCGGCGTTTGCACAGATGGTCGCTGTTGCACTCCTCACAGAACCGCCACCTTGCCCATGGAGTTCAAGTGCCCCGATGGCCAAGTCATGAAGAAGCAGATGATGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11839
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063028 | Nonsense | 260 | 345 | 5 | 5 |
ENSDART00000063028 | Nonsense | 260 | 345 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 25371942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 25443245 |
GRCz11 | 20 | 25342335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTATCTTTCCAGAAAGGGWAAAAGTGCATCCGCACACCAMGAGTCTCC[A/T]AACCCATGAAGTTTGAGATTWCCGGCTGTACCACTACCAAGTCTTACAGA
Long Flanking Sequence:
AATGTATTTAGACAAAGTAATGGTCTTGGTATTAGGGGGTTTAGAATGAATATCAGTATAACATCAGATGTAACAATAAGAATAGCAGGATGACATCATGCTGTTGGATGGAATGTGTTGAGTAACATCTTATTGCTTCTTGTAGCTTACAGAGAGGAGGAGACATACGGTCCCGATCCCTCCATGATGAGAGAGAACTGCCTGGTTCAGACTACAGAATGGAGCGCATGCTCAAAAACCTGTGGCTTGGGAATCTCTACTCGTGTGACCAATGACAACCGTGAGTGCCGCCTTGAGAAGCAGTCTCGCCTTTGCATGGTCCGCCCTTGCGAGTCACACCTGGAGGAGAAAATAAGGGTAAGGGGCTATCTACCGATAAAATGAAATCATGCCACAGCTTCAATCTTGCTTTCACCGTGATGTAACTGAGCTTTATGGTTAACCTTCATTTTTTATCTTTCCAGAAAGGGAAAAAGTGCATCCGCACACCACGAGTCTCC[A/T]AACCCATGAAGTTTGAGATTTCCGGCTGTACCACTACCAAGTCTTACAGACCCAAGTTCTGCGGCGTTTGCACAGATGGTCGCTGTTGCACTCCTCACAGAACCGCCACCTTGCCCATGGAGTTCAAGTGCCCCGATGGCCAAGTCATGAAGAAGCAGATGATGTTCATCAAGACCTGCGCATGCCACTACAACTGCCCTGGGGAGAACGACATCTTTGAATCCATGTACTACAAGAAGATGGTTGGCGACATGGCGTGAAAAGTCATGACCTGACAAGGAGTTCCATGCAGTGACTGTCCACTTGAATTGAACAGATATCCATCTCATATCTCAGCACAAATTACTTGTTTGTCTTTTTATGGTTTGTTGCTTTCATTTTACGTCTTTTTGCGTGTATGTGTTTGCATCTTGTTGGTGGACTCTGGATTTCTATGCTGTATGTGTATTCATTTGTCATGGTGGATGTCTAAGCCTAGGGGGTGGGGATCGTAAAATGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13699
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063028 | Nonsense | 260 | 345 | 5 | 5 |
ENSDART00000063028 | Nonsense | 260 | 345 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 25371942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 25443245 |
GRCz11 | 20 | 25342335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTATCTTTCCAGAAAGGGWAAAAGTGCATCCGCACACCAMGAGTCTCC[A/T]AACCCATGAAGTTTGAGATTWCCGGCTGTACCACTACCAAGTCTTACAGA
Long Flanking Sequence:
AATGTATTTAGACAAAGTAATGGTCTTGGTATTAGGGGGTTTAGAATGAATATCAGTATAACATCAGATGTAACAATAAGAATAGCAGGATGACATCATGCTGTTGGATGGAATGTGTTGAGTAACATCTTATTGCTTCTTGTAGCTTACAGAGAGGAGGAGACATACGGTCCCGATCCCTCCATGATGAGAGAGAACTGCCTGGTTCAGACTACAGAATGGAGCGCATGCTCAAAAACCTGTGGCTTGGGAATCTCTACTCGTGTGACCAATGACAACCGTGAGTGCCGCCTTGAGAAGCAGTCTCGCCTTTGCATGGTCCGCCCTTGCGAGTCACACCTGGAGGAGAAAATAAGGGTAAGGGGCTATCTACCGATAAAATGAAATCATGCCACAGCTTCAATCTTGCTTTCACCGTGATGTAACTGAGCTTTATGGTTAACCTTCATTTTTTATCTTTCCAGAAAGGGAAAAAGTGCATCCGCACACCACGAGTCTCC[A/T]AACCCATGAAGTTTGAGATTTCCGGCTGTACCACTACCAAGTCTTACAGACCCAAGTTCTGCGGCGTTTGCACAGATGGTCGCTGTTGCACTCCTCACAGAACCGCCACCTTGCCCATGGAGTTCAAGTGCCCCGATGGCCAAGTCATGAAGAAGCAGATGATGTTCATCAAGACCTGCGCATGCCACTACAACTGCCCTGGGGAGAACGACATCTTTGAATCCATGTACTACAAGAAGATGGTTGGCGACATGGCGTGAAAAGTCATGACCTGACAAGGAGTTCCATGCAGTGACTGTCCACTTGAATTGAACAGATATCCATCTCATATCTCAGCACAAATTACTTGTTTGTCTTTTTATGGTTTGTTGCTTTCATTTTACGTCTTTTTGCGTGTATGTGTTTGCATCTTGTTGGTGGACTCTGGATTTCTATGCTGTATGTGTATTCATTTGTCATGGTGGATGTCTAAGCCTAGGGGGTGGGGATCGTAAAATGAC
Associated Phenotype:
Not determined