Busch Lab

ZMP

creld2

Ensembl ID:
ENSDARG00000029071
ZFIN ID:
ZDB-GENE-040426-1626
Description:
Cysteine-rich with EGF-like domain protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXF6]
Human Orthologue:
CRELD2
Human Description:
cysteine-rich with EGF-like domains 2 [Source:HGNC Symbol;Acc:28150]
Mouse Orthologue:
Creld2
Mouse Description:
cysteine-rich with EGF-like domains 2 Gene [Source:MGI Symbol;Acc:MGI:1923987]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa12172 Nonsense Available for shipment Available now
sa20294 Nonsense Available for shipment Available now
sa40308 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26313
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048383 Nonsense 15 341 1 10

The following transcripts of ENSDARG00000029071 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 26395407)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 27109728
GRCz11 4 27099016
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACAACATGTTACTCTCATGTAGTATTTTTCGTTTATTTTGTATAATTT[T/A]GCTTCTGCAACTTGGATCTATTTATACAAAGGACTTTACAGCATTATGCT
Long Flanking Sequence:
ATATATTACAAACTAAAAATTCTTATTCTTAAGTATTTTGTTCAAAAATCATATTGATTAAACAATATATAATCATTCAATGAAATCGATTTGCATATAAAAGAACGCATAATCGCATACACTTCTAAATATCTTTGTTAAAGATACTATTGGACCTCCCGCGCGTGGCGGCAGTTCATTGGCTCATGCATTGATGTCCAGGAGAACCGTCCAATTACGTAAAGACACAATGTTACAGAGGGGCTGACGCGGAAATCCGAATATCTAACCGGTGAGAAGGCGGCATGCTAGTTTGTAAATGTGACGTGCTACATGTCTTGATAATAAACGTGTCGTAATCTCAGACGTTAGATGTTGATTAATATGTATATATTTTTAACTTGCTAAGGATAGCCCAGAAAAAAAACTAATATCTTATTGGGCAACATTTGTTGTAGACAGTACACTTGATGACAACATGTTACTCTCATGTAGTATTTTTCGTTTATTTTGTATAATTT[T/A]GCTTCTGCAACTTGGATCTATTTATACAAAGGACTTTACAGCATTATGCTCAACTTGCCGACAGCTAGTAGACGATTTTGACAAGGTATCTATCTATCTATCTATCTGTCTGTCTGTCTGATGTTAAATAGCTGGACGTTGTTACACTTAGCACGTTCATTGTTAATGATATGTGATTCCTCGTCTAAGGCACGTCAACTACTTTAGTGTTAAAAATATCCTTTTTTTCCTCCAGGGTTTGGAAAAAACAGCAAAGCAAAATTTTGGGGGTGGAAACACAGCGTGGGAAGAACGTAAACTATCTAAATATGAGACGAGGTGAGAAGAAAATTAAAATGAATTGAATTTATTAAAAAAGTATTAAATGTAGCACTTTAATATATTTAACGTTAATGCACCTAATTAATTAGTTTTTCACTCATACTTTTTGAGTTCTTACAATAATGCAGTCCTATTTGTGGTTTCTTCAGTGAGATTAGGCTGACGGAGATCCTGGAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12172
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
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048383 Nonsense 175 341 5 10

The following transcripts of ENSDARG00000029071 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 26387981)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 27102302
GRCz11 4 27091590
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTACAAGGGCTGGAAATGGGAAATGCAGTTGTGATGAAGGATATGATGGG[G/T]AGTTTTGTCTGGACTGCAGTGATGGATATTTTAATTCACTGAGGAATGAC
Long Flanking Sequence:
GTAAATGGGACCTTGTATATAGTTGACATGTTGAAAAATATGTCCCTTCTTTGAGTTTCCAGAGGGAACATAAACATGTTCCCTGTAAGTCGTTATAAACGTAATCAGGCCAACTTCCATTGATTCTAAAACAGTTAAGCCAGTGAAGCTTACCAGTGAAAACTGGGTTAGCAAATGCATTGATAAAACCATATCCTTGTACTAAAGTCGGCTATTGCATTTTTTTTTTGCATCATCACTGTCAAATGTAGTGTATAAATCTGTTATATAAGGAATAGTGCTTTGGTATTACTTGCATTCAATTTTTATGGGGAGTAACATTTTCGTTTAGGTACTTTATTCTTGCAAACTACTCACATTTTATGATTATTAATCCACTCTTATTATTTTAAGCTTGCATTGGAGGAGCTGACAGACCATGCCACGGGAATGGTAAATGCGATGGAGATGGTACAAGGGCTGGAAATGGGAAATGCAGTTGTGATGAAGGATATGATGGG[G/T]AGTTTTGTCTGGACTGCAGTGATGGATATTTTAATTCACTGAGGAATGACACATTCTTCTTGTGCAAAGGTATTCAAAAATACTGTCACACACAGATAGACTGTAAATGGTATATACAGTATTTAGAAAAGTTATTCTCAAGGCAATATGATAAAAAAAACTGAAAAAACACAGGACATAGATTTTAGTGATAGACATTTTTTTAAAATGTATATACCAAGAGAGTAAAAGTTAATGGGTGATTTAGGCAGCTTTTATTTAAAAATTTTTCTATGAATGTTTACTTTTAAGACTTTTTTTGAATACATATGCGTACCAAGTCAAAACAAGAGAAGTGACATATTTATTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCGTGTGCGTGTGCGCGGAAATGTTCACAGTATGTCTAATAATATTTTTTTCCCATAGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20294
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048383 Nonsense 263 341 8 10

The following transcripts of ENSDARG00000029071 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 26380707)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 27095028
GRCz11 4 27084316
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTAATTAATATTTTTGTCTGTGTTTGTCCATGTAAGCATGTGATATC[A/T]GATGCACTGGATGCAAAGGAGATGGTGCCAGTAGCTGCCTTAACTGTGCT
Long Flanking Sequence:
CGAGCGGGATATTTGCATTTGTTTATTTACAATAAATGCTCATGTTTTTCTGTGCATGTACTTGAGTTTTTAAAGATACAGTTCATACATCTGACTGCTTGTATTAAAGGACTACATTGTATTACAACTTATATTTAAATATATATTTATACATTTTAATATAAGAATTGTTGTGCTGTGAAGTAAAATATTGAATTGAACCGAACCGATGGCATAGAGGTTCACACCTCTTGTAACTGAGAACGAAGCTTAGCAAAGGGTCAGTTCAAGTCATATTAAACTCTGCATGAACTGATAGCTCCTTTTGTTTGTTTGTTTCTAGTATTGTGACTTAGAGAAACAGAATGAGAAAACAGTAGGTGTTTTTTTTCTACTGCAAGCAGACTGGATGTAGTGTAATAATTCGGAAAGATTAGGAAAAAGGTCTCAGGAGATATCAAGTAAAAAAAAAATGTAATTAATATTTTTGTCTGTGTTTGTCCATGTAAGCATGTGATATC[A/T]GATGCACTGGATGCAAAGGAGATGGTGCCAGTAGCTGCCTTAACTGTGCTGATGGCTATAAGGACGAAGAAGGCACTTGCACAGGTAGCATTTATTTTCATTCTCACGAATACCTTTTAACATTCCATGACTGTGTTTACTCTGTCCCTGGAACATTTCAAAAATGTAATGGTTTGATAATTGCTTGTTGATCCTGTCTTTCATGCCCTTGTGATTATCTGCAGTTAGAAGCAACGTGCAATTAAGAACAAAAGAAGTCAAGATATGTGCTTGTTTCCTATAGGTTTTAGCATATTCAGAGAGGTTTACACTTGGTGTAAATTTTTTGCATTCATTTTCTTACATATAGGGTGACTAAGTCCATAAAGCAGTGGTTGCAGTTCGTTTGTGTTAAACATTTTGTTGAATTCAATCACTTGAATATGAAAGAAATGTATTAATTAAAATATTATTTAGTGTCAAGTTGTAGACAACATTGTGGGCAAGTAAATAAAGGTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40308
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000048383 Essential Splice Site 318 341 9 10

The following transcripts of ENSDARG00000029071 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 26379874)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 27094195
GRCz11 4 27083483
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGATAACCAGCATTGCCTAAACACAGATGGTTCTTTCTCCTGTGAAG[G/A]TTTGTTGAAACAATATTATGTGCCCTTTGCAGAGATTACACTGGTTTTAT
Long Flanking Sequence:
CATTTTCTTACATATAGGGTGACTAAGTCCATAAAGCAGTGGTTGCAGTTCGTTTGTGTTAAACATTTTGTTGAATTCAATCACTTGAATATGAAAGAAATGTATTAATTAAAATATTATTTAGTGTCAAGTTGTAGACAACATTGTGGGCAAGTAAATAAAGGTATTGACTAGTGTGGACTATTCTTTTTGTTTGGAGATGCTTTTCTGGTACCTTGATTGAAACTGGTTGCCTTTCTCTCAGCTTAGAGTATTAAAGCTTTTATCCTCTGACTGTTGTCGTTAACATGAGGCAAGAAGTAAAATGATTACTGCATAAAAAGCCAACATTATTTGAAAACAATTGTGTATGTTCCATATATTTACCGTTCTATGTTGGTTCAGTTTTCTTATTTTCCAAAGTTTCTCTATTGCAGACATTGATGAATGCACTGAAGACCCAGCTTCATGCAGTGATAACCAGCATTGCCTAAACACAGATGGTTCTTTCTCCTGTGAAG[G/A]TTTGTTGAAACAATATTATGTGCCCTTTGCAGAGATTACACTGGTTTTATTTTAAAGTATCCTTGTTAGAGTGTAGTTACACAAAGTACTACATACTATTAACAAAATGTTGTTATGGTAGGTGTAGACTAGTACTTGAACATATAGCAGAAAGAGTCAGATGAGTAGTAGTAGAGTTGAATTCAGCCAGCGTTTCTGTAAATTATTTCTTTAAATCCGAGTTGTACCACCAGAGAAAATCACAGTTTTTATAGTAACTTTTAGACTTTTTTTTTCATATGTACATACATACATACATGCATACATATGTATGTGTGTGTGTGTGTATGTATGTATGTATGTATGTATGTATGTATGCATGTATGTGTGTATGTATGTATGTGTGTAATATATATATATATATATATATATATATAGTTTATGTATATATATATATAGTTTATGTATATATATATATATAGTTTATGTATATATATGTGTGTGTGTGTGTGTATATATGT
Associated Phenotype:
Not determined