ZMP
col14a1
Ensembl ID:
ZFIN ID:
Description:
Col14a1 protein [Source:UniProtKB/TrEMBL;Acc:Q6NW57]
Human Orthologue:
COL14A1
Human Description:
collagen, type XIV, alpha 1 [Source:HGNC Symbol;Acc:2191]
Mouse Orthologue:
Col14a1
Mouse Description:
collagen, type XIV, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:1341272]
Alleles
There are 14 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11768 | Splice Site, Nonsense | Available for shipment | Available now |
| sa11818 | Essential Splice Site | Available for shipment | Available now |
| sa12938 | Nonsense | Available for shipment | Available now |
| sa12349 | Nonsense | Available for shipment | Available now |
| sa22787 | Nonsense | Available for shipment | Available now |
| sa10929 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11768
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027982 | Splice Site, Nonsense | 347 | 1864 | 8 | 47 |
| ENSDART00000134087 | None | None | 1382 | None | 37 |
| ENSDART00000137912 | None | None | 253 | None | 8 |
| ENSDART00000138611 | None | None | 96 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 17096689)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 14911550 |
| GRCz11 | 16 | 14801670 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACYAGGACGGTGTGTGATGGAGYGGAGCAACAGGACAAAGAAATTAAA[C/T]GTGAGTRCTTATACCTAATGTAGATGTGTCATATGTGRAAAGGGATCAAA
Long Flanking Sequence:
TAACTATTAATCAAAACATATTTTAATCATAAGCATATTATATTGGGACTTGTGTGAACTAAGAGAAAAACAGAAACATGTCAAAGTTACAAACAGTGGAAAATTACACGCTTTGTTAATGTTGTTGCATTCTGTTTGTTTACCTTCAAATTGAATATTTTTTTTACATTTTAAATGATTTTCAAATCAATTAAAAATTATTTTAAATAAGTCTGTGATAATTAGATTTTATTATGATTTTTTATGTATAGTATTAGAAAGAAAATCGTAATTGTCAAAAATGTATATATTTCAGAAATGTGAAATATGACCTGGTGTGTGTATACCGCATGTGTGTAGGTGTGAAGAATGCTGATGAAAATGAGCTGAAGGCCATTGCGTCTGAACCAGAGGACACACATGTTTATAATGTGGCTGACTTCAGTATTATGGGCACCATAGTGGAAGGTTTGACCAGGACGGTGTGTGATGGAGTGGAGCAACAGGACAAAGAAATTAAA[C/T]GTGAGTACTTATACCTAATGTAGATGTGTCATATGTGGAAAGGGATCAAAAACCTCATGATTTCCTCGCAATTAACAGAAGATTCTGTCCCCGAGGAGACTGTGTCAACTCCTCTGAACCTGCTCATTTCTGAGGTGACGGCACACAGTTTCCGAGTGTCCTGGACTCATTCGGCTGGCAAGGTGGAAAAGTATCGTGTGGTTTACCATCCGACCGATGCAGACATTCCAGAAGAGGTGACTTGATGTTCATTTTAAGGTTATCTACAATATAAGCTAGTGTGCTACAGTTAAACAAAAACAGTTACACAGTTCACATTTAAAAGATTAAGAGCCCTATAACCCCGGCACAAGACACATTTGGCGCAGTTTGTTGCTATTTTCATACCAACACAACACAAATTTTCACGTTTTGCACCATGTTATTTAAATGGTAAATCTATTTGCGCCACTTTGTGGATTCATGGGTGTTCTGATCTAGAAAGGAGGAGTGTTTGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11818
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027982 | Essential Splice Site | 1000 | 1864 | 23 | 47 |
| ENSDART00000134087 | Essential Splice Site | 518 | 1382 | 13 | 37 |
| ENSDART00000137912 | None | None | 253 | None | 8 |
| ENSDART00000138611 | None | None | 96 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 17196940)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 15011801 |
| GRCz11 | 16 | 14901921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KTTTTWCAGGACACAGAGGGCCCTGCTGTCAYCACCATGGTCACCACTGG[T/A]AAATACACTCAGAAAAATTAAYACTATACTATTTACTTGAGWGRAAGAAA
Long Flanking Sequence:
TACATCAGGCTAACATGTCAAAACAGTTAAAGAGCATAGTGTAAAACTCAGAGAGTAAAATGCTGGTCCTTTTTTTAGCAGTGGAAAAATCATAGATGACAATTAGCTGAATTAGTGTTGAATTTTCCTTCATTTGCAGACAAATTTGTAAGCAGCAACTCATGCCTGTTAAAAAATAACAACACTTTGACGACTGCTGTGGTGCCACTTCTGTCATTTTGAGTCTTTGTTTGTTGGCTGAGGACTCTAATGACTCTCATTAATTAGGATGATTGTTTGCTTGAGGAAGCTGATGTGATTTTGTATTATACTTTTATTTGTTGTTTGAATGCCATTTGTCTTTATTTTGCAGACGGGCAGAAACAGGAGGTGAGGGTCGGTGGTGGTGCGTCCAGAGAGTGTTTCTTCAGACTTTCCCCCAACACCCAGTACAAGATAAGTGTATACACCGTTTTACAGGACACAGAGGGCCCTGCTGTCACCACCATGGTCACCACTGG[T/A]AAATACACTCAGAAAAATTAATACTATACTATTTACTTGAGTGGAAGAAAAATGCCTCAATAAATGTGAAATAAATTTGACAGGTGTGTGAGGATATTTTAAATACCAGTAATAGATGTGTTTTGTGGTAATGCAATTTCAGGGGTAAAAATAATAGACTAGAGACAATATTTAAATTTGGAACACTGCTTACATCTTGTGGGACCTGTGTCAAACTCTCAACTTTGGAGCTGTCTTACACACAAACATAAAAATAGAAAAGAAAAGTTAGAGGCTATTAAAAATAAAAAAATGCAGTTAGGGGCCATTCACACAGAGCAGAGTGCATGTTTTGCATTGAAAATTATGAGACACTGGCAGTGGAATGAGGAAAATGCAGGCTTCAAGATGTGTTTTGTGAAGTTGAACTTCTTTAAACTTGAAAACAACATTTGTGTTGTGGTCAGACACATCTGTCTAATATGTTTACTTTAAAAAACAATGGTTAAGTATTGGAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12938
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 |
|---|---|---|---|---|---|
| ENSDART00000027982 | Nonsense | 1376 | 1864 | 33 | 47 |
| ENSDART00000134087 | Nonsense | 894 | 1382 | 23 | 37 |
| ENSDART00000137912 | None | None | 253 | None | 8 |
| ENSDART00000138611 | None | None | 96 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 17268904)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 15083765 |
| GRCz11 | 16 | 14973885 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTCATGTGGCCATCAGCAAAACTGCTGCTAAAGTGGTGATCGACTGC[A/T]AGACRGTTGGAGAGAAATCCATCAATGCCGCAGGGAAYATCAGCATTGAT
Long Flanking Sequence:
TATTGTGTGACTGTACAATAGTAGTTATTGTTAAGCCACATTATTATTAACCTTTTTATTTGTTGGTATGTATTTGTTTTTTTTTCTCATTGTATGTGCTTAAGTTGATACTATTTCTTGATATACTATATATATATATATATATATATATATATGTATATATATATATATATATATATATATATATATACATACATACATACATACATACATACACATACATATATAAATATAAAAACATCTTTATAATTGATGAATGAAGAATAGTAATTAGGAAAGCAGGGGGTTTGTCTTTTTAACACAACAATTCTCAGTTTTTATTTTTAGTTATTTTTTAATCTTCTTTAACACTTAACTATATTTACTATGTCTCTCAAATAGTTATCCTCCATAAACATCAGAACATCCCTATTTGCCATTAAACCTTATTTGTCTCTTCTTGTCCCACACAGCTTCATGTGGCCATCAGCAAAACTGCTGCTAAAGTGGTGATCGACTGC[A/T]AGACGGTTGGAGAGAAATCCATCAATGCCGCAGGGAACATCAGCATTGATGGAGTGGAGGTTCTAGGGCGAATGGTCCGATCACGGGGACGGAAAGACAATTCAGCACCGGTAAGACTTTCAGTACACAAATCAAGCGGACTAAAAATAACAGATATCATAATAACACATAACTCCAGTAGGTAAGCTTACAAGGCCATCTTTTTAATTCCATAGTGCAAAGTAATAACCCTTCTGTTGACTTAAAATGACTCATGACCATTTTAAAAACTTGTTAATAAAAATGACCCTTAATGATGAAAATTTAATCGTCAATAATAATAAATGTACAAAAATATTGTCATAAACTGATAACCCTACTGATGATTAATGATTATTCAAACAAGTGTAAATGATAAAACATTGAAAATATAATTATAATAATTTATTTTTGCCAAAAAAAATGAATAAATGTGTGTAAAAACATGTATCACTGCAACATGTGTTAGCATTTTAATAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12349
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027982 | Nonsense | 1767 | 1864 | 46 | 47 |
| ENSDART00000134087 | Nonsense | 1285 | 1382 | 36 | 37 |
| ENSDART00000137912 | None | None | 253 | None | 8 |
| ENSDART00000138611 | None | None | 96 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 17332812)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 15147673 |
| GRCz11 | 16 | 15037793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCCTGCTGGACCGCCCGGCTACTGCGACCARAAYTCCTGCCTCGGRTA[C/A]AATGTTGGAGGTAATAATCTCATTCTCTACATCTGTTTCTCAAACTNTCT
Long Flanking Sequence:
GATCTGTTTTGGGTTCCTTTGATTCCTCTCTAGAATATCAAGCAGATATTGAAACAATATTTGGGTCTGGGAGAAATGTTTTCCTATCGATTTTTAGCTGTGCAGCTTGTCGGTAGATTTTGAAAAATGTCAGCGTCGCTCGCTGTTAATTGCGCTTTGATCAATACTCTTCACAAATGAGATTCATTGAAGCAACACAGCTATATGAGCTAGCGACATGTGAGAAGGATGTGGACTGGCATTAGCTGAAACTTGTATTTTGTGAGGAAGAGATCCAGACCCGCTGTGGGTGTGGAGTTTAGCTGCTTTCATTGTGTAGATACAGTATTAATGGCCAACATTATATCCCATTCAGGGCCTGCTGGAGAAGGGCGAACAGGAAGCCAGGGTCCACCAGGGAGACCTGGAATTCAAGGCACCCAAGGACGTCCAGGTACCCCAGGCAGTCCTGGTCCTGCTGGACCGCCCGGCTACTGCGACCAGAACTCCTGCCTCGGGTA[C/A]AATGTTGGAGGTAATAATCTCATTCTCTACATCTGTTTCTCAAACTCTCTCAGTGCGTCTGAAATCGCATACTTCGATTAATATATAGTACATGAAAAAGTAGTGAGCCAAGTAATGTTTAGTGTATGGTACTTGACAATAACACTCAATTGAACATATAAAGAATTTGTAACGTATTCCTATTCATTTCAAACACATTGGATTTATTGACCAGTTTACATAAATCTTATTCTTACTTATTTAATCGAGATTTAACTAACAAATGCATATTACATACAATTTATTGTAAAATTTGTATGTAATTTGAATACATAAATTCTTTTTCTTTGGCCTAATTATTTTTATTTTTTTGAGTGCATGTTCAAATTCATAGTATATGATAAACAGTGGGTAAAAATTCTTGGATTACCTACTACTTTCAGCAAGATGTGCACATCCATTGGAGAGACACATGGGACAATTTACAAATGCAAGTAAATCAATGCAAGTGAAGCATGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22787
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027982 | Nonsense | 1791 | 1864 | 47 | 47 |
| ENSDART00000134087 | Nonsense | 1309 | 1382 | 37 | 37 |
| ENSDART00000137912 | None | None | 253 | None | 8 |
| ENSDART00000138611 | None | None | 96 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 17343320)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 15158181 |
| GRCz11 | 16 | 15048301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCTCCAATCCCTACCAAAACTACGGCCCCGCCACCAACTACAACCCT[G/T]AGGATGAGGAGGAGGATGACCCTTATGGCGGCTACCGGGCCTACCCTCCT
Long Flanking Sequence:
TGTTACAAATTTTTGGTTTAACATAGGTTACTATTCACATGACGAAATTAGCATCATAAACACTATGCACTGACCTTCAAATATGCATACAAAAATGAAAGATACCTGGGGCTTGGAAACCCTCCAAAATCAATAAGTCACTGTATAGTATTAGAGCCACACTCATTCGTTATTAAAAAAAATGGCTGCCAGTAACAATTATTTCAGCCAGGTTCAACACTTAACAAGCAAGGGCTAAATAAGTCATGCTAACAATTAACTGTTGATCCATCAGTCCGAACTAATCTAATGACAATAACAACTCTCTTCTTCCTTTCTGCACTGACTTTGTTCCTTCATTCTTTGTCGTTTCCTTCACTCTTTCTAACTCGACACCTGCTCCCCTGGTGGTGGTGACTGAAAAAAGAAGGCAATCGATCTAATTCCCCCGTGTTCCCATAGTACAACAGTTGTCCTCCAATCCCTACCAAAACTACGGCCCCGCCACCAACTACAACCCT[G/T]AGGATGAGGAGGAGGATGACCCTTATGGCGGCTACCGGGCCTACCCTCCTCAATACTACCAACCCAGCTACCCCGACCCCCGTGGCGCCAGGCCTGGCCCCGTACACCCTGGTGACACGGCGGGCATGAGGGCACCCGGCGCACGCCGCTTCACCCGCAGCACAGCTGAAGAGGGCATCGTCCATCAGCCGCAGGAGCATGTGAAGGAAGAAGAGCTGTGGTGACCGACAGATCGTCCACATACAAACACTTTTCAGCAGAATGTCCTGCAGGATTGGACCGAGGGAAATCCGAAAAGTGCCTGCTATATGCATCCTTATTGGGGCGGGTGAGTGAAGATTAGGAAAAAAAAAAAAAAAAAAACTGTGCCGAAATTCATTCAGTGACTTTTCTGTCTTTTGTGAGGCTGCATGTAGCCAATGAAACGAAAAGCTGAAGGAGGAACTCTGCAAATACGTTTTCTTAATGAGTGTTTTTGAATTGTTGTCTAGGTAAAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10929
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027982 | Nonsense | 1864 | 1864 | 47 | 47 |
| ENSDART00000134087 | Nonsense | 1382 | 1382 | 37 | 37 |
| ENSDART00000137912 | None | None | 253 | None | 8 |
| ENSDART00000138611 | None | None | 96 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 17343541)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 15158402 |
| GRCz11 | 16 | 15048522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGGCATCGTCCATCAGCCGCAGGAGCATGTGAAGGAAGAAGAGCTGTG[G/A]TGACCGACAGAYCGTCCACATACAAACACTTTTCAGCAKAAYGTYCTGCA
Long Flanking Sequence:
TAACAAGCAAGGGCTAAATAAGTCATGCTAACAATTAACTGTTGATCCATCAGTCCGAACTAATCTAATGACAATAACAACTCTCTTCTTCCTTTCTGCACTGACTTTGTTCCTTCATTCTTTGTCGTTTCCTTCACTCTTTCTAACTCGACACCTGCTCCCCTGGTGGTGGTGACTGAAAAAAGAAGGCAATCGATCTAATTCCCCCGTGTTCCCATAGTACAACAGTTGTCCTCCAATCCCTACCAAAACTACGGCCCCGCCACCAACTACAACCCTGAGGATGAGGAGGAGGATGACCCTTATGGCGGCTACCGGGCCTACCCTCCTCAATACTACCAACCCAGCTACCCCGACCCCCGTGGCGCCAGGCCTGGCCCCGTACACCCTGGTGACACGGCGGGCATGAGGGCACCCGGCGCACGCCGCTTCACCCGCAGCACAGCTGAAGAGGGCATCGTCCATCAGCCGCAGGAGCATGTGAAGGAAGAAGAGCTGTG[G/A]TGACCGACAGATCGTCCACATACAAACACTTTTCAGCAGAATGTCCTGCAGGATTGGACCGAGGGAAATCCGAAAAGTGCCTGCTATATGCATCCTTATTGGGGCGGGTGAGTGAAGATTAGGAAAAAAAAAAAAAAAAAAACTGTGCCGAAATTCATTCAGTGACTTTTCTGTCTTTTGTGAGGCTGCATGTAGCCAATGAAACGAAAAGCTGAAGGAGGAACTCTGCAAATACGTTTTCTTAATGAGTGTTTTTGAATTGTTGTCTAGGTAAAATACACACAACATTCTGAAGATAAAGACAGACATTTTACAGCATAAATATGTATTATAATTGACAATCATTGGCAGATTAAATTTTTTTTTTCAGTGTAGCTTTACAATAATGATAATAATGAAATTTAAATGATAAATATTTAATATTATTGTTGTTGACGACAATGATAAAAAGAAATGACATCATAATGTTATTTAATTAAATCTTAATTAAATTTAATTTA
Associated Phenotype:
Not determined